Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 54778 |
| ensemblid | ENSG00000157450.16 |
| hgncid | 17384 |
| symbol | RNF111 |
| name | ring finger protein 111 |
| refseq_nuc | NM_017610.8 |
| refseq_prot | NP_060080.6 |
| ensembl_nuc | ENST00000348370.9 |
| ensembl_prot | ENSP00000288199.5 |
| mane_status | MANE Select |
| chr | chr15 |
| start | 58987663 |
| end | 59097419 |
| strand | + |
| ver | v1.2 |
| region | chr15:58987663-59097419 |
| region5000 | chr15:58982663-59102419 |
| regionname0 | RNF111_chr15_58987663_59097419 |
| regionname5000 | RNF111_chr15_58982663_59102419 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 986 | 281 | 84 | 44 | 120 | 10 | 21 | 93 | RNF111_chr15_58982663_59102419 | RNF111 | MSQWT others(981): Show |
chr15 | 58982663 | 59102419 |
| a0002 | 0/0 | 986 | 43 | 2 | 14 | 16 | 4 | 7 | 10 | RNF111_chr15_58982663_59102419 | RNF111 | MSQWT others(981): Show |
chr15 | 58982663 | 59102419 |
| a0003 | 0/0 | 986 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | MSQWT others(981): Show |
chr15 | 58982663 | 59102419 |
| a0004 | 0/0 | 986 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | MSQWT others(981): Show |
chr15 | 58982663 | 59102419 |
| a0005 | 0/0 | 986 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | MSQWT others(981): Show |
chr15 | 58982663 | 59102419 |
| a0006 | 0/0 | 986 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | MSQWT others(981): Show |
chr15 | 58982663 | 59102419 |
| a0007 | 0/0 | 986 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RNF111_chr15_58982663_59102419 | RNF111 | MSQWT others(981): Show |
chr15 | 58982663 | 59102419 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2958 | 185 | 61 | 32 | 75 | 5 | 12 | RNF111_chr15_58982663_59102419 | RNF111 | ATGTC others(2953): Show |
chr15 | 58982663 | 59102419 | ||
| a0001c0002 | 1/0 | 2958 | 82 | 21 | 6 | 42 | 3 | 9 | RNF111_chr15_58982663_59102419 | RNF111 | ATGTC others(2953): Show |
chr15 | 58982663 | 59102419 | ||
| a0001c0004 | 0/1 | 2958 | 8 | 1 | 4 | 0 | 2 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | ATGTC others(2953): Show |
chr15 | 58982663 | 59102419 | ||
| a0001c0005 | 0/0 | 2958 | 2 | 0 | 0 | 2 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | ATGTC others(2953): Show |
chr15 | 58982663 | 59102419 | ||
| a0001c0007 | 0/0 | 2958 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | ATGTC others(2953): Show |
chr15 | 58982663 | 59102419 | ||
| a0001c0008 | 0/0 | 2958 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | ATGTC others(2953): Show |
chr15 | 58982663 | 59102419 | ||
| a0001c0009 | 0/0 | 2958 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | ATGTC others(2953): Show |
chr15 | 58982663 | 59102419 | ||
| a0001c0010 | 0/0 | 2958 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | ATGTC others(2953): Show |
chr15 | 58982663 | 59102419 | ||
| a0002c0003 | 0/0 | 2958 | 39 | 2 | 14 | 13 | 4 | 6 | RNF111_chr15_58982663_59102419 | RNF111 | ATGTC others(2953): Show |
chr15 | 58982663 | 59102419 | ||
| a0002c0015 | 0/0 | 2958 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | ATGTC others(2953): Show |
chr15 | 58982663 | 59102419 | ||
| a0002c0016 | 0/0 | 2958 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | ATGTC others(2953): Show |
chr15 | 58982663 | 59102419 | ||
| a0002c0017 | 0/0 | 2958 | 1 | 0 | 0 | 0 | 0 | 1 | RNF111_chr15_58982663_59102419 | RNF111 | ATGTC others(2953): Show |
chr15 | 58982663 | 59102419 | ||
| a0002c0018 | 0/0 | 2958 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | ATGTC others(2953): Show |
chr15 | 58982663 | 59102419 | ||
| a0003c0006 | 0/0 | 2958 | 2 | 0 | 2 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | ATGTC others(2953): Show |
chr15 | 58982663 | 59102419 | ||
| a0004c0012 | 0/0 | 2958 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | ATGTC others(2953): Show |
chr15 | 58982663 | 59102419 | ||
| a0005c0011 | 0/0 | 2958 | 1 | 0 | 0 | 0 | 0 | 1 | RNF111_chr15_58982663_59102419 | RNF111 | ATGTC others(2953): Show |
chr15 | 58982663 | 59102419 | ||
| a0006c0013 | 0/0 | 2958 | 1 | 0 | 0 | 0 | 0 | 1 | RNF111_chr15_58982663_59102419 | RNF111 | ATGTC others(2953): Show |
chr15 | 58982663 | 59102419 | ||
| a0007c0014 | 0/0 | 2958 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | ATGTC others(2953): Show |
chr15 | 58982663 | 59102419 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5905 | 9 | 7 | 2 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | AGTGT others(5900): Show |
chr15 | 58982663 | 59102419 |
| a0001c0001t0002 | 0/0 | 5905 | 67 | 5 | 10 | 48 | 0 | 4 | RNF111_chr15_58982663_59102419 | RNF111 | AGTGT others(5900): Show |
chr15 | 58982663 | 59102419 |
| a0001c0001t0003 | 0/0 | 5905 | 26 | 25 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | AGTGT others(5900): Show |
chr15 | 58982663 | 59102419 |
| a0001c0001t0004 | 0/0 | 5905 | 28 | 9 | 13 | 3 | 0 | 3 | RNF111_chr15_58982663_59102419 | RNF111 | AGTGT others(5900): Show |
chr15 | 58982663 | 59102419 |
| a0001c0001t0005 | 0/0 | 5905 | 14 | 1 | 4 | 4 | 3 | 2 | RNF111_chr15_58982663_59102419 | RNF111 | AGTGT others(5900): Show |
chr15 | 58982663 | 59102419 |
| a0001c0001t0006 | 0/0 | 5905 | 8 | 0 | 0 | 7 | 0 | 1 | RNF111_chr15_58982663_59102419 | RNF111 | AGTGT others(5900): Show |
chr15 | 58982663 | 59102419 |
| a0001c0001t0007 | 0/0 | 5905 | 8 | 6 | 2 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | AGTGT others(5900): Show |
chr15 | 58982663 | 59102419 |
| a0001c0001t0008 | 0/0 | 5905 | 6 | 0 | 0 | 6 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | AGTGT others(5900): Show |
chr15 | 58982663 | 59102419 |
| a0001c0001t0009 | 0/0 | 5905 | 3 | 3 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | AGTGT others(5900): Show |
chr15 | 58982663 | 59102419 |
| a0001c0001t0010 | 0/0 | 5905 | 2 | 0 | 1 | 0 | 0 | 1 | RNF111_chr15_58982663_59102419 | RNF111 | AGTGT others(5900): Show |
chr15 | 58982663 | 59102419 |
| a0001c0001t0011 | 0/0 | 5905 | 2 | 0 | 0 | 0 | 2 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | AGTGT others(5900): Show |
chr15 | 58982663 | 59102419 |
| a0001c0001t0013 | 0/0 | 5905 | 2 | 0 | 0 | 2 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | AGTGT others(5900): Show |
chr15 | 58982663 | 59102419 |
| a0001c0001t0014 | 0/0 | 5905 | 2 | 2 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | AGTGT others(5900): Show |
chr15 | 58982663 | 59102419 |
| a0001c0001t0016 | 0/0 | 5905 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | AGTGT others(5900): Show |
chr15 | 58982663 | 59102419 |
| a0001c0001t0017 | 0/0 | 5905 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | AGTGT others(5900): Show |
chr15 | 58982663 | 59102419 |
| a0001c0001t0018 | 0/0 | 5905 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | AGTGT others(5900): Show |
chr15 | 58982663 | 59102419 |
| a0001c0001t0019 | 0/0 | 5905 | 1 | 0 | 0 | 0 | 0 | 1 | RNF111_chr15_58982663_59102419 | RNF111 | AGTGT others(5900): Show |
chr15 | 58982663 | 59102419 |
| a0001c0001t0020 | 0/0 | 5905 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | AGTGT others(5900): Show |
chr15 | 58982663 | 59102419 |
| a0001c0001t0021 | 0/0 | 5905 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | AGTGT others(5900): Show |
chr15 | 58982663 | 59102419 |
| a0001c0001t0022 | 0/0 | 5905 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | AGTGT others(5900): Show |
chr15 | 58982663 | 59102419 |
| a0001c0001t0023 | 0/0 | 5905 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | AGTGT others(5900): Show |
chr15 | 58982663 | 59102419 |
| a0001c0002t0001 | 1/0 | 5905 | 69 | 11 | 5 | 40 | 3 | 9 | RNF111_chr15_58982663_59102419 | RNF111 | AGTGT others(5900): Show |
chr15 | 58982663 | 59102419 |
| a0001c0002t0003 | 0/0 | 5905 | 10 | 8 | 0 | 2 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | AGTGT others(5900): Show |
chr15 | 58982663 | 59102419 |
| a0001c0002t0012 | 0/0 | 5905 | 2 | 2 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | AGTGT others(5900): Show |
chr15 | 58982663 | 59102419 |
| a0001c0002t0015 | 0/0 | 5905 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | AGTGT others(5900): Show |
chr15 | 58982663 | 59102419 |
| a0001c0004t0003 | 0/1 | 5905 | 8 | 1 | 4 | 0 | 2 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | AGTGT others(5900): Show |
chr15 | 58982663 | 59102419 |
| a0001c0005t0005 | 0/0 | 5905 | 2 | 0 | 0 | 2 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | AGTGT others(5900): Show |
chr15 | 58982663 | 59102419 |
| a0001c0007t0003 | 0/0 | 5905 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | AGTGT others(5900): Show |
chr15 | 58982663 | 59102419 |
| a0001c0008t0002 | 0/0 | 5905 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | AGTGT others(5900): Show |
chr15 | 58982663 | 59102419 |
| a0001c0009t0006 | 0/0 | 5905 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | AGTGT others(5900): Show |
chr15 | 58982663 | 59102419 |
| a0001c0010t0002 | 0/0 | 5905 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | AGTGT others(5900): Show |
chr15 | 58982663 | 59102419 |
| a0002c0003t0001 | 0/0 | 5905 | 34 | 2 | 13 | 11 | 3 | 5 | RNF111_chr15_58982663_59102419 | RNF111 | AGTGT others(5900): Show |
chr15 | 58982663 | 59102419 |
| a0002c0003t0003 | 0/0 | 5905 | 2 | 0 | 0 | 2 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | AGTGT others(5900): Show |
chr15 | 58982663 | 59102419 |
| a0002c0003t0015 | 0/0 | 5905 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | AGTGT others(5900): Show |
chr15 | 58982663 | 59102419 |
| a0002c0003t0024 | 0/0 | 5905 | 1 | 0 | 0 | 0 | 0 | 1 | RNF111_chr15_58982663_59102419 | RNF111 | AGTGT others(5900): Show |
chr15 | 58982663 | 59102419 |
| a0002c0003t0025 | 0/0 | 5905 | 1 | 0 | 0 | 0 | 1 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | AGTGT others(5900): Show |
chr15 | 58982663 | 59102419 |
| a0002c0015t0001 | 0/0 | 5905 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | AGTGT others(5900): Show |
chr15 | 58982663 | 59102419 |
| a0002c0016t0006 | 0/0 | 5905 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | AGTGT others(5900): Show |
chr15 | 58982663 | 59102419 |
| a0002c0017t0001 | 0/0 | 5905 | 1 | 0 | 0 | 0 | 0 | 1 | RNF111_chr15_58982663_59102419 | RNF111 | AGTGT others(5900): Show |
chr15 | 58982663 | 59102419 |
| a0002c0018t0001 | 0/0 | 5905 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | AGTGT others(5900): Show |
chr15 | 58982663 | 59102419 |
| a0003c0006t0006 | 0/0 | 5905 | 2 | 0 | 2 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | AGTGT others(5900): Show |
chr15 | 58982663 | 59102419 |
| a0004c0012t0002 | 0/0 | 5905 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | AGTGT others(5900): Show |
chr15 | 58982663 | 59102419 |
| a0005c0011t0010 | 0/0 | 5905 | 1 | 0 | 0 | 0 | 0 | 1 | RNF111_chr15_58982663_59102419 | RNF111 | AGTGT others(5900): Show |
chr15 | 58982663 | 59102419 |
| a0006c0013t0001 | 0/0 | 5905 | 1 | 0 | 0 | 0 | 0 | 1 | RNF111_chr15_58982663_59102419 | RNF111 | AGTGT others(5900): Show |
chr15 | 58982663 | 59102419 |
| a0007c0014t0001 | 0/0 | 5905 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | AGTGT others(5900): Show |
chr15 | 58982663 | 59102419 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0003g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0003g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0003g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0003g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0003g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0003g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0003g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0003g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0003g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0003g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0003g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0003g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0003g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0003g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0003g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0004g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0004g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0004g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0004g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0004g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0004g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0004g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0004g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0004g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0004g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0004g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0004g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0004g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0004g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0004g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0004g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0004g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0004g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0004g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0004g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0004g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0005g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0005g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0005g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0005g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0005g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0005g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0005g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0005g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0005g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0005g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0005g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0005g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0005g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0005g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0006g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0006g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0006g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0006g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0006g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0006g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0006g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0006g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0007g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0007g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0007g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0007g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0007g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0007g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0007g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0007g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0008g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0008g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0008g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0008g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0008g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0008g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0009g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0009g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0009g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0010g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0010g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0011g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0013g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0013g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0014g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0014g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0016g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0017g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0018g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0019g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0020g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0021g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0022g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0001t0023g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0001g0260 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0003g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0003g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0003g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0003g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0012g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0012g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0002t0015g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0004t0003g0002 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0004t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0004t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0004t0003g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0004t0003g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0004t0003g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0004t0003g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0004t0003g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0005t0005g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0005t0005g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0007t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0008t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0009t0006g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0001c0010t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0002c0003t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0002c0003t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0002c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0002c0003t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0002c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0002c0003t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0002c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0002c0003t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0002c0003t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0002c0003t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0002c0003t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0002c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0002c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0002c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0002c0003t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0002c0003t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0002c0003t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0002c0003t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0002c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0002c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0002c0003t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0002c0003t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0002c0003t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0002c0003t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0002c0003t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0002c0003t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0002c0003t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0002c0003t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0002c0003t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0002c0003t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0002c0003t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0002c0003t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0002c0003t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0002c0003t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0002c0003t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0002c0003t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0002c0003t0015g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0002c0003t0024g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0002c0003t0025g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0002c0015t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0002c0016t0006g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0002c0017t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0002c0018t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0003c0006t0006g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0003c0006t0006g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0004c0012t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0005c0011t0010g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0006c0013t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| a0007c0014t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0004 | t0003 | g0053 | EUR | GBR | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG00099 | hp2 | a0001 | c0001 | t0005 | g0323 | EUR | GBR | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0086 | EUR | GBR | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG00140 | hp2 | a0002 | c0003 | t0001 | g0174 | EUR | GBR | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG00280 | hp1 | a0001 | c0004 | t0003 | g0262 | EUR | FIN | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG00280 | hp2 | a0002 | c0003 | t0025 | g0274 | EUR | FIN | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG00408 | hp1 | a0001 | c0001 | t0008 | g0282 | EAS | CHS | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | CHS | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | CHS | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG00423 | hp2 | a0004 | c0012 | t0002 | g0194 | EAS | CHS | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0151 | EAS | CHS | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | CHS | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | CHS | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0167 | EAS | CHS | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0184 | EAS | CHS | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG00558 | hp2 | a0002 | c0003 | t0001 | g0067 | EAS | CHS | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | CHS | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0109 | EAS | CHS | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | CHS | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0133 | EAS | CHS | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0034 | AMR | PUR | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG00639 | hp2 | a0002 | c0003 | t0001 | g0175 | AMR | PUR | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG00733 | hp1 | a0002 | c0003 | t0001 | g0075 | AMR | PUR | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG00733 | hp2 | a0001 | c0001 | t0005 | g0329 | AMR | PUR | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG00741 | hp1 | a0002 | c0003 | t0001 | g0073 | AMR | PUR | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0245 | AMR | PUR | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01069 | hp2 | a0002 | c0003 | t0001 | g0143 | AMR | PUR | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01070 | hp1 | a0002 | c0003 | t0001 | g0083 | AMR | PUR | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0244 | AMR | PUR | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01071 | hp1 | a0002 | c0003 | t0001 | g0142 | AMR | PUR | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0249 | AMR | PUR | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01106 | hp1 | a0002 | c0003 | t0001 | g0076 | AMR | PUR | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01106 | hp2 | a0001 | c0004 | t0003 | g0202 | AMR | PUR | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01167 | hp1 | a0002 | c0003 | t0001 | g0069 | AMR | PUR | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01167 | hp2 | a0001 | c0001 | t0007 | g0026 | AMR | PUR | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0192 | AMR | PUR | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0198 | AMR | PUR | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01169 | hp2 | a0001 | c0001 | t0007 | g0025 | AMR | PUR | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0098 | AMR | PUR | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01175 | hp2 | a0001 | c0001 | t0010 | g0058 | AMR | PUR | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01192 | hp1 | a0001 | c0001 | t0004 | g0041 | AMR | PUR | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01192 | hp2 | a0002 | c0003 | t0001 | g0179 | AMR | PUR | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01256 | hp1 | a0001 | c0008 | t0002 | g0197 | AMR | CLM | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01256 | hp2 | a0001 | c0004 | t0003 | g0264 | AMR | CLM | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01258 | hp1 | a0001 | c0002 | t0015 | g0093 | AMR | CLM | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01258 | hp2 | a0001 | c0004 | t0003 | g0265 | AMR | CLM | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0200 | AMR | CLM | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01261 | hp2 | a0001 | c0001 | t0004 | g0048 | AMR | CLM | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0030 | AMR | CLM | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01346 | hp2 | a0002 | c0003 | t0001 | g0081 | AMR | CLM | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01358 | hp1 | a0001 | c0001 | t0005 | g0169 | AMR | CLM | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01358 | hp2 | a0001 | c0001 | t0004 | g0032 | AMR | CLM | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01361 | hp1 | a0002 | c0003 | t0001 | g0156 | AMR | CLM | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01361 | hp2 | a0001 | c0001 | t0005 | g0019 | AMR | CLM | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01433 | hp1 | a0002 | c0003 | t0001 | g0074 | AMR | CLM | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0047 | AMR | CLM | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0029 | AMR | CLM | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0125 | AMR | CLM | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01515 | hp1 | a0001 | c0001 | t0011 | g0001 | EUR | IBS | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01515 | hp2 | a0002 | c0003 | t0001 | g0161 | EUR | IBS | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0087 | EUR | IBS | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01517 | hp2 | a0001 | c0001 | t0011 | g0001 | EUR | IBS | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0178 | AFR | ACB | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0226 | AFR | ACB | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01891 | hp1 | a0001 | c0004 | t0003 | g0191 | AFR | ACB | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0054 | AFR | ACB | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01928 | hp1 | a0001 | c0001 | t0004 | g0031 | AMR | PEL | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0246 | AMR | PEL | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01934 | hp1 | a0003 | c0006 | t0006 | g0315 | AMR | PEL | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01934 | hp2 | a0002 | c0003 | t0001 | g0066 | AMR | PEL | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01943 | hp1 | a0001 | c0001 | t0005 | g0284 | AMR | PEL | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01943 | hp2 | a0001 | c0001 | t0004 | g0027 | AMR | PEL | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01952 | hp1 | a0003 | c0006 | t0006 | g0317 | AMR | PEL | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01952 | hp2 | a0001 | c0001 | t0004 | g0033 | AMR | PEL | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0251 | AMR | PEL | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01975 | hp2 | a0001 | c0001 | t0004 | g0028 | AMR | PEL | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0253 | AMR | PEL | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01978 | hp2 | a0001 | c0010 | t0002 | g0214 | AMR | PEL | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01993 | hp1 | a0001 | c0004 | t0003 | g0325 | AMR | PEL | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0100 | AMR | PEL | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02004 | hp1 | a0001 | c0001 | t0004 | g0044 | AMR | PEL | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0113 | AMR | PEL | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0110 | EAS | KHV | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02027 | hp2 | a0001 | c0001 | t0013 | g0146 | EAS | KHV | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | ACB | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02055 | hp2 | a0002 | c0003 | t0001 | g0082 | AFR | ACB | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0123 | EAS | KHV | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | KHV | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02074 | hp1 | a0002 | c0003 | t0001 | g0148 | EAS | KHV | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02074 | hp2 | a0001 | c0001 | t0008 | g0283 | EAS | KHV | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02080 | hp1 | a0001 | c0002 | t0003 | g0276 | EAS | KHV | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | KHV | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02083 | hp1 | a0002 | c0003 | t0001 | g0077 | EAS | KHV | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02083 | hp2 | a0001 | c0001 | t0008 | g0281 | EAS | KHV | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0138 | EAS | KHV | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02132 | hp2 | a0001 | c0001 | t0008 | g0287 | EAS | KHV | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0144 | EAS | KHV | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | KHV | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0164 | AMR | PEL | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0248 | AMR | PEL | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0149 | EAS | CDX | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02165 | hp2 | a0002 | c0003 | t0001 | g0170 | EAS | CDX | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02257 | hp1 | a0001 | c0002 | t0003 | g0013 | AFR | ACB | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02257 | hp2 | a0001 | c0002 | t0012 | g0229 | AFR | ACB | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0300 | AFR | ACB | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02258 | hp2 | a0001 | c0002 | t0003 | g0239 | AFR | ACB | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0153 | AFR | ACB | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0261 | AFR | ACB | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0301 | AFR | ACB | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | KHV | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02523 | hp2 | a0002 | c0016 | t0006 | g0173 | EAS | KHV | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02572 | hp1 | a0001 | c0001 | t0007 | g0240 | AFR | GWD | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0016 | AFR | GWD | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02615 | hp1 | a0001 | c0001 | t0007 | g0011 | AFR | GWD | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0327 | AFR | GWD | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0268 | AFR | GWD | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0298 | AFR | GWD | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0104 | AFR | GWD | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02717 | hp1 | a0001 | c0001 | t0007 | g0235 | AFR | GWD | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02717 | hp2 | a0001 | c0002 | t0003 | g0277 | AFR | GWD | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0152 | AFR | GWD | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0154 | SAS | PJL | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02735 | hp2 | a0005 | c0011 | t0010 | g0057 | SAS | PJL | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02738 | hp1 | a0001 | c0001 | t0010 | g0056 | SAS | PJL | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02738 | hp2 | a0002 | c0003 | t0024 | g0177 | SAS | PJL | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0326 | AFR | GWD | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0126 | AFR | GWD | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0278 | AFR | GWD | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0085 | AFR | GWD | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0039 | AFR | GWD | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0242 | AFR | GWD | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | GWD | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02896 | hp1 | a0001 | c0001 | t0009 | g0199 | AFR | GWD | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02896 | hp2 | a0001 | c0002 | t0003 | g0009 | AFR | GWD | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0243 | AFR | GWD | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02897 | hp2 | a0001 | c0002 | t0003 | g0010 | AFR | GWD | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | ESN | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0254 | AFR | ESN | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02970 | hp1 | a0001 | c0001 | t0007 | g0024 | AFR | ESN | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0105 | AFR | ESN | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0059 | SAS | PJL | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG03017 | hp2 | a0002 | c0003 | t0001 | g0061 | SAS | PJL | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0035 | AFR | GWD | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG03041 | hp2 | a0001 | c0002 | t0003 | g0236 | AFR | GWD | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | MSL | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0106 | AFR | MSL | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0162 | AFR | ESN | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0279 | AFR | ESN | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0050 | AFR | ESN | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | ESN | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG03209 | hp1 | a0001 | c0002 | t0003 | g0238 | AFR | MSL | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0310 | AFR | MSL | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0306 | AFR | MSL | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0049 | AFR | MSL | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0055 | SAS | PJL | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0188 | SAS | PJL | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0308 | AFR | MSL | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | MSL | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | MSL | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | MSL | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG03540 | hp1 | a0001 | c0007 | t0003 | g0237 | AFR | GWD | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0230 | AFR | GWD | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG03579 | hp1 | a0001 | c0002 | t0003 | g0304 | AFR | MSL | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0307 | AFR | MSL | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0117 | SAS | PJL | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0289 | SAS | PJL | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0291 | SAS | PJL | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG03669 | hp2 | a0006 | c0013 | t0001 | g0127 | SAS | PJL | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG03688 | hp1 | a0001 | c0001 | t0004 | g0037 | SAS | STU | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0084 | SAS | STU | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0060 | SAS | PJL | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG03710 | hp2 | a0002 | c0003 | t0001 | g0118 | SAS | PJL | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG03831 | hp1 | a0001 | c0001 | t0019 | g0187 | SAS | BEB | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG03831 | hp2 | a0002 | c0003 | t0001 | g0158 | SAS | BEB | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0092 | SAS | BEB | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG03834 | hp2 | a0001 | c0001 | t0005 | g0141 | SAS | BEB | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0116 | SAS | BEB | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0038 | SAS | BEB | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG03942 | hp1 | a0002 | c0017 | t0001 | g0140 | SAS | BEB | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG03942 | hp2 | a0001 | c0001 | t0006 | g0311 | SAS | BEB | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0097 | SAS | BEB | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0271 | SAS | BEB | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0022 | SAS | STU | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG04199 | hp2 | a0002 | c0003 | t0001 | g0080 | SAS | STU | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG04228 | hp1 | a0001 | c0001 | t0005 | g0020 | SAS | STU | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG04228 | hp2 | a0002 | c0003 | t0001 | g0111 | SAS | STU | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0045 | AFR | YRI | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18522 | hp2 | a0001 | c0001 | t0007 | g0234 | AFR | YRI | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0166 | EAS | CHB | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18612 | hp2 | a0002 | c0003 | t0001 | g0018 | EAS | CHB | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0266 | AFR | YRI | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18906 | hp2 | a0001 | c0001 | t0016 | g0008 | AFR | YRI | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0155 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18940 | hp1 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18940 | hp2 | a0001 | c0001 | t0013 | g0145 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0124 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0182 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18944 | hp1 | a0001 | c0001 | t0005 | g0290 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18944 | hp2 | a0001 | c0001 | t0022 | g0223 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18946 | hp1 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18949 | hp1 | a0002 | c0018 | t0001 | g0159 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18949 | hp2 | a0001 | c0002 | t0001 | g0130 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18951 | hp2 | a0002 | c0003 | t0001 | g0017 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18956 | hp1 | a0001 | c0001 | t0006 | g0313 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18957 | hp2 | a0001 | c0001 | t0006 | g0319 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18959 | hp1 | a0001 | c0001 | t0006 | g0316 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18960 | hp2 | a0001 | c0002 | t0003 | g0147 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18963 | hp1 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18964 | hp2 | a0002 | c0015 | t0001 | g0157 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18968 | hp1 | a0001 | c0001 | t0004 | g0043 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18970 | hp2 | a0001 | c0001 | t0005 | g0285 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18971 | hp2 | a0001 | c0001 | t0005 | g0267 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18984 | hp1 | a0002 | c0003 | t0001 | g0128 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18984 | hp2 | a0001 | c0001 | t0008 | g0280 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18985 | hp2 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18989 | hp2 | a0001 | c0001 | t0023 | g0320 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0185 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18995 | hp2 | a0001 | c0001 | t0017 | g0294 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18998 | hp1 | a0001 | c0005 | t0005 | g0096 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18998 | hp2 | a0002 | c0003 | t0001 | g0168 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA19000 | hp1 | a0001 | c0001 | t0004 | g0040 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0183 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA19002 | hp1 | a0001 | c0001 | t0008 | g0286 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA19002 | hp2 | a0002 | c0003 | t0003 | g0079 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA19006 | hp1 | a0001 | c0001 | t0005 | g0293 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA19006 | hp2 | a0001 | c0002 | t0001 | g0135 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA19012 | hp2 | a0007 | c0014 | t0001 | g0131 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA19030 | hp1 | a0001 | c0001 | t0014 | g0046 | AFR | LWK | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | LWK | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0103 | AFR | LWK | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA19043 | hp2 | a0001 | c0001 | t0009 | g0324 | AFR | LWK | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA19054 | hp2 | a0002 | c0003 | t0001 | g0122 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA19057 | hp1 | a0001 | c0001 | t0004 | g0042 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA19057 | hp2 | a0001 | c0001 | t0006 | g0321 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA19058 | hp1 | a0001 | c0001 | t0006 | g0312 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA19060 | hp1 | a0001 | c0009 | t0006 | g0318 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA19062 | hp2 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA19063 | hp2 | a0001 | c0001 | t0006 | g0322 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0150 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0165 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA19070 | hp2 | a0002 | c0003 | t0001 | g0139 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0180 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA19082 | hp1 | a0001 | c0002 | t0001 | g0134 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA19085 | hp2 | a0001 | c0001 | t0020 | g0208 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA19087 | hp2 | a0002 | c0003 | t0003 | g0309 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA19088 | hp1 | a0002 | c0003 | t0001 | g0078 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0121 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA19090 | hp2 | a0001 | c0005 | t0005 | g0120 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA19091 | hp1 | a0001 | c0001 | t0006 | g0314 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0288 | AFR | YRI | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0051 | AFR | YRI | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA20129 | hp1 | a0001 | c0002 | t0012 | g0012 | AFR | ASW | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA20129 | hp2 | a0001 | c0001 | t0021 | g0052 | AFR | ASW | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA20752 | hp1 | a0001 | c0001 | t0005 | g0071 | EUR | TSI | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA20752 | hp2 | a0002 | c0003 | t0001 | g0070 | EUR | TSI | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0112 | EUR | TSI | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA20805 | hp2 | a0001 | c0001 | t0005 | g0114 | EUR | TSI | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01123 | hp1 | a0002 | c0003 | t0015 | g0176 | AMR | CLM | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0036 | AMR | CLM | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02109 | hp1 | a0001 | c0001 | t0009 | g0263 | AFR | ACB | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0328 | AFR | ACB | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02559 | hp1 | a0001 | c0001 | t0018 | g0233 | AFR | ACB | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0163 | AFR | ACB | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0255 | AFR | MSL | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0303 | AFR | MSL | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0171 | AFR | USA | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| HG06807 | hp2 | a0001 | c0001 | t0014 | g0305 | AFR | USA | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA20300 | hp1 | a0001 | c0001 | t0007 | g0023 | AFR | USA | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0302 | AFR | USA | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA21309 | hp1 | a0002 | c0003 | t0001 | g0160 | AFR | LWK | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0273 | AFR | LWK | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| homoSapiens | chm13v2 | a0001 | c0004 | t0003 | g0002 | REF | REF | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0260 | REF | REF | RNF111_chr15_58982663_59102419 | RNF111 | chr15 | 58982663 | 59102419 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:59030849 | C | G | 1 | a0002 | 43 | HG00140.hp2 HG00280.hp2 HG00558.hp2 others(40): Show |
