Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9604 |
| ensemblid | ENSG00000013561.18 |
| hgncid | 10058 |
| symbol | RNF14 |
| name | ring finger protein 14 |
| refseq_nuc | NM_004290.5 |
| refseq_prot | NP_004281.1 |
| ensembl_nuc | ENST00000394520.7 |
| ensembl_prot | ENSP00000378028.2 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 141969105 |
| end | 141990292 |
| strand | + |
| ver | v1.2 |
| region | chr5:141969105-141990292 |
| region5000 | chr5:141964105-141995292 |
| regionname0 | RNF14_chr5_141969105_141990292 |
| regionname5000 | RNF14_chr5_141964105_141995292 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 474 | 280 | 88 | 79 | 59 | 12 | 40 | 41 | RNF14_chr5_141964105_141995292 | RNF14 | MSSED others(469): Show |
chr5 | 141964105 | 141995292 |
| a0002 | 0/0 | 474 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | MSSED others(469): Show |
chr5 | 141964105 | 141995292 |
| a0003 | 0/0 | 474 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RNF14_chr5_141964105_141995292 | RNF14 | MSSED others(469): Show |
chr5 | 141964105 | 141995292 |
| a0004 | 0/0 | 474 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | MSSED others(469): Show |
chr5 | 141964105 | 141995292 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1422 | 272 | 82 | 77 | 59 | 12 | 40 | RNF14_chr5_141964105_141995292 | RNF14 | ATGTC others(1417): Show |
chr5 | 141964105 | 141995292 | ||
| a0001c0002 | 0/0 | 1422 | 2 | 2 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | ATGTC others(1417): Show |
chr5 | 141964105 | 141995292 | ||
| a0001c0004 | 0/0 | 1422 | 2 | 0 | 2 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | ATGTC others(1417): Show |
chr5 | 141964105 | 141995292 | ||
| a0001c0005 | 0/0 | 1422 | 2 | 2 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | ATGTC others(1417): Show |
chr5 | 141964105 | 141995292 | ||
| a0001c0006 | 0/0 | 1422 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | ATGTC others(1417): Show |
chr5 | 141964105 | 141995292 | ||
| a0001c0007 | 0/0 | 1422 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | ATGTC others(1417): Show |
chr5 | 141964105 | 141995292 | ||
| a0002c0003 | 0/0 | 1422 | 2 | 1 | 1 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | ATGTC others(1417): Show |
chr5 | 141964105 | 141995292 | ||
| a0003c0009 | 0/0 | 1422 | 1 | 0 | 0 | 1 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | ATGTC others(1417): Show |
chr5 | 141964105 | 141995292 | ||
| a0004c0008 | 0/0 | 1422 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | ATGTC others(1417): Show |
chr5 | 141964105 | 141995292 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4167 | 145 | 22 | 43 | 51 | 3 | 26 | RNF14_chr5_141964105_141995292 | RNF14 | GAGAA others(4162): Show |
chr5 | 141964105 | 141995292 |
| a0001c0001t0002 | 0/0 | 4167 | 30 | 19 | 8 | 0 | 2 | 1 | RNF14_chr5_141964105_141995292 | RNF14 | GAGAA others(4162): Show |
chr5 | 141964105 | 141995292 |
| a0001c0001t0003 | 1/0 | 4170 | 20 | 4 | 9 | 1 | 1 | 4 | RNF14_chr5_141964105_141995292 | RNF14 | GAGAA others(4165): Show |
chr5 | 141964105 | 141995292 |
| a0001c0001t0004 | 0/1 | 4166 | 14 | 8 | 2 | 0 | 2 | 1 | RNF14_chr5_141964105_141995292 | RNF14 | GAGAA others(4161): Show |
chr5 | 141964105 | 141995292 |
| a0001c0001t0005 | 0/0 | 4166 | 13 | 2 | 6 | 0 | 1 | 4 | RNF14_chr5_141964105_141995292 | RNF14 | GAGAA others(4161): Show |
chr5 | 141964105 | 141995292 |
| a0001c0001t0006 | 0/0 | 4167 | 5 | 0 | 0 | 5 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | GAGAA others(4162): Show |
chr5 | 141964105 | 141995292 |
| a0001c0001t0007 | 0/0 | 4167 | 6 | 1 | 5 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | GAGAA others(4162): Show |
chr5 | 141964105 | 141995292 |
| a0001c0001t0008 | 0/0 | 4167 | 5 | 4 | 1 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | GAGAA others(4162): Show |
chr5 | 141964105 | 141995292 |
| a0001c0001t0009 | 0/0 | 4167 | 5 | 3 | 1 | 0 | 0 | 1 | RNF14_chr5_141964105_141995292 | RNF14 | GAGAA others(4162): Show |
chr5 | 141964105 | 141995292 |
| a0001c0001t0010 | 0/0 | 4170 | 2 | 2 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | GAGAA others(4165): Show |
chr5 | 141964105 | 141995292 |
| a0001c0001t0011 | 0/0 | 4167 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | GAGAA others(4162): Show |
chr5 | 141964105 | 141995292 |
| a0001c0001t0012 | 0/0 | 4167 | 3 | 3 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | GAGAA others(4162): Show |
chr5 | 141964105 | 141995292 |
| a0001c0001t0013 | 0/0 | 4170 | 2 | 0 | 0 | 0 | 2 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | GAGAA others(4165): Show |
chr5 | 141964105 | 141995292 |
| a0001c0001t0014 | 0/0 | 4170 | 2 | 2 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | GAGAA others(4165): Show |
chr5 | 141964105 | 141995292 |
| a0001c0001t0015 | 0/0 | 4167 | 2 | 1 | 1 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | GAGAA others(4162): Show |
chr5 | 141964105 | 141995292 |
| a0001c0001t0016 | 0/0 | 4170 | 2 | 2 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | GAGAA others(4165): Show |
chr5 | 141964105 | 141995292 |
| a0001c0001t0017 | 0/0 | 4167 | 1 | 0 | 0 | 1 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | GAGAA others(4162): Show |
chr5 | 141964105 | 141995292 |
| a0001c0001t0018 | 0/0 | 4167 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | GAGAA others(4162): Show |
chr5 | 141964105 | 141995292 |
| a0001c0001t0019 | 0/0 | 4170 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | GAGAA others(4165): Show |
chr5 | 141964105 | 141995292 |
| a0001c0001t0020 | 0/0 | 4170 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | GAGAA others(4165): Show |
chr5 | 141964105 | 141995292 |
| a0001c0001t0021 | 0/0 | 4170 | 1 | 0 | 1 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | GAGAA others(4165): Show |
chr5 | 141964105 | 141995292 |
| a0001c0001t0022 | 0/0 | 4170 | 1 | 0 | 0 | 0 | 0 | 1 | RNF14_chr5_141964105_141995292 | RNF14 | GAGAA others(4165): Show |
chr5 | 141964105 | 141995292 |
| a0001c0001t0023 | 0/0 | 4167 | 1 | 0 | 0 | 0 | 0 | 1 | RNF14_chr5_141964105_141995292 | RNF14 | GAGAA others(4162): Show |
chr5 | 141964105 | 141995292 |
| a0001c0001t0024 | 0/0 | 4167 | 1 | 0 | 0 | 0 | 1 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | GAGAA others(4162): Show |
chr5 | 141964105 | 141995292 |
| a0001c0001t0025 | 0/0 | 4167 | 1 | 0 | 0 | 0 | 0 | 1 | RNF14_chr5_141964105_141995292 | RNF14 | GAGAA others(4162): Show |
chr5 | 141964105 | 141995292 |
| a0001c0001t0026 | 0/0 | 4167 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | GAGAA others(4162): Show |
chr5 | 141964105 | 141995292 |
| a0001c0001t0027 | 0/0 | 4166 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | GAGAA others(4161): Show |
chr5 | 141964105 | 141995292 |
| a0001c0001t0028 | 0/0 | 4170 | 1 | 0 | 0 | 1 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | GAGAA others(4165): Show |
chr5 | 141964105 | 141995292 |
| a0001c0001t0029 | 0/0 | 4170 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | GAGAA others(4165): Show |
chr5 | 141964105 | 141995292 |
| a0001c0001t0030 | 0/0 | 4166 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | GAGAA others(4161): Show |
chr5 | 141964105 | 141995292 |
| a0001c0001t0031 | 0/0 | 4167 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | GAGAA others(4162): Show |
chr5 | 141964105 | 141995292 |
| a0001c0002t0002 | 0/0 | 4167 | 2 | 2 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | GAGAA others(4162): Show |
chr5 | 141964105 | 141995292 |
| a0001c0004t0011 | 0/0 | 4167 | 2 | 0 | 2 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | GAGAA others(4162): Show |
chr5 | 141964105 | 141995292 |
| a0001c0005t0002 | 0/0 | 4167 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | GAGAA others(4162): Show |
chr5 | 141964105 | 141995292 |
| a0001c0005t0032 | 0/0 | 4170 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | GAGAA others(4165): Show |
chr5 | 141964105 | 141995292 |
| a0001c0006t0001 | 0/0 | 4167 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | GAGAA others(4162): Show |
chr5 | 141964105 | 141995292 |
| a0001c0007t0010 | 0/0 | 4170 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | GAGAA others(4165): Show |
chr5 | 141964105 | 141995292 |
| a0002c0003t0001 | 0/0 | 4167 | 2 | 1 | 1 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | GAGAA others(4162): Show |
chr5 | 141964105 | 141995292 |
| a0003c0009t0006 | 0/0 | 4167 | 1 | 0 | 0 | 1 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | GAGAA others(4162): Show |
chr5 | 141964105 | 141995292 |
| a0004c0008t0002 | 0/0 | 4167 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | GAGAA others(4162): Show |
chr5 | 141964105 | 141995292 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 28 | 5 | 2 | 13 | 0 | 8 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0002 | 0/0 | 16 | 0 | 8 | 1 | 0 | 7 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0006 | 0/0 | 7 | 1 | 4 | 0 | 0 | 2 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0008 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0009 | 0/0 | 6 | 0 | 5 | 0 | 1 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0016 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0040 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0002g0007 | 0/0 | 6 | 4 | 2 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0002g0014 | 0/0 | 4 | 1 | 2 | 0 | 0 | 1 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0002g0015 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0002g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0003g0003 | 0/0 | 10 | 1 | 5 | 1 | 1 | 2 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0003g0011 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0003g0019 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0003g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0004g0017 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0004g0029 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0004g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0004g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0004g0075 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0004g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0005g0004 | 0/0 | 9 | 0 | 5 | 0 | 1 | 3 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0005g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0005g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0005g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0005g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0006g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0006g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0007g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0007g0005 | 0/0 | 5 | 1 | 4 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0008g0010 