Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 100507650 |
| ensemblid | ENSG00000215277.9 |
| hgncid | 20438 |
| symbol | RNF212B |
| name | ring finger protein 212B |
| refseq_nuc | NM_001282322.3 |
| refseq_prot | NP_001269251.1 |
| ensembl_nuc | ENST00000430154.7 |
| ensembl_prot | ENSP00000397830.2 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 23237936 |
| end | 23273477 |
| strand | + |
| ver | v1.2 |
| region | chr14:23237936-23273477 |
| region5000 | chr14:23232936-23278477 |
| regionname0 | RNF212B_chr14_23237936_23273477 |
| regionname5000 | RNF212B_chr14_23232936_23278477 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 300 | 366 | 96 | 61 | 171 | 18 | 18 | 128 | RNF212B_chr14_23232936_23278477 | RNF212B | MDWFH others(295): Show |
chr14 | 23232936 | 23278477 |
| a0002 | 0/0 | 300 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | MDWFH others(295): Show |
chr14 | 23232936 | 23278477 |
| a0003 | 0/0 | 300 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | MDWFH others(295): Show |
chr14 | 23232936 | 23278477 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 900 | 366 | 96 | 61 | 171 | 18 | 18 | RNF212B_chr14_23232936_23278477 | RNF212B | ATGGA others(895): Show |
chr14 | 23232936 | 23278477 | ||
| a0002c0002 | 0/0 | 900 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | ATGGA others(895): Show |
chr14 | 23232936 | 23278477 | ||
| a0003c0003 | 0/0 | 900 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | ATGGA others(895): Show |
chr14 | 23232936 | 23278477 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1609 | 209 | 72 | 25 | 92 | 9 | 10 | RNF212B_chr14_23232936_23278477 | RNF212B | CTCTT others(1604): Show |
chr14 | 23232936 | 23278477 |
| a0001c0001t0002 | 1/0 | 1609 | 145 | 23 | 29 | 78 | 7 | 7 | RNF212B_chr14_23232936_23278477 | RNF212B | CTCTT others(1604): Show |
chr14 | 23232936 | 23278477 |
| a0001c0001t0003 | 0/0 | 1609 | 7 | 0 | 6 | 0 | 1 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | CTCTT others(1604): Show |
chr14 | 23232936 | 23278477 |
| a0001c0001t0004 | 0/0 | 1609 | 1 | 0 | 0 | 0 | 1 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | CTCTT others(1604): Show |
chr14 | 23232936 | 23278477 |
| a0001c0001t0005 | 0/0 | 1609 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | CTCTT others(1604): Show |
chr14 | 23232936 | 23278477 |
| a0001c0001t0006 | 0/0 | 1582 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | CTCTT others(1577): Show |
chr14 | 23232936 | 23278477 |
| a0001c0001t0007 | 0/0 | 1599 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | CTCTT others(1594): Show |
chr14 | 23232936 | 23278477 |
| a0001c0001t0008 | 0/0 | 1609 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212B_chr14_23232936_23278477 | RNF212B | CTCTT others(1604): Show |
chr14 | 23232936 | 23278477 |
| a0002c0002t0002 | 0/0 | 1609 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | CTCTT others(1604): Show |
chr14 | 23232936 | 23278477 |
| a0003c0003t0002 | 0/0 | 1609 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | CTCTT others(1604): Show |
chr14 | 23232936 | 23278477 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0014 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0293 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0001 | 0/0 | 9 | 0 | 3 | 6 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0002 | 0/0 | 8 | 0 | 4 | 3 | 1 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0003 | 1/0 | 8 | 0 | 2 | 4 | 1 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0003g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0003g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0004g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0005g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0006g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0007g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0001c0001t0008g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| a0003c0003t0002g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0132 | EUR | GBR | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | GBR | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0197 | EUR | GBR | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0007 | EUR | GBR | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG00280 | hp1 | a0001 | c0001 | t0004 | g0236 | EUR | FIN | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0180 | EUR | FIN | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | FIN | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0179 | EUR | FIN | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | CHS | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG00438 | hp1 | a0002 | c0002 | t0002 | g0047 | EAS | CHS | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | CHS | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | CHS | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | CHS | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | CHS | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | CHS | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG00639 | hp2 | a0001 | c0001 | t0006 | g0015 | AMR | PUR | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0141 | AMR | PUR | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | CHS | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | CHS | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | PUR | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0137 | AMR | PUR | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0118 | AMR | PUR | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0120 | AMR | PUR | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0142 | AMR | PUR | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0020 | AMR | PUR | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0103 | AMR | PUR | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0170 | AMR | CLM | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0154 | AMR | CLM | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | CLM | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | CLM | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0114 | AMR | CLM | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | CLM | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | CLM | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0116 | AMR | CLM | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0089 | AMR | CLM | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0121 | AMR | CLM | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0112 | AMR | CLM | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0290 | AMR | CLM | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | CLM | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0131 | EUR | IBS | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0018 | EUR | IBS | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0172 | EUR | IBS | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0023 | EUR | IBS | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0018 | EUR | IBS | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0023 | EUR | IBS | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | ACB | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0303 | AFR | ACB | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | PEL | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PEL | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0043 | AMR | PEL | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0115 | AMR | PEL | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02004 | hp1 | a0003 | c0003 | t0002 | g0007 | AMR | PEL | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0104 | AMR | PEL | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | KHV | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | KHV | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | KHV | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0078 | AFR | ACB | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | ACB | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | KHV | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | KHV | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | KHV | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | KHV | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | KHV | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | KHV | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | CDX | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | CDX | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | ACB | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | ACB | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | ACB | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | ACB | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0068 | AMR | PEL | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0289 | AMR | PEL | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0071 | AFR | ACB | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | KHV | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | GWD | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0261 | AFR | GWD | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0088 | AFR | GWD | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0061 | AFR | GWD | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02647 | hp2 | a0001 | c0001 | t0005 | g0011 | AFR | GWD | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0035 | SAS | PJL | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02698 | hp2 | a0001 | c0001 | t0008 | g0206 | SAS | PJL | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0153 | SAS | PJL | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0079 | AFR | GWD | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0080 | AFR | GWD | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0302 | AFR | GWD | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0301 | AFR | GWD | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | ESN | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | ESN | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ESN | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0297 | AFR | ESN | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | ESN | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | ESN | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0291 | SAS | PJL | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0095 | SAS | PJL | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | MSL | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0106 | AFR | MSL | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0166 | AFR | ESN | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | ESN | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | ESN | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | ESN | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | ESN | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0161 | AFR | ESN | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | MSL | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | MSL | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | MSL | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | MSL | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | MSL | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | MSL | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | MSL | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0134 | AFR | ESN | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0081 | AFR | MSL | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | MSL | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0124 | SAS | PJL | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0094 | SAS | PJL | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | BEB | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0096 | SAS | BEB | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | STU | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | STU | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0274 | SAS | STU | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | STU | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0108 | AFR | YRI | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | YRI | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHB | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | CHB | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHB | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | YRI | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | YRI | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | LWK | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | LWK | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | LWK | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | LWK | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA19063 | hp2 | a0001 | c0001 | t0007 | g0229 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0107 | AFR | YRI | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ASW | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0054 | AFR | ASW | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0122 | EUR | TSI | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0020 | EUR | TSI | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0187 | EUR | TSI | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0133 | EUR | TSI | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0135 | AFR | ACB | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0091 | AFR | ACB | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | ACB | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | ACB | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | MSL | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | USA | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | USA | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0105 | AFR | USA | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | USA | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | LWK | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | LWK | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0293 | REF | REF | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0003 | REF | REF | RNF212B_chr14_23232936_23278477 | RNF212B | chr14 | 23232936 | 23278477 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:23268938 | G | C | 1 | a0002 | 1 | HG00438.hp1 | missense_variant | MODERATE | c.649G>C | p.Ala217Pro | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 12/15 | 770/1610 | 649/903 | 217/300 | chr14 | 23268938 | |||
| chr14:23270624 | T | C | 1 | a0003 | 1 | HG02004.hp1 | missense_variant | MODERATE | c.797T>C | p.Leu266Pro | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 14/15 | 918/1610 | 797/903 | 266/300 | chr14 | 23270624 | |||
| chr14:23272889 | T | C | 1 | a0001 | 1 | HG02647.hp2 | stop_lost | HIGH | c.901T>C | p.Ter301Glnext*? | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 15/15 | 1022/1610 | 901/903 | 301/300 | chr14 | 23272889 | |||
| chr14:23273450 | TAAAGACG others(43): Show |
T | 1 | a0001 | 1 | HG00639.hp2 | splice_region_variant | LOW | c.*560_*609delAAAGAC others(44): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 15/15 | chr14 | 23273450 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:23238020 | G | C | 1 | a0001c0001t0004 | 1 | HG00280.hp1 | 5_prime_UTR_variant | MODIFIER | c.-37G>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/15 | 2326 | chr14 | 23238020 | ||||||
| chr14:23273087 | A | G | 1 | a0001c0001t0003 | 7 | HG01069.hp1 HG01192.hp1 HG01255.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*196A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 15/15 | 196 | chr14 | 23273087 | ||||||
| chr14:23273126 | C | T | 6 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(3): Show |
219 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(216): Show |
3_prime_UTR_variant | MODIFIER | c.*235C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 15/15 | 235 | chr14 | 23273126 | ||||||
| chr14:23273228 | ATATACTC others(3): Show |
A | 1 | a0001c0001t0007 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*338_*347delTATACT others(4): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 15/15 | 338 | chr14 | 23273228 | ||||||
| chr14:23273277 | T | C | 1 | a0001c0001t0008 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*386T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 15/15 | 386 | chr14 | 23273277 | ||||||