missense_variant | MODERATE | c.27C>G | p.Asn9Lys | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/14 | 452/5905 | 27/2961 | 9/986 | chr15 | 59030849 | |||
| chr15:59030928 | A | T | 1 | a0003 | 2 | HG01934.hp1 HG01952.hp1 |
missense_variant | MODERATE | c.106A>T | p.Ile36Phe | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/14 | 531/5905 | 106/2961 | 36/986 | chr15 | 59030928 | |||
| chr15:59031082 | A | G | 1 | a0007 | 1 | NA19012.hp2 | missense_variant | MODERATE | c.260A>G | p.Lys87Arg | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/14 | 685/5905 | 260/2961 | 87/986 | chr15 | 59031082 | |||
| chr15:59058373 | A | G | 1 | a0004 | 1 | HG00423.hp2 | missense_variant | MODERATE | c.1189A>G | p.Thr397Ala | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/14 | 1614/5905 | 1189/2961 | 397/986 | chr15 | 59058373 | |||
| chr15:59058524 | A | G | 1 | a0005 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.1340A>G | p.Asn447Ser | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/14 | 1765/5905 | 1340/2961 | 447/986 | chr15 | 59058524 | |||
| chr15:59076119 | A | G | 1 | a0006 | 1 | HG03669.hp2 | missense_variant | MODERATE | c.1852A>G | p.Ile618Val | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/14 | 2277/5905 | 1852/2961 | 618/986 | chr15 | 59076119 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:59031011 | A | G | 1 | a0002c0018 | 1 | NA18949.hp1 | synonymous_variant | LOW | c.189A>G | p.Glu63Glu | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/14 | 614/5905 | 189/2961 | 63/986 | chr15 | 59031011 | |||
| chr15:59031362 | G | A | 1 | a0002c0015 | 1 | NA18964.hp2 | synonymous_variant | LOW | c.540G>A | p.Arg180Arg | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/14 | 965/5905 | 540/2961 | 180/986 | chr15 | 59031362 | |||
| chr15:59055715 | T | C | 1 | a0001c0007 | 1 | HG03540.hp1 | synonymous_variant | LOW | c.1041T>C | p.His347His | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 4/14 | 1466/5905 | 1041/2961 | 347/986 | chr15 | 59055715 | |||
| chr15:59055730 | C | A | 8 | a0001c0001 a0001c0004 a0001c0008 others(5): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
synonymous_variant | LOW | c.1056C>A | p.Ser352Ser | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 4/14 | 1481/5905 | 1056/2961 | 352/986 | chr15 | 59055730 | |||
| chr15:59055746 | C | A | 1 | a0001c0008 | 1 | HG01256.hp1 | synonymous_variant | LOW | c.1072C>A | p.Arg358Arg | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 4/14 | 1497/5905 | 1072/2961 | 358/986 | chr15 | 59055746 | |||
| chr15:59066972 | T | C | 1 | a0001c0009 | 1 | NA19060.hp1 | synonymous_variant | LOW | c.1575T>C | p.Ala525Ala | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/14 | 2000/5905 | 1575/2961 | 525/986 | chr15 | 59066972 | |||
| chr15:59075968 | G | A | 9 | a0001c0001 a0001c0005 a0001c0008 others(6): Show |
195 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(192): Show |
synonymous_variant | LOW | c.1701G>A | p.Val567Val | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/14 | 2126/5905 | 1701/2961 | 567/986 | chr15 | 59075968 | |||
| chr15:59076190 | A | G | 1 | a0001c0010 | 1 | HG01978.hp2 | synonymous_variant | LOW | c.1923A>G | p.Ser641Ser | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/14 | 2348/5905 | 1923/2961 | 641/986 | chr15 | 59076190 | |||
| chr15:59081021 | G | A | 1 | a0002c0017 | 1 | HG03942.hp1 | synonymous_variant | LOW | c.2034G>A | p.Pro678Pro | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 8/14 | 2459/5905 | 2034/2961 | 678/986 | chr15 | 59081021 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:58987672 | C | G | 2 | a0001c0002t0015 a0002c0003t0015 |
2 | HG01123.hp1 HG01258.hp1 |
5_prime_UTR_variant | MODIFIER | c.-416C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/14 | 43151 | chr15 | 58987672 | ||||||
| chr15:58987784 | C | T | 1 | a0001c0001t0014 | 2 | HG06807.hp2 NA19030.hp1 |
5_prime_UTR_variant | MODIFIER | c.-304C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/14 | 43039 | chr15 | 58987784 | ||||||
| chr15:58987920 | T | C | 27 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(24): Show |
181 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(178): Show |
5_prime_UTR_variant | MODIFIER | c.-168T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/14 | 42903 | chr15 | 58987920 | ||||||
| chr15:58987954 | G | A | 1 | a0001c0001t0016 | 1 | NA18906.hp2 | 5_prime_UTR_variant | MODIFIER | c.-134G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/14 | 42869 | chr15 | 58987954 | ||||||
| chr15:58988023 | A | C | 5 | a0001c0001t0006 a0001c0001t0023 a0001c0009t0006 others(2): Show |
13 | HG01934.hp1 HG01952.hp1 HG02523.hp2 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-65A>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/14 | 42800 | chr15 | 58988023 | ||||||
| chr15:59095182 | C | T | 1 | a0001c0001t0022 | 1 | NA18944.hp2 | 3_prime_UTR_variant | MODIFIER | c.*282C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 14/14 | 282 | chr15 | 59095182 | ||||||
| chr15:59095268 | T | G | 1 | a0001c0001t0023 | 1 | NA18989.hp2 | 3_prime_UTR_variant | MODIFIER | c.*368T>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 14/14 | 368 | chr15 | 59095268 | ||||||
| chr15:59095364 | T | G | 1 | a0002c0003t0024 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*464T>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 14/14 | 464 | chr15 | 59095364 | ||||||
| chr15:59095430 | A | T | 1 | a0002c0003t0025 | 1 | HG00280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*530A>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 14/14 | 530 | chr15 | 59095430 | ||||||
| chr15:59095577 | A | T | 1 | a0001c0001t0021 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*677A>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 14/14 | 677 | chr15 | 59095577 | ||||||
| chr15:59096014 | T | C | 1 | a0001c0001t0008 | 6 | HG00408.hp1 HG02074.hp2 HG02083.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1114T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 14/14 | 1114 | chr15 | 59096014 | ||||||
| chr15:59096520 | G | A | 1 | a0001c0001t0017 | 1 | NA18995.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1620G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 14/14 | 1620 | chr15 | 59096520 | ||||||
| chr15:59096546 | A | G | 8 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0013 others(5): Show |
25 | HG01167.hp2 HG01169.hp2 HG01934.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1646A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 14/14 | 1646 | chr15 | 59096546 | ||||||
| chr15:59096567 | T | C | 1 | a0001c0001t0011 | 2 | HG01515.hp1 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1667T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 14/14 | 1667 | chr15 | 59096567 | ||||||
| chr15:59096748 | G | C | 1 | a0001c0001t0018 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1848G>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 14/14 | 1848 | chr15 | 59096748 | ||||||
| chr15:59096796 | A | G | 8 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0013 others(5): Show |
25 | HG01167.hp2 HG01169.hp2 HG01934.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1896A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 14/14 | 1896 | chr15 | 59096796 | ||||||
| chr15:59096876 | C | A | 1 | a0001c0001t0019 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1976C>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 14/14 | 1976 | chr15 | 59096876 | ||||||
| chr15:59096897 | C | T | 26 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(23): Show |
159 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*1997C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 14/14 | 1997 | chr15 | 59096897 | ||||||
| chr15:59096988 | G | T | 1 | a0001c0001t0009 | 3 | HG02109.hp1 HG02896.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2088G>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 14/14 | 2088 | chr15 | 59096988 | ||||||
| chr15:59097083 | A | G | 1 | a0001c0001t0020 | 1 | NA19085.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2183A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 14/14 | 2183 | chr15 | 59097083 | ||||||
| chr15:59097267 | G | A | 5 | a0001c0001t0004 a0001c0001t0010 a0001c0001t0011 others(2): Show |
34 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*2367G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 14/14 | 2367 | chr15 | 59097267 | ||||||
| chr15:59097372 | C | G | 1 | a0001c0002t0012 | 2 | HG02257.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2472C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 14/14 | 2472 | chr15 | 59097372 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:58988079 | C | G | 1 | a0001c0001t0005g0329 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-20+11C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58988079 | |||||||
| chr15:58988079 | CG | C | 11 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0005 others(8): Show |
11 | HG02055.hp1 HG02257.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.-20+19delG | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 58988079 | ||||||
| chr15:58988080 | G | A | 128 | a0001c0001t0002g0186 a0001c0001t0002g0188 a0001c0001t0002g0189 others(125): Show |
128 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.-20+12G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58988080 | |||||||
| chr15:58988105 | C | T | 2 | a0001c0001t0003g0327 a0001c0001t0003g0328 |
2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-20+37C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58988105 | |||||||
| chr15:58988186 | T | C | 1 | a0001c0001t0002g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-20+118T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58988186 | |||||||
| chr15:58988271 | C | G | 1 | a0001c0001t0003g0326 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-20+203C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58988271 | |||||||
| chr15:58988398 | T | C | 1 | a0001c0001t0003g0015 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-20+330T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58988398 | |||||||
| chr15:58988450 | C | T | 1 | a0001c0004t0003g0325 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-20+382C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58988450 | |||||||
| chr15:58988565 | A | G | 1 | a0001c0001t0002g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-20+497A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58988565 | |||||||
| chr15:58988744 | C | T | 1 | a0001c0001t0002g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-20+676C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58988744 | |||||||
| chr15:58988914 | A | T | 1 | a0001c0001t0009g0324 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-20+846A>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58988914 | |||||||
| chr15:58988962 | T | G | 1 | a0001c0001t0003g0016 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-20+894T>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58988962 | |||||||
| chr15:58988987 | C | T | 1 | a0001c0001t0005g0323 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-20+919C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58988987 | |||||||
| chr15:58989138 | T | G | 2 | a0002c0003t0001g0017 a0002c0003t0001g0018 |
2 | NA18612.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.-20+1070T>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58989138 | |||||||
| chr15:58989170 | A | G | 14 | a0001c0001t0002g0014 a0001c0001t0003g0310 a0001c0001t0006g0311 others(11): Show |
14 | HG01934.hp1 HG01952.hp1 HG03209.hp2 others(11): Show |
intron_variant | MODIFIER | c.-20+1102A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58989170 | |||||||
| chr15:58989199 | C | T | 1 | a0002c0003t0003g0309 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-20+1131C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58989199 | |||||||
| chr15:58989274 | G | T | 3 | a0001c0001t0003g0306 a0001c0001t0003g0307 a0001c0001t0003g0308 |
3 | HG03225.hp1 HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-20+1206G>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58989274 | |||||||
| chr15:58989581 | A | G | 1 | a0001c0001t0014g0305 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-20+1513A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58989581 | |||||||
| chr15:58989605 | G | T | 1 | a0001c0001t0003g0016 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-20+1537G>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58989605 | |||||||
| chr15:58989746 | A | G | 1 | a0001c0002t0003g0304 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-20+1678A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58989746 | |||||||
| chr15:58989763 | T | G | 176 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0002g0072 others(173): Show |
177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.-20+1695T>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58989763 | |||||||
| chr15:58989874 | CT | C | 82 | a0001c0001t0002g0186 a0001c0001t0002g0188 a0001c0001t0002g0189 others(79): Show |
83 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.-20+1817delT | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 58989874 | ||||||
| chr15:58989883 | T | G | 1 | a0001c0001t0005g0019 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-20+1815T>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58989883 | |||||||
| chr15:58989886 | G | T | 6 | a0001c0002t0001g0180 a0001c0002t0001g0181 a0001c0002t0001g0182 others(3): Show |
6 | HG00558.hp1 NA18943.hp1 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.-20+1818G>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58989886 | |||||||
| chr15:58990090 | A | G | 39 | a0001c0001t0003g0016 a0001c0001t0003g0045 a0001c0001t0003g0049 others(36): Show |
40 | HG00639.hp1 HG01123.hp2 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.-20+2022A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58990090 | |||||||
| chr15:58990131 | A | C | 3 | a0001c0001t0004g0300 a0001c0001t0004g0301 a0001c0001t0004g0302 |
3 | HG02258.hp1 HG02451.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-20+2063A>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58990131 | |||||||
| chr15:58990131 | A | G | 1 | a0001c0001t0002g0228 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-20+2063A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58990131 | |||||||
| chr15:58990142 | C | G | 33 | a0001c0001t0003g0016 a0001c0001t0003g0045 a0001c0001t0003g0049 others(30): Show |
34 | HG00639.hp1 HG01123.hp2 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.-20+2074C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58990142 | |||||||
| chr15:58990145 | C | T | 1 | a0001c0001t0005g0178 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-20+2077C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58990145 | |||||||
| chr15:58990218 | G | A | 3 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0005 |
3 | HG02895.hp2 HG02965.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-20+2150G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58990218 | |||||||
| chr15:58990275 | A | G | 183 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0002g0072 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.-20+2207A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58990275 | |||||||
| chr15:58990276 | T | C | 1 | a0001c0001t0003g0310 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-20+2208T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58990276 | |||||||
| chr15:58990301 | C | T | 1 | a0001c0001t0004g0226 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-20+2233C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58990301 | |||||||
| chr15:58990317 | G | A | 1 | a0001c0001t0005g0267 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-20+2249G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58990317 | |||||||
| chr15:58990372 | G | A | 151 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(148): Show |
152 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.-20+2304G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58990372 | |||||||
| chr15:58990386 | G | T | 2 | a0001c0001t0004g0044 a0001c0001t0011g0001 |
3 | HG01515.hp1 HG01517.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.-20+2318G>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58990386 | |||||||
| chr15:58990412 | C | A | 1 | a0001c0001t0003g0326 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-20+2344C>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58990412 | |||||||
| chr15:58990424 | C | G | 1 | a0001c0001t0014g0305 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-20+2356C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58990424 | |||||||
| chr15:58990459 | G | A | 1 | a0001c0001t0002g0190 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-20+2391G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58990459 | |||||||
| chr15:58990477 | C | T | 39 | a0001c0001t0002g0189 a0001c0001t0002g0190 a0001c0001t0002g0200 others(36): Show |
39 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.-20+2409C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58990477 | |||||||
| chr15:58990582 | G | A | 1 | a0001c0001t0002g0273 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-20+2514G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58990582 | |||||||
| chr15:58990627 | T | C | 1 | a0001c0002t0001g0055 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-20+2559T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58990627 | |||||||
| chr15:58990648 | T | C | 255 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(252): Show |
255 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.-20+2580T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58990648 | |||||||
| chr15:58990869 | A | G | 2 | a0001c0001t0004g0042 a0001c0001t0004g0043 |
2 | NA18968.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.-20+2801A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58990869 | |||||||
| chr15:58990881 | T | TAG | 17 | a0001c0001t0003g0327 a0001c0001t0003g0328 a0001c0001t0006g0311 others(14): Show |
17 | HG01934.hp1 HG01952.hp1 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.-20+2814_-20+2815i others(4): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 58990881 | ||||||
| chr15:58990886 | C | T | 14 | a0001c0001t0002g0266 a0001c0001t0003g0016 a0001c0001t0003g0261 others(11): Show |
14 | HG00099.hp1 HG00280.hp1 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.-20+2818C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58990886 | |||||||
| chr15:58990919 | C | G | 1 | a0001c0002t0001g0144 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-20+2851C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58990919 | |||||||
| chr15:58990990 | A | G | 17 | a0001c0001t0003g0327 a0001c0001t0003g0328 a0001c0001t0006g0311 others(14): Show |
17 | HG01934.hp1 HG01952.hp1 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.-20+2922A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58990990 | |||||||
| chr15:58991052 | T | A | 4 | a0001c0001t0010g0056 a0001c0001t0010g0058 a0002c0003t0025g0274 others(1): Show |
4 | HG00280.hp2 HG01175.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20+2984T>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58991052 | |||||||
| chr15:58991084 | G | A | 1 | a0001c0001t0004g0300 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-20+3016G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58991084 | |||||||
| chr15:58991161 | G | A | 1 | a0001c0001t0003g0016 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-20+3093G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58991161 | |||||||
| chr15:58991195 | G | C | 7 | a0001c0001t0003g0045 a0001c0001t0003g0306 a0001c0001t0003g0307 others(4): Show |
7 | HG02717.hp1 HG03225.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.-20+3127G>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58991195 | |||||||
| chr15:58991356 | C | T | 1 | a0001c0001t0007g0235 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-20+3288C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58991356 | |||||||
| chr15:58991367 | C | T | 2 | a0002c0003t0001g0142 a0002c0003t0001g0143 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-20+3299C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58991367 | |||||||
| chr15:58991576 | G | A | 13 | a0001c0001t0002g0266 a0001c0001t0003g0261 a0001c0001t0003g0310 others(10): Show |
13 | HG00099.hp1 HG00280.hp1 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.-20+3508G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58991576 | |||||||
| chr15:58991615 | C | A | 1 | a0001c0002t0001g0152 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-20+3547C>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58991615 | |||||||
| chr15:58991683 | A | G | 1 | a0001c0002t0001g0172 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-20+3615A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58991683 | |||||||
| chr15:58991703 | A | T | 75 | a0001c0001t0002g0186 a0001c0001t0002g0188 a0001c0001t0002g0189 others(72): Show |
75 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.-20+3635A>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58991703 | |||||||
| chr15:58991717 | A | G | 1 | a0001c0001t0002g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-20+3649A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58991717 | |||||||
| chr15:58991719 | A | G | 1 | a0002c0003t0001g0018 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-20+3651A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58991719 | |||||||
| chr15:58991831 | T | G | 7 | a0001c0001t0007g0011 a0001c0001t0007g0023 a0001c0001t0007g0024 others(4): Show |
7 | HG01167.hp2 HG01169.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-20+3763T>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58991831 | |||||||
| chr15:58991875 | A | G | 1 | a0001c0001t0006g0322 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-20+3807A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58991875 | |||||||
| chr15:58992037 | G | GTATTT | 3 | a0001c0001t0002g0201 a0001c0001t0003g0327 a0001c0001t0003g0328 |
3 | HG02109.hp2 HG02615.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.-20+3991_-20+3995d others(7): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 58992037 | ||||||
| chr15:58992037 | GTATTTTA others(3): Show |
G | 1 | a0002c0003t0001g0018 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-20+3986_-20+3995d others(12): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 58992037 | ||||||
| chr15:58992075 | T | G | 1 | a0001c0001t0002g0275 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-20+4007T>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58992075 | |||||||
| chr15:58992255 | G | A | 2 | a0001c0002t0001g0059 a0001c0002t0001g0060 |
2 | HG03017.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.-20+4187G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58992255 | |||||||
| chr15:58992297 | G | A | 1 | a0001c0001t0004g0300 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-20+4229G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58992297 | |||||||
| chr15:58992335 | G | A | 1 | a0001c0001t0016g0008 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-20+4267G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58992335 | |||||||
| chr15:58992392 | T | G | 1 | a0002c0003t0001g0061 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-20+4324T>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58992392 | |||||||
| chr15:58992479 | T | C | 1 | a0001c0001t0003g0016 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-20+4411T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58992479 | |||||||
| chr15:58992551 | C | T | 4 | a0001c0001t0004g0054 a0001c0001t0004g0300 a0001c0001t0004g0301 others(1): Show |
4 | HG01891.hp2 HG02258.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+4483C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58992551 | |||||||
| chr15:58992585 | A | C | 44 | a0001c0001t0002g0186 a0001c0001t0002g0188 a0001c0001t0002g0189 others(41): Show |
44 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.-20+4517A>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58992585 | |||||||
| chr15:58992611 | A | G | 2 | a0001c0001t0003g0327 a0001c0001t0003g0328 |
2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-20+4543A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58992611 | |||||||
| chr15:58992712 | C | T | 1 | a0001c0001t0002g0225 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-20+4644C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58992712 | |||||||
| chr15:58992869 | G | A | 1 | a0001c0001t0002g0203 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-20+4801G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58992869 | |||||||
| chr15:58992883 | A | G | 1 | a0002c0003t0001g0139 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-20+4815A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58992883 | |||||||
| chr15:58992917 | C | G | 7 | a0001c0001t0007g0011 a0001c0001t0007g0023 a0001c0001t0007g0024 others(4): Show |
7 | HG01167.hp2 HG01169.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-20+4849C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58992917 | |||||||
| chr15:58992959 | A | G | 5 | a0001c0001t0007g0011 a0001c0001t0007g0023 a0001c0001t0007g0024 others(2): Show |
5 | HG01167.hp2 HG01169.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-20+4891A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58992959 | |||||||
| chr15:58992985 | G | A | 21 | a0001c0001t0006g0311 a0001c0001t0006g0312 a0001c0001t0006g0313 others(18): Show |
21 | HG01167.hp2 HG01169.hp2 HG01934.hp1 others(18): Show |
intron_variant | MODIFIER | c.-20+4917G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58992985 | |||||||
| chr15:58993027 | G | A | 5 | a0001c0002t0001g0180 a0001c0002t0001g0181 a0001c0002t0001g0182 others(2): Show |
5 | NA18943.hp1 NA18985.hp2 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.-20+4959G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58993027 | |||||||
| chr15:58993119 | A | G | 2 | a0001c0001t0004g0041 a0001c0001t0004g0254 |
2 | HG01192.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-20+5051A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58993119 | |||||||
| chr15:58993228 | G | T | 54 | a0001c0001t0002g0186 a0001c0001t0002g0188 a0001c0001t0002g0189 others(51): Show |
54 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.-20+5160G>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58993228 | |||||||
| chr15:58993338 | G | T | 21 | a0001c0001t0006g0311 a0001c0001t0006g0312 a0001c0001t0006g0313 others(18): Show |
21 | HG01167.hp2 HG01169.hp2 HG01934.hp1 others(18): Show |
intron_variant | MODIFIER | c.-20+5270G>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58993338 | |||||||
| chr15:58993368 | AT | A | 26 | a0001c0001t0004g0022 a0001c0001t0004g0027 a0001c0001t0004g0028 others(23): Show |
27 | HG00639.hp1 HG01123.hp2 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.-20+5301delT | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58993368 | |||||||
| chr15:58993450 | A | G | 2 | a0001c0002t0001g0021 a0001c0002t0001g0138 |
2 | HG02132.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.-20+5382A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58993450 | |||||||
| chr15:58993819 | C | T | 1 | a0001c0001t0002g0266 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-20+5751C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58993819 | |||||||
| chr15:58993820 | G | A | 147 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(144): Show |
147 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.-20+5752G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58993820 | |||||||
| chr15:58994033 | A | AT | 53 | a0001c0001t0001g0136 a0001c0001t0002g0192 a0001c0001t0002g0204 others(50): Show |
54 | HG00621.hp2 HG00639.hp1 HG01123.hp2 others(51): Show |
intron_variant | MODIFIER | c.-20+5989dupT | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 58994033 | ||||||
| chr15:58994033 | A | ATT | 78 | a0001c0001t0001g0137 a0001c0001t0002g0186 a0001c0001t0002g0188 others(75): Show |
78 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.-20+5988_-20+5989d others(4): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 58994033 | ||||||
| chr15:58994033 | A | ATTT | 9 | a0001c0001t0002g0198 a0001c0001t0002g0220 a0001c0001t0002g0221 others(6): Show |
9 | HG01169.hp1 NA18522.hp1 NA18939.hp2 others(6): Show |
intron_variant | MODIFIER | c.-20+5987_-20+5989d others(5): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 58994033 | ||||||
| chr15:58994033 | AT | A | 15 | a0001c0001t0001g0256 a0001c0001t0003g0327 a0001c0001t0006g0321 others(12): Show |
15 | HG00558.hp2 HG01069.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.-20+5989delT | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 58994033 | ||||||
| chr15:58994033 | ATT | A | 13 | a0001c0001t0006g0311 a0001c0001t0006g0312 a0001c0001t0006g0313 others(10): Show |
13 | HG01934.hp1 HG01952.hp1 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.-20+5988_-20+5989d others(4): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 58994033 | ||||||
| chr15:58994033 | ATTT | A | 6 | a0001c0001t0007g0011 a0001c0001t0007g0023 a0001c0001t0007g0025 others(3): Show |
6 | HG01167.hp2 HG01169.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20+5987_-20+5989d others(5): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 58994033 | ||||||
| chr15:58994102 | A | G | 87 | a0001c0001t0002g0186 a0001c0001t0002g0188 a0001c0001t0002g0189 others(84): Show |
88 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.-20+6034A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58994102 | |||||||
| chr15:58994156 | C | T | 1 | a0001c0002t0001g0155 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-20+6088C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58994156 | |||||||
| chr15:58994245 | G | A | 1 | a0001c0001t0002g0275 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-20+6177G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58994245 | |||||||
| chr15:58994285 | C | T | 1 | a0001c0001t0002g0298 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-20+6217C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58994285 | |||||||
| chr15:58994321 | G | A | 1 | a0001c0001t0008g0281 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-20+6253G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58994321 | |||||||
| chr15:58994359 | A | C | 39 | a0001c0001t0002g0200 a0001c0001t0002g0244 a0001c0001t0002g0245 others(36): Show |
39 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.-20+6291A>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58994359 | |||||||
| chr15:58994416 | A | T | 2 | a0001c0004t0003g0264 a0001c0004t0003g0265 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-20+6348A>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58994416 | |||||||
| chr15:58994437 | T | C | 1 | a0001c0001t0010g0056 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-20+6369T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58994437 | |||||||
| chr15:58994473 | CT | C | 256 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0002g0072 others(253): Show |
257 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.-20+6427delT | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 58994473 | ||||||
| chr15:58994473 | CTTTT | C | 9 | a0001c0001t0005g0284 a0001c0001t0005g0285 a0001c0001t0005g0323 others(6): Show |
9 | HG00099.hp2 HG00408.hp1 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+6424_-20+6427d others(6): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 58994473 | ||||||
| chr15:58994476 | T | C | 1 | a0001c0001t0003g0016 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-20+6408T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58994476 | |||||||
| chr15:58994681 | T | G | 1 | a0001c0001t0004g0054 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-20+6613T>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58994681 | |||||||
| chr15:58994809 | A | G | 1 | a0001c0001t0003g0015 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-20+6741A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58994809 | |||||||
| chr15:58994884 | C | T | 1 | a0001c0001t0002g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-20+6816C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58994884 | |||||||
| chr15:58994956 | G | A | 5 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0003g0003 others(2): Show |
5 | HG00741.hp2 HG01168.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20+6888G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58994956 | |||||||
| chr15:58995214 | C | G | 1 | a0001c0001t0003g0016 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-20+7146C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58995214 | |||||||
| chr15:58995260 | C | T | 1 | a0002c0003t0015g0176 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-20+7192C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58995260 | |||||||
| chr15:58995465 | G | GT | 150 | a0001c0001t0001g0231 a0001c0001t0002g0072 a0001c0001t0002g0088 others(147): Show |
150 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.-20+7409dupT | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 58995465 | ||||||
| chr15:58995563 | A | G | 4 | a0001c0001t0002g0295 a0001c0001t0002g0296 a0001c0001t0002g0297 others(1): Show |
4 | HG02523.hp1 NA18955.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20+7495A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58995563 | |||||||
| chr15:58995754 | G | T | 115 | a0001c0001t0002g0186 a0001c0001t0002g0188 a0001c0001t0002g0190 others(112): Show |
116 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.-20+7686G>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58995754 | |||||||
| chr15:58995764 | C | CT | 48 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(45): Show |
48 | HG00438.hp1 HG00741.hp2 HG01168.hp1 others(45): Show |
intron_variant | MODIFIER | c.-20+7720dupT | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 58995764 | ||||||
| chr15:58995764 | CT | C | 119 | a0001c0001t0002g0014 a0001c0001t0002g0186 a0001c0001t0002g0188 others(116): Show |
120 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.-20+7720delT | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 58995764 | ||||||
| chr15:58996147 | T | C | 1 | a0002c0003t0001g0174 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-20+8079T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58996147 | |||||||
| chr15:58996220 | A | T | 42 | a0001c0001t0002g0186 a0001c0001t0002g0188 a0001c0001t0002g0189 others(39): Show |
42 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.-20+8152A>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58996220 | |||||||
| chr15:58996338 | C | T | 1 | a0001c0001t0007g0011 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-20+8270C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58996338 | |||||||
| chr15:58996393 | T | G | 1 | a0001c0007t0003g0237 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-20+8325T>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58996393 | |||||||
| chr15:58996495 | C | T | 1 | a0001c0001t0002g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-20+8427C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58996495 | |||||||
| chr15:58996649 | C | CTTTTT | 7 | a0001c0001t0001g0231 a0001c0001t0003g0007 a0001c0001t0006g0311 others(4): Show |
7 | HG02027.hp2 HG02055.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-20+8606_-20+8610d others(7): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 58996649 | ||||||
| chr15:58996649 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0001g0136 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-20+8601_-20+8610d others(12): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 58996649 | ||||||
| chr15:58996649 | C | T | 1 | a0001c0001t0003g0303 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-20+8581C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58996649 | |||||||
| chr15:58996649 | CTTTTTTT | C | 9 | a0001c0001t0002g0115 a0001c0002t0001g0116 a0001c0002t0001g0117 others(6): Show |
9 | HG00558.hp1 HG02132.hp1 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.-20+8604_-20+8610d others(9): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 58996649 | ||||||
| chr15:58996649 | CTTTTTTT others(1): Show |
C | 129 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(126): Show |
129 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.-20+8603_-20+8610d others(10): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 58996649 | ||||||
| chr15:58996649 | CTTTTTTT others(2): Show |
C | 10 | a0001c0001t0002g0196 a0001c0001t0003g0045 a0001c0001t0008g0287 others(7): Show |
10 | HG01167.hp1 HG01934.hp2 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.-20+8602_-20+8610d others(11): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 58996649 | ||||||
| chr15:58996649 | CTTTTTTT others(3): Show |
C | 120 | a0001c0001t0002g0186 a0001c0001t0002g0188 a0001c0001t0002g0189 others(117): Show |
121 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.-20+8601_-20+8610d others(12): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 58996649 | ||||||
| chr15:58996649 | CTTTTTTT others(4): Show |
C | 4 | a0001c0001t0002g0192 a0001c0001t0002g0244 a0001c0001t0004g0028 others(1): Show |
4 | HG01070.hp2 HG01168.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20+8600_-20+8610d others(13): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 58996649 | ||||||
| chr15:58996678 | T | C | 1 | a0001c0002t0001g0021 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-20+8610T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58996678 | |||||||
| chr15:58996736 | A | G | 1 | a0001c0001t0002g0297 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-20+8668A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58996736 | |||||||
| chr15:58996868 | C | A | 1 | a0001c0002t0003g0276 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-20+8800C>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58996868 | |||||||
| chr15:58997040 | C | T | 2 | a0001c0001t0005g0114 a0001c0001t0005g0169 |
2 | HG01358.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.-20+8972C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58997040 | |||||||
| chr15:58997061 | A | T | 5 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0003g0003 others(2): Show |
5 | HG00741.hp2 HG01168.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20+8993A>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58997061 | |||||||
| chr15:58997130 | A | G | 1 | a0001c0002t0001g0113 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-20+9062A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58997130 | |||||||
| chr15:58997183 | C | G | 1 | a0001c0001t0013g0146 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-20+9115C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58997183 | |||||||
| chr15:58997419 | A | T | 1 | a0001c0001t0003g0045 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-20+9351A>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58997419 | |||||||
| chr15:58997516 | TA | T | 93 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0002g0088 others(90): Show |
93 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.-20+9464delA | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 58997516 | ||||||
| chr15:58997543 | G | A | 1 | a0001c0001t0002g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-20+9475G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58997543 | |||||||
| chr15:58997726 | G | A | 1 | a0001c0001t0003g0306 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-20+9658G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58997726 | |||||||
| chr15:58997772 | C | G | 1 | a0001c0001t0003g0016 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-20+9704C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58997772 | |||||||
| chr15:58997773 | G | A | 1 | a0001c0001t0002g0288 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-20+9705G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58997773 | |||||||
| chr15:58997799 | T | G | 2 | a0001c0001t0003g0327 a0001c0001t0003g0328 |
2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-20+9731T>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58997799 | |||||||
| chr15:58997814 | C | CA | 9 | a0001c0001t0002g0196 a0001c0001t0002g0270 a0001c0001t0002g0299 others(6): Show |
9 | HG00639.hp1 HG01433.hp2 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.-20+9757dupA | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 58997814 | ||||||
| chr15:58998182 | C | T | 1 | a0001c0001t0002g0296 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-20+10114C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58998182 | |||||||
