Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 154214 |
| ensemblid | ENSG00000146373.17 |
| hgncid | 21487 |
| symbol | RNF217 |
| name | ring finger protein 217 |
| refseq_nuc | NM_001286398.3 |
| refseq_prot | NP_001273327.1 |
| ensembl_nuc | ENST00000521654.7 |
| ensembl_prot | ENSP00000428698.2 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 124962437 |
| end | 125092633 |
| strand | + |
| ver | v1.2 |
| region | chr6:124962437-125092633 |
| region5000 | chr6:124957437-125097633 |
| regionname0 | RNF217_chr6_124962437_125092633 |
| regionname5000 | RNF217_chr6_124957437_125097633 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 542 | 215 | 67 | 43 | 75 | 5 | 25 | 56 | RNF217_chr6_124957437_125097633 | RNF217 | MGEEQ others(537): Show |
chr6 | 124957437 | 125097633 |
| a0002 | 1/1 | 542 | 33 | 6 | 7 | 12 | 1 | 5 | 10 | RNF217_chr6_124957437_125097633 | RNF217 | MGEEQ others(537): Show |
chr6 | 124957437 | 125097633 |
| a0003 | 0/0 | 542 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | MGEEQ others(537): Show |
chr6 | 124957437 | 125097633 |
| a0004 | 0/0 | 542 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | MGEEQ others(537): Show |
chr6 | 124957437 | 125097633 |
| a0005 | 0/0 | 542 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | MGEEQ others(537): Show |
chr6 | 124957437 | 125097633 |
| a0006 | 0/0 | 542 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | MGEEQ others(537): Show |
chr6 | 124957437 | 125097633 |
| a0007 | 0/0 | 542 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | MGEEQ others(537): Show |
chr6 | 124957437 | 125097633 |
| a0008 | 0/0 | 542 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | MGEEQ others(537): Show |
chr6 | 124957437 | 125097633 |
| a0009 | 0/0 | 542 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | MGEEQ others(537): Show |
chr6 | 124957437 | 125097633 |
| a0010 | 0/0 | 542 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | MGEEQ others(537): Show |
chr6 | 124957437 | 125097633 |
| a0011 | 0/0 | 542 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | MGEEQ others(537): Show |
chr6 | 124957437 | 125097633 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1626 | 198 | 52 | 41 | 75 | 5 | 25 | RNF217_chr6_124957437_125097633 | RNF217 | ATGGG others(1621): Show |
chr6 | 124957437 | 125097633 | ||
| a0001c0003 | 0/0 | 1626 | 14 | 12 | 2 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | ATGGG others(1621): Show |
chr6 | 124957437 | 125097633 | ||
| a0001c0008 | 0/0 | 1626 | 2 | 2 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | ATGGG others(1621): Show |
chr6 | 124957437 | 125097633 | ||
| a0001c0012 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | ATGGG others(1621): Show |
chr6 | 124957437 | 125097633 | ||
| a0002c0002 | 1/1 | 1626 | 30 | 5 | 7 | 10 | 1 | 5 | RNF217_chr6_124957437_125097633 | RNF217 | ATGGG others(1621): Show |
chr6 | 124957437 | 125097633 | ||
| a0002c0006 | 0/0 | 1626 | 3 | 1 | 0 | 2 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | ATGGG others(1621): Show |
chr6 | 124957437 | 125097633 | ||
| a0003c0004 | 0/0 | 1626 | 7 | 6 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | ATGGG others(1621): Show |
chr6 | 124957437 | 125097633 | ||
| a0004c0005 | 0/0 | 1626 | 3 | 0 | 3 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | ATGGG others(1621): Show |
chr6 | 124957437 | 125097633 | ||
| a0005c0007 | 0/0 | 1626 | 2 | 2 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | ATGGG others(1621): Show |
chr6 | 124957437 | 125097633 | ||
| a0006c0010 | 0/0 | 1626 | 2 | 2 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | ATGGG others(1621): Show |
chr6 | 124957437 | 125097633 | ||
| a0007c0009 | 0/0 | 1626 | 2 | 2 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | ATGGG others(1621): Show |
chr6 | 124957437 | 125097633 | ||
| a0008c0014 | 0/0 | 1626 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | ATGGG others(1621): Show |
chr6 | 124957437 | 125097633 | ||
| a0009c0015 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | ATGGG others(1621): Show |
chr6 | 124957437 | 125097633 | ||
| a0010c0013 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | ATGGG others(1621): Show |
chr6 | 124957437 | 125097633 | ||
| a0011c0011 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | ATGGG others(1621): Show |
chr6 | 124957437 | 125097633 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 11433 | 55 | 3 | 21 | 23 | 2 | 6 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11428): Show |
chr6 | 124957437 | 125097633 |
| a0001c0001t0002 | 0/0 | 11433 | 25 | 0 | 9 | 13 | 0 | 3 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11428): Show |
chr6 | 124957437 | 125097633 |
| a0001c0001t0003 | 0/0 | 11429 | 11 | 5 | 2 | 0 | 0 | 4 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11424): Show |
chr6 | 124957437 | 125097633 |
| a0001c0001t0004 | 0/0 | 11430 | 11 | 2 | 0 | 6 | 0 | 3 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11425): Show |
chr6 | 124957437 | 125097633 |
| a0001c0001t0005 | 0/0 | 11433 | 11 | 0 | 3 | 8 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11428): Show |
chr6 | 124957437 | 125097633 |
| a0001c0001t0006 | 0/0 | 11433 | 8 | 8 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11428): Show |
chr6 | 124957437 | 125097633 |
| a0001c0001t0008 | 0/0 | 11432 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11427): Show |
chr6 | 124957437 | 125097633 |
| a0001c0001t0010 | 0/0 | 11432 | 5 | 5 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11427): Show |
chr6 | 124957437 | 125097633 |
| a0001c0001t0012 | 0/0 | 11430 | 5 | 0 | 2 | 0 | 1 | 2 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11425): Show |
chr6 | 124957437 | 125097633 |
| a0001c0001t0014 | 0/0 | 11433 | 4 | 0 | 0 | 4 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11428): Show |
chr6 | 124957437 | 125097633 |
| a0001c0001t0015 | 0/0 | 11430 | 4 | 0 | 0 | 4 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11425): Show |
chr6 | 124957437 | 125097633 |
| a0001c0001t0016 | 0/0 | 11432 | 3 | 0 | 0 | 0 | 0 | 3 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11427): Show |
chr6 | 124957437 | 125097633 |
| a0001c0001t0017 | 0/0 | 11430 | 3 | 3 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11425): Show |
chr6 | 124957437 | 125097633 |
| a0001c0001t0018 | 0/0 | 11432 | 3 | 0 | 0 | 3 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11427): Show |
chr6 | 124957437 | 125097633 |
| a0001c0001t0019 | 0/0 | 11433 | 3 | 0 | 0 | 3 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11428): Show |
chr6 | 124957437 | 125097633 |
| a0001c0001t0021 | 0/0 | 11432 | 2 | 2 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11427): Show |
chr6 | 124957437 | 125097633 |
| a0001c0001t0022 | 0/0 | 11430 | 3 | 3 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11425): Show |
chr6 | 124957437 | 125097633 |
| a0001c0001t0023 | 0/0 | 11431 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11426): Show |
chr6 | 124957437 | 125097633 |
| a0001c0001t0024 | 0/0 | 11432 | 2 | 2 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11427): Show |
chr6 | 124957437 | 125097633 |
| a0001c0001t0025 | 0/0 | 11434 | 2 | 0 | 1 | 0 | 1 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11429): Show |
chr6 | 124957437 | 125097633 |
| a0001c0001t0026 | 0/0 | 11433 | 2 | 2 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11428): Show |
chr6 | 124957437 | 125097633 |
| a0001c0001t0032 | 0/0 | 11433 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11428): Show |
chr6 | 124957437 | 125097633 |
| a0001c0001t0033 | 0/0 | 11433 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11428): Show |
chr6 | 124957437 | 125097633 |
| a0001c0001t0034 | 0/0 | 11433 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11428): Show |
chr6 | 124957437 | 125097633 |
| a0001c0001t0035 | 0/0 | 11433 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11428): Show |
chr6 | 124957437 | 125097633 |
| a0001c0001t0036 | 0/0 | 11433 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11428): Show |
chr6 | 124957437 | 125097633 |
| a0001c0001t0037 | 0/0 | 11431 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11426): Show |
chr6 | 124957437 | 125097633 |
| a0001c0001t0038 | 0/0 | 11433 | 1 | 0 | 0 | 0 | 1 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11428): Show |
chr6 | 124957437 | 125097633 |
| a0001c0001t0039 | 0/0 | 11434 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11429): Show |
chr6 | 124957437 | 125097633 |
| a0001c0001t0040 | 0/0 | 11434 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11429): Show |
chr6 | 124957437 | 125097633 |
| a0001c0001t0041 | 0/0 | 11429 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11424): Show |
chr6 | 124957437 | 125097633 |
| a0001c0001t0042 | 0/0 | 11430 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11425): Show |
chr6 | 124957437 | 125097633 |
| a0001c0001t0043 | 0/0 | 11429 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11424): Show |
chr6 | 124957437 | 125097633 |
| a0001c0001t0045 | 0/0 | 11432 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11427): Show |
chr6 | 124957437 | 125097633 |
| a0001c0001t0046 | 0/0 | 11430 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11425): Show |
chr6 | 124957437 | 125097633 |
| a0001c0001t0047 | 0/0 | 11429 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11424): Show |
chr6 | 124957437 | 125097633 |
| a0001c0001t0048 | 0/0 | 11432 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11427): Show |
chr6 | 124957437 | 125097633 |
| a0001c0001t0049 | 0/0 | 11434 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11429): Show |
chr6 | 124957437 | 125097633 |
| a0001c0001t0050 | 0/0 | 11430 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11425): Show |
chr6 | 124957437 | 125097633 |
| a0001c0001t0051 | 0/0 | 11431 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11426): Show |
chr6 | 124957437 | 125097633 |
| a0001c0001t0052 | 0/0 | 11433 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11428): Show |
chr6 | 124957437 | 125097633 |
| a0001c0001t0054 | 0/0 | 11432 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11427): Show |
chr6 | 124957437 | 125097633 |
| a0001c0001t0055 | 0/0 | 11433 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11428): Show |
chr6 | 124957437 | 125097633 |
| a0001c0001t0056 | 0/0 | 11433 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11428): Show |
chr6 | 124957437 | 125097633 |
| a0001c0001t0057 | 0/0 | 11433 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11428): Show |
chr6 | 124957437 | 125097633 |
| a0001c0001t0058 | 0/0 | 11433 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11428): Show |
chr6 | 124957437 | 125097633 |
| a0001c0001t0059 | 0/0 | 11433 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11428): Show |
chr6 | 124957437 | 125097633 |
| a0001c0001t0060 | 0/0 | 11433 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11428): Show |
chr6 | 124957437 | 125097633 |
| a0001c0001t0061 | 0/0 | 11433 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11428): Show |
chr6 | 124957437 | 125097633 |
| a0001c0001t0062 | 0/0 | 11434 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11429): Show |
chr6 | 124957437 | 125097633 |
| a0001c0001t0063 | 0/0 | 11410 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11405): Show |
chr6 | 124957437 | 125097633 |
| a0001c0001t0066 | 0/0 | 11433 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11428): Show |
chr6 | 124957437 | 125097633 |
| a0001c0001t0067 | 0/0 | 11433 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11428): Show |
chr6 | 124957437 | 125097633 |
| a0001c0001t0068 | 0/0 | 11431 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11426): Show |
chr6 | 124957437 | 125097633 |
| a0001c0001t0069 | 0/0 | 11431 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11426): Show |
chr6 | 124957437 | 125097633 |
| a0001c0003t0008 | 0/0 | 11432 | 7 | 6 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11427): Show |
chr6 | 124957437 | 125097633 |
| a0001c0003t0010 | 0/0 | 11432 | 2 | 2 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11427): Show |
chr6 | 124957437 | 125097633 |
| a0001c0003t0013 | 0/0 | 11433 | 2 | 2 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11428): Show |
chr6 | 124957437 | 125097633 |
| a0001c0003t0023 | 0/0 | 11431 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11426): Show |
chr6 | 124957437 | 125097633 |
| a0001c0003t0064 | 0/0 | 11432 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11427): Show |
chr6 | 124957437 | 125097633 |
| a0001c0003t0065 | 0/0 | 11433 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11428): Show |
chr6 | 124957437 | 125097633 |
| a0001c0008t0003 | 0/0 | 11429 | 2 | 2 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11424): Show |
chr6 | 124957437 | 125097633 |
| a0001c0012t0031 | 0/0 | 11433 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11428): Show |
chr6 | 124957437 | 125097633 |
| a0002c0002t0007 | 1/0 | 11433 | 9 | 0 | 0 | 5 | 0 | 3 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11428): Show |
chr6 | 124957437 | 125097633 |
| a0002c0002t0009 | 0/1 | 11433 | 8 | 0 | 3 | 1 | 1 | 2 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11428): Show |
chr6 | 124957437 | 125097633 |
| a0002c0002t0013 | 0/0 | 11433 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11428): Show |
chr6 | 124957437 | 125097633 |
| a0002c0002t0027 | 0/0 | 11431 | 2 | 1 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11426): Show |
chr6 | 124957437 | 125097633 |
| a0002c0002t0029 | 0/0 | 11433 | 2 | 0 | 0 | 2 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11428): Show |
chr6 | 124957437 | 125097633 |
| a0002c0002t0070 | 0/0 | 11433 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11428): Show |
chr6 | 124957437 | 125097633 |
| a0002c0002t0071 | 0/0 | 11432 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11427): Show |
chr6 | 124957437 | 125097633 |
| a0002c0002t0072 | 0/0 | 11433 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11428): Show |
chr6 | 124957437 | 125097633 |
| a0002c0002t0073 | 0/0 | 11430 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11425): Show |
chr6 | 124957437 | 125097633 |
| a0002c0002t0074 | 0/0 | 11430 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11425): Show |
chr6 | 124957437 | 125097633 |
| a0002c0002t0075 | 0/0 | 11432 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11427): Show |
chr6 | 124957437 | 125097633 |
| a0002c0002t0076 | 0/0 | 11433 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11428): Show |
chr6 | 124957437 | 125097633 |
| a0002c0002t0077 | 0/0 | 11433 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11428): Show |
chr6 | 124957437 | 125097633 |
| a0002c0006t0013 | 0/0 | 11433 | 2 | 0 | 0 | 2 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11428): Show |
chr6 | 124957437 | 125097633 |
| a0002c0006t0078 | 0/0 | 11432 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11427): Show |
chr6 | 124957437 | 125097633 |
| a0003c0004t0011 | 0/0 | 11429 | 6 | 5 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11424): Show |
chr6 | 124957437 | 125097633 |
| a0003c0004t0044 | 0/0 | 11430 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11425): Show |
chr6 | 124957437 | 125097633 |
| a0004c0005t0020 | 0/0 | 11434 | 3 | 0 | 3 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11429): Show |
chr6 | 124957437 | 125097633 |
| a0005c0007t0006 | 0/0 | 11433 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11428): Show |
chr6 | 124957437 | 125097633 |
| a0005c0007t0021 | 0/0 | 11432 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11427): Show |
chr6 | 124957437 | 125097633 |
| a0006c0010t0028 | 0/0 | 11429 | 2 | 2 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11424): Show |
chr6 | 124957437 | 125097633 |
| a0007c0009t0001 | 0/0 | 11433 | 2 | 2 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11428): Show |
chr6 | 124957437 | 125097633 |
| a0008c0014t0001 | 0/0 | 11433 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11428): Show |
chr6 | 124957437 | 125097633 |
| a0009c0015t0053 | 0/0 | 11433 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11428): Show |
chr6 | 124957437 | 125097633 |
| a0010c0013t0030 | 0/0 | 11433 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11428): Show |
chr6 | 124957437 | 125097633 |
| a0011c0011t0079 | 0/0 | 11432 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | AGAAG others(11427): Show |
chr6 | 124957437 | 125097633 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0003g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0004g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0004g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0004g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0004g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0004g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0005g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0005g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0005g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0005g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0005g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0005g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0005g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0005g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0005g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0005g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0005g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0006g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0006g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0006g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0006g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0006g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0006g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0006g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0006g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0008g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0010g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0010g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0010g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0010g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0010g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0012g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0012g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0012g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0012g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0012g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0014g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0014g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0014g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0014g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0015g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0015g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0015g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0015g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0016g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0016g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0016g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0017g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0017g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0017g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0018g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0018g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0018g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0019g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0019g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0019g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0021g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0021g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0022g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0022g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0022g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0023g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0024g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0024g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0025g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0025g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0026g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0026g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0032g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0033g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0034g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0035g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0036g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0037g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0038g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0039g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0040g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0041g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0042g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0043g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0045g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0046g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0047g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0048g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0049g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0050g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0051g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0052g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0054g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0055g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0056g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0057g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0058g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0059g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0060g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0061g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0062g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0063g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0066g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0067g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0068g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0001t0069g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0003t0008g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0003t0008g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0003t0008g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0003t0008g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0003t0008g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0003t0008g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0003t0008g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0003t0010g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0003t0010g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0003t0013g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0003t0013g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0003t0023g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0003t0064g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0003t0065g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0008t0003g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0001c0012t0031g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0007g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0007g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0007g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0007g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0007g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0007g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0007g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0007g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0007g0030 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0009g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0009g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0009g0019 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0009g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0009g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0009g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0009g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0013g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0027g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0027g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0029g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0029g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0070g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0071g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0072g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0073g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0074g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0075g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0076g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0002t0077g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0006t0013g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0006t0013g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0002c0006t0078g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0003c0004t0011g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0003c0004t0011g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0003c0004t0011g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0003c0004t0011g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0003c0004t0011g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0003c0004t0011g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0003c0004t0044g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0004c0005t0020g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0004c0005t0020g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0004c0005t0020g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0005c0007t0006g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0005c0007t0021g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0006c0010t0028g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0006c0010t0028g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0007c0009t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0007c0009t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0008c0014t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0009c0015t0053g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0010c0013t0030g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| a0011c0011t0079g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0038 | g0203 | EUR | GBR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0136 | EUR | GBR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG00140 | hp1 | a0001 | c0001 | t0012 | g0125 | EUR | GBR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG00140 | hp2 | a0001 | c0001 | t0025 | g0141 | EUR | GBR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0230 | EUR | FIN | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG00323 | hp2 | a0002 | c0002 | t0009 | g0034 | EUR | FIN | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | CHS | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG00408 | hp2 | a0001 | c0001 | t0005 | g0091 | EAS | CHS | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG00423 | hp1 | a0002 | c0002 | t0007 | g0009 | EAS | CHS | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG00423 | hp2 | a0001 | c0001 | t0032 | g0078 | EAS | CHS | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG00609 | hp1 | a0001 | c0001 | t0014 | g0237 | EAS | CHS | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG00639 | hp1 | a0001 | c0003 | t0065 | g0166 | AMR | PUR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0233 | AMR | PUR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0084 | AMR | PUR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0066 | AMR | PUR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0065 | AMR | PUR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0197 | AMR | PUR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG00738 | hp2 | a0002 | c0002 | t0027 | g0021 | AMR | PUR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG00741 | hp1 | a0003 | c0004 | t0011 | g0155 | AMR | PUR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG00741 | hp2 | a0004 | c0005 | t0020 | g0087 | AMR | PUR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01069 | hp1 | a0002 | c0002 | t0072 | g0007 | AMR | PUR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01069 | hp2 | a0001 | c0001 | t0025 | g0164 | AMR | PUR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0204 | AMR | PUR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0211 | AMR | PUR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01106 | hp1 | a0002 | c0002 | t0013 | g0012 | AMR | PUR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01106 | hp2 | a0001 | c0001 | t0037 | g0138 | AMR | PUR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0140 | AMR | PUR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01169 | hp2 | a0004 | c0005 | t0020 | g0089 | AMR | PUR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01192 | hp2 | a0001 | c0001 | t0012 | g0064 | AMR | PUR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01243 | hp1 | a0001 | c0003 | t0008 | g0187 | AMR | PUR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0163 | AMR | CLM | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01257 | hp1 | a0002 | c0002 | t0009 | g0001 | AMR | CLM | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01257 | hp2 | a0004 | c0005 | t0020 | g0088 | AMR | CLM | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01258 | hp2 | a0002 | c0002 | t0009 | g0001 | AMR | CLM | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01346 | hp1 | a0002 | c0002 | t0009 | g0024 | AMR | CLM | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01433 | hp1 | a0001 | c0001 | t0005 | g0080 | AMR | CLM | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01433 | hp2 | a0001 | c0001 | t0056 | g0111 | AMR | CLM | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01884 | hp1 | a0005 | c0007 | t0006 | g0094 | AFR | ACB | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01884 | hp2 | a0001 | c0001 | t0017 | g0153 | AFR | ACB | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01891 | hp2 | a0001 | c0001 | t0010 | g0162 | AFR | ACB | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01928 | hp2 | a0001 | c0001 | t0005 | g0215 | AMR | PEL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01934 | hp1 | a0002 | c0002 | t0077 | g0033 | AMR | PEL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01952 | hp2 | a0001 | c0001 | t0055 | g0073 | AMR | PEL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01981 | hp1 | a0001 | c0001 | t0012 | g0216 | AMR | PEL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0085 | AMR | PEL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01993 | hp1 | a0001 | c0001 | t0005 | g0106 | AMR | PEL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0229 | AMR | PEL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02055 | hp1 | a0006 | c0010 | t0028 | g0031 | AFR | ACB | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02055 | hp2 | a0001 | c0001 | t0008 | g0181 | AFR | ACB | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02056 | hp1 | a0001 | c0001 | t0019 | g0076 | EAS | KHV | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | KHV | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02071 | hp2 | a0002 | c0002 | t0076 | g0016 | EAS | KHV | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0116 | EAS | KHV | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02083 | hp1 | a0001 | c0001 | t0047 | g0225 | EAS | KHV | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02083 | hp2 | a0008 | c0014 | t0001 | g0126 | EAS | KHV | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | KHV | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | CDX | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02155 | hp2 | a0001 | c0001 | t0060 | g0232 | EAS | CDX | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02257 | hp1 | a0007 | c0009 | t0001 | g0193 | AFR | ACB | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02257 | hp2 | a0001 | c0001 | t0040 | g0260 | AFR | ACB | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02258 | hp1 | a0001 | c0001 | t0049 | g0261 | AFR | ACB | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02258 | hp2 | a0001 | c0001 | t0017 | g0253 | AFR | ACB | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02280 | hp1 | a0001 | c0003 | t0008 | g0186 | AFR | ACB | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02280 | hp2 | a0001 | c0001 | t0006 | g0173 | AFR | ACB | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0177 | AFR | ACB | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02451 | hp2 | a0001 | c0003 | t0023 | g0142 | AFR | ACB | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02523 | hp2 | a0001 | c0001 | t0018 | g0214 | EAS | KHV | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0168 | AFR | GWD | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02572 | hp2 | a0001 | c0001 | t0006 | g0263 | AFR | GWD | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0086 | SAS | PJL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02602 | hp2 | a0001 | c0001 | t0016 | g0221 | SAS | PJL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0171 | AFR | GWD | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02615 | hp2 | a0002 | c0006 | t0078 | g0008 | AFR | GWD | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02622 | hp1 | a0001 | c0001 | t0010 | g0144 | AFR | GWD | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0182 | AFR | GWD | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02630 | hp1 | a0003 | c0004 | t0011 | g0148 | AFR | GWD | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02630 | hp2 | a0001 | c0001 | t0006 | g0176 | AFR | GWD | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02647 | hp1 | a0003 | c0004 | t0011 | g0149 | AFR | GWD | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02647 | hp2 | a0001 | c0001 | t0022 | g0041 | AFR | GWD | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0202 | SAS | PJL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02683 | hp2 | a0001 | c0001 | t0066 | g0165 | SAS | PJL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02698 | hp1 | a0001 | c0001 | t0036 | g0231 | SAS | PJL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02735 | hp1 | a0001 | c0001 | t0012 | g0061 | SAS | PJL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02809 | hp1 | a0005 | c0007 | t0021 | g0093 | AFR | GWD | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02809 | hp2 | a0001 | c0001 | t0051 | g0172 | AFR | GWD | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02818 | hp1 | a0001 | c0001 | t0010 | g0147 | AFR | GWD | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02818 | hp2 | a0003 | c0004 | t0011 | g0189 | AFR | GWD | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0175 | AFR | GWD | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02886 | hp2 | a0001 | c0001 | t0022 | g0131 | AFR | GWD | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02895 | hp1 | a0001 | c0001 | t0026 | g0159 | AFR | GWD | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02895 | hp2 | a0001 | c0003 | t0064 | g0188 | AFR | GWD | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02896 | hp1 | a0001 | c0001 | t0059 | g0170 | AFR | GWD | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02896 | hp2 | a0001 | c0008 | t0003 | g0002 | AFR | GWD | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02897 | hp1 | a0001 | c0008 | t0003 | g0002 | AFR | GWD | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02897 | hp2 | a0001 | c0001 | t0021 | g0158 | AFR | GWD | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02922 | hp1 | a0009 | c0015 | t0053 | g0247 | AFR | ESN | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02922 | hp2 | a0001 | c0003 | t0010 | g0265 | AFR | ESN | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02965 | hp1 | a0001 | c0001 | t0050 | g0040 | AFR | ESN | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02965 | hp2 | a0001 | c0001 | t0041 | g0098 | AFR | ESN | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02970 | hp1 | a0001 | c0001 | t0033 | g0133 | AFR | ESN | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02970 | hp2 | a0010 | c0013 | t0030 | g0191 | AFR | ESN | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02976 | hp1 | a0003 | c0004 | t0044 | g0099 | AFR | ESN | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02976 | hp2 | a0001 | c0001 | t0024 | g0169 | AFR | ESN | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03041 | hp1 | a0001 | c0003 | t0010 | g0258 | AFR | GWD | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03041 | hp2 | a0001 | c0001 | t0048 | g0161 | AFR | GWD | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03098 | hp1 | a0001 | c0003 | t0008 | g0150 | AFR | MSL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03098 | hp2 | a0001 | c0001 | t0023 | g0249 | AFR | MSL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03130 | hp1 | a0001 | c0001 | t0046 | g0195 | AFR | ESN | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03130 | hp2 | a0001 | c0003 | t0013 | g0184 | AFR | ESN | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03139 | hp1 | a0003 | c0004 | t0011 | g0257 | AFR | ESN | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03139 | hp2 | a0001 | c0001 | t0006 | g0190 | AFR | ESN | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03209 | hp1 | a0001 | c0001 | t0010 | g0194 | AFR | MSL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03209 | hp2 | a0002 | c0002 | t0071 | g0037 | AFR | MSL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03225 | hp1 | a0011 | c0011 | t0079 | g0035 | AFR | MSL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03225 | hp2 | a0002 | c0002 | t0073 | g0029 | AFR | MSL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03239 | hp1 | a0001 | c0001 | t0012 | g0200 | SAS | PJL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03239 | hp2 | a0001 | c0001 | t0035 | g0139 | SAS | PJL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03453 | hp1 | a0001 | c0001 | t0017 | g0100 | AFR | MSL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03453 | hp2 | a0001 | c0001 | t0034 | g0145 | AFR | MSL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03486 | hp1 | a0001 | c0001 | t0026 | g0167 | AFR | MSL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03486 | hp2 | a0001 | c0001 | t0010 | g0152 | AFR | MSL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03491 | hp1 | a0002 | c0002 | t0007 | g0027 | SAS | PJL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03492 | hp1 | a0001 | c0001 | t0067 | g0198 | SAS | PJL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03540 | hp1 | a0001 | c0001 | t0022 | g0179 | AFR | GWD | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03540 | hp2 | a0003 | c0004 | t0011 | g0259 | AFR | GWD | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03579 | hp1 | a0001 | c0012 | t0031 | g0255 | AFR | MSL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03579 | hp2 | a0001 | c0003 | t0008 | g0192 | AFR | MSL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03669 | hp1 | a0002 | c0002 | t0007 | g0026 | SAS | PJL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0239 | SAS | PJL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03688 | hp1 | a0001 | c0001 | t0004 | g0241 | SAS | STU | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | STU | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03704 | hp1 | a0001 | c0001 | t0016 | g0082 | SAS | PJL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03704 | hp2 | a0001 | c0001 | t0016 | g0143 | SAS | PJL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | BEB | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03834 | hp2 | a0001 | c0001 | t0004 | g0226 | SAS | BEB | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0220 | SAS | STU | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG04115 | hp2 | a0002 | c0002 | t0009 | g0025 | SAS | STU | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG04184 | hp1 | a0002 | c0002 | t0009 | g0023 | SAS | BEB | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | BEB | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0242 | SAS | STU | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG04204 | hp2 | a0002 | c0002 | t0007 | g0013 | SAS | STU | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0114 | SAS | STU | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | STU | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18522 | hp1 | a0001 | c0001 | t0021 | g0132 | AFR | YRI | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18522 | hp2 | a0001 | c0001 | t0039 | g0178 | AFR | YRI | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | CHB | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18747 | hp2 | a0001 | c0001 | t0052 | g0048 | EAS | CHB | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18906 | hp1 | a0001 | c0001 | t0006 | g0004 | AFR | YRI | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18906 | hp2 | a0007 | c0009 | t0001 | g0264 | AFR | YRI | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18942 | hp2 | a0001 | c0001 | t0015 | g0251 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18943 | hp1 | a0001 | c0001 | t0069 | g0117 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18943 | hp2 | a0001 | c0001 | t0018 | g0223 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18946 | hp1 | a0001 | c0001 | t0015 | g0224 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18946 | hp2 | a0001 | c0001 | t0005 | g0081 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18948 | hp1 | a0001 | c0001 | t0004 | g0075 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18949 | hp2 | a0001 | c0001 | t0005 | g0113 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18956 | hp1 | a0002 | c0002 | t0009 | g0010 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18959 | hp1 | a0001 | c0001 | t0004 | g0070 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18959 | hp2 | a0002 | c0002 | t0007 | g0014 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18962 | hp2 | a0001 | c0001 | t0005 | g0129 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0095 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18970 | hp2 | a0001 | c0001 | t0063 | g0090 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18971 | hp1 | a0001 | c0001 | t0019 | g0118 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18971 | hp2 | a0002 | c0002 | t0007 | g0017 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18975 | hp1 | a0001 | c0001 | t0005 | g0219 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18983 | hp1 | a0001 | c0001 | t0061 | g0252 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18983 | hp2 | a0001 | c0001 | t0015 | g0206 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18988 | hp1 | a0001 | c0001 | t0005 | g0060 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18988 | hp2 | a0002 | c0002 | t0074 | g0036 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18989 | hp2 | a0001 | c0001 | t0014 | g0096 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18994 | hp1 | a0001 | c0001 | t0058 | g0053 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18994 | hp2 | a0001 | c0001 | t0018 | g0222 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18999 | hp1 | a0001 | c0001 | t0015 | g0044 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA18999 | hp2 | a0002 | c0002 | t0007 | g0022 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19002 | hp1 | a0002 | c0006 | t0013 | g0018 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19002 | hp2 | a0001 | c0001 | t0019 | g0238 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19010 | hp1 | a0001 | c0001 | t0014 | g0059 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19010 | hp2 | a0001 | c0001 | t0057 | g0245 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19011 | hp2 | a0001 | c0001 | t0062 | g0196 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19030 | hp1 | a0001 | c0001 | t0024 | g0183 | AFR | LWK | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0154 | AFR | LWK | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19043 | hp1 | a0001 | c0003 | t0008 | g0256 | AFR | LWK | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19043 | hp2 | a0002 | c0002 | t0075 | g0039 | AFR | LWK | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19056 | hp1 | a0001 | c0001 | t0005 | g0207 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19056 | hp2 | a0002 | c0002 | t0029 | g0032 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19065 | hp1 | a0002 | c0002 | t0029 | g0006 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19066 | hp1 | a0002 | c0002 | t0007 | g0015 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19068 | hp2 | a0001 | c0001 | t0014 | g0102 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19070 | hp1 | a0002 | c0006 | t0013 | g0011 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19076 | hp1 | a0001 | c0001 | t0042 | g0052 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19083 | hp1 | a0001 | c0001 | t0004 | g0045 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19084 | hp1 | a0001 | c0001 | t0005 | g0201 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19085 | hp1 | a0001 | c0001 | t0004 | g0122 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA20129 | hp1 | a0006 | c0010 | t0028 | g0028 | AFR | ASW | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ASW | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02109 | hp1 | a0001 | c0001 | t0054 | g0180 | AFR | ACB | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0146 | AFR | ACB | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02486 | hp1 | a0001 | c0001 | t0043 | g0005 | AFR | ACB | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02559 | hp1 | a0001 | c0003 | t0013 | g0185 | AFR | ACB | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0254 | AFR | ACB | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03471 | hp1 | a0001 | c0001 | t0006 | g0250 | AFR | MSL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG03471 | hp2 | a0001 | c0003 | t0008 | g0174 | AFR | MSL | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG06807 | hp1 | a0001 | c0003 | t0008 | g0130 | AFR | USA | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| HG06807 | hp2 | a0002 | c0002 | t0070 | g0038 | AFR | USA | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA20300 | hp1 | a0001 | c0001 | t0045 | g0160 | AFR | USA | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA20300 | hp2 | a0001 | c0001 | t0068 | g0244 | AFR | USA | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA21309 | hp1 | a0001 | c0001 | t0006 | g0157 | AFR | LWK | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| NA21309 | hp2 | a0002 | c0002 | t0027 | g0020 | AFR | LWK | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0009 | g0019 | REF | REF | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0007 | g0030 | REF | REF | RNF217_chr6_124957437_125097633 | RNF217 | chr6 | 124957437 | 125097633 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:124962663 | C | A | 1 | a0011 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.119C>A | p.Ala40Glu | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/6 | 227/11433 | 119/1629 | 40/542 | chr6 | 124962663 | |||