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0009g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0009g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0009g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0009g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0010g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0010g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0011g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0012g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0013g0011 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0014g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0015g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0016g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0016g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0017g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0018g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0019g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0020g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0021g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0022g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0023g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0024g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0025g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0026g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0027g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0028g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0029g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0030g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0001t0031g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0002t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0002t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0004t0011g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0004t0011g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0005t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0005t0032g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0006t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0001c0007t0010g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0002c0003t0001g0001 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0003c0009t0006g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| a0004c0008t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0037 | EUR | GBR | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0069 | EUR | GBR | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0127 | EUR | FIN | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | FIN | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG00408 | hp2 | a0001 | c0001 | t0017 | g0002 | EAS | CHS | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG00639 | hp1 | a0001 | c0001 | t0007 | g0005 | AMR | PUR | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG00639 | hp2 | a0001 | c0001 | t0005 | g0004 | AMR | PUR | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG00642 | hp1 | a0001 | c0001 | t0007 | g0001 | AMR | PUR | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG00733 | hp1 | a0001 | c0001 | t0005 | g0004 | AMR | PUR | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG00735 | hp1 | a0001 | c0001 | t0007 | g0005 | AMR | PUR | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0073 | AMR | PUR | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01070 | hp2 | a0001 | c0001 | t0005 | g0004 | AMR | PUR | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01071 | hp2 | a0001 | c0001 | t0005 | g0004 | AMR | PUR | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01099 | hp2 | a0001 | c0004 | t0011 | g0065 | AMR | PUR | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0019 | AMR | PUR | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01168 | hp2 | a0001 | c0004 | t0011 | g0027 | AMR | PUR | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0099 | AMR | PUR | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01175 | hp2 | a0001 | c0001 | t0021 | g0077 | AMR | PUR | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01243 | hp1 | a0001 | c0001 | t0015 | g0028 | AMR | PUR | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01255 | hp2 | a0001 | c0001 | t0005 | g0055 | AMR | CLM | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01256 | hp1 | a0001 | c0001 | t0007 | g0005 | AMR | CLM | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | CLM | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0079 | AMR | CLM | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | CLM | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01496 | hp1 | a0001 | c0001 | t0008 | g0010 | AMR | CLM | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01515 | hp2 | a0001 | c0001 | t0013 | g0011 | EUR | IBS | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01516 | hp1 | a0001 | c0001 | t0024 | g0032 | EUR | IBS | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0086 | EUR | IBS | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0015 | EUR | IBS | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01517 | hp2 | a0001 | c0001 | t0013 | g0011 | EUR | IBS | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01884 | hp2 | a0001 | c0005 | t0002 | g0066 | AFR | ACB | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01891 | hp1 | a0001 | c0001 | t0031 | g0070 | AFR | ACB | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | ACB | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01934 | hp1 | a0001 | c0001 | t0005 | g0004 | AMR | PEL | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01934 | hp2 | a0001 | c0001 | t0004 | g0017 | AMR | PEL | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01943 | hp2 | a0001 | c0001 | t0009 | g0054 | AMR | PEL | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01952 | hp2 | a0002 | c0003 | t0001 | g0001 | AMR | PEL | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | PEL | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02055 | hp1 | a0001 | c0001 | t0010 | g0051 | AFR | ACB | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02132 | hp1 | a0001 | c0001 | t0006 | g0002 | EAS | KHV | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | CDX | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | ACB | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02257 | hp2 | a0001 | c0001 | t0008 | g0010 | AFR | ACB | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | ACB | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0017 | AFR | ACB | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02451 | hp1 | a0001 | c0001 | t0016 | g0062 | AFR | ACB | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02451 | hp2 | a0001 | c0001 | t0029 | g0018 | AFR | ACB | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02572 | hp2 | a0001 | c0002 | t0002 | g0058 | AFR | GWD | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0071 | AFR | GWD | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02647 | hp1 | a0001 | c0001 | t0012 | g0020 | AFR | GWD | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02647 | hp2 | a0001 | c0001 | t0019 | g0031 | AFR | GWD | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02717 | hp1 | a0001 | c0002 | t0002 | g0059 | AFR | GWD | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0068 | AFR | GWD | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02723 | hp1 | a0001 | c0001 | t0030 | g0074 | AFR | GWD | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02738 | hp2 | a0001 | c0001 | t0005 | g0004 | SAS | PJL | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0031 | AFR | GWD | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0064 | AFR | GWD | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0128 | AFR | GWD | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0106 | AFR | GWD | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0090 | AFR | GWD | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02895 | hp2 | a0001 | c0001 | t0009 | g0083 | AFR | GWD | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0048 | AFR | GWD | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02896 | hp2 | a0001 | c0001 | t0027 | g0038 | AFR | GWD | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0092 | AFR | GWD | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0052 | AFR | ESN | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02965 | hp1 | a0001 | c0001 | t0012 | g0020 | AFR | ESN | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0063 | AFR | ESN | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0101 | AFR | ESN | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | ESN | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02976 | hp1 | a0001 | c0001 | t0009 | g0018 | AFR | ESN | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | ESN | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG03041 | hp1 | a0001 | c0001 | t0015 | g0028 | AFR | GWD | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG03041 | hp2 | a0001 | c0001 | t0016 | g0061 | AFR | GWD | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0030 | AFR | ESN | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ESN | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG03139 | hp2 | a0001 | c0001 | t0008 | g0010 | AFR | ESN | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG03195 | hp1 | a0001 | c0001 | t0011 | g0027 | AFR | ESN | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0030 | AFR | ESN | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG03209 | hp1 | a0001 | c0005 | t0032 | g0057 | AFR | MSL | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | MSL | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG03225 | hp1 | a0001 | c0006 | t0001 | g0060 | AFR | MSL | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | MSL | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | MSL | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG03453 | hp2 | a0001 | c0001 | t0018 | g0082 | AFR | MSL | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG03486 | hp1 | a0001 | c0001 | t0014 | g0026 | AFR | MSL | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | MSL | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG03492 | hp2 | a0001 | c0001 | t0025 | g0008 | SAS | PJL | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG03516 | hp1 | a0001 | c0001 | t0008 | g0010 | AFR | ESN | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0047 | AFR | ESN | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG03540 | hp1 | a0001 | c0001 | t0009 | g0018 | AFR | GWD | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG03579 | hp2 | a0001 | c0007 | t0010 | g0044 | AFR | MSL | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG03669 | hp2 | a0001 | c0001 | t0022 | g0078 | SAS | PJL | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG03688 | hp1 | a0001 | c0001 | t0005 | g0004 | SAS | STU | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG03704 | hp1 | a0001 | c0001 | t0004 | g0029 | SAS | PJL | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0011 | SAS | BEB | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG03834 | hp1 | a0001 | c0001 | t0009 | g0076 | SAS | BEB | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0014 | SAS | BEB | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | BEB | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0081 | SAS | BEB | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | BEB | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG04115 | hp2 | a0001 | c0001 | t0023 | g0001 | SAS | STU | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | BEB | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG04204 | hp2 | a0001 | c0001 | t0005 | g0004 | SAS | STU | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | STU | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG04228 | hp2 | a0001 | c0001 | t0005 | g0056 | SAS | STU | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0093 | AFR | YRI | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA18522 | hp2 | a0001 | c0001 | t0008 | g0010 | AFR | YRI | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | YRI | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | YRI | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA18986 | hp2 | a0001 | c0001 | t0006 | g0002 | EAS | JPT | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA19011 | hp1 | a0001 | c0001 | t0006 | g0024 | EAS | JPT | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | LWK | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0100 | AFR | LWK | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA19055 | hp1 | a0001 | c0001 | t0006 | g0024 | EAS | JPT | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA19063 | hp1 | a0001 | c0001 | t0028 | g0002 | EAS | JPT | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA19079 | hp2 | a0001 | c0001 | t0006 | g0002 | EAS | JPT | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA19084 | hp2 | a0003 | c0009 | t0006 | g0024 | EAS | JPT | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | YRI | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA20129 | hp1 | a0001 | c0001 | t0026 | g0105 | AFR | ASW | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ASW | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA20752 | hp1 | a0001 | c0001 | t0005 | g0004 | EUR | TSI | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0029 | EUR | TSI | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | GIH | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01123 | hp1 | a0001 | c0001 | t0007 | g0005 | AMR | CLM | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0102 | AFR | ACB | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0098 | AFR | ACB | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG03471 | hp1 | a0001 | c0001 | t0010 | g0046 | AFR | MSL | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG06807 | hp1 | a0001 | c0001 | t0014 | g0026 | AFR | USA | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| HG06807 | hp2 | a0001 | c0001 | t0020 | g0019 | AFR | USA | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA20300 | hp1 | a0004 | c0008 | t0002 | g0025 | AFR | USA | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA20300 | hp2 | a0002 | c0003 | t0001 | g0001 | AFR | USA | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA21309 | hp1 | a0001 | c0001 | t0012 | g0020 | AFR | LWK | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| NA21309 | hp2 | a0001 | c0001 | t0007 | g0005 | AFR | LWK | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0004 | g0075 | REF | REF | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0019 | REF | REF | RNF14_chr5_141964105_141995292 | RNF14 | chr5 | 141964105 | 141995292 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:141978621 | C | A | 1 | a0004 | 1 | NA20300.hp1 | missense_variant | MODERATE | c.625C>A | p.Gln209Lys | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 5/9 | 868/4170 | 625/1425 | 209/474 | chr5 | 141978621 | |||
| chr5:141978825 | G | A | 1 | a0002 | 2 | HG01952.hp2 NA20300.hp2 |
missense_variant | MODERATE | c.829G>A | p.Gly277Ser | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 5/9 | 1072/4170 | 829/1425 | 277/474 | chr5 | 141978825 | |||
| chr5:141984932 | C | T | 1 | a0003 | 1 | NA19084.hp2 | missense_variant&splice_region_variant | MODERATE | c.1366C>T | p.Arg456Trp | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 8/9 | 1609/4170 | 1366/1425 | 456/474 | chr5 | 141984932 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:141973687 | T | G | 2 | a0001c0002 a0001c0006 |
3 | HG02572.hp2 HG02717.hp1 HG03225.hp1 |
synonymous_variant | LOW | c.99T>G | p.Gly33Gly | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 3/9 | 342/4170 | 99/1425 | 33/474 | chr5 | 141973687 | |||
| chr5:141974943 | G | A | 1 | a0001c0007 | 1 | HG03579.hp2 | synonymous_variant | LOW | c.294G>A | p.Leu98Leu | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 4/9 | 537/4170 | 294/1425 | 98/474 | chr5 | 141974943 | |||
| chr5:141980347 | T | G | 1 | a0001c0004 | 2 | HG01099.hp2 HG01168.hp2 |
synonymous_variant | LOW | c.1059T>G | p.Thr353Thr | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 6/9 | 1302/4170 | 1059/1425 | 353/474 | chr5 | 141980347 | |||
| chr5:141984874 | T | C | 2 | a0001c0002 a0001c0005 |
4 | HG01884.hp2 HG02572.hp2 HG02717.hp1 others(1): Show |
synonymous_variant | LOW | c.1308T>C | p.Ser436Ser | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 8/9 | 1551/4170 | 1308/1425 | 436/474 | chr5 | 141984874 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:141969110 | C | A | 1 | a0001c0001t0017 | 1 | HG00408.hp2 | 5_prime_UTR_variant | MODIFIER | c.-238C>A | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 1/9 | 4479 | chr5 | 141969110 | ||||||
| chr5:141969141 | G | T | 1 | a0001c0001t0012 | 3 | HG02647.hp1 HG02965.hp1 NA21309.hp1 |
5_prime_UTR_variant | MODIFIER | c.-207G>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 1/9 | 4448 | chr5 | 141969141 | ||||||
| chr5:141969143 | C | T | 32 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(29): Show |
254 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
5_prime_UTR_variant | MODIFIER | c.-205C>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 1/9 | 4446 | chr5 | 141969143 | ||||||
| chr5:141987801 | C | A | 1 | a0001c0001t0013 | 2 | HG01515.hp2 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*11C>A | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 9/9 | 11 | chr5 | 141987801 | ||||||
| chr5:141987992 | T | G | 1 | a0001c0001t0023 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*202T>G | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 9/9 | 202 | chr5 | 141987992 | ||||||
| chr5:141988034 | A | C | 1 | a0001c0005t0032 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*244A>C | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 9/9 | 244 | chr5 | 141988034 | ||||||
| chr5:141988242 | G | C | 33 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(30): Show |
250 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(247): Show |
3_prime_UTR_variant | MODIFIER | c.*452G>C | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 9/9 | 452 | chr5 | 141988242 | ||||||
| chr5:141988333 | G | A | 14 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(11): Show |
168 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*543G>A | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 9/9 | 543 | chr5 | 141988333 | ||||||
| chr5:141988526 | C | T | 32 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(29): Show |
253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
3_prime_UTR_variant | MODIFIER | c.*736C>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 9/9 | 736 | chr5 | 141988526 | ||||||
| chr5:141988543 | C | A | 1 | a0001c0001t0008 | 5 | HG01496.hp1 HG02257.hp2 HG03139.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*753C>A | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 9/9 | 753 | chr5 | 141988543 | ||||||
| chr5:141988771 | A | G | 1 | a0001c0001t0022 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*981A>G | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 9/9 | 981 | chr5 | 141988771 | ||||||
| chr5:141989218 | A | T | 1 | a0001c0001t0015 | 2 | HG01243.hp1 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1428A>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 9/9 | 1428 | chr5 | 141989218 | ||||||
| chr5:141989325 | T | C | 1 | a0001c0001t0014 | 2 | HG03486.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1535T>C | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 9/9 | 1535 | chr5 | 141989325 | ||||||
| chr5:141989341 | A | G | 1 | a0001c0001t0031 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1551A>G | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 9/9 | 1551 | chr5 | 141989341 | ||||||
| chr5:141989366 | C | A | 1 | a0001c0001t0024 | 1 | HG01516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1576C>A | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 9/9 | 1576 | chr5 | 141989366 | ||||||
| chr5:141989615 | C | T | 3 | a0001c0001t0006 a0001c0001t0028 a0003c0009t0006 |
7 | HG02132.hp1 NA18986.hp2 NA19011.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1825C>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 9/9 | 1825 | chr5 | 141989615 | ||||||
| chr5:141989647 | A | G | 1 | a0001c0001t0021 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1857A>G | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 9/9 | 1857 | chr5 | 141989647 | ||||||
| chr5:141989692 | CAAA | C | 23 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(20): Show |
219 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(216): Show |
3_prime_UTR_variant | MODIFIER | c.*1920_*1922delAAA | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 9/9 | 1920 | INFO_REALIGN_3_PRIME | chr5 | 141989692 | |||||
| chr5:141989692 | CAAAA | C | 4 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0027 others(1): Show |
28 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1919_*1922delAAAA | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 9/9 | 1919 | INFO_REALIGN_3_PRIME | chr5 | 141989692 | |||||
| chr5:141989806 | G | T | 1 | a0001c0001t0030 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2016G>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 9/9 | 2016 | chr5 | 141989806 | ||||||
| chr5:141989857 | G | A | 32 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(29): Show |
253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
3_prime_UTR_variant | MODIFIER | c.*2067G>A | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 9/9 | 2067 | chr5 | 141989857 | ||||||
| chr5:141989881 | G | T | 1 | a0001c0001t0026 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2091G>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 9/9 | 2091 | chr5 | 141989881 | ||||||
| chr5:141989900 | G | A | 28 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(25): Show |
233 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(230): Show |
3_prime_UTR_variant | MODIFIER | c.*2110G>A | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 9/9 | 2110 | chr5 | 141989900 | ||||||