| chr14:23273330 | T | C | 1 | a0001c0001t0008 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*439T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 15/15 | 439 | chr14 | 23273330 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:23238117 | T | C | 2 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
2 | HG01884.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-2+62T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | chr14 | 23238117 | |||||||
| chr14:23238123 | G | A | 1 | a0001c0001t0002g0035 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-2+68G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | chr14 | 23238123 | |||||||
| chr14:23238144 | G | C | 1 | a0001c0001t0002g0036 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-2+89G>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | chr14 | 23238144 | |||||||
| chr14:23238150 | C | A | 1 | a0001c0001t0002g0037 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-2+95C>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | chr14 | 23238150 | |||||||
| chr14:23238161 | T | A | 1 | a0001c0001t0002g0038 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-2+106T>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | chr14 | 23238161 | |||||||
| chr14:23238198 | A | G | 6 | a0001c0001t0001g0298 a0001c0001t0001g0299 a0001c0001t0001g0300 others(3): Show |
6 | HG01891.hp1 HG02717.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2+143A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | chr14 | 23238198 | |||||||
| chr14:23238265 | G | GT | 51 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(48): Show |
62 | HG00544.hp2 HG00738.hp2 HG01109.hp2 others(59): Show |
intron_variant | MODIFIER | c.-2+216dupT | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 23238265 | ||||||
| chr14:23238292 | G | A | 2 | a0001c0001t0001g0262 a0001c0001t0002g0261 |
2 | HG02572.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-2+237G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | chr14 | 23238292 | |||||||
| chr14:23238534 | C | G | 2 | a0001c0001t0001g0296 a0001c0001t0001g0297 |
2 | HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-2+479C>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | chr14 | 23238534 | |||||||
| chr14:23238598 | C | T | 48 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(45): Show |
54 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.-2+543C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | chr14 | 23238598 | |||||||
| chr14:23238632 | A | G | 54 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(51): Show |
64 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.-2+577A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | chr14 | 23238632 | |||||||
| chr14:23238700 | G | A | 2 | a0001c0001t0001g0296 a0001c0001t0001g0297 |
2 | HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-2+645G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | chr14 | 23238700 | |||||||
| chr14:23238708 | A | G | 71 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0027 others(68): Show |
80 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.-2+653A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | chr14 | 23238708 | |||||||
| chr14:23238737 | A | AAAT | 58 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0033 others(55): Show |
69 | HG00323.hp1 HG00438.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.-2+725_-2+727dupAA others(1): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 23238737 | ||||||
| chr14:23238737 | A | AAATAAT | 13 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 others(10): Show |
13 | HG00741.hp2 HG01978.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.-2+722_-2+727dupAA others(4): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 23238737 | ||||||
| chr14:23238737 | AAAT | A | 28 | a0001c0001t0001g0004 a0001c0001t0001g0031 a0001c0001t0001g0160 others(25): Show |
33 | HG00408.hp2 HG00544.hp2 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.-2+725_-2+727delAA others(1): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 23238737 | ||||||
| chr14:23238737 | AAATAAT | A | 9 | a0001c0001t0001g0011 a0001c0001t0001g0256 a0001c0001t0001g0257 others(6): Show |
10 | HG01168.hp1 HG01169.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.-2+722_-2+727delAA others(4): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 23238737 | ||||||
| chr14:23238737 | AAATAATA others(2): Show |
A | 8 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0164 others(5): Show |
12 | HG00609.hp1 HG02922.hp1 HG02970.hp1 others(9): Show |
intron_variant | MODIFIER | c.-2+719_-2+727delAA others(7): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 23238737 | ||||||
| chr14:23238737 | AAATAATA others(5): Show |
A | 1 | a0001c0001t0002g0166 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-2+716_-2+727delAA others(10): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 23238737 | ||||||
| chr14:23238737 | AAATAATA others(8): Show |
A | 1 | a0001c0001t0002g0167 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-2+713_-2+727delAA others(13): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 23238737 | ||||||
| chr14:23238737 | AAATAATA others(11): Show |
A | 1 | a0001c0001t0001g0169 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-2+710_-2+727delAA others(16): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 23238737 | ||||||
| chr14:23238745 | A | G | 1 | a0001c0001t0003g0170 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-2+690A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | chr14 | 23238745 | |||||||
| chr14:23238755 | T | TAAC | 5 | a0001c0001t0001g0032 a0001c0001t0001g0279 a0001c0001t0001g0280 others(2): Show |
6 | HG02486.hp2 HG02818.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2+702_-2+703insCA others(1): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 23238755 | ||||||
| chr14:23238758 | T | C | 7 | a0001c0001t0001g0014 a0001c0001t0001g0283 a0001c0001t0001g0284 others(4): Show |
9 | HG00738.hp2 HG01884.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.-2+703T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | chr14 | 23238758 | |||||||
| chr14:23238761 | T | C | 4 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(1): Show |
4 | HG01433.hp2 HG02300.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+706T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | chr14 | 23238761 | |||||||
| chr14:23238765 | A | C | 1 | a0001c0001t0001g0168 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-2+710A>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | chr14 | 23238765 | |||||||
| chr14:23238768 | A | AATCATCA others(2): Show |
7 | a0001c0001t0001g0025 a0001c0001t0001g0209 a0001c0001t0001g0210 others(4): Show |
8 | HG00597.hp1 HG02523.hp1 HG03942.hp1 others(5): Show |
intron_variant | MODIFIER | c.-2+715_-2+716insCA others(7): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 23238768 | ||||||
| chr14:23238768 | A | C | 4 | a0001c0001t0001g0026 a0001c0001t0001g0168 a0001c0001t0001g0216 others(1): Show |
5 | HG00438.hp2 HG00673.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2+713A>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | chr14 | 23238768 | |||||||
| chr14:23238771 | A | AATCATCA others(2): Show |
12 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0024 others(9): Show |
18 | HG00423.hp2 HG01069.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.-2+718_-2+719insCA others(7): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 23238771 | ||||||
| chr14:23238771 | A | AATCATCA others(5): Show |
2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG00738.hp1 NA18940.hp1 |
intron_variant | MODIFIER | c.-2+718_-2+719insCA others(10): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 23238771 | ||||||
| chr14:23238771 | A | C | 12 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0168 others(9): Show |
14 | HG00438.hp2 HG00597.hp1 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.-2+716A>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | chr14 | 23238771 | |||||||
| chr14:23238774 | A | AATCATCA others(2): Show |