| chr15:58998244 | GT | G | 7 | a0001c0001t0002g0198 a0001c0001t0002g0204 a0001c0001t0003g0015 others(4): Show |
7 | HG01169.hp1 HG06807.hp2 NA18957.hp1 others(4): Show |
intron_variant | MODIFIER | c.-20+10191delT | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 58998244 | ||||||
| chr15:58998346 | C | T | 16 | a0001c0001t0006g0311 a0001c0001t0006g0312 a0001c0001t0006g0313 others(13): Show |
16 | HG01934.hp1 HG01952.hp1 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.-20+10278C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58998346 | |||||||
| chr15:58998430 | G | A | 1 | a0001c0001t0002g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-20+10362G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58998430 | |||||||
| chr15:58998453 | G | A | 157 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0002g0072 others(154): Show |
157 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.-20+10385G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58998453 | |||||||
| chr15:58998547 | A | C | 17 | a0001c0001t0006g0311 a0001c0001t0006g0312 a0001c0001t0006g0313 others(14): Show |
17 | HG01934.hp1 HG01952.hp1 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.-20+10479A>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58998547 | |||||||
| chr15:58998636 | A | C | 1 | a0001c0001t0003g0016 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-20+10568A>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58998636 | |||||||
| chr15:58998706 | A | G | 321 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(318): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.-20+10638A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58998706 | |||||||
| chr15:58998739 | T | C | 4 | a0001c0001t0002g0246 a0001c0001t0003g0049 a0001c0001t0003g0050 others(1): Show |
4 | HG01928.hp2 HG03195.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20+10671T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58998739 | |||||||
| chr15:58998982 | A | G | 1 | a0001c0001t0005g0071 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-20+10914A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58998982 | |||||||
| chr15:58999059 | A | G | 9 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0003g0003 others(6): Show |
9 | HG00741.hp2 HG01168.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-20+10991A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58999059 | |||||||
| chr15:58999106 | T | A | 1 | a0001c0002t0001g0125 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-20+11038T>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58999106 | |||||||
| chr15:58999150 | T | C | 5 | a0001c0001t0007g0011 a0001c0001t0007g0023 a0001c0001t0007g0024 others(2): Show |
5 | HG01167.hp2 HG01169.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-20+11082T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58999150 | |||||||
| chr15:58999173 | A | G | 1 | a0002c0017t0001g0140 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-20+11105A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58999173 | |||||||
| chr15:58999196 | A | T | 1 | a0001c0001t0004g0022 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-20+11128A>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58999196 | |||||||
| chr15:58999400 | A | G | 3 | a0001c0001t0003g0049 a0001c0001t0003g0050 a0001c0001t0003g0051 |
3 | HG03195.hp1 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-20+11332A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58999400 | |||||||
| chr15:58999427 | C | T | 38 | a0001c0001t0002g0200 a0001c0001t0002g0244 a0001c0001t0002g0245 others(35): Show |
38 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(35): Show |
intron_variant | MODIFIER | c.-20+11359C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58999427 | |||||||
| chr15:58999546 | G | A | 1 | a0001c0001t0003g0003 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-20+11478G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58999546 | |||||||
| chr15:58999640 | A | G | 1 | a0002c0003t0001g0083 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-20+11572A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58999640 | |||||||
| chr15:58999768 | T | G | 1 | a0001c0002t0001g0085 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-20+11700T>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 58999768 | |||||||
| chr15:59000017 | A | C | 24 | a0001c0001t0004g0022 a0001c0001t0004g0027 a0001c0001t0004g0028 others(21): Show |
25 | HG00639.hp1 HG01123.hp2 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.-20+11949A>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59000017 | |||||||
| chr15:59000056 | C | T | 1 | a0001c0001t0004g0255 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-20+11988C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59000056 | |||||||
| chr15:59000091 | A | G | 1 | a0001c0002t0001g0084 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-20+12023A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59000091 | |||||||
| chr15:59000161 | C | T | 2 | a0001c0001t0003g0327 a0001c0001t0003g0328 |
2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-20+12093C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59000161 | |||||||
| chr15:59000163 | CT | C | 11 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0003g0003 others(8): Show |
11 | HG00741.hp2 HG01168.hp1 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.-20+12113delT | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59000163 | ||||||
| chr15:59000163 | CTTT | C | 27 | a0001c0001t0002g0014 a0001c0001t0002g0222 a0001c0001t0003g0049 others(24): Show |
27 | HG01167.hp2 HG01169.hp2 HG01934.hp1 others(24): Show |
intron_variant | MODIFIER | c.-20+12111_-20+1211 others(7): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59000163 | ||||||
| chr15:59000163 | CTTTT | C | 135 | a0001c0001t0001g0232 a0001c0001t0001g0241 a0001c0001t0001g0256 others(132): Show |
136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.-20+12110_-20+1211 others(8): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59000163 | ||||||
| chr15:59000167 | T | A | 1 | a0001c0001t0002g0222 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-20+12099T>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59000167 | |||||||
| chr15:59000167 | T | C | 2 | a0001c0001t0003g0327 a0001c0001t0003g0328 |
2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-20+12099T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59000167 | |||||||
| chr15:59000190 | G | T | 1 | a0001c0002t0001g0135 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-20+12122G>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59000190 | |||||||
| chr15:59000470 | G | T | 1 | a0001c0001t0009g0263 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-20+12402G>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59000470 | |||||||
| chr15:59000474 | G | A | 1 | a0001c0001t0017g0294 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-20+12406G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59000474 | |||||||
| chr15:59000475 | G | A | 24 | a0001c0001t0004g0022 a0001c0001t0004g0027 a0001c0001t0004g0028 others(21): Show |
25 | HG00639.hp1 HG01123.hp2 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.-20+12407G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59000475 | |||||||
| chr15:59000642 | G | T | 1 | a0001c0010t0002g0214 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-20+12574G>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59000642 | |||||||
| chr15:59000644 | T | C | 22 | a0001c0001t0006g0311 a0001c0001t0006g0312 a0001c0001t0006g0313 others(19): Show |
22 | HG01167.hp2 HG01169.hp2 HG01934.hp1 others(19): Show |
intron_variant | MODIFIER | c.-20+12576T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59000644 | |||||||
| chr15:59000708 | CA | C | 14 | a0001c0001t0002g0204 a0001c0001t0002g0218 a0001c0001t0002g0251 others(11): Show |
14 | HG01070.hp1 HG01515.hp2 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.-20+12656delA | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59000708 | ||||||
| chr15:59000733 | C | G | 42 | a0001c0001t0002g0186 a0001c0001t0002g0188 a0001c0001t0002g0189 others(39): Show |
42 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.-20+12665C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59000733 | |||||||
| chr15:59000763 | G | A | 5 | a0001c0002t0001g0055 a0001c0002t0001g0086 a0001c0002t0001g0087 others(2): Show |
5 | HG00140.hp1 HG01517.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.-20+12695G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59000763 | |||||||
| chr15:59001228 | TGAG | T | 4 | a0001c0001t0003g0242 a0001c0001t0003g0243 a0001c0001t0003g0278 others(1): Show |
4 | HG02818.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+13167_-20+1316 others(7): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59001228 | ||||||
| chr15:59001242 | G | A | 1 | a0001c0001t0002g0288 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-20+13174G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59001242 | |||||||
| chr15:59001249 | C | T | 1 | a0001c0001t0021g0052 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-20+13181C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59001249 | |||||||
| chr15:59001322 | A | G | 10 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0003g0003 others(7): Show |
10 | HG00741.hp2 HG01168.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-20+13254A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59001322 | |||||||
| chr15:59001406 | A | G | 144 | a0001c0001t0001g0231 a0001c0001t0002g0273 a0001c0001t0003g0230 others(141): Show |
144 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.-20+13338A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59001406 | |||||||
| chr15:59001618 | A | C | 1 | a0001c0001t0017g0294 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-20+13550A>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59001618 | |||||||
| chr15:59001627 | A | G | 3 | a0001c0001t0003g0049 a0001c0001t0003g0050 a0001c0001t0003g0051 |
3 | HG03195.hp1 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-20+13559A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59001627 | |||||||
| chr15:59001632 | A | G | 1 | a0001c0001t0002g0227 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-20+13564A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59001632 | |||||||
| chr15:59001677 | C | G | 9 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0003g0003 others(6): Show |
9 | HG00741.hp2 HG01168.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-20+13609C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59001677 | |||||||
| chr15:59001802 | C | G | 2 | a0002c0003t0001g0082 a0002c0003t0001g0161 |
2 | HG01515.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-20+13734C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59001802 | |||||||
| chr15:59001967 | A | C | 6 | a0001c0002t0001g0109 a0001c0002t0001g0110 a0001c0002t0001g0123 others(3): Show |
6 | HG00609.hp2 HG00621.hp2 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20+13899A>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59001967 | |||||||
| chr15:59001971 | C | T | 4 | a0001c0001t0004g0054 a0001c0001t0004g0300 a0001c0001t0004g0301 others(1): Show |
4 | HG01891.hp2 HG02258.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+13903C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59001971 | |||||||
| chr15:59002046 | A | G | 1 | a0001c0001t0005g0178 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-20+13978A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59002046 | |||||||
| chr15:59002232 | A | G | 1 | a0001c0001t0002g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-20+14164A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59002232 | |||||||
| chr15:59002332 | G | C | 1 | a0001c0001t0004g0255 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-20+14264G>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59002332 | |||||||
| chr15:59002418 | A | C | 310 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(307): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.-20+14350A>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59002418 | |||||||
| chr15:59002544 | G | A | 1 | a0001c0001t0008g0282 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-20+14476G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59002544 | |||||||
| chr15:59002555 | TA | T | 121 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(118): Show |
122 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.-20+14500delA | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59002555 | ||||||
| chr15:59002566 | A | C | 1 | a0004c0012t0002g0194 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-20+14498A>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59002566 | |||||||
| chr15:59002740 | C | T | 3 | a0001c0002t0001g0087 a0001c0002t0001g0112 a0002c0003t0001g0111 |
3 | HG01517.hp1 HG04228.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-20+14672C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59002740 | |||||||
| chr15:59002748 | T | C | 22 | a0001c0001t0006g0311 a0001c0001t0006g0312 a0001c0001t0006g0313 others(19): Show |
22 | HG01167.hp2 HG01169.hp2 HG01934.hp1 others(19): Show |
intron_variant | MODIFIER | c.-20+14680T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59002748 | |||||||
| chr15:59002853 | C | T | 1 | a0001c0001t0002g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-20+14785C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59002853 | |||||||
| chr15:59002951 | G | A | 1 | a0001c0001t0002g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-20+14883G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59002951 | |||||||
| chr15:59003015 | A | T | 1 | a0001c0002t0001g0107 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-20+14947A>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59003015 | |||||||
| chr15:59003025 | C | T | 136 | a0001c0001t0005g0019 a0001c0001t0005g0020 a0001c0001t0005g0071 others(133): Show |
136 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.-20+14957C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59003025 | |||||||
| chr15:59003204 | C | G | 1 | a0001c0001t0002g0091 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-20+15136C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59003204 | |||||||
| chr15:59003288 | A | G | 1 | a0001c0001t0007g0011 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-20+15220A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59003288 | |||||||
| chr15:59003296 | G | A | 1 | a0001c0001t0002g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-20+15228G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59003296 | |||||||
| chr15:59003384 | T | C | 321 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(318): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.-20+15316T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59003384 | |||||||
| chr15:59003417 | G | C | 1 | a0001c0001t0002g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-20+15349G>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59003417 | |||||||
| chr15:59003566 | T | A | 1 | a0002c0003t0001g0083 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-20+15498T>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59003566 | |||||||
| chr15:59003601 | C | G | 1 | a0001c0001t0003g0310 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-20+15533C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59003601 | |||||||
| chr15:59003608 | C | A | 87 | a0001c0001t0007g0234 a0001c0001t0007g0235 a0001c0001t0007g0240 others(84): Show |
87 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-20+15540C>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59003608 | |||||||
| chr15:59003726 | G | A | 9 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0003g0003 others(6): Show |
9 | HG00741.hp2 HG01168.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-20+15658G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59003726 | |||||||
| chr15:59003803 | G | A | 129 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(126): Show |
130 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.-20+15735G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59003803 | |||||||
| chr15:59003877 | C | T | 49 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(46): Show |
49 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.-20+15809C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59003877 | |||||||
| chr15:59003978 | T | C | 1 | a0001c0002t0001g0084 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-20+15910T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59003978 | |||||||
| chr15:59004089 | C | T | 1 | a0001c0001t0002g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-20+16021C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59004089 | |||||||
| chr15:59004143 | A | G | 1 | a0001c0002t0001g0144 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-20+16075A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59004143 | |||||||
| chr15:59004244 | C | G | 3 | a0001c0004t0003g0053 a0001c0004t0003g0262 a0001c0004t0003g0325 |
3 | HG00099.hp1 HG00280.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.-20+16176C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59004244 | |||||||
| chr15:59004292 | G | T | 87 | a0001c0001t0007g0234 a0001c0001t0007g0235 a0001c0001t0007g0240 others(84): Show |
87 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-20+16224G>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59004292 | |||||||
| chr15:59004416 | T | C | 1 | a0001c0001t0002g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-20+16348T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59004416 | |||||||
| chr15:59004489 | G | A | 1 | a0002c0003t0001g0156 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-20+16421G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59004489 | |||||||
| chr15:59004520 | G | C | 1 | a0001c0002t0001g0084 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-20+16452G>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59004520 | |||||||
| chr15:59004639 | T | C | 38 | a0001c0001t0002g0200 a0001c0001t0002g0244 a0001c0001t0002g0245 others(35): Show |
38 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(35): Show |
intron_variant | MODIFIER | c.-20+16571T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59004639 | |||||||
| chr15:59004686 | G | C | 1 | a0001c0001t0002g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-20+16618G>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59004686 | |||||||
| chr15:59004891 | A | G | 1 | a0001c0001t0003g0003 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-20+16823A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59004891 | |||||||
| chr15:59004938 | G | A | 321 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(318): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.-20+16870G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59004938 | |||||||
| chr15:59005061 | A | G | 1 | a0001c0001t0002g0190 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-20+16993A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59005061 | |||||||
| chr15:59005129 | A | G | 51 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(48): Show |
51 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.-20+17061A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59005129 | |||||||
| chr15:59005212 | G | A | 3 | a0001c0001t0003g0049 a0001c0001t0003g0050 a0001c0001t0003g0051 |
3 | HG03195.hp1 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-20+17144G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59005212 | |||||||
| chr15:59005234 | C | G | 1 | a0001c0001t0002g0219 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-20+17166C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59005234 | |||||||
| chr15:59005248 | A | G | 2 | a0001c0001t0014g0046 a0001c0001t0014g0305 |
2 | HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-20+17180A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59005248 | |||||||
| chr15:59005251 | T | C | 3 | a0001c0001t0003g0049 a0001c0001t0003g0050 a0001c0001t0003g0051 |
3 | HG03195.hp1 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-20+17183T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59005251 | |||||||
| chr15:59005300 | C | G | 1 | a0001c0001t0021g0052 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-20+17232C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59005300 | |||||||
| chr15:59005300 | C | T | 1 | a0001c0001t0004g0040 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-20+17232C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59005300 | |||||||
| chr15:59005308 | T | C | 2 | a0001c0001t0014g0046 a0001c0001t0014g0305 |
2 | HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-20+17240T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59005308 | |||||||
| chr15:59005313 | CCAGCCTC others(5): Show |
C | 38 | a0001c0001t0002g0200 a0001c0001t0002g0244 a0001c0001t0002g0245 others(35): Show |
38 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(35): Show |
intron_variant | MODIFIER | c.-20+17248_-20+1725 others(16): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59005313 | ||||||
| chr15:59005499 | C | T | 6 | a0001c0001t0003g0242 a0001c0001t0003g0243 a0001c0001t0003g0268 others(3): Show |
6 | HG02630.hp1 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20+17431C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59005499 | |||||||
| chr15:59005666 | C | T | 1 | a0001c0001t0004g0226 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-20+17598C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59005666 | |||||||
| chr15:59005804 | A | G | 1 | a0001c0001t0003g0016 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-20+17736A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59005804 | |||||||
| chr15:59006034 | G | A | 14 | a0001c0001t0006g0311 a0001c0001t0006g0312 a0001c0001t0006g0313 others(11): Show |
14 | HG01934.hp1 HG01952.hp1 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.-20+17966G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59006034 | |||||||
| chr15:59006071 | C | T | 16 | a0001c0001t0006g0311 a0001c0001t0006g0312 a0001c0001t0006g0313 others(13): Show |
16 | HG01934.hp1 HG01952.hp1 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.-20+18003C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59006071 | |||||||
| chr15:59006231 | A | G | 3 | a0001c0001t0003g0049 a0001c0001t0003g0050 a0001c0001t0003g0051 |
3 | HG03195.hp1 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-20+18163A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59006231 | |||||||
| chr15:59006248 | T | C | 1 | a0001c0002t0001g0092 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-20+18180T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59006248 | |||||||
| chr15:59006393 | A | G | 1 | a0001c0010t0002g0214 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-20+18325A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59006393 | |||||||
| chr15:59006546 | T | A | 2 | a0001c0001t0003g0327 a0001c0001t0003g0328 |
2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-20+18478T>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59006546 | |||||||
| chr15:59006547 | G | A | 2 | a0001c0001t0003g0327 a0001c0001t0003g0328 |
2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-20+18479G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59006547 | |||||||
| chr15:59006557 | C | T | 7 | a0001c0004t0003g0053 a0001c0004t0003g0191 a0001c0004t0003g0202 others(4): Show |
7 | HG00099.hp1 HG00280.hp1 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.-20+18489C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59006557 | |||||||
| chr15:59006703 | A | G | 2 | a0001c0001t0003g0327 a0001c0001t0003g0328 |
2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-20+18635A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59006703 | |||||||
| chr15:59006826 | G | T | 7 | a0001c0004t0003g0053 a0001c0004t0003g0191 a0001c0004t0003g0202 others(4): Show |
7 | HG00099.hp1 HG00280.hp1 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.-20+18758G>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59006826 | |||||||
| chr15:59006889 | C | T | 2 | a0001c0001t0003g0327 a0001c0001t0003g0328 |
2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-20+18821C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59006889 | |||||||
| chr15:59006943 | G | A | 131 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(128): Show |
132 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.-20+18875G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59006943 | |||||||
| chr15:59006974 | A | G | 1 | a0001c0002t0001g0134 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-20+18906A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59006974 | |||||||
| chr15:59006979 | G | A | 16 | a0001c0001t0006g0311 a0001c0001t0006g0312 a0001c0001t0006g0313 others(13): Show |
16 | HG01934.hp1 HG01952.hp1 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.-20+18911G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59006979 | |||||||
| chr15:59007005 | C | A | 1 | a0002c0003t0001g0073 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-20+18937C>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59007005 | |||||||
| chr15:59007065 | C | T | 1 | a0001c0001t0004g0226 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-20+18997C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59007065 | |||||||
| chr15:59007267 | A | AT | 10 | a0001c0001t0001g0137 a0001c0001t0002g0014 a0001c0001t0003g0242 others(7): Show |
10 | HG00741.hp2 HG02630.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.-20+19215dupT | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59007267 | ||||||
| chr15:59007267 | AT | A | 8 | a0001c0001t0002g0193 a0001c0001t0004g0029 a0001c0001t0004g0042 others(5): Show |
8 | HG00099.hp1 HG01258.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.-20+19215delT | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59007267 | ||||||
| chr15:59007451 | A | G | 2 | a0001c0001t0003g0327 a0001c0001t0003g0328 |
2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-20+19383A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59007451 | |||||||
| chr15:59007631 | CAT | C | 10 | a0001c0001t0001g0232 a0001c0001t0001g0241 a0001c0001t0001g0256 others(7): Show |
10 | HG02055.hp1 HG02451.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.-20+19564_-20+1956 others(6): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59007631 | |||||||
| chr15:59007700 | C | G | 4 | a0001c0002t0003g0236 a0001c0002t0003g0238 a0001c0002t0003g0304 others(1): Show |
4 | HG02257.hp2 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+19632C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59007700 | |||||||
| chr15:59007710 | G | A | 6 | a0001c0002t0001g0062 a0001c0002t0001g0063 a0001c0002t0001g0064 others(3): Show |
6 | NA18940.hp1 NA18942.hp1 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20+19642G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59007710 | |||||||
| chr15:59007722 | A | G | 2 | a0001c0001t0003g0327 a0001c0001t0003g0328 |
2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-20+19654A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59007722 | |||||||
| chr15:59007825 | A | G | 5 | a0001c0001t0007g0011 a0001c0001t0007g0023 a0001c0001t0007g0024 others(2): Show |
5 | HG01167.hp2 HG01169.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-20+19757A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59007825 | |||||||
| chr15:59007885 | C | T | 1 | a0001c0001t0002g0292 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-20+19817C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59007885 | |||||||
| chr15:59007989 | C | T | 1 | a0001c0002t0001g0144 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-20+19921C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59007989 | |||||||
| chr15:59008038 | T | C | 2 | a0001c0001t0014g0046 a0001c0001t0014g0305 |
2 | HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-20+19970T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59008038 | |||||||
| chr15:59008248 | T | G | 1 | a0001c0001t0004g0300 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-20+20180T>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59008248 | |||||||
| chr15:59008365 | G | A | 1 | a0001c0002t0001g0144 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-20+20297G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59008365 | |||||||
| chr15:59008417 | C | T | 4 | a0002c0003t0001g0066 a0002c0003t0001g0070 a0002c0003t0001g0073 others(1): Show |
4 | HG00741.hp1 HG01934.hp2 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20+20349C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59008417 | |||||||
| chr15:59008448 | G | C | 2 | a0001c0001t0003g0327 a0001c0001t0003g0328 |
2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-20+20380G>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59008448 | |||||||
| chr15:59008508 | C | T | 1 | a0001c0001t0004g0300 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-20+20440C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59008508 | |||||||
| chr15:59008612 | C | T | 1 | a0001c0002t0001g0144 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-20+20544C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59008612 | |||||||
| chr15:59008637 | A | G | 1 | a0001c0001t0002g0190 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-20+20569A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59008637 | |||||||
| chr15:59008755 | C | G | 1 | a0001c0001t0004g0226 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-20+20687C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59008755 | |||||||
| chr15:59008770 | A | G | 3 | a0001c0001t0003g0049 a0001c0001t0003g0050 a0001c0001t0003g0051 |
3 | HG03195.hp1 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-20+20702A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59008770 | |||||||
| chr15:59008859 | A | G | 7 | a0001c0001t0002g0014 a0001c0001t0003g0242 a0001c0001t0003g0243 others(4): Show |
7 | HG02630.hp1 HG02818.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-20+20791A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59008859 | |||||||
| chr15:59008948 | GTATTTTA others(3): Show |
G | 3 | a0001c0004t0003g0053 a0001c0004t0003g0262 a0001c0004t0003g0325 |
3 | HG00099.hp1 HG00280.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.-20+20897_-20+2090 others(14): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59008948 | ||||||
| chr15:59009161 | A | T | 23 | a0001c0001t0006g0311 a0001c0001t0006g0312 a0001c0001t0006g0313 others(20): Show |
23 | HG01167.hp2 HG01169.hp2 HG01934.hp1 others(20): Show |
intron_variant | MODIFIER | c.-20+21093A>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59009161 | |||||||
| chr15:59009261 | G | A | 5 | a0001c0001t0004g0034 a0001c0001t0004g0036 a0001c0001t0004g0037 others(2): Show |
5 | HG00639.hp1 HG01123.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20+21193G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59009261 | |||||||
| chr15:59009373 | A | G | 2 | a0001c0001t0001g0232 a0001c0001t0001g0259 |
2 | HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-20+21305A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59009373 | |||||||
| chr15:59009412 | A | T | 1 | a0001c0001t0007g0011 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-20+21344A>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59009412 | |||||||
| chr15:59009485 | C | A | 5 | a0001c0001t0007g0011 a0001c0001t0007g0023 a0001c0001t0007g0024 others(2): Show |
5 | HG01167.hp2 HG01169.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19-21319C>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59009485 | |||||||
| chr15:59009535 | G | T | 22 | a0001c0001t0006g0311 a0001c0001t0006g0312 a0001c0001t0006g0313 others(19): Show |
22 | HG01167.hp2 HG01169.hp2 HG01934.hp1 others(19): Show |
intron_variant | MODIFIER | c.-19-21269G>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59009535 | |||||||
| chr15:59009583 | A | ATAGAACG others(10): Show |
6 | a0001c0001t0006g0312 a0001c0001t0006g0313 a0001c0001t0006g0314 others(3): Show |
6 | NA18956.hp1 NA18989.hp2 NA19057.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19-21214_-19-2119 others(21): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59009583 | ||||||
| chr15:59009597 | A | G | 1 | a0001c0002t0003g0239 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-19-21207A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59009597 | |||||||
| chr15:59009633 | G | A | 6 | a0001c0001t0001g0232 a0001c0001t0001g0241 a0001c0001t0001g0256 others(3): Show |
6 | HG02451.hp2 HG02723.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19-21171G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59009633 | |||||||
| chr15:59009703 | T | C | 191 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(188): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.-19-21101T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59009703 | |||||||
| chr15:59009815 | G | A | 1 | a0001c0001t0002g0273 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-19-20989G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59009815 | |||||||
| chr15:59010046 | T | C | 321 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(318): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.-19-20758T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59010046 | |||||||
| chr15:59010263 | G | T | 173 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0002g0014 others(170): Show |
174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.-19-20541G>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59010263 | |||||||
| chr15:59010549 | C | G | 1 | a0001c0002t0001g0151 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-19-20255C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59010549 | |||||||
| chr15:59010668 | T | C | 24 | a0001c0001t0003g0327 a0001c0001t0003g0328 a0001c0001t0006g0311 others(21): Show |
24 | HG01167.hp2 HG01169.hp2 HG01934.hp1 others(21): Show |
intron_variant | MODIFIER | c.-19-20136T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59010668 | |||||||
| chr15:59010908 | T | TTTTGTAA others(54): Show |
1 | a0001c0001t0006g0314 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-19-19894_-19-1983 others(65): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59010908 | ||||||
| chr15:59010995 | G | A | 1 | a0002c0003t0001g0179 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-19-19809G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59010995 | |||||||
| chr15:59011041 | A | T | 1 | a0002c0003t0025g0274 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-19-19763A>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59011041 | |||||||
| chr15:59011156 | G | A | 16 | a0001c0001t0006g0311 a0001c0001t0006g0312 a0001c0001t0006g0313 others(13): Show |
16 | HG01934.hp1 HG01952.hp1 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.-19-19648G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59011156 | |||||||
| chr15:59011205 | T | C | 2 | a0001c0001t0003g0327 a0001c0001t0003g0328 |
2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-19-19599T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59011205 | |||||||
| chr15:59011285 | C | T | 2 | a0001c0001t0003g0327 a0001c0001t0003g0328 |
2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-19-19519C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59011285 | |||||||
| chr15:59011809 | G | T | 1 | a0002c0003t0024g0177 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-19-18995G>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59011809 | |||||||
| chr15:59011920 | G | A | 1 | a0001c0010t0002g0214 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-19-18884G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59011920 | |||||||
| chr15:59011949 | T | G | 1 | a0001c0001t0005g0178 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-19-18855T>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59011949 | |||||||
| chr15:59011953 | T | TTA | 3 | a0001c0001t0003g0049 a0001c0001t0003g0050 a0001c0001t0003g0051 |
3 | HG03195.hp1 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-19-18846_-19-1884 others(6): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59011953 | ||||||
| chr15:59011981 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-19-18823G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59011981 | |||||||
| chr15:59012003 | C | CT | 7 | a0001c0001t0004g0027 a0001c0001t0004g0028 a0001c0001t0004g0029 others(4): Show |
7 | HG01346.hp1 HG01496.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19-18772dupT | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59012003 | ||||||
| chr15:59012003 | C | CTT | 19 | a0001c0001t0004g0032 a0001c0001t0004g0033 a0001c0001t0004g0034 others(16): Show |
19 | HG00639.hp1 HG01123.hp2 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.-19-18773_-19-1877 others(6): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59012003 | ||||||
| chr15:59012003 | C | CTTT | 6 | a0001c0001t0003g0326 a0001c0001t0004g0022 a0001c0001t0004g0037 others(3): Show |
7 | HG01175.hp2 HG01192.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19-18774_-19-1877 others(7): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59012003 | ||||||
| chr15:59012003 | C | CTTTTT | 7 | a0001c0001t0002g0272 a0001c0001t0002g0273 a0001c0001t0002g0292 others(4): Show |
7 | HG03195.hp1 HG03225.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19-18776_-19-1877 others(9): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59012003 | ||||||
| chr15:59012003 | C | CTTTTTT | 33 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0091 others(30): Show |
33 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(30): Show |
intron_variant | MODIFIER | c.-19-18777_-19-1877 others(10): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59012003 | ||||||
| chr15:59012003 | C | CTTTTTTT | 44 | a0001c0001t0001g0136 a0001c0001t0002g0089 a0001c0001t0002g0090 others(41): Show |
44 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.-19-18778_-19-1877 others(11): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59012003 | ||||||
| chr15:59012003 | C | CTTTTTTT others(1): Show |
17 | a0001c0001t0002g0188 a0001c0001t0002g0195 a0001c0001t0002g0196 others(14): Show |
17 | HG00438.hp2 HG00544.hp1 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.-19-18779_-19-1877 others(12): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59012003 | ||||||
| chr15:59012003 | C | CTTTTTTT others(4): Show |
2 | a0001c0001t0007g0025 a0001c0001t0007g0026 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-19-18782_-19-1877 others(15): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59012003 | ||||||
| chr15:59012003 | C | CTTTTTTT others(5): Show |
3 | a0001c0001t0007g0011 a0001c0001t0007g0023 a0001c0001t0007g0024 |
3 | HG02615.hp1 HG02970.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-19-18783_-19-1877 others(16): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59012003 | ||||||
| chr15:59012003 | C | CTTTTTTT others(7): Show |
1 | a0001c0001t0016g0008 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-19-18785_-19-1877 others(18): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59012003 | ||||||
| chr15:59012003 | C | CTTTTTTT others(14): Show |
1 | a0001c0001t0001g0231 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-19-18792_-19-1877 others(25): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59012003 | ||||||
| chr15:59012003 | C | CTTTTTTT others(15): Show |
1 | a0001c0001t0003g0230 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-19-18793_-19-1877 others(26): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59012003 | ||||||
| chr15:59012003 | CT | C | 104 | a0001c0001t0003g0310 a0001c0002t0001g0021 a0001c0002t0001g0055 others(101): Show |
104 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.-19-18772delT | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59012003 | ||||||
| chr15:59012003 | CTTTTTTT | C | 22 | a0001c0001t0002g0205 a0001c0001t0002g0275 a0001c0001t0003g0003 others(19): Show |
22 | HG01934.hp1 HG01952.hp1 HG02027.hp2 others(19): Show |
intron_variant | MODIFIER | c.-19-18778_-19-1877 others(11): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59012003 | ||||||
| chr15:59012003 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0003g0016 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-19-18782_-19-1877 others(15): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59012003 | ||||||
| chr15:59012003 | CTTTTTTT others(5): Show |
C | 9 | a0001c0001t0002g0014 a0001c0001t0003g0243 a0001c0001t0003g0268 others(6): Show |
9 | HG02109.hp1 HG02630.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.-19-18783_-19-1877 others(16): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59012003 | ||||||
| chr15:59012003 | CTTTTTTT others(6): Show |
C | 3 | a0001c0001t0002g0246 a0001c0001t0003g0242 a0001c0002t0003g0239 |
3 | HG01928.hp2 HG02258.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-19-18784_-19-1877 others(17): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59012003 | ||||||
| chr15:59012003 | CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0002g0209 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-19-18786_-19-1877 others(19): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59012003 | ||||||
| chr15:59012003 | CTTTTTTT others(10): Show |
C | 2 | a0001c0001t0003g0327 a0001c0001t0003g0328 |
2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-19-18788_-19-1877 others(21): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59012003 | ||||||
| chr15:59012061 | C | T | 5 | a0001c0001t0007g0011 a0001c0001t0007g0023 a0001c0001t0007g0024 others(2): Show |
5 | HG01167.hp2 HG01169.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19-18743C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59012061 | |||||||
| chr15:59012178 | C | T | 1 | a0002c0003t0001g0082 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-19-18626C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59012178 | |||||||
| chr15:59012179 | C | T | 1 | a0001c0001t0002g0216 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-19-18625C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59012179 | |||||||
| chr15:59012199 | A | G | 1 | a0001c0001t0004g0226 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-19-18605A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59012199 | |||||||
| chr15:59012307 | C | T | 13 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0241 others(10): Show |
13 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19-18497C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59012307 | |||||||
| chr15:59012400 | A | G | 1 | a0001c0001t0003g0015 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-19-18404A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59012400 | |||||||