| chr5:141989904 | T | C | 1 | a0001c0005t0032 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2114T>C | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 9/9 | 2114 | chr5 | 141989904 | ||||||
| chr5:141990052 | T | A | 1 | a0001c0001t0020 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2262T>A | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 9/9 | 2262 | chr5 | 141990052 | ||||||
| chr5:141990070 | T | C | 4 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0029 others(1): Show |
20 | HG00140.hp2 HG00741.hp1 HG01934.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2280T>C | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 9/9 | 2280 | chr5 | 141990070 | ||||||
| chr5:141990127 | C | T | 4 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0029 others(1): Show |
20 | HG00140.hp2 HG00741.hp1 HG01934.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2337C>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 9/9 | 2337 | chr5 | 141990127 | ||||||
| chr5:141990129 | T | G | 2 | a0001c0001t0011 a0001c0004t0011 |
3 | HG01099.hp2 HG01168.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2339T>G | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 9/9 | 2339 | chr5 | 141990129 | ||||||
| chr5:141990156 | T | C | 1 | a0001c0001t0025 | 1 | HG03492.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2366T>C | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 9/9 | 2366 | chr5 | 141990156 | ||||||
| chr5:141990222 | A | T | 1 | a0001c0001t0018 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2432A>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 9/9 | 2432 | chr5 | 141990222 | ||||||
| chr5:141990224 | A | C | 1 | a0001c0001t0018 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2434A>C | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 9/9 | 2434 | chr5 | 141990224 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:141969384 | A | C | 1 | a0001c0001t0001g0043 | 2 | NA19012.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.-181+217A>C | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 1/8 | chr5 | 141969384 | |||||||
| chr5:141969411 | C | A | 1 | a0001c0001t0008g0010 | 5 | HG01496.hp1 HG02257.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.-181+244C>A | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 1/8 | chr5 | 141969411 | |||||||
| chr5:141969631 | A | G | 83 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(80): Show |
183 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.-181+464A>G | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 1/8 | chr5 | 141969631 | |||||||
| chr5:141969836 | G | A | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(115): Show |
237 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.-181+669G>A | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 1/8 | chr5 | 141969836 | |||||||
| chr5:141970067 | G | T | 6 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0004g0069 others(3): Show |
7 | HG00140.hp2 HG01243.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.-180-637G>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 1/8 | chr5 | 141970067 | |||||||
| chr5:141970281 | A | T | 3 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 |
3 | HG00280.hp1 HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-180-423A>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 1/8 | chr5 | 141970281 | |||||||
| chr5:141970498 | T | TA | 19 | a0001c0001t0001g0045 a0001c0001t0001g0053 a0001c0001t0002g0007 others(16): Show |
37 | HG00639.hp2 HG00733.hp1 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.-180-201dupA | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr5 | 141970498 | ||||||
| chr5:141970607 | A | C | 11 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0004g0063 others(8): Show |
12 | HG00140.hp2 HG01099.hp2 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.-180-97A>C | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 1/8 | chr5 | 141970607 | |||||||
| chr5:141971196 | C | T | 3 | a0001c0001t0011g0027 a0001c0004t0011g0027 a0001c0004t0011g0065 |
3 | HG01099.hp2 HG01168.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-7+319C>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 2/8 | chr5 | 141971196 | |||||||
| chr5:141971364 | C | T | 4 | a0001c0001t0005g0004 a0001c0001t0005g0055 a0001c0001t0005g0056 others(1): Show |
12 | HG00639.hp2 HG00733.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.-7+487C>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 2/8 | chr5 | 141971364 | |||||||
| chr5:141971388 | C | T | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(116): Show |
240 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.-7+511C>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 2/8 | chr5 | 141971388 | |||||||
| chr5:141971563 | TTTTC | T | 7 | a0001c0001t0001g0080 a0001c0001t0003g0011 a0001c0001t0003g0030 others(4): Show |
12 | HG00738.hp2 HG01192.hp2 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.-7+731_-7+734delTT others(2): Show |
RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr5 | 141971563 | ||||||
| chr5:141971563 | TTTTCTTT others(5): Show |
T | 3 | a0001c0001t0001g0124 a0001c0001t0021g0077 a0001c0001t0022g0078 |
3 | HG01175.hp2 HG03669.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.-7+723_-7+734delTT others(10): Show |
RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr5 | 141971563 | ||||||
| chr5:141971563 | TTTTCTTT others(9): Show |
T | 2 | a0001c0001t0004g0029 a0001c0001t0009g0076 |
3 | HG03704.hp1 HG03834.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-7+719_-7+734delTT others(14): Show |
RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr5 | 141971563 | ||||||
| chr5:141971563 | TTTTCTTT others(13): Show |
T | 6 | a0001c0001t0001g0072 a0001c0001t0002g0071 a0001c0001t0004g0017 others(3): Show |
8 | HG00741.hp1 HG01934.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-7+715_-7+734delTT others(18): Show |
RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr5 | 141971563 | ||||||
| chr5:141971564 | TTTCTTTC others(4): Show |
T | 1 | a0001c0001t0001g0002 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-7+690_-7+700delCT others(9): Show |
RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr5 | 141971564 | ||||||
| chr5:141971564 | TTTCTTTC others(8): Show |
T | 1 | a0001c0001t0001g0001 | 2 | HG01099.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.-7+690_-7+704delCT others(13): Show |
RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr5 | 141971564 | ||||||
| chr5:141971565 | TTCTTTCT others(3): Show |
T | 24 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(21): Show |
58 | HG00408.hp2 HG00597.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.-7+690_-7+699delCT others(8): Show |
RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr5 | 141971565 | ||||||
| chr5:141971565 | TTCTTTCT others(7): Show |
T | 90 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(87): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.-7+690_-7+703delCT others(12): Show |
RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr5 | 141971565 | ||||||
| chr5:141971566 | TCTTTCTT others(6): Show |
T | 2 | a0001c0001t0001g0084 a0001c0001t0014g0026 |
3 | HG01981.hp1 HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-7+690_-7+702delCT others(11): Show |
RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 2/8 | chr5 | 141971566 | |||||||
| chr5:141971571 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-7+694C>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 2/8 | chr5 | 141971571 | |||||||
| chr5:141971575 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-7+698C>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 2/8 | chr5 | 141971575 | |||||||
| chr5:141971579 | C | T | 25 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(22): Show |
60 | HG00408.hp2 HG00597.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.-7+702C>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 2/8 | chr5 | 141971579 | |||||||
| chr5:141971583 | C | T | 91 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(88): Show |
177 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.-7+706C>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 2/8 | chr5 | 141971583 | |||||||
| chr5:141971587 | C | T | 3 | a0001c0001t0001g0039 a0001c0001t0001g0113 a0001c0001t0005g0052 |
4 | HG01978.hp2 HG02922.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7+710C>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 2/8 | chr5 | 141971587 | |||||||
| chr5:141971636 | C | CT | 13 | a0001c0001t0001g0080 a0001c0001t0003g0079 a0001c0001t0004g0017 others(10): Show |
17 | HG00741.hp1 HG01175.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.-7+781dupT | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr5 | 141971636 | ||||||
| chr5:141971636 | CT | C | 6 | a0001c0001t0005g0004 a0001c0001t0005g0052 a0001c0001t0005g0055 others(3): Show |
14 | HG00639.hp2 HG00733.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.-7+781delT | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr5 | 141971636 | ||||||
| chr5:141971636 | CTT | C | 6 | a0001c0001t0010g0051 a0001c0001t0012g0020 a0001c0001t0031g0070 others(3): Show |
8 | HG01891.hp1 HG02055.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.-7+780_-7+781delTT | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr5 | 141971636 | ||||||
| chr5:141971636 | CTTT | C | 23 | a0001c0001t0001g0045 a0001c0001t0002g0007 a0001c0001t0002g0025 others(20): Show |
34 | HG00140.hp2 HG01099.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.-7+779_-7+781delTT others(1): Show |
RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr5 | 141971636 | ||||||
| chr5:141971636 | CTTTTTTT others(7): Show |
C | 83 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(80): Show |
183 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.-7+768_-7+781delTT others(12): Show |
RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr5 | 141971636 | ||||||
| chr5:141971658 | T | G | 1 | a0001c0001t0031g0070 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-7+781T>G | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 2/8 | chr5 | 141971658 | |||||||
| chr5:141971808 | C | T | 5 | a0001c0001t0001g0016 a0001c0001t0001g0023 a0001c0001t0001g0038 others(2): Show |
10 | HG01069.hp2 HG01071.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.-7+931C>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 2/8 | chr5 | 141971808 | |||||||
| chr5:141971819 | T | TTTATTTT others(9): Show |
2 | a0001c0001t0003g0030 a0001c0001t0018g0082 |
3 | HG03130.hp2 HG03195.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-7+944_-7+959dupTA others(14): Show |
RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr5 | 141971819 | ||||||
| chr5:141971852 | T | C | 8 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0004g0063 others(5): Show |
9 | HG00140.hp2 HG01243.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.-7+975T>C | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 2/8 | chr5 | 141971852 | |||||||