| chr6:124963010 | T | C | 1 | a0005 | 2 | HG01884.hp1 HG02809.hp1 |
missense_variant | MODERATE | c.466T>C | p.Ser156Pro | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/6 | 574/11433 | 466/1629 | 156/542 | chr6 | 124963010 | |||
| chr6:124963149 | C | G | 1 | a0009 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.605C>G | p.Ser202Cys | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/6 | 713/11433 | 605/1629 | 202/542 | chr6 | 124963149 | |||
| chr6:124963311 | T | C | 8 | a0001 a0003 a0004 others(5): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
missense_variant | MODERATE | c.767T>C | p.Val256Ala | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/6 | 875/11433 | 767/1629 | 256/542 | chr6 | 124963311 | |||
| chr6:125057966 | G | A | 3 | a0003 a0006 a0009 |
10 | HG00741.hp1 HG02055.hp1 HG02630.hp1 others(7): Show |
missense_variant | MODERATE | c.1141G>A | p.Val381Ile | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/6 | 1249/11433 | 1141/1629 | 381/542 | chr6 | 125057966 | |||
| chr6:125058056 | A | G | 1 | a0004 | 3 | HG00741.hp2 HG01169.hp2 HG01257.hp2 |
missense_variant | MODERATE | c.1231A>G | p.Ser411Gly | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/6 | 1339/11433 | 1231/1629 | 411/542 | chr6 | 125058056 | |||
| chr6:125076745 | G | A | 1 | a0007 | 2 | HG02257.hp1 NA18906.hp2 |
missense_variant | MODERATE | c.1370G>A | p.Arg457His | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/6 | 1478/11433 | 1370/1629 | 457/542 | chr6 | 125076745 | |||
| chr6:125081449 | C | A | 1 | a0010 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.1497C>A | p.Phe499Leu | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 5/6 | 1605/11433 | 1497/1629 | 499/542 | chr6 | 125081449 | |||
| chr6:125082926 | A | G | 1 | a0008 | 1 | HG02083.hp2 | missense_variant | MODERATE | c.1618A>G | p.Met540Val | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 1726/11433 | 1618/1629 | 540/542 | chr6 | 125082926 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:125057980 | G | A | 4 | a0001c0003 a0001c0008 a0001c0012 others(1): Show |
20 | HG00639.hp1 HG01243.hp1 HG02280.hp1 others(17): Show |
synonymous_variant | LOW | c.1155G>A | p.Lys385Lys | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/6 | 1263/11433 | 1155/1629 | 385/542 | chr6 | 125057980 | |||
| chr6:125076686 | C | T | 1 | a0001c0008 | 2 | HG02896.hp2 HG02897.hp1 |
synonymous_variant | LOW | c.1311C>T | p.Asp437Asp | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/6 | 1419/11433 | 1311/1629 | 437/542 | chr6 | 125076686 | |||
| chr6:125081497 | G | A | 1 | a0001c0012 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.1545G>A | p.Ala515Ala | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 5/6 | 1653/11433 | 1545/1629 | 515/542 | chr6 | 125081497 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:124962484 | G | C | 71 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(68): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
5_prime_UTR_variant | MODIFIER | c.-61G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/6 | 61 | chr6 | 124962484 | ||||||
| chr6:125083165 | A | G | 2 | a0001c0001t0015 a0001c0001t0069 |
5 | NA18942.hp2 NA18943.hp1 NA18946.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*228A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 228 | chr6 | 125083165 | ||||||
| chr6:125083257 | G | A | 2 | a0002c0002t0070 a0010c0013t0030 |
2 | HG02970.hp2 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*320G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 320 | chr6 | 125083257 | ||||||
| chr6:125083275 | T | G | 1 | a0001c0012t0031 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*338T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 338 | chr6 | 125083275 | ||||||
| chr6:125083505 | T | C | 1 | a0001c0001t0032 | 1 | HG00423.hp2 | 3_prime_UTR_variant | MODIFIER | c.*568T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 568 | chr6 | 125083505 | ||||||
| chr6:125083672 | G | A | 1 | a0001c0001t0033 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*735G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 735 | chr6 | 125083672 | ||||||
| chr6:125083918 | A | G | 2 | a0002c0002t0070 a0010c0013t0030 |
2 | HG02970.hp2 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*981A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 981 | chr6 | 125083918 | ||||||
| chr6:125084060 | C | A | 12 | a0001c0001t0002 a0001c0001t0016 a0001c0001t0033 others(9): Show |
45 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1123C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 1123 | chr6 | 125084060 | ||||||
| chr6:125084085 | A | G | 1 | a0001c0001t0022 | 3 | HG02647.hp2 HG02886.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1148A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 1148 | chr6 | 125084085 | ||||||
| chr6:125084100 | C | G | 1 | a0002c0002t0070 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1163C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 1163 | chr6 | 125084100 | ||||||
| chr6:125084325 | A | G | 7 | a0001c0001t0008 a0001c0001t0021 a0001c0001t0026 others(4): Show |
15 | HG01243.hp1 HG02055.hp2 HG02280.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1388A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 1388 | chr6 | 125084325 | ||||||
| chr6:125084850 | T | C | 1 | a0001c0001t0041 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1913T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 1913 | chr6 | 125084850 | ||||||
| chr6:125085101 | G | A | 7 | a0001c0001t0008 a0001c0001t0021 a0001c0001t0026 others(4): Show |
15 | HG01243.hp1 HG02055.hp2 HG02280.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2164G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 2164 | chr6 | 125085101 | ||||||
| chr6:125085288 | A | G | 1 | a0001c0001t0068 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2351A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 2351 | chr6 | 125085288 | ||||||
| chr6:125085364 | A | G | 1 | a0001c0001t0067 | 1 | HG03492.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2427A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 2427 | chr6 | 125085364 | ||||||
| chr6:125085453 | T | C | 1 | a0001c0001t0042 | 1 | NA19076.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2516T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 2516 | chr6 | 125085453 | ||||||
| chr6:125085845 | T | C | 3 | a0001c0001t0023 a0001c0001t0068 a0001c0003t0023 |
3 | HG02451.hp2 HG03098.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2908T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 2908 | chr6 | 125085845 | ||||||
| chr6:125085861 | ACT | A | 1 | a0001c0001t0022 | 3 | HG02647.hp2 HG02886.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2927_*2928delCT | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 2927 | INFO_REALIGN_3_PRIME | chr6 | 125085861 | |||||
| chr6:125085938 | A | G | 4 | a0001c0001t0021 a0001c0001t0026 a0005c0007t0021 others(1): Show |
6 | HG02809.hp1 HG02895.hp1 HG02897.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3001A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 3001 | chr6 | 125085938 | ||||||
| chr6:125086091 | C | T | 3 | a0001c0001t0008 a0001c0003t0008 a0002c0006t0078 |
9 | HG01243.hp1 HG02055.hp2 HG02280.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3154C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 3154 | chr6 | 125086091 | ||||||
| chr6:125086097 | G | A | 9 | a0001c0001t0023 a0001c0001t0043 a0001c0001t0045 others(6): Show |
15 | HG00741.hp1 HG02055.hp1 HG02451.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3160G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 3160 | chr6 | 125086097 | ||||||
| chr6:125086319 | A | G | 20 | a0001c0001t0002 a0001c0001t0016 a0001c0001t0025 others(17): Show |
58 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*3382A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 3382 | chr6 | 125086319 | ||||||
| chr6:125086334 | TGAG | T | 5 | a0001c0001t0003 a0001c0001t0041 a0001c0001t0046 others(2): Show |
16 | HG00642.hp1 HG00735.hp2 HG02083.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*3401_*3403delGAG | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 3401 | INFO_REALIGN_3_PRIME | chr6 | 125086334 | |||||
| chr6:125086368 | G | A | 3 | a0001c0001t0023 a0001c0001t0068 a0001c0003t0023 |
3 | HG02451.hp2 HG03098.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3431G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 3431 | chr6 | 125086368 | ||||||
| chr6:125086399 | CTT | C | 4 | a0001c0001t0043 a0003c0004t0011 a0003c0004t0044 others(1): Show |
10 | HG00741.hp1 HG02055.hp1 HG02486.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3463_*3464delTT | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 3463 | chr6 | 125086399 | ||||||
| chr6:125086510 | T | C | 1 | a0002c0002t0072 | 1 | HG01069.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3573T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 3573 | chr6 | 125086510 | ||||||
| chr6:125086521 | A | C | 1 | a0001c0003t0064 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3584A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 3584 | chr6 | 125086521 | ||||||
| chr6:125086671 | G | A | 1 | a0001c0001t0012 | 5 | HG00140.hp1 HG01192.hp2 HG01981.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3734G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 3734 | chr6 | 125086671 | ||||||
| chr6:125086779 | C | A | 4 | a0001c0001t0006 a0001c0001t0048 a0001c0001t0049 others(1): Show |
11 | HG01884.hp1 HG02109.hp2 HG02258.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3842C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 3842 | chr6 | 125086779 | ||||||
| chr6:125086960 | A | C | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4023A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4023 | chr6 | 125086960 | ||||||
| chr6:125086961 | C | G | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4024C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4024 | chr6 | 125086961 | ||||||
| chr6:125086962 | C | A | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4025C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4025 | chr6 | 125086962 | ||||||
| chr6:125086963 | A | T | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4026A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4026 | chr6 | 125086963 | ||||||
| chr6:125086964 | C | T | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4027C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4027 | chr6 | 125086964 | ||||||
| chr6:125086966 | G | A | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4029G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4029 | chr6 | 125086966 | ||||||
| chr6:125086971 | C | T | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4034C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4034 | chr6 | 125086971 | ||||||
| chr6:125086974 | T | C | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4037T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4037 | chr6 | 125086974 | ||||||
| chr6:125086975 | T | A | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4038T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4038 | chr6 | 125086975 | ||||||
| chr6:125086977 | C | A | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4040C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4040 | chr6 | 125086977 | ||||||
| chr6:125086979 | G | A | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4042G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4042 | chr6 | 125086979 | ||||||
| chr6:125086982 | C | A | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4045C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4045 | chr6 | 125086982 | ||||||
| chr6:125086985 | G | A | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4048G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4048 | chr6 | 125086985 | ||||||
| chr6:125086987 | T | C | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4050T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4050 | chr6 | 125086987 | ||||||
| chr6:125086989 | C | T | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4052C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4052 | chr6 | 125086989 | ||||||
| chr6:125086990 | C | A | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4053C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4053 | chr6 | 125086990 | ||||||
| chr6:125086992 | C | A | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4055C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4055 | chr6 | 125086992 | ||||||
| chr6:125086994 | C | A | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4057C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4057 | chr6 | 125086994 | ||||||
| chr6:125086995 | T | A | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4058T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4058 | chr6 | 125086995 | ||||||
| chr6:125086998 | A | T | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4061A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4061 | chr6 | 125086998 | ||||||
| chr6:125087000 | C | A | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4063C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4063 | chr6 | 125087000 | ||||||
| chr6:125087001 | C | T | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4064C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4064 | chr6 | 125087001 | ||||||
| chr6:125087002 | T | G | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4065T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4065 | chr6 | 125087002 | ||||||
| chr6:125087003 | C | T | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4066C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4066 | chr6 | 125087003 | ||||||
| chr6:125087012 | C | G | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4075C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4075 | chr6 | 125087012 | ||||||
| chr6:125087013 | C | A | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4076C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4076 | chr6 | 125087013 | ||||||
| chr6:125087016 | A | T | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4079A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4079 | chr6 | 125087016 | ||||||
| chr6:125087017 | C | G | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4080C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4080 | chr6 | 125087017 | ||||||
| chr6:125087020 | C | G | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4083C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4083 | chr6 | 125087020 | ||||||
| chr6:125087024 | T | A | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4087T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4087 | chr6 | 125087024 | ||||||
| chr6:125087025 | A | T | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4088A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4088 | chr6 | 125087025 | ||||||
| chr6:125087028 | C | A | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4091C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4091 | chr6 | 125087028 | ||||||
| chr6:125087032 | C | A | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4095C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4095 | chr6 | 125087032 | ||||||
| chr6:125087035 | T | C | 1 | a0001c0001t0022 | 3 | HG02647.hp2 HG02886.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4098T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4098 | chr6 | 125087035 | ||||||
| chr6:125087040 | C | T | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4103C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4103 | chr6 | 125087040 | ||||||
| chr6:125087045 | CTGAAGGA others(16): Show |
C | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4109_*4131delTGAA others(19): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4109 | chr6 | 125087045 | ||||||
| chr6:125087070 | G | A | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4133G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4133 | chr6 | 125087070 | ||||||
| chr6:125087071 | G | T | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4134G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4134 | chr6 | 125087071 | ||||||
| chr6:125087075 | C | A | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4138C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4138 | chr6 | 125087075 | ||||||
| chr6:125087075 | C | G | 5 | a0001c0001t0003 a0001c0001t0041 a0001c0001t0046 others(2): Show |
16 | HG00642.hp1 HG00735.hp2 HG02083.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*4138C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4138 | chr6 | 125087075 | ||||||
| chr6:125087079 | A | T | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4142A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4142 | chr6 | 125087079 | ||||||
| chr6:125087082 | C | G | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4145C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4145 | chr6 | 125087082 | ||||||
| chr6:125087084 | C | T | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4147C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4147 | chr6 | 125087084 | ||||||
| chr6:125087085 | A | C | 1 | a0001c0001t0063 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4148A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4148 | chr6 | 125087085 | ||||||
| chr6:125087098 | G | A | 1 | a0002c0002t0070 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4161G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4161 | chr6 | 125087098 | ||||||
| chr6:125087117 | C | G | 5 | a0001c0001t0003 a0001c0001t0041 a0001c0001t0046 others(2): Show |
16 | HG00642.hp1 HG00735.hp2 HG02083.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*4180C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4180 | chr6 | 125087117 | ||||||
| chr6:125087292 | G | T | 6 | a0001c0001t0043 a0001c0001t0045 a0002c0002t0071 others(3): Show |
12 | HG00741.hp1 HG02055.hp1 HG02486.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*4355G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4355 | chr6 | 125087292 | ||||||
| chr6:125087304 | AC | A | 1 | a0001c0001t0016 | 3 | HG02602.hp2 HG03704.hp1 HG03704.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4368delC | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4368 | chr6 | 125087304 | ||||||
| chr6:125087306 | G | A | 4 | a0001c0001t0017 a0001c0001t0050 a0001c0001t0051 others(1): Show |
6 | HG01884.hp2 HG02258.hp2 HG02809.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4369G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4369 | chr6 | 125087306 | ||||||
| chr6:125087347 | T | G | 1 | a0001c0001t0052 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4410T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4410 | chr6 | 125087347 | ||||||
| chr6:125087421 | G | A | 66 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(63): Show |
163 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(160): Show |
3_prime_UTR_variant | MODIFIER | c.*4484G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4484 | chr6 | 125087421 | ||||||
| chr6:125087572 | A | G | 9 | a0001c0001t0023 a0001c0001t0043 a0001c0001t0045 others(6): Show |
15 | HG00741.hp1 HG02055.hp1 HG02451.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*4635A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4635 | chr6 | 125087572 | ||||||
| chr6:125087885 | C | G | 34 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0008 others(31): Show |
73 | HG00642.hp1 HG00735.hp2 HG00741.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*4948C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4948 | chr6 | 125087885 | ||||||
| chr6:125087899 | T | G | 3 | a0001c0001t0022 a0002c0002t0070 a0010c0013t0030 |
5 | HG02647.hp2 HG02886.hp2 HG02970.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4962T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4962 | chr6 | 125087899 | ||||||
| chr6:125087925 | C | G | 1 | a0001c0001t0047 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4988C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 4988 | chr6 | 125087925 | ||||||
| chr6:125087987 | CT | C | 9 | a0001c0001t0023 a0001c0001t0043 a0001c0001t0045 others(6): Show |
15 | HG00741.hp1 HG02055.hp1 HG02451.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*5051delT | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 5051 | chr6 | 125087987 | ||||||
| chr6:125088014 | C | CT | 6 | a0001c0001t0025 a0001c0001t0039 a0001c0001t0040 others(3): Show |
9 | HG00140.hp2 HG00741.hp2 HG01069.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5099dupT | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 5100 | INFO_REALIGN_3_PRIME | chr6 | 125088014 | |||||
| chr6:125088014 | CT | C | 33 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0008 others(30): Show |
86 | HG00140.hp1 HG00642.hp1 HG00735.hp2 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*5099delT | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 5099 | INFO_REALIGN_3_PRIME | chr6 | 125088014 | |||||
| chr6:125088038 | A | G | 11 | a0001c0001t0002 a0001c0001t0016 a0001c0001t0025 others(8): Show |
47 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*5101A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 5101 | chr6 | 125088038 | ||||||
| chr6:125088053 | C | T | 1 | a0001c0001t0054 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5116C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 5116 | chr6 | 125088053 | ||||||
| chr6:125088070 | G | T | 4 | a0001c0001t0043 a0003c0004t0011 a0003c0004t0044 others(1): Show |
10 | HG00741.hp1 HG02055.hp1 HG02486.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*5133G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 5133 | chr6 | 125088070 | ||||||
| chr6:125088301 | G | C | 1 | a0001c0001t0055 | 1 | HG01952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5364G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 5364 | chr6 | 125088301 | ||||||
| chr6:125088358 | C | T | 2 | a0001c0001t0019 a0002c0002t0076 |
4 | HG02056.hp1 HG02071.hp2 NA18971.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5421C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 5421 | chr6 | 125088358 | ||||||
| chr6:125088504 | C | T | 2 | a0001c0001t0015 a0001c0001t0069 |
5 | NA18942.hp2 NA18943.hp1 NA18946.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5567C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 5567 | chr6 | 125088504 | ||||||
| chr6:125088611 | A | G | 1 | a0001c0001t0038 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5674A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 5674 | chr6 | 125088611 | ||||||
| chr6:125088818 | T | G | 1 | a0001c0001t0035 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5881T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 5881 | chr6 | 125088818 | ||||||
| chr6:125088914 | A | G | 1 | a0004c0005t0020 | 3 | HG00741.hp2 HG01169.hp2 HG01257.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5977A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 5977 | chr6 | 125088914 | ||||||
| chr6:125089513 | T | C | 1 | a0001c0001t0056 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6576T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 6576 | chr6 | 125089513 | ||||||
| chr6:125089531 | A | G | 1 | a0001c0001t0061 | 1 | NA18983.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6594A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 6594 | chr6 | 125089531 | ||||||
| chr6:125089609 | C | T | 5 | a0001c0001t0003 a0001c0001t0041 a0001c0001t0046 others(2): Show |
16 | HG00642.hp1 HG00735.hp2 HG02083.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*6672C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 6672 | chr6 | 125089609 | ||||||
| chr6:125089661 | A | G | 4 | a0001c0001t0021 a0001c0001t0026 a0005c0007t0021 others(1): Show |
6 | HG02809.hp1 HG02895.hp1 HG02897.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6724A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 6724 | chr6 | 125089661 | ||||||
| chr6:125089698 | G | T | 1 | a0001c0012t0031 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6761G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 6761 | chr6 | 125089698 | ||||||
| chr6:125089888 | C | A | 1 | a0001c0012t0031 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6951C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 6951 | chr6 | 125089888 | ||||||
| chr6:125090334 | T | C | 1 | a0001c0001t0039 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7397T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 7397 | chr6 | 125090334 | ||||||
| chr6:125090375 | A | C | 1 | a0001c0001t0060 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7438A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 7438 | chr6 | 125090375 | ||||||
| chr6:125090484 | T | C | 1 | a0001c0001t0057 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7547T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 7547 | chr6 | 125090484 | ||||||
| chr6:125090503 | C | T | 66 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(63): Show |
163 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(160): Show |
3_prime_UTR_variant | MODIFIER | c.*7566C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 7566 | chr6 | 125090503 | ||||||
| chr6:125090613 | T | C | 1 | a0010c0013t0030 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7676T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 7676 | chr6 | 125090613 | ||||||
| chr6:125090630 | T | C | 1 | a0001c0001t0043 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7693T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 7693 | chr6 | 125090630 | ||||||
| chr6:125090702 | G | A | 1 | a0001c0001t0050 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7765G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 7765 | chr6 | 125090702 | ||||||
| chr6:125090764 | A | G | 2 | a0001c0001t0014 a0002c0002t0029 |
6 | HG00609.hp1 NA18989.hp2 NA19010.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*7827A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 7827 | chr6 | 125090764 | ||||||
| chr6:125090773 | G | T | 66 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(63): Show |
163 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(160): Show |
3_prime_UTR_variant | MODIFIER | c.*7836G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 7836 | chr6 | 125090773 | ||||||
| chr6:125090873 | A | T | 12 | a0001c0001t0002 a0001c0001t0016 a0001c0001t0033 others(9): Show |
45 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*7936A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 7936 | chr6 | 125090873 | ||||||
| chr6:125090900 | A | G | 4 | a0001c0001t0006 a0001c0001t0048 a0001c0001t0049 others(1): Show |
11 | HG01884.hp1 HG02109.hp2 HG02258.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*7963A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 7963 | chr6 | 125090900 | ||||||
| chr6:125091071 | A | G | 1 | a0001c0001t0059 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8134A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 8134 | chr6 | 125091071 | ||||||
| chr6:125091073 | A | G | 5 | a0001c0001t0003 a0001c0001t0041 a0001c0001t0046 others(2): Show |
16 | HG00642.hp1 HG00735.hp2 HG02083.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*8136A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 8136 | chr6 | 125091073 | ||||||
| chr6:125091085 | A | C | 5 | a0001c0001t0003 a0001c0001t0041 a0001c0001t0046 others(2): Show |
16 | HG00642.hp1 HG00735.hp2 HG02083.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*8148A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 8148 | chr6 | 125091085 | ||||||
| chr6:125091204 | G | A | 6 | a0001c0001t0043 a0001c0001t0045 a0002c0002t0071 others(3): Show |
12 | HG00741.hp1 HG02055.hp1 HG02486.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*8267G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 8267 | chr6 | 125091204 | ||||||
| chr6:125091564 | A | G | 2 | a0001c0001t0005 a0001c0001t0032 |
12 | HG00408.hp2 HG00423.hp2 HG01433.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*8627A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 8627 | chr6 | 125091564 | ||||||
| chr6:125091645 | TCA | T | 12 | a0001c0001t0004 a0001c0001t0012 a0001c0001t0015 others(9): Show |
32 | HG00140.hp1 HG00738.hp2 HG01106.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*8709_*8710delCA | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 8709 | chr6 | 125091645 | ||||||
| chr6:125091721 | C | T | 1 | a0001c0001t0058 | 1 | NA18994.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8784C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 8784 | chr6 | 125091721 | ||||||
| chr6:125092107 | A | G | 12 | a0001c0001t0006 a0001c0001t0023 a0001c0001t0043 others(9): Show |
25 | HG00741.hp1 HG01884.hp1 HG02055.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*9170A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 9170 | chr6 | 125092107 | ||||||
| chr6:125092517 | G | T | 4 | a0001c0001t0043 a0002c0002t0071 a0003c0004t0011 others(1): Show |
10 | HG00741.hp1 HG02055.hp1 HG02486.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*9580G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 9580 | chr6 | 125092517 | ||||||
| chr6:125092577 | C | T | 1 | a0001c0001t0036 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9640C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 9640 | chr6 | 125092577 | ||||||
| chr6:125092591 | A | G | 1 | a0002c0002t0077 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9654A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 6/6 | 9654 | chr6 | 125092591 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:124963785 | G | A | 2 | a0001c0001t0006g0004 a0001c0001t0043g0005 |
2 | HG02486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.882+359G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124963785 | |||||||
| chr6:124963829 | A | G | 8 | a0001c0001t0001g0262 a0001c0001t0006g0263 a0001c0001t0040g0260 others(5): Show |
8 | HG01192.hp1 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.882+403A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124963829 | |||||||
| chr6:124963893 | A | C | 1 | a0003c0004t0011g0257 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.882+467A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124963893 | |||||||
| chr6:124963977 | C | T | 230 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(227): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.882+551C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124963977 | |||||||
| chr6:124964314 | T | C | 2 | a0001c0001t0006g0004 a0001c0001t0043g0005 |
2 | HG02486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.882+888T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124964314 | |||||||
| chr6:124964441 | T | TA | 58 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(55): Show |
58 | HG00408.hp2 HG00423.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.882+1016dupA | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 124964441 | ||||||
| chr6:124964475 | C | T | 4 | a0001c0001t0003g0254 a0001c0001t0017g0253 a0001c0003t0008g0256 others(1): Show |
4 | HG02258.hp2 HG02559.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+1049C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124964475 | |||||||
| chr6:124964612 | A | G | 1 | a0001c0001t0061g0252 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.882+1186A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124964612 | |||||||
| chr6:124964658 | G | T | 1 | a0001c0001t0015g0251 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.882+1232G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124964658 | |||||||
| chr6:124964738 | A | T | 1 | a0002c0002t0075g0039 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.882+1312A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124964738 | |||||||
| chr6:124964841 | C | T | 2 | a0001c0001t0002g0097 a0001c0001t0014g0096 |
2 | NA18952.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.882+1415C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124964841 | |||||||
| chr6:124965105 | A | G | 2 | a0001c0001t0006g0250 a0001c0001t0023g0249 |
2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.882+1679A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124965105 | |||||||
| chr6:124965114 | A | C | 1 | a0001c0001t0004g0095 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.882+1688A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124965114 | |||||||
| chr6:124965249 | A | G | 1 | a0001c0001t0002g0248 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.882+1823A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124965249 | |||||||
| chr6:124965447 | C | T | 1 | a0009c0015t0053g0247 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.882+2021C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124965447 | |||||||
| chr6:124965866 | A | G | 1 | a0001c0001t0001g0246 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.882+2440A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124965866 | |||||||
| chr6:124965933 | C | T | 1 | a0001c0003t0008g0256 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.882+2507C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124965933 | |||||||
| chr6:124965937 | G | A | 3 | a0001c0001t0017g0100 a0001c0001t0041g0098 a0003c0004t0044g0099 |
3 | HG02965.hp2 HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.882+2511G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124965937 | |||||||
| chr6:124965963 | A | G | 2 | a0005c0007t0006g0094 a0005c0007t0021g0093 |
2 | HG01884.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.882+2537A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124965963 | |||||||
| chr6:124966194 | G | T | 54 | a0001c0001t0001g0199 a0001c0001t0001g0208 a0001c0001t0001g0209 others(51): Show |
55 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.882+2768G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124966194 | |||||||
| chr6:124966249 | T | A | 3 | a0001c0001t0017g0100 a0001c0001t0041g0098 a0003c0004t0044g0099 |
3 | HG02965.hp2 HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.882+2823T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124966249 | |||||||
| chr6:124966313 | A | C | 1 | a0001c0001t0057g0245 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.882+2887A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124966313 | |||||||
| chr6:124966314 | T | A | 1 | a0001c0001t0057g0245 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.882+2888T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124966314 | |||||||
| chr6:124966357 | A | G | 1 | a0001c0001t0062g0196 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.882+2931A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124966357 | |||||||
| chr6:124966415 | G | A | 81 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0104 others(78): Show |
81 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.882+2989G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124966415 | |||||||
| chr6:124966629 | A | G | 2 | a0005c0007t0006g0094 a0005c0007t0021g0093 |
2 | HG01884.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.882+3203A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124966629 | |||||||
| chr6:124966750 | A | G | 1 | a0001c0001t0001g0092 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.882+3324A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124966750 | |||||||
| chr6:124966876 | A | G | 1 | a0001c0003t0065g0166 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.882+3450A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124966876 | |||||||
| chr6:124967020 | C | T | 2 | a0005c0007t0006g0094 a0005c0007t0021g0093 |
2 | HG01884.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.882+3594C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124967020 | |||||||
| chr6:124967116 | A | G | 1 | a0001c0001t0068g0244 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.882+3690A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124967116 | |||||||
| chr6:124967362 | C | T | 3 | a0001c0001t0002g0163 a0001c0001t0025g0164 a0001c0001t0066g0165 |
3 | HG01069.hp2 HG01255.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.882+3936C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124967362 | |||||||
| chr6:124967802 | G | T | 1 | a0002c0002t0070g0038 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.882+4376G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124967802 | |||||||
| chr6:124967843 | A | G | 12 | a0001c0001t0006g0190 a0001c0001t0010g0194 a0001c0001t0046g0195 others(9): Show |
13 | HG01243.hp1 HG02257.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.882+4417A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124967843 | |||||||
| chr6:124967858 | A | G | 54 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(51): Show |
54 | HG00408.hp2 HG00423.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.882+4432A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124967858 | |||||||
| chr6:124967903 | T | C | 2 | a0005c0007t0006g0094 a0005c0007t0021g0093 |
2 | HG01884.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.882+4477T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124967903 | |||||||
| chr6:124967996 | T | C | 2 | a0005c0007t0006g0094 a0005c0007t0021g0093 |
2 | HG01884.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.882+4570T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124967996 | |||||||
| chr6:124968032 | G | A | 1 | a0002c0002t0029g0006 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.882+4606G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124968032 | |||||||
| chr6:124968073 | T | C | 143 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(140): Show |
145 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.882+4647T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124968073 | |||||||
| chr6:124968463 | C | T | 2 | a0005c0007t0006g0094 a0005c0007t0021g0093 |