| chr15:59012436 | C | T | 195 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(192): Show |
196 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.-19-18368C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59012436 | |||||||
| chr15:59012500 | C | T | 19 | a0001c0001t0006g0311 a0001c0001t0006g0312 a0001c0001t0006g0313 others(16): Show |
19 | HG01952.hp1 HG02027.hp2 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.-19-18304C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59012500 | |||||||
| chr15:59012591 | A | T | 7 | a0001c0004t0003g0053 a0001c0004t0003g0191 a0001c0004t0003g0202 others(4): Show |
7 | HG00099.hp1 HG00280.hp1 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19-18213A>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59012591 | |||||||
| chr15:59012743 | C | CT | 136 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(133): Show |
137 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.-19-18048dupT | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59012743 | ||||||
| chr15:59012743 | C | CTT | 6 | a0001c0001t0002g0206 a0001c0001t0004g0054 a0001c0001t0004g0300 others(3): Show |
6 | HG01256.hp2 HG01258.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19-18049_-19-1804 others(6): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59012743 | ||||||
| chr15:59012889 | A | C | 191 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0241 others(188): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.-19-17915A>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59012889 | |||||||
| chr15:59012945 | G | A | 1 | a0001c0001t0004g0038 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-19-17859G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59012945 | |||||||
| chr15:59013018 | C | T | 19 | a0001c0001t0006g0311 a0001c0001t0006g0312 a0001c0001t0006g0313 others(16): Show |
19 | HG01952.hp1 HG02027.hp2 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.-19-17786C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59013018 | |||||||
| chr15:59013024 | C | G | 1 | a0002c0003t0001g0080 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-19-17780C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59013024 | |||||||
| chr15:59013138 | C | T | 2 | a0001c0001t0010g0056 a0005c0011t0010g0057 |
2 | HG02735.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.-19-17666C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59013138 | |||||||
| chr15:59013167 | A | C | 7 | a0001c0001t0002g0014 a0001c0001t0003g0242 a0001c0001t0003g0243 others(4): Show |
7 | HG02630.hp1 HG02818.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19-17637A>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59013167 | |||||||
| chr15:59013313 | A | G | 25 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0241 others(22): Show |
25 | HG01167.hp2 HG01169.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.-19-17491A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59013313 | |||||||
| chr15:59013321 | C | A | 16 | a0001c0001t0006g0311 a0001c0001t0006g0312 a0001c0001t0006g0313 others(13): Show |
16 | HG01952.hp1 HG02027.hp2 HG02523.hp2 others(13): Show |
intron_variant | MODIFIER | c.-19-17483C>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59013321 | |||||||
| chr15:59013331 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-19-17473C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59013331 | |||||||
| chr15:59013500 | G | T | 1 | a0001c0001t0006g0314 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-19-17304G>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59013500 | |||||||
| chr15:59013707 | C | T | 17 | a0001c0001t0001g0232 a0001c0001t0001g0241 a0001c0001t0001g0256 others(14): Show |
17 | HG01167.hp2 HG01169.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.-19-17097C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59013707 | |||||||
| chr15:59013822 | T | C | 2 | a0001c0001t0002g0289 a0001c0001t0002g0291 |
2 | HG03654.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-19-16982T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59013822 | |||||||
| chr15:59013902 | C | A | 2 | a0001c0001t0003g0327 a0001c0001t0003g0328 |
2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-19-16902C>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59013902 | |||||||
| chr15:59013913 | C | G | 19 | a0001c0001t0006g0311 a0001c0001t0006g0312 a0001c0001t0006g0313 others(16): Show |
19 | HG01952.hp1 HG02027.hp2 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.-19-16891C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59013913 | |||||||
| chr15:59013949 | T | C | 191 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0241 others(188): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.-19-16855T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59013949 | |||||||
| chr15:59014030 | A | G | 1 | a0001c0008t0002g0197 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-19-16774A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59014030 | |||||||
| chr15:59014054 | A | G | 192 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0241 others(189): Show |
193 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.-19-16750A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59014054 | |||||||
| chr15:59014120 | A | G | 1 | a0002c0003t0001g0081 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-19-16684A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59014120 | |||||||
| chr15:59014125 | A | G | 27 | a0001c0001t0004g0022 a0001c0001t0004g0027 a0001c0001t0004g0028 others(24): Show |
28 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(25): Show |
intron_variant | MODIFIER | c.-19-16679A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59014125 | |||||||
| chr15:59014169 | G | C | 1 | a0001c0001t0003g0268 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-19-16635G>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59014169 | |||||||
| chr15:59014296 | T | C | 6 | a0001c0001t0003g0242 a0001c0001t0003g0243 a0001c0001t0003g0268 others(3): Show |
6 | HG02630.hp1 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-16508T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59014296 | |||||||
| chr15:59014581 | A | G | 200 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(197): Show |
201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.-19-16223A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59014581 | |||||||
| chr15:59014758 | C | CT | 12 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0003g0003 others(9): Show |
12 | HG00741.hp2 HG01168.hp1 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.-19-16030dupT | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59014758 | ||||||
| chr15:59014865 | C | T | 6 | a0001c0002t0001g0109 a0001c0002t0001g0110 a0001c0002t0001g0123 others(3): Show |
6 | HG00609.hp2 HG00621.hp2 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-15939C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59014865 | |||||||
| chr15:59014995 | T | C | 1 | a0002c0003t0001g0073 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-19-15809T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59014995 | |||||||
| chr15:59015008 | G | A | 1 | a0001c0001t0007g0011 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-19-15796G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59015008 | |||||||
| chr15:59015197 | T | A | 1 | a0001c0001t0006g0314 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-19-15607T>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59015197 | |||||||
| chr15:59015198 | A | T | 1 | a0001c0001t0006g0314 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-19-15606A>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59015198 | |||||||
| chr15:59015472 | C | T | 1 | a0001c0002t0001g0138 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-19-15332C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59015472 | |||||||
| chr15:59015578 | A | C | 7 | a0001c0001t0002g0014 a0001c0001t0003g0242 a0001c0001t0003g0243 others(4): Show |
7 | HG02630.hp1 HG02818.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19-15226A>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59015578 | |||||||
| chr15:59015745 | A | G | 3 | a0001c0001t0003g0049 a0001c0001t0003g0050 a0001c0001t0003g0051 |
3 | HG03195.hp1 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-19-15059A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59015745 | |||||||
| chr15:59015818 | A | G | 1 | a0001c0001t0004g0031 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-19-14986A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59015818 | |||||||
| chr15:59015886 | C | A | 1 | a0001c0001t0004g0041 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-19-14918C>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59015886 | |||||||
| chr15:59015896 | G | C | 3 | a0001c0002t0001g0121 a0001c0005t0005g0096 a0001c0005t0005g0120 |
3 | NA18998.hp1 NA19090.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.-19-14908G>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59015896 | |||||||
| chr15:59016008 | A | G | 197 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(194): Show |
198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.-19-14796A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59016008 | |||||||
| chr15:59016145 | T | C | 1 | a0002c0003t0001g0017 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-19-14659T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59016145 | |||||||
| chr15:59016154 | A | T | 1 | a0001c0001t0003g0016 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-19-14650A>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59016154 | |||||||
| chr15:59016162 | G | GTA | 9 | a0001c0001t0002g0072 a0001c0001t0002g0089 a0001c0001t0002g0090 others(6): Show |
9 | HG01168.hp2 HG01169.hp1 NA18951.hp1 others(6): Show |
intron_variant | MODIFIER | c.-19-14631_-19-1463 others(6): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59016162 | ||||||
| chr15:59016175 | G | GT | 7 | a0001c0001t0002g0190 a0001c0001t0002g0209 a0001c0001t0004g0042 others(4): Show |
7 | HG00639.hp2 HG06807.hp2 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19-14617dupT | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59016175 | ||||||
| chr15:59016316 | C | T | 6 | a0001c0001t0001g0232 a0001c0001t0001g0241 a0001c0001t0001g0256 others(3): Show |
6 | HG02451.hp2 HG02723.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19-14488C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59016316 | |||||||
| chr15:59016500 | C | G | 2 | a0001c0001t0006g0321 a0001c0001t0006g0322 |
2 | NA19057.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.-19-14304C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59016500 | |||||||
| chr15:59016739 | G | C | 5 | a0002c0003t0001g0074 a0002c0003t0001g0075 a0002c0003t0001g0076 others(2): Show |
5 | HG00733.hp1 HG01106.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19-14065G>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59016739 | |||||||
| chr15:59016768 | G | A | 6 | a0001c0001t0003g0242 a0001c0001t0003g0243 a0001c0001t0003g0268 others(3): Show |
6 | HG02630.hp1 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-14036G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59016768 | |||||||
| chr15:59016939 | T | G | 186 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0241 others(183): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.-19-13865T>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59016939 | |||||||
| chr15:59016990 | C | G | 1 | a0001c0002t0001g0134 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-19-13814C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59016990 | |||||||
| chr15:59017092 | A | G | 22 | a0001c0001t0006g0311 a0001c0001t0006g0312 a0001c0001t0006g0313 others(19): Show |
22 | HG01167.hp2 HG01169.hp2 HG01934.hp1 others(19): Show |
intron_variant | MODIFIER | c.-19-13712A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59017092 | |||||||
| chr15:59017160 | G | A | 2 | a0001c0001t0002g0217 a0007c0014t0001g0131 |
2 | NA19012.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.-19-13644G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59017160 | |||||||
| chr15:59017274 | C | T | 193 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(190): Show |
194 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.-19-13530C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59017274 | |||||||
| chr15:59017311 | T | C | 9 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0003g0003 others(6): Show |
9 | HG00741.hp2 HG01168.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-19-13493T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59017311 | |||||||
| chr15:59017572 | A | G | 2 | a0002c0003t0001g0075 a0002c0003t0001g0076 |
2 | HG00733.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.-19-13232A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59017572 | |||||||
| chr15:59017753 | C | CT | 35 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(32): Show |
35 | HG00741.hp2 HG01167.hp2 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.-19-13030dupT | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59017753 | ||||||
| chr15:59017753 | C | CTTTTTTT | 30 | a0001c0001t0004g0022 a0001c0001t0004g0027 a0001c0001t0004g0028 others(27): Show |
31 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.-19-13036_-19-1303 others(11): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59017753 | ||||||
| chr15:59017753 | C | CTTTTTTT others(2): Show |
12 | a0001c0001t0006g0312 a0001c0001t0006g0313 a0001c0001t0006g0319 others(9): Show |
12 | HG01934.hp1 HG01952.hp1 HG02027.hp2 others(9): Show |
intron_variant | MODIFIER | c.-19-13038_-19-1303 others(13): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59017753 | ||||||
| chr15:59017753 | C | CTTTTTTT others(3): Show |
3 | a0001c0001t0006g0311 a0001c0001t0013g0145 a0002c0016t0006g0173 |
3 | HG02523.hp2 HG03942.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.-19-13039_-19-1303 others(14): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59017753 | ||||||
| chr15:59017753 | CTTTTTTT others(1): Show |
C | 104 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(101): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.-19-13037_-19-1303 others(12): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59017753 | ||||||
| chr15:59017783 | G | T | 1 | a0002c0003t0001g0083 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-19-13021G>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59017783 | |||||||
| chr15:59017807 | G | T | 1 | a0001c0001t0013g0146 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-19-12997G>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59017807 | |||||||
| chr15:59017880 | C | T | 1 | a0001c0002t0001g0167 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-19-12924C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59017880 | |||||||
| chr15:59017888 | G | A | 137 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(134): Show |
138 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.-19-12916G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59017888 | |||||||
| chr15:59017947 | C | T | 152 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0088 others(149): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.-19-12857C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59017947 | |||||||
| chr15:59017979 | G | A | 1 | a0001c0001t0002g0266 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-19-12825G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59017979 | |||||||
| chr15:59018051 | G | A | 1 | a0001c0002t0001g0103 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-19-12753G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59018051 | |||||||
| chr15:59018053 | C | A | 137 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(134): Show |
138 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.-19-12751C>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59018053 | |||||||
| chr15:59018054 | C | T | 3 | a0001c0001t0003g0306 a0001c0001t0003g0307 a0001c0001t0003g0308 |
3 | HG03225.hp1 HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-19-12750C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59018054 | |||||||
| chr15:59018169 | G | A | 3 | a0001c0001t0003g0306 a0001c0001t0003g0307 a0001c0001t0003g0308 |
3 | HG03225.hp1 HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-19-12635G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59018169 | |||||||
| chr15:59018171 | G | A | 6 | a0001c0001t0003g0242 a0001c0001t0003g0243 a0001c0001t0003g0268 others(3): Show |
6 | HG02630.hp1 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-12633G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59018171 | |||||||
| chr15:59018181 | T | G | 2 | a0001c0001t0014g0046 a0001c0001t0014g0305 |
2 | HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-19-12623T>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59018181 | |||||||
| chr15:59018269 | C | G | 2 | a0001c0001t0002g0266 a0001c0001t0003g0261 |
2 | HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-19-12535C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59018269 | |||||||
| chr15:59018330 | G | A | 19 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0241 others(16): Show |
19 | HG02055.hp1 HG02258.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.-19-12474G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59018330 | |||||||
| chr15:59018377 | C | G | 7 | a0001c0004t0003g0053 a0001c0004t0003g0191 a0001c0004t0003g0202 others(4): Show |
7 | HG00099.hp1 HG00280.hp1 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19-12427C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59018377 | |||||||
| chr15:59018403 | G | C | 2 | a0001c0002t0003g0013 a0001c0002t0012g0012 |
2 | HG02257.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-19-12401G>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59018403 | |||||||
| chr15:59018486 | A | T | 1 | a0001c0001t0009g0199 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-19-12318A>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59018486 | |||||||
| chr15:59018488 | G | A | 6 | a0001c0001t0003g0242 a0001c0001t0003g0243 a0001c0001t0003g0268 others(3): Show |
6 | HG02630.hp1 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-12316G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59018488 | |||||||
| chr15:59018500 | T | C | 1 | a0001c0002t0003g0147 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-19-12304T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59018500 | |||||||
| chr15:59018551 | G | GA | 21 | a0001c0001t0006g0311 a0001c0001t0006g0312 a0001c0001t0006g0313 others(18): Show |
21 | HG01167.hp2 HG01169.hp2 HG01934.hp1 others(18): Show |
intron_variant | MODIFIER | c.-19-12245dupA | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59018551 | ||||||
| chr15:59018693 | C | T | 1 | a0001c0001t0002g0200 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-19-12111C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59018693 | |||||||
| chr15:59018782 | C | T | 3 | a0001c0001t0003g0049 a0001c0001t0003g0050 a0001c0001t0003g0051 |
3 | HG03195.hp1 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-19-12022C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59018782 | |||||||
| chr15:59018963 | G | T | 27 | a0001c0001t0004g0022 a0001c0001t0004g0027 a0001c0001t0004g0028 others(24): Show |
28 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(25): Show |
intron_variant | MODIFIER | c.-19-11841G>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59018963 | |||||||
| chr15:59019016 | C | T | 15 | a0001c0001t0006g0311 a0001c0001t0006g0312 a0001c0001t0006g0313 others(12): Show |
15 | HG01934.hp1 HG01952.hp1 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.-19-11788C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59019016 | |||||||
| chr15:59019065 | A | T | 2 | a0001c0001t0014g0046 a0001c0001t0014g0305 |
2 | HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-19-11739A>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59019065 | |||||||
| chr15:59019103 | G | T | 1 | a0001c0001t0006g0313 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-19-11701G>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59019103 | |||||||
| chr15:59019105 | A | ATTTTTTT | 12 | a0001c0001t0006g0312 a0001c0001t0006g0314 a0001c0001t0006g0319 others(9): Show |
12 | HG01934.hp1 HG01952.hp1 HG02027.hp2 others(9): Show |
intron_variant | MODIFIER | c.-19-11688_-19-1168 others(11): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59019105 | ||||||
| chr15:59019105 | A | ATTTTTTT others(3): Show |
1 | a0001c0001t0002g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-19-11691_-19-1168 others(14): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59019105 | ||||||
| chr15:59019105 | A | T | 1 | a0001c0001t0006g0313 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-19-11699A>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59019105 | |||||||
| chr15:59019105 | AT | A | 145 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0002g0072 others(142): Show |
146 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.-19-11682delT | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59019105 | ||||||
| chr15:59019244 | ATTAAGTT others(16): Show |
A | 1 | a0001c0001t0006g0314 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-19-11558_-19-1153 others(27): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59019244 | ||||||
| chr15:59019250 | T | G | 1 | a0001c0002t0001g0134 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-19-11554T>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59019250 | |||||||
| chr15:59019378 | G | A | 1 | a0001c0002t0001g0126 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-19-11426G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59019378 | |||||||
| chr15:59019485 | G | A | 1 | a0001c0001t0008g0287 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-19-11319G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59019485 | |||||||
| chr15:59019557 | A | ATTCTTGT others(7): Show |
195 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(192): Show |
196 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.-19-11234_-19-1123 others(18): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59019557 | ||||||
| chr15:59019684 | C | T | 137 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(134): Show |
138 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.-19-11120C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59019684 | |||||||
| chr15:59019763 | G | A | 5 | a0002c0003t0001g0156 a0002c0003t0001g0174 a0002c0003t0001g0175 others(2): Show |
5 | HG00140.hp2 HG00639.hp2 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19-11041G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59019763 | |||||||
| chr15:59019771 | C | G | 1 | a0002c0017t0001g0140 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-19-11033C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59019771 | |||||||
| chr15:59019783 | A | G | 1 | a0001c0001t0003g0310 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-19-11021A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59019783 | |||||||
| chr15:59019818 | G | T | 5 | a0001c0002t0003g0236 a0001c0002t0003g0238 a0001c0002t0003g0277 others(2): Show |
5 | HG02257.hp2 HG02717.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-19-10986G>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59019818 | |||||||
| chr15:59019875 | C | T | 138 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0088 others(135): Show |
139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.-19-10929C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59019875 | |||||||
| chr15:59019913 | C | T | 7 | a0001c0002t0001g0117 a0001c0002t0001g0180 a0001c0002t0001g0181 others(4): Show |
7 | HG00558.hp1 HG03654.hp1 NA18943.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19-10891C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59019913 | |||||||
| chr15:59019925 | C | T | 138 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0088 others(135): Show |
139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.-19-10879C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59019925 | |||||||
| chr15:59020048 | C | T | 1 | a0001c0001t0003g0261 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-19-10756C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59020048 | |||||||
| chr15:59020134 | TTA | T | 3 | a0001c0001t0004g0054 a0001c0001t0004g0301 a0001c0001t0004g0302 |
3 | HG01891.hp2 HG02451.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-19-10664_-19-1066 others(6): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59020134 | ||||||
| chr15:59020209 | T | G | 1 | a0001c0001t0002g0224 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-19-10595T>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59020209 | |||||||
| chr15:59020226 | A | G | 1 | a0001c0001t0002g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-19-10578A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59020226 | |||||||
| chr15:59020689 | G | A | 136 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(133): Show |
137 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.-19-10115G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59020689 | |||||||
| chr15:59020751 | G | A | 1 | a0001c0002t0001g0086 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-19-10053G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59020751 | |||||||
| chr15:59020976 | G | A | 9 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0003g0003 others(6): Show |
9 | HG00741.hp2 HG01168.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-19-9828G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59020976 | |||||||
| chr15:59021231 | A | G | 1 | a0001c0001t0002g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-19-9573A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59021231 | |||||||
| chr15:59021235 | C | G | 1 | a0001c0002t0001g0100 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-19-9569C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59021235 | |||||||
| chr15:59021381 | C | T | 2 | a0001c0001t0009g0199 a0001c0001t0009g0263 |
2 | HG02109.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-19-9423C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59021381 | |||||||
| chr15:59021402 | C | T | 1 | a0001c0001t0004g0226 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-19-9402C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59021402 | |||||||
| chr15:59021445 | C | T | 2 | a0003c0006t0006g0315 a0003c0006t0006g0317 |
2 | HG01934.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.-19-9359C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59021445 | |||||||
| chr15:59021526 | T | A | 1 | a0001c0001t0002g0295 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-19-9278T>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59021526 | |||||||
| chr15:59021626 | G | A | 2 | a0002c0003t0001g0066 a0002c0003t0001g0073 |
2 | HG00741.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.-19-9178G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59021626 | |||||||
| chr15:59021629 | C | CTAT | 3 | a0001c0002t0001g0125 a0001c0002t0001g0126 a0001c0002t0001g0171 |
3 | HG01496.hp2 HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-19-9167_-19-9165d others(5): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59021629 | ||||||
| chr15:59021656 | A | G | 199 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(196): Show |
200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.-19-9148A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59021656 | |||||||
| chr15:59021728 | G | A | 182 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0241 others(179): Show |
183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.-19-9076G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59021728 | |||||||
| chr15:59021895 | C | T | 1 | a0001c0001t0002g0295 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-19-8909C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59021895 | |||||||
| chr15:59022199 | T | A | 16 | a0001c0001t0006g0311 a0001c0001t0006g0312 a0001c0001t0006g0313 others(13): Show |
16 | HG01934.hp1 HG01952.hp1 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.-19-8605T>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59022199 | |||||||
| chr15:59022359 | G | A | 52 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(49): Show |
52 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.-19-8445G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59022359 | |||||||
| chr15:59022364 | G | C | 186 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0241 others(183): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.-19-8440G>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59022364 | |||||||
| chr15:59022365 | G | A | 1 | a0002c0003t0001g0139 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-19-8439G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59022365 | |||||||
| chr15:59022754 | G | A | 1 | a0001c0001t0002g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-19-8050G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59022754 | |||||||
| chr15:59022974 | C | T | 1 | a0001c0002t0001g0166 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-19-7830C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59022974 | |||||||
| chr15:59022985 | G | A | 1 | a0001c0001t0007g0023 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-19-7819G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59022985 | |||||||
| chr15:59023109 | A | G | 9 | a0001c0001t0002g0244 a0001c0001t0002g0245 a0001c0001t0002g0246 others(6): Show |
9 | HG00408.hp2 HG00438.hp2 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.-19-7695A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59023109 | |||||||
| chr15:59023115 | G | C | 154 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0088 others(151): Show |
155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.-19-7689G>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59023115 | |||||||
| chr15:59023119 | G | A | 2 | a0001c0001t0014g0046 a0001c0001t0014g0305 |
2 | HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-19-7685G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59023119 | |||||||
| chr15:59023351 | G | A | 15 | a0001c0001t0006g0312 a0001c0001t0006g0313 a0001c0001t0006g0314 others(12): Show |
15 | HG01934.hp1 HG01952.hp1 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.-19-7453G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59023351 | |||||||
| chr15:59023436 | C | A | 39 | a0001c0001t0002g0200 a0001c0001t0002g0244 a0001c0001t0002g0245 others(36): Show |
39 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.-19-7368C>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59023436 | |||||||
| chr15:59023469 | G | T | 9 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0003g0003 others(6): Show |
9 | HG00741.hp2 HG01168.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-19-7335G>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59023469 | |||||||
| chr15:59023534 | TTA | T | 139 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(136): Show |
140 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.-19-7264_-19-7263d others(4): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59023534 | ||||||
| chr15:59023603 | G | A | 1 | a0001c0001t0003g0310 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-19-7201G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59023603 | |||||||
| chr15:59023685 | G | C | 155 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0088 others(152): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.-19-7119G>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59023685 | |||||||
| chr15:59023702 | G | A | 15 | a0001c0001t0006g0312 a0001c0001t0006g0313 a0001c0001t0006g0314 others(12): Show |
15 | HG01934.hp1 HG01952.hp1 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.-19-7102G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59023702 | |||||||
| chr15:59023956 | T | G | 2 | a0001c0001t0014g0046 a0001c0001t0014g0305 |
2 | HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-19-6848T>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59023956 | |||||||
| chr15:59024062 | G | A | 1 | a0002c0017t0001g0140 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-19-6742G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59024062 | |||||||
| chr15:59024146 | A | G | 2 | a0001c0001t0004g0041 a0001c0001t0004g0254 |
2 | HG01192.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-19-6658A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59024146 | |||||||
| chr15:59024156 | A | T | 1 | a0002c0003t0001g0128 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-19-6648A>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59024156 | |||||||
| chr15:59024296 | T | C | 1 | a0001c0001t0004g0226 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-19-6508T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59024296 | |||||||
| chr15:59024462 | C | CAGTTAGT | 248 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(245): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.-19-6340_-19-6339i others(9): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59024462 | ||||||
| chr15:59024519 | A | AT | 5 | a0001c0001t0007g0011 a0001c0001t0007g0023 a0001c0001t0007g0024 others(2): Show |
5 | HG01167.hp2 HG01169.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19-6279dupT | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59024519 | ||||||
| chr15:59024544 | G | C | 1 | a0001c0001t0007g0024 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-19-6260G>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59024544 | |||||||
| chr15:59024811 | T | A | 7 | a0001c0002t0001g0117 a0001c0002t0001g0180 a0001c0002t0001g0181 others(4): Show |
7 | HG00558.hp1 HG03654.hp1 NA18943.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19-5993T>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59024811 | |||||||
| chr15:59024837 | C | G | 1 | a0001c0001t0016g0008 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-19-5967C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59024837 | |||||||
| chr15:59024909 | A | G | 2 | a0001c0001t0003g0268 a0001c0001t0003g0279 |
2 | HG02630.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-19-5895A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59024909 | |||||||
| chr15:59024940 | T | C | 1 | a0001c0002t0001g0135 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-19-5864T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59024940 | |||||||
| chr15:59024959 | A | G | 1 | a0001c0004t0003g0325 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-19-5845A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59024959 | |||||||
| chr15:59025159 | A | G | 2 | a0001c0001t0003g0327 a0001c0001t0003g0328 |
2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-19-5645A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59025159 | |||||||
| chr15:59025165 | G | A | 1 | a0001c0004t0003g0053 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-19-5639G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59025165 | |||||||
| chr15:59025271 | A | G | 1 | a0001c0001t0003g0308 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-19-5533A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59025271 | |||||||
| chr15:59025319 | C | G | 1 | a0001c0010t0002g0214 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-19-5485C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59025319 | |||||||
| chr15:59025488 | G | T | 2 | a0001c0001t0002g0200 a0001c0001t0002g0271 |
2 | HG01261.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-19-5316G>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59025488 | |||||||
| chr15:59025814 | G | T | 198 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(195): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.-19-4990G>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59025814 | |||||||
| chr15:59025834 | G | A | 1 | a0001c0002t0001g0097 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-19-4970G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59025834 | |||||||
| chr15:59025945 | G | C | 3 | a0001c0001t0003g0049 a0001c0001t0003g0050 a0001c0001t0003g0051 |
3 | HG03195.hp1 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-19-4859G>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59025945 | |||||||
| chr15:59026029 | C | T | 7 | a0001c0001t0002g0244 a0001c0001t0002g0245 a0001c0001t0002g0246 others(4): Show |
7 | HG01069.hp1 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19-4775C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59026029 | |||||||
| chr15:59026032 | C | CT | 6 | a0001c0001t0001g0232 a0001c0001t0001g0241 a0001c0001t0001g0256 others(3): Show |
6 | HG02451.hp2 HG02723.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19-4761dupT | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59026032 | ||||||
| chr15:59026193 | A | G | 1 | a0001c0001t0014g0046 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-19-4611A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59026193 | |||||||
| chr15:59026211 | T | G | 19 | a0001c0001t0006g0312 a0001c0001t0006g0313 a0001c0001t0006g0314 others(16): Show |
19 | HG01934.hp1 HG01952.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.-19-4593T>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59026211 | |||||||
| chr15:59026268 | C | A | 19 | a0001c0001t0006g0312 a0001c0001t0006g0313 a0001c0001t0006g0314 others(16): Show |
19 | HG01934.hp1 HG01952.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.-19-4536C>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59026268 | |||||||
| chr15:59026532 | T | G | 2 | a0001c0001t0002g0266 a0001c0001t0003g0261 |
2 | HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-19-4272T>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59026532 | |||||||
| chr15:59026723 | G | GA | 140 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(137): Show |
141 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.-19-4072dupA | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59026723 | ||||||
| chr15:59026882 | A | G | 2 | a0001c0001t0003g0327 a0001c0001t0003g0328 |
2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-19-3922A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59026882 | |||||||
| chr15:59026951 | G | A | 1 | a0001c0010t0002g0214 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-19-3853G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59026951 | |||||||
| chr15:59026992 | A | T | 99 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(96): Show |
100 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.-19-3812A>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59026992 | |||||||
| chr15:59027061 | T | C | 3 | a0001c0001t0003g0049 a0001c0001t0003g0050 a0001c0001t0003g0051 |
3 | HG03195.hp1 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-19-3743T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59027061 | |||||||
| chr15:59027289 | C | T | 1 | a0001c0001t0002g0190 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-19-3515C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59027289 | |||||||
| chr15:59027298 | A | G | 3 | a0001c0002t0001g0129 a0001c0002t0001g0130 a0001c0002t0001g0132 |
3 | NA18949.hp2 NA19005.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.-19-3506A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59027298 | |||||||
| chr15:59027298 | A | T | 1 | a0001c0001t0001g0241 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-19-3506A>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59027298 | |||||||
| chr15:59027339 | G | A | 2 | a0001c0001t0003g0327 a0001c0001t0003g0328 |
2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-19-3465G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59027339 | |||||||
| chr15:59027340 | C | T | 2 | a0001c0001t0003g0327 a0001c0001t0003g0328 |
2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-19-3464C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59027340 | |||||||
| chr15:59027516 | A | G | 9 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0003g0003 others(6): Show |
9 | HG00741.hp2 HG01168.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-19-3288A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59027516 | |||||||
| chr15:59027533 | C | CT | 26 | a0001c0001t0002g0014 a0001c0001t0002g0213 a0001c0001t0006g0312 others(23): Show |
26 | HG01167.hp2 HG01169.hp2 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.-19-3260dupT | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59027533 | ||||||
| chr15:59027544 | T | G | 2 | a0001c0001t0003g0327 a0001c0001t0003g0328 |
2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-19-3260T>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59027544 | |||||||
| chr15:59027554 | A | C | 1 | a0001c0001t0002g0190 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-19-3250A>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59027554 | |||||||
| chr15:59027731 | C | G | 3 | a0001c0001t0003g0049 a0001c0001t0003g0050 a0001c0001t0003g0051 |
3 | HG03195.hp1 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-19-3073C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59027731 | |||||||
| chr15:59027836 | C | CT | 9 | a0001c0001t0001g0259 a0001c0001t0005g0169 a0001c0002t0001g0097 others(6): Show |
9 | HG00438.hp1 HG01358.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.-19-2953dupT | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59027836 | ||||||
| chr15:59027876 | A | C | 1 | a0001c0002t0001g0124 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-19-2928A>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59027876 | |||||||
| chr15:59027887 | G | A | 5 | a0001c0001t0007g0011 a0001c0001t0007g0023 a0001c0001t0007g0024 others(2): Show |
5 | HG01167.hp2 HG01169.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19-2917G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59027887 | |||||||
| chr15:59027895 | A | G | 9 | a0001c0001t0005g0284 a0001c0001t0005g0285 a0001c0001t0005g0323 others(6): Show |
9 | HG00099.hp2 HG00408.hp1 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.-19-2909A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59027895 | |||||||
| chr15:59027906 | A | G | 1 | a0001c0004t0003g0202 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-19-2898A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59027906 | |||||||
| chr15:59027933 | C | G | 2 | a0001c0001t0002g0289 a0001c0001t0002g0291 |
2 | HG03654.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-19-2871C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59027933 | |||||||
| chr15:59028008 | G | A | 2 | a0001c0001t0003g0327 a0001c0001t0003g0328 |
2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-19-2796G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59028008 | |||||||
| chr15:59028021 | T | G | 13 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0241 others(10): Show |