| chr5:141971900 | G | A | 1 | a0001c0001t0001g0085 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-7+1023G>A | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 2/8 | chr5 | 141971900 | |||||||
| chr5:141972019 | T | A | 17 | a0001c0001t0001g0045 a0001c0001t0002g0007 a0001c0001t0002g0025 others(14): Show |
34 | HG00639.hp2 HG00733.hp1 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.-7+1142T>A | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 2/8 | chr5 | 141972019 | |||||||
| chr5:141972054 | C | G | 3 | a0001c0001t0002g0007 a0001c0001t0002g0049 a0001c0001t0002g0050 |
8 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.-7+1177C>G | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 2/8 | chr5 | 141972054 | |||||||
| chr5:141972076 | A | G | 1 | a0001c0001t0001g0111 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-7+1199A>G | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 2/8 | chr5 | 141972076 | |||||||
| chr5:141972236 | A | AT | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(120): Show |
247 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.-6-1336dupT | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr5 | 141972236 | ||||||
| chr5:141972236 | A | T | 2 | a0001c0001t0001g0110 a0001c0001t0031g0070 |
2 | HG01891.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.-6-1347A>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 2/8 | chr5 | 141972236 | |||||||
| chr5:141972578 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-6-1005G>A | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 2/8 | chr5 | 141972578 | |||||||
| chr5:141972664 | C | T | 16 | a0001c0001t0001g0045 a0001c0001t0002g0007 a0001c0001t0002g0025 others(13): Show |
33 | HG00639.hp2 HG00733.hp1 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.-6-919C>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 2/8 | chr5 | 141972664 | |||||||
| chr5:141972678 | C | T | 1 | a0001c0001t0016g0061 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-6-905C>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 2/8 | chr5 | 141972678 | |||||||
| chr5:141972698 | C | T | 1 | a0001c0001t0001g0009 | 6 | HG00642.hp2 HG01074.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.-6-885C>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 2/8 | chr5 | 141972698 | |||||||
| chr5:141972709 | A | G | 1 | a0001c0001t0001g0022 | 3 | HG01106.hp2 HG01123.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.-6-874A>G | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 2/8 | chr5 | 141972709 | |||||||
| chr5:141972822 | T | C | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(128): Show |
256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.-6-761T>C | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 2/8 | chr5 | 141972822 | |||||||
| chr5:141972843 | G | A | 1 | a0001c0005t0032g0057 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-6-740G>A | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 2/8 | chr5 | 141972843 | |||||||
| chr5:141972873 | G | T | 1 | a0001c0001t0001g0109 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-6-710G>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 2/8 | chr5 | 141972873 | |||||||
| chr5:141972932 | T | C | 2 | a0001c0001t0003g0031 a0001c0001t0019g0031 |
2 | HG02647.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-6-651T>C | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 2/8 | chr5 | 141972932 | |||||||
| chr5:141972934 | C | A | 1 | a0001c0005t0002g0066 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-6-649C>A | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 2/8 | chr5 | 141972934 | |||||||
| chr5:141972985 | T | C | 1 | a0001c0001t0001g0088 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-6-598T>C | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 2/8 | chr5 | 141972985 | |||||||
| chr5:141973031 | A | C | 1 | a0001c0005t0032g0057 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-6-552A>C | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 2/8 | chr5 | 141973031 | |||||||
| chr5:141973037 | G | T | 1 | a0001c0005t0032g0057 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-6-546G>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 2/8 | chr5 | 141973037 | |||||||
| chr5:141973170 | T | G | 1 | a0001c0007t0010g0044 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-6-413T>G | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 2/8 | chr5 | 141973170 | |||||||
| chr5:141973177 | G | A | 4 | a0001c0001t0001g0045 a0001c0001t0004g0047 a0001c0001t0010g0046 others(1): Show |
4 | HG02055.hp1 HG03471.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-6-406G>A | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 2/8 | chr5 | 141973177 | |||||||
| chr5:141973195 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-6-388G>A | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 2/8 | chr5 | 141973195 | |||||||
| chr5:141973241 | C | CT | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(104): Show |
226 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.-6-328dupT | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr5 | 141973241 | ||||||
| chr5:141973241 | C | CTT | 10 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0004g0064 others(7): Show |
12 | HG00140.hp2 HG01243.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.-6-329_-6-328dupTT | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr5 | 141973241 | ||||||
| chr5:141973309 | G | C | 6 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0004g0063 others(3): Show |
6 | HG00140.hp2 HG01884.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-6-274G>C | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 2/8 | chr5 | 141973309 | |||||||
| chr5:141973480 | C | T | 3 | a0001c0001t0004g0073 a0001c0001t0009g0054 a0001c0007t0010g0044 |
3 | HG00741.hp1 HG01943.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-6-103C>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 2/8 | chr5 | 141973480 | |||||||
| chr5:141973766 | G | T | 4 | a0001c0001t0005g0004 a0001c0001t0005g0052 a0001c0001t0005g0055 others(1): Show |
12 | HG00639.hp2 HG00733.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.154+24G>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 3/8 | chr5 | 141973766 | |||||||
| chr5:141973774 | T | C | 1 | a0001c0001t0001g0091 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.154+32T>C | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 3/8 | chr5 | 141973774 | |||||||
| chr5:141973913 | A | G | 1 | a0001c0001t0001g0042 | 2 | HG02683.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.154+171A>G | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 3/8 | chr5 | 141973913 | |||||||
| chr5:141973988 | CAGT | C | 2 | a0001c0001t0001g0012 a0001c0001t0001g0114 |
6 | HG00597.hp1 NA18980.hp2 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.154+247_154+249del others(3): Show |
RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 3/8 | chr5 | 141973988 | |||||||
| chr5:141973993 | T | G | 2 | a0001c0001t0001g0012 a0001c0001t0001g0114 |
6 | HG00597.hp1 NA18980.hp2 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.154+251T>G | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 3/8 | chr5 | 141973993 | |||||||
| chr5:141973996 | C | A | 2 | a0001c0001t0001g0012 a0001c0001t0001g0114 |
6 | HG00597.hp1 NA18980.hp2 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.154+254C>A | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 3/8 | chr5 | 141973996 | |||||||
| chr5:141974206 | T | G | 2 | a0001c0001t0006g0024 a0003c0009t0006g0024 |
3 | NA19011.hp1 NA19055.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.154+464T>G | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 3/8 | chr5 | 141974206 | |||||||
| chr5:141974223 | C | G | 1 | a0001c0001t0005g0052 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.154+481C>G | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 3/8 | chr5 | 141974223 | |||||||
| chr5:141974344 | C | T | 4 | a0001c0001t0001g0080 a0001c0001t0009g0018 a0001c0001t0009g0083 others(1): Show |
5 | HG02451.hp2 HG02895.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.155-460C>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 3/8 | chr5 | 141974344 | |||||||
| chr5:141974375 | T | G | 8 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0004g0063 others(5): Show |
9 | HG00140.hp2 HG01243.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.155-429T>G | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 3/8 | chr5 | 141974375 | |||||||
| chr5:141974475 | C | T | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(114): Show |
236 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.155-329C>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 3/8 | chr5 | 141974475 | |||||||
| chr5:141974551 | T | C | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(128): Show |
256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.155-253T>C | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 3/8 | chr5 | 141974551 | |||||||
| chr5:141974622 | G | A | 1 | a0001c0001t0001g0006 | 7 | HG01361.hp1 HG01433.hp2 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.155-182G>A | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 3/8 | chr5 | 141974622 | |||||||
| chr5:141974655 | G | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(116): Show |
240 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.155-149G>C | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 3/8 | chr5 | 141974655 | |||||||
| chr5:141975076 | A | C | 1 | a0001c0005t0002g0066 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.306+121A>C | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 4/8 | chr5 | 141975076 | |||||||
| chr5:141975370 | A | C | 1 | a0001c0001t0001g0108 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.306+415A>C | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 4/8 | chr5 | 141975370 | |||||||
| chr5:141975383 | A | C | 1 | a0001c0001t0001g0107 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.306+428A>C | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 4/8 | chr5 | 141975383 | |||||||
| chr5:141975428 | T | C | 4 | a0001c0001t0001g0080 a0001c0001t0009g0018 a0001c0001t0009g0083 others(1): Show |
5 | HG02451.hp2 HG02895.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.306+473T>C | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 4/8 | chr5 | 141975428 | |||||||
| chr5:141975829 | G | C | 2 | a0001c0001t0003g0030 a0001c0001t0018g0082 |
3 | HG03130.hp2 HG03195.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.306+874G>C | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 4/8 | chr5 | 141975829 | |||||||
| chr5:141975916 | C | A | 1 | a0001c0001t0002g0048 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.306+961C>A | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 4/8 | chr5 | 141975916 | |||||||
| chr5:141975924 | CA | C | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(120): Show |
239 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.306+985delA | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 141975924 | ||||||