12 | a0001c0001t0001g0023 a0001c0001t0001g0188 a0001c0001t0001g0189 others(9): Show |
13 | HG00140.hp1 HG01516.hp2 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.-2+721_-2+722insCA others(7): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 23238774 | ||||||
| chr14:23238774 | A | AATCATCA others(5): Show |
3 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 |
3 | HG02040.hp2 NA18957.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.-2+721_-2+722insCA others(10): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 23238774 | ||||||
| chr14:23238774 | A | C | 26 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0024 others(23): Show |
34 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.-2+719A>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | chr14 | 23238774 | |||||||
| chr14:23238777 | A | AATCATCA others(2): Show |
5 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(2): Show |
5 | HG00280.hp2 HG00323.hp2 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2+724_-2+725insCA others(7): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 23238777 | ||||||
| chr14:23238777 | A | AATCATCA others(5): Show |
1 | a0001c0001t0001g0178 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-2+724_-2+725insCA others(10): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 23238777 | ||||||
| chr14:23238777 | A | AATCATCA others(8): Show |
1 | a0001c0001t0001g0177 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-2+724_-2+725insCA others(13): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 23238777 | ||||||
| chr14:23238777 | A | C | 41 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0023 others(38): Show |
50 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.-2+722A>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | chr14 | 23238777 | |||||||
| chr14:23238780 | A | AATAATAA others(11): Show |
1 | a0001c0001t0001g0171 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-2+727_-2+728insAA others(16): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 23238780 | ||||||
| chr14:23238780 | A | AATAATCA others(8): Show |
1 | a0001c0001t0001g0173 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-2+727_-2+728insAA others(13): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 23238780 | ||||||
| chr14:23238780 | A | AATAATCA others(11): Show |
1 | a0001c0001t0001g0172 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-2+727_-2+728insAA others(16): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 23238780 | ||||||
| chr14:23238780 | A | AATCATCA others(5): Show |
3 | a0001c0001t0001g0022 a0001c0001t0001g0175 a0001c0001t0001g0176 |
4 | HG00642.hp1 HG01106.hp1 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2+728_-2+729insAT others(10): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 23238780 | ||||||
| chr14:23238780 | A | AATCATCA others(8): Show |
1 | a0001c0001t0001g0174 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-2+728_-2+729insAT others(13): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 23238780 | ||||||
| chr14:23238780 | A | C | 48 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0023 others(45): Show |
57 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.-2+725A>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | chr14 | 23238780 | |||||||
| chr14:23239033 | A | G | 155 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(152): Show |
182 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.-2+978A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | chr14 | 23239033 | |||||||
| chr14:23239178 | T | C | 155 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(152): Show |
182 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.-2+1123T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | chr14 | 23239178 | |||||||
| chr14:23239274 | G | A | 1 | a0001c0001t0001g0168 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-1-1071G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | chr14 | 23239274 | |||||||
| chr14:23239312 | G | A | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-1-1033G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | chr14 | 23239312 | |||||||
| chr14:23239339 | T | C | 1 | a0002c0002t0002g0047 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-1-1006T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | chr14 | 23239339 | |||||||
| chr14:23239351 | T | C | 154 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(151): Show |
181 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.-1-994T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | chr14 | 23239351 | |||||||
| chr14:23239426 | C | A | 1 | a0001c0001t0001g0283 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-1-919C>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | chr14 | 23239426 | |||||||
| chr14:23239560 | G | T | 24 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0029 others(21): Show |
31 | HG00544.hp2 HG01243.hp2 HG02015.hp1 others(28): Show |
intron_variant | MODIFIER | c.-1-785G>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | chr14 | 23239560 | |||||||
| chr14:23239597 | G | T | 1 | a0001c0001t0002g0076 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-1-748G>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | chr14 | 23239597 | |||||||
| chr14:23239598 | A | T | 1 | a0001c0001t0002g0076 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-1-747A>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | chr14 | 23239598 | |||||||
| chr14:23239600 | T | G | 1 | a0001c0001t0002g0076 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-1-745T>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | chr14 | 23239600 | |||||||
| chr14:23239601 | G | T | 1 | a0001c0001t0002g0076 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-1-744G>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | chr14 | 23239601 | |||||||
| chr14:23239628 | T | C | 1 | a0001c0001t0002g0076 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-1-717T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | chr14 | 23239628 | |||||||
| chr14:23239658 | G | A | 17 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0279 others(14): Show |
20 | HG00738.hp2 HG01433.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.-1-687G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | chr14 | 23239658 | |||||||
| chr14:23239785 | A | G | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-1-560A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | chr14 | 23239785 | |||||||
| chr14:23239993 | A | AAC | 61 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0012 others(58): Show |
72 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.-1-329_-1-328dupAC | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 23239993 | ||||||
| chr14:23239993 | A | AACAC | 4 | a0001c0001t0001g0026 a0001c0001t0001g0209 a0001c0001t0001g0296 others(1): Show |
5 | HG01346.hp1 HG01496.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1-331_-1-328dupAC others(2): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 23239993 | ||||||
| chr14:23240034 | C | CA | 7 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0262 others(4): Show |
7 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1-298dupA | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 23240034 | ||||||
| chr14:23240034 | C | CAA | 43 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(40): Show |
49 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.-1-299_-1-298dupAA | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 23240034 | ||||||
| chr14:23240048 | T | A | 55 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(52): Show |
65 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.-1-297T>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | chr14 | 23240048 | |||||||
| chr14:23240106 | C | T | 70 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0027 others(67): Show |
79 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.-1-239C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | chr14 | 23240106 | |||||||
| chr14:23240192 | T | C | 2 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