2 | HG01884.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.882+5037C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124968463 | |||||||
| chr6:124968733 | G | A | 35 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(32): Show |
35 | HG00140.hp1 HG00609.hp2 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.882+5307G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124968733 | |||||||
| chr6:124968738 | T | G | 2 | a0005c0007t0006g0094 a0005c0007t0021g0093 |
2 | HG01884.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.882+5312T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124968738 | |||||||
| chr6:124969016 | A | G | 1 | a0001c0001t0005g0129 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.882+5590A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124969016 | |||||||
| chr6:124969049 | T | A | 1 | a0001c0001t0001g0042 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.882+5623T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124969049 | |||||||
| chr6:124969363 | A | G | 2 | a0005c0007t0006g0094 a0005c0007t0021g0093 |
2 | HG01884.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.882+5937A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124969363 | |||||||
| chr6:124969382 | T | C | 1 | a0001c0001t0001g0092 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.882+5956T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124969382 | |||||||
| chr6:124969506 | C | T | 1 | a0001c0001t0004g0182 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.882+6080C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124969506 | |||||||
| chr6:124969572 | G | A | 227 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(224): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.882+6146G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124969572 | |||||||
| chr6:124969612 | G | A | 4 | a0001c0001t0001g0043 a0001c0001t0001g0046 a0001c0001t0004g0045 others(1): Show |
4 | HG02523.hp1 NA18999.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+6186G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124969612 | |||||||
| chr6:124969660 | T | C | 3 | a0005c0007t0006g0094 a0005c0007t0021g0093 a0009c0015t0053g0247 |
3 | HG01884.hp1 HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.882+6234T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124969660 | |||||||
| chr6:124969663 | A | T | 4 | a0001c0001t0008g0181 a0001c0001t0022g0179 a0001c0001t0039g0178 others(1): Show |
4 | HG02055.hp2 HG02109.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+6237A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124969663 | |||||||
| chr6:124969766 | T | C | 1 | a0001c0001t0026g0167 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.882+6340T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124969766 | |||||||
| chr6:124969871 | GGGGTTGT others(22): Show |
G | 1 | a0001c0001t0026g0167 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.882+6449_882+6477d others(31): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 124969871 | ||||||
| chr6:124969990 | A | G | 3 | a0005c0007t0006g0094 a0005c0007t0021g0093 a0009c0015t0053g0247 |
3 | HG01884.hp1 HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.882+6564A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124969990 | |||||||
| chr6:124970339 | C | T | 1 | a0001c0001t0048g0161 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.882+6913C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124970339 | |||||||
| chr6:124970398 | A | G | 2 | a0005c0007t0006g0094 a0005c0007t0021g0093 |
2 | HG01884.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.882+6972A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124970398 | |||||||
| chr6:124970404 | G | A | 1 | a0001c0003t0008g0130 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.882+6978G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124970404 | |||||||
| chr6:124970551 | C | T | 1 | a0002c0002t0070g0038 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.882+7125C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124970551 | |||||||
| chr6:124970741 | A | G | 1 | a0001c0001t0045g0160 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.882+7315A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124970741 | |||||||
| chr6:124970766 | C | T | 1 | a0002c0002t0071g0037 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.882+7340C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124970766 | |||||||
| chr6:124970779 | A | C | 2 | a0001c0001t0021g0158 a0001c0001t0026g0159 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.882+7353A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124970779 | |||||||
| chr6:124970867 | G | T | 1 | a0001c0001t0002g0128 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.882+7441G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124970867 | |||||||
| chr6:124971327 | G | A | 1 | a0002c0002t0072g0007 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.882+7901G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124971327 | |||||||
| chr6:124971558 | C | A | 3 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0052g0048 |
3 | HG02132.hp2 NA18747.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.882+8132C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124971558 | |||||||
| chr6:124971563 | C | A | 1 | a0009c0015t0053g0247 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.882+8137C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124971563 | |||||||
| chr6:124971663 | C | T | 2 | a0001c0001t0001g0243 a0001c0001t0004g0242 |
2 | HG03834.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.882+8237C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124971663 | |||||||
| chr6:124971714 | G | T | 2 | a0001c0001t0005g0091 a0001c0001t0063g0090 |
2 | HG00408.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.882+8288G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124971714 | |||||||
| chr6:124971766 | A | T | 3 | a0004c0005t0020g0087 a0004c0005t0020g0088 a0004c0005t0020g0089 |
3 | HG00741.hp2 HG01169.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.882+8340A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124971766 | |||||||
| chr6:124971930 | C | A | 1 | a0002c0006t0078g0008 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.882+8504C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124971930 | |||||||
| chr6:124972012 | C | T | 56 | a0001c0001t0001g0101 a0001c0001t0001g0127 a0001c0001t0001g0199 others(53): Show |
57 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.882+8586C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124972012 | |||||||
| chr6:124972312 | C | T | 2 | a0005c0007t0006g0094 a0005c0007t0021g0093 |
2 | HG01884.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.882+8886C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124972312 | |||||||
| chr6:124972515 | G | A | 1 | a0002c0006t0078g0008 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.882+9089G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124972515 | |||||||
| chr6:124972588 | C | T | 1 | a0001c0001t0002g0086 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.882+9162C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124972588 | |||||||
| chr6:124972589 | C | T | 1 | a0008c0014t0001g0126 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.882+9163C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124972589 | |||||||
| chr6:124972705 | C | T | 2 | a0001c0001t0002g0097 a0001c0001t0014g0096 |
2 | NA18952.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.882+9279C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124972705 | |||||||
| chr6:124972922 | A | G | 2 | a0005c0007t0006g0094 a0005c0007t0021g0093 |
2 | HG01884.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.882+9496A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124972922 | |||||||
| chr6:124973094 | G | T | 1 | a0001c0001t0026g0167 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.882+9668G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124973094 | |||||||
| chr6:124973129 | G | A | 4 | a0002c0002t0075g0039 a0005c0007t0006g0094 a0005c0007t0021g0093 others(1): Show |
4 | HG01884.hp1 HG02809.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+9703G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124973129 | |||||||
| chr6:124973234 | A | G | 2 | a0002c0002t0075g0039 a0009c0015t0053g0247 |
2 | HG02922.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.882+9808A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124973234 | |||||||
| chr6:124973487 | A | C | 1 | a0002c0002t0074g0036 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.882+10061A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124973487 | |||||||
| chr6:124973539 | C | T | 1 | a0001c0001t0004g0241 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.882+10113C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124973539 | |||||||
| chr6:124973563 | TTATAA | T | 4 | a0002c0002t0075g0039 a0005c0007t0006g0094 a0005c0007t0021g0093 others(1): Show |
4 | HG01884.hp1 HG02809.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+10141_882+1014 others(9): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 124973563 | ||||||
| chr6:124973665 | A | G | 1 | a0002c0002t0075g0039 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.882+10239A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124973665 | |||||||
| chr6:124973669 | A | G | 1 | a0001c0001t0002g0085 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.882+10243A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124973669 | |||||||
| chr6:124973901 | C | T | 1 | a0001c0001t0046g0195 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.882+10475C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124973901 | |||||||
| chr6:124973962 | C | T | 1 | a0002c0002t0071g0037 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.882+10536C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124973962 | |||||||
| chr6:124973985 | T | G | 1 | a0001c0001t0062g0196 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.882+10559T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124973985 | |||||||
| chr6:124974091 | G | A | 2 | a0001c0001t0002g0163 a0001c0001t0025g0164 |
2 | HG01069.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.882+10665G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124974091 | |||||||
| chr6:124974312 | A | T | 1 | a0002c0002t0071g0037 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.882+10886A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124974312 | |||||||
| chr6:124974388 | T | G | 1 | a0001c0001t0003g0197 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.882+10962T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124974388 | |||||||
| chr6:124974626 | G | A | 1 | a0002c0002t0075g0039 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.882+11200G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124974626 | |||||||
| chr6:124974754 | A | C | 1 | a0001c0001t0003g0177 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.882+11328A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124974754 | |||||||
| chr6:124974880 | T | C | 2 | a0001c0001t0003g0254 a0001c0001t0017g0253 |
2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.882+11454T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124974880 | |||||||
| chr6:124974894 | G | A | 1 | a0001c0001t0039g0178 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.882+11468G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124974894 | |||||||
| chr6:124975012 | C | T | 1 | a0001c0001t0026g0167 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.882+11586C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124975012 | |||||||
| chr6:124975107 | A | G | 2 | a0001c0001t0006g0004 a0001c0001t0043g0005 |
2 | HG02486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.882+11681A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124975107 | |||||||
| chr6:124975892 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.882+12466T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124975892 | |||||||
| chr6:124975953 | TC | T | 12 | a0001c0001t0006g0190 a0001c0001t0010g0194 a0001c0001t0046g0195 others(9): Show |
13 | HG01243.hp1 HG02257.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.882+12528delC | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124975953 | |||||||
| chr6:124976036 | T | C | 1 | a0009c0015t0053g0247 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.882+12610T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124976036 | |||||||
| chr6:124976190 | C | G | 1 | a0001c0001t0010g0162 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.882+12764C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124976190 | |||||||
| chr6:124976231 | G | A | 1 | a0001c0001t0010g0162 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.882+12805G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124976231 | |||||||
| chr6:124976250 | A | C | 1 | a0002c0006t0078g0008 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.882+12824A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124976250 | |||||||
| chr6:124976250 | ACTCC | A | 5 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(2): Show |
5 | HG00423.hp1 HG01243.hp2 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.882+12846_882+1284 others(8): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 124976250 | ||||||
| chr6:124976275 | C | T | 61 | a0001c0001t0001g0101 a0001c0001t0001g0124 a0001c0001t0001g0127 others(58): Show |
62 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.882+12849C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124976275 | |||||||
| chr6:124976276 | G | T | 1 | a0001c0001t0026g0167 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.882+12850G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124976276 | |||||||
| chr6:124976290 | C | G | 61 | a0001c0001t0001g0101 a0001c0001t0001g0124 a0001c0001t0001g0127 others(58): Show |
62 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.882+12864C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124976290 | |||||||
| chr6:124976302 | C | CCTTCCTT others(3): Show |
216 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(213): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.882+12878_882+1287 others(14): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 124976302 | ||||||
| chr6:124976373 | A | G | 1 | a0009c0015t0053g0247 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.882+12947A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124976373 | |||||||
| chr6:124976534 | C | T | 1 | a0001c0001t0043g0005 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.882+13108C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124976534 | |||||||
| chr6:124976609 | C | G | 1 | a0001c0001t0010g0194 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.882+13183C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124976609 | |||||||
| chr6:124976624 | C | T | 2 | a0001c0001t0068g0244 a0002c0002t0075g0039 |
2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.882+13198C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124976624 | |||||||
| chr6:124976695 | G | A | 8 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(5): Show |
8 | HG00609.hp2 HG01358.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.882+13269G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124976695 | |||||||
| chr6:124976750 | C | A | 3 | a0001c0001t0017g0100 a0001c0001t0041g0098 a0003c0004t0044g0099 |
3 | HG02965.hp2 HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.882+13324C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124976750 | |||||||
| chr6:124976890 | C | A | 216 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(213): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.882+13464C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124976890 | |||||||
| chr6:124977194 | C | A | 215 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(212): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.882+13768C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124977194 | |||||||
| chr6:124977225 | T | C | 1 | a0002c0002t0070g0038 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.882+13799T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124977225 | |||||||
| chr6:124977445 | TAATG | T | 58 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(55): Show |
58 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.882+14022_882+1402 others(8): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 124977445 | ||||||
| chr6:124977611 | C | T | 2 | a0001c0003t0013g0184 a0001c0003t0013g0185 |
2 | HG02559.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.882+14185C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124977611 | |||||||
| chr6:124977813 | C | A | 3 | a0001c0001t0017g0100 a0001c0001t0041g0098 a0003c0004t0044g0099 |
3 | HG02965.hp2 HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.882+14387C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124977813 | |||||||
| chr6:124977848 | T | C | 3 | a0001c0001t0001g0243 a0001c0001t0004g0242 a0001c0001t0067g0198 |
3 | HG03492.hp1 HG03834.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.882+14422T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124977848 | |||||||
| chr6:124977900 | A | G | 1 | a0001c0001t0001g0240 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.882+14474A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124977900 | |||||||
| chr6:124978083 | A | T | 1 | a0001c0001t0026g0167 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.882+14657A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124978083 | |||||||
| chr6:124978100 | C | T | 1 | a0002c0002t0075g0039 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.882+14674C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124978100 | |||||||
| chr6:124978227 | T | A | 37 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(34): Show |
37 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.882+14801T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124978227 | |||||||
| chr6:124978229 | C | T | 17 | a0001c0001t0003g0168 a0001c0001t0003g0171 a0001c0001t0003g0175 others(14): Show |
17 | HG02055.hp2 HG02109.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.882+14803C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124978229 | |||||||
| chr6:124978313 | G | C | 60 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(57): Show |
60 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.882+14887G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124978313 | |||||||
| chr6:124978314 | C | A | 8 | a0001c0001t0001g0051 a0001c0001t0001g0056 a0001c0001t0002g0054 others(5): Show |
8 | HG01261.hp1 HG02132.hp1 NA18942.hp1 others(5): Show |
intron_variant | MODIFIER | c.882+14888C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124978314 | |||||||
| chr6:124978367 | G | A | 1 | a0001c0001t0017g0153 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.882+14941G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124978367 | |||||||
| chr6:124978408 | C | T | 1 | a0002c0002t0075g0039 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.882+14982C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124978408 | |||||||
| chr6:124978512 | C | G | 1 | a0001c0001t0010g0152 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.882+15086C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124978512 | |||||||
| chr6:124978618 | A | G | 5 | a0001c0001t0001g0119 a0001c0001t0002g0120 a0001c0001t0002g0121 others(2): Show |
5 | NA18964.hp2 NA18968.hp2 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.882+15192A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124978618 | |||||||
| chr6:124978749 | C | G | 1 | a0001c0001t0001g0083 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.882+15323C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124978749 | |||||||
| chr6:124978882 | G | C | 1 | a0009c0015t0053g0247 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.882+15456G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124978882 | |||||||
| chr6:124978967 | G | A | 3 | a0001c0001t0021g0132 a0001c0001t0022g0131 a0001c0001t0033g0133 |
3 | HG02886.hp2 HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.882+15541G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124978967 | |||||||
| chr6:124979111 | G | A | 2 | a0001c0001t0006g0004 a0001c0001t0043g0005 |
2 | HG02486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.882+15685G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124979111 | |||||||
| chr6:124979133 | T | C | 62 | a0001c0001t0001g0101 a0001c0001t0001g0124 a0001c0001t0001g0127 others(59): Show |
63 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.882+15707T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124979133 | |||||||
| chr6:124979177 | C | T | 2 | a0001c0001t0006g0004 a0001c0001t0043g0005 |
2 | HG02486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.882+15751C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124979177 | |||||||
| chr6:124979705 | A | T | 2 | a0001c0003t0010g0265 a0007c0009t0001g0264 |
2 | HG02922.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.882+16279A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124979705 | |||||||
| chr6:124979740 | C | G | 1 | a0001c0001t0006g0176 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.882+16314C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124979740 | |||||||
| chr6:124979928 | C | T | 3 | a0001c0001t0021g0132 a0001c0001t0022g0131 a0001c0001t0033g0133 |
3 | HG02886.hp2 HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.882+16502C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124979928 | |||||||
| chr6:124979981 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.882+16555G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124979981 | |||||||
| chr6:124980029 | G | C | 58 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(55): Show |
58 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.882+16603G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124980029 | |||||||
| chr6:124980074 | T | C | 2 | a0005c0007t0006g0094 a0005c0007t0021g0093 |
2 | HG01884.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.882+16648T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124980074 | |||||||
| chr6:124980516 | G | T | 2 | a0001c0001t0001g0262 a0001c0001t0006g0263 |
2 | HG01192.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.882+17090G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124980516 | |||||||
| chr6:124980575 | C | T | 1 | a0003c0004t0011g0257 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.882+17149C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124980575 | |||||||
| chr6:124980655 | A | C | 1 | a0001c0001t0010g0152 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.882+17229A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124980655 | |||||||
| chr6:124980694 | TTAGAG | T | 38 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(35): Show |
38 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.882+17275_882+1727 others(9): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 124980694 | ||||||
| chr6:124980751 | G | A | 1 | a0011c0011t0079g0035 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.882+17325G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124980751 | |||||||
| chr6:124980986 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.882+17560C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124980986 | |||||||
| chr6:124981091 | T | A | 3 | a0001c0001t0001g0101 a0001c0001t0001g0199 a0001c0001t0012g0200 |
3 | HG01928.hp1 HG03239.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.882+17665T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124981091 | |||||||
| chr6:124981135 | A | C | 12 | a0001c0001t0006g0190 a0001c0001t0010g0194 a0001c0001t0046g0195 others(9): Show |
13 | HG01243.hp1 HG02257.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.882+17709A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124981135 | |||||||
| chr6:124981207 | T | C | 12 | a0001c0001t0006g0190 a0001c0001t0010g0194 a0001c0001t0046g0195 others(9): Show |
13 | HG01243.hp1 HG02257.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.882+17781T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124981207 | |||||||
| chr6:124981462 | G | A | 13 | a0001c0001t0006g0004 a0001c0001t0006g0190 a0001c0001t0010g0194 others(10): Show |
14 | HG01243.hp1 HG02280.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.882+18036G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124981462 | |||||||
| chr6:124981468 | G | A | 1 | a0001c0003t0008g0186 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.882+18042G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124981468 | |||||||
| chr6:124981536 | G | A | 1 | a0001c0001t0001g0042 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.882+18110G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124981536 | |||||||
| chr6:124981586 | A | C | 1 | a0002c0002t0075g0039 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.882+18160A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124981586 | |||||||
| chr6:124981689 | T | C | 77 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(74): Show |
77 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.882+18263T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124981689 | |||||||
| chr6:124981726 | G | A | 1 | a0002c0002t0075g0039 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.882+18300G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124981726 | |||||||
| chr6:124981884 | C | T | 1 | a0002c0002t0075g0039 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.882+18458C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124981884 | |||||||
| chr6:124981888 | C | T | 1 | a0001c0001t0012g0200 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.882+18462C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124981888 | |||||||
| chr6:124981889 | G | A | 61 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(58): Show |
61 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.882+18463G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124981889 | |||||||
| chr6:124981953 | G | A | 1 | a0002c0002t0075g0039 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.882+18527G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124981953 | |||||||
| chr6:124981957 | G | A | 1 | a0001c0001t0005g0201 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.882+18531G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124981957 | |||||||
| chr6:124981977 | G | A | 1 | a0001c0001t0022g0179 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.882+18551G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124981977 | |||||||
| chr6:124982013 | C | T | 7 | a0001c0001t0006g0146 a0001c0001t0010g0144 a0001c0001t0010g0147 others(4): Show |
7 | HG02109.hp2 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.882+18587C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124982013 | |||||||
| chr6:124982026 | C | CA | 69 | a0001c0001t0001g0101 a0001c0001t0001g0124 a0001c0001t0001g0127 others(66): Show |
70 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.882+18621dupA | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 124982026 | ||||||
| chr6:124982026 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0016g0143 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.882+18610_882+1862 others(16): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 124982026 | ||||||
| chr6:124982075 | T | C | 1 | a0001c0001t0006g0176 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.882+18649T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124982075 | |||||||
| chr6:124982187 | C | G | 1 | a0002c0002t0075g0039 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.882+18761C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124982187 | |||||||
| chr6:124982307 | C | A | 56 | a0001c0001t0001g0124 a0001c0001t0001g0127 a0001c0001t0001g0199 others(53): Show |
57 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.882+18881C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124982307 | |||||||
| chr6:124982337 | A | G | 232 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(229): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.882+18911A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124982337 | |||||||
| chr6:124982436 | T | G | 1 | a0002c0002t0075g0039 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.882+19010T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124982436 | |||||||
| chr6:124982456 | T | C | 2 | a0005c0007t0006g0094 a0005c0007t0021g0093 |
2 | HG01884.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.882+19030T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124982456 | |||||||
| chr6:124982599 | A | T | 1 | a0001c0001t0017g0153 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.882+19173A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124982599 | |||||||
| chr6:124982607 | C | T | 1 | a0001c0001t0004g0241 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.882+19181C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124982607 | |||||||
| chr6:124982608 | G | A | 1 | a0001c0001t0005g0060 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.882+19182G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124982608 | |||||||
| chr6:124982844 | C | T | 1 | a0001c0001t0056g0111 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.882+19418C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124982844 | |||||||
| chr6:124983062 | A | G | 2 | a0001c0001t0021g0158 a0001c0001t0026g0159 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.882+19636A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124983062 | |||||||
| chr6:124983148 | G | T | 1 | a0002c0006t0078g0008 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.882+19722G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124983148 | |||||||
| chr6:124983160 | T | C | 3 | a0001c0001t0017g0100 a0001c0001t0041g0098 a0003c0004t0044g0099 |
3 | HG02965.hp2 HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.882+19734T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124983160 | |||||||
| chr6:124983600 | G | A | 1 | a0002c0002t0075g0039 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.882+20174G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124983600 | |||||||
| chr6:124983785 | T | C | 63 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(60): Show |
63 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.882+20359T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124983785 | |||||||
| chr6:124984123 | C | A | 1 | a0001c0001t0003g0084 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.882+20697C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124984123 | |||||||
| chr6:124984181 | G | C | 1 | a0001c0001t0012g0061 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.882+20755G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124984181 | |||||||
| chr6:124984423 | C | T | 1 | a0001c0001t0016g0143 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.882+20997C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124984423 | |||||||
| chr6:124984501 | A | G | 1 | a0001c0001t0001g0046 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.882+21075A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124984501 | |||||||
| chr6:124984541 | CA | C | 89 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(86): Show |
89 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.882+21135delA | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 124984541 | ||||||
| chr6:124984546 | A | AAAT | 62 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(59): Show |
62 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.882+21122_882+2112 others(7): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 124984546 | ||||||
| chr6:124984554 | A | G | 62 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(59): Show |
62 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.882+21128A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124984554 | |||||||
| chr6:124984558 | A | G | 64 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(61): Show |
64 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.882+21132A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124984558 | |||||||
| chr6:124984705 | A | C | 72 | a0001c0001t0001g0101 a0001c0001t0001g0124 a0001c0001t0001g0127 others(69): Show |
74 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.882+21279A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124984705 | |||||||
| chr6:124984865 | A | G | 1 | a0001c0003t0008g0174 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.882+21439A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124984865 | |||||||
| chr6:124985301 | A | G | 1 | a0001c0001t0067g0198 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.882+21875A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124985301 | |||||||
| chr6:124985316 | G | A | 1 | a0009c0015t0053g0247 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.882+21890G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124985316 | |||||||
| chr6:124985668 | A | G | 57 | a0001c0001t0001g0101 a0001c0001t0001g0124 a0001c0001t0001g0127 others(54): Show |
58 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.882+22242A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124985668 | |||||||
| chr6:124985738 | A | G | 62 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(59): Show |
62 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.882+22312A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124985738 | |||||||
| chr6:124985889 | T | G | 1 | a0001c0001t0002g0202 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.882+22463T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124985889 | |||||||
| chr6:124985940 | A | G | 1 | a0001c0001t0036g0231 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.882+22514A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124985940 | |||||||
| chr6:124986000 | T | C | 2 | a0001c0001t0001g0119 a0001c0001t0002g0120 |
2 | NA18964.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.882+22574T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124986000 | |||||||
| chr6:124986136 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.882+22710T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124986136 | |||||||
| chr6:124986288 | G | A | 3 | a0001c0001t0017g0100 a0001c0001t0041g0098 a0003c0004t0044g0099 |
3 | HG02965.hp2 HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.882+22862G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124986288 | |||||||
| chr6:124986840 | A | G | 2 | a0001c0001t0006g0173 a0001c0001t0051g0172 |
2 | HG02280.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.882+23414A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124986840 | |||||||
| chr6:124986940 | G | A | 62 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(59): Show |
62 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.882+23514G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124986940 | |||||||
| chr6:124987019 | A | G | 2 | a0001c0001t0003g0254 a0001c0001t0017g0253 |
2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.882+23593A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124987019 | |||||||
| chr6:124987042 | T | C | 1 | a0001c0001t0001g0063 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.882+23616T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124987042 | |||||||
| chr6:124987066 | C | A | 58 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(55): Show |
58 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.882+23640C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124987066 | |||||||
| chr6:124987241 | G | A | 39 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(36): Show |
39 | HG00423.hp1 HG00609.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.882+23815G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124987241 | |||||||
| chr6:124987339 | C | T | 2 | a0001c0001t0008g0181 a0001c0001t0022g0179 |
2 | HG02055.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.882+23913C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124987339 | |||||||
| chr6:124987367 | A | G | 1 | a0001c0001t0016g0082 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.882+23941A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124987367 | |||||||
| chr6:124987370 | A | G | 1 | a0007c0009t0001g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.882+23944A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124987370 | |||||||
| chr6:124987414 | C | T | 2 | a0005c0007t0006g0094 a0005c0007t0021g0093 |
2 | HG01884.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.882+23988C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124987414 | |||||||
| chr6:124987612 | C | T | 1 | a0002c0002t0070g0038 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.882+24186C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124987612 | |||||||
| chr6:124987668 | G | T | 1 | a0009c0015t0053g0247 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.882+24242G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124987668 | |||||||
| chr6:124987731 | C | A | 2 | a0001c0001t0004g0242 a0001c0001t0067g0198 |
2 | HG03492.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.882+24305C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124987731 | |||||||
| chr6:124987733 | G | A | 2 | a0001c0001t0006g0004 a0001c0001t0043g0005 |
2 | HG02486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.882+24307G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124987733 | |||||||
| chr6:124987750 | A | G | 1 | a0001c0001t0049g0261 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.882+24324A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124987750 | |||||||
| chr6:124987835 | T | A | 1 | a0001c0001t0038g0203 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.882+24409T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124987835 | |||||||
| chr6:124987915 | A | G | 62 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(59): Show |
62 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.882+24489A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124987915 | |||||||
| chr6:124987974 | A | G | 1 | a0001c0001t0026g0167 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.882+24548A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124987974 | |||||||
| chr6:124988150 | C | T | 9 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(6): Show |
9 | HG00323.hp1 HG00609.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.882+24724C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124988150 | |||||||
| chr6:124988794 | A | T | 2 | a0001c0001t0001g0230 a0001c0001t0003g0197 |
2 | HG00323.hp1 HG00735.hp2 |
intron_variant | MODIFIER | c.882+25368A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124988794 | |||||||
| chr6:124988868 | G | A | 58 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(55): Show |
58 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.882+25442G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124988868 | |||||||
| chr6:124988871 | T | C | 58 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(55): Show |
58 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.882+25445T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124988871 | |||||||
| chr6:124988879 | T | A | 1 | a0001c0001t0001g0050 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.882+25453T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124988879 | |||||||
| chr6:124988959 | A | T | 1 | a0001c0001t0002g0229 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.882+25533A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124988959 | |||||||
| chr6:124989019 | AT | A | 5 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(2): Show |
5 | HG00423.hp1 HG01243.hp2 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.882+25600delT | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 124989019 | ||||||
| chr6:124989057 | A | ATTACCTT others(20): Show |
62 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(59): Show |
62 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.882+25633_882+2563 others(31): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 124989057 | ||||||
| chr6:124989214 | C | T | 62 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(59): Show |
62 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.882+25788C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124989214 | |||||||
| chr6:124989269 | C | T | 11 | a0001c0001t0001g0262 a0001c0001t0006g0263 a0001c0001t0010g0152 others(8): Show |
11 | HG01192.hp1 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.882+25843C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124989269 | |||||||
| chr6:124989281 | A | T | 1 | a0001c0001t0001g0056 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.882+25855A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124989281 | |||||||
| chr6:124989306 | C | T | 2 | a0001c0001t0001g0199 a0001c0001t0012g0200 |
2 | HG01928.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.882+25880C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124989306 | |||||||
| chr6:124989389 | G | T | 58 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(55): Show |
58 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.882+25963G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124989389 | |||||||
| chr6:124989391 | A | G | 1 | a0001c0001t0001g0240 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.882+25965A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124989391 | |||||||
| chr6:124989572 | C | G | 1 | a0002c0002t0075g0039 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.882+26146C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124989572 | |||||||
| chr6:124989617 | C | T | 1 | a0001c0001t0005g0091 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.882+26191C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124989617 | |||||||
| chr6:124989637 | A | ATTTGAG | 260 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(257): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.882+26216_882+2621 others(10): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 124989637 | ||||||
| chr6:124989815 | T | C | 1 | a0001c0001t0003g0177 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.882+26389T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124989815 | |||||||
| chr6:124989867 | G | GA | 13 | a0001c0001t0001g0050 a0001c0001t0001g0057 a0001c0001t0001g0067 others(10): Show |
13 | HG00642.hp2 HG00735.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.882+26451dupA | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 124989867 | ||||||
| chr6:124989883 | A | T | 11 | a0001c0001t0006g0190 a0001c0001t0010g0194 a0001c0001t0046g0195 others(8): Show |
