Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 63891 |
| ensemblid | ENSG00000164068.16 |
| hgncid | 21148 |
| symbol | RNF123 |
| name | ring finger protein 123 |
| refseq_nuc | NM_022064.5 |
| refseq_prot | NP_071347.2 |
| ensembl_nuc | ENST00000327697.11 |
| ensembl_prot | ENSP00000328287.6 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 49689557 |
| end | 49721529 |
| strand | + |
| ver | v1.2 |
| region | chr3:49689557-49721529 |
| region5000 | chr3:49684557-49726529 |
| regionname0 | RNF123_chr3_49689557_49721529 |
| regionname5000 | RNF123_chr3_49684557_49726529 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 1314 | 242 | 81 | 43 | 72 | 15 | 31 | 58 | RNF123_chr3_49684557_49726529 | RNF123 | MASKG others(1309): Show |
chr3 | 49684557 | 49726529 |
| a0002 | 0/0 | 1314 | 15 | 0 | 6 | 5 | 2 | 2 | 4 | RNF123_chr3_49684557_49726529 | RNF123 | MASKG others(1309): Show |
chr3 | 49684557 | 49726529 |
| a0003 | 0/0 | 1314 | 7 | 0 | 7 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | MASKG others(1309): Show |
chr3 | 49684557 | 49726529 |
| a0004 | 0/0 | 1314 | 7 | 6 | 0 | 0 | 0 | 1 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | MASKG others(1309): Show |
chr3 | 49684557 | 49726529 |
| a0005 | 0/0 | 1314 | 3 | 0 | 0 | 2 | 0 | 1 | 1 | RNF123_chr3_49684557_49726529 | RNF123 | MASKG others(1309): Show |
chr3 | 49684557 | 49726529 |
| a0006 | 0/0 | 1314 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | RNF123_chr3_49684557_49726529 | RNF123 | MASKG others(1309): Show |
chr3 | 49684557 | 49726529 |
| a0007 | 0/0 | 1314 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | MASKG others(1309): Show |
chr3 | 49684557 | 49726529 |
| a0008 | 0/0 | 1314 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | MASKG others(1309): Show |
chr3 | 49684557 | 49726529 |
| a0009 | 0/0 | 1314 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | MASKG others(1309): Show |
chr3 | 49684557 | 49726529 |
| a0010 | 0/0 | 1314 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | MASKG others(1309): Show |
chr3 | 49684557 | 49726529 |
| a0011 | 0/0 | 1314 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | MASKG others(1309): Show |
chr3 | 49684557 | 49726529 |
| a0012 | 0/0 | 1314 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | MASKG others(1309): Show |
chr3 | 49684557 | 49726529 |
| a0013 | 0/0 | 1314 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | MASKG others(1309): Show |
chr3 | 49684557 | 49726529 |
| a0014 | 0/0 | 1314 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | MASKG others(1309): Show |
chr3 | 49684557 | 49726529 |
| a0015 | 0/0 | 738 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RNF123_chr3_49684557_49726529 | RNF123 | MASKG others(733): Show |
chr3 | 49684557 | 49726529 |
| a0016 | 0/0 | 411 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RNF123_chr3_49684557_49726529 | RNF123 | MASKG others(406): Show |
chr3 | 49684557 | 49726529 |
| a0017 | 0/0 | 1314 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RNF123_chr3_49684557_49726529 | RNF123 | MASKG others(1309): Show |
chr3 | 49684557 | 49726529 |
| a0018 | 0/0 | 1314 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | MASKG others(1309): Show |
chr3 | 49684557 | 49726529 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 3942 | 152 | 52 | 28 | 43 | 12 | 17 | RNF123_chr3_49684557_49726529 | RNF123 | ATGGC others(3937): Show |
chr3 | 49684557 | 49726529 | ||
| a0001c0002 | 0/0 | 3942 | 76 | 20 | 15 | 28 | 1 | 12 | RNF123_chr3_49684557_49726529 | RNF123 | ATGGC others(3937): Show |
chr3 | 49684557 | 49726529 | ||
| a0001c0006 | 0/0 | 3942 | 4 | 4 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | ATGGC others(3937): Show |
chr3 | 49684557 | 49726529 | ||
| a0001c0008 | 0/0 | 3942 | 3 | 2 | 0 | 1 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | ATGGC others(3937): Show |
chr3 | 49684557 | 49726529 | ||
| a0001c0010 | 0/0 | 3942 | 2 | 2 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | ATGGC others(3937): Show |
chr3 | 49684557 | 49726529 | ||
| a0001c0011 | 0/0 | 3942 | 2 | 0 | 0 | 0 | 0 | 2 | RNF123_chr3_49684557_49726529 | RNF123 | ATGGC others(3937): Show |
chr3 | 49684557 | 49726529 | ||
| a0001c0012 | 0/0 | 3942 | 2 | 0 | 0 | 0 | 2 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | ATGGC others(3937): Show |
chr3 | 49684557 | 49726529 | ||
| a0001c0023 | 0/0 | 3942 | 1 | 1 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | ATGGC others(3937): Show |
chr3 | 49684557 | 49726529 | ||
| a0002c0003 | 0/0 | 3942 | 15 | 0 | 6 | 5 | 2 | 2 | RNF123_chr3_49684557_49726529 | RNF123 | ATGGC others(3937): Show |
chr3 | 49684557 | 49726529 | ||
| a0003c0004 | 0/0 | 3942 | 7 | 0 | 7 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | ATGGC others(3937): Show |
chr3 | 49684557 | 49726529 | ||
| a0004c0005 | 0/0 | 3942 | 7 | 6 | 0 | 0 | 0 | 1 | RNF123_chr3_49684557_49726529 | RNF123 | ATGGC others(3937): Show |
chr3 | 49684557 | 49726529 | ||
| a0005c0007 | 0/0 | 3942 | 3 | 0 | 0 | 2 | 0 | 1 | RNF123_chr3_49684557_49726529 | RNF123 | ATGGC others(3937): Show |
chr3 | 49684557 | 49726529 | ||
| a0006c0009 | 0/0 | 3942 | 2 | 0 | 0 | 2 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | ATGGC others(3937): Show |
chr3 | 49684557 | 49726529 | ||
| a0007c0025 | 0/0 | 3942 | 1 | 0 | 0 | 1 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | ATGGC others(3937): Show |
chr3 | 49684557 | 49726529 | ||
| a0008c0015 | 0/0 | 3942 | 1 | 0 | 1 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | ATGGC others(3937): Show |
chr3 | 49684557 | 49726529 | ||
| a0009c0016 | 0/0 | 3942 | 1 | 0 | 1 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | ATGGC others(3937): Show |
chr3 | 49684557 | 49726529 | ||
| a0010c0024 | 0/0 | 3942 | 1 | 0 | 0 | 1 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | ATGGC others(3937): Show |
chr3 | 49684557 | 49726529 | ||
| a0011c0018 | 0/0 | 3942 | 1 | 0 | 0 | 0 | 0 | 1 | RNF123_chr3_49684557_49726529 | RNF123 | ATGGC others(3937): Show |
chr3 | 49684557 | 49726529 | ||
| a0012c0019 | 0/0 | 3942 | 1 | 1 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | ATGGC others(3937): Show |
chr3 | 49684557 | 49726529 | ||
| a0013c0014 | 0/0 | 3942 | 1 | 1 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | ATGGC others(3937): Show |
chr3 | 49684557 | 49726529 | ||
| a0014c0020 | 0/0 | 3942 | 1 | 1 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | ATGGC others(3937): Show |
chr3 | 49684557 | 49726529 | ||
| a0015c0017 | 0/0 | 3943 | 1 | 0 | 0 | 1 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | ATGGC others(3938): Show |
chr3 | 49684557 | 49726529 | ||
| a0016c0021 | 0/0 | 3941 | 1 | 0 | 0 | 1 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | ATGGC others(3936): Show |
chr3 | 49684557 | 49726529 | ||
| a0017c0022 | 0/0 | 3942 | 1 | 0 | 0 | 1 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | ATGGC others(3937): Show |
chr3 | 49684557 | 49726529 | ||
| a0018c0013 | 0/0 | 3942 | 1 | 0 | 0 | 0 | 1 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | ATGGC others(3937): Show |
chr3 | 49684557 | 49726529 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4255 | 151 | 51 | 28 | 43 | 12 | 17 | RNF123_chr3_49684557_49726529 | RNF123 | AAGAG others(4250): Show |
chr3 | 49684557 | 49726529 |
| a0001c0001t0004 | 0/0 | 4255 | 1 | 1 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | AAGAG others(4250): Show |
chr3 | 49684557 | 49726529 |
| a0001c0002t0002 | 0/0 | 4255 | 76 | 20 | 15 | 28 | 1 | 12 | RNF123_chr3_49684557_49726529 | RNF123 | AAGAG others(4250): Show |
chr3 | 49684557 | 49726529 |
| a0001c0006t0001 | 0/0 | 4255 | 4 | 4 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | AAGAG others(4250): Show |
chr3 | 49684557 | 49726529 |
| a0001c0008t0001 | 0/0 | 4255 | 2 | 2 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | AAGAG others(4250): Show |
chr3 | 49684557 | 49726529 |
| a0001c0008t0002 | 0/0 | 4255 | 1 | 0 | 0 | 1 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | AAGAG others(4250): Show |
chr3 | 49684557 | 49726529 |
| a0001c0010t0001 | 0/0 | 4255 | 2 | 2 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | AAGAG others(4250): Show |
chr3 | 49684557 | 49726529 |
| a0001c0011t0001 | 0/0 | 4255 | 2 | 0 | 0 | 0 | 0 | 2 | RNF123_chr3_49684557_49726529 | RNF123 | AAGAG others(4250): Show |
chr3 | 49684557 | 49726529 |
| a0001c0012t0001 | 0/0 | 4255 | 2 | 0 | 0 | 0 | 2 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | AAGAG others(4250): Show |
chr3 | 49684557 | 49726529 |
| a0001c0023t0003 | 0/0 | 4255 | 1 | 1 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | AAGAG others(4250): Show |
chr3 | 49684557 | 49726529 |
| a0002c0003t0001 | 0/0 | 4255 | 15 | 0 | 6 | 5 | 2 | 2 | RNF123_chr3_49684557_49726529 | RNF123 | AAGAG others(4250): Show |
chr3 | 49684557 | 49726529 |
| a0003c0004t0001 | 0/0 | 4255 | 7 | 0 | 7 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | AAGAG others(4250): Show |
chr3 | 49684557 | 49726529 |
| a0004c0005t0001 | 0/0 | 4255 | 7 | 6 | 0 | 0 | 0 | 1 | RNF123_chr3_49684557_49726529 | RNF123 | AAGAG others(4250): Show |
chr3 | 49684557 | 49726529 |
| a0005c0007t0001 | 0/0 | 4255 | 3 | 0 | 0 | 2 | 0 | 1 | RNF123_chr3_49684557_49726529 | RNF123 | AAGAG others(4250): Show |
chr3 | 49684557 | 49726529 |
| a0006c0009t0001 | 0/0 | 4255 | 2 | 0 | 0 | 2 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | AAGAG others(4250): Show |
chr3 | 49684557 | 49726529 |
| a0007c0025t0001 | 0/0 | 4255 | 1 | 0 | 0 | 1 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | AAGAG others(4250): Show |
chr3 | 49684557 | 49726529 |
| a0008c0015t0001 | 0/0 | 4255 | 1 | 0 | 1 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | AAGAG others(4250): Show |
chr3 | 49684557 | 49726529 |
| a0009c0016t0002 | 0/0 | 4255 | 1 | 0 | 1 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | AAGAG others(4250): Show |
chr3 | 49684557 | 49726529 |
| a0010c0024t0001 | 0/0 | 4255 | 1 | 0 | 0 | 1 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | AAGAG others(4250): Show |
chr3 | 49684557 | 49726529 |
| a0011c0018t0002 | 0/0 | 4255 | 1 | 0 | 0 | 0 | 0 | 1 | RNF123_chr3_49684557_49726529 | RNF123 | AAGAG others(4250): Show |