2 | HG01884.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-1-153T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | chr14 | 23240192 | |||||||
| chr14:23240324 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-1-21C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | chr14 | 23240324 | |||||||
| chr14:23240327 | T | G | 1 | a0001c0001t0002g0222 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-1-18T>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 1/14 | chr14 | 23240327 | |||||||
| chr14:23240519 | T | C | 1 | a0001c0001t0001g0248 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.100+74T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 2/14 | chr14 | 23240519 | |||||||
| chr14:23240631 | A | G | 28 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(25): Show |
36 | HG00544.hp2 HG01243.hp2 HG02015.hp1 others(33): Show |
intron_variant | MODIFIER | c.100+186A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 2/14 | chr14 | 23240631 | |||||||
| chr14:23240716 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.100+271G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 2/14 | chr14 | 23240716 | |||||||
| chr14:23240907 | C | T | 3 | a0001c0001t0001g0262 a0001c0001t0001g0303 a0001c0001t0002g0261 |
3 | HG01891.hp1 HG02572.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.100+462C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 2/14 | chr14 | 23240907 | |||||||
| chr14:23241488 | A | G | 2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | NA18940.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.100+1043A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 2/14 | chr14 | 23241488 | |||||||
| chr14:23241500 | T | C | 5 | a0001c0001t0002g0017 a0001c0001t0002g0048 a0001c0001t0002g0077 others(2): Show |
6 | HG00423.hp1 NA18957.hp2 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.100+1055T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 2/14 | chr14 | 23241500 | |||||||
| chr14:23241519 | G | A | 1 | a0001c0001t0001g0249 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.100+1074G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 2/14 | chr14 | 23241519 | |||||||
| chr14:23241579 | A | G | 1 | a0001c0001t0001g0298 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.100+1134A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 2/14 | chr14 | 23241579 | |||||||
| chr14:23241616 | G | T | 1 | a0001c0001t0001g0292 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.100+1171G>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 2/14 | chr14 | 23241616 | |||||||
| chr14:23241666 | C | T | 2 | a0001c0001t0002g0155 a0001c0001t0002g0156 |
2 | NA19064.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.100+1221C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 2/14 | chr14 | 23241666 | |||||||
| chr14:23241667 | G | A | 7 | a0001c0001t0001g0169 a0001c0001t0002g0049 a0001c0001t0002g0050 others(4): Show |
7 | NA18982.hp2 NA18987.hp2 NA18989.hp2 others(4): Show |
intron_variant | MODIFIER | c.100+1222G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 2/14 | chr14 | 23241667 | |||||||
| chr14:23241910 | A | G | 127 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(124): Show |
146 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.101-1346A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 2/14 | chr14 | 23241910 | |||||||
| chr14:23242036 | C | T | 29 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(26): Show |
37 | HG00544.hp2 HG01243.hp2 HG02015.hp1 others(34): Show |
intron_variant | MODIFIER | c.101-1220C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 2/14 | chr14 | 23242036 | |||||||
| chr14:23242061 | G | T | 3 | a0001c0001t0001g0262 a0001c0001t0001g0303 a0001c0001t0002g0261 |
3 | HG01891.hp1 HG02572.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.101-1195G>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 2/14 | chr14 | 23242061 | |||||||
| chr14:23242081 | C | CA | 9 | a0001c0001t0001g0053 a0001c0001t0001g0086 a0001c0001t0002g0049 others(6): Show |
9 | HG02074.hp2 NA18967.hp1 NA18973.hp1 others(6): Show |
intron_variant | MODIFIER | c.101-1149dupA | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr14 | 23242081 | ||||||
| chr14:23242081 | CA | C | 31 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0044 others(28): Show |
33 | HG01109.hp1 HG01256.hp1 HG02055.hp1 others(30): Show |
intron_variant | MODIFIER | c.101-1149delA | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr14 | 23242081 | ||||||
| chr14:23242095 | A | AAAG | 12 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0279 others(9): Show |
15 | HG00738.hp2 HG01884.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.101-1159_101-1158i others(5): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr14 | 23242095 | ||||||
| chr14:23242098 | A | G | 28 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(25): Show |
36 | HG00544.hp2 HG01243.hp2 HG02015.hp1 others(33): Show |
intron_variant | MODIFIER | c.101-1158A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 2/14 | chr14 | 23242098 | |||||||
| chr14:23242102 | A | AAAAAGAA others(3): Show |
42 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(39): Show |
52 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.101-1150_101-1149i others(12): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr14 | 23242102 | ||||||
| chr14:23242107 | A | AAAAAGAA others(3): Show |
2 | a0001c0001t0001g0292 a0001c0001t0002g0261 |
2 | HG02559.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.101-1149_101-1148i others(12): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 2/14 | chr14 | 23242107 | |||||||
| chr14:23242107 | A | AAGAAAAG others(6): Show |
1 | a0001c0001t0001g0200 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.101-1149_101-1148i others(15): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 2/14 | chr14 | 23242107 | |||||||
| chr14:23242107 | A | AAGAAAAG others(12): Show |
1 | a0001c0001t0001g0173 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.101-1149_101-1148i others(21): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 2/14 | chr14 | 23242107 | |||||||
| chr14:23242108 | G | A | 11 | a0001c0001t0001g0173 a0001c0001t0001g0200 a0001c0001t0001g0223 others(8): Show |
11 | HG01109.hp2 HG01433.hp2 HG02300.hp2 others(8): Show |
intron_variant | MODIFIER | c.101-1148G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 2/14 | chr14 | 23242108 | |||||||
| chr14:23242108 | G | GA | 47 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(44): Show |
57 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.101-1144dupA | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr14 | 23242108 | ||||||
| chr14:23242108 | G | GAAAAGA | 58 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0027 others(55): Show |
67 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.101-1131_101-1126d others(8): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr14 | 23242108 | ||||||
| chr14:23242108 | G | GAAAAGAA others(5): Show |
10 | a0001c0001t0001g0168 a0001c0001t0001g0179 a0001c0001t0001g0180 others(7): Show |
10 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(7): Show |
intron_variant | MODIFIER | c.101-1137_101-1126d others(14): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr14 | 23242108 | ||||||
| chr14:23242108 | G | GAAAAGAA others(11): Show |
1 | a0001c0001t0001g0171 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.101-1143_101-1126d others(20): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr14 | 23242108 | ||||||
| chr14:23242160 | G | C | 5 | a0001c0001t0002g0039 a0001c0001t0002g0078 a0001c0001t0002g0079 others(2): Show |
5 | HG02055.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.101-1096G>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 2/14 | chr14 | 23242160 | |||||||
| chr14:23242215 | A | AT | 55 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(52): Show |
65 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.101-1041_101-1040i others(3): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 2/14 | chr14 | 23242215 | |||||||
| chr14:23242216 | G | T | 55 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(52): Show |