12 | HG01243.hp1 HG02280.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.882+26457A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124989883 | |||||||
| chr6:124990326 | T | C | 56 | a0001c0001t0001g0101 a0001c0001t0001g0124 a0001c0001t0001g0127 others(53): Show |
57 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.882+26900T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124990326 | |||||||
| chr6:124990332 | A | G | 6 | a0002c0002t0007g0026 a0002c0002t0007g0027 a0002c0002t0009g0023 others(3): Show |
6 | HG00323.hp2 HG01346.hp1 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.882+26906A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124990332 | |||||||
| chr6:124990352 | C | T | 1 | a0002c0006t0078g0008 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.882+26926C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124990352 | |||||||
| chr6:124990633 | A | C | 61 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(58): Show |
61 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.882+27207A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124990633 | |||||||
| chr6:124990863 | G | A | 1 | a0001c0001t0001g0063 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.882+27437G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124990863 | |||||||
| chr6:124991006 | G | T | 9 | a0001c0001t0006g0004 a0001c0001t0006g0190 a0001c0001t0010g0194 others(6): Show |
10 | HG02486.hp1 HG02818.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.882+27580G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124991006 | |||||||
| chr6:124991248 | G | C | 6 | a0001c0001t0001g0156 a0001c0001t0004g0154 a0001c0001t0006g0157 others(3): Show |
6 | HG00741.hp1 HG01891.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.882+27822G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124991248 | |||||||
| chr6:124991423 | C | T | 1 | a0001c0001t0002g0228 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.882+27997C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124991423 | |||||||
| chr6:124991504 | T | C | 60 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(57): Show |
60 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.882+28078T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124991504 | |||||||
| chr6:124991556 | C | T | 1 | a0001c0001t0026g0167 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.882+28130C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124991556 | |||||||
| chr6:124991664 | T | C | 2 | a0002c0002t0029g0006 a0002c0006t0013g0011 |
2 | NA19065.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.882+28238T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124991664 | |||||||
| chr6:124992116 | A | G | 1 | a0001c0001t0010g0194 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.882+28690A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124992116 | |||||||
| chr6:124992137 | A | G | 1 | a0001c0001t0026g0167 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.882+28711A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124992137 | |||||||
| chr6:124992144 | C | G | 6 | a0001c0001t0040g0260 a0001c0001t0049g0261 a0001c0003t0010g0265 others(3): Show |
6 | HG02257.hp2 HG02258.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.882+28718C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124992144 | |||||||
| chr6:124992177 | CT | C | 60 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(57): Show |
60 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.882+28752delT | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124992177 | |||||||
| chr6:124992405 | C | A | 1 | a0001c0001t0004g0095 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.882+28979C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124992405 | |||||||
| chr6:124992407 | A | G | 1 | a0002c0002t0075g0039 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.882+28981A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124992407 | |||||||
| chr6:124992417 | A | G | 3 | a0001c0001t0017g0100 a0001c0001t0041g0098 a0003c0004t0044g0099 |
3 | HG02965.hp2 HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.882+28991A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124992417 | |||||||
| chr6:124992420 | A | G | 9 | a0001c0001t0006g0190 a0001c0001t0010g0194 a0001c0001t0046g0195 others(6): Show |
10 | HG01884.hp1 HG02809.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.882+28994A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124992420 | |||||||
| chr6:124992529 | C | T | 60 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(57): Show |
60 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.882+29103C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124992529 | |||||||
| chr6:124992566 | T | G | 60 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(57): Show |
60 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.882+29140T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124992566 | |||||||
| chr6:124992645 | G | A | 1 | a0001c0001t0002g0236 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.882+29219G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124992645 | |||||||
| chr6:124992735 | C | T | 5 | a0001c0001t0008g0181 a0001c0001t0022g0179 a0001c0001t0039g0178 others(2): Show |
5 | HG02055.hp2 HG02109.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.882+29309C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124992735 | |||||||
| chr6:124992894 | C | T | 1 | a0001c0001t0002g0055 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.882+29468C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124992894 | |||||||
| chr6:124992903 | T | A | 86 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(83): Show |
86 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.882+29477T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124992903 | |||||||
| chr6:124993009 | C | A | 1 | a0001c0001t0004g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.882+29583C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124993009 | |||||||
| chr6:124993088 | G | A | 1 | a0001c0001t0010g0194 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.882+29662G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124993088 | |||||||
| chr6:124993404 | T | G | 84 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0104 others(81): Show |
84 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.882+29978T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124993404 | |||||||
| chr6:124993564 | A | G | 1 | a0011c0011t0079g0035 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.882+30138A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124993564 | |||||||
| chr6:124993576 | A | C | 1 | a0001c0001t0039g0178 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.882+30150A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124993576 | |||||||
| chr6:124993704 | G | A | 10 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(7): Show |
10 | HG00099.hp2 HG00639.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.882+30278G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124993704 | |||||||
| chr6:124994277 | G | A | 60 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(57): Show |
60 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.882+30851G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124994277 | |||||||
| chr6:124994368 | C | T | 215 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(212): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.882+30942C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124994368 | |||||||
| chr6:124994376 | G | A | 60 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(57): Show |
60 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.882+30950G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124994376 | |||||||
| chr6:124994719 | A | G | 1 | a0002c0006t0078g0008 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.882+31293A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124994719 | |||||||
| chr6:124994725 | A | C | 3 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 |
3 | HG01243.hp2 HG01934.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.882+31299A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124994725 | |||||||
| chr6:124994850 | G | C | 1 | a0001c0001t0001g0068 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.882+31424G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124994850 | |||||||
| chr6:124994922 | G | T | 1 | a0009c0015t0053g0247 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.882+31496G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124994922 | |||||||
| chr6:124995129 | C | T | 1 | a0002c0006t0078g0008 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.882+31703C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124995129 | |||||||
| chr6:124995215 | T | C | 9 | a0001c0001t0006g0190 a0001c0001t0010g0194 a0001c0001t0046g0195 others(6): Show |
10 | HG01884.hp1 HG02809.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.882+31789T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124995215 | |||||||
| chr6:124995261 | A | G | 3 | a0001c0001t0017g0100 a0001c0001t0041g0098 a0003c0004t0044g0099 |
3 | HG02965.hp2 HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.882+31835A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124995261 | |||||||
| chr6:124995410 | G | A | 1 | a0001c0001t0003g0168 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.882+31984G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124995410 | |||||||
| chr6:124995895 | C | G | 1 | a0001c0001t0002g0054 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.882+32469C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124995895 | |||||||
| chr6:124995947 | A | G | 59 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(56): Show |
59 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.882+32521A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124995947 | |||||||
| chr6:124996132 | G | A | 3 | a0001c0001t0017g0100 a0001c0001t0041g0098 a0003c0004t0044g0099 |
3 | HG02965.hp2 HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.882+32706G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124996132 | |||||||
| chr6:124997017 | GCAAGTTT others(5): Show |
G | 11 | a0001c0001t0006g0004 a0001c0001t0006g0190 a0001c0001t0010g0194 others(8): Show |
12 | HG01884.hp1 HG02486.hp1 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.882+33593_882+3360 others(16): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 124997017 | ||||||
| chr6:124997026 | G | T | 60 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(57): Show |
60 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.882+33600G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124997026 | |||||||
| chr6:124997233 | C | T | 81 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(78): Show |
81 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.882+33807C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124997233 | |||||||
| chr6:124997396 | G | T | 1 | a0001c0001t0001g0227 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.882+33970G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124997396 | |||||||
| chr6:124997418 | A | G | 1 | a0009c0015t0053g0247 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.882+33992A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124997418 | |||||||
| chr6:124997461 | C | CAA | 174 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(171): Show |
175 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.882+34035_882+3403 others(6): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124997461 | |||||||
| chr6:124997547 | T | G | 57 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(54): Show |
57 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.882+34121T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124997547 | |||||||
| chr6:124997557 | C | G | 61 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(58): Show |
61 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.882+34131C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124997557 | |||||||
| chr6:124997671 | C | T | 16 | a0001c0001t0003g0168 a0001c0001t0003g0171 a0001c0001t0003g0175 others(13): Show |
16 | HG02055.hp2 HG02109.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.882+34245C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124997671 | |||||||
| chr6:124997686 | A | G | 2 | a0001c0001t0003g0171 a0001c0001t0059g0170 |
2 | HG02615.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.882+34260A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124997686 | |||||||
| chr6:124997735 | A | G | 1 | a0002c0002t0071g0037 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.882+34309A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124997735 | |||||||
| chr6:124997818 | A | G | 2 | a0001c0001t0005g0091 a0001c0001t0063g0090 |
2 | HG00408.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.882+34392A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124997818 | |||||||
| chr6:124997858 | A | G | 1 | a0002c0002t0007g0022 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.882+34432A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124997858 | |||||||
| chr6:124997902 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.882+34476G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124997902 | |||||||
| chr6:124997924 | C | T | 1 | a0002c0002t0070g0038 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.882+34498C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124997924 | |||||||
| chr6:124997966 | A | C | 8 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(5): Show |
8 | HG00609.hp2 HG01358.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.882+34540A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124997966 | |||||||
| chr6:124998069 | C | G | 175 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(172): Show |
176 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.882+34643C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124998069 | |||||||
| chr6:124998263 | T | A | 1 | a0011c0011t0079g0035 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.882+34837T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124998263 | |||||||
| chr6:124998404 | G | C | 8 | a0001c0001t0003g0168 a0001c0001t0003g0171 a0001c0001t0003g0175 others(5): Show |
8 | HG02451.hp1 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.882+34978G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124998404 | |||||||
| chr6:124998412 | A | T | 44 | a0001c0001t0001g0101 a0001c0001t0001g0134 a0001c0001t0001g0135 others(41): Show |
44 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.882+34986A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124998412 | |||||||
| chr6:124998417 | C | T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0067 |
2 | HG01070.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.882+34991C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124998417 | |||||||
| chr6:124998474 | A | G | 1 | a0001c0001t0026g0167 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.882+35048A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124998474 | |||||||
| chr6:124998545 | G | A | 229 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(226): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.882+35119G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124998545 | |||||||
| chr6:124998548 | G | A | 1 | a0001c0001t0026g0167 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.882+35122G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124998548 | |||||||
| chr6:124998753 | G | A | 2 | a0009c0015t0053g0247 a0011c0011t0079g0035 |
2 | HG02922.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.882+35327G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124998753 | |||||||
| chr6:124998797 | C | G | 62 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(59): Show |
62 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.882+35371C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124998797 | |||||||
| chr6:124998837 | G | A | 82 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(79): Show |
82 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.882+35411G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124998837 | |||||||
| chr6:124998893 | T | C | 1 | a0002c0002t0013g0012 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.882+35467T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124998893 | |||||||
| chr6:124998901 | A | G | 87 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(84): Show |
87 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.882+35475A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124998901 | |||||||
| chr6:124999094 | C | T | 1 | a0001c0001t0026g0167 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.882+35668C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124999094 | |||||||
| chr6:124999398 | A | C | 1 | a0011c0011t0079g0035 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.882+35972A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124999398 | |||||||
| chr6:124999939 | C | T | 1 | a0008c0014t0001g0126 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.882+36513C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 124999939 | |||||||
| chr6:125000245 | A | C | 1 | a0001c0003t0008g0192 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.882+36819A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125000245 | |||||||
| chr6:125000345 | A | C | 2 | a0001c0001t0015g0224 a0001c0001t0047g0225 |
2 | HG02083.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.882+36919A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125000345 | |||||||
| chr6:125000437 | C | T | 23 | a0001c0001t0003g0168 a0001c0001t0003g0171 a0001c0001t0003g0175 others(20): Show |
23 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.882+37011C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125000437 | |||||||
| chr6:125000484 | A | G | 4 | a0001c0001t0001g0101 a0001c0001t0002g0163 a0001c0001t0003g0084 others(1): Show |
4 | HG00642.hp1 HG01069.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+37058A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125000484 | |||||||
| chr6:125000599 | C | T | 1 | a0002c0002t0075g0039 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.882+37173C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125000599 | |||||||
| chr6:125000648 | A | G | 3 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0052g0048 |
3 | HG02132.hp2 NA18747.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.882+37222A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125000648 | |||||||
| chr6:125000734 | T | C | 1 | a0001c0001t0017g0153 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.882+37308T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125000734 | |||||||
| chr6:125001201 | T | C | 33 | a0001c0001t0003g0168 a0001c0001t0003g0171 a0001c0001t0003g0175 others(30): Show |
33 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(30): Show |
intron_variant | MODIFIER | c.882+37775T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125001201 | |||||||
| chr6:125001346 | T | C | 1 | a0002c0002t0070g0038 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.882+37920T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125001346 | |||||||
| chr6:125001394 | C | G | 1 | a0009c0015t0053g0247 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.882+37968C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125001394 | |||||||
| chr6:125001456 | A | T | 32 | a0001c0001t0003g0168 a0001c0001t0003g0171 a0001c0001t0003g0175 others(29): Show |
32 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.882+38030A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125001456 | |||||||
| chr6:125001655 | C | T | 11 | a0001c0001t0010g0194 a0001c0001t0040g0260 a0001c0001t0046g0195 others(8): Show |
11 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.882+38229C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125001655 | |||||||
| chr6:125001890 | A | AT | 6 | a0001c0001t0006g0004 a0001c0001t0006g0190 a0001c0001t0017g0153 others(3): Show |
6 | HG01884.hp2 HG02486.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.882+38466dupT | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125001890 | ||||||
| chr6:125002018 | T | C | 3 | a0001c0001t0021g0132 a0001c0001t0022g0131 a0001c0001t0033g0133 |
3 | HG02886.hp2 HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.882+38592T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125002018 | |||||||
| chr6:125002100 | G | C | 1 | a0001c0001t0001g0101 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.882+38674G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125002100 | |||||||
| chr6:125002102 | G | A | 1 | a0001c0001t0001g0042 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.882+38676G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125002102 | |||||||
| chr6:125002445 | CT | C | 28 | a0001c0001t0003g0168 a0001c0001t0003g0171 a0001c0001t0003g0175 others(25): Show |
28 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.882+39020delT | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125002445 | |||||||
| chr6:125002482 | G | C | 59 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(56): Show |
60 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.882+39056G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125002482 | |||||||
| chr6:125002599 | C | T | 10 | a0001c0001t0001g0119 a0001c0001t0002g0120 a0001c0001t0002g0121 others(7): Show |
10 | HG02080.hp2 NA18943.hp1 NA18946.hp2 others(7): Show |
intron_variant | MODIFIER | c.882+39173C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125002599 | |||||||
| chr6:125002606 | C | T | 1 | a0001c0001t0002g0228 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.882+39180C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125002606 | |||||||
| chr6:125003043 | G | A | 11 | a0001c0001t0010g0194 a0001c0001t0040g0260 a0001c0001t0046g0195 others(8): Show |
11 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.882+39617G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125003043 | |||||||
| chr6:125003104 | G | A | 32 | a0001c0001t0003g0168 a0001c0001t0003g0171 a0001c0001t0003g0175 others(29): Show |
32 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.882+39678G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125003104 | |||||||
| chr6:125003129 | T | C | 1 | a0001c0001t0049g0261 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.882+39703T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125003129 | |||||||
| chr6:125003183 | G | A | 31 | a0001c0001t0003g0168 a0001c0001t0003g0171 a0001c0001t0003g0175 others(28): Show |
31 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.882+39757G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125003183 | |||||||
| chr6:125003258 | G | A | 61 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(58): Show |
62 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.882+39832G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125003258 | |||||||
| chr6:125003373 | T | TG | 11 | a0001c0001t0010g0194 a0001c0001t0040g0260 a0001c0001t0046g0195 others(8): Show |
11 | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.882+39948dupG | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125003373 | ||||||
| chr6:125003546 | A | G | 31 | a0001c0001t0003g0168 a0001c0001t0003g0171 a0001c0001t0003g0175 others(28): Show |
31 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.882+40120A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125003546 | |||||||
| chr6:125003615 | A | G | 231 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(228): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.882+40189A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125003615 | |||||||
| chr6:125003719 | C | G | 60 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(57): Show |
61 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.882+40293C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125003719 | |||||||
| chr6:125003761 | A | G | 1 | a0001c0001t0045g0160 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.882+40335A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125003761 | |||||||
| chr6:125004051 | A | G | 1 | a0001c0001t0067g0198 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.882+40625A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125004051 | |||||||
| chr6:125004064 | G | GT | 220 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(217): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.882+40645dupT | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125004064 | ||||||
| chr6:125004064 | G | T | 15 | a0001c0001t0003g0168 a0001c0001t0003g0171 a0001c0001t0003g0175 others(12): Show |
15 | HG02055.hp2 HG02109.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.882+40638G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125004064 | |||||||
| chr6:125004064 | GTT | G | 7 | a0001c0001t0006g0004 a0001c0001t0006g0190 a0001c0001t0017g0153 others(4): Show |
7 | HG01884.hp2 HG02486.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.882+40644_882+4064 others(6): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125004064 | ||||||
| chr6:125004113 | G | A | 1 | a0002c0002t0075g0039 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.882+40687G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125004113 | |||||||
| chr6:125004186 | A | G | 1 | a0001c0001t0036g0231 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.882+40760A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125004186 | |||||||
| chr6:125004708 | G | A | 32 | a0001c0001t0003g0168 a0001c0001t0003g0171 a0001c0001t0003g0175 others(29): Show |
32 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.883-40503G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125004708 | |||||||
| chr6:125004955 | A | C | 259 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(256): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.883-40256A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125004955 | |||||||
| chr6:125005038 | G | A | 1 | a0001c0001t0023g0249 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.883-40173G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125005038 | |||||||
| chr6:125005270 | G | A | 33 | a0001c0001t0003g0168 a0001c0001t0003g0171 a0001c0001t0003g0175 others(30): Show |
33 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(30): Show |
intron_variant | MODIFIER | c.883-39941G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125005270 | |||||||
| chr6:125005399 | A | G | 2 | a0001c0001t0004g0242 a0001c0001t0016g0221 |
2 | HG02602.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.883-39812A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125005399 | |||||||
| chr6:125005478 | A | G | 2 | a0001c0001t0012g0061 a0001c0001t0016g0143 |
2 | HG02735.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.883-39733A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125005478 | |||||||
| chr6:125005704 | A | G | 1 | a0001c0001t0001g0092 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.883-39507A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125005704 | |||||||
| chr6:125005755 | T | C | 1 | a0001c0003t0008g0192 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.883-39456T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125005755 | |||||||
| chr6:125005869 | G | A | 2 | a0001c0001t0021g0158 a0001c0001t0026g0159 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.883-39342G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125005869 | |||||||
| chr6:125005931 | T | G | 1 | a0001c0001t0014g0096 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.883-39280T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125005931 | |||||||
| chr6:125006406 | C | T | 7 | a0001c0001t0006g0004 a0001c0001t0006g0190 a0001c0001t0017g0153 others(4): Show |
7 | HG01884.hp2 HG02486.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.883-38805C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125006406 | |||||||
| chr6:125006570 | A | G | 1 | a0002c0002t0072g0007 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.883-38641A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125006570 | |||||||
| chr6:125006601 | C | T | 1 | a0001c0003t0023g0142 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.883-38610C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125006601 | |||||||
| chr6:125006639 | G | A | 24 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(21): Show |
24 | HG00609.hp2 HG01358.hp1 HG01433.hp2 others(21): Show |
intron_variant | MODIFIER | c.883-38572G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125006639 | |||||||
| chr6:125006852 | G | C | 1 | a0002c0002t0007g0009 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.883-38359G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125006852 | |||||||
| chr6:125006881 | A | G | 110 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0104 others(107): Show |
110 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.883-38330A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125006881 | |||||||
| chr6:125006898 | G | A | 33 | a0001c0001t0003g0168 a0001c0001t0003g0171 a0001c0001t0003g0175 others(30): Show |
33 | HG01192.hp2 HG01884.hp1 HG02055.hp2 others(30): Show |
intron_variant | MODIFIER | c.883-38313G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125006898 | |||||||
| chr6:125007059 | A | T | 77 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0104 others(74): Show |
77 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.883-38152A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125007059 | |||||||
| chr6:125007062 | A | G | 77 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0104 others(74): Show |
77 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.883-38149A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125007062 | |||||||
| chr6:125007249 | A | AT | 111 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(108): Show |
113 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.883-37949dupT | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125007249 | ||||||
| chr6:125007249 | A | ATT | 6 | a0001c0001t0002g0220 a0001c0001t0002g0228 a0001c0001t0002g0248 others(3): Show |
6 | HG03492.hp1 HG04115.hp1 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.883-37950_883-3794 others(6): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125007249 | ||||||
| chr6:125007249 | ATT | A | 33 | a0001c0001t0003g0168 a0001c0001t0003g0171 a0001c0001t0003g0175 others(30): Show |
33 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(30): Show |
intron_variant | MODIFIER | c.883-37950_883-3794 others(6): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125007249 | ||||||
| chr6:125007266 | A | T | 1 | a0001c0001t0005g0080 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.883-37945A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125007266 | |||||||
| chr6:125007322 | C | T | 1 | a0001c0001t0004g0241 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.883-37889C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125007322 | |||||||
| chr6:125007323 | G | A | 1 | a0011c0011t0079g0035 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.883-37888G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125007323 | |||||||
| chr6:125007654 | T | C | 1 | a0001c0001t0036g0231 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.883-37557T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125007654 | |||||||
| chr6:125007704 | C | T | 33 | a0001c0001t0003g0168 a0001c0001t0003g0171 a0001c0001t0003g0175 others(30): Show |
33 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(30): Show |
intron_variant | MODIFIER | c.883-37507C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125007704 | |||||||
| chr6:125007797 | A | G | 33 | a0001c0001t0003g0168 a0001c0001t0003g0171 a0001c0001t0003g0175 others(30): Show |
33 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(30): Show |
intron_variant | MODIFIER | c.883-37414A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125007797 | |||||||
| chr6:125007979 | G | A | 77 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0104 others(74): Show |
77 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.883-37232G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125007979 | |||||||
| chr6:125008041 | G | A | 33 | a0001c0001t0003g0168 a0001c0001t0003g0171 a0001c0001t0003g0175 others(30): Show |
33 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(30): Show |
intron_variant | MODIFIER | c.883-37170G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125008041 | |||||||
| chr6:125008047 | T | G | 1 | a0006c0010t0028g0028 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.883-37164T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125008047 | |||||||
| chr6:125008131 | C | T | 77 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0104 others(74): Show |
77 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.883-37080C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125008131 | |||||||
| chr6:125008255 | C | CA | 32 | a0001c0001t0003g0168 a0001c0001t0003g0175 a0001c0001t0003g0177 others(29): Show |
32 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.883-36943dupA | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125008255 | ||||||
| chr6:125008369 | C | G | 1 | a0001c0003t0008g0192 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.883-36842C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125008369 | |||||||
| chr6:125008467 | G | A | 239 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(236): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.883-36744G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125008467 | |||||||
| chr6:125008479 | C | T | 1 | a0001c0003t0008g0256 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.883-36732C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125008479 | |||||||
| chr6:125008738 | C | CT | 136 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(133): Show |
138 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.883-36455dupT | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125008738 | ||||||
| chr6:125008738 | C | CTT | 9 | a0001c0001t0001g0079 a0001c0001t0001g0227 a0001c0001t0002g0097 others(6): Show |
9 | HG01891.hp2 HG02293.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.883-36456_883-3645 others(6): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125008738 | ||||||
| chr6:125008982 | G | C | 38 | a0001c0001t0001g0101 a0001c0001t0001g0134 a0001c0001t0001g0135 others(35): Show |
38 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.883-36229G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125008982 | |||||||
| chr6:125009285 | A | G | 1 | a0001c0001t0017g0153 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.883-35926A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125009285 | |||||||
| chr6:125009461 | T | C | 3 | a0001c0001t0001g0043 a0001c0001t0001g0046 a0001c0001t0015g0044 |
3 | HG02523.hp1 NA18999.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.883-35750T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125009461 | |||||||
| chr6:125009473 | GA | G | 77 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0104 others(74): Show |
77 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.883-35728delA | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125009473 | ||||||
| chr6:125009765 | G | A | 1 | a0001c0003t0008g0130 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.883-35446G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125009765 | |||||||
| chr6:125009775 | G | A | 60 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(57): Show |
61 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.883-35436G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125009775 | |||||||
| chr6:125009985 | CT | C | 178 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(175): Show |
179 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.883-35210delT | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125009985 | ||||||
| chr6:125010146 | A | C | 1 | a0001c0001t0002g0202 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.883-35065A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125010146 | |||||||
| chr6:125010292 | G | A | 1 | a0001c0003t0023g0142 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.883-34919G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125010292 | |||||||
| chr6:125010383 | G | A | 1 | a0001c0001t0023g0249 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.883-34828G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125010383 | |||||||
| chr6:125010481 | G | T | 1 | a0001c0001t0045g0160 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.883-34730G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125010481 | |||||||
| chr6:125010517 | C | T | 3 | a0001c0001t0001g0115 a0001c0001t0004g0095 a0001c0001t0005g0113 |
3 | NA18949.hp2 NA18956.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.883-34694C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125010517 | |||||||
| chr6:125010878 | A | G | 78 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0104 others(75): Show |
78 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.883-34333A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125010878 | |||||||
| chr6:125010882 | C | T | 231 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(228): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.883-34329C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125010882 | |||||||
| chr6:125010937 | A | G | 1 | a0001c0003t0010g0258 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.883-34274A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125010937 | |||||||
| chr6:125011030 | C | T | 78 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0104 others(75): Show |
78 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.883-34181C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125011030 | |||||||
| chr6:125011379 | G | T | 5 | a0001c0001t0015g0224 a0001c0001t0018g0222 a0001c0001t0018g0223 others(2): Show |
5 | HG00423.hp2 HG02083.hp1 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-33832G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125011379 | |||||||
| chr6:125011665 | A | G | 113 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(110): Show |
115 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.883-33546A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125011665 | |||||||
| chr6:125011706 | A | T | 1 | a0001c0001t0002g0228 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.883-33505A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125011706 | |||||||
| chr6:125011830 | G | A | 49 | a0001c0001t0001g0083 a0001c0001t0001g0124 a0001c0001t0001g0127 others(46): Show |
50 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.883-33381G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125011830 | |||||||
| chr6:125011857 | G | A | 1 | a0001c0001t0002g0163 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.883-33354G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125011857 | |||||||
| chr6:125011858 | G | C | 32 | a0001c0001t0003g0168 a0001c0001t0003g0171 a0001c0001t0003g0175 others(29): Show |
32 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.883-33353G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125011858 | |||||||
| chr6:125011876 | G | A | 1 | a0009c0015t0053g0247 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.883-33335G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125011876 | |||||||
| chr6:125011961 | G | C | 1 | a0001c0001t0017g0253 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.883-33250G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125011961 | |||||||
| chr6:125012064 | G | A | 32 | a0001c0001t0003g0168 a0001c0001t0003g0171 a0001c0001t0003g0175 others(29): Show |
32 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.883-33147G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125012064 | |||||||
| chr6:125012100 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.883-33111C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125012100 | |||||||
| chr6:125012527 | G | A | 231 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(228): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.883-32684G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125012527 | |||||||
| chr6:125012622 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.883-32589A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125012622 | |||||||
| chr6:125012651 | T | C | 63 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(60): Show |
64 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.883-32560T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125012651 | |||||||
| chr6:125013062 | G | C | 1 | a0001c0001t0015g0206 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.883-32149G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125013062 | |||||||
| chr6:125013188 | G | T | 1 | a0001c0001t0001g0235 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.883-32023G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125013188 | |||||||
| chr6:125013345 | TTGTGTA | T | 24 | a0001c0001t0003g0168 a0001c0001t0003g0171 a0001c0001t0003g0177 others(21): Show |
24 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.883-31860_883-3185 others(10): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125013345 | ||||||
| chr6:125013347 | GTGTA | G | 4 | a0001c0001t0003g0175 a0001c0001t0006g0173 a0001c0001t0051g0172 others(1): Show |
4 | HG02280.hp2 HG02809.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.883-31860_883-3185 others(8): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125013347 | ||||||
| chr6:125013351 | A | ATG | 17 | a0001c0001t0001g0243 a0001c0001t0012g0216 a0001c0001t0061g0252 others(14): Show |
17 | HG00738.hp2 HG01069.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.883-31823_883-3182 others(6): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125013351 | ||||||
| chr6:125013351 | A | ATGTG | 6 | a0001c0001t0017g0153 a0001c0001t0026g0167 a0001c0001t0043g0005 others(3): Show |
6 | HG01884.hp2 HG02071.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.883-31825_883-3182 others(8): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125013351 | ||||||
| chr6:125013351 | A | ATGTGTG | 4 | a0001c0001t0006g0004 a0002c0002t0007g0015 a0002c0002t0007g0017 others(1): Show |
4 | NA18906.hp1 NA18956.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.883-31827_883-3182 others(10): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125013351 | ||||||
| chr6:125013351 | A | ATGTGTGT others(1): Show |
3 | a0001c0001t0006g0190 a0003c0004t0011g0189 a0010c0013t0030g0191 |
3 | HG02818.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.883-31829_883-3182 others(12): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125013351 | ||||||