| chr5:141975924 | CAA | C | 4 | a0001c0001t0005g0004 a0001c0001t0005g0052 a0001c0001t0005g0055 others(1): Show |
12 | HG00639.hp2 HG00733.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.306+984_306+985del others(2): Show |
RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 141975924 | ||||||
| chr5:141975941 | G | A | 1 | a0001c0001t0015g0028 | 2 | HG01243.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.306+986G>A | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 4/8 | chr5 | 141975941 | |||||||
| chr5:141976031 | A | G | 7 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0004g0063 others(4): Show |
8 | HG00140.hp2 HG01243.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.306+1076A>G | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 4/8 | chr5 | 141976031 | |||||||
| chr5:141976081 | T | C | 9 | a0001c0001t0001g0080 a0001c0001t0004g0029 a0001c0001t0004g0073 others(6): Show |
13 | HG00741.hp1 HG01943.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.306+1126T>C | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 4/8 | chr5 | 141976081 | |||||||
| chr5:141976245 | T | A | 3 | a0001c0001t0002g0033 a0001c0001t0002g0090 a0001c0001t0005g0092 |
4 | HG02895.hp1 HG02897.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.306+1290T>A | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 4/8 | chr5 | 141976245 | |||||||
| chr5:141976297 | C | CCACGCAT others(3): Show |
2 | a0001c0001t0001g0040 a0001c0001t0001g0115 |
3 | HG02109.hp1 HG02109.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.306+1344_306+1353d others(12): Show |
RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 141976297 | ||||||
| chr5:141976303 | A | G | 1 | a0001c0001t0002g0050 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.306+1348A>G | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 4/8 | chr5 | 141976303 | |||||||
| chr5:141976307 | GCGTGCAT others(3): Show |
G | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.306+1364_306+1373d others(12): Show |
RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 141976307 | ||||||
| chr5:141976339 | A | G | 1 | a0001c0001t0002g0106 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.306+1384A>G | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 4/8 | chr5 | 141976339 | |||||||
| chr5:141976383 | T | C | 9 | a0001c0001t0001g0080 a0001c0001t0004g0029 a0001c0001t0004g0073 others(6): Show |
13 | HG00741.hp1 HG01943.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.306+1428T>C | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 4/8 | chr5 | 141976383 | |||||||
| chr5:141976395 | G | A | 4 | a0001c0001t0005g0004 a0001c0001t0005g0052 a0001c0001t0005g0055 others(1): Show |
12 | HG00639.hp2 HG00733.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.306+1440G>A | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 4/8 | chr5 | 141976395 | |||||||
| chr5:141976734 | G | A | 6 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0004g0069 others(3): Show |
7 | HG00140.hp2 HG01243.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.307-1569G>A | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 4/8 | chr5 | 141976734 | |||||||
| chr5:141976776 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0005g0056 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.307-1507_307-1497d others(13): Show |
RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 141976776 | ||||||
| chr5:141976776 | CTTTTTTT others(5): Show |
C | 18 | a0001c0001t0001g0072 a0001c0001t0002g0067 a0001c0001t0002g0068 others(15): Show |
27 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.307-1508_307-1497d others(14): Show |
RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 141976776 | ||||||
| chr5:141976776 | CTTTTTTT others(6): Show |
C | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(96): Show |
210 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.307-1509_307-1497d others(15): Show |
RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 141976776 | ||||||
| chr5:141976776 | CTTTTTTT others(7): Show |
C | 4 | a0001c0001t0001g0035 a0001c0001t0001g0117 a0001c0001t0001g0125 others(1): Show |
5 | HG01167.hp1 HG01167.hp2 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.307-1510_307-1497d others(16): Show |
RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 141976776 | ||||||
| chr5:141976790 | T | C | 1 | a0001c0001t0002g0093 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.307-1513T>C | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 4/8 | chr5 | 141976790 | |||||||
| chr5:141976796 | T | G | 3 | a0001c0001t0001g0034 a0001c0001t0001g0094 a0001c0001t0001g0116 |
4 | HG00438.hp2 NA18945.hp2 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.307-1507T>G | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 4/8 | chr5 | 141976796 | |||||||
| chr5:141976903 | C | G | 1 | a0001c0001t0015g0028 | 2 | HG01243.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.307-1400C>G | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 4/8 | chr5 | 141976903 | |||||||
| chr5:141976933 | C | T | 1 | a0001c0001t0030g0074 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.307-1370C>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 4/8 | chr5 | 141976933 | |||||||
| chr5:141977038 | G | A | 1 | a0001c0001t0009g0083 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.307-1265G>A | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 4/8 | chr5 | 141977038 | |||||||
| chr5:141977082 | C | T | 4 | a0001c0001t0005g0004 a0001c0001t0005g0052 a0001c0001t0005g0055 others(1): Show |
12 | HG00639.hp2 HG00733.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.307-1221C>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 4/8 | chr5 | 141977082 | |||||||
| chr5:141977193 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.307-1110G>A | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 4/8 | chr5 | 141977193 | |||||||
| chr5:141977323 | C | T | 1 | a0001c0005t0032g0057 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.307-980C>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 4/8 | chr5 | 141977323 | |||||||
| chr5:141977441 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.307-862A>G | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 4/8 | chr5 | 141977441 | |||||||
| chr5:141977481 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0116 |
3 | HG00438.hp2 NA19058.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.307-822C>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 4/8 | chr5 | 141977481 | |||||||
| chr5:141977518 | T | C | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(130): Show |
259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.307-785T>C | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 4/8 | chr5 | 141977518 | |||||||
| chr5:141977714 | T | C | 3 | a0001c0001t0002g0007 a0001c0001t0002g0049 a0001c0001t0002g0050 |
8 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.307-589T>C | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 4/8 | chr5 | 141977714 | |||||||
| chr5:141978063 | G | A | 122 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(119): Show |
244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.307-240G>A | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 4/8 | chr5 | 141978063 | |||||||
| chr5:141978154 | TTGTA | T | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(128): Show |
256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.307-144_307-141del others(4): Show |
RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr5 | 141978154 | ||||||
| chr5:141978911 | G | A | 1 | a0001c0001t0002g0067 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.834+81G>A | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 5/8 | chr5 | 141978911 | |||||||
| chr5:141979084 | T | C | 1 | a0001c0001t0005g0055 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.834+254T>C | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 5/8 | chr5 | 141979084 | |||||||
| chr5:141979089 | A | T | 2 | a0001c0001t0002g0015 a0001c0001t0002g0086 |
5 | HG01081.hp2 HG01106.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.834+259A>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 5/8 | chr5 | 141979089 | |||||||
| chr5:141979111 | A | T | 1 | a0001c0001t0001g0039 | 2 | HG01978.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.834+281A>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 5/8 | chr5 | 141979111 | |||||||
| chr5:141979222 | AGGT | A | 17 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0004g0029 others(14): Show |
22 | HG00140.hp2 HG00741.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.834+403_834+405del others(3): Show |
RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr5 | 141979222 | ||||||
| chr5:141979224 | G | GTTT | 6 | a0001c0001t0001g0005 a0001c0001t0001g0032 a0001c0001t0001g0085 others(3): Show |
13 | HG00639.hp1 HG00735.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.834+395_834+396ins others(3): Show |
RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr5 | 141979224 | ||||||
| chr5:141979226 | G | T | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(96): Show |
209 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.834+396G>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 5/8 | chr5 | 141979226 | |||||||
| chr5:141979227 | G | GTGT | 4 | a0001c0001t0001g0080 a0001c0001t0009g0018 a0001c0001t0009g0083 others(1): Show |
5 | HG02451.hp2 HG02895.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.834+399_834+400ins others(3): Show |
RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr5 | 141979227 | ||||||
| chr5:141979227 | G | T | 105 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(102): Show |
222 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.834+397G>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 5/8 | chr5 | 141979227 | |||||||
| chr5:141979229 | G | T | 12 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0004g0069 others(9): Show |
14 | HG00140.hp2 HG01099.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.834+399G>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 5/8 | chr5 | 141979229 | |||||||
| chr5:141979230 | G | GTGT | 2 | a0001c0001t0004g0017 a0001c0001t0030g0074 |
4 | HG01934.hp2 HG02258.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.834+402_834+403ins others(3): Show |
RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr5 | 141979230 | ||||||
| chr5:141979230 | G | GTGTTGTT others(5): Show |
1 | a0001c0001t0001g0072 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.834+402_834+403ins others(12): Show |
RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr5 | 141979230 | ||||||
| chr5:141979230 | G | T | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(123): Show |
249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.834+400G>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 5/8 | chr5 | 141979230 | |||||||
| chr5:141979233 | G | GTGT | 3 | a0001c0001t0003g0031 a0001c0001t0003g0081 a0001c0001t0019g0031 |