13 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19-2783T>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59028021 | |||||||
| chr15:59028044 | C | T | 1 | a0001c0001t0004g0226 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-19-2760C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59028044 | |||||||
| chr15:59028046 | C | T | 5 | a0001c0001t0002g0014 a0001c0001t0003g0242 a0001c0001t0003g0243 others(2): Show |
5 | HG02818.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19-2758C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59028046 | |||||||
| chr15:59028066 | A | G | 2 | a0001c0001t0003g0006 a0001c0001t0003g0007 |
2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-19-2738A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59028066 | |||||||
| chr15:59028099 | T | TTGG | 24 | a0001c0001t0006g0312 a0001c0001t0006g0313 a0001c0001t0006g0314 others(21): Show |
24 | HG01167.hp2 HG01169.hp2 HG01934.hp1 others(21): Show |
intron_variant | MODIFIER | c.-19-2704_-19-2702d others(5): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59028099 | ||||||
| chr15:59028261 | T | C | 1 | a0001c0008t0002g0197 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-19-2543T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59028261 | |||||||
| chr15:59028272 | T | A | 1 | a0001c0001t0003g0326 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-19-2532T>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59028272 | |||||||
| chr15:59028356 | A | G | 2 | a0001c0001t0001g0231 a0001c0001t0003g0230 |
2 | HG02647.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-19-2448A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59028356 | |||||||
| chr15:59028380 | G | A | 1 | a0001c0002t0001g0134 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-19-2424G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59028380 | |||||||
| chr15:59028519 | C | G | 1 | a0001c0001t0002g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-19-2285C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59028519 | |||||||
| chr15:59028571 | C | G | 2 | a0001c0001t0003g0327 a0001c0001t0003g0328 |
2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-19-2233C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59028571 | |||||||
| chr15:59028781 | A | AT | 258 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(255): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.-19-2010dupT | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59028781 | ||||||
| chr15:59028781 | A | ATT | 55 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(52): Show |
55 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.-19-2011_-19-2010d others(4): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59028781 | ||||||
| chr15:59028893 | C | G | 2 | a0001c0001t0003g0327 a0001c0001t0003g0328 |
2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-19-1911C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59028893 | |||||||
| chr15:59028920 | C | T | 139 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(136): Show |
140 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.-19-1884C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59028920 | |||||||
| chr15:59028945 | A | C | 1 | a0001c0002t0003g0277 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-19-1859A>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59028945 | |||||||
| chr15:59029002 | A | T | 2 | a0002c0003t0001g0066 a0002c0003t0001g0073 |
2 | HG00741.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.-19-1802A>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59029002 | |||||||
| chr15:59029018 | G | A | 8 | a0001c0001t0001g0232 a0001c0001t0001g0241 a0001c0001t0001g0256 others(5): Show |
8 | HG02451.hp2 HG02723.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-19-1786G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59029018 | |||||||
| chr15:59029110 | G | A | 3 | a0001c0001t0002g0269 a0001c0001t0002g0270 a0001c0001t0002g0272 |
3 | HG00423.hp1 HG02056.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.-19-1694G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59029110 | |||||||
| chr15:59029284 | T | C | 1 | a0001c0001t0016g0008 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-19-1520T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59029284 | |||||||
| chr15:59029722 | C | A | 1 | a0001c0004t0003g0053 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-19-1082C>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59029722 | |||||||
| chr15:59029757 | G | C | 38 | a0002c0003t0001g0017 a0002c0003t0001g0018 a0002c0003t0001g0061 others(35): Show |
38 | HG00140.hp2 HG00280.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.-19-1047G>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59029757 | |||||||
| chr15:59029777 | G | A | 1 | a0001c0001t0002g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-19-1027G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59029777 | |||||||
| chr15:59029833 | GTTCA | G | 4 | a0001c0001t0002g0203 a0001c0001t0002g0217 a0001c0001t0002g0227 others(1): Show |
4 | HG00423.hp2 NA19005.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-965_-19-962del others(4): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | 59029833 | ||||||
| chr15:59029865 | T | A | 1 | a0001c0002t0001g0104 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-19-939T>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59029865 | |||||||
| chr15:59029899 | G | A | 1 | a0002c0003t0001g0081 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-19-905G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59029899 | |||||||
| chr15:59029973 | T | C | 1 | a0001c0001t0001g0259 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-19-831T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59029973 | |||||||
| chr15:59030005 | C | T | 3 | a0001c0002t0001g0062 a0001c0002t0001g0063 a0001c0002t0001g0064 |
3 | NA18940.hp1 NA18942.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.-19-799C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59030005 | |||||||
| chr15:59030163 | A | G | 1 | a0001c0001t0004g0022 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-19-641A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59030163 | |||||||
| chr15:59030243 | G | C | 1 | a0001c0001t0002g0210 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-19-561G>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59030243 | |||||||
| chr15:59030516 | G | C | 1 | a0001c0001t0002g0273 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-19-288G>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59030516 | |||||||
| chr15:59030521 | G | A | 2 | a0001c0001t0002g0203 a0004c0012t0002g0194 |
2 | HG00423.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.-19-283G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59030521 | |||||||
| chr15:59030630 | A | G | 143 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(140): Show |
144 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.-19-174A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59030630 | |||||||
| chr15:59030649 | G | A | 6 | a0001c0002t0001g0062 a0001c0002t0001g0063 a0001c0002t0001g0064 others(3): Show |
6 | NA18940.hp1 NA18942.hp1 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-155G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 1/13 | chr15 | 59030649 | |||||||
| chr15:59031845 | T | C | 1 | a0001c0002t0001g0086 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.880+143T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59031845 | |||||||
| chr15:59031859 | A | G | 5 | a0001c0001t0007g0011 a0001c0001t0007g0023 a0001c0001t0007g0024 others(2): Show |
5 | HG01167.hp2 HG01169.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.880+157A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59031859 | |||||||
| chr15:59031965 | G | A | 1 | a0001c0001t0002g0248 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.880+263G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59031965 | |||||||
| chr15:59032024 | C | T | 1 | a0006c0013t0001g0127 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.880+322C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59032024 | |||||||
| chr15:59032114 | T | C | 19 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0241 others(16): Show |
19 | HG02055.hp1 HG02451.hp2 HG02630.hp1 others(16): Show |
intron_variant | MODIFIER | c.880+412T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59032114 | |||||||
| chr15:59032154 | G | A | 106 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(103): Show |
106 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.880+452G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59032154 | |||||||
| chr15:59032191 | A | G | 63 | a0001c0001t0002g0014 a0001c0001t0003g0049 a0001c0001t0003g0050 others(60): Show |
64 | HG00639.hp1 HG01123.hp2 HG01167.hp2 others(61): Show |
intron_variant | MODIFIER | c.880+489A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59032191 | |||||||
| chr15:59032278 | G | A | 1 | a0001c0002t0003g0304 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.880+576G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59032278 | |||||||
| chr15:59032535 | C | T | 13 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0241 others(10): Show |
13 | HG02055.hp1 HG02451.hp2 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.880+833C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59032535 | |||||||
| chr15:59032543 | C | T | 1 | a0002c0003t0001g0179 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.880+841C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59032543 | |||||||
| chr15:59032574 | A | G | 1 | a0001c0001t0002g0273 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.880+872A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59032574 | |||||||
| chr15:59032713 | G | T | 1 | a0001c0001t0003g0310 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.880+1011G>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59032713 | |||||||
| chr15:59032918 | A | C | 1 | a0001c0001t0004g0040 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.880+1216A>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59032918 | |||||||
| chr15:59032965 | A | G | 1 | a0001c0001t0003g0278 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.880+1263A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59032965 | |||||||
| chr15:59033051 | G | A | 1 | a0001c0001t0014g0046 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.880+1349G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59033051 | |||||||
| chr15:59033234 | T | C | 140 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(137): Show |
141 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.880+1532T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59033234 | |||||||
| chr15:59033264 | T | C | 167 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0088 others(164): Show |
168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.880+1562T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59033264 | |||||||
| chr15:59033548 | A | T | 2 | a0001c0001t0003g0327 a0001c0001t0003g0328 |
2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.880+1846A>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59033548 | |||||||
| chr15:59033591 | C | T | 161 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0088 others(158): Show |
162 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.880+1889C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59033591 | |||||||
| chr15:59033616 | A | G | 1 | a0001c0002t0001g0108 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.880+1914A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59033616 | |||||||
| chr15:59033655 | G | C | 2 | a0001c0004t0003g0264 a0001c0004t0003g0265 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.880+1953G>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59033655 | |||||||
| chr15:59033677 | T | C | 1 | a0001c0001t0003g0015 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.880+1975T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59033677 | |||||||
| chr15:59033704 | T | C | 1 | a0002c0003t0001g0168 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.880+2002T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59033704 | |||||||
| chr15:59033773 | G | A | 4 | a0001c0001t0004g0054 a0001c0001t0004g0300 a0001c0001t0004g0301 others(1): Show |
4 | HG01891.hp2 HG02258.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.880+2071G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59033773 | |||||||
| chr15:59034026 | T | G | 27 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0241 others(24): Show |
27 | HG01167.hp2 HG01169.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.880+2324T>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59034026 | |||||||
| chr15:59034120 | A | G | 1 | a0001c0001t0002g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.880+2418A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59034120 | |||||||
| chr15:59034131 | G | A | 27 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0241 others(24): Show |
27 | HG01167.hp2 HG01169.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.880+2429G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59034131 | |||||||
| chr15:59034238 | G | A | 1 | a0001c0001t0013g0146 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.880+2536G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59034238 | |||||||
| chr15:59034251 | T | A | 1 | a0001c0001t0003g0016 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.880+2549T>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59034251 | |||||||
| chr15:59034259 | C | T | 10 | a0001c0001t0001g0232 a0001c0001t0001g0241 a0001c0001t0001g0256 others(7): Show |
10 | HG02055.hp1 HG02451.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.880+2557C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59034259 | |||||||
| chr15:59034271 | G | A | 9 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0003g0003 others(6): Show |
9 | HG00741.hp2 HG01168.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.880+2569G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59034271 | |||||||
| chr15:59034341 | A | G | 27 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0241 others(24): Show |
27 | HG01167.hp2 HG01169.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.880+2639A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59034341 | |||||||
| chr15:59034356 | G | A | 321 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(318): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.880+2654G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59034356 | |||||||
| chr15:59034411 | C | T | 1 | a0001c0001t0003g0005 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.880+2709C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59034411 | |||||||
| chr15:59034715 | T | A | 1 | a0002c0003t0001g0118 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.880+3013T>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59034715 | |||||||
| chr15:59034844 | T | C | 1 | a0002c0003t0001g0074 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.880+3142T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59034844 | |||||||
| chr15:59035049 | C | T | 3 | a0001c0002t0001g0062 a0001c0002t0001g0063 a0001c0002t0001g0064 |
3 | NA18940.hp1 NA18942.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.880+3347C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59035049 | |||||||
| chr15:59035099 | A | G | 1 | a0001c0001t0002g0247 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.880+3397A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59035099 | |||||||
| chr15:59035123 | C | T | 1 | a0001c0001t0003g0310 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.880+3421C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59035123 | |||||||
| chr15:59035203 | C | T | 9 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0003g0003 others(6): Show |
9 | HG00741.hp2 HG01168.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.880+3501C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59035203 | |||||||
| chr15:59035331 | A | C | 1 | a0004c0012t0002g0194 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.880+3629A>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59035331 | |||||||
| chr15:59035353 | C | A | 2 | a0001c0001t0014g0046 a0001c0001t0014g0305 |
2 | HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.880+3651C>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59035353 | |||||||
| chr15:59035419 | C | T | 1 | a0001c0001t0005g0019 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.880+3717C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59035419 | |||||||
| chr15:59035912 | A | G | 2 | a0001c0001t0003g0327 a0001c0001t0003g0328 |
2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.880+4210A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59035912 | |||||||
| chr15:59035919 | C | T | 2 | a0001c0001t0014g0046 a0001c0001t0014g0305 |
2 | HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.880+4217C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59035919 | |||||||
| chr15:59036018 | C | T | 1 | a0001c0001t0003g0016 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.880+4316C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59036018 | |||||||
| chr15:59036048 | G | A | 1 | a0001c0001t0003g0016 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.880+4346G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59036048 | |||||||
| chr15:59036111 | G | A | 1 | a0001c0009t0006g0318 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.880+4409G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59036111 | |||||||
| chr15:59036230 | A | G | 177 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0088 others(174): Show |
178 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.880+4528A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59036230 | |||||||
| chr15:59036351 | G | A | 9 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0003g0003 others(6): Show |
9 | HG00741.hp2 HG01168.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.880+4649G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59036351 | |||||||
| chr15:59036552 | G | A | 1 | a0001c0001t0007g0011 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.880+4850G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59036552 | |||||||
| chr15:59036826 | T | C | 13 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0241 others(10): Show |
13 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.880+5124T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59036826 | |||||||
| chr15:59037000 | A | AT | 8 | a0001c0001t0002g0275 a0001c0002t0001g0068 a0001c0002t0001g0167 others(5): Show |
8 | HG00544.hp2 NA18943.hp1 NA18950.hp1 others(5): Show |
intron_variant | MODIFIER | c.880+5314dupT | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr15 | 59037000 | ||||||
| chr15:59037025 | CAG | C | 4 | a0001c0001t0010g0056 a0001c0004t0003g0264 a0001c0004t0003g0265 others(1): Show |
4 | HG01256.hp2 HG01258.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.880+5324_880+5325d others(4): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59037025 | |||||||
| chr15:59037056 | C | T | 1 | a0002c0003t0001g0174 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.880+5354C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59037056 | |||||||
| chr15:59037129 | C | T | 1 | a0001c0001t0004g0040 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.880+5427C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59037129 | |||||||
| chr15:59037191 | A | G | 1 | a0001c0002t0003g0239 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.880+5489A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59037191 | |||||||
| chr15:59037231 | T | A | 1 | a0006c0013t0001g0127 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.880+5529T>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59037231 | |||||||
| chr15:59037421 | A | G | 2 | a0001c0001t0002g0247 a0001c0001t0002g0250 |
2 | HG00408.hp2 HG00438.hp2 |
intron_variant | MODIFIER | c.880+5719A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59037421 | |||||||
| chr15:59037558 | C | T | 5 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0003g0003 others(2): Show |
5 | HG00741.hp2 HG01168.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.880+5856C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59037558 | |||||||
| chr15:59037559 | G | A | 147 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0088 others(144): Show |
148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.880+5857G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59037559 | |||||||
| chr15:59037664 | C | T | 1 | a0001c0001t0002g0266 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.880+5962C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59037664 | |||||||
| chr15:59037763 | G | A | 5 | a0001c0001t0005g0020 a0001c0001t0005g0071 a0001c0001t0005g0114 others(2): Show |
5 | HG01358.hp1 HG01884.hp1 HG04228.hp1 others(2): Show |
intron_variant | MODIFIER | c.880+6061G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59037763 | |||||||
| chr15:59037834 | C | T | 2 | a0001c0001t0014g0046 a0001c0001t0014g0305 |
2 | HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.880+6132C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59037834 | |||||||
| chr15:59037897 | C | T | 1 | a0001c0001t0004g0044 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.880+6195C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59037897 | |||||||
| chr15:59038070 | T | C | 16 | a0001c0001t0006g0311 a0001c0001t0006g0312 a0001c0001t0006g0313 others(13): Show |
16 | HG01934.hp1 HG01952.hp1 HG01978.hp2 others(13): Show |
intron_variant | MODIFIER | c.880+6368T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59038070 | |||||||
| chr15:59038116 | A | G | 1 | a0001c0002t0001g0126 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.880+6414A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59038116 | |||||||
| chr15:59038177 | T | C | 1 | a0001c0002t0001g0155 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.880+6475T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59038177 | |||||||
| chr15:59038221 | G | A | 1 | a0002c0003t0001g0111 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.880+6519G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59038221 | |||||||
| chr15:59038233 | T | C | 9 | a0001c0002t0001g0065 a0001c0002t0001g0101 a0001c0002t0001g0102 others(6): Show |
9 | NA18941.hp1 NA18957.hp1 NA18962.hp1 others(6): Show |
intron_variant | MODIFIER | c.880+6531T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59038233 | |||||||
| chr15:59038330 | A | G | 1 | a0001c0001t0003g0303 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.880+6628A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59038330 | |||||||
| chr15:59038714 | T | C | 176 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0088 others(173): Show |
177 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.880+7012T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59038714 | |||||||
| chr15:59038867 | T | C | 154 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0088 others(151): Show |
155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.880+7165T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59038867 | |||||||
| chr15:59038949 | A | G | 1 | a0001c0001t0003g0261 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.880+7247A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59038949 | |||||||
| chr15:59039033 | C | G | 1 | a0001c0001t0021g0052 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.880+7331C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59039033 | |||||||
| chr15:59039041 | C | T | 5 | a0002c0003t0001g0156 a0002c0003t0001g0174 a0002c0003t0001g0175 others(2): Show |
5 | HG00140.hp2 HG00639.hp2 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.880+7339C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59039041 | |||||||
| chr15:59039111 | C | T | 1 | a0001c0001t0005g0329 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.880+7409C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59039111 | |||||||
| chr15:59039131 | A | T | 1 | a0001c0001t0002g0225 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.880+7429A>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59039131 | |||||||
| chr15:59039262 | C | T | 1 | a0001c0001t0013g0146 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.880+7560C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59039262 | |||||||
| chr15:59039558 | A | C | 4 | a0001c0001t0003g0045 a0001c0001t0003g0306 a0001c0001t0003g0307 others(1): Show |
4 | HG03225.hp1 HG03453.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.880+7856A>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59039558 | |||||||
| chr15:59039590 | G | A | 17 | a0001c0001t0006g0311 a0001c0001t0006g0312 a0001c0001t0006g0313 others(14): Show |
17 | HG01934.hp1 HG01952.hp1 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.880+7888G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59039590 | |||||||
| chr15:59039599 | C | T | 6 | a0002c0003t0001g0017 a0002c0003t0001g0018 a0002c0003t0001g0083 others(3): Show |
6 | HG01070.hp1 NA18612.hp2 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.880+7897C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59039599 | |||||||
| chr15:59039721 | A | AT | 11 | a0001c0001t0003g0016 a0001c0001t0003g0242 a0001c0001t0003g0243 others(8): Show |
11 | HG01884.hp2 HG02572.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.880+8033dupT | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr15 | 59039721 | ||||||
| chr15:59039721 | AT | A | 18 | a0001c0001t0002g0244 a0001c0001t0006g0311 a0001c0001t0006g0312 others(15): Show |
18 | HG01070.hp2 HG01934.hp1 HG01952.hp1 others(15): Show |
intron_variant | MODIFIER | c.880+8033delT | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr15 | 59039721 | ||||||
| chr15:59039785 | T | G | 1 | a0001c0001t0003g0310 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.880+8083T>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59039785 | |||||||
| chr15:59039829 | G | T | 4 | a0001c0004t0003g0191 a0001c0004t0003g0202 a0001c0004t0003g0264 others(1): Show |
4 | HG01106.hp2 HG01256.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.880+8127G>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59039829 | |||||||
| chr15:59039872 | G | A | 2 | a0001c0001t0003g0006 a0001c0001t0003g0007 |
2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.880+8170G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59039872 | |||||||
| chr15:59039888 | T | G | 2 | a0001c0001t0003g0327 a0001c0001t0003g0328 |
2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.880+8186T>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59039888 | |||||||
| chr15:59040079 | C | T | 1 | a0001c0001t0002g0298 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.880+8377C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59040079 | |||||||
| chr15:59040131 | T | G | 1 | a0001c0002t0001g0116 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.880+8429T>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59040131 | |||||||
| chr15:59040246 | C | G | 1 | a0001c0008t0002g0197 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.880+8544C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59040246 | |||||||
| chr15:59040516 | A | G | 3 | a0001c0001t0002g0269 a0001c0001t0002g0270 a0001c0001t0002g0272 |
3 | HG00423.hp1 HG02056.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.880+8814A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59040516 | |||||||
| chr15:59040915 | C | G | 1 | a0001c0001t0002g0298 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.880+9213C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59040915 | |||||||
| chr15:59041037 | A | T | 2 | a0001c0001t0003g0327 a0001c0001t0003g0328 |
2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.880+9335A>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59041037 | |||||||
| chr15:59041081 | A | T | 1 | a0001c0001t0002g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.880+9379A>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59041081 | |||||||
| chr15:59041112 | A | G | 9 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0003g0003 others(6): Show |
9 | HG00741.hp2 HG01168.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.880+9410A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59041112 | |||||||
| chr15:59041230 | T | C | 1 | a0001c0001t0004g0038 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.880+9528T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59041230 | |||||||
| chr15:59041399 | G | C | 187 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0241 others(184): Show |
188 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.880+9697G>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59041399 | |||||||
| chr15:59041425 | C | T | 1 | a0001c0001t0002g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.880+9723C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59041425 | |||||||
| chr15:59041478 | A | T | 6 | a0001c0001t0003g0242 a0001c0001t0003g0243 a0001c0001t0003g0268 others(3): Show |
6 | HG02630.hp1 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.880+9776A>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59041478 | |||||||
| chr15:59041524 | G | A | 2 | a0001c0001t0003g0306 a0001c0001t0003g0307 |
2 | HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.880+9822G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59041524 | |||||||
| chr15:59041565 | GA | G | 5 | a0001c0001t0002g0014 a0001c0001t0004g0054 a0001c0001t0004g0300 others(2): Show |
5 | HG01891.hp2 HG02258.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.880+9873delA | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr15 | 59041565 | ||||||
| chr15:59041733 | T | C | 1 | a0001c0001t0005g0284 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.880+10031T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59041733 | |||||||
| chr15:59041735 | C | T | 174 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(171): Show |
175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.880+10033C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59041735 | |||||||
| chr15:59041961 | A | AT | 28 | a0001c0001t0001g0231 a0001c0001t0002g0211 a0001c0001t0002g0266 others(25): Show |
28 | HG00609.hp1 HG01167.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.880+10277dupT | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr15 | 59041961 | ||||||
| chr15:59041961 | A | ATT | 21 | a0001c0001t0002g0014 a0001c0001t0003g0007 a0001c0001t0003g0050 others(18): Show |
21 | HG00639.hp1 HG01934.hp1 HG01952.hp1 others(18): Show |
intron_variant | MODIFIER | c.880+10276_880+1027 others(6): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr15 | 59041961 | ||||||
| chr15:59041961 | A | ATTT | 8 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0016 others(5): Show |
8 | HG02572.hp2 HG02895.hp2 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.880+10275_880+1027 others(7): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr15 | 59041961 | ||||||
| chr15:59041961 | A | T | 3 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0002t0003g0147 |
3 | HG00741.hp2 HG01168.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.880+10259A>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59041961 | |||||||
| chr15:59041961 | AT | A | 44 | a0001c0001t0002g0186 a0001c0001t0002g0188 a0001c0001t0002g0200 others(41): Show |
44 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.880+10277delT | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr15 | 59041961 | ||||||
| chr15:59041963 | T | A | 1 | a0001c0001t0009g0324 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.880+10261T>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59041963 | |||||||
| chr15:59042036 | T | A | 1 | a0001c0001t0009g0324 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.881-10269T>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59042036 | |||||||
| chr15:59042041 | A | G | 1 | a0001c0001t0002g0271 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.881-10264A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59042041 | |||||||
| chr15:59042377 | C | T | 1 | a0001c0001t0002g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.881-9928C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59042377 | |||||||
| chr15:59042508 | C | T | 139 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(136): Show |
140 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.881-9797C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59042508 | |||||||
| chr15:59042609 | C | T | 195 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(192): Show |
196 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.881-9696C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59042609 | |||||||
| chr15:59042610 | G | A | 1 | a0001c0002t0001g0117 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.881-9695G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59042610 | |||||||
| chr15:59042815 | A | G | 1 | a0001c0001t0005g0293 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.881-9490A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59042815 | |||||||
| chr15:59043020 | T | G | 1 | a0001c0001t0002g0188 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.881-9285T>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59043020 | |||||||
| chr15:59043056 | G | A | 1 | a0001c0004t0003g0053 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.881-9249G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59043056 | |||||||
| chr15:59043157 | A | AT | 9 | a0001c0001t0002g0266 a0001c0001t0003g0242 a0001c0001t0003g0243 others(6): Show |
9 | HG02630.hp1 HG02818.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.881-9133dupT | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr15 | 59043157 | ||||||
| chr15:59043157 | AT | A | 35 | a0001c0001t0002g0201 a0001c0001t0004g0022 a0001c0001t0004g0027 others(32): Show |
36 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.881-9133delT | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr15 | 59043157 | ||||||
| chr15:59043180 | G | T | 1 | a0001c0002t0001g0166 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.881-9125G>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59043180 | |||||||
| chr15:59043385 | G | A | 138 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(135): Show |
139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.881-8920G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59043385 | |||||||
| chr15:59043464 | T | A | 1 | a0001c0002t0001g0135 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.881-8841T>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59043464 | |||||||
| chr15:59043549 | A | G | 139 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(136): Show |
140 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.881-8756A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59043549 | |||||||
| chr15:59043759 | T | C | 2 | a0001c0001t0003g0327 a0001c0001t0003g0328 |
2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.881-8546T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59043759 | |||||||
| chr15:59044016 | A | G | 6 | a0001c0001t0003g0242 a0001c0001t0003g0243 a0001c0001t0003g0268 others(3): Show |
6 | HG02630.hp1 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.881-8289A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59044016 | |||||||
| chr15:59044037 | T | TC | 3 | a0001c0002t0001g0129 a0001c0002t0001g0130 a0001c0002t0001g0132 |
3 | NA18949.hp2 NA19005.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.881-8267dupC | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr15 | 59044037 | ||||||
| chr15:59044043 | G | A | 139 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(136): Show |
140 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.881-8262G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59044043 | |||||||
| chr15:59044123 | C | G | 1 | a0001c0001t0002g0215 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.881-8182C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59044123 | |||||||
| chr15:59044180 | A | G | 33 | a0001c0001t0004g0022 a0001c0001t0004g0027 a0001c0001t0004g0028 others(30): Show |
34 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.881-8125A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59044180 | |||||||
| chr15:59044311 | A | C | 2 | a0001c0002t0001g0129 a0001c0002t0001g0130 |
2 | NA18949.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.881-7994A>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59044311 | |||||||
| chr15:59044322 | C | T | 1 | a0001c0001t0004g0226 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.881-7983C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59044322 | |||||||
| chr15:59044369 | A | C | 5 | a0001c0002t0001g0153 a0001c0002t0001g0162 a0001c0002t0001g0163 others(2): Show |
5 | HG02280.hp1 HG02559.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.881-7936A>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59044369 | |||||||
| chr15:59044376 | A | G | 28 | a0001c0001t0004g0022 a0001c0001t0004g0027 a0001c0001t0004g0028 others(25): Show |
29 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.881-7929A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59044376 | |||||||
| chr15:59044630 | A | G | 5 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0003g0003 others(2): Show |
5 | HG00741.hp2 HG01168.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.881-7675A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59044630 | |||||||
| chr15:59044880 | A | G | 4 | a0001c0001t0004g0054 a0001c0001t0004g0300 a0001c0001t0004g0301 others(1): Show |
4 | HG01891.hp2 HG02258.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.881-7425A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59044880 | |||||||
| chr15:59045098 | A | T | 1 | a0001c0001t0004g0030 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.881-7207A>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59045098 | |||||||
| chr15:59045130 | T | C | 1 | a0001c0001t0021g0052 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.881-7175T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59045130 | |||||||
| chr15:59045138 | G | A | 1 | a0001c0002t0001g0150 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.881-7167G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59045138 | |||||||
| chr15:59045168 | G | GT | 201 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(198): Show |
202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.881-7126dupT | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr15 | 59045168 | ||||||
| chr15:59045485 | G | A | 2 | a0001c0001t0003g0306 a0001c0001t0003g0307 |
2 | HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.881-6820G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59045485 | |||||||
| chr15:59045540 | A | G | 2 | a0001c0001t0005g0329 a0001c0008t0002g0197 |
2 | HG00733.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.881-6765A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59045540 | |||||||
| chr15:59045598 | G | A | 51 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(48): Show |
51 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.881-6707G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59045598 | |||||||
| chr15:59045677 | T | C | 4 | a0001c0001t0002g0203 a0001c0001t0002g0217 a0001c0001t0002g0227 others(1): Show |
4 | HG00423.hp2 NA19005.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.881-6628T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59045677 | |||||||
| chr15:59045772 | C | G | 1 | a0001c0002t0001g0109 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.881-6533C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59045772 | |||||||
| chr15:59045831 | A | T | 1 | a0001c0001t0002g0225 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.881-6474A>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59045831 | |||||||
| chr15:59045904 | T | C | 5 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0003g0003 others(2): Show |
5 | HG00741.hp2 HG01168.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.881-6401T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59045904 | |||||||
| chr15:59045954 | T | G | 1 | a0001c0001t0002g0190 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.881-6351T>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59045954 | |||||||
| chr15:59046069 | G | A | 1 | a0001c0001t0004g0254 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.881-6236G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59046069 | |||||||
| chr15:59046183 | CT | C | 138 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0088 others(135): Show |
139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.881-6108delT | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr15 | 59046183 | ||||||
| chr15:59046197 | T | C | 16 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(13): Show |
16 | HG00741.hp2 HG01168.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.881-6108T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59046197 | |||||||
| chr15:59046276 | C | T | 1 | a0001c0002t0001g0098 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.881-6029C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59046276 | |||||||
| chr15:59046329 | T | TA | 60 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(57): Show |
60 | HG00741.hp2 HG01167.hp2 HG01168.hp1 others(57): Show |
intron_variant | MODIFIER | c.881-5975dupA | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr15 | 59046329 | ||||||
| chr15:59046401 | C | T | 2 | a0001c0001t0004g0022 a0001c0001t0004g0038 |
2 | HG03927.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.881-5904C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59046401 | |||||||
| chr15:59046429 | G | A | 1 | a0001c0002t0001g0109 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.881-5876G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59046429 | |||||||
| chr15:59046522 | A | G | 60 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(57): Show |
60 | HG00741.hp2 HG01167.hp2 HG01168.hp1 others(57): Show |
intron_variant | MODIFIER | c.881-5783A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59046522 | |||||||
| chr15:59046529 | G | C | 5 | a0001c0002t0001g0153 a0001c0002t0001g0162 a0001c0002t0001g0163 others(2): Show |
5 | HG02280.hp1 HG02559.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.881-5776G>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59046529 | |||||||
| chr15:59046746 | C | T | 200 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(197): Show |
201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.881-5559C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59046746 | |||||||
| chr15:59047038 | G | T | 4 | a0001c0001t0003g0306 a0001c0001t0003g0307 a0001c0001t0003g0308 others(1): Show |