| chr6:125013351 | A | G | 3 | a0002c0002t0075g0039 a0009c0015t0053g0247 a0011c0011t0079g0035 |
3 | HG02922.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.883-31860A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125013351 | |||||||
| chr6:125013351 | ATG | A | 66 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(63): Show |
67 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.883-31823_883-3182 others(6): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125013351 | ||||||
| chr6:125013351 | ATGTG | A | 116 | a0001c0001t0001g0083 a0001c0001t0001g0101 a0001c0001t0001g0103 others(113): Show |
117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.883-31825_883-3182 others(8): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125013351 | ||||||
| chr6:125013351 | ATGTGTGT others(7): Show |
A | 1 | a0001c0001t0060g0232 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.883-31835_883-3182 others(18): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125013351 | ||||||
| chr6:125013459 | C | G | 1 | a0001c0001t0004g0226 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.883-31752C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125013459 | |||||||
| chr6:125013550 | G | GA | 54 | a0001c0001t0001g0050 a0001c0001t0001g0067 a0001c0001t0001g0083 others(51): Show |
55 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.883-31649dupA | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125013550 | ||||||
| chr6:125013551 | A | G | 7 | a0001c0001t0006g0004 a0001c0001t0006g0190 a0001c0001t0017g0153 others(4): Show |
7 | HG01884.hp2 HG02486.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.883-31660A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125013551 | |||||||
| chr6:125013556 | A | AG | 3 | a0001c0001t0001g0101 a0001c0001t0001g0199 a0001c0001t0012g0200 |
3 | HG01928.hp1 HG03239.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.883-31655_883-3165 others(5): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125013556 | |||||||
| chr6:125013574 | G | A | 28 | a0001c0001t0003g0168 a0001c0001t0003g0171 a0001c0001t0003g0175 others(25): Show |
28 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.883-31637G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125013574 | |||||||
| chr6:125013607 | G | C | 32 | a0001c0001t0003g0168 a0001c0001t0003g0171 a0001c0001t0003g0175 others(29): Show |
32 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.883-31604G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125013607 | |||||||
| chr6:125013942 | C | T | 3 | a0002c0002t0071g0037 a0009c0015t0053g0247 a0011c0011t0079g0035 |
3 | HG02922.hp1 HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.883-31269C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125013942 | |||||||
| chr6:125014111 | C | G | 2 | a0002c0002t0071g0037 a0009c0015t0053g0247 |
2 | HG02922.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.883-31100C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125014111 | |||||||
| chr6:125014243 | G | C | 1 | a0011c0011t0079g0035 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.883-30968G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125014243 | |||||||
| chr6:125014266 | G | A | 32 | a0001c0001t0003g0168 a0001c0001t0003g0171 a0001c0001t0003g0175 others(29): Show |
32 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.883-30945G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125014266 | |||||||
| chr6:125014307 | A | G | 1 | a0001c0001t0015g0206 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.883-30904A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125014307 | |||||||
| chr6:125014627 | C | T | 1 | a0001c0001t0005g0113 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.883-30584C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125014627 | |||||||
| chr6:125014772 | G | A | 1 | a0002c0002t0070g0038 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.883-30439G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125014772 | |||||||
| chr6:125014977 | G | A | 7 | a0001c0001t0006g0004 a0001c0001t0006g0190 a0001c0001t0017g0153 others(4): Show |
7 | HG01884.hp2 HG02486.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.883-30234G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125014977 | |||||||
| chr6:125015081 | A | T | 2 | a0001c0003t0013g0184 a0001c0003t0013g0185 |
2 | HG02559.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.883-30130A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125015081 | |||||||
| chr6:125015277 | G | C | 28 | a0001c0001t0003g0168 a0001c0001t0003g0171 a0001c0001t0003g0175 others(25): Show |
28 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.883-29934G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125015277 | |||||||
| chr6:125015340 | T | G | 1 | a0001c0001t0002g0163 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.883-29871T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125015340 | |||||||
| chr6:125015611 | C | T | 1 | a0001c0001t0025g0141 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.883-29600C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125015611 | |||||||
| chr6:125015653 | T | C | 159 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(156): Show |
161 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.883-29558T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125015653 | |||||||
| chr6:125015774 | A | G | 1 | a0001c0001t0014g0059 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.883-29437A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125015774 | |||||||
| chr6:125015984 | G | A | 3 | a0002c0002t0071g0037 a0009c0015t0053g0247 a0011c0011t0079g0035 |
3 | HG02922.hp1 HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.883-29227G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125015984 | |||||||
| chr6:125016021 | T | A | 1 | a0001c0001t0001g0068 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.883-29190T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125016021 | |||||||
| chr6:125016036 | T | C | 1 | a0002c0002t0070g0038 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.883-29175T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125016036 | |||||||
| chr6:125016179 | A | G | 1 | a0002c0002t0075g0039 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.883-29032A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125016179 | |||||||
| chr6:125016303 | G | A | 2 | a0002c0002t0075g0039 a0002c0002t0077g0033 |
2 | HG01934.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.883-28908G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125016303 | |||||||
| chr6:125016745 | G | T | 1 | a0001c0001t0005g0219 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.883-28466G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125016745 | |||||||
| chr6:125016830 | T | C | 1 | a0001c0001t0010g0144 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.883-28381T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125016830 | |||||||
| chr6:125016841 | T | A | 175 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0047 others(172): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.883-28370T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125016841 | |||||||
| chr6:125016956 | A | G | 3 | a0001c0003t0010g0265 a0002c0002t0071g0037 a0007c0009t0001g0264 |
3 | HG02922.hp2 HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.883-28255A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125016956 | |||||||
| chr6:125017164 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.883-28047C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125017164 | |||||||
| chr6:125017165 | A | T | 101 | a0001c0001t0001g0063 a0001c0001t0001g0083 a0001c0001t0001g0101 others(98): Show |
102 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(99): Show |
intron_variant | MODIFIER | c.883-28046A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125017165 | |||||||
| chr6:125017207 | C | T | 128 | a0001c0001t0001g0083 a0001c0001t0001g0101 a0001c0001t0001g0107 others(125): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.883-28004C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125017207 | |||||||
| chr6:125017418 | T | C | 194 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0047 others(191): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.883-27793T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125017418 | |||||||
| chr6:125017507 | G | A | 1 | a0001c0001t0022g0131 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.883-27704G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125017507 | |||||||
| chr6:125017853 | G | A | 2 | a0001c0001t0017g0100 a0001c0001t0041g0098 |
2 | HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.883-27358G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125017853 | |||||||
| chr6:125017957 | C | T | 1 | a0001c0001t0002g0054 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.883-27254C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125017957 | |||||||
| chr6:125018028 | G | A | 196 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0047 others(193): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.883-27183G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125018028 | |||||||
| chr6:125018123 | A | T | 1 | a0002c0002t0071g0037 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.883-27088A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125018123 | |||||||
| chr6:125018244 | T | C | 3 | a0001c0001t0006g0146 a0005c0007t0006g0094 a0005c0007t0021g0093 |
3 | HG01884.hp1 HG02109.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.883-26967T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125018244 | |||||||
| chr6:125018362 | C | T | 1 | a0009c0015t0053g0247 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.883-26849C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125018362 | |||||||
| chr6:125018813 | A | C | 1 | a0001c0001t0001g0227 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.883-26398A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125018813 | |||||||
| chr6:125018907 | G | C | 1 | a0001c0001t0001g0069 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.883-26304G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125018907 | |||||||
| chr6:125018920 | G | A | 1 | a0001c0001t0017g0253 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.883-26291G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125018920 | |||||||
| chr6:125019267 | T | G | 1 | a0001c0001t0004g0070 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.883-25944T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125019267 | |||||||
| chr6:125019269 | G | T | 1 | a0001c0001t0004g0070 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.883-25942G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125019269 | |||||||
| chr6:125019270 | T | A | 1 | a0001c0001t0004g0070 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.883-25941T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125019270 | |||||||
| chr6:125019308 | A | G | 1 | a0001c0001t0004g0242 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.883-25903A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125019308 | |||||||
| chr6:125019445 | C | T | 196 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0047 others(193): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.883-25766C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125019445 | |||||||
| chr6:125019503 | T | C | 203 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0047 others(200): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.883-25708T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125019503 | |||||||
| chr6:125019541 | T | G | 1 | a0002c0002t0009g0023 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.883-25670T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125019541 | |||||||
| chr6:125019692 | T | C | 2 | a0001c0001t0017g0100 a0001c0001t0041g0098 |
2 | HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.883-25519T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125019692 | |||||||
| chr6:125019830 | C | CG | 10 | a0001c0001t0001g0110 a0001c0001t0001g0210 a0001c0001t0001g0234 others(7): Show |
10 | HG01358.hp1 HG01433.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.883-25381_883-2538 others(5): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125019830 | |||||||
| chr6:125019831 | A | AG | 20 | a0001c0001t0001g0156 a0001c0001t0001g0208 a0001c0001t0001g0217 others(17): Show |
21 | HG00408.hp1 HG00408.hp2 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.883-25379dupG | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125019831 | ||||||
| chr6:125019831 | A | AGG | 6 | a0001c0001t0003g0254 a0001c0001t0006g0004 a0001c0001t0006g0190 others(3): Show |
6 | HG02486.hp1 HG02559.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.883-25379_883-2537 others(6): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125019831 | ||||||
| chr6:125019831 | A | G | 60 | a0001c0001t0001g0057 a0001c0001t0001g0083 a0001c0001t0001g0107 others(57): Show |
61 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.883-25380A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125019831 | |||||||
| chr6:125019833 | T | C | 3 | a0001c0001t0001g0208 a0001c0001t0005g0201 a0001c0001t0015g0206 |
3 | NA18983.hp2 NA19004.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.883-25378T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125019833 | |||||||
| chr6:125019833 | T | G | 238 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0047 others(235): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.883-25378T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125019833 | |||||||
| chr6:125019836 | G | C | 3 | a0001c0003t0010g0265 a0002c0002t0071g0037 a0007c0009t0001g0264 |
3 | HG02922.hp2 HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.883-25375G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125019836 | |||||||
| chr6:125019837 | G | C | 1 | a0001c0001t0001g0047 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.883-25374G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125019837 | |||||||
| chr6:125019843 | G | A | 1 | a0001c0001t0001g0071 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.883-25368G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125019843 | |||||||
| chr6:125020193 | G | A | 97 | a0001c0001t0001g0057 a0001c0001t0001g0083 a0001c0001t0001g0101 others(94): Show |
98 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
intron_variant | MODIFIER | c.883-25018G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125020193 | |||||||
| chr6:125020335 | A | G | 1 | a0001c0001t0023g0249 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.883-24876A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125020335 | |||||||
| chr6:125020373 | G | A | 1 | a0011c0011t0079g0035 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.883-24838G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125020373 | |||||||
| chr6:125020431 | T | G | 1 | a0001c0001t0061g0252 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.883-24780T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125020431 | |||||||
| chr6:125020935 | T | A | 1 | a0001c0001t0015g0206 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.883-24276T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125020935 | |||||||
| chr6:125020984 | A | G | 97 | a0001c0001t0001g0057 a0001c0001t0001g0083 a0001c0001t0001g0101 others(94): Show |
98 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
intron_variant | MODIFIER | c.883-24227A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125020984 | |||||||
| chr6:125021268 | CT | C | 126 | a0001c0001t0001g0049 a0001c0001t0001g0057 a0001c0001t0001g0083 others(123): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.883-23927delT | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125021268 | ||||||
| chr6:125021268 | CTT | C | 63 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0047 others(60): Show |
64 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.883-23928_883-2392 others(6): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125021268 | ||||||
| chr6:125021327 | C | T | 2 | a0001c0003t0008g0186 a0001c0003t0008g0187 |
2 | HG01243.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.883-23884C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125021327 | |||||||
| chr6:125021480 | T | C | 1 | a0001c0001t0001g0051 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.883-23731T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125021480 | |||||||
| chr6:125021481 | G | C | 1 | a0001c0001t0001g0051 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.883-23730G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125021481 | |||||||
| chr6:125021482 | G | T | 1 | a0001c0001t0001g0051 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.883-23729G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125021482 | |||||||
| chr6:125021512 | A | G | 138 | a0001c0001t0001g0057 a0001c0001t0001g0083 a0001c0001t0001g0101 others(135): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.883-23699A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125021512 | |||||||
| chr6:125021512 | A | T | 65 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0047 others(62): Show |
66 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.883-23699A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125021512 | |||||||
| chr6:125021565 | A | G | 203 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0047 others(200): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.883-23646A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125021565 | |||||||
| chr6:125021581 | A | G | 2 | a0002c0002t0013g0012 a0007c0009t0001g0193 |
2 | HG01106.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.883-23630A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125021581 | |||||||
| chr6:125021629 | G | A | 8 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(5): Show |
8 | HG00423.hp1 HG01243.hp2 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.883-23582G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125021629 | |||||||
| chr6:125021728 | C | A | 1 | a0001c0001t0012g0064 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.883-23483C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125021728 | |||||||
| chr6:125021748 | A | G | 14 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(11): Show |
14 | HG00099.hp2 HG00639.hp1 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.883-23463A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125021748 | |||||||
| chr6:125021854 | C | A | 2 | a0001c0001t0001g0199 a0001c0001t0005g0080 |
2 | HG01433.hp1 HG01928.hp1 |
intron_variant | MODIFIER | c.883-23357C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125021854 | |||||||
| chr6:125021959 | G | A | 2 | a0001c0001t0017g0100 a0001c0001t0041g0098 |
2 | HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.883-23252G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125021959 | |||||||
| chr6:125022139 | C | T | 6 | a0001c0001t0003g0254 a0001c0001t0006g0004 a0001c0001t0006g0190 others(3): Show |
6 | HG02486.hp1 HG02559.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.883-23072C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125022139 | |||||||
| chr6:125022381 | A | G | 3 | a0001c0003t0010g0265 a0002c0002t0071g0037 a0007c0009t0001g0264 |
3 | HG02922.hp2 HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.883-22830A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125022381 | |||||||
| chr6:125022389 | C | T | 3 | a0001c0003t0010g0265 a0002c0002t0071g0037 a0007c0009t0001g0264 |
3 | HG02922.hp2 HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.883-22822C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125022389 | |||||||
| chr6:125022451 | G | T | 96 | a0001c0001t0001g0057 a0001c0001t0001g0083 a0001c0001t0001g0101 others(93): Show |
97 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(94): Show |
intron_variant | MODIFIER | c.883-22760G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125022451 | |||||||
| chr6:125022717 | G | A | 6 | a0001c0001t0003g0254 a0001c0001t0006g0004 a0001c0001t0006g0190 others(3): Show |
6 | HG02486.hp1 HG02559.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.883-22494G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125022717 | |||||||
| chr6:125022992 | C | A | 202 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0047 others(199): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.883-22219C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125022992 | |||||||
| chr6:125023059 | T | C | 97 | a0001c0001t0001g0057 a0001c0001t0001g0083 a0001c0001t0001g0101 others(94): Show |
98 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
intron_variant | MODIFIER | c.883-22152T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125023059 | |||||||
| chr6:125023133 | C | T | 2 | a0001c0001t0010g0144 a0001c0001t0022g0131 |
2 | HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.883-22078C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125023133 | |||||||
| chr6:125023150 | T | G | 222 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0047 others(219): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.883-22061T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125023150 | |||||||
| chr6:125023367 | T | C | 22 | a0001c0001t0003g0168 a0001c0001t0003g0171 a0001c0001t0003g0175 others(19): Show |
23 | HG01257.hp1 HG01258.hp2 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.883-21844T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125023367 | |||||||
| chr6:125023409 | G | A | 222 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0047 others(219): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.883-21802G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125023409 | |||||||
| chr6:125023428 | G | T | 222 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0047 others(219): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.883-21783G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125023428 | |||||||
| chr6:125023678 | C | T | 2 | a0002c0002t0029g0006 a0002c0006t0013g0011 |
2 | NA19065.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.883-21533C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125023678 | |||||||
| chr6:125023754 | A | G | 1 | a0001c0001t0004g0045 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.883-21457A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125023754 | |||||||
| chr6:125023912 | G | C | 1 | a0001c0001t0005g0081 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.883-21299G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125023912 | |||||||
| chr6:125024228 | G | A | 1 | a0011c0011t0079g0035 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.883-20983G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125024228 | |||||||
| chr6:125024362 | C | T | 4 | a0001c0001t0001g0051 a0001c0001t0001g0063 a0001c0001t0002g0055 others(1): Show |
4 | NA18942.hp1 NA19057.hp2 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.883-20849C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125024362 | |||||||
| chr6:125024416 | C | T | 53 | a0001c0001t0001g0043 a0001c0001t0001g0050 a0001c0001t0001g0051 others(50): Show |
54 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.883-20795C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125024416 | |||||||
| chr6:125024492 | C | T | 112 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0047 others(109): Show |
114 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.883-20719C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125024492 | |||||||
| chr6:125024493 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.883-20718G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125024493 | |||||||
| chr6:125024584 | G | A | 1 | a0001c0001t0017g0253 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.883-20627G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125024584 | |||||||
| chr6:125024632 | A | G | 1 | a0001c0001t0003g0114 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.883-20579A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125024632 | |||||||
| chr6:125024635 | T | G | 19 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(16): Show |
19 | HG00099.hp2 HG00735.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.883-20576T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125024635 | |||||||
| chr6:125024706 | T | C | 1 | a0001c0001t0004g0075 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.883-20505T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125024706 | |||||||
| chr6:125024719 | C | CA | 10 | a0001c0001t0001g0243 a0001c0001t0003g0168 a0001c0001t0019g0238 others(7): Show |
10 | HG00741.hp1 HG00741.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.883-20471dupA | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125024719 | ||||||
| chr6:125024719 | CA | C | 84 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0049 others(81): Show |
85 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.883-20471delA | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125024719 | ||||||
| chr6:125024719 | CAA | C | 6 | a0001c0001t0003g0254 a0001c0001t0006g0190 a0001c0001t0010g0162 others(3): Show |
6 | HG01891.hp2 HG02559.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.883-20472_883-2047 others(6): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125024719 | ||||||
| chr6:125024721 | A | C | 1 | a0001c0001t0001g0199 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.883-20490A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125024721 | |||||||
| chr6:125024929 | G | C | 1 | a0001c0001t0002g0233 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.883-20282G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125024929 | |||||||
| chr6:125025038 | C | T | 20 | a0001c0001t0003g0168 a0001c0001t0003g0171 a0001c0001t0003g0175 others(17): Show |
21 | HG01257.hp1 HG01258.hp2 HG01346.hp1 others(18): Show |
intron_variant | MODIFIER | c.883-20173C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125025038 | |||||||
| chr6:125025367 | TTTTTTGT others(4): Show |
T | 2 | a0001c0001t0001g0156 a0003c0004t0011g0155 |
2 | HG00741.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.883-19839_883-1982 others(15): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125025367 | ||||||
| chr6:125025521 | G | C | 19 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(16): Show |
19 | HG00099.hp2 HG00735.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.883-19690G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125025521 | |||||||
| chr6:125025576 | A | AAGGG | 64 | a0001c0001t0001g0042 a0001c0001t0001g0156 a0001c0001t0001g0227 others(61): Show |
65 | HG00423.hp1 HG00741.hp1 HG01243.hp1 others(62): Show |
intron_variant | MODIFIER | c.883-19617_883-1961 others(8): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125025576 | ||||||
| chr6:125025666 | T | G | 144 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0047 others(141): Show |
146 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.883-19545T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125025666 | |||||||
| chr6:125025755 | AGGAG | A | 15 | a0001c0001t0001g0050 a0001c0001t0003g0168 a0001c0001t0003g0171 others(12): Show |
15 | HG01346.hp2 HG02055.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.883-19436_883-1943 others(8): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125025755 | ||||||
| chr6:125025802 | T | C | 6 | a0001c0001t0010g0144 a0001c0001t0017g0100 a0001c0001t0021g0132 others(3): Show |
6 | HG02622.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.883-19409T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125025802 | |||||||
| chr6:125025817 | T | C | 16 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(13): Show |
16 | HG00099.hp2 HG00735.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.883-19394T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125025817 | |||||||
| chr6:125025862 | C | T | 1 | a0001c0001t0003g0239 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.883-19349C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125025862 | |||||||
| chr6:125025877 | T | G | 1 | a0002c0002t0075g0039 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.883-19334T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125025877 | |||||||
| chr6:125025993 | C | T | 1 | a0001c0001t0001g0077 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.883-19218C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125025993 | |||||||
| chr6:125026353 | G | T | 19 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(16): Show |
19 | HG00099.hp2 HG00735.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.883-18858G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125026353 | |||||||
| chr6:125026533 | T | C | 5 | a0001c0001t0006g0173 a0001c0001t0008g0181 a0001c0001t0022g0179 others(2): Show |
5 | HG02055.hp2 HG02109.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-18678T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125026533 | |||||||
| chr6:125026545 | C | T | 1 | a0001c0001t0056g0111 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.883-18666C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125026545 | |||||||
| chr6:125026547 | T | A | 16 | a0001c0001t0003g0168 a0001c0001t0003g0171 a0001c0001t0003g0175 others(13): Show |
16 | HG02055.hp2 HG02109.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.883-18664T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125026547 | |||||||
| chr6:125026550 | C | T | 6 | a0001c0001t0010g0144 a0001c0001t0017g0100 a0001c0001t0021g0132 others(3): Show |
6 | HG02622.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.883-18661C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125026550 | |||||||
| chr6:125026656 | A | T | 244 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(241): Show |
247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.883-18555A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125026656 | |||||||
| chr6:125026702 | G | C | 1 | a0001c0001t0001g0107 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.883-18509G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125026702 | |||||||
| chr6:125026781 | A | G | 13 | a0001c0001t0001g0262 a0001c0001t0004g0182 a0001c0001t0004g0226 others(10): Show |
13 | HG00140.hp2 HG01192.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.883-18430A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125026781 | |||||||
| chr6:125026901 | A | C | 1 | a0001c0001t0003g0003 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.883-18310A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125026901 | |||||||
| chr6:125026911 | G | A | 6 | a0001c0001t0003g0254 a0001c0001t0006g0004 a0001c0001t0006g0190 others(3): Show |
6 | HG02486.hp1 HG02559.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.883-18300G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125026911 | |||||||
| chr6:125026918 | G | A | 2 | a0001c0001t0001g0230 a0001c0001t0002g0086 |
2 | HG00323.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.883-18293G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125026918 | |||||||
| chr6:125026944 | G | A | 1 | a0001c0001t0003g0114 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.883-18267G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125026944 | |||||||
| chr6:125026995 | A | T | 244 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(241): Show |
247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.883-18216A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125026995 | |||||||
| chr6:125027007 | C | T | 249 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(246): Show |
252 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.883-18204C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125027007 | |||||||
| chr6:125027033 | A | T | 1 | a0001c0012t0031g0255 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.883-18178A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125027033 | |||||||
| chr6:125027294 | C | T | 181 | a0001c0001t0001g0043 a0001c0001t0001g0046 a0001c0001t0001g0047 others(178): Show |
183 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.883-17917C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125027294 | |||||||
| chr6:125027300 | T | C | 244 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(241): Show |
247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.883-17911T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125027300 | |||||||
| chr6:125027352 | C | T | 14 | a0001c0001t0003g0168 a0001c0001t0003g0171 a0001c0001t0003g0175 others(11): Show |
14 | HG02055.hp2 HG02109.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.883-17859C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125027352 | |||||||
| chr6:125027578 | C | T | 1 | a0001c0001t0036g0231 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.883-17633C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125027578 | |||||||
| chr6:125027781 | A | G | 32 | a0001c0001t0001g0042 a0001c0001t0001g0227 a0001c0001t0001g0235 others(29): Show |
33 | HG00423.hp1 HG01243.hp1 HG01257.hp1 others(30): Show |
intron_variant | MODIFIER | c.883-17430A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125027781 | |||||||
| chr6:125027862 | C | T | 244 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(241): Show |
247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.883-17349C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125027862 | |||||||
| chr6:125027911 | G | A | 54 | a0001c0001t0001g0043 a0001c0001t0001g0047 a0001c0001t0001g0049 others(51): Show |
55 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.883-17300G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125027911 | |||||||
| chr6:125027958 | A | AT | 3 | a0001c0001t0026g0167 a0001c0001t0045g0160 a0001c0001t0046g0195 |
3 | HG03130.hp1 HG03486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.883-17247dupT | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125027958 | ||||||
| chr6:125028034 | A | G | 244 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(241): Show |
247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.883-17177A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125028034 | |||||||
| chr6:125028273 | C | T | 1 | a0001c0001t0005g0129 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.883-16938C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125028273 | |||||||
| chr6:125028315 | G | T | 2 | a0001c0001t0001g0156 a0003c0004t0011g0155 |
2 | HG00741.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.883-16896G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125028315 | |||||||
| chr6:125028361 | A | G | 1 | a0001c0001t0067g0198 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.883-16850A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125028361 | |||||||
| chr6:125028414 | C | T | 244 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(241): Show |
247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.883-16797C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125028414 | |||||||
| chr6:125028423 | A | G | 3 | a0001c0001t0026g0167 a0001c0001t0045g0160 a0001c0001t0046g0195 |
3 | HG03130.hp1 HG03486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.883-16788A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125028423 | |||||||
| chr6:125028630 | TA | T | 3 | a0001c0001t0006g0157 a0001c0003t0008g0130 a0001c0003t0008g0174 |
3 | HG03471.hp2 HG06807.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.883-16577delA | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125028630 | ||||||
| chr6:125028741 | T | G | 60 | a0001c0001t0001g0042 a0001c0001t0001g0227 a0001c0001t0002g0058 others(57): Show |
61 | HG00423.hp1 HG01243.hp1 HG01257.hp1 others(58): Show |
intron_variant | MODIFIER | c.883-16470T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125028741 | |||||||
| chr6:125028989 | A | G | 244 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(241): Show |
247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.883-16222A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125028989 | |||||||
| chr6:125029282 | C | T | 1 | a0001c0001t0010g0162 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.883-15929C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125029282 | |||||||
| chr6:125029286 | G | T | 183 | a0001c0001t0001g0043 a0001c0001t0001g0046 a0001c0001t0001g0047 others(180): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.883-15925G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125029286 | |||||||
| chr6:125029479 | G | A | 1 | a0001c0003t0008g0192 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.883-15732G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125029479 | |||||||
| chr6:125029542 | G | C | 1 | a0001c0001t0004g0241 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.883-15669G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125029542 | |||||||
| chr6:125029665 | A | G | 6 | a0001c0001t0006g0146 a0001c0001t0006g0190 a0001c0001t0039g0178 others(3): Show |
6 | HG01884.hp1 HG02109.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.883-15546A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125029665 | |||||||
| chr6:125029671 | T | A | 1 | a0001c0001t0021g0132 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.883-15540T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125029671 | |||||||
| chr6:125030028 | C | T | 4 | a0001c0001t0063g0090 a0002c0002t0029g0006 a0002c0006t0013g0011 others(1): Show |
4 | NA18970.hp2 NA19002.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.883-15183C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125030028 | |||||||
| chr6:125030032 | A | T | 2 | a0001c0003t0010g0265 a0007c0009t0001g0264 |
2 | HG02922.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.883-15179A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125030032 | |||||||
| chr6:125030052 | A | C | 2 | a0001c0001t0010g0144 a0001c0001t0022g0131 |
2 | HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.883-15159A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125030052 | |||||||
| chr6:125030070 | A | G | 23 | a0001c0001t0001g0262 a0001c0001t0003g0003 a0001c0001t0004g0154 others(20): Show |
24 | HG00140.hp2 HG01192.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.883-15141A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125030070 | |||||||
| chr6:125030075 | A | G | 1 | a0001c0001t0043g0005 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.883-15136A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125030075 | |||||||
| chr6:125030251 | G | T | 1 | a0001c0001t0002g0065 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.883-14960G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125030251 | |||||||
| chr6:125030356 | A | T | 1 | a0001c0001t0004g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.883-14855A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125030356 | |||||||
| chr6:125030516 | A | G | 2 | a0001c0001t0021g0132 a0001c0001t0033g0133 |
2 | HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.883-14695A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125030516 | |||||||
| chr6:125030765 | G | A | 10 | a0001c0001t0003g0168 a0001c0001t0003g0171 a0001c0001t0003g0175 others(7): Show |
10 | HG02109.hp1 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.883-14446G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125030765 | |||||||
| chr6:125030784 | T | A | 3 | a0001c0001t0010g0144 a0001c0001t0021g0132 a0001c0001t0033g0133 |
3 | HG02622.hp1 HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.883-14427T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125030784 | |||||||
| chr6:125030836 | GA | G | 3 | a0001c0001t0006g0146 a0005c0007t0006g0094 a0005c0007t0021g0093 |
3 | HG01884.hp1 HG02109.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.883-14374delA | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125030836 | |||||||
| chr6:125030848 | A | G | 10 | a0001c0001t0001g0151 a0001c0001t0001g0156 a0001c0001t0001g0218 others(7): Show |
10 | HG00741.hp1 HG01358.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.883-14363A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125030848 | |||||||
| chr6:125030891 | G | A | 2 | a0001c0003t0008g0130 a0001c0003t0008g0174 |
2 | HG03471.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.883-14320G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125030891 | |||||||
| chr6:125030912 | T | G | 1 | a0001c0001t0022g0041 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.883-14299T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125030912 | |||||||
| chr6:125031031 | C | T | 128 | a0001c0001t0001g0043 a0001c0001t0001g0047 a0001c0001t0001g0049 others(125): Show |
130 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.883-14180C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125031031 | |||||||
| chr6:125031086 | C | T | 62 | a0001c0001t0001g0042 a0001c0001t0001g0062 a0001c0001t0001g0069 others(59): Show |
63 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.883-14125C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125031086 | |||||||
| chr6:125031215 | G | A | 110 | a0001c0001t0001g0043 a0001c0001t0001g0047 a0001c0001t0001g0049 others(107): Show |
112 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.883-13996G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125031215 | |||||||
| chr6:125031244 | G | C | 236 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(233): Show |
239 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.883-13967G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125031244 | |||||||
| chr6:125031412 | C | T | 15 | a0001c0001t0001g0046 a0001c0001t0001g0240 a0001c0001t0002g0054 others(12): Show |
15 | HG01106.hp1 HG02055.hp1 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.883-13799C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125031412 | |||||||
| chr6:125031626 | T | A | 10 | a0001c0001t0001g0151 a0001c0001t0001g0156 a0001c0001t0001g0218 others(7): Show |
10 | HG00741.hp1 HG01358.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.883-13585T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125031626 | |||||||
| chr6:125031719 | A | G | 1 | a0007c0009t0001g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.883-13492A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125031719 | |||||||
| chr6:125031884 | T | G | 102 | a0001c0001t0001g0042 a0001c0001t0001g0046 a0001c0001t0001g0062 others(99): Show |
103 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(100): Show |
intron_variant | MODIFIER | c.883-13327T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125031884 | |||||||
| chr6:125031885 | T | C | 102 | a0001c0001t0001g0042 a0001c0001t0001g0046 a0001c0001t0001g0062 others(99): Show |
103 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(100): Show |