chr3 | 49684557 | 49726529 |
| a0012c0019t0002 | 0/0 | 4255 | 1 | 1 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | AAGAG others(4250): Show |
chr3 | 49684557 | 49726529 |
| a0013c0014t0001 | 0/0 | 4255 | 1 | 1 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | AAGAG others(4250): Show |
chr3 | 49684557 | 49726529 |
| a0014c0020t0002 | 0/0 | 4255 | 1 | 1 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | AAGAG others(4250): Show |
chr3 | 49684557 | 49726529 |
| a0015c0017t0002 | 0/0 | 4256 | 1 | 0 | 0 | 1 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | AAGAG others(4251): Show |
chr3 | 49684557 | 49726529 |
| a0016c0021t0001 | 0/0 | 4254 | 1 | 0 | 0 | 1 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | AAGAG others(4249): Show |
chr3 | 49684557 | 49726529 |
| a0017c0022t0001 | 0/0 | 4255 | 1 | 0 | 0 | 1 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | AAGAG others(4250): Show |
chr3 | 49684557 | 49726529 |
| a0018c0013t0001 | 0/0 | 4255 | 1 | 0 | 0 | 0 | 1 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | AAGAG others(4250): Show |
chr3 | 49684557 | 49726529 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 21 | 0 | 2 | 10 | 3 | 6 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0002 | 0/0 | 22 | 0 | 3 | 19 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0005 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0007 | 0/0 | 7 | 5 | 2 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0008 | 0/0 | 4 | 2 | 0 | 0 | 1 | 1 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0009 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0012 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 1 | 2 | 1 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0001t0004g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0002t0002g0003 | 0/0 | 22 | 1 | 7 | 9 | 0 | 5 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0002t0002g0004 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0002t0002g0006 | 0/0 | 7 | 5 | 2 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0002t0002g0011 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0002t0002g0016 | 0/0 | 4 | 0 | 0 | 0 | 0 | 4 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0002t0002g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0002t0002g0036 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0002t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0002t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0002t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0002t0002g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0002t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0002t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0002t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0002t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0002t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0002t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0006t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0006t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0006t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0008t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0008t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0010t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0011t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0012t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0001c0023t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0002c0003t0001g0015 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0002c0003t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0002c0003t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0002c0003t0001g0028 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0002c0003t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0002c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0002c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0002c0003t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0003c0004t0001g0014 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0003c0004t0001g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0004c0005t0001g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0004c0005t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0004c0005t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0004c0005t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0005c0007t0001g0018 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0006c0009t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0007c0025t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0008c0015t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0009c0016t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0010c0024t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0011c0018t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0012c0019t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0013c0014t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0014c0020t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0015c0017t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0016c0021t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0017c0022t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| a0018c0013t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | GBR | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0085 | EUR | GBR | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | GBR | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0079 | EUR | FIN | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | FIN | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG00323 | hp2 | a0001 | c0002 | t0002 | g0036 | EUR | FIN | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG00544 | hp1 | a0007 | c0025 | t0001 | g0002 | EAS | CHS | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG00544 | hp2 | a0005 | c0007 | t0001 | g0018 | EAS | CHS | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG00597 | hp2 | a0001 | c0002 | t0002 | g0098 | EAS | CHS | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG00609 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | CHS | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG00639 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG00639 | hp2 | a0002 | c0003 | t0001 | g0049 | AMR | PUR | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG00735 | hp1 | a0002 | c0003 | t0001 | g0015 | AMR | PUR | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG00738 | hp1 | a0003 | c0004 | t0001 | g0021 | AMR | PUR | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG00741 | hp1 | a0001 | c0002 | t0002 | g0023 | AMR | PUR | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG00741 | hp2 | a0001 | c0002 | t0002 | g0101 | AMR | PUR | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01070 | hp1 | a0002 | c0003 | t0001 | g0056 | AMR | PUR | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01071 | hp1 | a0002 | c0003 | t0001 | g0015 | AMR | PUR | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01099 | hp1 | a0003 | c0004 | t0001 | g0014 | AMR | PUR | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01099 | hp2 | a0002 | c0003 | t0001 | g0015 | AMR | PUR | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01106 | hp1 | a0001 | c0002 | t0002 | g0036 | AMR | PUR | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01109 | hp1 | a0002 | c0003 | t0001 | g0028 | AMR | PUR | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01109 | hp2 | a0001 | c0002 | t0002 | g0006 | AMR | PUR | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01167 | hp1 | a0001 | c0002 | t0002 | g0023 | AMR | PUR | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01168 | hp1 | a0003 | c0004 | t0001 | g0014 | AMR | PUR | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01169 | hp1 | a0003 | c0004 | t0001 | g0014 | AMR | PUR | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01175 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01243 | hp1 | a0001 | c0002 | t0002 | g0006 | AMR | PUR | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01256 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | CLM | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01257 | hp1 | a0003 | c0004 | t0001 | g0021 | AMR | CLM | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | CLM | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01258 | hp1 | a0003 | c0004 | t0001 | g0021 | AMR | CLM | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01346 | hp1 | a0008 | c0015 | t0001 | g0096 | AMR | CLM | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01346 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | CLM | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01433 | hp2 | a0003 | c0004 | t0001 | g0014 | AMR | CLM | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01496 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | CLM | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01515 | hp2 | a0002 | c0003 | t0001 | g0027 | EUR | IBS | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0057 | EUR | IBS | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01516 | hp2 | a0001 | c0012 | t0001 | g0008 | EUR | IBS | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01517 | hp1 | a0001 | c0012 | t0001 | g0008 | EUR | IBS | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01517 | hp2 | a0002 | c0003 | t0001 | g0027 | EUR | IBS | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0078 | AFR | ACB | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01928 | hp2 | a0001 | c0002 | t0002 | g0011 | AMR | PEL | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01934 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PEL | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01952 | hp2 | a0001 | c0002 | t0002 | g0100 | AMR | PEL | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02004 | hp1 | a0009 | c0016 | t0002 | g0109 | AMR | PEL | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02027 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | KHV | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02071 | hp1 | a0010 | c0024 | t0001 | g0002 | EAS | KHV | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02074 | hp2 | a0001 | c0002 | t0002 | g0037 | EAS | KHV | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02257 | hp2 | a0001 | c0006 | t0001 | g0026 | AFR | ACB | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02258 | hp2 | a0001 | c0002 | t0002 | g0004 | AFR | ACB | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02451 | hp1 | a0004 | c0005 | t0001 | g0120 | AFR | ACB | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02451 | hp2 | a0001 | c0006 | t0001 | g0026 | AFR | ACB | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02572 | hp1 | a0001 | c0002 | t0002 | g0106 | AFR | GWD | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02572 | hp2 | a0001 | c0008 | t0001 | g0042 | AFR | GWD | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02622 | hp1 | a0001 | c0002 | t0002 | g0041 | AFR | GWD | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02683 | hp1 | a0004 | c0005 | t0001 | g0119 | SAS | PJL | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02717 | hp2 | a0001 | c0002 | t0002 | g0006 | AFR | GWD | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02723 | hp1 | a0001 | c0023 | t0003 | g0046 | AFR | GWD | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02723 | hp2 | a0001 | c0006 | t0001 | g0043 | AFR | GWD | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02735 | hp1 | a0005 | c0007 | t0001 | g0018 | SAS | PJL | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02735 | hp2 | a0011 | c0018 | t0002 | g0083 | SAS | PJL | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02738 | hp1 | a0001 | c0011 | t0001 | g0001 | SAS | PJL | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02809 | hp2 | a0001 | c0002 | t0002 | g0004 | AFR | GWD | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02886 | hp1 | a0001 | c0002 | t0002 | g0116 | AFR | GWD | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02895 | hp2 | a0004 | c0005 | t0001 | g0017 | AFR | GWD | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02896 | hp1 | a0001 | c0002 | t0002 | g0041 | AFR | GWD | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02897 | hp1 | a0001 | c0002 | t0002 | g0006 | AFR | GWD | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02897 | hp2 | a0004 | c0005 | t0001 | g0017 | AFR | GWD | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0006 | AFR | ESN | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02922 | hp2 | a0001 | c0008 | t0001 | g0042 | AFR | ESN | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02970 | hp2 | a0001 | c0006 | t0001 | g0044 | AFR | ESN | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG03017 | hp1 | a0001 | c0002 | t0002 | g0003 | SAS | PJL | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG03017 | hp2 | a0001 | c0002 | t0002 | g0016 | SAS | PJL | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG03041 | hp1 | a0001 | c0010 | t0001 | g0032 | AFR | GWD | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG03041 | hp2 | a0001 | c0002 | t0002 | g0006 | AFR | GWD | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | MSL | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG03130 | hp1 | a0004 | c0005 | t0001 | g0017 | AFR | ESN | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG03139 | hp1 | a0001 | c0002 | t0002 | g0006 | AFR | ESN | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG03195 | hp2 | a0012 | c0019 | t0002 | g0006 | AFR | ESN | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | MSL | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG03453 | hp1 | a0001 | c0010 | t0001 | g0032 | AFR | MSL | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG03453 | hp2 | a0001 | c0002 | t0002 | g0102 | AFR | MSL | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG03486 | hp1 | a0001 | c0002 | t0002 | g0003 | AFR | MSL | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | MSL | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG03490 | hp2 | a0001 | c0002 | t0002 | g0003 | SAS | PJL | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG03491 | hp1 | a0001 | c0002 | t0002 | g0003 | SAS | PJL | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG03491 | hp2 | a0001 | c0002 | t0002 | g0016 | SAS | PJL | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0016 | SAS | PJL | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ESN | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0004 | AFR | GWD | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG03579 | hp2 | a0001 | c0002 | t0002 | g0004 | AFR | MSL | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG03654 | hp2 | a0001 | c0002 | t0002 | g0003 | SAS | PJL | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG03688 | hp2 | a0001 | c0002 | t0002 | g0016 | SAS | STU | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG03710 | hp1 | a0001 | c0011 | t0001 | g0001 | SAS | PJL | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG03710 | hp2 | a0001 | c0002 | t0002 | g0110 | SAS | PJL | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | BEB | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG03831 | hp2 | a0002 | c0003 | t0001 | g0028 | SAS | BEB | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG03834 | hp1 | a0002 | c0003 | t0001 | g0015 | SAS | BEB | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | BEB | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | BEB | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG04184 | hp2 | a0001 | c0002 | t0002 | g0003 | SAS | BEB | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG04204 | hp1 | a0001 | c0002 | t0002 | g0104 | SAS | STU | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | STU | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG04228 | hp1 | a0001 | c0002 | t0002 | g0103 | SAS | STU | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | STU | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA18522 | hp2 | a0001 | c0002 | t0002 | g0004 | AFR | YRI | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA18612 | hp1 | a0001 | c0002 | t0002 | g0107 | EAS | CHB | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA18612 | hp2 | a0002 | c0003 | t0001 | g0053 | EAS | CHB | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | YRI | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA18939 | hp2 | a0001 | c0002 | t0002 | g0108 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA18944 | hp1 | a0002 | c0003 | t0001 | g0020 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA18949 | hp2 | a0015 | c0017 | t0002 | g0035 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA18952 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA18953 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA18954 | hp1 | a0001 | c0002 | t0002 | g0038 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0035 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA18965 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA18967 | hp2 | a0001 | c0002 | t0002 | g0099 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA18968 | hp1 | a0001 | c0002 | t0002 | g0040 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA18971 | hp1 | a0001 | c0008 | t0002 | g0086 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA18972 | hp1 | a0016 | c0021 | t0001 | g0001 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA18972 | hp2 | a0002 | c0003 | t0001 | g0020 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA18979 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA18982 | hp2 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA18983 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA18984 | hp1 | a0001 | c0002 | t0002 | g0080 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA18986 | hp1 | a0001 | c0002 | t0002 | g0082 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA18995 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA18998 | hp2 | a0001 | c0002 | t0002 | g0105 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA18999 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA19012 | hp2 | a0017 | c0022 | t0001 | g0062 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | LWK | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | LWK | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | LWK | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA19043 | hp2 | a0001 | c0002 | t0002 | g0004 | AFR | LWK | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA19057 | hp1 | a0001 | c0002 | t0002 | g0038 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA19057 | hp2 | a0002 | c0003 | t0001 | g0020 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA19063 | hp2 | a0002 | c0003 | t0001 | g0055 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA19064 | hp2 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA19065 | hp2 | a0005 | c0007 | t0001 | g0018 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA19079 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA19079 | hp2 | a0006 | c0009 | t0001 | g0001 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA19085 | hp1 | a0001 | c0002 | t0002 | g0037 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA19088 | hp2 | a0001 | c0002 | t0002 | g0040 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA19090 | hp1 | a0006 | c0009 | t0001 | g0001 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA19091 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ASW | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ASW | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | TSI | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA20752 | hp2 | a0018 | c0013 | t0001 | g0058 | EUR | TSI | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0088 | EUR | TSI | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0045 | EUR | TSI | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02486 | hp1 | a0001 | c0002 | t0002 | g0004 | AFR | ACB | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02486 | hp2 | a0004 | c0005 | t0001 | g0017 | AFR | ACB | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02559 | hp1 | a0001 | c0002 | t0002 | g0004 | AFR | ACB | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG03471 | hp2 | a0013 | c0014 | t0001 | g0064 | AFR | MSL | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG06807 | hp1 | a0014 | c0020 | t0002 | g0004 | AFR | USA | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | USA | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA18955 | hp2 | a0001 | c0002 | t0002 | g0081 | EAS | JPT | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA20300 | hp1 | a0001 | c0002 | t0002 | g0084 | AFR | USA | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA20300 | hp2 | a0004 | c0005 | t0001 | g0121 | AFR | USA | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | LWK | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | LWK | RNF123_chr3_49684557_49726529 | RNF123 | chr3 | 49684557 | 49726529 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:49691437 | A | G | 1 | a0019 | 1 | homoSapiens_chm13v2.hp1 | missense_variant | MODERATE | c.95A>G | p.Glu32Gly | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 3/39 | 181/4255 | 95/3945 | 32/1314 | chr3 | 49691437 | |||