4 | HG03209.hp2 HG03225.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.881-5267G>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59047038 | |||||||
| chr15:59047130 | C | G | 5 | a0001c0001t0007g0011 a0001c0001t0007g0023 a0001c0001t0007g0024 others(2): Show |
5 | HG01167.hp2 HG01169.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.881-5175C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59047130 | |||||||
| chr15:59047196 | A | C | 1 | a0001c0001t0004g0041 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.881-5109A>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59047196 | |||||||
| chr15:59047324 | A | G | 2 | a0001c0002t0001g0059 a0001c0002t0001g0060 |
2 | HG03017.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.881-4981A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59047324 | |||||||
| chr15:59047377 | C | T | 1 | a0001c0001t0002g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.881-4928C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59047377 | |||||||
| chr15:59047450 | G | C | 27 | a0001c0001t0004g0022 a0001c0001t0004g0027 a0001c0001t0004g0028 others(24): Show |
28 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(25): Show |
intron_variant | MODIFIER | c.881-4855G>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59047450 | |||||||
| chr15:59047566 | G | A | 197 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(194): Show |
198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.881-4739G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59047566 | |||||||
| chr15:59047608 | C | T | 1 | a0001c0002t0001g0144 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.881-4697C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59047608 | |||||||
| chr15:59047641 | T | C | 1 | a0001c0001t0003g0303 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.881-4664T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59047641 | |||||||
| chr15:59047657 | C | T | 5 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0003g0003 others(2): Show |
5 | HG00741.hp2 HG01168.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.881-4648C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59047657 | |||||||
| chr15:59047661 | C | T | 1 | a0001c0001t0021g0052 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.881-4644C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59047661 | |||||||
| chr15:59047707 | C | A | 1 | a0002c0003t0001g0174 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.881-4598C>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59047707 | |||||||
| chr15:59047832 | C | T | 1 | a0002c0003t0001g0139 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.881-4473C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59047832 | |||||||
| chr15:59047854 | C | T | 21 | a0001c0001t0006g0311 a0001c0001t0006g0312 a0001c0001t0006g0313 others(18): Show |
21 | HG01934.hp1 HG01952.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.881-4451C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59047854 | |||||||
| chr15:59048048 | G | A | 138 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(135): Show |
139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.881-4257G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59048048 | |||||||
| chr15:59048397 | C | A | 1 | a0001c0001t0002g0206 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.881-3908C>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59048397 | |||||||
| chr15:59048463 | A | G | 1 | a0001c0001t0002g0225 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.881-3842A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59048463 | |||||||
| chr15:59048495 | G | A | 1 | a0001c0002t0001g0138 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.881-3810G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59048495 | |||||||
| chr15:59048851 | A | C | 1 | a0001c0001t0002g0206 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.881-3454A>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59048851 | |||||||
| chr15:59048852 | C | T | 1 | a0001c0001t0002g0206 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.881-3453C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59048852 | |||||||
| chr15:59048889 | G | A | 1 | a0001c0002t0001g0097 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.881-3416G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59048889 | |||||||
| chr15:59048927 | T | A | 199 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(196): Show |
200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.881-3378T>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59048927 | |||||||
| chr15:59049061 | C | T | 1 | a0001c0002t0001g0098 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.881-3244C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59049061 | |||||||
| chr15:59049351 | A | G | 1 | a0001c0001t0002g0091 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.881-2954A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59049351 | |||||||
| chr15:59049362 | A | AT | 18 | a0001c0001t0003g0242 a0001c0001t0003g0243 a0001c0001t0003g0310 others(15): Show |
18 | HG00609.hp2 HG01169.hp2 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.881-2919dupT | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr15 | 59049362 | ||||||
| chr15:59049362 | AT | A | 36 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0002g0115 others(33): Show |
36 | HG00741.hp2 HG01168.hp1 HG01496.hp2 others(33): Show |
intron_variant | MODIFIER | c.881-2919delT | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr15 | 59049362 | ||||||
| chr15:59049362 | ATT | A | 130 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0088 others(127): Show |
131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.881-2920_881-2919d others(4): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr15 | 59049362 | ||||||
| chr15:59049362 | ATTT | A | 6 | a0001c0001t0002g0203 a0001c0001t0004g0300 a0001c0001t0004g0301 others(3): Show |
6 | HG02258.hp1 HG02451.hp1 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.881-2921_881-2919d others(5): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr15 | 59049362 | ||||||
| chr15:59049447 | A | G | 140 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(137): Show |
141 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.881-2858A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59049447 | |||||||
| chr15:59049745 | C | CT | 149 | a0001c0001t0002g0088 a0001c0001t0002g0089 a0001c0001t0002g0090 others(146): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.881-2540dupT | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr15 | 59049745 | ||||||
| chr15:59049745 | C | CTT | 28 | a0001c0001t0002g0014 a0001c0001t0002g0207 a0001c0001t0002g0270 others(25): Show |
28 | HG00621.hp1 HG01934.hp1 HG01952.hp1 others(25): Show |
intron_variant | MODIFIER | c.881-2541_881-2540d others(4): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr15 | 59049745 | ||||||
| chr15:59049745 | C | T | 1 | a0001c0001t0002g0206 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.881-2560C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59049745 | |||||||
| chr15:59049779 | G | C | 1 | a0001c0001t0002g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.881-2526G>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59049779 | |||||||
| chr15:59049811 | G | A | 139 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0088 others(136): Show |
140 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.881-2494G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59049811 | |||||||
| chr15:59049888 | C | T | 2 | a0001c0002t0001g0125 a0001c0002t0001g0126 |
2 | HG01496.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.881-2417C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59049888 | |||||||
| chr15:59050006 | C | G | 1 | a0001c0001t0004g0226 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.881-2299C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59050006 | |||||||
| chr15:59050066 | C | CT | 56 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(53): Show |
56 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.881-2228dupT | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr15 | 59050066 | ||||||
| chr15:59050078 | G | C | 1 | a0001c0001t0002g0206 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.881-2227G>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59050078 | |||||||
| chr15:59050121 | T | A | 1 | a0001c0001t0019g0187 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.881-2184T>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59050121 | |||||||
| chr15:59050166 | G | A | 5 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0003g0003 others(2): Show |
5 | HG00741.hp2 HG01168.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.881-2139G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59050166 | |||||||
| chr15:59050184 | C | T | 2 | a0001c0001t0003g0327 a0001c0001t0003g0328 |
2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.881-2121C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59050184 | |||||||
| chr15:59050235 | T | C | 2 | a0001c0001t0003g0327 a0001c0001t0003g0328 |
2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.881-2070T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59050235 | |||||||
| chr15:59050323 | G | A | 1 | a0001c0002t0001g0164 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.881-1982G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59050323 | |||||||
| chr15:59050335 | C | G | 1 | a0002c0003t0025g0274 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.881-1970C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59050335 | |||||||
| chr15:59050421 | G | A | 1 | a0001c0001t0021g0052 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.881-1884G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59050421 | |||||||
| chr15:59050475 | A | C | 6 | a0001c0001t0003g0242 a0001c0001t0003g0243 a0001c0001t0003g0268 others(3): Show |
6 | HG02630.hp1 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.881-1830A>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59050475 | |||||||
| chr15:59050500 | C | G | 1 | a0001c0001t0003g0016 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.881-1805C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59050500 | |||||||
| chr15:59050575 | A | C | 1 | a0001c0001t0002g0091 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.881-1730A>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59050575 | |||||||
| chr15:59050712 | G | T | 1 | a0001c0001t0019g0187 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.881-1593G>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59050712 | |||||||
| chr15:59050821 | C | T | 1 | a0001c0001t0013g0146 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.881-1484C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59050821 | |||||||
| chr15:59051092 | T | C | 25 | a0001c0001t0006g0311 a0001c0001t0006g0312 a0001c0001t0006g0313 others(22): Show |
25 | HG01167.hp2 HG01169.hp2 HG01934.hp1 others(22): Show |
intron_variant | MODIFIER | c.881-1213T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59051092 | |||||||
| chr15:59051219 | T | C | 1 | a0002c0003t0001g0077 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.881-1086T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59051219 | |||||||
| chr15:59051430 | A | C | 199 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(196): Show |
200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.881-875A>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59051430 | |||||||
| chr15:59051451 | C | CT | 54 | a0001c0001t0002g0188 a0001c0001t0002g0200 a0001c0001t0002g0244 others(51): Show |
54 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.881-853dupT | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr15 | 59051451 | ||||||
| chr15:59051457 | C | CA | 43 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(40): Show |
43 | HG00741.hp2 HG01167.hp2 HG01168.hp1 others(40): Show |
intron_variant | MODIFIER | c.881-837dupA | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr15 | 59051457 | ||||||
| chr15:59051469 | G | A | 13 | a0001c0001t0001g0232 a0001c0001t0001g0241 a0001c0001t0001g0256 others(10): Show |
13 | HG02451.hp2 HG02630.hp1 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.881-836G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59051469 | |||||||
| chr15:59051470 | G | A | 1 | a0001c0001t0003g0016 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.881-835G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59051470 | |||||||
| chr15:59051471 | A | G | 13 | a0001c0001t0001g0232 a0001c0001t0001g0241 a0001c0001t0001g0256 others(10): Show |
13 | HG02451.hp2 HG02630.hp1 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.881-834A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59051471 | |||||||
| chr15:59051496 | C | T | 1 | a0001c0001t0002g0289 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.881-809C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59051496 | |||||||
| chr15:59051572 | T | C | 2 | a0001c0001t0003g0327 a0001c0001t0003g0328 |
2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.881-733T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59051572 | |||||||
| chr15:59051667 | G | T | 1 | a0002c0003t0001g0139 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.881-638G>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59051667 | |||||||
| chr15:59051675 | A | G | 3 | a0001c0001t0003g0049 a0001c0001t0003g0051 a0001c0001t0003g0310 |
3 | HG03209.hp2 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.881-630A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59051675 | |||||||
| chr15:59051738 | C | T | 1 | a0001c0002t0001g0084 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.881-567C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59051738 | |||||||
| chr15:59051771 | C | CAATA | 4 | a0001c0001t0003g0016 a0001c0002t0001g0123 a0001c0002t0001g0125 others(1): Show |
4 | HG01496.hp2 HG02056.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.881-502_881-499dup others(4): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr15 | 59051771 | ||||||
| chr15:59051771 | CAATA | C | 54 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(51): Show |
54 | HG00741.hp2 HG01167.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.881-502_881-499del others(4): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr15 | 59051771 | ||||||
| chr15:59051771 | CAATAAAT others(9): Show |
C | 142 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0088 others(139): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.881-514_881-499del others(16): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr15 | 59051771 | ||||||
| chr15:59052098 | G | A | 6 | a0001c0001t0001g0232 a0001c0001t0001g0241 a0001c0001t0001g0256 others(3): Show |
6 | HG02451.hp2 HG02723.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.881-207G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59052098 | |||||||
| chr15:59052156 | C | T | 1 | a0001c0001t0002g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.881-149C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59052156 | |||||||
| chr15:59052178 | C | A | 1 | a0002c0018t0001g0159 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.881-127C>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | chr15 | 59052178 | |||||||
| chr15:59052284 | G | GT | 55 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(52): Show |
55 | HG00741.hp2 HG01167.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.881-15dupT | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr15 | 59052284 | ||||||
| chr15:59052552 | A | G | 6 | a0001c0002t0001g0062 a0001c0002t0001g0063 a0001c0002t0001g0064 others(3): Show |
6 | NA18940.hp1 NA18942.hp1 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.1007+121A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 3/13 | chr15 | 59052552 | |||||||
| chr15:59052569 | A | AT | 20 | a0001c0001t0002g0196 a0001c0001t0002g0203 a0001c0001t0002g0204 others(17): Show |
20 | HG00280.hp2 HG01978.hp2 HG02004.hp1 others(17): Show |
intron_variant | MODIFIER | c.1007+160dupT | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr15 | 59052569 | ||||||
| chr15:59052569 | AT | A | 42 | a0001c0001t0001g0231 a0001c0001t0002g0014 a0001c0001t0003g0003 others(39): Show |
42 | HG01106.hp2 HG01167.hp2 HG01169.hp2 others(39): Show |
intron_variant | MODIFIER | c.1007+160delT | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr15 | 59052569 | ||||||
| chr15:59052603 | G | A | 141 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(138): Show |
142 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.1007+172G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 3/13 | chr15 | 59052603 | |||||||
| chr15:59052740 | A | G | 1 | a0001c0001t0003g0016 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1007+309A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 3/13 | chr15 | 59052740 | |||||||
| chr15:59052916 | T | C | 1 | a0001c0008t0002g0197 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1007+485T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 3/13 | chr15 | 59052916 | |||||||
| chr15:59053008 | A | G | 13 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0241 others(10): Show |
13 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1007+577A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 3/13 | chr15 | 59053008 | |||||||
| chr15:59053062 | T | G | 4 | a0001c0001t0004g0054 a0001c0001t0004g0300 a0001c0001t0004g0301 others(1): Show |
4 | HG01891.hp2 HG02258.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1007+631T>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 3/13 | chr15 | 59053062 | |||||||
| chr15:59053157 | C | CTCAGTAA others(88): Show |
2 | a0001c0001t0006g0312 a0001c0001t0006g0313 |
2 | NA18956.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.1007+760_1007+761i others(97): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr15 | 59053157 | ||||||
| chr15:59053192 | T | C | 200 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(197): Show |
201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.1007+761T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 3/13 | chr15 | 59053192 | |||||||
| chr15:59053249 | G | A | 199 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(196): Show |
200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.1007+818G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 3/13 | chr15 | 59053249 | |||||||
| chr15:59053310 | T | C | 1 | a0001c0001t0009g0324 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1007+879T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 3/13 | chr15 | 59053310 | |||||||
| chr15:59053758 | C | T | 1 | a0001c0001t0002g0195 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1007+1327C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 3/13 | chr15 | 59053758 | |||||||
| chr15:59053813 | A | G | 140 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0088 others(137): Show |
141 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.1007+1382A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 3/13 | chr15 | 59053813 | |||||||
| chr15:59053863 | T | C | 2 | a0001c0001t0004g0047 a0001c0001t0004g0048 |
2 | HG01261.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1007+1432T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 3/13 | chr15 | 59053863 | |||||||
| chr15:59053872 | T | C | 1 | a0001c0002t0001g0086 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1007+1441T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 3/13 | chr15 | 59053872 | |||||||
| chr15:59053877 | AT | A | 199 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(196): Show |
200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.1007+1448delT | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr15 | 59053877 | ||||||
| chr15:59053880 | A | C | 199 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(196): Show |
200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.1007+1449A>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 3/13 | chr15 | 59053880 | |||||||
| chr15:59053881 | A | T | 199 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(196): Show |
200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.1007+1450A>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 3/13 | chr15 | 59053881 | |||||||
| chr15:59053930 | A | G | 1 | a0001c0002t0001g0106 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1007+1499A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 3/13 | chr15 | 59053930 | |||||||
| chr15:59054018 | C | G | 139 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(136): Show |
140 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.1007+1587C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 3/13 | chr15 | 59054018 | |||||||
| chr15:59054022 | A | G | 198 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(195): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1007+1591A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 3/13 | chr15 | 59054022 | |||||||
| chr15:59054180 | A | G | 1 | a0001c0001t0003g0016 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1008-1502A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 3/13 | chr15 | 59054180 | |||||||
| chr15:59054465 | A | G | 4 | a0001c0001t0004g0054 a0001c0001t0004g0300 a0001c0001t0004g0301 others(1): Show |
4 | HG01891.hp2 HG02258.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1008-1217A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 3/13 | chr15 | 59054465 | |||||||
| chr15:59054521 | C | T | 1 | a0001c0001t0016g0008 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1008-1161C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 3/13 | chr15 | 59054521 | |||||||
| chr15:59054637 | CCTT | C | 143 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0088 others(140): Show |
144 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.1008-1041_1008-103 others(7): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr15 | 59054637 | ||||||
| chr15:59054649 | T | C | 1 | a0001c0001t0003g0310 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1008-1033T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 3/13 | chr15 | 59054649 | |||||||
| chr15:59054777 | A | G | 1 | a0001c0001t0004g0022 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1008-905A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 3/13 | chr15 | 59054777 | |||||||
| chr15:59054949 | A | G | 2 | a0001c0002t0012g0012 a0001c0002t0012g0229 |
2 | HG02257.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1008-733A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 3/13 | chr15 | 59054949 | |||||||
| chr15:59055159 | G | A | 188 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(185): Show |
189 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.1008-523G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 3/13 | chr15 | 59055159 | |||||||
| chr15:59055328 | T | C | 1 | a0001c0002t0015g0093 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1008-354T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 3/13 | chr15 | 59055328 | |||||||
| chr15:59055523 | T | TAGTTGGT others(14): Show |
198 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(195): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1008-155_1008-154i others(23): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr15 | 59055523 | ||||||
| chr15:59055558 | G | A | 140 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0088 others(137): Show |
141 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.1008-124G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 3/13 | chr15 | 59055558 | |||||||
| chr15:59055886 | T | C | 2 | a0003c0006t0006g0315 a0003c0006t0006g0317 |
2 | HG01934.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.1171+41T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 4/13 | chr15 | 59055886 | |||||||
| chr15:59055969 | A | G | 2 | a0003c0006t0006g0315 a0003c0006t0006g0317 |
2 | HG01934.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.1171+124A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 4/13 | chr15 | 59055969 | |||||||
| chr15:59056063 | C | T | 1 | a0001c0001t0002g0288 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1171+218C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 4/13 | chr15 | 59056063 | |||||||
| chr15:59056182 | T | C | 1 | a0001c0001t0004g0036 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1171+337T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 4/13 | chr15 | 59056182 | |||||||
| chr15:59056221 | T | G | 2 | a0001c0001t0003g0327 a0001c0001t0003g0328 |
2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1171+376T>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 4/13 | chr15 | 59056221 | |||||||
| chr15:59056432 | C | G | 1 | a0001c0001t0003g0268 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1171+587C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 4/13 | chr15 | 59056432 | |||||||
| chr15:59056750 | A | C | 1 | a0001c0001t0002g0193 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1171+905A>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 4/13 | chr15 | 59056750 | |||||||
| chr15:59056778 | C | T | 5 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0003g0003 others(2): Show |
5 | HG00741.hp2 HG01168.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1171+933C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 4/13 | chr15 | 59056778 | |||||||
| chr15:59056789 | T | C | 3 | a0001c0002t0001g0099 a0001c0002t0001g0167 a0007c0014t0001g0131 |
3 | HG00544.hp2 NA19012.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1171+944T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 4/13 | chr15 | 59056789 | |||||||
| chr15:59056858 | G | A | 1 | a0001c0002t0001g0101 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1171+1013G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 4/13 | chr15 | 59056858 | |||||||
| chr15:59056858 | G | T | 1 | a0002c0003t0001g0168 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1171+1013G>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 4/13 | chr15 | 59056858 | |||||||
| chr15:59056934 | A | T | 1 | a0001c0001t0002g0288 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1171+1089A>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 4/13 | chr15 | 59056934 | |||||||
| chr15:59056948 | TG | T | 5 | a0001c0002t0001g0062 a0001c0002t0001g0063 a0001c0002t0001g0064 others(2): Show |
5 | NA18940.hp1 NA18942.hp1 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.1171+1106delG | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr15 | 59056948 | ||||||
| chr15:59057016 | C | T | 137 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(134): Show |
138 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.1171+1171C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 4/13 | chr15 | 59057016 | |||||||
| chr15:59057197 | T | G | 2 | a0001c0001t0004g0301 a0001c0001t0004g0302 |
2 | HG02451.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1172-1159T>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 4/13 | chr15 | 59057197 | |||||||
| chr15:59057222 | C | T | 3 | a0001c0001t0007g0234 a0001c0001t0007g0235 a0001c0001t0007g0240 |
3 | HG02572.hp1 HG02717.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1172-1134C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 4/13 | chr15 | 59057222 | |||||||
| chr15:59057321 | C | T | 1 | a0001c0001t0002g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1172-1035C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 4/13 | chr15 | 59057321 | |||||||
| chr15:59057388 | T | C | 1 | a0001c0001t0003g0016 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1172-968T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 4/13 | chr15 | 59057388 | |||||||
| chr15:59057508 | C | T | 2 | a0001c0001t0001g0232 a0001c0001t0001g0259 |
2 | HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1172-848C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 4/13 | chr15 | 59057508 | |||||||
| chr15:59057540 | C | T | 165 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0088 others(162): Show |
166 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.1172-816C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 4/13 | chr15 | 59057540 | |||||||
| chr15:59057542 | T | C | 4 | a0001c0001t0004g0054 a0001c0001t0004g0300 a0001c0001t0004g0301 others(1): Show |
4 | HG01891.hp2 HG02258.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1172-814T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 4/13 | chr15 | 59057542 | |||||||
| chr15:59057715 | G | T | 141 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0088 others(138): Show |
142 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.1172-641G>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 4/13 | chr15 | 59057715 | |||||||
| chr15:59057773 | C | T | 1 | a0001c0001t0010g0058 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1172-583C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 4/13 | chr15 | 59057773 | |||||||
| chr15:59057787 | A | G | 24 | a0001c0001t0006g0311 a0001c0001t0006g0312 a0001c0001t0006g0313 others(21): Show |
24 | HG01167.hp2 HG01169.hp2 HG01934.hp1 others(21): Show |
intron_variant | MODIFIER | c.1172-569A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 4/13 | chr15 | 59057787 | |||||||
| chr15:59058137 | C | T | 1 | a0001c0001t0002g0207 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1172-219C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 4/13 | chr15 | 59058137 | |||||||
| chr15:59058138 | G | A | 2 | a0001c0001t0003g0327 a0001c0001t0003g0328 |
2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1172-218G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 4/13 | chr15 | 59058138 | |||||||
| chr15:59058168 | T | C | 1 | a0006c0013t0001g0127 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1172-188T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 4/13 | chr15 | 59058168 | |||||||
| chr15:59058584 | G | A | 19 | a0001c0001t0006g0311 a0001c0001t0006g0312 a0001c0001t0006g0313 others(16): Show |
19 | HG01934.hp1 HG01952.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.1366+34G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59058584 | |||||||
| chr15:59058773 | G | A | 1 | a0001c0002t0001g0105 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1366+223G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59058773 | |||||||
| chr15:59058835 | T | C | 1 | a0001c0002t0001g0126 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1366+285T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59058835 | |||||||
| chr15:59058861 | T | C | 1 | a0001c0002t0001g0117 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1366+311T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59058861 | |||||||
| chr15:59058950 | A | C | 1 | a0001c0002t0001g0144 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1366+400A>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59058950 | |||||||
| chr15:59059160 | C | T | 2 | a0003c0006t0006g0315 a0003c0006t0006g0317 |
2 | HG01934.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.1366+610C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59059160 | |||||||
| chr15:59059474 | G | C | 6 | a0001c0001t0001g0232 a0001c0001t0001g0241 a0001c0001t0001g0256 others(3): Show |
6 | HG02451.hp2 HG02723.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1366+924G>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59059474 | |||||||
| chr15:59059498 | A | G | 1 | a0001c0001t0002g0289 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1366+948A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59059498 | |||||||
| chr15:59059553 | T | C | 7 | a0001c0001t0002g0014 a0001c0001t0003g0242 a0001c0001t0003g0243 others(4): Show |
7 | HG02630.hp1 HG02818.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1366+1003T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59059553 | |||||||
| chr15:59059622 | G | A | 51 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(48): Show |
51 | HG00741.hp2 HG01167.hp2 HG01168.hp1 others(48): Show |
intron_variant | MODIFIER | c.1366+1072G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59059622 | |||||||
| chr15:59059635 | G | A | 140 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0088 others(137): Show |
141 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.1366+1085G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59059635 | |||||||
| chr15:59059656 | G | A | 1 | a0001c0001t0004g0226 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1366+1106G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59059656 | |||||||
| chr15:59059679 | TATCTC | T | 7 | a0001c0001t0002g0014 a0001c0001t0003g0242 a0001c0001t0003g0243 others(4): Show |
7 | HG02630.hp1 HG02818.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1366+1131_1366+113 others(9): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr15 | 59059679 | ||||||
| chr15:59059690 | A | T | 1 | a0001c0001t0002g0210 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1366+1140A>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59059690 | |||||||
| chr15:59059691 | G | T | 1 | a0001c0001t0002g0210 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1366+1141G>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59059691 | |||||||
| chr15:59059790 | A | G | 5 | a0001c0001t0004g0034 a0001c0001t0004g0036 a0001c0001t0004g0037 others(2): Show |
5 | HG00639.hp1 HG01123.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.1366+1240A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59059790 | |||||||
| chr15:59059962 | G | C | 10 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(7): Show |
10 | HG01168.hp2 HG01169.hp1 NA18951.hp1 others(7): Show |
intron_variant | MODIFIER | c.1366+1412G>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59059962 | |||||||
| chr15:59060281 | T | C | 146 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0088 others(143): Show |
147 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.1366+1731T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59060281 | |||||||
| chr15:59060307 | TA | T | 7 | a0001c0001t0002g0292 a0001c0001t0003g0243 a0001c0001t0003g0306 others(4): Show |
7 | HG01069.hp2 HG01167.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1366+1770delA | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr15 | 59060307 | ||||||
| chr15:59060376 | C | T | 1 | a0002c0003t0001g0080 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1366+1826C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59060376 | |||||||
| chr15:59060415 | G | A | 12 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0241 others(9): Show |
12 | HG02055.hp1 HG02451.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.1366+1865G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59060415 | |||||||
| chr15:59060458 | C | T | 1 | a0001c0001t0002g0246 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1366+1908C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59060458 | |||||||
| chr15:59060785 | C | CATT | 110 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(107): Show |
111 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.1366+2257_1366+225 others(7): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr15 | 59060785 | ||||||
| chr15:59060804 | A | ATTT | 8 | a0001c0001t0001g0232 a0001c0001t0001g0241 a0001c0001t0001g0256 others(5): Show |
8 | HG00408.hp2 HG00438.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1366+2256_1366+225 others(7): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr15 | 59060804 | ||||||
| chr15:59060804 | A | T | 2 | a0001c0001t0002g0275 a0001c0001t0003g0045 |
2 | NA18522.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.1366+2254A>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59060804 | |||||||
| chr15:59060807 | A | ATTT | 58 | a0001c0001t0001g0231 a0001c0001t0001g0258 a0001c0001t0002g0188 others(55): Show |
58 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.1366+2266_1366+226 others(7): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr15 | 59060807 | ||||||
| chr15:59060807 | A | T | 17 | a0001c0001t0001g0232 a0001c0001t0001g0241 a0001c0001t0001g0256 others(14): Show |
17 | HG00408.hp2 HG00438.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.1366+2257A>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59060807 | |||||||
| chr15:59060810 | T | A | 3 | a0001c0001t0004g0032 a0001c0001t0007g0240 a0002c0015t0001g0157 |
3 | HG01358.hp2 HG02572.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.1366+2260T>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59060810 | |||||||
| chr15:59061009 | C | A | 2 | a0001c0001t0003g0327 a0001c0001t0003g0328 |
2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1366+2459C>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59061009 | |||||||
| chr15:59061163 | A | C | 1 | a0001c0001t0021g0052 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1366+2613A>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59061163 | |||||||
| chr15:59061256 | C | A | 2 | a0001c0001t0002g0266 a0001c0001t0003g0261 |
2 | HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1366+2706C>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59061256 | |||||||
| chr15:59061258 | A | G | 2 | a0001c0001t0003g0278 a0001c0002t0001g0110 |
2 | HG02027.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1366+2708A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59061258 | |||||||
| chr15:59061308 | C | G | 6 | a0001c0001t0002g0204 a0001c0001t0002g0212 a0001c0001t0002g0213 others(3): Show |
6 | HG00544.hp1 NA18941.hp2 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.1366+2758C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59061308 | |||||||
| chr15:59061355 | A | C | 1 | a0002c0018t0001g0159 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1366+2805A>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59061355 | |||||||
| chr15:59061398 | A | T | 1 | a0001c0002t0001g0138 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1366+2848A>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59061398 | |||||||
| chr15:59061498 | C | T | 1 | a0002c0003t0001g0139 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1366+2948C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59061498 | |||||||
| chr15:59061499 | A | C | 1 | a0001c0002t0003g0276 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1366+2949A>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59061499 | |||||||
| chr15:59061642 | T | A | 10 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0003g0003 others(7): Show |
10 | HG00741.hp2 HG01168.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.1366+3092T>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59061642 | |||||||
| chr15:59061664 | C | A | 79 | a0001c0001t0002g0188 a0001c0001t0002g0200 a0001c0001t0002g0244 others(76): Show |
80 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.1366+3114C>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59061664 | |||||||
| chr15:59061947 | C | G | 1 | a0001c0001t0004g0226 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1366+3397C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59061947 | |||||||
| chr15:59061949 | T | A | 1 | a0001c0001t0004g0226 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1366+3399T>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59061949 | |||||||
| chr15:59061986 | C | T | 2 | a0001c0001t0004g0301 a0001c0001t0004g0302 |
2 | HG02451.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1366+3436C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59061986 | |||||||
| chr15:59062051 | C | CT | 13 | a0001c0001t0002g0221 a0001c0001t0002g0269 a0001c0001t0003g0327 others(10): Show |
13 | HG00423.hp1 HG01346.hp1 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.1366+3520dupT | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr15 | 59062051 | ||||||
| chr15:59062051 | C | CTT | 59 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0088 others(56): Show |
59 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.1366+3519_1366+352 others(6): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr15 | 59062051 | ||||||
| chr15:59062051 | CT | C | 13 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0002g0291 others(10): Show |
13 | HG00741.hp2 HG01168.hp1 HG02735.hp2 others(10): Show |
intron_variant | MODIFIER | c.1366+3520delT | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr15 | 59062051 | ||||||
| chr15:59062097 | C | T | 1 | a0001c0001t0004g0226 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1366+3547C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59062097 | |||||||
| chr15:59062414 | A | G | 1 | a0002c0003t0001g0061 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1366+3864A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59062414 | |||||||
| chr15:59062422 | C | G | 2 | a0001c0002t0001g0068 a0001c0002t0001g0121 |
2 | NA19084.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1366+3872C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59062422 | |||||||
| chr15:59062452 | A | G | 6 | a0001c0001t0001g0232 a0001c0001t0001g0241 a0001c0001t0001g0256 others(3): Show |
6 | HG02451.hp2 HG02723.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1366+3902A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59062452 | |||||||
| chr15:59062656 | A | G | 1 | a0001c0001t0007g0234 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1366+4106A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59062656 | |||||||
| chr15:59062735 | A | C | 25 | a0001c0001t0006g0311 a0001c0001t0006g0312 a0001c0001t0006g0313 others(22): Show |
25 | HG01167.hp2 HG01169.hp2 HG01934.hp1 others(22): Show |
intron_variant | MODIFIER | c.1367-4029A>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59062735 | |||||||
| chr15:59062743 | A | G | 10 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(7): Show |
10 | HG01168.hp2 HG01169.hp1 NA18951.hp1 others(7): Show |
intron_variant | MODIFIER | c.1367-4021A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59062743 | |||||||
| chr15:59062782 | G | T | 9 | a0001c0001t0002g0195 a0001c0001t0002g0204 a0001c0001t0002g0210 others(6): Show |
9 | HG00544.hp1 NA18941.hp2 NA18956.hp2 others(6): Show |
intron_variant | MODIFIER | c.1367-3982G>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59062782 | |||||||
| chr15:59062920 | A | G | 25 | a0001c0001t0006g0311 a0001c0001t0006g0312 a0001c0001t0006g0313 others(22): Show |
25 | HG01167.hp2 HG01169.hp2 HG01934.hp1 others(22): Show |
intron_variant | MODIFIER | c.1367-3844A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59062920 | |||||||
| chr15:59062994 | C | G | 7 | a0001c0001t0002g0014 a0001c0001t0003g0242 a0001c0001t0003g0243 others(4): Show |
7 | HG02630.hp1 HG02818.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1367-3770C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59062994 | |||||||
| chr15:59063153 | C | T | 6 | a0001c0001t0001g0232 a0001c0001t0001g0241 a0001c0001t0001g0256 others(3): Show |
6 | HG02451.hp2 HG02723.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1367-3611C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59063153 | |||||||