intron_variant | MODIFIER | c.883-13326T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125031885 | |||||||
| chr6:125031892 | A | G | 1 | a0001c0003t0008g0192 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.883-13319A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125031892 | |||||||
| chr6:125031943 | C | T | 1 | a0001c0001t0046g0195 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.883-13268C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125031943 | |||||||
| chr6:125031997 | A | G | 15 | a0001c0001t0001g0046 a0001c0001t0001g0240 a0001c0001t0002g0054 others(12): Show |
15 | HG01106.hp1 HG02055.hp1 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.883-13214A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125031997 | |||||||
| chr6:125032094 | C | T | 15 | a0001c0001t0001g0046 a0001c0001t0001g0240 a0001c0001t0002g0054 others(12): Show |
15 | HG01106.hp1 HG02055.hp1 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.883-13117C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125032094 | |||||||
| chr6:125032340 | A | G | 4 | a0001c0003t0008g0150 a0001c0003t0008g0186 a0001c0003t0008g0187 others(1): Show |
4 | HG01243.hp1 HG02280.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.883-12871A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125032340 | |||||||
| chr6:125032664 | A | G | 1 | a0001c0001t0005g0060 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.883-12547A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125032664 | |||||||
| chr6:125032812 | A | C | 2 | a0001c0001t0001g0209 a0001c0001t0001g0217 |
2 | HG00408.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.883-12399A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125032812 | |||||||
| chr6:125033008 | A | C | 137 | a0001c0001t0001g0043 a0001c0001t0001g0047 a0001c0001t0001g0049 others(134): Show |
139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.883-12203A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125033008 | |||||||
| chr6:125033106 | T | C | 15 | a0001c0001t0001g0046 a0001c0001t0001g0240 a0001c0001t0002g0054 others(12): Show |
15 | HG01106.hp1 HG02055.hp1 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.883-12105T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125033106 | |||||||
| chr6:125033128 | G | A | 15 | a0001c0001t0004g0154 a0001c0001t0004g0182 a0001c0001t0006g0004 others(12): Show |
15 | HG00140.hp2 HG02486.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.883-12083G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125033128 | |||||||
| chr6:125033221 | T | C | 137 | a0001c0001t0001g0043 a0001c0001t0001g0047 a0001c0001t0001g0049 others(134): Show |
139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.883-11990T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125033221 | |||||||
| chr6:125033444 | G | A | 1 | a0001c0001t0006g0263 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.883-11767G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125033444 | |||||||
| chr6:125033449 | G | GT | 56 | a0001c0001t0001g0042 a0001c0001t0001g0062 a0001c0001t0001g0069 others(53): Show |
57 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.883-11756dupT | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125033449 | ||||||
| chr6:125033505 | C | T | 78 | a0001c0001t0001g0042 a0001c0001t0001g0062 a0001c0001t0001g0069 others(75): Show |
79 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.883-11706C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125033505 | |||||||
| chr6:125033516 | A | G | 1 | a0001c0001t0012g0216 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.883-11695A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125033516 | |||||||
| chr6:125033571 | C | T | 68 | a0001c0001t0001g0042 a0001c0001t0001g0062 a0001c0001t0001g0069 others(65): Show |
69 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.883-11640C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125033571 | |||||||
| chr6:125033644 | G | A | 3 | a0001c0001t0026g0167 a0001c0001t0045g0160 a0001c0001t0046g0195 |
3 | HG03130.hp1 HG03486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.883-11567G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125033644 | |||||||
| chr6:125033646 | AATAAACA others(9): Show |
A | 1 | a0001c0003t0008g0192 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.883-11562_883-1154 others(20): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125033646 | ||||||
| chr6:125033655 | A | G | 1 | a0001c0001t0002g0248 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.883-11556A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125033655 | |||||||
| chr6:125033825 | T | C | 3 | a0001c0001t0001g0151 a0001c0001t0001g0218 a0001c0001t0004g0045 |
3 | HG01358.hp2 HG04228.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.883-11386T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125033825 | |||||||
| chr6:125033891 | G | C | 1 | a0001c0001t0002g0086 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.883-11320G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125033891 | |||||||
| chr6:125034150 | A | G | 1 | a0001c0001t0023g0249 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.883-11061A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125034150 | |||||||
| chr6:125034155 | T | C | 1 | a0001c0001t0023g0249 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.883-11056T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125034155 | |||||||
| chr6:125034229 | G | A | 1 | a0002c0002t0071g0037 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.883-10982G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125034229 | |||||||
| chr6:125034370 | G | A | 15 | a0001c0001t0001g0046 a0001c0001t0001g0240 a0001c0001t0002g0054 others(12): Show |
15 | HG01106.hp1 HG02055.hp1 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.883-10841G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125034370 | |||||||
| chr6:125034477 | G | C | 1 | a0001c0003t0008g0192 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.883-10734G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125034477 | |||||||
| chr6:125034513 | C | T | 54 | a0001c0001t0001g0042 a0001c0001t0001g0062 a0001c0001t0001g0069 others(51): Show |
55 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.883-10698C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125034513 | |||||||
| chr6:125034514 | G | A | 1 | a0001c0001t0002g0233 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.883-10697G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125034514 | |||||||
| chr6:125034515 | A | G | 23 | a0001c0001t0001g0046 a0001c0001t0001g0240 a0001c0001t0002g0054 others(20): Show |
23 | HG01106.hp1 HG01884.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.883-10696A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125034515 | |||||||
| chr6:125034604 | T | A | 5 | a0001c0001t0006g0004 a0001c0001t0021g0158 a0001c0001t0026g0159 others(2): Show |
5 | HG02486.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-10607T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125034604 | |||||||
| chr6:125034645 | G | T | 136 | a0001c0001t0001g0043 a0001c0001t0001g0047 a0001c0001t0001g0049 others(133): Show |
138 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.883-10566G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125034645 | |||||||
| chr6:125034764 | C | T | 1 | a0001c0003t0008g0192 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.883-10447C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125034764 | |||||||
| chr6:125034772 | A | G | 7 | a0001c0001t0006g0146 a0001c0001t0010g0162 a0001c0003t0010g0265 others(4): Show |
7 | HG01884.hp1 HG01891.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.883-10439A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125034772 | |||||||
| chr6:125034850 | G | C | 1 | a0001c0003t0008g0192 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.883-10361G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125034850 | |||||||
| chr6:125034894 | C | G | 1 | a0002c0002t0071g0037 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.883-10317C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125034894 | |||||||
| chr6:125034915 | C | A | 135 | a0001c0001t0001g0043 a0001c0001t0001g0047 a0001c0001t0001g0049 others(132): Show |
137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.883-10296C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125034915 | |||||||
| chr6:125035015 | T | C | 12 | a0001c0001t0003g0168 a0001c0001t0003g0171 a0001c0001t0003g0175 others(9): Show |
12 | HG02109.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.883-10196T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125035015 | |||||||
| chr6:125035022 | G | T | 1 | a0001c0001t0001g0243 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.883-10189G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125035022 | |||||||
| chr6:125035086 | G | A | 4 | a0001c0001t0003g0168 a0001c0001t0003g0175 a0001c0001t0003g0177 others(1): Show |
4 | HG02451.hp1 HG02572.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.883-10125G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125035086 | |||||||
| chr6:125035104 | C | T | 1 | a0001c0001t0010g0162 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.883-10107C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125035104 | |||||||
| chr6:125035247 | G | A | 15 | a0001c0001t0001g0046 a0001c0001t0001g0240 a0001c0001t0002g0054 others(12): Show |
15 | HG01106.hp1 HG02055.hp1 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.883-9964G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125035247 | |||||||
| chr6:125035501 | T | G | 1 | a0001c0001t0026g0167 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.883-9710T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125035501 | |||||||
| chr6:125035520 | T | C | 15 | a0001c0001t0001g0046 a0001c0001t0001g0240 a0001c0001t0002g0054 others(12): Show |
15 | HG01106.hp1 HG02055.hp1 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.883-9691T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125035520 | |||||||
| chr6:125035732 | T | C | 1 | a0002c0006t0078g0008 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.883-9479T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125035732 | |||||||
| chr6:125035755 | A | G | 15 | a0001c0001t0001g0046 a0001c0001t0001g0240 a0001c0001t0002g0054 others(12): Show |
15 | HG01106.hp1 HG02055.hp1 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.883-9456A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125035755 | |||||||
| chr6:125036129 | G | A | 4 | a0001c0001t0006g0157 a0001c0001t0048g0161 a0001c0003t0008g0130 others(1): Show |
4 | HG03041.hp2 HG03471.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.883-9082G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125036129 | |||||||
| chr6:125036371 | G | T | 1 | a0002c0002t0077g0033 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.883-8840G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125036371 | |||||||
| chr6:125036432 | G | A | 6 | a0001c0001t0001g0156 a0001c0001t0008g0181 a0001c0001t0017g0253 others(3): Show |
6 | HG00741.hp1 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.883-8779G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125036432 | |||||||
| chr6:125036496 | C | T | 15 | a0001c0001t0001g0046 a0001c0001t0001g0240 a0001c0001t0002g0054 others(12): Show |
15 | HG01106.hp1 HG02055.hp1 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.883-8715C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125036496 | |||||||
| chr6:125036523 | G | T | 1 | a0001c0001t0035g0139 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.883-8688G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125036523 | |||||||
| chr6:125036553 | A | G | 1 | a0001c0003t0008g0192 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.883-8658A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125036553 | |||||||
| chr6:125036660 | G | A | 1 | a0001c0001t0017g0153 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.883-8551G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125036660 | |||||||
| chr6:125036773 | G | A | 22 | a0001c0001t0001g0046 a0001c0001t0001g0240 a0001c0001t0002g0054 others(19): Show |
22 | HG01106.hp1 HG01884.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.883-8438G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125036773 | |||||||
| chr6:125036838 | C | T | 1 | a0001c0003t0008g0192 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.883-8373C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125036838 | |||||||
| chr6:125036844 | A | G | 54 | a0001c0001t0001g0042 a0001c0001t0001g0062 a0001c0001t0001g0069 others(51): Show |
55 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.883-8367A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125036844 | |||||||
| chr6:125036891 | T | G | 15 | a0001c0001t0001g0046 a0001c0001t0001g0240 a0001c0001t0002g0054 others(12): Show |
15 | HG01106.hp1 HG02055.hp1 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.883-8320T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125036891 | |||||||
| chr6:125036925 | A | C | 1 | a0001c0001t0004g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.883-8286A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125036925 | |||||||
| chr6:125036926 | G | A | 54 | a0001c0001t0001g0042 a0001c0001t0001g0062 a0001c0001t0001g0069 others(51): Show |
55 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.883-8285G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125036926 | |||||||
| chr6:125037037 | G | A | 1 | a0002c0002t0071g0037 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.883-8174G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125037037 | |||||||
| chr6:125037077 | GA | G | 15 | a0001c0001t0001g0046 a0001c0001t0001g0240 a0001c0001t0002g0054 others(12): Show |
15 | HG01106.hp1 HG02055.hp1 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.883-8121delA | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125037077 | ||||||
| chr6:125037181 | A | T | 1 | a0001c0001t0005g0080 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.883-8030A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125037181 | |||||||
| chr6:125037326 | C | G | 1 | a0001c0001t0001g0199 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.883-7885C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125037326 | |||||||
| chr6:125037541 | G | A | 1 | a0001c0003t0008g0192 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.883-7670G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125037541 | |||||||
| chr6:125037626 | G | T | 2 | a0001c0001t0005g0060 a0001c0001t0062g0196 |
2 | NA18988.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.883-7585G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125037626 | |||||||
| chr6:125037737 | A | T | 1 | a0001c0001t0019g0118 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.883-7474A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125037737 | |||||||
| chr6:125037767 | C | G | 10 | a0001c0001t0001g0151 a0001c0001t0001g0156 a0001c0001t0001g0218 others(7): Show |
10 | HG00741.hp1 HG01358.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.883-7444C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125037767 | |||||||
| chr6:125037953 | G | A | 16 | a0001c0001t0001g0046 a0001c0001t0001g0240 a0001c0001t0002g0054 others(13): Show |
16 | HG01106.hp1 HG02055.hp1 HG02132.hp1 others(13): Show |
intron_variant | MODIFIER | c.883-7258G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125037953 | |||||||
| chr6:125037955 | C | A | 16 | a0001c0001t0001g0046 a0001c0001t0001g0240 a0001c0001t0002g0054 others(13): Show |
16 | HG01106.hp1 HG02055.hp1 HG02132.hp1 others(13): Show |
intron_variant | MODIFIER | c.883-7256C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125037955 | |||||||
| chr6:125038242 | T | G | 255 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(252): Show |
258 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.883-6969T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125038242 | |||||||
| chr6:125038243 | T | A | 255 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(252): Show |
258 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.883-6968T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125038243 | |||||||
| chr6:125038547 | G | T | 5 | a0001c0001t0001g0062 a0001c0001t0001g0079 a0001c0001t0001g0199 others(2): Show |
5 | HG01928.hp1 HG01952.hp1 HG02080.hp1 others(2): Show |
intron_variant | MODIFIER | c.883-6664G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125038547 | |||||||
| chr6:125038739 | A | G | 1 | a0001c0001t0002g0066 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.883-6472A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125038739 | |||||||
| chr6:125038895 | G | A | 15 | a0001c0001t0001g0046 a0001c0001t0001g0240 a0001c0001t0002g0054 others(12): Show |
15 | HG01106.hp1 HG02055.hp1 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.883-6316G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125038895 | |||||||
| chr6:125039053 | A | C | 138 | a0001c0001t0001g0043 a0001c0001t0001g0047 a0001c0001t0001g0049 others(135): Show |
140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.883-6158A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125039053 | |||||||
| chr6:125039332 | A | G | 1 | a0001c0001t0022g0131 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.883-5879A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125039332 | |||||||
| chr6:125039443 | C | G | 1 | a0007c0009t0001g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.883-5768C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125039443 | |||||||
| chr6:125039516 | A | C | 236 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0046 others(233): Show |
239 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.883-5695A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125039516 | |||||||
| chr6:125039562 | A | G | 17 | a0001c0001t0001g0046 a0001c0001t0001g0240 a0001c0001t0002g0054 others(14): Show |
17 | HG01106.hp1 HG02055.hp1 HG02132.hp1 others(14): Show |
intron_variant | MODIFIER | c.883-5649A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125039562 | |||||||
| chr6:125039861 | C | T | 99 | a0001c0001t0001g0043 a0001c0001t0001g0047 a0001c0001t0001g0049 others(96): Show |
101 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.883-5350C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125039861 | |||||||
| chr6:125039908 | A | G | 1 | a0001c0001t0015g0251 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.883-5303A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125039908 | |||||||
| chr6:125040119 | T | A | 15 | a0001c0001t0001g0046 a0001c0001t0001g0240 a0001c0001t0002g0054 others(12): Show |
15 | HG01106.hp1 HG02055.hp1 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.883-5092T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125040119 | |||||||
| chr6:125040267 | C | T | 133 | a0001c0001t0001g0043 a0001c0001t0001g0047 a0001c0001t0001g0049 others(130): Show |
135 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.883-4944C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125040267 | |||||||
| chr6:125040406 | C | T | 3 | a0001c0001t0010g0144 a0001c0001t0021g0132 a0001c0001t0033g0133 |
3 | HG02622.hp1 HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.883-4805C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125040406 | |||||||
| chr6:125040422 | C | T | 1 | a0001c0001t0005g0207 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.883-4789C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125040422 | |||||||
| chr6:125040734 | A | G | 1 | a0001c0001t0022g0179 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.883-4477A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125040734 | |||||||
| chr6:125040938 | A | G | 1 | a0001c0003t0008g0192 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.883-4273A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125040938 | |||||||
| chr6:125040964 | A | T | 1 | a0002c0006t0013g0011 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.883-4247A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125040964 | |||||||
| chr6:125040967 | A | G | 1 | a0007c0009t0001g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.883-4244A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125040967 | |||||||
| chr6:125041047 | T | C | 10 | a0001c0001t0001g0151 a0001c0001t0001g0156 a0001c0001t0001g0218 others(7): Show |
10 | HG00741.hp1 HG01358.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.883-4164T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125041047 | |||||||
| chr6:125041395 | C | G | 1 | a0001c0003t0008g0192 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.883-3816C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125041395 | |||||||
| chr6:125041414 | A | T | 1 | a0001c0001t0005g0129 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.883-3797A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125041414 | |||||||
| chr6:125041437 | A | G | 15 | a0001c0001t0001g0046 a0001c0001t0001g0240 a0001c0001t0002g0054 others(12): Show |
15 | HG01106.hp1 HG02055.hp1 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.883-3774A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125041437 | |||||||
| chr6:125041478 | T | C | 1 | a0001c0001t0015g0044 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.883-3733T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125041478 | |||||||
| chr6:125041583 | C | T | 1 | a0001c0001t0062g0196 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.883-3628C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125041583 | |||||||
| chr6:125042454 | A | T | 1 | a0001c0003t0008g0192 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.883-2757A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125042454 | |||||||
| chr6:125042557 | T | C | 1 | a0001c0001t0004g0116 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.883-2654T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125042557 | |||||||
| chr6:125042744 | C | A | 21 | a0001c0001t0001g0046 a0001c0001t0001g0240 a0001c0001t0002g0054 others(18): Show |
21 | HG01106.hp1 HG01884.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.883-2467C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125042744 | |||||||
| chr6:125042927 | T | G | 12 | a0001c0001t0003g0168 a0001c0001t0003g0171 a0001c0001t0003g0175 others(9): Show |
12 | HG02109.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.883-2284T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125042927 | |||||||
| chr6:125042993 | A | C | 1 | a0002c0002t0009g0001 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.883-2218A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125042993 | |||||||
| chr6:125043056 | T | C | 7 | a0001c0001t0001g0156 a0001c0001t0008g0181 a0001c0001t0017g0253 others(4): Show |
7 | HG00741.hp1 HG01891.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.883-2155T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125043056 | |||||||
| chr6:125043388 | G | A | 1 | a0001c0001t0052g0048 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.883-1823G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125043388 | |||||||
| chr6:125043412 | A | G | 1 | a0002c0002t0071g0037 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.883-1799A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125043412 | |||||||
| chr6:125043504 | C | G | 2 | a0001c0001t0001g0230 a0002c0002t0009g0024 |
2 | HG00323.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.883-1707C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125043504 | |||||||
| chr6:125043561 | A | G | 1 | a0001c0001t0012g0125 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.883-1650A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125043561 | |||||||
| chr6:125043712 | G | A | 4 | a0001c0001t0002g0085 a0002c0002t0007g0026 a0002c0002t0009g0023 others(1): Show |
4 | HG01981.hp2 HG03669.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.883-1499G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125043712 | |||||||
| chr6:125043859 | A | G | 135 | a0001c0001t0001g0043 a0001c0001t0001g0047 a0001c0001t0001g0049 others(132): Show |
137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.883-1352A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125043859 | |||||||
| chr6:125043959 | A | G | 1 | a0001c0001t0019g0238 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.883-1252A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125043959 | |||||||
| chr6:125044058 | GT | G | 139 | a0001c0001t0001g0043 a0001c0001t0001g0047 a0001c0001t0001g0049 others(136): Show |
141 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.883-1142delT | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125044058 | ||||||
| chr6:125044149 | C | T | 132 | a0001c0001t0001g0043 a0001c0001t0001g0047 a0001c0001t0001g0049 others(129): Show |
134 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.883-1062C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125044149 | |||||||
| chr6:125044327 | C | T | 129 | a0001c0001t0001g0043 a0001c0001t0001g0047 a0001c0001t0001g0049 others(126): Show |
130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.883-884C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125044327 | |||||||
| chr6:125044402 | T | C | 3 | a0001c0001t0001g0156 a0001c0001t0008g0181 a0001c0001t0022g0179 |
3 | HG01891.hp1 HG02055.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.883-809T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125044402 | |||||||
| chr6:125044486 | T | G | 78 | a0001c0001t0001g0042 a0001c0001t0001g0057 a0001c0001t0001g0062 others(75): Show |
80 | HG00408.hp1 HG00408.hp2 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.883-725T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125044486 | |||||||
| chr6:125044502 | A | T | 151 | a0001c0001t0001g0043 a0001c0001t0001g0047 a0001c0001t0001g0049 others(148): Show |
152 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.883-709A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125044502 | |||||||
| chr6:125044541 | A | T | 1 | a0001c0001t0041g0098 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.883-670A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125044541 | |||||||
| chr6:125044620 | G | T | 126 | a0001c0001t0001g0043 a0001c0001t0001g0047 a0001c0001t0001g0049 others(123): Show |
127 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.883-591G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125044620 | |||||||
| chr6:125044716 | A | G | 1 | a0001c0001t0068g0244 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.883-495A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125044716 | |||||||
| chr6:125045143 | C | CA | 18 | a0001c0001t0001g0046 a0001c0001t0001g0208 a0001c0001t0002g0054 others(15): Show |
18 | HG01106.hp1 HG02056.hp1 HG02132.hp1 others(15): Show |
intron_variant | MODIFIER | c.883-57dupA | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125045143 | ||||||
| chr6:125045143 | CA | C | 72 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0057 others(69): Show |
74 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.883-57delA | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 125045143 | ||||||
| chr6:125045179 | T | G | 1 | a0001c0001t0054g0180 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.883-32T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 1/5 | chr6 | 125045179 | |||||||
| chr6:125045784 | T | C | 13 | a0001c0001t0001g0056 a0001c0001t0001g0103 a0001c0001t0001g0104 others(10): Show |
13 | HG01243.hp2 HG01261.hp1 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.1116+340T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125045784 | |||||||
| chr6:125045955 | G | A | 69 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0057 others(66): Show |
71 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.1116+511G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125045955 | |||||||
| chr6:125046237 | G | A | 3 | a0001c0001t0001g0083 a0001c0001t0001g0124 a0001c0001t0012g0125 |
3 | HG00140.hp1 HG02486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1116+793G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125046237 | |||||||
| chr6:125046277 | G | A | 1 | a0001c0001t0002g0055 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1116+833G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125046277 | |||||||
| chr6:125046307 | A | G | 1 | a0001c0001t0002g0220 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1116+863A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125046307 | |||||||
| chr6:125046510 | C | G | 11 | a0001c0001t0003g0168 a0001c0001t0003g0171 a0001c0001t0003g0175 others(8): Show |
11 | HG02109.hp1 HG02280.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1116+1066C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125046510 | |||||||
| chr6:125046647 | T | C | 1 | a0001c0001t0016g0221 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1116+1203T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125046647 | |||||||
| chr6:125046727 | G | A | 1 | a0002c0002t0007g0022 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1116+1283G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125046727 | |||||||
| chr6:125046854 | T | G | 1 | a0002c0006t0078g0008 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1116+1410T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125046854 | |||||||
| chr6:125046857 | C | T | 90 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0050 others(87): Show |
91 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.1116+1413C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125046857 | |||||||
| chr6:125047134 | G | A | 71 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0057 others(68): Show |
73 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.1116+1690G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125047134 | |||||||
| chr6:125047265 | T | C | 3 | a0001c0001t0006g0146 a0005c0007t0006g0094 a0005c0007t0021g0093 |
3 | HG01884.hp1 HG02109.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1116+1821T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125047265 | |||||||
| chr6:125047278 | T | C | 3 | a0001c0001t0006g0146 a0005c0007t0006g0094 a0005c0007t0021g0093 |
3 | HG01884.hp1 HG02109.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1116+1834T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125047278 | |||||||
| chr6:125047320 | T | C | 1 | a0001c0001t0001g0083 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1116+1876T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125047320 | |||||||
| chr6:125047328 | G | A | 70 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0057 others(67): Show |
72 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.1116+1884G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125047328 | |||||||
| chr6:125047502 | G | A | 13 | a0001c0001t0001g0046 a0001c0001t0002g0054 a0001c0001t0010g0144 others(10): Show |
13 | HG01106.hp1 HG02056.hp1 HG02132.hp1 others(10): Show |
intron_variant | MODIFIER | c.1116+2058G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125047502 | |||||||
| chr6:125047532 | T | A | 1 | a0001c0001t0004g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1116+2088T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125047532 | |||||||
| chr6:125047532 | T | G | 27 | a0001c0001t0003g0254 a0001c0001t0004g0182 a0001c0001t0006g0004 others(24): Show |
27 | HG00140.hp2 HG00741.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.1116+2088T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125047532 | |||||||
| chr6:125047563 | G | A | 69 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0057 others(66): Show |
71 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.1116+2119G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125047563 | |||||||
| chr6:125047610 | T | C | 1 | a0001c0001t0001g0156 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1116+2166T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125047610 | |||||||
| chr6:125048216 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1116+2772C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125048216 | |||||||
| chr6:125048466 | A | T | 3 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 |
3 | HG01243.hp2 HG01934.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.1116+3022A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125048466 | |||||||
| chr6:125048528 | T | C | 68 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0057 others(65): Show |
69 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.1116+3084T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125048528 | |||||||
| chr6:125048552 | T | C | 1 | a0001c0001t0001g0262 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1116+3108T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125048552 | |||||||
| chr6:125048590 | T | C | 1 | a0002c0002t0009g0001 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1116+3146T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125048590 | |||||||
| chr6:125048608 | G | A | 11 | a0001c0001t0003g0168 a0001c0001t0003g0171 a0001c0001t0003g0175 others(8): Show |
11 | HG02109.hp1 HG02280.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1116+3164G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125048608 | |||||||
| chr6:125048650 | GAGTA | G | 3 | a0001c0001t0006g0176 a0001c0001t0010g0162 a0001c0001t0045g0160 |
3 | HG01891.hp2 HG02630.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1116+3210_1116+321 others(8): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 125048650 | ||||||
| chr6:125048720 | C | T | 1 | a0001c0008t0003g0002 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1116+3276C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125048720 | |||||||
| chr6:125048891 | C | T | 9 | a0001c0001t0003g0168 a0001c0001t0003g0171 a0001c0001t0003g0175 others(6): Show |
9 | HG02109.hp1 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1116+3447C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125048891 | |||||||
| chr6:125049115 | G | A | 1 | a0001c0001t0010g0194 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1116+3671G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125049115 | |||||||
| chr6:125049480 | T | C | 117 | a0001c0001t0001g0043 a0001c0001t0001g0057 a0001c0001t0001g0069 others(114): Show |
120 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.1116+4036T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125049480 | |||||||
| chr6:125049572 | G | A | 1 | a0001c0001t0002g0065 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1116+4128G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125049572 | |||||||
| chr6:125049643 | CACACATA others(22): Show |
C | 34 | a0001c0001t0001g0156 a0001c0001t0001g0208 a0001c0001t0001g0243 others(31): Show |
34 | HG00741.hp1 HG01884.hp1 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.1116+4200_1116+422 others(33): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125049643 | |||||||
| chr6:125049658 | C | G | 1 | a0001c0001t0001g0063 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1116+4214C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125049658 | |||||||
| chr6:125049706 | T | C | 56 | a0001c0001t0001g0156 a0001c0001t0001g0208 a0001c0001t0001g0243 others(53): Show |
56 | HG00741.hp1 HG01106.hp1 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.1116+4262T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125049706 | |||||||
| chr6:125049765 | A | G | 27 | a0001c0001t0002g0065 a0001c0001t0003g0171 a0001c0001t0004g0226 others(24): Show |
27 | HG00735.hp1 HG00741.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.1116+4321A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125049765 | |||||||
| chr6:125049791 | A | G | 6 | a0001c0001t0001g0083 a0001c0001t0025g0141 a0001c0001t0025g0164 others(3): Show |
6 | HG00140.hp2 HG00741.hp2 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.1116+4347A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125049791 | |||||||
| chr6:125049839 | A | G | 13 | a0001c0001t0006g0176 a0001c0001t0006g0250 a0001c0001t0010g0194 others(10): Show |
13 | HG01884.hp2 HG02630.hp2 HG03041.hp2 others(10): Show |
intron_variant | MODIFIER | c.1116+4395A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125049839 | |||||||
| chr6:125049851 | G | A | 2 | a0001c0001t0010g0162 a0011c0011t0079g0035 |
2 | HG01891.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1116+4407G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125049851 | |||||||
| chr6:125049883 | T | C | 1 | a0001c0001t0008g0181 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1116+4439T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125049883 | |||||||
| chr6:125049885 | A | C | 1 | a0001c0003t0008g0192 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1116+4441A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125049885 | |||||||
| chr6:125050155 | G | A | 36 | a0001c0001t0003g0171 a0001c0001t0003g0254 a0001c0001t0004g0075 others(33): Show |
36 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(33): Show |
intron_variant | MODIFIER | c.1116+4711G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125050155 | |||||||
| chr6:125050157 | G | A | 7 | a0001c0001t0017g0100 a0001c0001t0017g0153 a0001c0001t0017g0253 others(4): Show |
7 | HG01884.hp2 HG02258.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1116+4713G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125050157 | |||||||
| chr6:125050184 | G | T | 95 | a0001c0001t0001g0134 a0001c0001t0001g0136 a0001c0001t0001g0156 others(92): Show |
96 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.1116+4740G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125050184 | |||||||
| chr6:125050187 | T | G | 95 | a0001c0001t0001g0134 a0001c0001t0001g0136 a0001c0001t0001g0156 others(92): Show |
96 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.1116+4743T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125050187 | |||||||
| chr6:125050317 | C | T | 17 | a0001c0001t0004g0075 a0001c0001t0004g0122 a0001c0001t0034g0145 others(14): Show |
18 | HG01243.hp1 HG02280.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.1116+4873C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125050317 | |||||||
| chr6:125050320 | C | T | 1 | a0002c0002t0071g0037 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1116+4876C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125050320 | |||||||
| chr6:125050473 | A | C | 3 | a0001c0001t0023g0249 a0001c0001t0043g0005 a0001c0001t0068g0244 |
3 | HG02486.hp1 HG03098.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1116+5029A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125050473 | |||||||
| chr6:125050478 | C | T | 12 | a0002c0002t0070g0038 a0003c0004t0011g0148 a0003c0004t0011g0149 others(9): Show |
12 | HG00741.hp1 HG02055.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1116+5034C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125050478 | |||||||
| chr6:125050517 | A | G | 3 | a0001c0001t0008g0181 a0001c0001t0022g0131 a0001c0001t0022g0179 |
3 | HG02055.hp2 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1116+5073A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125050517 | |||||||
| chr6:125050654 | A | G | 13 | a0001c0001t0010g0194 a0002c0002t0070g0038 a0003c0004t0011g0148 others(10): Show |
13 | HG00741.hp1 HG02055.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1116+5210A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125050654 | |||||||
| chr6:125050669 | A | G | 1 | a0001c0001t0005g0215 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1116+5225A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125050669 | |||||||
| chr6:125050985 | A | G | 153 | a0001c0001t0001g0046 a0001c0001t0001g0101 a0001c0001t0001g0134 others(150): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.1116+5541A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125050985 | |||||||
| chr6:125051054 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1116+5610G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125051054 | |||||||
| chr6:125051280 | T | C | 121 | a0001c0001t0001g0046 a0001c0001t0001g0101 a0001c0001t0001g0208 others(118): Show |
124 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(121): Show |
intron_variant | MODIFIER | c.1116+5836T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125051280 | |||||||
| chr6:125051441 | A | G | 3 | a0001c0001t0019g0076 a0001c0001t0019g0118 a0001c0001t0019g0238 |
3 | HG02056.hp1 NA18971.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.1116+5997A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125051441 | |||||||
| chr6:125051721 | T | A | 1 | a0001c0001t0036g0231 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1117-6221T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125051721 | |||||||
| chr6:125051756 | T | C | 10 | a0003c0004t0011g0148 a0003c0004t0011g0149 a0003c0004t0011g0155 others(7): Show |
10 | HG00741.hp1 HG02055.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1117-6186T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125051756 | |||||||
| chr6:125051891 | C | T | 1 | a0001c0001t0054g0180 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1117-6051C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125051891 | |||||||
| chr6:125051920 | C | T | 9 | a0001c0001t0001g0050 a0001c0001t0001g0056 a0001c0001t0001g0068 others(6): Show |
9 | HG01255.hp1 HG01261.hp1 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.1117-6022C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125051920 | |||||||
| chr6:125052284 | T | G | 3 | a0001c0001t0008g0181 a0001c0001t0022g0131 a0001c0001t0022g0179 |
3 | HG02055.hp2 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1117-5658T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125052284 | |||||||
| chr6:125052284 | T | TTG | 8 | a0001c0001t0001g0046 a0001c0001t0001g0051 a0001c0001t0002g0086 others(5): Show |
8 | HG01981.hp1 HG02523.hp1 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.1117-5623_1117-562 others(6): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 125052284 | ||||||
| chr6:125052284 | T | TTGTG | 11 | a0001c0001t0004g0182 a0001c0001t0014g0059 a0001c0001t0024g0169 others(8): Show |
11 | HG00140.hp2 HG00741.hp2 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.1117-5625_1117-562 others(8): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 125052284 | ||||||
| chr6:125052284 | T | TTGTGTG | 7 | a0001c0001t0003g0003 a0001c0001t0003g0114 a0001c0001t0003g0197 others(4): Show |
8 | HG00735.hp2 HG02970.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.1117-5627_1117-562 others(10): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 125052284 | ||||||
| chr6:125052284 | T | TTGTGTGT others(1): Show |
19 | a0001c0001t0003g0168 a0001c0001t0003g0171 a0001c0001t0003g0175 others(16): Show |