65 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.101-1040G>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 2/14 | chr14 | 23242216 | |||||||
| chr14:23242279 | C | T | 1 | a0001c0001t0002g0087 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.101-977C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 2/14 | chr14 | 23242279 | |||||||
| chr14:23242282 | G | A | 1 | a0001c0001t0001g0294 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.101-974G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 2/14 | chr14 | 23242282 | |||||||
| chr14:23242917 | T | TG | 57 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(54): Show |
67 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.101-338dupG | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr14 | 23242917 | ||||||
| chr14:23243026 | G | A | 1 | a0001c0001t0001g0250 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.101-230G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 2/14 | chr14 | 23243026 | |||||||
| chr14:23243029 | C | T | 1 | a0001c0001t0002g0038 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.101-227C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 2/14 | chr14 | 23243029 | |||||||
| chr14:23243185 | A | G | 3 | a0001c0001t0001g0028 a0001c0001t0001g0244 a0001c0001t0001g0245 |
4 | NA18984.hp2 NA18987.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-71A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 2/14 | chr14 | 23243185 | |||||||
| chr14:23243249 | C | T | 3 | a0001c0001t0001g0221 a0001c0001t0001g0243 a0001c0001t0001g0255 |
3 | NA18992.hp1 NA18997.hp1 NA18999.hp1 |
splice_region_variant&intron_variant | LOW | c.101-7C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 2/14 | chr14 | 23243249 | |||||||
| chr14:23243332 | A | T | 1 | a0001c0001t0001g0174 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.153+24A>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 3/14 | chr14 | 23243332 | |||||||
| chr14:23243341 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.153+33C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 3/14 | chr14 | 23243341 | |||||||
| chr14:23243418 | G | A | 28 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(25): Show |
36 | HG00544.hp2 HG01243.hp2 HG02015.hp1 others(33): Show |
intron_variant | MODIFIER | c.153+110G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 3/14 | chr14 | 23243418 | |||||||
| chr14:23243540 | T | C | 155 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(152): Show |
182 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.153+232T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 3/14 | chr14 | 23243540 | |||||||
| chr14:23243589 | G | C | 1 | a0001c0001t0002g0037 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.153+281G>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 3/14 | chr14 | 23243589 | |||||||
| chr14:23243650 | C | G | 3 | a0001c0001t0001g0262 a0001c0001t0001g0303 a0001c0001t0002g0261 |
3 | HG01891.hp1 HG02572.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.153+342C>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 3/14 | chr14 | 23243650 | |||||||
| chr14:23243680 | G | C | 1 | a0001c0001t0001g0055 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.153+372G>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 3/14 | chr14 | 23243680 | |||||||
| chr14:23243694 | C | CA | 21 | a0001c0001t0001g0082 a0001c0001t0002g0050 a0001c0001t0002g0056 others(18): Show |
21 | HG01109.hp1 HG01261.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.153+411dupA | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr14 | 23243694 | ||||||
| chr14:23243694 | CA | C | 8 | a0001c0001t0001g0188 a0001c0001t0001g0201 a0001c0001t0001g0202 others(5): Show |
8 | HG01169.hp1 HG01256.hp1 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.153+411delA | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr14 | 23243694 | ||||||
| chr14:23243694 | CAA | C | 49 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(46): Show |
59 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.153+410_153+411del others(2): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr14 | 23243694 | ||||||
| chr14:23243694 | CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.153+400_153+411del others(12): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr14 | 23243694 | ||||||
| chr14:23243707 | AAAAAAAA others(7): Show |
A | 1 | a0001c0001t0001g0234 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.153+402_153+415del others(14): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr14 | 23243707 | ||||||
| chr14:23243716 | A | G | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.153+408A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 3/14 | chr14 | 23243716 | |||||||
| chr14:23243717 | A | AGC | 22 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0022 others(19): Show |
28 | HG00544.hp2 HG01106.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.153+409_153+410ins others(2): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 3/14 | chr14 | 23243717 | |||||||
| chr14:23243717 | A | AGCAAGC | 4 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0267 others(1): Show |
4 | HG02257.hp1 HG02258.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.153+409_153+410ins others(6): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 3/14 | chr14 | 23243717 | |||||||
| chr14:23243717 | A | C | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.153+409A>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 3/14 | chr14 | 23243717 | |||||||
| chr14:23243717 | AAAGC | A | 22 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0262 others(19): Show |
25 | HG00738.hp2 HG01109.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.153+436_153+439del others(4): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr14 | 23243717 | ||||||
| chr14:23243719 | AG | A | 12 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(9): Show |
12 | HG01256.hp2 HG02080.hp2 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.153+412delG | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 3/14 | chr14 | 23243719 | |||||||
| chr14:23243719 | AGC | A | 31 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(28): Show |
36 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.153+412_153+413del others(2): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 3/14 | chr14 | 23243719 | |||||||
| chr14:23243721 | C | A | 12 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(9): Show |
12 | HG01256.hp2 HG02080.hp2 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.153+413C>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 3/14 | chr14 | 23243721 | |||||||
| chr14:23243736 | G | A | 17 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0279 others(14): Show |
20 | HG00738.hp2 HG01433.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.153+428G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 3/14 | chr14 | 23243736 | |||||||
| chr14:23243892 | C | A | 57 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(54): Show |
67 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.154-430C>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 3/14 | chr14 | 23243892 | |||||||
| chr14:23243907 | G | A | 8 | a0001c0001t0002g0058 a0001c0001t0002g0059 a0001c0001t0002g0070 others(5): Show |
8 | HG00609.hp2 HG02071.hp2 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.154-415G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 3/14 | chr14 | 23243907 | |||||||
| chr14:23243911 | C | G | 98 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(95): Show |
115 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(112): Show |
intron_variant | MODIFIER | c.154-411C>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 3/14 | chr14 | 23243911 | |||||||
| chr14:23243995 | T | C | 3 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG00280.hp2 HG00323.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.154-327T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 3/14 | chr14 | 23243995 | |||||||
| chr14:23244007 | G | A | 2 | a0001c0001t0001g0223 a0001c0001t0001g0225 |