| chr3:49698753 | A | AG | 1 | a0001 | 1 | NA18967.hp2 | frameshift_variant&splice_region_variant | HIGH | c.571dupG | p.Ala191fs | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 9/39 | 658/4255 | 572/3945 | 191/1314 | INFO_REALIGN_3_PRIME | chr3 | 49698753 | ||
| chr3:49699104 | C | T | 2 | a0007 a0010 |
2 | HG00544.hp1 HG02071.hp1 |
missense_variant&splice_region_variant | MODERATE | c.763C>T | p.Arg255Cys | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 10/39 | 849/4255 | 763/3945 | 255/1314 | chr3 | 49699104 | |||
| chr3:49699704 | C | T | 1 | a0017 | 1 | NA19012.hp2 | missense_variant | MODERATE | c.916C>T | p.Arg306Trp | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 12/39 | 1002/4255 | 916/3945 | 306/1314 | chr3 | 49699704 | |||
| chr3:49700227 | C | T | 1 | a0004 | 7 | HG02451.hp1 HG02486.hp2 HG02683.hp1 others(4): Show |
missense_variant&splice_region_variant | MODERATE | c.985C>T | p.Arg329Cys | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 13/39 | 1071/4255 | 985/3945 | 329/1314 | chr3 | 49700227 | |||
| chr3:49700521 | G | A | 2 | a0003 a0017 |
8 | HG00738.hp1 HG01099.hp1 HG01168.hp1 others(5): Show |
missense_variant | MODERATE | c.1160G>A | p.Arg387Gln | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 14/39 | 1246/4255 | 1160/3945 | 387/1314 | chr3 | 49700521 | |||
| chr3:49700527 | AC | A | 1 | a0016 | 1 | NA18972.hp1 | frameshift_variant | HIGH | c.1168delC | p.Arg390fs | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 14/39 | 1254/4255 | 1168/3945 | 390/1314 | INFO_REALIGN_3_PRIME | chr3 | 49700527 | ||
| chr3:49701540 | C | T | 1 | a0008 | 1 | HG01346.hp1 | missense_variant | MODERATE | c.1327C>T | p.Arg443Cys | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 16/39 | 1413/4255 | 1327/3945 | 443/1314 | chr3 | 49701540 | |||
| chr3:49701844 | G | A | 1 | a0009 | 1 | HG02004.hp1 | missense_variant | MODERATE | c.1429G>A | p.Ala477Thr | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 17/39 | 1515/4255 | 1429/3945 | 477/1314 | chr3 | 49701844 | |||
| chr3:49702699 | C | T | 1 | a0013 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.1696C>T | p.Arg566Cys | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 20/39 | 1782/4255 | 1696/3945 | 566/1314 | chr3 | 49702699 | |||
| chr3:49703513 | C | T | 1 | a0014 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.1837C>T | p.Arg613Trp | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 21/39 | 1923/4255 | 1837/3945 | 613/1314 | chr3 | 49703513 | |||
| chr3:49704984 | C | T | 1 | a0018 | 1 | NA20752.hp2 | missense_variant&splice_region_variant | MODERATE | c.1960C>T | p.Arg654Cys | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 23/39 | 2046/4255 | 1960/3945 | 654/1314 | chr3 | 49704984 | |||
| chr3:49705574 | G | GC | 1 | a0015 | 1 | NA18949.hp2 | frameshift_variant | HIGH | c.2205dupC | p.Glu736fs | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 24/39 | 2292/4255 | 2206/3945 | 736/1314 | INFO_REALIGN_3_PRIME | chr3 | 49705574 | ||
| chr3:49712543 | G | A | 1 | a0002 | 15 | HG00639.hp2 HG00735.hp1 HG01070.hp1 others(12): Show |
missense_variant | MODERATE | c.2561G>A | p.Arg854His | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 27/39 | 2647/4255 | 2561/3945 | 854/1314 | chr3 | 49712543 | |||
| chr3:49713791 | T | A | 1 | a0006 | 2 | NA19079.hp2 NA19090.hp1 |
missense_variant | MODERATE | c.2803T>A | p.Ser935Thr | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 29/39 | 2889/4255 | 2803/3945 | 935/1314 | chr3 | 49713791 | |||
| chr3:49715850 | G | A | 1 | a0011 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.3179G>A | p.Arg1060Gln | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 33/39 | 3265/4255 | 3179/3945 | 1060/1314 | chr3 | 49715850 | |||
| chr3:49716402 | G | A | 1 | a0010 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.3425G>A | p.Ser1142Asn | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 35/39 | 3511/4255 | 3425/3945 | 1142/1314 | chr3 | 49716402 | |||
| chr3:49720606 | G | C | 1 | a0012 | 1 | HG03195.hp2 | missense_variant | MODERATE | c.3596G>C | p.Gly1199Ala | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 36/39 | 3682/4255 | 3596/3945 | 1199/1314 | chr3 | 49720606 | |||
| chr3:49720630 | G | A | 2 | a0005 a0006 |
5 | HG00544.hp2 HG02735.hp1 NA19065.hp2 others(2): Show |
missense_variant | MODERATE | c.3620G>A | p.Arg1207Gln | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 36/39 | 3706/4255 | 3620/3945 | 1207/1314 | chr3 | 49720630 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:49699474 | A | G | 1 | a0001c0023 | 1 | HG02723.hp1 | synonymous_variant | LOW | c.771A>G | p.Pro257Pro | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 11/39 | 857/4255 | 771/3945 | 257/1314 | chr3 | 49699474 | |||
| chr3:49701512 | C | T | 7 | a0001c0002 a0009c0016 a0011c0018 others(4): Show |
82 | HG00323.hp2 HG00597.hp2 HG00609.hp2 others(79): Show |
synonymous_variant | LOW | c.1299C>T | p.Val433Val | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 16/39 | 1385/4255 | 1299/3945 | 433/1314 | chr3 | 49701512 | |||
| chr3:49702671 | C | T | 1 | a0001c0006 | 4 | HG02257.hp2 HG02451.hp2 HG02723.hp2 others(1): Show |
synonymous_variant | LOW | c.1668C>T | p.Cys556Cys | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 20/39 | 1754/4255 | 1668/3945 | 556/1314 | chr3 | 49702671 | |||
| chr3:49702719 | C | T | 1 | a0001c0012 | 2 | HG01516.hp2 HG01517.hp1 |
synonymous_variant | LOW | c.1716C>T | p.Tyr572Tyr | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 20/39 | 1802/4255 | 1716/3945 | 572/1314 | chr3 | 49702719 | |||
| chr3:49713562 | T | C | 1 | a0017c0022 | 1 | NA19012.hp2 | synonymous_variant | LOW | c.2724T>C | p.Phe908Phe | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 28/39 | 2810/4255 | 2724/3945 | 908/1314 | chr3 | 49713562 | |||
| chr3:49714152 | C | T | 9 | a0001c0002 a0001c0006 a0001c0008 others(6): Show |
89 | HG00323.hp2 HG00597.hp2 HG00609.hp2 others(86): Show |
synonymous_variant | LOW | c.2988C>T | p.Asp996Asp | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 31/39 | 3074/4255 | 2988/3945 | 996/1314 | chr3 | 49714152 | |||
| chr3:49715666 | C | T | 1 | a0001c0011 | 2 | HG02738.hp1 HG03710.hp1 |
synonymous_variant | LOW | c.3102C>T | p.Leu1034Leu | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 32/39 | 3188/4255 | 3102/3945 | 1034/1314 | chr3 | 49715666 | |||
| chr3:49721064 | C | T | 1 | a0001c0010 | 2 | HG03041.hp1 HG03453.hp1 |
synonymous_variant | LOW | c.3783C>T | p.Pro1261Pro | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 38/39 | 3869/4255 | 3783/3945 | 1261/1314 | chr3 | 49721064 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:49721331 | A | G | 8 | a0001c0002t0002 a0001c0008t0002 a0009c0016t0002 others(5): Show |
83 | HG00323.hp2 HG00597.hp2 HG00609.hp2 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*26A>G | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 39/39 | 26 | chr3 | 49721331 | ||||||
| chr3:49721347 | C | G | 1 | a0001c0001t0004 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*42C>G | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 39/39 | 42 | chr3 | 49721347 | ||||||
| chr3:49721387 | C | T | 1 | a0001c0023t0003 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*82C>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 39/39 | 82 | chr3 | 49721387 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:49689649 | C | A | 3 | a0001c0006t0001g0026 a0001c0006t0001g0043 a0001c0006t0001g0044 |
4 | HG02257.hp2 HG02451.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37+43C>A | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 1/38 | chr3 | 49689649 | |||||||
| chr3:49689668 | G | A | 1 | a0001c0001t0001g0045 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-37+62G>A | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 1/38 | chr3 | 49689668 | |||||||
| chr3:49689772 | G | C | 1 | a0001c0023t0003g0046 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-37+166G>C | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 1/38 | chr3 | 49689772 | |||||||
| chr3:49689889 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-37+283C>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 1/38 | chr3 | 49689889 | |||||||
| chr3:49689899 | C | A | 1 | a0001c0001t0001g0047 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-37+293C>A | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 1/38 | chr3 | 49689899 | |||||||
| chr3:49689945 | C | T | 3 | a0001c0001t0001g0025 a0001c0001t0001g0122 a0001c0001t0001g0123 |
5 | HG02055.hp1 HG02602.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.-37+339C>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 1/38 | chr3 | 49689945 | |||||||
| chr3:49690238 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-37+632G>A | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 1/38 | chr3 | 49690238 | |||||||
| chr3:49690269 | C | T | 1 | a0001c0001t0001g0024 | 3 | HG02559.hp2 HG03098.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-37+663C>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 1/38 | chr3 | 49690269 | |||||||