19 | HG01891.hp2 HG02055.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1117-5629_1117-562 others(12): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 125052284 | ||||||
| chr6:125052284 | T | TTGTGTGT others(3): Show |
12 | a0001c0001t0010g0144 a0001c0001t0021g0132 a0001c0001t0021g0158 others(9): Show |
12 | HG00741.hp1 HG02083.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1117-5631_1117-562 others(14): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 125052284 | ||||||
| chr6:125052284 | T | TTGTGTGT others(5): Show |
1 | a0001c0001t0039g0178 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1117-5633_1117-562 others(16): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 125052284 | ||||||
| chr6:125052284 | T | TTGTGTGT others(7): Show |
2 | a0001c0001t0010g0152 a0011c0011t0079g0035 |
2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1117-5635_1117-562 others(18): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 125052284 | ||||||
| chr6:125052288 | G | A | 10 | a0001c0001t0003g0254 a0001c0001t0006g0004 a0001c0001t0006g0146 others(7): Show |
10 | HG01884.hp1 HG02109.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1117-5654G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125052288 | |||||||
| chr6:125052292 | G | GTA | 3 | a0001c0001t0008g0181 a0001c0001t0022g0131 a0001c0001t0022g0179 |
3 | HG02055.hp2 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1117-5649_1117-564 others(6): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 125052292 | ||||||
| chr6:125052306 | GTGTGTGT others(2): Show |
G | 19 | a0001c0001t0034g0145 a0001c0003t0008g0130 a0001c0003t0008g0174 others(16): Show |
20 | HG00639.hp1 HG01243.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.1117-5635_1117-562 others(13): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125052306 | |||||||
| chr6:125052318 | G | T | 20 | a0001c0001t0034g0145 a0001c0003t0008g0130 a0001c0003t0008g0150 others(17): Show |
21 | HG00639.hp1 HG01243.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.1117-5624G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125052318 | |||||||
| chr6:125052320 | G | GTGTGTGT | 3 | a0001c0001t0017g0253 a0001c0001t0045g0160 a0001c0001t0051g0172 |
3 | HG02258.hp2 HG02809.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1117-5622_1117-562 others(11): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125052320 | |||||||
| chr6:125052320 | G | GTGTGTGT others(2): Show |
7 | a0001c0001t0003g0254 a0001c0001t0006g0004 a0001c0001t0006g0146 others(4): Show |
7 | HG01884.hp1 HG02109.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1117-5622_1117-562 others(13): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125052320 | |||||||
| chr6:125052320 | G | GTGTGTGT others(6): Show |
1 | a0002c0002t0071g0037 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1117-5622_1117-562 others(17): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125052320 | |||||||
| chr6:125052320 | G | T | 20 | a0001c0001t0034g0145 a0001c0003t0008g0130 a0001c0003t0008g0150 others(17): Show |
21 | HG00639.hp1 HG01243.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.1117-5622G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125052320 | |||||||
| chr6:125052321 | G | A | 20 | a0001c0001t0034g0145 a0001c0003t0008g0130 a0001c0003t0008g0150 others(17): Show |
21 | HG00639.hp1 HG01243.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.1117-5621G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125052321 | |||||||
| chr6:125052321 | G | T | 1 | a0002c0002t0073g0029 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1117-5621G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125052321 | |||||||
| chr6:125052323 | T | G | 17 | a0001c0001t0003g0254 a0001c0001t0006g0004 a0001c0001t0006g0146 others(14): Show |
17 | HG01884.hp1 HG01884.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1117-5619T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125052323 | |||||||
| chr6:125052325 | T | G | 38 | a0001c0001t0003g0254 a0001c0001t0006g0004 a0001c0001t0006g0146 others(35): Show |
39 | HG00639.hp1 HG01243.hp1 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.1117-5617T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125052325 | |||||||
| chr6:125052326 | A | ATTTGTTT others(3): Show |
16 | a0001c0001t0008g0181 a0001c0001t0010g0194 a0001c0001t0022g0131 others(13): Show |
16 | HG00741.hp1 HG02055.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.1117-5596_1117-558 others(14): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 125052326 | ||||||
| chr6:125052326 | A | G | 17 | a0001c0001t0003g0254 a0001c0001t0006g0004 a0001c0001t0006g0146 others(14): Show |
17 | HG01884.hp1 HG01884.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1117-5616A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125052326 | |||||||
| chr6:125052326 | A | T | 21 | a0001c0001t0034g0145 a0001c0003t0008g0130 a0001c0003t0008g0150 others(18): Show |
22 | HG00639.hp1 HG01243.hp1 HG02280.hp1 others(19): Show |
intron_variant | MODIFIER | c.1117-5616A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125052326 | |||||||
| chr6:125052330 | G | T | 17 | a0001c0001t0003g0254 a0001c0001t0006g0004 a0001c0001t0006g0146 others(14): Show |
17 | HG01884.hp1 HG01884.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1117-5612G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125052330 | |||||||
| chr6:125052331 | T | A | 17 | a0001c0001t0003g0254 a0001c0001t0006g0004 a0001c0001t0006g0146 others(14): Show |
17 | HG01884.hp1 HG01884.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1117-5611T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125052331 | |||||||
| chr6:125052517 | G | T | 3 | a0001c0001t0008g0181 a0001c0001t0022g0131 a0001c0001t0022g0179 |
3 | HG02055.hp2 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1117-5425G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125052517 | |||||||
| chr6:125052715 | A | G | 2 | a0001c0001t0045g0160 a0002c0002t0071g0037 |
2 | HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1117-5227A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125052715 | |||||||
| chr6:125052926 | A | C | 3 | a0001c0001t0012g0061 a0001c0001t0012g0200 a0001c0001t0012g0216 |
3 | HG01981.hp1 HG02735.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1117-5016A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125052926 | |||||||
| chr6:125053092 | C | A | 1 | a0001c0001t0004g0241 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1117-4850C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125053092 | |||||||
| chr6:125053210 | T | G | 12 | a0001c0001t0003g0254 a0001c0001t0006g0004 a0001c0001t0006g0146 others(9): Show |
12 | HG01884.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1117-4732T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125053210 | |||||||
| chr6:125053320 | A | G | 132 | a0001c0001t0001g0046 a0001c0001t0001g0101 a0001c0001t0001g0134 others(129): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.1117-4622A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125053320 | |||||||
| chr6:125053473 | A | G | 3 | a0001c0001t0008g0181 a0001c0001t0022g0131 a0001c0001t0022g0179 |
3 | HG02055.hp2 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1117-4469A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125053473 | |||||||
| chr6:125053636 | TC | T | 13 | a0001c0001t0010g0194 a0002c0002t0070g0038 a0003c0004t0011g0148 others(10): Show |
13 | HG00741.hp1 HG02055.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1117-4304delC | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 125053636 | ||||||
| chr6:125053644 | C | T | 13 | a0001c0001t0010g0194 a0002c0002t0070g0038 a0003c0004t0011g0148 others(10): Show |
13 | HG00741.hp1 HG02055.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1117-4298C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125053644 | |||||||
| chr6:125053674 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1117-4268A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125053674 | |||||||
| chr6:125053730 | G | A | 5 | a0001c0001t0021g0158 a0001c0001t0026g0159 a0001c0001t0026g0167 others(2): Show |
5 | HG02809.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1117-4212G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125053730 | |||||||
| chr6:125053883 | C | T | 12 | a0001c0001t0003g0003 a0001c0001t0003g0114 a0001c0001t0003g0168 others(9): Show |
13 | HG00735.hp2 HG02083.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1117-4059C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125053883 | |||||||
| chr6:125054124 | G | A | 15 | a0001c0001t0001g0134 a0001c0001t0001g0136 a0001c0001t0002g0065 others(12): Show |
15 | HG00099.hp2 HG00140.hp1 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.1117-3818G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125054124 | |||||||
| chr6:125054151 | T | C | 13 | a0001c0001t0010g0194 a0002c0002t0070g0038 a0003c0004t0011g0148 others(10): Show |
13 | HG00741.hp1 HG02055.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1117-3791T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125054151 | |||||||
| chr6:125054333 | G | A | 13 | a0001c0001t0010g0194 a0002c0002t0070g0038 a0003c0004t0011g0148 others(10): Show |
13 | HG00741.hp1 HG02055.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1117-3609G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125054333 | |||||||
| chr6:125054343 | G | A | 1 | a0002c0002t0071g0037 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1117-3599G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125054343 | |||||||
| chr6:125054346 | G | A | 1 | a0001c0001t0010g0194 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1117-3596G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125054346 | |||||||
| chr6:125054366 | C | A | 1 | a0001c0001t0004g0045 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1117-3576C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125054366 | |||||||
| chr6:125054414 | C | G | 10 | a0001c0001t0017g0100 a0001c0001t0017g0153 a0001c0001t0017g0253 others(7): Show |
10 | HG01884.hp2 HG02258.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1117-3528C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125054414 | |||||||
| chr6:125054603 | A | G | 3 | a0001c0001t0008g0181 a0001c0001t0022g0131 a0001c0001t0022g0179 |
3 | HG02055.hp2 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1117-3339A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125054603 | |||||||
| chr6:125054755 | T | C | 1 | a0001c0001t0069g0117 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1117-3187T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125054755 | |||||||
| chr6:125054869 | C | A | 5 | a0001c0001t0021g0158 a0001c0001t0026g0159 a0001c0001t0026g0167 others(2): Show |
5 | HG02809.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1117-3073C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125054869 | |||||||
| chr6:125054955 | T | A | 2 | a0001c0001t0001g0109 a0001c0001t0001g0209 |
2 | HG00609.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1117-2987T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125054955 | |||||||
| chr6:125054956 | A | C | 95 | a0001c0001t0001g0046 a0001c0001t0001g0101 a0001c0001t0001g0208 others(92): Show |
96 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.1117-2986A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125054956 | |||||||
| chr6:125054958 | G | A | 3 | a0001c0001t0008g0181 a0001c0001t0022g0131 a0001c0001t0022g0179 |
3 | HG02055.hp2 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1117-2984G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125054958 | |||||||
| chr6:125055265 | C | T | 13 | a0001c0001t0010g0194 a0002c0002t0070g0038 a0003c0004t0011g0148 others(10): Show |
13 | HG00741.hp1 HG02055.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1117-2677C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125055265 | |||||||
| chr6:125055353 | T | C | 1 | a0001c0001t0024g0183 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1117-2589T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125055353 | |||||||
| chr6:125055486 | C | T | 2 | a0001c0001t0016g0082 a0001c0001t0016g0221 |
2 | HG02602.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1117-2456C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125055486 | |||||||
| chr6:125055490 | T | A | 1 | a0001c0003t0008g0174 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1117-2452T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125055490 | |||||||
| chr6:125055543 | G | A | 3 | a0001c0001t0008g0181 a0001c0001t0022g0131 a0001c0001t0022g0179 |
3 | HG02055.hp2 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1117-2399G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125055543 | |||||||
| chr6:125055683 | A | G | 1 | a0001c0001t0002g0163 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1117-2259A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125055683 | |||||||
| chr6:125055694 | G | A | 19 | a0001c0001t0001g0134 a0001c0001t0001g0136 a0001c0001t0002g0065 others(16): Show |
19 | HG00099.hp2 HG00140.hp1 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.1117-2248G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125055694 | |||||||
| chr6:125055733 | A | G | 1 | a0002c0002t0073g0029 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1117-2209A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125055733 | |||||||
| chr6:125055748 | T | A | 3 | a0001c0001t0008g0181 a0001c0001t0022g0131 a0001c0001t0022g0179 |
3 | HG02055.hp2 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1117-2194T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125055748 | |||||||
| chr6:125055767 | TTTCA | T | 5 | a0001c0001t0021g0158 a0001c0001t0026g0159 a0001c0001t0026g0167 others(2): Show |
5 | HG02809.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1117-2168_1117-216 others(8): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 125055767 | ||||||
| chr6:125055843 | G | A | 3 | a0001c0001t0008g0181 a0001c0001t0022g0131 a0001c0001t0022g0179 |
3 | HG02055.hp2 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1117-2099G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125055843 | |||||||
| chr6:125056330 | T | G | 1 | a0001c0001t0001g0105 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1117-1612T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125056330 | |||||||
| chr6:125056339 | A | G | 9 | a0001c0001t0010g0144 a0001c0001t0010g0147 a0001c0001t0010g0152 others(6): Show |
9 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1117-1603A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125056339 | |||||||
| chr6:125056579 | G | T | 2 | a0001c0001t0024g0169 a0001c0001t0033g0133 |
2 | HG02970.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1117-1363G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125056579 | |||||||
| chr6:125057040 | T | C | 3 | a0001c0001t0008g0181 a0001c0001t0022g0131 a0001c0001t0022g0179 |
3 | HG02055.hp2 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1117-902T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125057040 | |||||||
| chr6:125057218 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1117-724C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125057218 | |||||||
| chr6:125057222 | C | A | 1 | a0005c0007t0021g0093 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1117-720C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125057222 | |||||||
| chr6:125057362 | C | A | 78 | a0001c0001t0001g0046 a0001c0001t0001g0101 a0001c0001t0001g0208 others(75): Show |
79 | HG00099.hp1 HG00639.hp2 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.1117-580C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125057362 | |||||||
| chr6:125057428 | C | T | 1 | a0001c0001t0004g0226 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1117-514C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125057428 | |||||||
| chr6:125057769 | A | G | 68 | a0001c0001t0001g0046 a0001c0001t0001g0101 a0001c0001t0001g0208 others(65): Show |
69 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.1117-173A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125057769 | |||||||
| chr6:125057821 | T | C | 20 | a0001c0001t0034g0145 a0001c0003t0008g0130 a0001c0003t0008g0150 others(17): Show |
21 | HG00639.hp1 HG01243.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.1117-121T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 2/5 | chr6 | 125057821 | |||||||
| chr6:125058280 | C | A | 146 | a0001c0001t0001g0046 a0001c0001t0001g0134 a0001c0001t0001g0136 others(143): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.1281+174C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125058280 | |||||||
| chr6:125058283 | G | A | 1 | a0002c0002t0071g0037 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1281+177G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125058283 | |||||||
| chr6:125058445 | C | A | 1 | a0001c0001t0004g0182 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1281+339C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125058445 | |||||||
| chr6:125058490 | C | T | 5 | a0001c0001t0021g0158 a0001c0001t0026g0159 a0001c0001t0026g0167 others(2): Show |
5 | HG02809.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1281+384C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125058490 | |||||||
| chr6:125058788 | C | T | 94 | a0001c0001t0001g0046 a0001c0001t0001g0101 a0001c0001t0001g0208 others(91): Show |
95 | HG00099.hp1 HG00639.hp2 HG00642.hp2 others(92): Show |
intron_variant | MODIFIER | c.1281+682C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125058788 | |||||||
| chr6:125058789 | T | C | 1 | a0001c0001t0001g0246 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1281+683T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125058789 | |||||||
| chr6:125058798 | A | G | 1 | a0001c0001t0010g0194 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1281+692A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125058798 | |||||||
| chr6:125058850 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1281+744A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125058850 | |||||||
| chr6:125059143 | GA | G | 9 | a0001c0001t0010g0144 a0001c0001t0010g0147 a0001c0001t0010g0152 others(6): Show |
9 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1281+1041delA | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125059143 | ||||||
| chr6:125059227 | T | C | 13 | a0001c0001t0010g0194 a0002c0002t0070g0038 a0003c0004t0011g0148 others(10): Show |
13 | HG00741.hp1 HG02055.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1281+1121T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125059227 | |||||||
| chr6:125059299 | G | T | 1 | a0001c0001t0068g0244 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1281+1193G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125059299 | |||||||
| chr6:125059402 | C | G | 12 | a0001c0001t0001g0109 a0001c0001t0001g0209 a0003c0004t0011g0148 others(9): Show |
12 | HG00609.hp2 HG00741.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1281+1296C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125059402 | |||||||
| chr6:125059477 | A | C | 1 | a0001c0001t0001g0108 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1281+1371A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125059477 | |||||||
| chr6:125059567 | T | C | 1 | a0001c0001t0043g0005 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1281+1461T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125059567 | |||||||
| chr6:125059623 | T | C | 9 | a0001c0001t0010g0144 a0001c0001t0010g0147 a0001c0001t0010g0152 others(6): Show |
9 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1281+1517T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125059623 | |||||||
| chr6:125059747 | A | G | 2 | a0001c0001t0001g0119 a0001c0001t0057g0245 |
2 | NA18968.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.1281+1641A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125059747 | |||||||
| chr6:125059992 | G | C | 1 | a0010c0013t0030g0191 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1281+1886G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125059992 | |||||||
| chr6:125060304 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1281+2198A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125060304 | |||||||
| chr6:125060356 | T | TAC | 28 | a0001c0001t0001g0049 a0001c0001t0001g0115 a0001c0001t0001g0134 others(25): Show |
28 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.1281+2274_1281+227 others(6): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125060356 | ||||||
| chr6:125060356 | T | TACACACA others(3): Show |
1 | a0001c0001t0033g0133 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1281+2266_1281+227 others(14): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125060356 | ||||||
| chr6:125060356 | TAC | T | 105 | a0001c0001t0001g0046 a0001c0001t0001g0101 a0001c0001t0001g0208 others(102): Show |
107 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(104): Show |
intron_variant | MODIFIER | c.1281+2274_1281+227 others(6): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125060356 | ||||||
| chr6:125060382 | T | C | 17 | a0001c0001t0001g0134 a0001c0001t0001g0136 a0001c0001t0002g0065 others(14): Show |
17 | HG00099.hp2 HG00140.hp1 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.1281+2276T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125060382 | |||||||
| chr6:125060596 | C | A | 28 | a0001c0001t0001g0134 a0001c0001t0001g0136 a0001c0001t0002g0065 others(25): Show |
28 | HG00099.hp2 HG00140.hp1 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.1281+2490C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125060596 | |||||||
| chr6:125060633 | C | T | 5 | a0001c0001t0021g0158 a0001c0001t0026g0159 a0001c0001t0026g0167 others(2): Show |
5 | HG02809.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1281+2527C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125060633 | |||||||
| chr6:125060892 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1281+2786C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125060892 | |||||||
| chr6:125060977 | T | C | 107 | a0001c0001t0001g0046 a0001c0001t0001g0101 a0001c0001t0001g0240 others(104): Show |
109 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(106): Show |
intron_variant | MODIFIER | c.1281+2871T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125060977 | |||||||
| chr6:125061242 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1281+3136G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125061242 | |||||||
| chr6:125061521 | A | G | 4 | a0002c0002t0013g0012 a0002c0002t0077g0033 a0007c0009t0001g0193 others(1): Show |
4 | HG01106.hp1 HG01934.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1281+3415A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125061521 | |||||||
| chr6:125061525 | T | A | 18 | a0001c0001t0010g0144 a0001c0001t0010g0147 a0001c0001t0010g0152 others(15): Show |
18 | HG01891.hp2 HG02109.hp1 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.1281+3419T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125061525 | |||||||
| chr6:125061552 | A | G | 26 | a0001c0001t0001g0134 a0001c0001t0001g0136 a0001c0001t0004g0045 others(23): Show |
26 | HG00099.hp2 HG00140.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.1281+3446A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125061552 | |||||||
| chr6:125061629 | G | A | 18 | a0001c0001t0010g0144 a0001c0001t0010g0147 a0001c0001t0010g0152 others(15): Show |
18 | HG01891.hp2 HG02109.hp1 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.1281+3523G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125061629 | |||||||
| chr6:125061705 | C | A | 3 | a0001c0001t0023g0249 a0001c0001t0068g0244 a0001c0003t0023g0142 |
3 | HG02451.hp2 HG03098.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1281+3599C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125061705 | |||||||
| chr6:125061792 | T | C | 82 | a0001c0001t0001g0046 a0001c0001t0001g0101 a0001c0001t0001g0134 others(79): Show |
83 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(80): Show |
intron_variant | MODIFIER | c.1281+3686T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125061792 | |||||||
| chr6:125061804 | G | A | 99 | a0001c0001t0001g0046 a0001c0001t0001g0101 a0001c0001t0001g0134 others(96): Show |
100 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(97): Show |
intron_variant | MODIFIER | c.1281+3698G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125061804 | |||||||
| chr6:125061844 | TTTTC | T | 5 | a0001c0001t0021g0158 a0001c0001t0026g0159 a0001c0001t0026g0167 others(2): Show |
5 | HG02809.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1281+3746_1281+374 others(8): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125061844 | ||||||
| chr6:125062000 | A | G | 54 | a0001c0001t0001g0046 a0001c0001t0001g0101 a0001c0001t0002g0054 others(51): Show |
55 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.1281+3894A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125062000 | |||||||
| chr6:125062252 | C | T | 18 | a0001c0001t0010g0144 a0001c0001t0010g0147 a0001c0001t0010g0152 others(15): Show |
18 | HG01891.hp2 HG02109.hp1 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.1281+4146C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125062252 | |||||||
| chr6:125062360 | T | C | 18 | a0001c0001t0010g0144 a0001c0001t0010g0147 a0001c0001t0010g0152 others(15): Show |
18 | HG01891.hp2 HG02109.hp1 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.1281+4254T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125062360 | |||||||
| chr6:125062416 | ATACT | A | 10 | a0001c0001t0023g0249 a0003c0004t0011g0148 a0003c0004t0011g0149 others(7): Show |
10 | HG00741.hp1 HG02055.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1281+4318_1281+432 others(8): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125062416 | ||||||
| chr6:125062420 | T | C | 2 | a0001c0001t0003g0197 a0001c0001t0003g0239 |
2 | HG00735.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1281+4314T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125062420 | |||||||
| chr6:125062447 | C | T | 2 | a0001c0001t0045g0160 a0002c0002t0071g0037 |
2 | HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1281+4341C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125062447 | |||||||
| chr6:125062513 | A | G | 15 | a0001c0001t0010g0144 a0001c0001t0010g0147 a0001c0001t0010g0152 others(12): Show |
15 | HG01891.hp2 HG02109.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.1281+4407A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125062513 | |||||||
| chr6:125062559 | T | A | 1 | a0001c0001t0034g0145 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1281+4453T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125062559 | |||||||
| chr6:125062610 | C | T | 13 | a0001c0001t0003g0003 a0001c0001t0003g0084 a0001c0001t0003g0114 others(10): Show |
15 | HG00642.hp1 HG00735.hp2 HG02083.hp1 others(12): Show |
intron_variant | MODIFIER | c.1281+4504C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125062610 | |||||||
| chr6:125062625 | G | A | 1 | a0001c0003t0065g0166 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1281+4519G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125062625 | |||||||
| chr6:125062664 | T | C | 1 | a0001c0001t0019g0118 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1281+4558T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125062664 | |||||||
| chr6:125062757 | A | G | 9 | a0001c0001t0008g0181 a0001c0003t0008g0130 a0001c0003t0008g0150 others(6): Show |
9 | HG01243.hp1 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1281+4651A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125062757 | |||||||
| chr6:125062765 | C | T | 12 | a0001c0001t0001g0071 a0001c0001t0005g0060 a0001c0001t0005g0080 others(9): Show |
12 | HG00408.hp2 HG00423.hp2 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.1281+4659C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125062765 | |||||||
| chr6:125062796 | G | A | 1 | a0001c0001t0003g0171 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1281+4690G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125062796 | |||||||
| chr6:125062809 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1281+4703C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125062809 | |||||||
| chr6:125062835 | C | G | 3 | a0001c0001t0021g0132 a0001c0001t0033g0133 a0001c0001t0034g0145 |
3 | HG02970.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1281+4729C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125062835 | |||||||
| chr6:125062891 | T | G | 19 | a0001c0001t0010g0144 a0001c0001t0010g0147 a0001c0001t0010g0152 others(16): Show |
19 | HG01891.hp2 HG02109.hp1 HG02622.hp1 others(16): Show |
intron_variant | MODIFIER | c.1281+4785T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125062891 | |||||||
| chr6:125062925 | T | C | 1 | a0001c0001t0002g0236 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1281+4819T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125062925 | |||||||
| chr6:125063057 | C | T | 5 | a0001c0001t0021g0158 a0001c0001t0026g0159 a0001c0001t0026g0167 others(2): Show |
5 | HG02809.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1281+4951C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125063057 | |||||||
| chr6:125063073 | T | C | 15 | a0001c0001t0010g0144 a0001c0001t0010g0147 a0001c0001t0010g0152 others(12): Show |
15 | HG01891.hp2 HG02109.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.1281+4967T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125063073 | |||||||
| chr6:125063080 | A | T | 9 | a0001c0001t0008g0181 a0001c0003t0008g0130 a0001c0003t0008g0150 others(6): Show |
9 | HG01243.hp1 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1281+4974A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125063080 | |||||||
| chr6:125063111 | A | G | 2 | a0001c0001t0001g0101 a0001c0001t0002g0211 |
2 | HG01074.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1281+5005A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125063111 | |||||||
| chr6:125063276 | C | T | 1 | a0002c0002t0071g0037 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1281+5170C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125063276 | |||||||
| chr6:125063360 | C | T | 1 | a0001c0001t0002g0085 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1281+5254C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125063360 | |||||||
| chr6:125063373 | T | C | 1 | a0002c0002t0027g0021 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1281+5267T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125063373 | |||||||
| chr6:125063442 | C | T | 18 | a0001c0001t0010g0144 a0001c0001t0010g0147 a0001c0001t0010g0152 others(15): Show |
18 | HG01891.hp2 HG02109.hp1 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.1281+5336C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125063442 | |||||||
| chr6:125063443 | G | A | 2 | a0001c0001t0002g0204 a0002c0002t0009g0024 |
2 | HG01070.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.1281+5337G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125063443 | |||||||
| chr6:125063578 | C | T | 1 | a0001c0001t0039g0178 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1281+5472C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125063578 | |||||||
| chr6:125063677 | TATAAC | T | 82 | a0001c0001t0001g0046 a0001c0001t0001g0134 a0001c0001t0001g0136 others(79): Show |
83 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(80): Show |
intron_variant | MODIFIER | c.1281+5578_1281+558 others(9): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125063677 | ||||||
| chr6:125063688 | A | G | 5 | a0001c0001t0022g0041 a0001c0001t0022g0131 a0001c0001t0022g0179 others(2): Show |
5 | HG02647.hp2 HG02886.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1281+5582A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125063688 | |||||||
| chr6:125063778 | A | C | 1 | a0011c0011t0079g0035 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1281+5672A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125063778 | |||||||
| chr6:125064018 | T | C | 1 | a0001c0001t0038g0203 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1281+5912T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125064018 | |||||||
| chr6:125064324 | G | A | 81 | a0001c0001t0001g0046 a0001c0001t0001g0101 a0001c0001t0001g0134 others(78): Show |
82 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(79): Show |
intron_variant | MODIFIER | c.1281+6218G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125064324 | |||||||
| chr6:125064350 | T | C | 2 | a0001c0001t0001g0134 a0001c0001t0001g0136 |
2 | HG00099.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.1281+6244T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125064350 | |||||||
| chr6:125064504 | C | T | 1 | a0001c0001t0002g0236 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1281+6398C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125064504 | |||||||
| chr6:125064663 | A | C | 2 | a0002c0002t0070g0038 a0010c0013t0030g0191 |
2 | HG02970.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1281+6557A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125064663 | |||||||
| chr6:125064729 | A | T | 9 | a0001c0001t0008g0181 a0001c0003t0008g0130 a0001c0003t0008g0150 others(6): Show |
9 | HG01243.hp1 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1281+6623A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125064729 | |||||||
| chr6:125064739 | C | A | 2 | a0001c0001t0001g0134 a0001c0001t0001g0136 |
2 | HG00099.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.1281+6633C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125064739 | |||||||
| chr6:125064745 | A | C | 1 | a0001c0001t0001g0108 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1281+6639A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125064745 | |||||||
| chr6:125064791 | T | G | 2 | a0001c0001t0016g0082 a0001c0001t0016g0221 |
2 | HG02602.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1281+6685T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125064791 | |||||||
| chr6:125064806 | A | G | 1 | a0002c0002t0007g0013 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1281+6700A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125064806 | |||||||
| chr6:125064931 | C | G | 19 | a0001c0001t0010g0144 a0001c0001t0010g0147 a0001c0001t0010g0152 others(16): Show |
19 | HG01891.hp2 HG02109.hp1 HG02622.hp1 others(16): Show |
intron_variant | MODIFIER | c.1281+6825C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125064931 | |||||||
| chr6:125064947 | A | G | 1 | a0001c0001t0025g0141 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1281+6841A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125064947 | |||||||
| chr6:125065057 | C | T | 6 | a0001c0001t0004g0154 a0001c0001t0015g0044 a0001c0001t0015g0206 others(3): Show |
6 | NA18942.hp2 NA18943.hp1 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.1281+6951C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125065057 | |||||||
| chr6:125065084 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1281+6978G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125065084 | |||||||
| chr6:125065103 | G | A | 5 | a0001c0001t0003g0168 a0001c0001t0003g0175 a0001c0001t0003g0177 others(2): Show |
5 | HG02451.hp1 HG02572.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1281+6997G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125065103 | |||||||
| chr6:125065163 | C | T | 1 | a0001c0001t0038g0203 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1281+7057C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125065163 | |||||||
| chr6:125065166 | T | C | 155 | a0001c0001t0001g0046 a0001c0001t0001g0101 a0001c0001t0001g0134 others(152): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.1281+7060T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125065166 | |||||||
| chr6:125065269 | C | T | 1 | a0001c0003t0013g0185 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1281+7163C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125065269 | |||||||
| chr6:125065290 | C | CA | 33 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0003g0254 others(30): Show |
33 | HG00140.hp2 HG00741.hp2 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.1281+7204dupA | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125065290 | ||||||
| chr6:125065290 | C | CAA | 11 | a0001c0001t0010g0144 a0001c0001t0010g0147 a0001c0001t0010g0152 others(8): Show |
11 | HG01891.hp2 HG02109.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1281+7203_1281+720 others(6): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125065290 | ||||||
| chr6:125065317 | G | C | 101 | a0001c0001t0001g0046 a0001c0001t0001g0101 a0001c0001t0001g0134 others(98): Show |
102 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(99): Show |
intron_variant | MODIFIER | c.1281+7211G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125065317 | |||||||
| chr6:125065527 | C | T | 3 | a0001c0001t0021g0132 a0001c0001t0033g0133 a0001c0001t0034g0145 |
3 | HG02970.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1281+7421C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125065527 | |||||||
| chr6:125065541 | G | A | 1 | a0001c0001t0022g0131 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1281+7435G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125065541 | |||||||
| chr6:125065580 | A | G | 19 | a0001c0001t0010g0144 a0001c0001t0010g0147 a0001c0001t0010g0152 others(16): Show |
19 | HG01891.hp2 HG02109.hp1 HG02622.hp1 others(16): Show |
intron_variant | MODIFIER | c.1281+7474A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125065580 | |||||||
| chr6:125065831 | G | A | 9 | a0003c0004t0011g0148 a0003c0004t0011g0149 a0003c0004t0011g0155 others(6): Show |
9 | HG00741.hp1 HG02055.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1281+7725G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125065831 | |||||||
| chr6:125066016 | C | G | 1 | a0001c0001t0001g0151 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1281+7910C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125066016 | |||||||
| chr6:125066034 | C | T | 10 | a0001c0001t0010g0144 a0001c0001t0010g0147 a0001c0001t0010g0152 others(7): Show |
10 | HG01891.hp2 HG02109.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1281+7928C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125066034 | |||||||
| chr6:125066158 | G | C | 11 | a0001c0001t0006g0004 a0001c0001t0006g0146 a0001c0001t0006g0157 others(8): Show |
11 | HG01884.hp1 HG02109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1281+8052G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125066158 | |||||||
| chr6:125066252 | T | C | 5 | a0001c0001t0010g0162 a0001c0001t0010g0194 a0001c0003t0010g0258 others(2): Show |
5 | HG01891.hp2 HG02922.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1281+8146T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125066252 | |||||||
| chr6:125066329 | T | C | 160 | a0001c0001t0001g0046 a0001c0001t0001g0101 a0001c0001t0001g0134 others(157): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.1281+8223T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125066329 | |||||||
| chr6:125066404 | C | T | 1 | a0001c0003t0023g0142 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1281+8298C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125066404 | |||||||
| chr6:125066447 | G | A | 1 | a0001c0003t0023g0142 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1281+8341G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125066447 | |||||||
| chr6:125066466 | C | T | 1 | a0001c0001t0024g0183 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1281+8360C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125066466 | |||||||
| chr6:125066727 | T | C | 16 | a0001c0001t0010g0144 a0001c0001t0010g0147 a0001c0001t0010g0152 others(13): Show |
16 | HG01891.hp2 HG02109.hp1 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.1281+8621T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125066727 | |||||||
| chr6:125066737 | GA | G | 15 | a0001c0001t0010g0144 a0001c0001t0010g0147 a0001c0001t0010g0152 others(12): Show |
15 | HG01891.hp2 HG02109.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.1281+8632delA | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125066737 | |||||||
| chr6:125066995 | A | AG | 161 | a0001c0001t0001g0046 a0001c0001t0001g0101 a0001c0001t0001g0134 others(158): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.1281+8891dupG | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125066995 | ||||||
| chr6:125067001 | A | G | 90 | a0001c0001t0001g0046 a0001c0001t0001g0101 a0001c0001t0001g0134 others(87): Show |
91 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(88): Show |
intron_variant | MODIFIER | c.1281+8895A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125067001 | |||||||
| chr6:125067020 | C | A | 29 | a0001c0001t0008g0181 a0001c0001t0021g0132 a0001c0001t0021g0158 others(26): Show |
29 | HG00741.hp1 HG01243.hp1 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.1281+8914C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125067020 | |||||||
| chr6:125067048 | T | A | 1 | a0001c0003t0064g0188 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1281+8942T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125067048 | |||||||
| chr6:125067054 | G | C | 89 | a0001c0001t0001g0046 a0001c0001t0001g0134 a0001c0001t0001g0136 others(86): Show |
90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.1281+8948G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125067054 | |||||||
| chr6:125067127 | T | C | 1 | a0001c0001t0002g0236 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1281+9021T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125067127 | |||||||
| chr6:125067135 | C | T | 1 | a0001c0001t0068g0244 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1281+9029C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125067135 | |||||||
| chr6:125067560 | G | A | 2 | a0007c0009t0001g0193 a0007c0009t0001g0264 |
2 | HG02257.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1282-9097G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125067560 | |||||||
| chr6:125067607 | A | G | 16 | a0001c0001t0010g0144 a0001c0001t0010g0147 a0001c0001t0010g0152 others(13): Show |
16 | HG01891.hp2 HG02109.hp1 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.1282-9050A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125067607 | |||||||
| chr6:125067632 | G | A | 1 | a0001c0001t0003g0084 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1282-9025G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125067632 | |||||||
| chr6:125067783 | T | C | 16 | a0001c0001t0010g0144 a0001c0001t0010g0147 a0001c0001t0010g0152 others(13): Show |