| chr15:59063368 | A | T | 1 | a0001c0001t0003g0308 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1367-3396A>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59063368 | |||||||
| chr15:59063664 | C | T | 1 | a0001c0001t0004g0254 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1367-3100C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59063664 | |||||||
| chr15:59063755 | A | T | 1 | a0001c0001t0002g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1367-3009A>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59063755 | |||||||
| chr15:59063881 | G | T | 1 | a0001c0001t0003g0016 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1367-2883G>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59063881 | |||||||
| chr15:59063883 | A | C | 1 | a0001c0001t0002g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1367-2881A>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59063883 | |||||||
| chr15:59063904 | A | G | 172 | a0001c0001t0001g0232 a0001c0001t0001g0241 a0001c0001t0001g0256 others(169): Show |
173 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.1367-2860A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59063904 | |||||||
| chr15:59064093 | C | T | 1 | a0001c0002t0001g0098 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1367-2671C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59064093 | |||||||
| chr15:59064156 | G | A | 6 | a0001c0001t0001g0232 a0001c0001t0001g0241 a0001c0001t0001g0256 others(3): Show |
6 | HG02451.hp2 HG02723.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1367-2608G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59064156 | |||||||
| chr15:59064251 | T | C | 40 | a0001c0001t0002g0200 a0001c0001t0002g0244 a0001c0001t0002g0245 others(37): Show |
40 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.1367-2513T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59064251 | |||||||
| chr15:59064258 | G | T | 1 | a0001c0001t0003g0016 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1367-2506G>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59064258 | |||||||
| chr15:59064331 | C | T | 13 | a0001c0001t0001g0232 a0001c0001t0001g0241 a0001c0001t0001g0256 others(10): Show |
13 | HG02451.hp2 HG02630.hp1 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.1367-2433C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59064331 | |||||||
| chr15:59064360 | C | T | 1 | a0001c0001t0002g0296 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1367-2404C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59064360 | |||||||
| chr15:59064363 | G | A | 1 | a0001c0001t0002g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1367-2401G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59064363 | |||||||
| chr15:59064458 | C | G | 1 | a0001c0001t0005g0141 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1367-2306C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59064458 | |||||||
| chr15:59064460 | C | T | 20 | a0001c0001t0006g0311 a0001c0001t0006g0312 a0001c0001t0006g0313 others(17): Show |
20 | HG01934.hp1 HG01952.hp1 HG02027.hp2 others(17): Show |
intron_variant | MODIFIER | c.1367-2304C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59064460 | |||||||
| chr15:59064535 | C | CA | 43 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0002g0210 others(40): Show |
43 | HG00621.hp2 HG00741.hp2 HG01168.hp1 others(40): Show |
intron_variant | MODIFIER | c.1367-2211dupA | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr15 | 59064535 | ||||||
| chr15:59064535 | C | CAA | 113 | a0001c0001t0001g0232 a0001c0001t0001g0241 a0001c0001t0001g0256 others(110): Show |
113 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.1367-2212_1367-221 others(6): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr15 | 59064535 | ||||||
| chr15:59064535 | C | CAAA | 51 | a0001c0001t0001g0231 a0001c0001t0002g0188 a0001c0001t0002g0201 others(48): Show |
52 | HG00423.hp1 HG00423.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.1367-2213_1367-221 others(7): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr15 | 59064535 | ||||||
| chr15:59064535 | C | CAAAA | 6 | a0001c0001t0002g0014 a0001c0001t0004g0028 a0001c0001t0004g0040 others(3): Show |
6 | HG01175.hp2 HG01433.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.1367-2214_1367-221 others(8): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr15 | 59064535 | ||||||
| chr15:59064548 | A | G | 1 | a0001c0002t0001g0092 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1367-2216A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59064548 | |||||||
| chr15:59064616 | G | A | 1 | a0001c0001t0002g0252 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1367-2148G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59064616 | |||||||
| chr15:59064651 | C | T | 1 | a0001c0002t0003g0013 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1367-2113C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59064651 | |||||||
| chr15:59064739 | C | T | 2 | a0001c0001t0004g0041 a0001c0001t0004g0254 |
2 | HG01192.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1367-2025C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59064739 | |||||||
| chr15:59064849 | C | T | 1 | a0001c0001t0017g0294 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1367-1915C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59064849 | |||||||
| chr15:59064908 | A | G | 1 | a0001c0001t0002g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1367-1856A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59064908 | |||||||
| chr15:59064980 | T | C | 2 | a0001c0001t0002g0192 a0001c0001t0002g0198 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1367-1784T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59064980 | |||||||
| chr15:59065158 | C | T | 2 | a0001c0001t0001g0231 a0001c0001t0003g0230 |
2 | HG02647.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1367-1606C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59065158 | |||||||
| chr15:59065191 | G | T | 1 | a0001c0001t0002g0251 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1367-1573G>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59065191 | |||||||
| chr15:59065198 | G | A | 1 | a0001c0002t0001g0108 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1367-1566G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59065198 | |||||||
| chr15:59065331 | C | A | 6 | a0001c0001t0001g0232 a0001c0001t0001g0241 a0001c0001t0001g0256 others(3): Show |
6 | HG02451.hp2 HG02723.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1367-1433C>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59065331 | |||||||
| chr15:59065410 | C | T | 1 | a0001c0002t0001g0149 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1367-1354C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59065410 | |||||||
| chr15:59065467 | A | G | 17 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(14): Show |
17 | HG00741.hp2 HG01168.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1367-1297A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59065467 | |||||||
| chr15:59065694 | G | A | 134 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0088 others(131): Show |
135 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.1367-1070G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59065694 | |||||||
| chr15:59065888 | A | G | 2 | a0001c0001t0003g0327 a0001c0001t0003g0328 |
2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1367-876A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59065888 | |||||||
| chr15:59065968 | T | C | 138 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(135): Show |
139 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.1367-796T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59065968 | |||||||
| chr15:59066181 | C | T | 174 | a0001c0001t0001g0232 a0001c0001t0001g0241 a0001c0001t0001g0256 others(171): Show |
175 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.1367-583C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59066181 | |||||||
| chr15:59066273 | G | A | 176 | a0001c0001t0001g0232 a0001c0001t0001g0241 a0001c0001t0001g0256 others(173): Show |
177 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.1367-491G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59066273 | |||||||
| chr15:59066330 | C | A | 134 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0088 others(131): Show |
135 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.1367-434C>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59066330 | |||||||
| chr15:59066343 | G | A | 3 | a0001c0002t0001g0062 a0001c0002t0001g0063 a0001c0002t0001g0064 |
3 | NA18940.hp1 NA18942.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.1367-421G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59066343 | |||||||
| chr15:59066381 | C | T | 5 | a0001c0002t0003g0013 a0001c0002t0003g0236 a0001c0002t0003g0238 others(2): Show |
5 | HG02257.hp1 HG02717.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1367-383C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59066381 | |||||||
| chr15:59066394 | T | C | 1 | a0001c0001t0003g0050 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1367-370T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59066394 | |||||||
| chr15:59066414 | C | G | 1 | a0001c0001t0016g0008 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1367-350C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59066414 | |||||||
| chr15:59066508 | G | T | 5 | a0002c0003t0001g0156 a0002c0003t0001g0174 a0002c0003t0001g0175 others(2): Show |
5 | HG00140.hp2 HG00639.hp2 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.1367-256G>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59066508 | |||||||
| chr15:59066525 | G | A | 1 | a0001c0001t0001g0258 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1367-239G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59066525 | |||||||
| chr15:59066646 | A | C | 133 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(130): Show |
134 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.1367-118A>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59066646 | |||||||
| chr15:59066663 | G | A | 134 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0088 others(131): Show |
135 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.1367-101G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 5/13 | chr15 | 59066663 | |||||||
| chr15:59067235 | C | T | 18 | a0001c0001t0006g0311 a0001c0001t0006g0312 a0001c0001t0006g0313 others(15): Show |
18 | HG01934.hp1 HG01952.hp1 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.1686+152C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59067235 | |||||||
| chr15:59067241 | C | CT | 6 | a0001c0001t0001g0232 a0001c0001t0001g0241 a0001c0001t0001g0256 others(3): Show |
6 | HG02451.hp2 HG02723.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1686+171dupT | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr15 | 59067241 | ||||||
| chr15:59067241 | CTT | C | 15 | a0001c0001t0004g0022 a0001c0001t0004g0034 a0001c0001t0004g0035 others(12): Show |
16 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.1686+170_1686+171d others(4): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr15 | 59067241 | ||||||
| chr15:59067254 | T | A | 143 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0088 others(140): Show |
143 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1686+171T>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59067254 | |||||||
| chr15:59067255 | AACTCC | A | 143 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0088 others(140): Show |
143 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1686+173_1686+177d others(7): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59067255 | |||||||
| chr15:59067256 | ACTCC | A | 16 | a0001c0001t0004g0022 a0001c0001t0004g0034 a0001c0001t0004g0035 others(13): Show |
17 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.1686+179_1686+182d others(6): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr15 | 59067256 | ||||||
| chr15:59067334 | C | T | 1 | a0001c0002t0001g0107 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1686+251C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59067334 | |||||||
| chr15:59067399 | C | G | 2 | a0001c0002t0003g0009 a0001c0002t0003g0010 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1686+316C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59067399 | |||||||
| chr15:59067407 | G | A | 6 | a0001c0001t0003g0242 a0001c0001t0003g0243 a0001c0001t0003g0268 others(3): Show |
6 | HG02630.hp1 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1686+324G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59067407 | |||||||
| chr15:59067452 | T | C | 1 | a0001c0001t0018g0233 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1686+369T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59067452 | |||||||
| chr15:59067525 | C | T | 159 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0088 others(156): Show |
160 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.1686+442C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59067525 | |||||||
| chr15:59067527 | C | T | 1 | a0002c0003t0001g0018 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1686+444C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59067527 | |||||||
| chr15:59067727 | C | T | 160 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0088 others(157): Show |
161 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.1686+644C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59067727 | |||||||
| chr15:59067809 | C | G | 14 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(11): Show |
14 | HG00741.hp2 HG01168.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.1686+726C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59067809 | |||||||
| chr15:59067824 | C | T | 20 | a0001c0001t0006g0311 a0001c0001t0006g0312 a0001c0001t0006g0313 others(17): Show |
20 | HG01934.hp1 HG01952.hp1 HG02027.hp2 others(17): Show |
intron_variant | MODIFIER | c.1686+741C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59067824 | |||||||
| chr15:59067891 | G | A | 2 | a0001c0001t0003g0327 a0001c0001t0003g0328 |
2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1686+808G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59067891 | |||||||
| chr15:59067983 | A | C | 1 | a0001c0002t0001g0110 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1686+900A>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59067983 | |||||||
| chr15:59067990 | A | G | 15 | a0001c0001t0001g0232 a0001c0001t0001g0241 a0001c0001t0001g0256 others(12): Show |
15 | HG02451.hp2 HG02630.hp1 HG02723.hp1 others(12): Show |
intron_variant | MODIFIER | c.1686+907A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59067990 | |||||||
| chr15:59068018 | C | G | 1 | a0001c0001t0005g0141 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1686+935C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59068018 | |||||||
| chr15:59068039 | C | T | 1 | a0001c0002t0001g0149 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1686+956C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59068039 | |||||||
| chr15:59068066 | T | G | 1 | a0002c0003t0001g0082 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1686+983T>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59068066 | |||||||
| chr15:59068286 | T | C | 25 | a0001c0001t0006g0311 a0001c0001t0006g0312 a0001c0001t0006g0313 others(22): Show |
25 | HG01167.hp2 HG01169.hp2 HG01934.hp1 others(22): Show |
intron_variant | MODIFIER | c.1686+1203T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59068286 | |||||||
| chr15:59068434 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1686+1351C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59068434 | |||||||
| chr15:59068612 | T | G | 1 | a0002c0003t0001g0179 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1686+1529T>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59068612 | |||||||
| chr15:59068943 | G | A | 1 | a0001c0001t0002g0248 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1686+1860G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59068943 | |||||||
| chr15:59069005 | C | T | 135 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0088 others(132): Show |
136 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.1686+1922C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59069005 | |||||||
| chr15:59069056 | A | G | 25 | a0001c0001t0006g0311 a0001c0001t0006g0312 a0001c0001t0006g0313 others(22): Show |
25 | HG01167.hp2 HG01169.hp2 HG01934.hp1 others(22): Show |
intron_variant | MODIFIER | c.1686+1973A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59069056 | |||||||
| chr15:59069073 | C | CA | 13 | a0001c0001t0001g0231 a0001c0001t0003g0045 a0001c0002t0001g0098 others(10): Show |
13 | HG00741.hp1 HG01167.hp1 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.1686+2010dupA | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr15 | 59069073 | ||||||
| chr15:59069073 | CA | C | 65 | a0001c0001t0001g0232 a0001c0001t0001g0241 a0001c0001t0001g0256 others(62): Show |
65 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.1686+2010delA | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr15 | 59069073 | ||||||
| chr15:59069073 | CAA | C | 101 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0088 others(98): Show |
102 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.1686+2009_1686+201 others(6): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr15 | 59069073 | ||||||
| chr15:59069075 | A | G | 1 | a0001c0001t0002g0188 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1686+1992A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59069075 | |||||||
| chr15:59069266 | G | T | 1 | a0001c0002t0001g0116 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1686+2183G>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59069266 | |||||||
| chr15:59069413 | G | A | 12 | a0001c0001t0005g0267 a0001c0001t0005g0284 a0001c0001t0005g0285 others(9): Show |
12 | HG00099.hp2 HG00408.hp1 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.1686+2330G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59069413 | |||||||
| chr15:59069478 | A | G | 40 | a0001c0001t0002g0200 a0001c0001t0002g0244 a0001c0001t0002g0245 others(37): Show |
40 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.1686+2395A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59069478 | |||||||
| chr15:59069573 | C | G | 1 | a0001c0001t0002g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1686+2490C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59069573 | |||||||
| chr15:59069712 | T | A | 6 | a0001c0001t0001g0232 a0001c0001t0001g0241 a0001c0001t0001g0256 others(3): Show |
6 | HG02451.hp2 HG02723.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1686+2629T>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59069712 | |||||||
| chr15:59070029 | C | CT | 26 | a0001c0001t0003g0242 a0001c0001t0003g0268 a0001c0001t0003g0279 others(23): Show |
26 | HG00438.hp1 HG00609.hp2 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.1686+2976dupT | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr15 | 59070029 | ||||||
| chr15:59070029 | C | CTT | 6 | a0001c0001t0003g0016 a0001c0001t0003g0278 a0001c0001t0003g0303 others(3): Show |
6 | HG01891.hp1 HG02055.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1686+2975_1686+297 others(6): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr15 | 59070029 | ||||||
| chr15:59070029 | C | CTTT | 10 | a0001c0001t0001g0232 a0001c0001t0001g0241 a0001c0001t0001g0256 others(7): Show |
10 | HG00741.hp1 HG02451.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1686+2974_1686+297 others(7): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr15 | 59070029 | ||||||
| chr15:59070029 | C | CTTTT | 6 | a0001c0001t0001g0231 a0001c0001t0001g0257 a0001c0001t0001g0258 others(3): Show |
6 | HG02055.hp1 HG02647.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1686+2973_1686+297 others(8): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr15 | 59070029 | ||||||
| chr15:59070029 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0007g0024 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1686+2967_1686+297 others(14): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr15 | 59070029 | ||||||
| chr15:59070029 | CT | C | 6 | a0001c0002t0001g0021 a0001c0002t0001g0103 a0001c0002t0003g0147 others(3): Show |
6 | HG01256.hp2 NA18951.hp2 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.1686+2976delT | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr15 | 59070029 | ||||||
| chr15:59070029 | CTTT | C | 32 | a0001c0001t0002g0115 a0001c0001t0002g0188 a0001c0001t0002g0201 others(29): Show |
33 | HG00621.hp1 HG00639.hp1 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.1686+2974_1686+297 others(7): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr15 | 59070029 | ||||||
| chr15:59070029 | CTTTT | C | 94 | a0001c0001t0002g0014 a0001c0001t0002g0088 a0001c0001t0002g0089 others(91): Show |
94 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.1686+2973_1686+297 others(8): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr15 | 59070029 | ||||||
| chr15:59070029 | CTTTTT | C | 8 | a0001c0001t0002g0072 a0001c0001t0002g0189 a0001c0001t0002g0198 others(5): Show |
8 | HG01070.hp1 HG01169.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.1686+2972_1686+297 others(9): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr15 | 59070029 | ||||||
| chr15:59070029 | CTTTTTTT others(7): Show |
C | 1 | a0001c0002t0001g0150 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1686+2963_1686+297 others(18): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr15 | 59070029 | ||||||
| chr15:59070029 | CTTTTTTT others(10): Show |
C | 1 | a0001c0002t0003g0239 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1686+2960_1686+297 others(21): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr15 | 59070029 | ||||||
| chr15:59070035 | T | TTC | 7 | a0001c0001t0007g0234 a0001c0001t0007g0235 a0001c0001t0007g0240 others(4): Show |
7 | HG02027.hp2 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1686+2953_1686+295 others(6): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr15 | 59070035 | ||||||
| chr15:59070036 | T | TC | 10 | a0001c0001t0006g0311 a0001c0001t0006g0312 a0001c0001t0006g0313 others(7): Show |
10 | HG01934.hp1 HG01952.hp1 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.1686+2953_1686+295 others(5): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59070036 | |||||||
| chr15:59070037 | T | C | 3 | a0001c0001t0006g0316 a0001c0001t0006g0321 a0001c0001t0023g0320 |
3 | NA18959.hp1 NA18989.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1686+2954T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59070037 | |||||||
| chr15:59070059 | T | A | 137 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0088 others(134): Show |
138 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.1686+2976T>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59070059 | |||||||
| chr15:59070061 | G | A | 5 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0003g0003 others(2): Show |
5 | HG00741.hp2 HG01168.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1686+2978G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59070061 | |||||||
| chr15:59070087 | C | G | 11 | a0001c0001t0001g0231 a0001c0001t0003g0006 a0001c0001t0003g0007 others(8): Show |
11 | HG02055.hp1 HG02647.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.1686+3004C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59070087 | |||||||
| chr15:59070101 | C | T | 1 | a0001c0002t0001g0144 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1686+3018C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59070101 | |||||||
| chr15:59070117 | C | G | 135 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0088 others(132): Show |
136 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.1686+3034C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59070117 | |||||||
| chr15:59070169 | C | T | 1 | a0001c0002t0001g0163 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1686+3086C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59070169 | |||||||
| chr15:59070269 | G | A | 224 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(221): Show |
225 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.1686+3186G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59070269 | |||||||
| chr15:59070357 | G | T | 1 | a0001c0001t0004g0226 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1686+3274G>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59070357 | |||||||
| chr15:59070556 | C | A | 133 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0088 others(130): Show |
134 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.1686+3473C>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59070556 | |||||||
| chr15:59070644 | T | C | 2 | a0001c0002t0001g0087 a0002c0003t0001g0111 |
2 | HG01517.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1686+3561T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59070644 | |||||||
| chr15:59070707 | G | T | 1 | a0001c0001t0002g0217 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1686+3624G>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59070707 | |||||||
| chr15:59070734 | A | C | 3 | a0001c0001t0002g0188 a0001c0001t0004g0022 a0001c0001t0004g0038 |
3 | HG03239.hp2 HG03927.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1686+3651A>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59070734 | |||||||
| chr15:59070891 | A | G | 20 | a0001c0001t0001g0232 a0001c0001t0001g0241 a0001c0001t0001g0256 others(17): Show |
20 | HG01167.hp2 HG01169.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.1686+3808A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59070891 | |||||||
| chr15:59070938 | T | C | 12 | a0001c0001t0001g0231 a0001c0001t0003g0006 a0001c0001t0003g0007 others(9): Show |
12 | HG02055.hp1 HG02258.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.1686+3855T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59070938 | |||||||
| chr15:59071008 | G | A | 1 | a0001c0001t0002g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1686+3925G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59071008 | |||||||
| chr15:59071150 | T | C | 1 | a0001c0002t0015g0093 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1686+4067T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59071150 | |||||||
| chr15:59071215 | C | T | 1 | a0001c0001t0002g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1686+4132C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59071215 | |||||||
| chr15:59071298 | C | CA | 21 | a0001c0001t0001g0232 a0001c0001t0001g0241 a0001c0001t0001g0256 others(18): Show |
21 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.1686+4234dupA | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr15 | 59071298 | ||||||
| chr15:59071298 | C | T | 1 | a0001c0001t0002g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1686+4215C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59071298 | |||||||
| chr15:59071298 | CA | C | 167 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(164): Show |
168 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.1686+4234delA | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr15 | 59071298 | ||||||
| chr15:59071414 | G | A | 1 | a0001c0001t0004g0036 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1686+4331G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59071414 | |||||||
| chr15:59071470 | C | T | 1 | a0001c0001t0002g0228 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1686+4387C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59071470 | |||||||
| chr15:59071481 | G | A | 1 | a0001c0004t0003g0202 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1686+4398G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59071481 | |||||||
| chr15:59071488 | C | G | 1 | a0001c0002t0001g0117 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1686+4405C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59071488 | |||||||
| chr15:59071554 | G | C | 140 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0088 others(137): Show |
141 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.1687-4400G>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59071554 | |||||||
| chr15:59071690 | C | CA | 19 | a0001c0001t0003g0327 a0001c0001t0003g0328 a0001c0001t0006g0311 others(16): Show |
19 | HG01934.hp1 HG01952.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.1687-4249dupA | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr15 | 59071690 | ||||||
| chr15:59071702 | A | T | 138 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(135): Show |
139 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.1687-4252A>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59071702 | |||||||
| chr15:59071780 | G | C | 4 | a0001c0001t0004g0054 a0001c0001t0004g0300 a0001c0001t0004g0301 others(1): Show |
4 | HG01891.hp2 HG02258.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1687-4174G>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59071780 | |||||||
| chr15:59071815 | G | A | 140 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0088 others(137): Show |
141 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.1687-4139G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59071815 | |||||||
| chr15:59071836 | G | C | 2 | a0001c0001t0002g0192 a0001c0001t0002g0198 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1687-4118G>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59071836 | |||||||
| chr15:59072208 | G | A | 6 | a0001c0001t0001g0232 a0001c0001t0001g0241 a0001c0001t0001g0256 others(3): Show |
6 | HG02451.hp2 HG02723.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1687-3746G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59072208 | |||||||
| chr15:59072270 | A | C | 236 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(233): Show |
237 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.1687-3684A>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59072270 | |||||||
| chr15:59072315 | T | C | 195 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(192): Show |
196 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.1687-3639T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59072315 | |||||||
| chr15:59072352 | A | G | 17 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(14): Show |
17 | HG00741.hp2 HG01168.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1687-3602A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59072352 | |||||||
| chr15:59072450 | C | CT | 20 | a0001c0001t0001g0232 a0001c0001t0001g0241 a0001c0001t0001g0256 others(17): Show |
20 | HG01123.hp1 HG01175.hp1 HG01256.hp2 others(17): Show |
intron_variant | MODIFIER | c.1687-3481dupT | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr15 | 59072450 | ||||||
| chr15:59072450 | C | CTT | 11 | a0001c0001t0001g0231 a0001c0001t0003g0006 a0001c0001t0003g0007 others(8): Show |
11 | HG02055.hp1 HG02258.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.1687-3482_1687-348 others(6): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr15 | 59072450 | ||||||
| chr15:59072450 | C | CTTT | 6 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0003g0003 others(3): Show |
6 | HG00741.hp2 HG01168.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1687-3483_1687-348 others(7): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr15 | 59072450 | ||||||
| chr15:59072450 | CT | C | 9 | a0001c0001t0002g0014 a0001c0001t0002g0115 a0001c0001t0002g0206 others(6): Show |
9 | HG01167.hp2 HG02897.hp2 HG03453.hp2 others(6): Show |
intron_variant | MODIFIER | c.1687-3481delT | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr15 | 59072450 | ||||||
| chr15:59072450 | CTT | C | 130 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(127): Show |
131 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.1687-3482_1687-348 others(6): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr15 | 59072450 | ||||||
| chr15:59072507 | G | A | 1 | a0001c0002t0001g0097 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1687-3447G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59072507 | |||||||
| chr15:59072515 | G | A | 134 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(131): Show |
135 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.1687-3439G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59072515 | |||||||
| chr15:59072541 | C | T | 1 | a0001c0001t0004g0226 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1687-3413C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59072541 | |||||||
| chr15:59072653 | C | T | 1 | a0002c0003t0001g0083 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1687-3301C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59072653 | |||||||
| chr15:59072731 | C | T | 1 | a0001c0001t0010g0058 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1687-3223C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59072731 | |||||||
| chr15:59072785 | T | A | 195 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(192): Show |
196 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.1687-3169T>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59072785 | |||||||
| chr15:59072823 | G | GGTT | 4 | a0001c0001t0001g0231 a0001c0001t0003g0006 a0001c0001t0003g0007 others(1): Show |
4 | HG02055.hp1 HG02647.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1687-3131_1687-313 others(7): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59072823 | |||||||
| chr15:59072826 | T | G | 4 | a0001c0001t0001g0231 a0001c0001t0003g0006 a0001c0001t0003g0007 others(1): Show |
4 | HG02055.hp1 HG02647.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1687-3128T>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59072826 | |||||||
| chr15:59072880 | T | TA | 137 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0088 others(134): Show |
138 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.1687-3061dupA | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr15 | 59072880 | ||||||
| chr15:59072880 | T | TAA | 6 | a0001c0001t0002g0206 a0001c0001t0004g0037 a0001c0001t0004g0040 others(3): Show |
6 | HG02109.hp1 HG02896.hp1 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.1687-3062_1687-306 others(6): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr15 | 59072880 | ||||||
| chr15:59072894 | C | A | 175 | a0001c0001t0001g0232 a0001c0001t0001g0241 a0001c0001t0001g0256 others(172): Show |
176 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.1687-3060C>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59072894 | |||||||
| chr15:59072932 | G | T | 1 | a0001c0001t0003g0050 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1687-3022G>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59072932 | |||||||
| chr15:59073064 | T | C | 236 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(233): Show |
237 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.1687-2890T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59073064 | |||||||
| chr15:59073139 | C | T | 2 | a0001c0002t0001g0184 a0002c0003t0001g0077 |
2 | HG00558.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.1687-2815C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59073139 | |||||||
| chr15:59073206 | G | C | 173 | a0001c0001t0001g0232 a0001c0001t0001g0241 a0001c0001t0001g0256 others(170): Show |
174 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.1687-2748G>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59073206 | |||||||
| chr15:59073260 | C | T | 2 | a0001c0001t0003g0327 a0001c0001t0003g0328 |
2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1687-2694C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59073260 | |||||||
| chr15:59073266 | G | C | 1 | a0001c0001t0004g0034 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1687-2688G>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59073266 | |||||||
| chr15:59073324 | A | G | 1 | a0002c0003t0001g0122 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1687-2630A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59073324 | |||||||
| chr15:59073397 | C | T | 140 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0088 others(137): Show |
141 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.1687-2557C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59073397 | |||||||
| chr15:59073481 | C | CA | 35 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(32): Show |
35 | HG00741.hp2 HG01168.hp1 HG01934.hp1 others(32): Show |
intron_variant | MODIFIER | c.1687-2459dupA | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr15 | 59073481 | ||||||
| chr15:59073492 | A | AAT | 136 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(133): Show |
137 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.1687-2461_1687-246 others(6): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr15 | 59073492 | ||||||
| chr15:59073492 | A | AT | 14 | a0001c0001t0001g0232 a0001c0001t0001g0241 a0001c0001t0001g0256 others(11): Show |
14 | HG02451.hp2 HG02630.hp1 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.1687-2462_1687-246 others(5): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59073492 | |||||||
| chr15:59073492 | A | T | 3 | a0001c0001t0002g0115 a0001c0001t0003g0016 a0001c0001t0005g0141 |
3 | HG02572.hp2 HG03834.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1687-2462A>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59073492 | |||||||
| chr15:59073522 | C | G | 1 | a0001c0002t0001g0132 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1687-2432C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59073522 | |||||||
| chr15:59073583 | T | G | 235 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(232): Show |
236 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.1687-2371T>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59073583 | |||||||
| chr15:59073782 | G | A | 2 | a0001c0001t0004g0035 a0001c0001t0004g0039 |
2 | HG02886.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1687-2172G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59073782 | |||||||
| chr15:59073855 | T | C | 2 | a0001c0001t0003g0327 a0001c0001t0003g0328 |
2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1687-2099T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59073855 | |||||||
| chr15:59073862 | G | A | 194 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(191): Show |
195 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(192): Show |
intron_variant | MODIFIER | c.1687-2092G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59073862 | |||||||
| chr15:59073900 | T | G | 139 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(136): Show |
140 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.1687-2054T>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59073900 | |||||||
| chr15:59074170 | G | A | 1 | a0001c0001t0004g0036 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1687-1784G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59074170 | |||||||
| chr15:59074239 | T | A | 4 | a0001c0002t0003g0013 a0001c0002t0003g0236 a0001c0002t0003g0238 others(1): Show |
4 | HG02257.hp1 HG03041.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1687-1715T>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59074239 | |||||||
| chr15:59074303 | G | A | 1 | a0001c0001t0003g0310 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1687-1651G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59074303 | |||||||
| chr15:59074312 | T | C | 1 | a0001c0001t0003g0310 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1687-1642T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59074312 | |||||||
| chr15:59074364 | A | G | 140 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0088 others(137): Show |
141 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.1687-1590A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59074364 | |||||||
| chr15:59074478 | C | A | 139 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0088 others(136): Show |
140 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.1687-1476C>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59074478 | |||||||
| chr15:59074792 | GC | G | 139 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(136): Show |
140 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.1687-1161delC | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59074792 | |||||||
| chr15:59074926 | A | G | 1 | a0002c0003t0001g0074 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1687-1028A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59074926 | |||||||
| chr15:59075132 | G | A | 139 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0088 others(136): Show |
140 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.1687-822G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59075132 | |||||||
| chr15:59075634 | A | G | 1 | a0002c0003t0003g0309 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1687-320A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59075634 | |||||||
| chr15:59075717 | A | T | 1 | a0001c0001t0004g0033 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1687-237A>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59075717 | |||||||
| chr15:59075735 | A | G | 2 | a0001c0001t0003g0268 a0001c0001t0003g0279 |
2 | HG02630.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1687-219A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59075735 | |||||||
| chr15:59075812 | G | T | 1 | a0002c0003t0003g0309 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1687-142G>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 6/13 | chr15 | 59075812 | |||||||
| chr15:59076311 | T | G | 148 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(145): Show |
149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.1948+96T>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | chr15 | 59076311 | |||||||
| chr15:59076688 | C | T | 18 | a0001c0001t0006g0311 a0001c0001t0006g0312 a0001c0001t0006g0313 others(15): Show |
18 | HG01934.hp1 HG01952.hp1 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.1948+473C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | chr15 | 59076688 | |||||||
| chr15:59076744 | C | T | 3 | a0001c0001t0002g0269 a0001c0001t0002g0270 a0001c0001t0002g0272 |
3 | HG00423.hp1 HG02056.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1948+529C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | chr15 | 59076744 | |||||||
| chr15:59076773 | T | C | 194 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(191): Show |
195 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(192): Show |
intron_variant | MODIFIER | c.1948+558T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | chr15 | 59076773 | |||||||
| chr15:59076798 | A | G | 3 | a0001c0001t0007g0234 a0001c0001t0007g0235 a0001c0001t0007g0240 |
3 | HG02572.hp1 HG02717.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1948+583A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | chr15 | 59076798 | |||||||
| chr15:59077002 | G | A | 5 | a0001c0001t0007g0011 a0001c0001t0007g0023 a0001c0001t0007g0024 others(2): Show |