| chr3:49690421 | G | C | 1 | a0001c0023t0003g0046 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-36-709G>C | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 1/38 | chr3 | 49690421 | |||||||
| chr3:49690728 | C | T | 4 | a0004c0005t0001g0017 a0004c0005t0001g0119 a0004c0005t0001g0120 others(1): Show |
7 | HG02451.hp1 HG02486.hp2 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.-36-402C>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 1/38 | chr3 | 49690728 | |||||||
| chr3:49691072 | G | A | 1 | a0005c0007t0001g0018 | 3 | HG00544.hp2 HG02735.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.-36-58G>A | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 1/38 | chr3 | 49691072 | |||||||
| chr3:49691671 | C | G | 2 | a0001c0001t0001g0118 a0001c0008t0001g0042 |
3 | HG02572.hp2 HG02922.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.167+162C>G | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 3/38 | chr3 | 49691671 | |||||||
| chr3:49691838 | C | T | 3 | a0001c0006t0001g0026 a0001c0006t0001g0043 a0001c0006t0001g0044 |
4 | HG02257.hp2 HG02451.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.167+329C>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 3/38 | chr3 | 49691838 | |||||||
| chr3:49692625 | A | G | 74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(71): Show |
177 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.167+1116A>G | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 3/38 | chr3 | 49692625 | |||||||
| chr3:49692722 | A | T | 1 | a0001c0001t0001g0117 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.167+1213A>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 3/38 | chr3 | 49692722 | |||||||
| chr3:49692842 | A | G | 1 | a0001c0006t0001g0044 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.167+1333A>G | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 3/38 | chr3 | 49692842 | |||||||
| chr3:49693020 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.167+1511C>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 3/38 | chr3 | 49693020 | |||||||
| chr3:49693119 | G | C | 1 | a0001c0006t0001g0044 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.167+1610G>C | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 3/38 | chr3 | 49693119 | |||||||
| chr3:49693192 | G | A | 30 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0013 others(27): Show |
61 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.167+1683G>A | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 3/38 | chr3 | 49693192 | |||||||
| chr3:49693347 | C | CT | 11 | a0001c0001t0001g0048 a0001c0001t0001g0073 a0001c0001t0001g0074 others(8): Show |
14 | HG00639.hp2 HG02027.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.167+1864dupT | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr3 | 49693347 | ||||||
| chr3:49693347 | C | CTT | 21 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0013 others(18): Show |
51 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(48): Show |
intron_variant | MODIFIER | c.167+1863_167+1864d others(4): Show |
RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr3 | 49693347 | ||||||
| chr3:49693347 | C | CTTT | 9 | a0001c0001t0001g0057 a0001c0001t0001g0059 a0001c0001t0001g0060 others(6): Show |
10 | HG01109.hp1 HG01516.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.167+1862_167+1864d others(5): Show |
RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr3 | 49693347 | ||||||
| chr3:49693347 | CT | C | 66 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0022 others(63): Show |
163 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.167+1864delT | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr3 | 49693347 | ||||||
| chr3:49693547 | G | T | 1 | a0001c0001t0001g0111 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.167+2038G>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 3/38 | chr3 | 49693547 | |||||||
| chr3:49694196 | C | T | 3 | a0001c0002t0002g0006 a0001c0002t0002g0041 a0012c0019t0002g0006 |
10 | HG01109.hp2 HG01243.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.167+2687C>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 3/38 | chr3 | 49694196 | |||||||
| chr3:49694428 | G | T | 30 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0013 others(27): Show |
61 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.168-2715G>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 3/38 | chr3 | 49694428 | |||||||
| chr3:49694628 | C | T | 1 | a0001c0001t0001g0024 | 3 | HG02559.hp2 HG03098.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.168-2515C>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 3/38 | chr3 | 49694628 | |||||||
| chr3:49695266 | C | T | 5 | a0002c0003t0001g0015 a0002c0003t0001g0027 a0002c0003t0001g0028 others(2): Show |
10 | HG00639.hp2 HG00735.hp1 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.168-1877C>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 3/38 | chr3 | 49695266 | |||||||
| chr3:49695448 | A | G | 1 | a0001c0023t0003g0046 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.168-1695A>G | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 3/38 | chr3 | 49695448 | |||||||
| chr3:49695663 | C | G | 4 | a0004c0005t0001g0017 a0004c0005t0001g0119 a0004c0005t0001g0120 others(1): Show |
7 | HG02451.hp1 HG02486.hp2 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.168-1480C>G | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 3/38 | chr3 | 49695663 | |||||||
| chr3:49695757 | G | A | 1 | a0001c0001t0001g0009 | 5 | HG01934.hp1 HG02970.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.168-1386G>A | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 3/38 | chr3 | 49695757 | |||||||
| chr3:49695820 | G | C | 6 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0063 others(3): Show |
17 | HG01074.hp1 HG01243.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.168-1323G>C | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 3/38 | chr3 | 49695820 | |||||||
| chr3:49695873 | C | T | 1 | a0001c0002t0002g0110 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.168-1270C>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 3/38 | chr3 | 49695873 | |||||||
| chr3:49695937 | C | T | 3 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0077 |
3 | HG02647.hp2 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.168-1206C>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 3/38 | chr3 | 49695937 | |||||||
| chr3:49696088 | C | T | 1 | a0001c0001t0001g0039 | 2 | NA18974.hp1 NA19059.hp1 |
intron_variant | MODIFIER | c.168-1055C>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 3/38 | chr3 | 49696088 | |||||||
| chr3:49696203 | C | T | 1 | a0009c0016t0002g0109 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.168-940C>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 3/38 | chr3 | 49696203 | |||||||
| chr3:49696349 | CT | C | 8 | a0001c0001t0001g0063 a0001c0001t0001g0066 a0001c0001t0001g0074 others(5): Show |
8 | HG01070.hp1 HG01070.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.168-777delT | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr3 | 49696349 | ||||||
| chr3:49696410 | A | G | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(130): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.168-733A>G | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 3/38 | chr3 | 49696410 | |||||||
| chr3:49696607 | G | T | 39 | a0001c0001t0001g0118 a0001c0002t0002g0003 a0001c0002t0002g0004 others(36): Show |
88 | HG00323.hp2 HG00597.hp2 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.168-536G>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 3/38 | chr3 | 49696607 | |||||||
| chr3:49696610 | T | C | 2 | a0001c0002t0002g0016 a0001c0002t0002g0110 |
5 | HG03017.hp2 HG03491.hp2 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.168-533T>C | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 3/38 | chr3 | 49696610 | |||||||
| chr3:49696642 | C | CT | 66 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(63): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.168-482dupT | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr3 | 49696642 | ||||||
| chr3:49696771 | C | T | 2 | a0003c0004t0001g0014 a0003c0004t0001g0021 |
7 | HG00738.hp1 HG01099.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.168-372C>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 3/38 | chr3 | 49696771 | |||||||
| chr3:49696796 | G | A | 64 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(61): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.168-347G>A | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 3/38 | chr3 | 49696796 | |||||||
| chr3:49696829 | T | C | 1 | a0001c0001t0001g0051 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.168-314T>C | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 3/38 | chr3 | 49696829 | |||||||
| chr3:49696992 | C | T | 1 | a0003c0004t0001g0014 | 4 | HG01099.hp1 HG01168.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.168-151C>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 3/38 | chr3 | 49696992 | |||||||
| chr3:49697252 | G | C | 1 | a0001c0001t0001g0067 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.247+30G>C | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 4/38 | chr3 | 49697252 | |||||||
| chr3:49698289 | G | C | 1 | a0001c0002t0002g0098 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.484-151G>C | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 7/38 | chr3 | 49698289 | |||||||
| chr3:49698313 | C | G | 40 | a0001c0001t0001g0118 a0001c0002t0002g0003 a0001c0002t0002g0004 others(37): Show |
89 | HG00323.hp2 HG00597.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.484-127C>G | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 7/38 | chr3 | 49698313 | |||||||
| chr3:49698374 | G | T | 4 | a0004c0005t0001g0017 a0004c0005t0001g0119 a0004c0005t0001g0120 others(1): Show |
7 | HG02451.hp1 HG02486.hp2 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.484-66G>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 7/38 | chr3 | 49698374 | |||||||
| chr3:49698739 | C | A | 35 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0006 others(32): Show |