16 | HG01891.hp2 HG02109.hp1 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.1282-8874T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125067783 | |||||||
| chr6:125067820 | G | A | 1 | a0001c0001t0001g0083 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1282-8837G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125067820 | |||||||
| chr6:125067953 | A | G | 16 | a0001c0001t0010g0144 a0001c0001t0010g0147 a0001c0001t0010g0152 others(13): Show |
16 | HG01891.hp2 HG02109.hp1 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.1282-8704A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125067953 | |||||||
| chr6:125068065 | A | G | 55 | a0001c0001t0003g0003 a0001c0001t0003g0084 a0001c0001t0003g0114 others(52): Show |
57 | HG00642.hp1 HG00735.hp2 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.1282-8592A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125068065 | |||||||
| chr6:125068153 | C | A | 16 | a0001c0001t0010g0144 a0001c0001t0010g0147 a0001c0001t0010g0152 others(13): Show |
16 | HG01891.hp2 HG02109.hp1 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.1282-8504C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125068153 | |||||||
| chr6:125068280 | C | T | 1 | a0002c0002t0070g0038 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1282-8377C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125068280 | |||||||
| chr6:125068449 | G | T | 2 | a0001c0001t0001g0230 a0008c0014t0001g0126 |
2 | HG00323.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.1282-8208G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125068449 | |||||||
| chr6:125068666 | T | A | 1 | a0001c0001t0001g0108 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1282-7991T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125068666 | |||||||
| chr6:125068709 | A | G | 2 | a0001c0001t0001g0074 a0001c0001t0001g0218 |
2 | HG01255.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.1282-7948A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125068709 | |||||||
| chr6:125068920 | A | G | 1 | a0001c0001t0006g0004 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1282-7737A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125068920 | |||||||
| chr6:125068963 | G | A | 16 | a0001c0001t0010g0144 a0001c0001t0010g0147 a0001c0001t0010g0152 others(13): Show |
16 | HG01891.hp2 HG02109.hp1 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.1282-7694G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125068963 | |||||||
| chr6:125069213 | A | C | 1 | a0001c0001t0004g0182 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1282-7444A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125069213 | |||||||
| chr6:125069239 | A | G | 1 | a0007c0009t0001g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1282-7418A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125069239 | |||||||
| chr6:125069287 | T | C | 2 | a0001c0001t0045g0160 a0002c0002t0071g0037 |
2 | HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1282-7370T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125069287 | |||||||
| chr6:125069538 | C | A | 15 | a0001c0001t0003g0003 a0001c0001t0003g0084 a0001c0001t0003g0114 others(12): Show |
17 | HG00642.hp1 HG00735.hp2 HG02083.hp1 others(14): Show |
intron_variant | MODIFIER | c.1282-7119C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125069538 | |||||||
| chr6:125069547 | G | A | 87 | a0001c0001t0001g0134 a0001c0001t0001g0136 a0001c0001t0002g0054 others(84): Show |
88 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(85): Show |
intron_variant | MODIFIER | c.1282-7110G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125069547 | |||||||
| chr6:125069679 | G | A | 1 | a0002c0002t0009g0001 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1282-6978G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125069679 | |||||||
| chr6:125069831 | A | G | 9 | a0001c0001t0008g0181 a0001c0003t0008g0130 a0001c0003t0008g0150 others(6): Show |
9 | HG01243.hp1 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1282-6826A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125069831 | |||||||
| chr6:125069858 | A | AT | 14 | a0001c0001t0003g0003 a0001c0001t0003g0084 a0001c0001t0003g0114 others(11): Show |
16 | HG00642.hp1 HG00735.hp2 HG02083.hp1 others(13): Show |
intron_variant | MODIFIER | c.1282-6791dupT | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125069858 | ||||||
| chr6:125069889 | C | T | 1 | a0001c0001t0004g0154 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1282-6768C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125069889 | |||||||
| chr6:125069922 | G | A | 14 | a0001c0001t0003g0003 a0001c0001t0003g0084 a0001c0001t0003g0114 others(11): Show |
16 | HG00642.hp1 HG00735.hp2 HG02083.hp1 others(13): Show |
intron_variant | MODIFIER | c.1282-6735G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125069922 | |||||||
| chr6:125070008 | T | A | 9 | a0003c0004t0011g0148 a0003c0004t0011g0149 a0003c0004t0011g0155 others(6): Show |
9 | HG00741.hp1 HG02055.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1282-6649T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125070008 | |||||||
| chr6:125070033 | C | T | 3 | a0001c0001t0023g0249 a0001c0001t0068g0244 a0001c0003t0023g0142 |
3 | HG02451.hp2 HG03098.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1282-6624C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125070033 | |||||||
| chr6:125070258 | T | A | 159 | a0001c0001t0001g0134 a0001c0001t0001g0136 a0001c0001t0002g0054 others(156): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.1282-6399T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125070258 | |||||||
| chr6:125070462 | C | T | 6 | a0001c0001t0001g0042 a0001c0001t0001g0127 a0001c0001t0052g0048 others(3): Show |
6 | HG02056.hp2 NA18747.hp2 NA18994.hp1 others(3): Show |
intron_variant | MODIFIER | c.1282-6195C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125070462 | |||||||
| chr6:125070500 | A | T | 3 | a0001c0001t0023g0249 a0001c0001t0068g0244 a0001c0003t0023g0142 |
3 | HG02451.hp2 HG03098.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1282-6157A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125070500 | |||||||
| chr6:125070507 | A | G | 1 | a0001c0001t0002g0220 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1282-6150A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125070507 | |||||||
| chr6:125070541 | G | A | 9 | a0003c0004t0011g0148 a0003c0004t0011g0149 a0003c0004t0011g0155 others(6): Show |
9 | HG00741.hp1 HG02055.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1282-6116G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125070541 | |||||||
| chr6:125070547 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1282-6110G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125070547 | |||||||
| chr6:125070549 | A | G | 29 | a0001c0001t0008g0181 a0001c0001t0021g0132 a0001c0001t0021g0158 others(26): Show |
29 | HG00741.hp1 HG01243.hp1 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.1282-6108A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125070549 | |||||||
| chr6:125070839 | A | T | 2 | a0001c0001t0024g0169 a0009c0015t0053g0247 |
2 | HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1282-5818A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125070839 | |||||||
| chr6:125070942 | T | C | 3 | a0001c0001t0001g0151 a0001c0001t0001g0230 a0008c0014t0001g0126 |
3 | HG00323.hp1 HG02083.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1282-5715T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125070942 | |||||||
| chr6:125070947 | G | T | 88 | a0001c0001t0001g0134 a0001c0001t0001g0136 a0001c0001t0002g0054 others(85): Show |
89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): Show |
intron_variant | MODIFIER | c.1282-5710G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125070947 | |||||||
| chr6:125070948 | T | C | 1 | a0001c0001t0015g0224 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1282-5709T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125070948 | |||||||
| chr6:125071045 | A | T | 3 | a0001c0001t0001g0079 a0001c0001t0001g0104 a0001c0001t0001g0212 |
3 | HG01952.hp1 HG02273.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.1282-5612A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125071045 | |||||||
| chr6:125071129 | C | A | 29 | a0001c0001t0008g0181 a0001c0001t0021g0132 a0001c0001t0021g0158 others(26): Show |
29 | HG00741.hp1 HG01243.hp1 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.1282-5528C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125071129 | |||||||
| chr6:125071148 | G | A | 1 | a0001c0001t0001g0042 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1282-5509G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125071148 | |||||||
| chr6:125071208 | A | G | 1 | a0001c0001t0001g0208 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1282-5449A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125071208 | |||||||
| chr6:125071231 | C | A | 1 | a0001c0001t0001g0210 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1282-5426C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125071231 | |||||||
| chr6:125071253 | T | C | 159 | a0001c0001t0001g0134 a0001c0001t0001g0136 a0001c0001t0002g0054 others(156): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.1282-5404T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125071253 | |||||||
| chr6:125071260 | T | A | 1 | a0003c0004t0011g0155 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1282-5397T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125071260 | |||||||
| chr6:125071335 | G | A | 1 | a0001c0001t0021g0132 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1282-5322G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125071335 | |||||||
| chr6:125071344 | C | T | 2 | a0001c0001t0016g0082 a0001c0001t0016g0221 |
2 | HG02602.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1282-5313C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125071344 | |||||||
| chr6:125071365 | C | T | 1 | a0001c0001t0039g0178 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1282-5292C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125071365 | |||||||
| chr6:125071454 | A | C | 1 | a0001c0012t0031g0255 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1282-5203A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125071454 | |||||||
| chr6:125071482 | ATATGTGT others(1): Show |
A | 6 | a0001c0001t0017g0100 a0001c0001t0017g0153 a0001c0001t0017g0253 others(3): Show |
6 | HG01884.hp2 HG02258.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1282-5173_1282-516 others(12): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125071482 | ||||||
| chr6:125071484 | A | ATG | 14 | a0001c0001t0001g0062 a0001c0001t0001g0071 a0001c0001t0001g0108 others(11): Show |
14 | HG00408.hp2 HG00423.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.1282-5121_1282-512 others(6): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125071484 | ||||||
| chr6:125071484 | A | ATGTG | 7 | a0001c0001t0005g0081 a0001c0001t0005g0207 a0001c0001t0005g0219 others(4): Show |
7 | NA18946.hp2 NA18975.hp1 NA18989.hp2 others(4): Show |
intron_variant | MODIFIER | c.1282-5123_1282-512 others(8): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125071484 | ||||||
| chr6:125071484 | A | ATGTGTGT others(3): Show |
2 | a0001c0001t0014g0059 a0001c0001t0057g0245 |
2 | NA19010.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1282-5129_1282-512 others(14): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125071484 | ||||||
| chr6:125071484 | ATG | A | 38 | a0001c0001t0001g0042 a0001c0001t0001g0046 a0001c0001t0001g0056 others(35): Show |
38 | HG00323.hp1 HG00609.hp2 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.1282-5121_1282-512 others(6): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125071484 | ||||||
| chr6:125071484 | ATGTG | A | 39 | a0001c0001t0001g0043 a0001c0001t0001g0050 a0001c0001t0001g0051 others(36): Show |
39 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(36): Show |
intron_variant | MODIFIER | c.1282-5123_1282-512 others(8): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125071484 | ||||||
| chr6:125071484 | ATGTGTG | A | 72 | a0001c0001t0001g0049 a0001c0001t0001g0115 a0001c0001t0002g0054 others(69): Show |
73 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.1282-5125_1282-512 others(10): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125071484 | ||||||
| chr6:125071484 | ATGTGTGT others(1): Show |
A | 28 | a0001c0001t0003g0003 a0001c0001t0003g0084 a0001c0001t0003g0114 others(25): Show |
30 | HG00642.hp1 HG00735.hp2 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.1282-5127_1282-512 others(12): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125071484 | ||||||
| chr6:125071484 | ATGTGTGT others(3): Show |
A | 3 | a0001c0001t0046g0195 a0001c0003t0008g0130 a0002c0002t0071g0037 |
3 | HG03130.hp1 HG03209.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1282-5129_1282-512 others(14): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125071484 | ||||||
| chr6:125071484 | ATGTGTGT others(5): Show |
A | 14 | a0001c0001t0021g0132 a0001c0001t0021g0158 a0001c0001t0026g0159 others(11): Show |
14 | HG00741.hp1 HG02630.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.1282-5131_1282-512 others(16): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125071484 | ||||||
| chr6:125071484 | ATGTGTGT others(7): Show |
A | 11 | a0001c0001t0008g0181 a0001c0003t0008g0150 a0001c0003t0008g0174 others(8): Show |
11 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1282-5133_1282-512 others(18): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125071484 | ||||||
| chr6:125071484 | ATGTGTGT others(9): Show |
A | 1 | a0001c0001t0023g0249 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1282-5135_1282-512 others(20): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125071484 | ||||||
| chr6:125071484 | ATGTGTGT others(13): Show |
A | 4 | a0001c0001t0001g0103 a0001c0001t0001g0234 a0001c0001t0006g0176 others(1): Show |
4 | HG01243.hp2 HG01993.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1282-5139_1282-512 others(24): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125071484 | ||||||
| chr6:125071528 | G | A | 4 | a0001c0001t0024g0169 a0001c0001t0040g0260 a0002c0002t0027g0021 others(1): Show |
4 | HG00738.hp2 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1282-5129G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125071528 | |||||||
| chr6:125071530 | G | A | 78 | a0001c0001t0001g0134 a0001c0001t0001g0136 a0001c0001t0002g0054 others(75): Show |
79 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(76): Show |
intron_variant | MODIFIER | c.1282-5127G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125071530 | |||||||
| chr6:125071532 | G | A | 87 | a0001c0001t0001g0134 a0001c0001t0001g0136 a0001c0001t0002g0054 others(84): Show |
88 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(85): Show |
intron_variant | MODIFIER | c.1282-5125G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125071532 | |||||||
| chr6:125071534 | G | A | 101 | a0001c0001t0001g0134 a0001c0001t0001g0136 a0001c0001t0002g0054 others(98): Show |
102 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(99): Show |
intron_variant | MODIFIER | c.1282-5123G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125071534 | |||||||
| chr6:125071536 | G | A | 129 | a0001c0001t0001g0134 a0001c0001t0001g0136 a0001c0001t0002g0054 others(126): Show |
132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.1282-5121G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125071536 | |||||||
| chr6:125071538 | A | G | 1 | a0001c0001t0001g0108 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1282-5119A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125071538 | |||||||
| chr6:125071689 | C | A | 1 | a0001c0003t0008g0150 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1282-4968C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125071689 | |||||||
| chr6:125071810 | A | G | 88 | a0001c0001t0001g0134 a0001c0001t0001g0136 a0001c0001t0002g0054 others(85): Show |
89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): Show |
intron_variant | MODIFIER | c.1282-4847A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125071810 | |||||||
| chr6:125071828 | G | A | 159 | a0001c0001t0001g0134 a0001c0001t0001g0136 a0001c0001t0002g0054 others(156): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.1282-4829G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125071828 | |||||||
| chr6:125072028 | C | A | 1 | a0001c0001t0001g0069 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1282-4629C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125072028 | |||||||
| chr6:125072041 | G | T | 22 | a0001c0001t0001g0134 a0001c0001t0001g0136 a0001c0001t0004g0045 others(19): Show |
22 | HG00099.hp2 HG00140.hp1 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.1282-4616G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125072041 | |||||||
| chr6:125072060 | A | G | 88 | a0001c0001t0001g0134 a0001c0001t0001g0136 a0001c0001t0002g0054 others(85): Show |
89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): Show |
intron_variant | MODIFIER | c.1282-4597A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125072060 | |||||||
| chr6:125072261 | A | G | 1 | a0001c0001t0037g0138 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1282-4396A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125072261 | |||||||
| chr6:125072278 | T | A | 15 | a0001c0001t0003g0003 a0001c0001t0003g0084 a0001c0001t0003g0114 others(12): Show |
17 | HG00642.hp1 HG00735.hp2 HG02083.hp1 others(14): Show |
intron_variant | MODIFIER | c.1282-4379T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125072278 | |||||||
| chr6:125072450 | A | G | 1 | a0010c0013t0030g0191 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1282-4207A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125072450 | |||||||
| chr6:125072626 | T | A | 1 | a0001c0001t0024g0183 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1282-4031T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125072626 | |||||||
| chr6:125072654 | T | C | 11 | a0001c0001t0045g0160 a0002c0002t0071g0037 a0003c0004t0011g0148 others(8): Show |
11 | HG00741.hp1 HG02055.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1282-4003T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125072654 | |||||||
| chr6:125072669 | C | T | 1 | a0001c0001t0023g0249 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1282-3988C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125072669 | |||||||
| chr6:125072854 | C | CAG | 159 | a0001c0001t0001g0134 a0001c0001t0001g0136 a0001c0001t0002g0054 others(156): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.1282-3802_1282-380 others(6): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125072854 | ||||||
| chr6:125072972 | G | A | 1 | a0001c0012t0031g0255 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1282-3685G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125072972 | |||||||
| chr6:125073012 | G | A | 6 | a0001c0001t0021g0132 a0001c0001t0021g0158 a0001c0001t0026g0159 others(3): Show |
6 | HG02809.hp1 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1282-3645G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125073012 | |||||||
| chr6:125073049 | G | A | 1 | a0001c0001t0040g0260 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1282-3608G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125073049 | |||||||
| chr6:125073453 | G | A | 11 | a0001c0001t0006g0004 a0001c0001t0006g0146 a0001c0001t0006g0157 others(8): Show |
11 | HG01884.hp1 HG02109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1282-3204G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125073453 | |||||||
| chr6:125073609 | A | G | 159 | a0001c0001t0001g0134 a0001c0001t0001g0136 a0001c0001t0002g0054 others(156): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.1282-3048A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125073609 | |||||||
| chr6:125073628 | C | T | 99 | a0001c0001t0001g0134 a0001c0001t0001g0136 a0001c0001t0002g0054 others(96): Show |
100 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(97): Show |
intron_variant | MODIFIER | c.1282-3029C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125073628 | |||||||
| chr6:125073676 | A | C | 88 | a0001c0001t0001g0134 a0001c0001t0001g0136 a0001c0001t0002g0054 others(85): Show |
89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): Show |
intron_variant | MODIFIER | c.1282-2981A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125073676 | |||||||
| chr6:125073942 | A | T | 1 | a0001c0001t0050g0040 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1282-2715A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125073942 | |||||||
| chr6:125074000 | T | C | 88 | a0001c0001t0001g0134 a0001c0001t0001g0136 a0001c0001t0002g0054 others(85): Show |
89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): Show |
intron_variant | MODIFIER | c.1282-2657T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125074000 | |||||||
| chr6:125074044 | A | T | 99 | a0001c0001t0001g0134 a0001c0001t0001g0136 a0001c0001t0002g0054 others(96): Show |
100 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(97): Show |
intron_variant | MODIFIER | c.1282-2613A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125074044 | |||||||
| chr6:125074048 | G | C | 99 | a0001c0001t0001g0134 a0001c0001t0001g0136 a0001c0001t0002g0054 others(96): Show |
100 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(97): Show |
intron_variant | MODIFIER | c.1282-2609G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125074048 | |||||||
| chr6:125074198 | G | A | 30 | a0001c0001t0001g0062 a0001c0001t0001g0071 a0001c0001t0001g0092 others(27): Show |
30 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.1282-2459G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125074198 | |||||||
| chr6:125074226 | T | C | 1 | a0001c0012t0031g0255 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1282-2431T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125074226 | |||||||
| chr6:125074297 | G | GTAGA | 20 | a0001c0001t0001g0230 a0001c0001t0002g0058 a0001c0001t0002g0085 others(17): Show |
21 | HG00323.hp1 HG00741.hp1 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.1282-2308_1282-230 others(8): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125074297 | ||||||
| chr6:125074297 | G | GTAGATAG others(1): Show |
3 | a0001c0001t0002g0140 a0001c0001t0004g0122 a0001c0001t0022g0179 |
3 | HG01169.hp1 HG03540.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1282-2312_1282-230 others(12): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125074297 | ||||||
| chr6:125074297 | GTAGA | G | 95 | a0001c0001t0001g0049 a0001c0001t0001g0056 a0001c0001t0001g0063 others(92): Show |
96 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(93): Show |
intron_variant | MODIFIER | c.1282-2308_1282-230 others(8): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125074297 | ||||||
| chr6:125074297 | GTAGATAG others(1): Show |
G | 31 | a0001c0001t0001g0079 a0001c0001t0001g0092 a0001c0001t0001g0105 others(28): Show |
31 | HG00408.hp2 HG00609.hp2 HG01346.hp1 others(28): Show |
intron_variant | MODIFIER | c.1282-2312_1282-230 others(12): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125074297 | ||||||
| chr6:125074297 | GTAGATAG others(5): Show |
G | 30 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0062 others(27): Show |
30 | HG00423.hp1 HG00738.hp1 HG01433.hp1 others(27): Show |
intron_variant | MODIFIER | c.1282-2316_1282-230 others(16): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125074297 | ||||||
| chr6:125074297 | GTAGATAG others(9): Show |
G | 1 | a0001c0001t0017g0253 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1282-2320_1282-230 others(20): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125074297 | ||||||
| chr6:125074317 | A | ATAGGTAG others(13): Show |
1 | a0001c0001t0033g0133 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1282-2337_1282-233 others(24): Show |
RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 125074317 | ||||||
| chr6:125074388 | T | G | 15 | a0001c0001t0010g0144 a0001c0001t0010g0147 a0001c0001t0010g0152 others(12): Show |
15 | HG01891.hp2 HG02109.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.1282-2269T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125074388 | |||||||
| chr6:125074533 | A | C | 11 | a0001c0001t0006g0004 a0001c0001t0006g0146 a0001c0001t0006g0157 others(8): Show |
11 | HG01884.hp1 HG02109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1282-2124A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125074533 | |||||||
| chr6:125074585 | C | T | 1 | a0005c0007t0006g0094 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1282-2072C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125074585 | |||||||
| chr6:125075070 | A | G | 157 | a0001c0001t0002g0054 a0001c0001t0002g0055 a0001c0001t0002g0058 others(154): Show |
160 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.1282-1587A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125075070 | |||||||
| chr6:125075188 | G | A | 1 | a0003c0004t0011g0149 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1282-1469G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125075188 | |||||||
| chr6:125075235 | T | A | 102 | a0001c0001t0002g0054 a0001c0001t0002g0055 a0001c0001t0002g0058 others(99): Show |
103 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(100): Show |
intron_variant | MODIFIER | c.1282-1422T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125075235 | |||||||
| chr6:125075406 | C | A | 1 | a0001c0001t0040g0260 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1282-1251C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125075406 | |||||||
| chr6:125075407 | G | A | 1 | a0001c0008t0003g0002 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1282-1250G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125075407 | |||||||
| chr6:125075528 | C | T | 1 | a0001c0001t0002g0097 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1282-1129C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125075528 | |||||||
| chr6:125075764 | C | T | 155 | a0001c0001t0002g0054 a0001c0001t0002g0055 a0001c0001t0002g0058 others(152): Show |
158 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.1282-893C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125075764 | |||||||
| chr6:125075781 | C | T | 11 | a0001c0001t0006g0004 a0001c0001t0006g0146 a0001c0001t0006g0157 others(8): Show |
11 | HG01884.hp1 HG02109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1282-876C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125075781 | |||||||
| chr6:125075790 | C | A | 14 | a0001c0001t0023g0249 a0001c0001t0045g0160 a0001c0001t0068g0244 others(11): Show |
14 | HG00741.hp1 HG02055.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1282-867C>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125075790 | |||||||
| chr6:125075847 | G | A | 100 | a0001c0001t0002g0054 a0001c0001t0002g0055 a0001c0001t0002g0058 others(97): Show |
101 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.1282-810G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125075847 | |||||||
| chr6:125075899 | C | G | 25 | a0001c0001t0006g0004 a0001c0001t0006g0146 a0001c0001t0006g0157 others(22): Show |
25 | HG00741.hp1 HG01884.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.1282-758C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125075899 | |||||||
| chr6:125075940 | A | G | 1 | a0001c0001t0001g0243 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1282-717A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125075940 | |||||||
| chr6:125076034 | A | T | 1 | a0001c0001t0017g0253 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1282-623A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125076034 | |||||||
| chr6:125076066 | C | T | 30 | a0001c0001t0003g0003 a0001c0001t0003g0084 a0001c0001t0003g0114 others(27): Show |
32 | HG00642.hp1 HG00735.hp2 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.1282-591C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125076066 | |||||||
| chr6:125076144 | A | C | 11 | a0001c0001t0006g0004 a0001c0001t0006g0146 a0001c0001t0006g0157 others(8): Show |
11 | HG01884.hp1 HG02109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1282-513A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125076144 | |||||||
| chr6:125076414 | A | G | 100 | a0001c0001t0002g0054 a0001c0001t0002g0055 a0001c0001t0002g0058 others(97): Show |
101 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.1282-243A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125076414 | |||||||
| chr6:125076594 | C | T | 1 | a0001c0012t0031g0255 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1282-63C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 3/5 | chr6 | 125076594 | |||||||
| chr6:125076907 | G | A | 1 | a0001c0012t0031g0255 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1483+49G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125076907 | |||||||
| chr6:125077167 | G | A | 1 | a0001c0001t0024g0183 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1483+309G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125077167 | |||||||
| chr6:125077173 | T | C | 6 | a0001c0001t0004g0070 a0001c0001t0004g0075 a0001c0001t0004g0095 others(3): Show |
6 | HG02080.hp2 NA18948.hp1 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.1483+315T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125077173 | |||||||
| chr6:125077228 | T | C | 14 | a0001c0001t0023g0249 a0001c0001t0045g0160 a0001c0001t0068g0244 others(11): Show |
14 | HG00741.hp1 HG02055.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1483+370T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125077228 | |||||||
| chr6:125077409 | A | G | 3 | a0001c0001t0023g0249 a0001c0001t0068g0244 a0001c0003t0023g0142 |
3 | HG02451.hp2 HG03098.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1483+551A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125077409 | |||||||
| chr6:125077456 | G | A | 3 | a0001c0001t0022g0041 a0001c0001t0022g0131 a0001c0001t0022g0179 |
3 | HG02647.hp2 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1483+598G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125077456 | |||||||
| chr6:125077556 | C | T | 14 | a0001c0001t0003g0003 a0001c0001t0003g0084 a0001c0001t0003g0114 others(11): Show |
16 | HG00642.hp1 HG00735.hp2 HG02083.hp1 others(13): Show |
intron_variant | MODIFIER | c.1483+698C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125077556 | |||||||
| chr6:125077621 | G | A | 5 | a0001c0001t0022g0041 a0001c0001t0022g0131 a0001c0001t0022g0179 others(2): Show |
5 | HG02647.hp2 HG02886.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1483+763G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125077621 | |||||||
| chr6:125077721 | CT | C | 5 | a0001c0001t0015g0044 a0001c0001t0015g0206 a0001c0001t0015g0224 others(2): Show |
5 | NA18942.hp2 NA18943.hp1 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.1483+864delT | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125077721 | |||||||
| chr6:125077886 | C | T | 9 | a0003c0004t0011g0148 a0003c0004t0011g0149 a0003c0004t0011g0155 others(6): Show |
9 | HG00741.hp1 HG02055.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1483+1028C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125077886 | |||||||
| chr6:125077937 | T | C | 2 | a0002c0002t0070g0038 a0010c0013t0030g0191 |
2 | HG02970.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1483+1079T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125077937 | |||||||
| chr6:125077971 | A | G | 1 | a0001c0003t0064g0188 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1483+1113A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125077971 | |||||||
| chr6:125078061 | A | G | 15 | a0001c0001t0003g0003 a0001c0001t0003g0084 a0001c0001t0003g0114 others(12): Show |
17 | HG00642.hp1 HG00735.hp2 HG02083.hp1 others(14): Show |
intron_variant | MODIFIER | c.1483+1203A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125078061 | |||||||
| chr6:125078081 | G | A | 1 | a0001c0001t0010g0194 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1483+1223G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125078081 | |||||||
| chr6:125078224 | C | T | 11 | a0001c0001t0006g0004 a0001c0001t0006g0146 a0001c0001t0006g0157 others(8): Show |
11 | HG01884.hp1 HG02109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1483+1366C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125078224 | |||||||
| chr6:125078384 | C | T | 11 | a0001c0001t0006g0004 a0001c0001t0006g0146 a0001c0001t0006g0157 others(8): Show |
11 | HG01884.hp1 HG02109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1483+1526C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125078384 | |||||||
| chr6:125078442 | C | T | 19 | a0001c0001t0003g0168 a0001c0001t0003g0175 a0001c0001t0003g0177 others(16): Show |
19 | HG00741.hp1 HG02055.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.1483+1584C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125078442 | |||||||
| chr6:125078546 | C | G | 160 | a0001c0001t0002g0054 a0001c0001t0002g0055 a0001c0001t0002g0058 others(157): Show |
163 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1483+1688C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125078546 | |||||||
| chr6:125078605 | C | T | 1 | a0002c0002t0077g0033 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1483+1747C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125078605 | |||||||
| chr6:125078713 | T | C | 5 | a0001c0001t0022g0041 a0001c0001t0022g0131 a0001c0001t0022g0179 others(2): Show |
5 | HG02647.hp2 HG02886.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1483+1855T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125078713 | |||||||
| chr6:125078824 | G | A | 14 | a0001c0001t0003g0003 a0001c0001t0003g0084 a0001c0001t0003g0114 others(11): Show |
16 | HG00642.hp1 HG00735.hp2 HG02083.hp1 others(13): Show |
intron_variant | MODIFIER | c.1483+1966G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125078824 | |||||||
| chr6:125078981 | C | T | 2 | a0001c0001t0016g0082 a0001c0001t0016g0221 |
2 | HG02602.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1483+2123C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125078981 | |||||||
| chr6:125079065 | G | A | 1 | a0001c0001t0038g0203 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1483+2207G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125079065 | |||||||
| chr6:125079141 | G | A | 14 | a0001c0001t0003g0003 a0001c0001t0003g0084 a0001c0001t0003g0114 others(11): Show |
16 | HG00642.hp1 HG00735.hp2 HG02083.hp1 others(13): Show |
intron_variant | MODIFIER | c.1483+2283G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125079141 | |||||||
| chr6:125079329 | T | C | 12 | a0001c0001t0043g0005 a0001c0001t0045g0160 a0002c0002t0071g0037 others(9): Show |
12 | HG00741.hp1 HG02055.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.1484-2107T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125079329 | |||||||
| chr6:125079382 | C | T | 5 | a0001c0001t0002g0054 a0001c0001t0002g0055 a0001c0001t0002g0097 others(2): Show |
5 | HG02132.hp1 NA18952.hp2 NA18956.hp1 others(2): Show |
intron_variant | MODIFIER | c.1484-2054C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125079382 | |||||||
| chr6:125079438 | T | TA | 17 | a0001c0001t0003g0084 a0001c0001t0008g0181 a0001c0001t0021g0132 others(14): Show |
17 | HG00642.hp1 HG01243.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1484-1983dupA | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr6 | 125079438 | ||||||
| chr6:125079792 | A | G | 15 | a0001c0001t0023g0249 a0001c0001t0043g0005 a0001c0001t0045g0160 others(12): Show |
15 | HG00741.hp1 HG02055.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1484-1644A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125079792 | |||||||
| chr6:125079833 | T | C | 5 | a0001c0001t0015g0044 a0001c0001t0015g0206 a0001c0001t0015g0224 others(2): Show |
5 | NA18942.hp2 NA18943.hp1 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.1484-1603T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125079833 | |||||||
| chr6:125079888 | A | T | 15 | a0001c0001t0023g0249 a0001c0001t0043g0005 a0001c0001t0045g0160 others(12): Show |
15 | HG00741.hp1 HG02055.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1484-1548A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125079888 | |||||||
| chr6:125080124 | T | A | 3 | a0001c0001t0023g0249 a0001c0001t0068g0244 a0001c0003t0023g0142 |
3 | HG02451.hp2 HG03098.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1484-1312T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125080124 | |||||||
| chr6:125080174 | C | G | 1 | a0001c0001t0001g0213 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1484-1262C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125080174 | |||||||
| chr6:125080355 | C | G | 14 | a0001c0001t0003g0003 a0001c0001t0003g0084 a0001c0001t0003g0114 others(11): Show |
16 | HG00642.hp1 HG00735.hp2 HG02083.hp1 others(13): Show |
intron_variant | MODIFIER | c.1484-1081C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125080355 | |||||||
| chr6:125080418 | C | T | 10 | a0001c0001t0043g0005 a0003c0004t0011g0148 a0003c0004t0011g0149 others(7): Show |
10 | HG00741.hp1 HG02055.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1484-1018C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125080418 | |||||||
| chr6:125080574 | C | T | 1 | a0001c0001t0055g0073 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1484-862C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125080574 | |||||||
| chr6:125080575 | G | A | 3 | a0001c0001t0023g0249 a0001c0001t0068g0244 a0001c0003t0023g0142 |
3 | HG02451.hp2 HG03098.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1484-861G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125080575 | |||||||
| chr6:125080686 | G | C | 3 | a0001c0001t0023g0249 a0001c0001t0068g0244 a0001c0003t0023g0142 |
3 | HG02451.hp2 HG03098.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1484-750G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 4/5 | chr6 | 125080686 | |||||||
| chr6:125081542 | A | T | 1 | a0001c0001t0033g0133 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1555+35A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 5/5 | chr6 | 125081542 | |||||||
| chr6:125081565 | C | T | 132 | a0001c0001t0001g0134 a0001c0001t0001g0136 a0001c0001t0002g0054 others(129): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.1555+58C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 5/5 | chr6 | 125081565 | |||||||
| chr6:125081625 | T | G | 1 | a0001c0001t0017g0253 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1555+118T>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 5/5 | chr6 | 125081625 | |||||||
| chr6:125081732 | C | T | 132 | a0001c0001t0001g0134 a0001c0001t0001g0136 a0001c0001t0002g0054 others(129): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.1555+225C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 5/5 | chr6 | 125081732 | |||||||
| chr6:125081733 | C | G | 3 | a0001c0001t0017g0100 a0001c0001t0017g0153 a0002c0002t0073g0029 |
3 | HG01884.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1555+226C>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 5/5 | chr6 | 125081733 | |||||||
| chr6:125081863 | C | T | 26 | a0001c0001t0006g0004 a0001c0001t0006g0146 a0001c0001t0006g0157 others(23): Show |
26 | HG00741.hp1 HG01884.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1555+356C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 5/5 | chr6 | 125081863 | |||||||
| chr6:125082133 | A | G | 46 | a0001c0001t0002g0054 a0001c0001t0002g0055 a0001c0001t0002g0058 others(43): Show |
47 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.1555+626A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 5/5 | chr6 | 125082133 | |||||||
| chr6:125082203 | A | T | 1 | a0001c0003t0064g0188 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1556-661A>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 5/5 | chr6 | 125082203 | |||||||
| chr6:125082248 | T | C | 91 | a0001c0001t0001g0134 a0001c0001t0001g0136 a0001c0001t0002g0054 others(88): Show |
92 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(89): Show |
intron_variant | MODIFIER | c.1556-616T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 5/5 | chr6 | 125082248 | |||||||
| chr6:125082293 | G | T | 2 | a0001c0001t0012g0064 a0001c0001t0012g0125 |
2 | HG00140.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1556-571G>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 5/5 | chr6 | 125082293 | |||||||
| chr6:125082320 | G | A | 9 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0051 others(6): Show |
9 | HG01255.hp1 HG01358.hp2 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.1556-544G>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 5/5 | chr6 | 125082320 | |||||||
| chr6:125082347 | T | C | 1 | a0001c0003t0064g0188 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1556-517T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 5/5 | chr6 | 125082347 | |||||||
| chr6:125082478 | A | G | 1 | a0001c0003t0064g0188 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1556-386A>G | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 5/5 | chr6 | 125082478 | |||||||
| chr6:125082545 | T | A | 1 | a0001c0001t0001g0262 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1556-319T>A | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 5/5 | chr6 | 125082545 | |||||||
| chr6:125082661 | G | C | 2 | a0001c0001t0001g0049 a0001c0001t0001g0115 |
2 | NA18956.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.1556-203G>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 5/5 | chr6 | 125082661 | |||||||
| chr6:125082720 | T | C | 15 | a0001c0001t0023g0249 a0001c0001t0043g0005 a0001c0001t0045g0160 others(12): Show |
15 | HG00741.hp1 HG02055.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1556-144T>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 5/5 | chr6 | 125082720 | |||||||
| chr6:125082771 | C | T | 26 | a0001c0001t0006g0004 a0001c0001t0006g0146 a0001c0001t0006g0157 others(23): Show |
26 | HG00741.hp1 HG01884.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1556-93C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 5/5 | chr6 | 125082771 | |||||||
| chr6:125082777 | C | T | 26 | a0001c0001t0006g0004 a0001c0001t0006g0146 a0001c0001t0006g0157 others(23): Show |
26 | HG00741.hp1 HG01884.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1556-87C>T | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 5/5 | chr6 | 125082777 | |||||||
| chr6:125082793 | A | C | 9 | a0001c0001t0010g0144 a0001c0001t0010g0147 a0001c0001t0010g0152 others(6): Show |
9 | HG01891.hp2 HG02109.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1556-71A>C | RNF217 | ENSG00000146373.17 | transcript | ENST00000521654.7 | protein_coding | 5/5 | chr6 | 125082793 |