2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.154-315G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 3/14 | chr14 | 23244007 | |||||||
| chr14:23244069 | A | T | 3 | a0001c0001t0001g0284 a0001c0001t0001g0287 a0001c0001t0001g0288 |
3 | HG01884.hp2 HG02055.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.154-253A>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 3/14 | chr14 | 23244069 | |||||||
| chr14:23244205 | A | G | 1 | a0001c0001t0002g0141 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.154-117A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 3/14 | chr14 | 23244205 | |||||||
| chr14:23244282 | A | G | 1 | a0001c0001t0001g0197 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.154-40A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 3/14 | chr14 | 23244282 | |||||||
| chr14:23244545 | A | T | 1 | a0001c0001t0001g0215 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.228+149A>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23244545 | |||||||
| chr14:23244743 | C | T | 1 | a0001c0001t0001g0294 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.228+347C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23244743 | |||||||
| chr14:23244937 | A | G | 2 | a0001c0001t0001g0296 a0001c0001t0001g0297 |
2 | HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.228+541A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23244937 | |||||||
| chr14:23245037 | T | A | 1 | a0001c0001t0001g0184 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.228+641T>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23245037 | |||||||
| chr14:23245038 | C | A | 1 | a0001c0001t0001g0184 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.228+642C>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23245038 | |||||||
| chr14:23245039 | C | T | 155 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(152): Show |
182 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.228+643C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23245039 | |||||||
| chr14:23245179 | A | G | 3 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0269 |
3 | HG02257.hp1 HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.228+783A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23245179 | |||||||
| chr14:23245190 | T | C | 2 | a0001c0001t0002g0088 a0001c0001t0002g0166 |
2 | HG02615.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.228+794T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23245190 | |||||||
| chr14:23245239 | C | T | 7 | a0001c0001t0001g0032 a0001c0001t0001g0279 a0001c0001t0001g0280 others(4): Show |
8 | HG02486.hp2 HG02818.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.228+843C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23245239 | |||||||
| chr14:23245241 | A | G | 3 | a0001c0001t0002g0058 a0001c0001t0002g0059 a0001c0001t0002g0102 |
3 | HG00609.hp2 HG02071.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.228+845A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23245241 | |||||||
| chr14:23245258 | G | A | 9 | a0001c0001t0001g0044 a0001c0001t0001g0060 a0001c0001t0001g0144 others(6): Show |
9 | HG02257.hp2 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.228+862G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23245258 | |||||||
| chr14:23245473 | G | C | 70 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0027 others(67): Show |
79 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.228+1077G>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23245473 | |||||||
| chr14:23245531 | G | C | 2 | a0001c0001t0001g0262 a0001c0001t0002g0261 |
2 | HG02572.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.228+1135G>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23245531 | |||||||
| chr14:23245724 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.228+1328A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23245724 | |||||||
| chr14:23245750 | C | T | 28 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(25): Show |
36 | HG00544.hp2 HG01243.hp2 HG02015.hp1 others(33): Show |
intron_variant | MODIFIER | c.228+1354C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23245750 | |||||||
| chr14:23245869 | T | C | 3 | a0001c0001t0002g0058 a0001c0001t0002g0059 a0001c0001t0002g0102 |
3 | HG00609.hp2 HG02071.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.228+1473T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23245869 | |||||||
| chr14:23245905 | G | A | 5 | a0001c0001t0002g0039 a0001c0001t0002g0078 a0001c0001t0002g0079 others(2): Show |
5 | HG02055.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.228+1509G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23245905 | |||||||
| chr14:23245914 | G | A | 1 | a0001c0001t0002g0155 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.228+1518G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23245914 | |||||||
| chr14:23245972 | A | G | 13 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0279 others(10): Show |
16 | HG00738.hp2 HG01884.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.228+1576A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23245972 | |||||||
| chr14:23246036 | T | A | 1 | a0001c0001t0001g0216 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.228+1640T>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23246036 | |||||||
| chr14:23246134 | C | CT | 10 | a0001c0001t0001g0044 a0001c0001t0001g0060 a0001c0001t0001g0144 others(7): Show |
10 | HG01891.hp1 HG02257.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.228+1751dupT | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr14 | 23246134 | ||||||
| chr14:23246237 | C | T | 2 | a0001c0001t0001g0296 a0001c0001t0001g0297 |
2 | HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.228+1841C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23246237 | |||||||
| chr14:23246259 | A | G | 1 | a0001c0001t0001g0267 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.228+1863A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23246259 | |||||||
| chr14:23246369 | G | A | 17 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0279 others(14): Show |
20 | HG00738.hp2 HG01433.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.228+1973G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23246369 | |||||||
| chr14:23246463 | T | A | 9 | a0001c0001t0001g0044 a0001c0001t0001g0060 a0001c0001t0001g0144 others(6): Show |
9 | HG02257.hp2 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.228+2067T>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23246463 | |||||||
| chr14:23246474 | C | A | 17 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0279 others(14): Show |
20 | HG00738.hp2 HG01433.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.228+2078C>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23246474 | |||||||
| chr14:23246694 | C | T | 2 | a0001c0001t0002g0139 a0001c0001t0002g0140 |
2 | NA18959.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.228+2298C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23246694 | |||||||
| chr14:23246702 | A | G | 1 | a0001c0001t0001g0217 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.228+2306A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23246702 | |||||||
| chr14:23246724 | A | G | 1 | a0001c0001t0001g0268 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.228+2328A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23246724 | |||||||
| chr14:23246757 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.228+2361T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23246757 | |||||||
| chr14:23246999 | G | C | 5 | a0001c0001t0001g0032 a0001c0001t0001g0279 a0001c0001t0001g0280 others(2): Show |
6 | HG02486.hp2 HG02818.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.228+2603G>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23246999 | |||||||
| chr14:23247062 | C | T | 2 | a0001c0001t0001g0242 a0001c0001t0001g0256 |
2 | HG01099.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.228+2666C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23247062 | |||||||
| chr14:23247094 | C | T | 5 | a0001c0001t0002g0039 a0001c0001t0002g0078 a0001c0001t0002g0079 others(2): Show |
5 | HG02055.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.228+2698C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23247094 | |||||||