82 | HG00323.hp2 HG00597.hp2 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.571-16C>A | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 8/38 | chr3 | 49698739 | |||||||
| chr3:49698836 | C | T | 4 | a0004c0005t0001g0017 a0004c0005t0001g0119 a0004c0005t0001g0120 others(1): Show |
7 | HG02451.hp1 HG02486.hp2 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.638+14C>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 9/38 | chr3 | 49698836 | |||||||
| chr3:49699123 | T | C | 2 | a0001c0006t0001g0026 a0001c0006t0001g0043 |
3 | HG02257.hp2 HG02451.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.764+18T>C | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 10/38 | chr3 | 49699123 | |||||||
| chr3:49699132 | G | A | 66 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(63): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.764+27G>A | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 10/38 | chr3 | 49699132 | |||||||
| chr3:49699259 | C | G | 1 | a0001c0002t0002g0107 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.764+154C>G | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 10/38 | chr3 | 49699259 | |||||||
| chr3:49699446 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.765-22G>A | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 10/38 | chr3 | 49699446 | |||||||
| chr3:49699633 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.880-35C>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 11/38 | chr3 | 49699633 | |||||||
| chr3:49699890 | A | G | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(108): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.984+118A>G | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 12/38 | chr3 | 49699890 | |||||||
| chr3:49699925 | C | G | 1 | a0001c0001t0001g0072 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.984+153C>G | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 12/38 | chr3 | 49699925 | |||||||
| chr3:49699942 | A | G | 1 | a0001c0023t0003g0046 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.984+170A>G | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 12/38 | chr3 | 49699942 | |||||||
| chr3:49700038 | T | TA | 2 | a0001c0001t0001g0118 a0001c0008t0001g0042 |
3 | HG02572.hp2 HG02922.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.985-188dupA | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 12/38 | INFO_REALIGN_3_PRIME | chr3 | 49700038 | ||||||
| chr3:49700085 | G | A | 4 | a0004c0005t0001g0017 a0004c0005t0001g0119 a0004c0005t0001g0120 others(1): Show |
7 | HG02451.hp1 HG02486.hp2 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.985-142G>A | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 12/38 | chr3 | 49700085 | |||||||
| chr3:49700812 | A | G | 5 | a0001c0001t0001g0005 a0001c0001t0001g0063 a0001c0001t0001g0065 others(2): Show |
12 | HG01074.hp1 HG01243.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1277+103A>G | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 15/38 | chr3 | 49700812 | |||||||
| chr3:49700863 | C | T | 1 | a0001c0001t0001g0047 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1277+154C>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 15/38 | chr3 | 49700863 | |||||||
| chr3:49700957 | C | T | 1 | a0008c0015t0001g0096 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1277+248C>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 15/38 | chr3 | 49700957 | |||||||
| chr3:49701121 | G | T | 1 | a0001c0010t0001g0032 | 2 | HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1278-370G>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 15/38 | chr3 | 49701121 | |||||||
| chr3:49701329 | T | G | 1 | a0002c0003t0001g0027 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1278-162T>G | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 15/38 | chr3 | 49701329 | |||||||
| chr3:49701383 | G | A | 3 | a0001c0002t0002g0100 a0001c0002t0002g0101 a0009c0016t0002g0109 |
3 | HG00741.hp2 HG01952.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.1278-108G>A | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 15/38 | chr3 | 49701383 | |||||||
| chr3:49701653 | C | T | 65 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(62): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.1395+45C>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 16/38 | chr3 | 49701653 | |||||||
| chr3:49701755 | A | G | 3 | a0001c0006t0001g0026 a0001c0006t0001g0043 a0001c0006t0001g0044 |
4 | HG02257.hp2 HG02451.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1396-56A>G | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 16/38 | chr3 | 49701755 | |||||||
| chr3:49702025 | C | T | 1 | a0001c0001t0004g0078 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1496-58C>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 17/38 | chr3 | 49702025 | |||||||
| chr3:49702074 | G | C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(104): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1496-9G>C | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 17/38 | chr3 | 49702074 | |||||||
| chr3:49702309 | A | C | 1 | a0001c0001t0001g0022 | 3 | HG02055.hp2 HG02258.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1558-25A>C | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 18/38 | chr3 | 49702309 | |||||||
| chr3:49702801 | C | T | 1 | a0001c0008t0001g0042 | 2 | HG02572.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1750+48C>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 20/38 | chr3 | 49702801 | |||||||
| chr3:49703236 | G | A | 1 | a0001c0001t0001g0087 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1751-191G>A | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 20/38 | chr3 | 49703236 | |||||||
| chr3:49703572 | G | T | 1 | a0001c0001t0001g0095 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1852+44G>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 21/38 | chr3 | 49703572 | |||||||
| chr3:49704301 | G | A | 1 | a0001c0001t0001g0074 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1853-349G>A | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 21/38 | chr3 | 49704301 | |||||||
| chr3:49704398 | T | G | 1 | a0001c0006t0001g0026 | 2 | HG02257.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1853-252T>G | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 21/38 | chr3 | 49704398 | |||||||
| chr3:49704462 | C | T | 1 | a0001c0002t0002g0038 | 2 | NA18954.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.1853-188C>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 21/38 | chr3 | 49704462 | |||||||
| chr3:49704567 | G | C | 1 | a0001c0001t0004g0078 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1853-83G>C | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 21/38 | chr3 | 49704567 | |||||||
| chr3:49705220 | C | G | 1 | a0001c0001t0001g0070 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2158+38C>G | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 23/38 | chr3 | 49705220 | |||||||
| chr3:49705357 | TCCTGGCA others(13): Show |
T | 1 | a0001c0002t0002g0080 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2159-172_2159-153d others(22): Show |
RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 23/38 | INFO_REALIGN_3_PRIME | chr3 | 49705357 | ||||||
| chr3:49705530 | C | T | 1 | a0001c0001t0001g0094 | 1 | NA18983.hp1 | splice_region_variant&intron_variant | LOW | c.2159-4C>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 23/38 | chr3 | 49705530 | |||||||
| chr3:49706174 | C | A | 1 | a0001c0002t0002g0080 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2388+109C>A | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 25/38 | chr3 | 49706174 | |||||||
| chr3:49706263 | C | T | 6 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0063 others(3): Show |
17 | HG01074.hp1 HG01243.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.2388+198C>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 25/38 | chr3 | 49706263 | |||||||
| chr3:49706279 | T | C | 1 | a0001c0001t0001g0019 | 3 | HG00323.hp1 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.2388+214T>C | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 25/38 | chr3 | 49706279 | |||||||
| chr3:49706959 | A | G | 66 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(63): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.2496+61A>G | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 26/38 | chr3 | 49706959 | |||||||
| chr3:49707087 | G | A | 1 | a0001c0001t0001g0039 | 2 | NA18974.hp1 NA19059.hp1 |
intron_variant | MODIFIER | c.2496+189G>A | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 26/38 | chr3 | 49707087 | |||||||
| chr3:49707230 | T | C | 7 | a0001c0002t0002g0011 a0001c0002t0002g0035 a0001c0002t0002g0081 others(4): Show |
11 | HG01928.hp2 NA18939.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.2496+332T>C | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 26/38 | chr3 | 49707230 | |||||||
| chr3:49707457 | A | G | 65 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(62): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.2496+559A>G | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 26/38 | chr3 | 49707457 | |||||||
| chr3:49707674 | C | T | 1 | a0001c0001t0001g0034 | 2 | HG01192.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.2496+776C>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 26/38 | chr3 | 49707674 | |||||||
| chr3:49707755 | C | T | 65 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(62): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.2496+857C>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 26/38 | chr3 | 49707755 | |||||||
| chr3:49707802 | G | A | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(104): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.2496+904G>A | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 26/38 | chr3 | 49707802 | |||||||
| chr3:49708038 | C | G | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(129): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.2496+1140C>G | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 26/38 | chr3 | 49708038 | |||||||
| chr3:49708244 | G | A | 63 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(60): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.2496+1346G>A | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 26/38 | chr3 | 49708244 | |||||||