3 | HG02647.hp2 HG02809.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.834+429_834+431dup others(3): Show |
RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr5 | 141979233 | ||||||
| chr5:141979233 | G | T | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(129): Show |
258 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.834+403G>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 5/8 | chr5 | 141979233 | |||||||
| chr5:141979235 | G | T | 1 | a0001c0001t0026g0105 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.834+405G>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 5/8 | chr5 | 141979235 | |||||||
| chr5:141979270 | G | A | 5 | a0001c0001t0004g0063 a0001c0001t0004g0064 a0001c0001t0014g0026 others(2): Show |
6 | HG02451.hp1 HG02809.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.834+440G>A | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 5/8 | chr5 | 141979270 | |||||||
| chr5:141979332 | C | T | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(111): Show |
233 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.834+502C>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 5/8 | chr5 | 141979332 | |||||||
| chr5:141979380 | C | T | 4 | a0001c0001t0001g0072 a0001c0001t0002g0071 a0001c0001t0004g0017 others(1): Show |
6 | HG01934.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.834+550C>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 5/8 | chr5 | 141979380 | |||||||
| chr5:141979398 | G | A | 1 | a0001c0001t0001g0036 | 2 | HG02055.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.834+568G>A | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 5/8 | chr5 | 141979398 | |||||||
| chr5:141979409 | C | T | 1 | a0001c0001t0031g0070 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.834+579C>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 5/8 | chr5 | 141979409 | |||||||
| chr5:141979544 | T | G | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(125): Show |
251 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.835-579T>G | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 5/8 | chr5 | 141979544 | |||||||
| chr5:141979600 | A | G | 4 | a0001c0001t0001g0072 a0001c0001t0002g0071 a0001c0001t0004g0017 others(1): Show |
6 | HG01934.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.835-523A>G | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 5/8 | chr5 | 141979600 | |||||||
| chr5:141979615 | A | G | 1 | a0001c0001t0015g0028 | 2 | HG01243.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.835-508A>G | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 5/8 | chr5 | 141979615 | |||||||
| chr5:141979677 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.835-446C>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 5/8 | chr5 | 141979677 | |||||||
| chr5:141979772 | C | T | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(125): Show |
251 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.835-351C>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 5/8 | chr5 | 141979772 | |||||||
| chr5:141979960 | A | G | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(121): Show |
245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.835-163A>G | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 5/8 | chr5 | 141979960 | |||||||
| chr5:141979968 | C | T | 7 | a0001c0001t0004g0029 a0001c0001t0004g0073 a0001c0001t0009g0018 others(4): Show |
9 | HG00741.hp1 HG01943.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.835-155C>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 5/8 | chr5 | 141979968 | |||||||
| chr5:141980418 | G | C | 1 | a0001c0001t0002g0068 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1063+67G>C | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 6/8 | chr5 | 141980418 | |||||||
| chr5:141980484 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1063+133A>G | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 6/8 | chr5 | 141980484 | |||||||
| chr5:141980686 | CAG | C | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(111): Show |
232 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.1063+336_1063+337d others(4): Show |
RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 6/8 | chr5 | 141980686 | |||||||
| chr5:141980720 | A | T | 2 | a0001c0001t0004g0017 a0001c0001t0030g0074 |
4 | HG01934.hp2 HG02258.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.1063+369A>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 6/8 | chr5 | 141980720 | |||||||
| chr5:141980821 | A | G | 1 | a0001c0001t0008g0010 | 5 | HG01496.hp1 HG02257.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1063+470A>G | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 6/8 | chr5 | 141980821 | |||||||
| chr5:141980909 | T | C | 2 | a0001c0001t0002g0090 a0001c0001t0005g0092 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1063+558T>C | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 6/8 | chr5 | 141980909 | |||||||
| chr5:141981014 | C | T | 1 | a0001c0001t0003g0030 | 2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1063+663C>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 6/8 | chr5 | 141981014 | |||||||
| chr5:141981072 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1063+721T>C | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 6/8 | chr5 | 141981072 | |||||||
| chr5:141981083 | C | T | 3 | a0001c0001t0001g0016 a0001c0001t0001g0038 a0001c0001t0027g0038 |
6 | HG01069.hp2 HG01071.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1063+732C>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 6/8 | chr5 | 141981083 | |||||||
| chr5:141981184 | G | C | 2 | a0001c0001t0004g0017 a0001c0001t0030g0074 |
4 | HG01934.hp2 HG02258.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.1063+833G>C | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 6/8 | chr5 | 141981184 | |||||||
| chr5:141981418 | T | G | 1 | a0001c0002t0002g0058 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1063+1067T>G | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 6/8 | chr5 | 141981418 | |||||||
| chr5:141981419 | G | A | 4 | a0001c0001t0004g0029 a0001c0001t0004g0073 a0001c0001t0009g0054 others(1): Show |
5 | HG00741.hp1 HG01943.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.1063+1068G>A | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 6/8 | chr5 | 141981419 | |||||||
| chr5:141981516 | T | C | 1 | a0001c0001t0001g0096 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1063+1165T>C | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 6/8 | chr5 | 141981516 | |||||||
| chr5:141981626 | G | A | 4 | a0001c0001t0004g0029 a0001c0001t0004g0073 a0001c0001t0009g0054 others(1): Show |
5 | HG00741.hp1 HG01943.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.1063+1275G>A | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 6/8 | chr5 | 141981626 | |||||||
| chr5:141981667 | T | C | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(129): Show |
257 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.1063+1316T>C | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 6/8 | chr5 | 141981667 | |||||||
| chr5:141981820 | C | G | 1 | a0001c0001t0001g0080 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1063+1469C>G | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 6/8 | chr5 | 141981820 | |||||||
| chr5:141981851 | C | CA | 5 | a0001c0001t0001g0038 a0001c0001t0015g0028 a0001c0001t0027g0038 others(2): Show |
6 | HG01243.hp1 HG01891.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1063+1513dupA | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr5 | 141981851 | ||||||
| chr5:141981860 | A | G | 1 | a0001c0005t0032g0057 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1063+1509A>G | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 6/8 | chr5 | 141981860 | |||||||
| chr5:141981863 | A | AG | 4 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0004g0069 others(1): Show |
4 | HG00140.hp2 HG01884.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1063+1512_1063+151 others(5): Show |
RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 6/8 | chr5 | 141981863 | |||||||
| chr5:141981982 | A | G | 1 | a0001c0001t0031g0070 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1064-1398A>G | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 6/8 | chr5 | 141981982 | |||||||
| chr5:141982123 | A | G | 4 | a0001c0001t0004g0029 a0001c0001t0004g0073 a0001c0001t0009g0054 others(1): Show |
5 | HG00741.hp1 HG01943.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.1064-1257A>G | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 6/8 | chr5 | 141982123 | |||||||
| chr5:141982138 | A | T | 7 | a0001c0001t0004g0029 a0001c0001t0004g0073 a0001c0001t0009g0018 others(4): Show |
9 | HG00741.hp1 HG01943.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1064-1242A>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 6/8 | chr5 | 141982138 | |||||||
| chr5:141982206 | A | G | 4 | a0001c0001t0002g0025 a0001c0001t0002g0048 a0001c0001t0008g0010 others(1): Show |
8 | HG01496.hp1 HG02257.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1064-1174A>G | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 6/8 | chr5 | 141982206 | |||||||
| chr5:141982213 | A | G | 1 | a0001c0001t0008g0010 | 5 | HG01496.hp1 HG02257.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1064-1167A>G | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 6/8 | chr5 | 141982213 | |||||||
| chr5:141982289 | A | T | 15 | a0001c0001t0002g0007 a0001c0001t0002g0025 a0001c0001t0002g0048 others(12): Show |
32 | HG00639.hp2 HG00733.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.1064-1091A>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 6/8 | chr5 | 141982289 | |||||||
| chr5:141982543 | T | C | 7 | a0001c0001t0004g0029 a0001c0001t0004g0073 a0001c0001t0009g0018 others(4): Show |
9 | HG00741.hp1 HG01943.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1064-837T>C | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 6/8 | chr5 | 141982543 | |||||||
| chr5:141982597 | A | G | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(129): Show |
257 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.1064-783A>G | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 6/8 | chr5 | 141982597 | |||||||
| chr5:141982707 | G | A | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(130): Show |
259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.1064-673G>A | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 6/8 | chr5 | 141982707 | |||||||
| chr5:141982724 | C | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(127): Show |
253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.1064-656C>G | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 6/8 | chr5 | 141982724 | |||||||
| chr5:141982741 | AT | A | 122 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(119): Show |
244 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(241): Show |
intron_variant | MODIFIER | c.1064-627delT | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr5 | 141982741 | ||||||