5 | HG01167.hp2 HG01169.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1948+787G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | chr15 | 59077002 | |||||||
| chr15:59077009 | C | T | 2 | a0001c0001t0014g0046 a0001c0001t0014g0305 |
2 | HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1948+794C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | chr15 | 59077009 | |||||||
| chr15:59077116 | A | AAC | 165 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0088 others(162): Show |
166 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.1948+902_1948+903i others(4): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr15 | 59077116 | ||||||
| chr15:59077549 | T | G | 1 | a0001c0002t0001g0021 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1948+1334T>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | chr15 | 59077549 | |||||||
| chr15:59077550 | G | T | 1 | a0001c0002t0001g0021 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1948+1335G>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | chr15 | 59077550 | |||||||
| chr15:59077551 | T | G | 1 | a0001c0002t0001g0021 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1948+1336T>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | chr15 | 59077551 | |||||||
| chr15:59077618 | T | A | 2 | a0001c0001t0003g0327 a0001c0001t0003g0328 |
2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1948+1403T>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | chr15 | 59077618 | |||||||
| chr15:59077628 | A | T | 1 | a0001c0002t0001g0021 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1948+1413A>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | chr15 | 59077628 | |||||||
| chr15:59077811 | G | T | 2 | a0001c0002t0001g0021 a0001c0002t0001g0138 |
2 | HG02132.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1948+1596G>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | chr15 | 59077811 | |||||||
| chr15:59077849 | A | G | 1 | a0001c0001t0003g0045 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1948+1634A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | chr15 | 59077849 | |||||||
| chr15:59077880 | C | G | 2 | a0001c0001t0003g0327 a0001c0001t0003g0328 |
2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1948+1665C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | chr15 | 59077880 | |||||||
| chr15:59077909 | G | A | 135 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0088 others(132): Show |
136 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.1948+1694G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | chr15 | 59077909 | |||||||
| chr15:59077927 | A | C | 1 | a0001c0002t0001g0021 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1948+1712A>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | chr15 | 59077927 | |||||||
| chr15:59078037 | T | C | 1 | a0001c0001t0002g0193 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1948+1822T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | chr15 | 59078037 | |||||||
| chr15:59078043 | A | G | 18 | a0001c0001t0006g0311 a0001c0001t0006g0312 a0001c0001t0006g0313 others(15): Show |
18 | HG01934.hp1 HG01952.hp1 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.1948+1828A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | chr15 | 59078043 | |||||||
| chr15:59078156 | T | A | 5 | a0001c0002t0001g0153 a0001c0002t0001g0162 a0001c0002t0001g0163 others(2): Show |
5 | HG02280.hp1 HG02559.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1948+1941T>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | chr15 | 59078156 | |||||||
| chr15:59078200 | A | T | 1 | a0001c0001t0002g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1948+1985A>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | chr15 | 59078200 | |||||||
| chr15:59078277 | C | G | 3 | a0001c0001t0009g0199 a0001c0001t0009g0263 a0001c0001t0009g0324 |
3 | HG02109.hp1 HG02896.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1948+2062C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | chr15 | 59078277 | |||||||
| chr15:59078510 | T | C | 1 | a0001c0002t0003g0147 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1948+2295T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | chr15 | 59078510 | |||||||
| chr15:59078525 | C | T | 1 | a0001c0001t0005g0178 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1948+2310C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | chr15 | 59078525 | |||||||
| chr15:59078552 | T | TA | 11 | a0001c0001t0001g0259 a0001c0001t0003g0310 a0001c0001t0003g0327 others(8): Show |
11 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(8): Show |
intron_variant | MODIFIER | c.1948+2360dupA | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr15 | 59078552 | ||||||
| chr15:59078552 | TA | T | 39 | a0001c0001t0002g0210 a0001c0001t0004g0033 a0001c0001t0004g0040 others(36): Show |
39 | HG01167.hp1 HG01167.hp2 HG01169.hp2 others(36): Show |
intron_variant | MODIFIER | c.1948+2360delA | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr15 | 59078552 | ||||||
| chr15:59078552 | TAA | T | 125 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0088 others(122): Show |
126 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.1948+2359_1948+236 others(6): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr15 | 59078552 | ||||||
| chr15:59078595 | C | T | 3 | a0001c0002t0001g0125 a0001c0002t0001g0126 a0001c0002t0001g0171 |
3 | HG01496.hp2 HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1949-2341C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | chr15 | 59078595 | |||||||
| chr15:59078625 | G | A | 134 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(131): Show |
135 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.1949-2311G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | chr15 | 59078625 | |||||||
| chr15:59078703 | T | A | 194 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(191): Show |
195 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(192): Show |
intron_variant | MODIFIER | c.1949-2233T>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | chr15 | 59078703 | |||||||
| chr15:59078838 | G | A | 2 | a0001c0001t0003g0327 a0001c0001t0003g0328 |
2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1949-2098G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | chr15 | 59078838 | |||||||
| chr15:59078866 | GA | G | 138 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(135): Show |
138 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.1949-2054delA | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr15 | 59078866 | ||||||
| chr15:59078881 | A | G | 133 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(130): Show |
134 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.1949-2055A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | chr15 | 59078881 | |||||||
| chr15:59078908 | G | A | 1 | a0001c0001t0007g0235 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1949-2028G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | chr15 | 59078908 | |||||||
| chr15:59079130 | T | C | 1 | a0001c0002t0001g0126 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1949-1806T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | chr15 | 59079130 | |||||||
| chr15:59079464 | A | G | 49 | a0001c0001t0005g0293 a0001c0002t0001g0117 a0001c0002t0001g0180 others(46): Show |
49 | HG00140.hp2 HG00280.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.1949-1472A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | chr15 | 59079464 | |||||||
| chr15:59079619 | C | T | 1 | a0002c0003t0001g0148 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1949-1317C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | chr15 | 59079619 | |||||||
| chr15:59079641 | A | C | 1 | a0001c0001t0006g0322 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1949-1295A>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | chr15 | 59079641 | |||||||
| chr15:59079655 | C | CT | 10 | a0001c0001t0001g0232 a0001c0001t0001g0241 a0001c0001t0001g0256 others(7): Show |
10 | HG01070.hp1 HG02451.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1949-1266dupT | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr15 | 59079655 | ||||||
| chr15:59079655 | CT | C | 135 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0088 others(132): Show |
136 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.1949-1266delT | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr15 | 59079655 | ||||||
| chr15:59079766 | T | G | 1 | a0001c0004t0003g0262 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1949-1170T>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | chr15 | 59079766 | |||||||
| chr15:59079829 | G | T | 135 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0088 others(132): Show |
136 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.1949-1107G>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | chr15 | 59079829 | |||||||
| chr15:59079831 | T | C | 135 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0088 others(132): Show |
136 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.1949-1105T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | chr15 | 59079831 | |||||||
| chr15:59079916 | A | G | 3 | a0001c0001t0003g0016 a0001c0001t0003g0049 a0001c0001t0003g0051 |
3 | HG02572.hp2 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1949-1020A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | chr15 | 59079916 | |||||||
| chr15:59080077 | T | C | 1 | a0001c0001t0004g0226 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1949-859T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | chr15 | 59080077 | |||||||
| chr15:59080112 | TCC | T | 3 | a0001c0001t0003g0243 a0001c0001t0003g0268 a0001c0001t0003g0279 |
3 | HG02630.hp1 HG02897.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1949-823_1949-822d others(4): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | chr15 | 59080112 | |||||||
| chr15:59080114 | C | CT | 82 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(79): Show |
83 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(80): Show |
intron_variant | MODIFIER | c.1949-798dupT | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr15 | 59080114 | ||||||
| chr15:59080114 | C | CTT | 8 | a0001c0001t0002g0273 a0001c0001t0003g0006 a0001c0001t0004g0022 others(5): Show |
8 | HG01175.hp2 HG01256.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.1949-799_1949-798d others(4): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr15 | 59080114 | ||||||
| chr15:59080114 | C | CTTT | 28 | a0001c0001t0002g0200 a0001c0001t0002g0245 a0001c0001t0002g0246 others(25): Show |
28 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(25): Show |
intron_variant | MODIFIER | c.1949-800_1949-798d others(5): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr15 | 59080114 | ||||||
| chr15:59080114 | C | CTTTT | 12 | a0001c0001t0002g0244 a0001c0001t0002g0249 a0001c0001t0002g0252 others(9): Show |
12 | HG00423.hp1 HG01070.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.1949-801_1949-798d others(6): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr15 | 59080114 | ||||||
| chr15:59080114 | C | T | 1 | a0001c0001t0003g0242 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1949-822C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | chr15 | 59080114 | |||||||
| chr15:59080114 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0004g0041 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1949-809_1949-798d others(14): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr15 | 59080114 | ||||||
| chr15:59080160 | G | A | 2 | a0001c0005t0005g0096 a0001c0005t0005g0120 |
2 | NA18998.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1949-776G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | chr15 | 59080160 | |||||||
| chr15:59080305 | G | C | 1 | a0001c0001t0003g0310 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1949-631G>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | chr15 | 59080305 | |||||||
| chr15:59080363 | C | G | 49 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0241 others(46): Show |
49 | HG01167.hp2 HG01169.hp2 HG01934.hp1 others(46): Show |
intron_variant | MODIFIER | c.1949-573C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | chr15 | 59080363 | |||||||
| chr15:59080367 | C | G | 25 | a0001c0001t0002g0188 a0001c0001t0002g0201 a0001c0001t0004g0022 others(22): Show |
26 | HG00639.hp1 HG01123.hp2 HG01175.hp2 others(23): Show |
intron_variant | MODIFIER | c.1949-569C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | chr15 | 59080367 | |||||||
| chr15:59080798 | G | T | 3 | a0001c0001t0010g0056 a0001c0001t0010g0058 a0005c0011t0010g0057 |
3 | HG01175.hp2 HG02735.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1949-138G>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 7/13 | chr15 | 59080798 | |||||||
| chr15:59081364 | A | G | 1 | a0001c0001t0003g0310 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2297+80A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 8/13 | chr15 | 59081364 | |||||||
| chr15:59081389 | A | C | 5 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0003g0003 others(2): Show |
5 | HG00741.hp2 HG01168.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2297+105A>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 8/13 | chr15 | 59081389 | |||||||
| chr15:59081531 | C | A | 1 | a0001c0001t0004g0226 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2297+247C>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 8/13 | chr15 | 59081531 | |||||||
| chr15:59081531 | C | CA | 28 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0241 others(25): Show |
28 | HG01361.hp1 HG02055.hp1 HG02135.hp1 others(25): Show |
intron_variant | MODIFIER | c.2297+255dupA | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr15 | 59081531 | ||||||
| chr15:59081595 | T | A | 137 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0088 others(134): Show |
138 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.2297+311T>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 8/13 | chr15 | 59081595 | |||||||
| chr15:59081616 | A | G | 49 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0241 others(46): Show |
49 | HG01167.hp2 HG01169.hp2 HG01934.hp1 others(46): Show |
intron_variant | MODIFIER | c.2297+332A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 8/13 | chr15 | 59081616 | |||||||
| chr15:59081670 | A | T | 134 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(131): Show |
135 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.2297+386A>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 8/13 | chr15 | 59081670 | |||||||
| chr15:59081917 | G | C | 195 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(192): Show |
196 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.2297+633G>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 8/13 | chr15 | 59081917 | |||||||
| chr15:59082069 | C | T | 1 | a0001c0001t0002g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2297+785C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 8/13 | chr15 | 59082069 | |||||||
| chr15:59082126 | G | T | 39 | a0001c0001t0002g0200 a0001c0001t0002g0244 a0001c0001t0002g0245 others(36): Show |
39 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.2297+842G>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 8/13 | chr15 | 59082126 | |||||||
| chr15:59082248 | T | C | 2 | a0001c0001t0002g0292 a0001c0001t0002g0299 |
2 | NA18943.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.2297+964T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 8/13 | chr15 | 59082248 | |||||||
| chr15:59082349 | A | G | 16 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(13): Show |
16 | HG00741.hp2 HG01168.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.2297+1065A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 8/13 | chr15 | 59082349 | |||||||
| chr15:59082369 | T | C | 2 | a0001c0001t0003g0327 a0001c0001t0003g0328 |
2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.2297+1085T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 8/13 | chr15 | 59082369 | |||||||
| chr15:59082698 | C | T | 9 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0003g0003 others(6): Show |
9 | HG00741.hp2 HG01168.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.2297+1414C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 8/13 | chr15 | 59082698 | |||||||
| chr15:59082733 | C | A | 9 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0003g0003 others(6): Show |
9 | HG00741.hp2 HG01168.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.2298-1396C>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 8/13 | chr15 | 59082733 | |||||||
| chr15:59082810 | G | A | 1 | a0001c0001t0007g0234 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2298-1319G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 8/13 | chr15 | 59082810 | |||||||
| chr15:59082904 | T | C | 244 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(241): Show |
245 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.2298-1225T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 8/13 | chr15 | 59082904 | |||||||
| chr15:59082909 | G | A | 1 | a0001c0001t0002g0273 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2298-1220G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 8/13 | chr15 | 59082909 | |||||||
| chr15:59083034 | A | G | 2 | a0001c0001t0003g0327 a0001c0001t0003g0328 |
2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.2298-1095A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 8/13 | chr15 | 59083034 | |||||||
| chr15:59083073 | C | T | 38 | a0001c0001t0002g0200 a0001c0001t0002g0244 a0001c0001t0002g0245 others(35): Show |
38 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(35): Show |
intron_variant | MODIFIER | c.2298-1056C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 8/13 | chr15 | 59083073 | |||||||
| chr15:59083107 | C | T | 1 | a0001c0001t0003g0051 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2298-1022C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 8/13 | chr15 | 59083107 | |||||||
| chr15:59083115 | C | G | 1 | a0001c0001t0003g0051 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2298-1014C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 8/13 | chr15 | 59083115 | |||||||
| chr15:59083139 | C | T | 2 | a0001c0001t0003g0327 a0001c0001t0003g0328 |
2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.2298-990C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 8/13 | chr15 | 59083139 | |||||||
| chr15:59083143 | T | TA | 182 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0241 others(179): Show |
183 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.2298-975dupA | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr15 | 59083143 | ||||||
| chr15:59083246 | A | G | 195 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(192): Show |
196 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.2298-883A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 8/13 | chr15 | 59083246 | |||||||
| chr15:59083520 | G | A | 1 | a0001c0001t0002g0271 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2298-609G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 8/13 | chr15 | 59083520 | |||||||
| chr15:59083535 | C | CA | 22 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0241 others(19): Show |
22 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.2298-580dupA | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr15 | 59083535 | ||||||
| chr15:59083577 | C | G | 3 | a0001c0001t0002g0228 a0001c0005t0005g0096 a0001c0005t0005g0120 |
3 | NA18998.hp1 NA19062.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.2298-552C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 8/13 | chr15 | 59083577 | |||||||
| chr15:59083875 | A | AC | 195 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(192): Show |
196 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.2298-253dupC | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr15 | 59083875 | ||||||
| chr15:59083935 | A | G | 5 | a0001c0001t0006g0311 a0001c0009t0006g0318 a0002c0016t0006g0173 others(2): Show |
5 | HG01934.hp1 HG01952.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.2298-194A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 8/13 | chr15 | 59083935 | |||||||
| chr15:59083978 | A | G | 1 | a0001c0001t0003g0045 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2298-151A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 8/13 | chr15 | 59083978 | |||||||
| chr15:59084003 | ATTTAT | A | 5 | a0002c0003t0001g0156 a0002c0003t0001g0174 a0002c0003t0001g0175 others(2): Show |
5 | HG00140.hp2 HG00639.hp2 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.2298-120_2298-116d others(7): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr15 | 59084003 | ||||||
| chr15:59084018 | A | C | 1 | a0001c0001t0007g0024 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2298-111A>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 8/13 | chr15 | 59084018 | |||||||
| chr15:59084307 | A | G | 1 | a0001c0001t0003g0045 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2423+53A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 9/13 | chr15 | 59084307 | |||||||
| chr15:59084332 | T | C | 139 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(136): Show |
140 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.2423+78T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 9/13 | chr15 | 59084332 | |||||||
| chr15:59084362 | C | G | 1 | a0001c0001t0004g0226 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2423+108C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 9/13 | chr15 | 59084362 | |||||||
| chr15:59084378 | C | G | 1 | a0001c0002t0001g0099 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2423+124C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 9/13 | chr15 | 59084378 | |||||||
| chr15:59084509 | A | T | 5 | a0001c0001t0007g0011 a0001c0001t0007g0023 a0001c0001t0007g0024 others(2): Show |
5 | HG01167.hp2 HG01169.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.2423+255A>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 9/13 | chr15 | 59084509 | |||||||
| chr15:59084696 | G | A | 2 | a0001c0001t0006g0316 a0001c0001t0006g0319 |
2 | NA18957.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.2423+442G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 9/13 | chr15 | 59084696 | |||||||
| chr15:59084863 | G | A | 2 | a0001c0001t0003g0327 a0001c0001t0003g0328 |
2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.2423+609G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 9/13 | chr15 | 59084863 | |||||||
| chr15:59084912 | C | T | 1 | a0001c0002t0001g0060 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2423+658C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 9/13 | chr15 | 59084912 | |||||||
| chr15:59085126 | T | G | 2 | a0001c0001t0006g0312 a0001c0001t0006g0313 |
2 | NA18956.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.2424-533T>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 9/13 | chr15 | 59085126 | |||||||
| chr15:59085242 | C | G | 1 | a0001c0001t0002g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2424-417C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 9/13 | chr15 | 59085242 | |||||||
| chr15:59085247 | C | T | 192 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(189): Show |
193 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.2424-412C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 9/13 | chr15 | 59085247 | |||||||
| chr15:59085254 | A | C | 51 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0241 others(48): Show |
51 | HG01167.hp2 HG01169.hp2 HG01934.hp1 others(48): Show |
intron_variant | MODIFIER | c.2424-405A>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 9/13 | chr15 | 59085254 | |||||||
| chr15:59085340 | A | G | 3 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0005 |
3 | HG02895.hp2 HG02965.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2424-319A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 9/13 | chr15 | 59085340 | |||||||
| chr15:59085654 | G | C | 1 | a0002c0003t0001g0179 | 1 | HG01192.hp2 | splice_region_variant&intron_variant | LOW | c.2424-5G>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 9/13 | chr15 | 59085654 | |||||||
| chr15:59086022 | T | C | 1 | a0001c0001t0002g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2550+237T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 10/13 | chr15 | 59086022 | |||||||
| chr15:59086052 | G | GTA | 14 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0241 others(11): Show |
14 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.2550+270_2550+271d others(4): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr15 | 59086052 | ||||||
| chr15:59086095 | C | G | 144 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(141): Show |
145 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.2550+310C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 10/13 | chr15 | 59086095 | |||||||
| chr15:59086146 | G | T | 9 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0003g0003 others(6): Show |
9 | HG00741.hp2 HG01168.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.2550+361G>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 10/13 | chr15 | 59086146 | |||||||
| chr15:59086154 | C | T | 1 | a0001c0001t0002g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2550+369C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 10/13 | chr15 | 59086154 | |||||||
| chr15:59086175 | A | G | 2 | a0001c0001t0014g0046 a0001c0001t0014g0305 |
2 | HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2550+390A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 10/13 | chr15 | 59086175 | |||||||
| chr15:59086417 | C | A | 1 | a0001c0001t0003g0015 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2550+632C>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 10/13 | chr15 | 59086417 | |||||||
| chr15:59086957 | G | A | 1 | a0001c0001t0003g0050 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2550+1172G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 10/13 | chr15 | 59086957 | |||||||
| chr15:59087322 | T | G | 1 | a0001c0001t0021g0052 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2550+1537T>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 10/13 | chr15 | 59087322 | |||||||
| chr15:59087386 | A | G | 2 | a0001c0005t0005g0096 a0001c0005t0005g0120 |
2 | NA18998.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.2550+1601A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 10/13 | chr15 | 59087386 | |||||||
| chr15:59087415 | C | A | 50 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(47): Show |
50 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.2550+1630C>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 10/13 | chr15 | 59087415 | |||||||
| chr15:59087567 | T | C | 1 | a0001c0002t0003g0276 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2550+1782T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 10/13 | chr15 | 59087567 | |||||||
| chr15:59087734 | G | T | 1 | a0001c0001t0002g0201 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2551-1933G>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 10/13 | chr15 | 59087734 | |||||||
| chr15:59087752 | G | GA | 20 | a0001c0001t0006g0311 a0001c0001t0006g0312 a0001c0001t0006g0313 others(17): Show |
20 | HG01934.hp1 HG01952.hp1 HG02027.hp2 others(17): Show |
intron_variant | MODIFIER | c.2551-1911dupA | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr15 | 59087752 | ||||||
| chr15:59087904 | G | T | 1 | a0002c0003t0025g0274 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2551-1763G>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 10/13 | chr15 | 59087904 | |||||||
| chr15:59088010 | T | A | 15 | a0001c0001t0006g0311 a0001c0001t0006g0312 a0001c0001t0006g0313 others(12): Show |
15 | HG01934.hp1 HG01952.hp1 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.2551-1657T>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 10/13 | chr15 | 59088010 | |||||||
| chr15:59088012 | A | G | 9 | a0001c0001t0005g0284 a0001c0001t0005g0285 a0001c0001t0005g0323 others(6): Show |
9 | HG00099.hp2 HG00408.hp1 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.2551-1655A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 10/13 | chr15 | 59088012 | |||||||
| chr15:59088305 | G | C | 1 | a0001c0001t0003g0310 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2551-1362G>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 10/13 | chr15 | 59088305 | |||||||
| chr15:59088388 | G | A | 1 | a0001c0001t0002g0272 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2551-1279G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 10/13 | chr15 | 59088388 | |||||||
| chr15:59088452 | C | T | 4 | a0001c0001t0004g0054 a0001c0001t0004g0300 a0001c0001t0004g0301 others(1): Show |
4 | HG01891.hp2 HG02258.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.2551-1215C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 10/13 | chr15 | 59088452 | |||||||
| chr15:59088541 | G | T | 1 | a0002c0003t0001g0078 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2551-1126G>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 10/13 | chr15 | 59088541 | |||||||
| chr15:59088661 | T | G | 1 | a0002c0003t0025g0274 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2551-1006T>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 10/13 | chr15 | 59088661 | |||||||
| chr15:59088761 | C | G | 12 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0241 others(9): Show |
12 | HG02055.hp1 HG02451.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.2551-906C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 10/13 | chr15 | 59088761 | |||||||
| chr15:59088853 | C | G | 130 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(127): Show |
131 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.2551-814C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 10/13 | chr15 | 59088853 | |||||||
| chr15:59088913 | T | A | 4 | a0001c0001t0007g0023 a0001c0001t0007g0024 a0001c0001t0007g0025 others(1): Show |
4 | HG01167.hp2 HG01169.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2551-754T>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 10/13 | chr15 | 59088913 | |||||||
| chr15:59089066 | C | T | 2 | a0002c0003t0001g0142 a0002c0003t0001g0143 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.2551-601C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 10/13 | chr15 | 59089066 | |||||||
| chr15:59089259 | T | C | 2 | a0001c0001t0003g0327 a0001c0001t0003g0328 |
2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.2551-408T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 10/13 | chr15 | 59089259 | |||||||
| chr15:59089435 | A | C | 23 | a0001c0001t0003g0016 a0001c0001t0003g0049 a0001c0001t0003g0051 others(20): Show |
23 | HG01934.hp1 HG01952.hp1 HG02027.hp2 others(20): Show |
intron_variant | MODIFIER | c.2551-232A>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 10/13 | chr15 | 59089435 | |||||||
| chr15:59089570 | A | T | 138 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(135): Show |
139 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.2551-97A>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 10/13 | chr15 | 59089570 | |||||||
| chr15:59089648 | A | G | 9 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0003g0003 others(6): Show |
9 | HG00741.hp2 HG01168.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.2551-19A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 10/13 | chr15 | 59089648 | |||||||
| chr15:59090006 | T | G | 1 | a0001c0001t0002g0209 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2643+247T>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 11/13 | chr15 | 59090006 | |||||||
| chr15:59090135 | T | C | 3 | a0001c0001t0003g0306 a0001c0001t0003g0307 a0001c0001t0003g0308 |
3 | HG03225.hp1 HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2643+376T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 11/13 | chr15 | 59090135 | |||||||
| chr15:59090208 | TTTTG | T | 166 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0088 others(163): Show |
167 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.2643+472_2643+475d others(6): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr15 | 59090208 | ||||||
| chr15:59090212 | G | T | 1 | a0002c0018t0001g0159 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2643+453G>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 11/13 | chr15 | 59090212 | |||||||
| chr15:59090244 | T | G | 2 | a0001c0001t0002g0014 a0001c0001t0007g0023 |
2 | HG03453.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2643+485T>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 11/13 | chr15 | 59090244 | |||||||
| chr15:59090370 | C | T | 1 | a0001c0001t0002g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2643+611C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 11/13 | chr15 | 59090370 | |||||||
| chr15:59090671 | A | G | 182 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0241 others(179): Show |
183 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.2644-388A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 11/13 | chr15 | 59090671 | |||||||
| chr15:59090702 | T | C | 9 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0003g0003 others(6): Show |
9 | HG00741.hp2 HG01168.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.2644-357T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 11/13 | chr15 | 59090702 | |||||||
| chr15:59091352 | A | T | 138 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(135): Show |
139 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.2739+198A>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 12/13 | chr15 | 59091352 | |||||||
| chr15:59091441 | A | G | 1 | a0001c0001t0003g0049 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2739+287A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 12/13 | chr15 | 59091441 | |||||||
| chr15:59091499 | G | A | 1 | a0001c0002t0003g0276 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2739+345G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 12/13 | chr15 | 59091499 | |||||||
| chr15:59091503 | A | G | 138 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(135): Show |
139 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.2739+349A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 12/13 | chr15 | 59091503 | |||||||
| chr15:59091688 | C | T | 1 | a0001c0001t0007g0234 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2739+534C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 12/13 | chr15 | 59091688 | |||||||
| chr15:59091874 | A | G | 4 | a0001c0001t0004g0054 a0001c0001t0004g0300 a0001c0001t0004g0301 others(1): Show |
4 | HG01891.hp2 HG02258.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.2740-663A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 12/13 | chr15 | 59091874 | |||||||
| chr15:59091888 | A | G | 162 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0088 others(159): Show |
163 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.2740-649A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 12/13 | chr15 | 59091888 | |||||||
| chr15:59091923 | T | C | 194 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(191): Show |
195 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(192): Show |
intron_variant | MODIFIER | c.2740-614T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 12/13 | chr15 | 59091923 | |||||||
| chr15:59092056 | A | G | 1 | a0001c0004t0003g0202 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2740-481A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 12/13 | chr15 | 59092056 | |||||||
| chr15:59092135 | T | A | 13 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0241 others(10): Show |
13 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.2740-402T>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 12/13 | chr15 | 59092135 | |||||||
| chr15:59092156 | T | C | 139 | a0001c0001t0002g0072 a0001c0001t0002g0088 a0001c0001t0002g0089 others(136): Show |
140 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.2740-381T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 12/13 | chr15 | 59092156 | |||||||
| chr15:59092782 | C | T | 139 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0088 others(136): Show |
140 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.2843+142C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 13/13 | chr15 | 59092782 | |||||||
| chr15:59092970 | C | G | 1 | a0001c0001t0002g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2843+330C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 13/13 | chr15 | 59092970 | |||||||
| chr15:59093200 | C | T | 162 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0088 others(159): Show |
163 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.2843+560C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 13/13 | chr15 | 59093200 | |||||||
| chr15:59093337 | C | CT | 16 | a0001c0001t0001g0231 a0001c0001t0001g0259 a0001c0001t0003g0007 others(13): Show |
16 | HG01175.hp1 HG02055.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.2843+721dupT | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr15 | 59093337 | ||||||
| chr15:59093337 | CT | C | 7 | a0001c0001t0003g0306 a0001c0001t0003g0308 a0001c0002t0003g0236 others(4): Show |
7 | HG02717.hp2 HG03041.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.2843+721delT | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr15 | 59093337 | ||||||
| chr15:59093361 | T | C | 6 | a0001c0001t0004g0027 a0001c0001t0004g0028 a0001c0001t0004g0029 others(3): Show |
6 | HG01346.hp1 HG01358.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.2843+721T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 13/13 | chr15 | 59093361 | |||||||
| chr15:59093361 | T | TC | 75 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0088 others(72): Show |
76 | HG00423.hp2 HG00639.hp1 HG01123.hp2 others(73): Show |
intron_variant | MODIFIER | c.2843+723dupC | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr15 | 59093361 | ||||||
| chr15:59093361 | T | TCTC | 15 | a0001c0001t0006g0312 a0001c0001t0006g0313 a0001c0001t0006g0314 others(12): Show |
15 | HG01934.hp1 HG01952.hp1 HG02523.hp2 others(12): Show |
intron_variant | MODIFIER | c.2843+722_2843+723i others(5): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr15 | 59093361 | ||||||
| chr15:59093361 | T | TTC | 51 | a0001c0001t0002g0090 a0001c0001t0002g0188 a0001c0001t0002g0196 others(48): Show |
51 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.2843+721_2843+722i others(4): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 13/13 | chr15 | 59093361 | |||||||
| chr15:59093361 | T | TTTC | 11 | a0001c0001t0002g0269 a0001c0001t0002g0272 a0001c0001t0005g0284 others(8): Show |
11 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(8): Show |
intron_variant | MODIFIER | c.2843+721_2843+722i others(5): Show |
RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 13/13 | chr15 | 59093361 | |||||||
| chr15:59093363 | C | G | 1 | a0001c0002t0001g0104 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2843+723C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 13/13 | chr15 | 59093363 | |||||||
| chr15:59093384 | T | G | 1 | a0001c0002t0001g0104 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2843+744T>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 13/13 | chr15 | 59093384 | |||||||
| chr15:59093427 | C | T | 1 | a0001c0001t0002g0228 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2843+787C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 13/13 | chr15 | 59093427 | |||||||
| chr15:59093455 | C | A | 3 | a0001c0001t0003g0016 a0001c0001t0003g0049 a0001c0001t0003g0051 |
3 | HG02572.hp2 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2843+815C>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 13/13 | chr15 | 59093455 | |||||||
| chr15:59093469 | C | T | 9 | a0001c0001t0003g0242 a0001c0001t0003g0243 a0001c0001t0003g0268 others(6): Show |
9 | HG02109.hp2 HG02615.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.2843+829C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 13/13 | chr15 | 59093469 | |||||||
| chr15:59093646 | A | G | 1 | a0001c0001t0004g0226 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2843+1006A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 13/13 | chr15 | 59093646 | |||||||
| chr15:59093712 | G | A | 3 | a0001c0001t0007g0234 a0001c0001t0007g0235 a0001c0001t0007g0240 |
3 | HG02572.hp1 HG02717.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2844-1071G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 13/13 | chr15 | 59093712 | |||||||
| chr15:59093935 | G | A | 162 | a0001c0001t0002g0014 a0001c0001t0002g0072 a0001c0001t0002g0088 others(159): Show |
163 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.2844-848G>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 13/13 | chr15 | 59093935 | |||||||
| chr15:59093949 | C | G | 1 | a0001c0001t0018g0233 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2844-834C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 13/13 | chr15 | 59093949 | |||||||
| chr15:59094151 | T | C | 194 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0231 others(191): Show |
195 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(192): Show |
intron_variant | MODIFIER | c.2844-632T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 13/13 | chr15 | 59094151 | |||||||
| chr15:59094198 | C | A | 6 | a0001c0002t0001g0109 a0001c0002t0001g0110 a0001c0002t0001g0123 others(3): Show |
6 | HG00609.hp2 HG00621.hp2 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.2844-585C>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 13/13 | chr15 | 59094198 | |||||||
| chr15:59094320 | T | C | 1 | a0001c0001t0003g0016 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2844-463T>C | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 13/13 | chr15 | 59094320 | |||||||
| chr15:59094360 | A | G | 4 | a0001c0001t0004g0054 a0001c0001t0004g0300 a0001c0001t0004g0301 others(1): Show |
4 | HG01891.hp2 HG02258.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.2844-423A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 13/13 | chr15 | 59094360 | |||||||
| chr15:59094474 | C | T | 22 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0241 others(19): Show |
22 | HG02055.hp1 HG02109.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.2844-309C>T | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 13/13 | chr15 | 59094474 | |||||||
| chr15:59094500 | A | G | 1 | a0001c0001t0003g0050 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2844-283A>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 13/13 | chr15 | 59094500 | |||||||
| chr15:59094510 | C | G | 1 | a0001c0001t0002g0205 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2844-273C>G | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 13/13 | chr15 | 59094510 | |||||||
| chr15:59094632 | C | A | 6 | a0001c0001t0001g0232 a0001c0001t0001g0241 a0001c0001t0001g0256 others(3): Show |
6 | HG02451.hp2 HG02723.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2844-151C>A | RNF111 | ENSG00000157450.16 | transcript | ENST00000348370.9 | protein_coding | 13/13 | chr15 | 59094632 |