| chr3:49708248 | G | A | 2 | a0001c0001t0001g0057 a0018c0013t0001g0058 |
2 | HG01516.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.2496+1350G>A | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 26/38 | chr3 | 49708248 | |||||||
| chr3:49708389 | C | T | 65 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(62): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.2496+1491C>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 26/38 | chr3 | 49708389 | |||||||
| chr3:49708508 | A | AC | 36 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0006 others(33): Show |
83 | HG00323.hp2 HG00597.hp2 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.2496+1615dupC | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr3 | 49708508 | ||||||
| chr3:49708707 | G | A | 1 | a0001c0002t0002g0016 | 4 | HG03017.hp2 HG03491.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.2496+1809G>A | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 26/38 | chr3 | 49708707 | |||||||
| chr3:49708714 | A | G | 1 | a0001c0001t0004g0078 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2496+1816A>G | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 26/38 | chr3 | 49708714 | |||||||
| chr3:49708809 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2496+1911C>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 26/38 | chr3 | 49708809 | |||||||
| chr3:49708812 | G | C | 1 | a0001c0002t0002g0102 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2496+1914G>C | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 26/38 | chr3 | 49708812 | |||||||
| chr3:49708970 | A | T | 1 | a0001c0001t0001g0093 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2496+2072A>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 26/38 | chr3 | 49708970 | |||||||
| chr3:49709036 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2496+2138C>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 26/38 | chr3 | 49709036 | |||||||
| chr3:49709079 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2496+2181C>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 26/38 | chr3 | 49709079 | |||||||
| chr3:49709130 | A | AT | 6 | a0001c0001t0004g0078 a0001c0002t0002g0004 a0001c0002t0002g0102 others(3): Show |
13 | HG01884.hp1 HG02258.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.2496+2242dupT | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr3 | 49709130 | ||||||
| chr3:49709137 | T | C | 1 | a0001c0002t0002g0036 | 2 | HG00323.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.2496+2239T>C | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 26/38 | chr3 | 49709137 | |||||||
| chr3:49709143 | T | C | 1 | a0001c0002t0002g0106 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2496+2245T>C | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 26/38 | chr3 | 49709143 | |||||||
| chr3:49709348 | C | T | 1 | a0002c0003t0001g0055 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2496+2450C>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 26/38 | chr3 | 49709348 | |||||||
| chr3:49709386 | C | T | 63 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(60): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.2496+2488C>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 26/38 | chr3 | 49709386 | |||||||
| chr3:49709426 | G | A | 1 | a0001c0002t0002g0103 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2496+2528G>A | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 26/38 | chr3 | 49709426 | |||||||
| chr3:49709462 | G | A | 4 | a0001c0001t0001g0007 a0001c0001t0001g0050 a0001c0001t0001g0052 others(1): Show |
10 | HG01167.hp2 HG01169.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.2496+2564G>A | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 26/38 | chr3 | 49709462 | |||||||
| chr3:49709522 | G | A | 1 | a0001c0002t0002g0107 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2496+2624G>A | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 26/38 | chr3 | 49709522 | |||||||
| chr3:49709568 | G | T | 1 | a0001c0001t0001g0054 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2496+2670G>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 26/38 | chr3 | 49709568 | |||||||
| chr3:49709599 | C | A | 1 | a0013c0014t0001g0064 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2496+2701C>A | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 26/38 | chr3 | 49709599 | |||||||
| chr3:49709609 | A | G | 12 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0034 others(9): Show |
39 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.2496+2711A>G | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 26/38 | chr3 | 49709609 | |||||||
| chr3:49709772 | C | T | 2 | a0001c0006t0001g0026 a0001c0006t0001g0043 |
3 | HG02257.hp2 HG02451.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.2497-2707C>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 26/38 | chr3 | 49709772 | |||||||
| chr3:49710127 | C | T | 3 | a0003c0004t0001g0014 a0003c0004t0001g0021 a0017c0022t0001g0062 |
8 | HG00738.hp1 HG01099.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.2497-2352C>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 26/38 | chr3 | 49710127 | |||||||
| chr3:49710132 | G | A | 1 | a0001c0001t0001g0074 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2497-2347G>A | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 26/38 | chr3 | 49710132 | |||||||
| chr3:49710211 | T | A | 1 | a0001c0002t0002g0104 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2497-2268T>A | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 26/38 | chr3 | 49710211 | |||||||
| chr3:49710226 | C | T | 1 | a0002c0003t0001g0053 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2497-2253C>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 26/38 | chr3 | 49710226 | |||||||
| chr3:49710382 | C | T | 1 | a0001c0001t0001g0010 | 5 | HG02622.hp2 HG02895.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.2497-2097C>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 26/38 | chr3 | 49710382 | |||||||
| chr3:49710569 | C | T | 1 | a0001c0002t0002g0101 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2497-1910C>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 26/38 | chr3 | 49710569 | |||||||
| chr3:49710570 | G | A | 1 | a0001c0010t0001g0032 | 2 | HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2497-1909G>A | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 26/38 | chr3 | 49710570 | |||||||
| chr3:49711004 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2497-1475G>A | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 26/38 | chr3 | 49711004 | |||||||
| chr3:49711400 | C | T | 65 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(62): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.2497-1079C>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 26/38 | chr3 | 49711400 | |||||||
| chr3:49711416 | C | A | 1 | a0001c0001t0001g0010 | 5 | HG02622.hp2 HG02895.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.2497-1063C>A | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 26/38 | chr3 | 49711416 | |||||||
| chr3:49711540 | C | T | 1 | a0004c0005t0001g0120 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2497-939C>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 26/38 | chr3 | 49711540 | |||||||
| chr3:49711566 | T | C | 1 | a0001c0002t0002g0080 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2497-913T>C | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 26/38 | chr3 | 49711566 | |||||||
| chr3:49711567 | C | T | 1 | a0001c0002t0002g0080 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2497-912C>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 26/38 | chr3 | 49711567 | |||||||
| chr3:49711646 | G | T | 1 | a0004c0005t0001g0120 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2497-833G>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 26/38 | chr3 | 49711646 | |||||||
| chr3:49711748 | G | A | 1 | a0001c0010t0001g0032 | 2 | HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2497-731G>A | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 26/38 | chr3 | 49711748 | |||||||
| chr3:49712087 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2497-392C>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 26/38 | chr3 | 49712087 | |||||||
| chr3:49712118 | G | A | 1 | a0001c0001t0001g0088 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2497-361G>A | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 26/38 | chr3 | 49712118 | |||||||
| chr3:49712183 | G | A | 2 | a0001c0002t0002g0023 a0019c0026t0002g0023 |
3 | HG00741.hp1 HG01167.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2497-296G>A | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 26/38 | chr3 | 49712183 | |||||||
| chr3:49712215 | C | CA | 40 | a0001c0001t0001g0019 a0001c0001t0001g0118 a0001c0002t0002g0003 others(37): Show |
91 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.2497-250dupA | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr3 | 49712215 | ||||||
| chr3:49712272 | A | C | 10 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0025 others(7): Show |
17 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(14): Show |
intron_variant | MODIFIER | c.2497-207A>C | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 26/38 | chr3 | 49712272 | |||||||
| chr3:49712371 | G | A | 3 | a0001c0001t0001g0030 a0001c0001t0001g0066 a0001c0001t0001g0068 |
4 | HG01069.hp1 HG01070.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.2497-108G>A | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 26/38 | chr3 | 49712371 | |||||||
| chr3:49712755 | T | A | 66 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(63): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.2674+99T>A | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 27/38 | chr3 | 49712755 | |||||||
| chr3:49712828 | C | T | 4 | a0001c0001t0001g0007 a0001c0001t0001g0050 a0001c0001t0001g0052 others(1): Show |
10 | HG01167.hp2 HG01169.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.2674+172C>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 27/38 | chr3 | 49712828 | |||||||