| chr5:141983128 | G | A | 1 | a0001c0001t0021g0077 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1064-252G>A | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 6/8 | chr5 | 141983128 | |||||||
| chr5:141983170 | A | G | 17 | a0001c0001t0001g0053 a0001c0001t0002g0007 a0001c0001t0002g0025 others(14): Show |
34 | HG00639.hp2 HG00733.hp1 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.1064-210A>G | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 6/8 | chr5 | 141983170 | |||||||
| chr5:141983601 | TATG | T | 7 | a0001c0001t0001g0095 a0001c0001t0004g0029 a0001c0001t0004g0073 others(4): Show |
8 | HG00741.hp1 HG01943.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1236+52_1236+54del others(3): Show |
RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr5 | 141983601 | ||||||
| chr5:141983642 | T | TA | 4 | a0001c0001t0012g0020 a0001c0002t0002g0058 a0001c0002t0002g0059 others(1): Show |
6 | HG01884.hp2 HG02572.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1236+91dupA | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr5 | 141983642 | ||||||
| chr5:141983954 | TAGAC | T | 3 | a0001c0001t0004g0017 a0001c0001t0004g0047 a0001c0001t0030g0074 |
5 | HG01934.hp2 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1236+406_1236+409d others(6): Show |
RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr5 | 141983954 | ||||||
| chr5:141984034 | C | G | 3 | a0001c0001t0002g0007 a0001c0001t0002g0049 a0001c0001t0002g0050 |
8 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1236+482C>G | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 7/8 | chr5 | 141984034 | |||||||
| chr5:141984101 | C | CT | 18 | a0001c0001t0001g0013 a0001c0001t0001g0041 a0001c0001t0001g0108 others(15): Show |
30 | HG00609.hp1 HG00609.hp2 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.1236+567dupT | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr5 | 141984101 | ||||||
| chr5:141984152 | C | T | 4 | a0001c0001t0001g0036 a0001c0001t0001g0045 a0001c0001t0018g0082 others(1): Show |
5 | HG02055.hp2 HG03130.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1236+600C>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 7/8 | chr5 | 141984152 | |||||||
| chr5:141984246 | A | G | 10 | a0001c0001t0004g0029 a0001c0001t0004g0073 a0001c0001t0004g0101 others(7): Show |
12 | HG00741.hp1 HG01943.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1237-557A>G | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 7/8 | chr5 | 141984246 | |||||||
| chr5:141984428 | A | G | 4 | a0001c0001t0002g0033 a0001c0001t0002g0090 a0001c0001t0002g0100 others(1): Show |
5 | HG02895.hp1 HG02897.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1237-375A>G | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 7/8 | chr5 | 141984428 | |||||||
| chr5:141984502 | C | T | 3 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0086 |
9 | HG01081.hp2 HG01106.hp1 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.1237-301C>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 7/8 | chr5 | 141984502 | |||||||
| chr5:141984544 | T | G | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(126): Show |
253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.1237-259T>G | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 7/8 | chr5 | 141984544 | |||||||
| chr5:141984675 | T | G | 1 | a0001c0001t0015g0028 | 2 | HG01243.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1237-128T>G | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 7/8 | chr5 | 141984675 | |||||||
| chr5:141984946 | A | G | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(126): Show |
253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.1367+13A>G | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 8/8 | chr5 | 141984946 | |||||||
| chr5:141985072 | C | T | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(126): Show |
253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.1367+139C>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 8/8 | chr5 | 141985072 | |||||||
| chr5:141985148 | AAC | A | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(126): Show |
253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.1367+219_1367+220d others(4): Show |
RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr5 | 141985148 | ||||||
| chr5:141985187 | G | A | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(112): Show |
235 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.1367+254G>A | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 8/8 | chr5 | 141985187 | |||||||
| chr5:141985304 | C | T | 4 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0004g0069 others(1): Show |
4 | HG00140.hp2 HG01891.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1367+371C>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 8/8 | chr5 | 141985304 | |||||||
| chr5:141985372 | C | A | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(73): Show |
169 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.1367+439C>A | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 8/8 | chr5 | 141985372 | |||||||
| chr5:141985476 | T | C | 1 | a0001c0001t0001g0097 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1367+543T>C | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 8/8 | chr5 | 141985476 | |||||||
| chr5:141985536 | T | G | 16 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0021 others(13): Show |
44 | HG00408.hp2 HG00597.hp1 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.1367+603T>G | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 8/8 | chr5 | 141985536 | |||||||
| chr5:141985648 | C | T | 3 | a0001c0001t0002g0007 a0001c0001t0002g0049 a0001c0001t0002g0050 |
8 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1367+715C>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 8/8 | chr5 | 141985648 | |||||||
| chr5:141985649 | G | A | 1 | a0001c0001t0009g0076 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1367+716G>A | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 8/8 | chr5 | 141985649 | |||||||
| chr5:141985770 | G | A | 14 | a0001c0001t0004g0017 a0001c0001t0004g0029 a0001c0001t0004g0047 others(11): Show |
18 | HG00741.hp1 HG01934.hp2 HG01943.hp2 others(15): Show |
intron_variant | MODIFIER | c.1367+837G>A | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 8/8 | chr5 | 141985770 | |||||||
| chr5:141985775 | G | A | 1 | a0001c0001t0002g0068 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1367+842G>A | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 8/8 | chr5 | 141985775 | |||||||
| chr5:141985776 | A | G | 8 | a0001c0001t0002g0033 a0001c0001t0002g0090 a0001c0001t0002g0093 others(5): Show |
9 | HG01175.hp1 HG02559.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1367+843A>G | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 8/8 | chr5 | 141985776 | |||||||
| chr5:141986028 | C | T | 3 | a0001c0002t0002g0058 a0001c0002t0002g0059 a0001c0005t0002g0066 |
3 | HG01884.hp2 HG02572.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1367+1095C>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 8/8 | chr5 | 141986028 | |||||||
| chr5:141986343 | T | C | 1 | a0001c0001t0012g0020 | 3 | HG02647.hp1 HG02965.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1368-1390T>C | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 8/8 | chr5 | 141986343 | |||||||
| chr5:141986455 | G | A | 142 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(139): Show |
280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.1368-1278G>A | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 8/8 | chr5 | 141986455 | |||||||
| chr5:141986561 | A | G | 1 | a0001c0001t0002g0099 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1368-1172A>G | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 8/8 | chr5 | 141986561 | |||||||
| chr5:141986622 | T | G | 1 | a0001c0002t0002g0058 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1368-1111T>G | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 8/8 | chr5 | 141986622 | |||||||
| chr5:141986679 | C | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0114 |
6 | HG00597.hp1 NA18980.hp2 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.1368-1054C>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 8/8 | chr5 | 141986679 | |||||||
| chr5:141986845 | A | G | 1 | a0001c0001t0010g0051 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1368-888A>G | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 8/8 | chr5 | 141986845 | |||||||
| chr5:141986850 | A | T | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(126): Show |
253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.1368-883A>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 8/8 | chr5 | 141986850 | |||||||
| chr5:141986991 | A | G | 1 | a0001c0001t0015g0028 | 2 | HG01243.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1368-742A>G | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 8/8 | chr5 | 141986991 | |||||||
| chr5:141986996 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1368-737C>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 8/8 | chr5 | 141986996 | |||||||
| chr5:141987071 | G | A | 1 | a0001c0001t0004g0101 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1368-662G>A | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 8/8 | chr5 | 141987071 | |||||||
| chr5:141987086 | A | G | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(126): Show |
253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.1368-647A>G | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 8/8 | chr5 | 141987086 | |||||||
| chr5:141987109 | C | T | 7 | a0001c0001t0002g0033 a0001c0001t0002g0090 a0001c0001t0002g0093 others(4): Show |
8 | HG01175.hp1 HG02559.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1368-624C>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 8/8 | chr5 | 141987109 | |||||||
| chr5:141987303 | G | A | 1 | a0001c0001t0005g0052 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1368-430G>A | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 8/8 | chr5 | 141987303 | |||||||
| chr5:141987461 | C | T | 1 | a0001c0001t0026g0105 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1368-272C>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 8/8 | chr5 | 141987461 | |||||||
| chr5:141987637 | G | T | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(108): Show |
226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1368-96G>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 8/8 | chr5 | 141987637 | |||||||
| chr5:141987638 | A | T | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(108): Show |
226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1368-95A>T | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 8/8 | chr5 | 141987638 | |||||||
| chr5:141987670 | G | A | 2 | a0001c0001t0001g0037 a0001c0001t0001g0119 |
3 | HG00140.hp1 HG01074.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1368-63G>A | RNF14 | ENSG00000013561.18 | transcript | ENST00000394520.7 | protein_coding | 8/8 | chr5 | 141987670 |