| chr3:49713165 | C | T | 3 | a0001c0006t0001g0026 a0001c0006t0001g0043 a0001c0006t0001g0044 |
4 | HG02257.hp2 HG02451.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.2675-348C>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 27/38 | chr3 | 49713165 | |||||||
| chr3:49713392 | G | T | 2 | a0001c0001t0001g0033 a0001c0001t0001g0092 |
3 | HG01168.hp2 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.2675-121G>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 27/38 | chr3 | 49713392 | |||||||
| chr3:49714067 | G | A | 1 | a0001c0001t0001g0031 | 2 | HG01123.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.2926-23G>A | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 30/38 | chr3 | 49714067 | |||||||
| chr3:49714321 | T | A | 1 | a0001c0001t0001g0061 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3010+147T>A | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 31/38 | chr3 | 49714321 | |||||||
| chr3:49714423 | T | C | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(108): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.3010+249T>C | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 31/38 | chr3 | 49714423 | |||||||
| chr3:49714450 | G | A | 1 | a0001c0002t0002g0105 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.3010+276G>A | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 31/38 | chr3 | 49714450 | |||||||
| chr3:49714467 | C | A | 41 | a0001c0001t0001g0118 a0001c0002t0002g0003 a0001c0002t0002g0004 others(38): Show |
90 | HG00323.hp2 HG00597.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.3010+293C>A | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 31/38 | chr3 | 49714467 | |||||||
| chr3:49714529 | C | A | 1 | a0001c0001t0001g0089 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.3010+355C>A | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 31/38 | chr3 | 49714529 | |||||||
| chr3:49714542 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3010+368A>G | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 31/38 | chr3 | 49714542 | |||||||
| chr3:49714939 | C | T | 63 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(60): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.3011-636C>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 31/38 | chr3 | 49714939 | |||||||
| chr3:49714943 | C | A | 1 | a0001c0001t0001g0068 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3011-632C>A | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 31/38 | chr3 | 49714943 | |||||||
| chr3:49714994 | C | T | 65 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(62): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.3011-581C>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 31/38 | chr3 | 49714994 | |||||||
| chr3:49715050 | C | T | 1 | a0001c0001t0001g0047 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3011-525C>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 31/38 | chr3 | 49715050 | |||||||
| chr3:49715088 | C | A | 1 | a0001c0010t0001g0032 | 2 | HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.3011-487C>A | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 31/38 | chr3 | 49715088 | |||||||
| chr3:49715356 | G | C | 3 | a0002c0003t0001g0020 a0002c0003t0001g0053 a0002c0003t0001g0055 |
5 | NA18612.hp2 NA18944.hp1 NA18972.hp2 others(2): Show |
intron_variant | MODIFIER | c.3011-219G>C | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 31/38 | chr3 | 49715356 | |||||||
| chr3:49715535 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.3011-40A>G | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 31/38 | chr3 | 49715535 | |||||||
| chr3:49715570 | T | G | 65 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(62): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
splice_region_variant&intron_variant | LOW | c.3011-5T>G | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 31/38 | chr3 | 49715570 | |||||||
| chr3:49716344 | G | A | 1 | a0001c0002t0002g0100 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.3416-49G>A | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 34/38 | chr3 | 49716344 | |||||||
| chr3:49716355 | A | G | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(105): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.3416-38A>G | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 34/38 | chr3 | 49716355 | |||||||
| chr3:49716370 | C | G | 1 | a0001c0001t0001g0068 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3416-23C>G | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 34/38 | chr3 | 49716370 | |||||||
| chr3:49716909 | G | A | 1 | a0001c0023t0003g0046 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3500+432G>A | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 35/38 | chr3 | 49716909 | |||||||
| chr3:49717007 | C | A | 1 | a0001c0001t0001g0052 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3500+530C>A | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 35/38 | chr3 | 49717007 | |||||||
| chr3:49717076 | G | A | 1 | a0001c0001t0001g0074 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3500+599G>A | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 35/38 | chr3 | 49717076 | |||||||
| chr3:49717254 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3500+777C>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 35/38 | chr3 | 49717254 | |||||||
| chr3:49717469 | C | T | 3 | a0001c0002t0002g0037 a0001c0002t0002g0098 a0001c0002t0002g0105 |
4 | HG00597.hp2 HG02074.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.3500+992C>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 35/38 | chr3 | 49717469 | |||||||
| chr3:49717528 | C | T | 1 | a0018c0013t0001g0058 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.3500+1051C>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 35/38 | chr3 | 49717528 | |||||||
| chr3:49717537 | T | C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(104): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.3500+1060T>C | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 35/38 | chr3 | 49717537 | |||||||
| chr3:49718038 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3500+1561G>A | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 35/38 | chr3 | 49718038 | |||||||
| chr3:49718065 | G | A | 1 | a0001c0002t0002g0100 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.3500+1588G>A | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 35/38 | chr3 | 49718065 | |||||||
| chr3:49718223 | G | A | 1 | a0001c0001t0004g0078 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3500+1746G>A | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 35/38 | chr3 | 49718223 | |||||||
| chr3:49718309 | G | T | 1 | a0001c0002t0002g0082 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.3500+1832G>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 35/38 | chr3 | 49718309 | |||||||
| chr3:49718440 | T | C | 1 | a0001c0001t0001g0039 | 2 | NA18974.hp1 NA19059.hp1 |
intron_variant | MODIFIER | c.3500+1963T>C | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 35/38 | chr3 | 49718440 | |||||||
| chr3:49718696 | G | A | 1 | a0001c0006t0001g0044 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3501-1815G>A | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 35/38 | chr3 | 49718696 | |||||||
| chr3:49718727 | G | T | 1 | a0001c0001t0001g0076 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3501-1784G>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 35/38 | chr3 | 49718727 | |||||||
| chr3:49718779 | G | A | 1 | a0001c0010t0001g0032 | 2 | HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.3501-1732G>A | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 35/38 | chr3 | 49718779 | |||||||
| chr3:49718927 | A | G | 1 | a0004c0005t0001g0119 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3501-1584A>G | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 35/38 | chr3 | 49718927 | |||||||
| chr3:49719078 | C | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0114 |
4 | HG02559.hp2 HG03098.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.3501-1433C>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 35/38 | chr3 | 49719078 | |||||||
| chr3:49719653 | G | C | 1 | a0001c0001t0001g0091 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3501-858G>C | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 35/38 | chr3 | 49719653 | |||||||
| chr3:49719774 | A | G | 1 | a0001c0002t0002g0098 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3501-737A>G | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 35/38 | chr3 | 49719774 | |||||||
| chr3:49720159 | T | TACA | 66 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(63): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.3501-347_3501-345d others(5): Show |
RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 35/38 | INFO_REALIGN_3_PRIME | chr3 | 49720159 | ||||||
| chr3:49720365 | A | G | 1 | a0001c0001t0001g0033 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.3501-146A>G | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 35/38 | chr3 | 49720365 | |||||||
| chr3:49720391 | G | A | 2 | a0001c0001t0001g0048 a0001c0001t0001g0060 |
2 | HG02886.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3501-120G>A | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 35/38 | chr3 | 49720391 | |||||||
| chr3:49720678 | A | G | 4 | a0004c0005t0001g0017 a0004c0005t0001g0119 a0004c0005t0001g0120 others(1): Show |
7 | HG02451.hp1 HG02486.hp2 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.3643+25A>G | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 36/38 | chr3 | 49720678 | |||||||
| chr3:49720722 | A | AAAGTC | 2 | a0001c0001t0001g0033 a0001c0001t0001g0092 |
3 | HG01168.hp2 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.3643+70_3644-73dup others(5): Show |
RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr3 | 49720722 | ||||||
| chr3:49720961 | C | T | 5 | a0001c0002t0002g0035 a0001c0002t0002g0081 a0001c0002t0002g0082 others(2): Show |
5 | NA18939.hp2 NA18949.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.3739-59C>T | RNF123 | ENSG00000164068.16 | transcript | ENST00000327697.11 | protein_coding | 37/38 | chr3 | 49720961 |