| chr14:23247123 | C | T | 2 | a0001c0001t0002g0097 a0001c0001t0002g0138 |
2 | HG02027.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.228+2727C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23247123 | |||||||
| chr14:23247140 | C | CA | 125 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(122): Show |
142 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.228+2758dupA | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr14 | 23247140 | ||||||
| chr14:23247140 | CA | C | 5 | a0001c0001t0001g0160 a0001c0001t0003g0006 a0001c0001t0003g0020 others(2): Show |
8 | HG01069.hp1 HG01192.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.228+2758delA | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr14 | 23247140 | ||||||
| chr14:23247184 | A | G | 17 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0279 others(14): Show |
20 | HG00738.hp2 HG01433.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.228+2788A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23247184 | |||||||
| chr14:23247462 | A | G | 1 | a0001c0001t0002g0136 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.228+3066A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23247462 | |||||||
| chr14:23247482 | C | G | 18 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0279 others(15): Show |
21 | HG00738.hp2 HG01109.hp2 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.228+3086C>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23247482 | |||||||
| chr14:23247581 | T | A | 1 | a0001c0001t0001g0023 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.228+3185T>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23247581 | |||||||
| chr14:23248022 | G | T | 68 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0027 others(65): Show |
77 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.228+3626G>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23248022 | |||||||
| chr14:23248025 | G | T | 68 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0027 others(65): Show |
77 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.228+3629G>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23248025 | |||||||
| chr14:23248029 | G | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0276 a0001c0001t0005g0011 |
4 | HG02280.hp2 HG02647.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.228+3633G>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23248029 | |||||||
| chr14:23248051 | T | A | 1 | a0001c0001t0001g0267 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.228+3655T>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23248051 | |||||||
| chr14:23248080 | C | T | 8 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0268 others(5): Show |
12 | HG00544.hp2 HG02559.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.228+3684C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23248080 | |||||||
| chr14:23248121 | G | T | 171 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(168): Show |
198 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.228+3725G>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23248121 | |||||||
| chr14:23248201 | C | T | 2 | a0001c0001t0002g0095 a0001c0001t0002g0096 |
2 | HG03017.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.228+3805C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23248201 | |||||||
| chr14:23248302 | G | GT | 5 | a0001c0001t0002g0085 a0001c0001t0003g0006 a0001c0001t0003g0020 others(2): Show |
8 | HG01069.hp1 HG01192.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.228+3919dupT | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr14 | 23248302 | ||||||
| chr14:23248302 | G | T | 1 | a0001c0001t0001g0233 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.228+3906G>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23248302 | |||||||
| chr14:23248315 | T | A | 17 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0279 others(14): Show |
20 | HG00738.hp2 HG01433.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.228+3919T>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23248315 | |||||||
| chr14:23248346 | G | C | 28 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(25): Show |
36 | HG00544.hp2 HG01243.hp2 HG02015.hp1 others(33): Show |
intron_variant | MODIFIER | c.228+3950G>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23248346 | |||||||
| chr14:23248351 | C | T | 2 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
2 | HG01884.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.228+3955C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23248351 | |||||||
| chr14:23248378 | C | T | 57 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(54): Show |
67 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.228+3982C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23248378 | |||||||
| chr14:23248438 | C | T | 17 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0279 others(14): Show |
20 | HG00738.hp2 HG01433.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.228+4042C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23248438 | |||||||
| chr14:23248440 | C | CT | 58 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0012 others(55): Show |
70 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.228+4063dupT | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr14 | 23248440 | ||||||
| chr14:23248440 | C | CTT | 7 | a0001c0001t0001g0172 a0001c0001t0001g0174 a0001c0001t0001g0178 others(4): Show |
7 | HG00140.hp1 HG01516.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.228+4062_228+4063d others(4): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr14 | 23248440 | ||||||
| chr14:23248440 | CT | C | 71 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0027 others(68): Show |
80 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.228+4063delT | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr14 | 23248440 | ||||||
| chr14:23248503 | A | G | 57 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(54): Show |
67 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.228+4107A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23248503 | |||||||
| chr14:23248528 | G | A | 54 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(51): Show |
64 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.228+4132G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23248528 | |||||||
| chr14:23248661 | C | T | 1 | a0001c0001t0001g0195 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.228+4265C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23248661 | |||||||
| chr14:23248681 | C | T | 1 | a0001c0001t0001g0294 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.228+4285C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23248681 | |||||||
| chr14:23248735 | C | T | 2 | a0001c0001t0001g0296 a0001c0001t0001g0297 |
2 | HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.228+4339C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23248735 | |||||||
| chr14:23248831 | C | T | 57 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(54): Show |
67 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.228+4435C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23248831 | |||||||
| chr14:23248870 | G | A | 2 | a0001c0001t0001g0296 a0001c0001t0001g0297 |
2 | HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.228+4474G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23248870 | |||||||
| chr14:23248896 | C | T | 17 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0279 others(14): Show |
20 | HG00738.hp2 HG01433.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.228+4500C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23248896 | |||||||
| chr14:23249053 | T | G | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.228+4657T>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23249053 | |||||||
| chr14:23249061 | C | A | 17 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0279 others(14): Show |
20 | HG00738.hp2 HG01433.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.228+4665C>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23249061 | |||||||
| chr14:23249190 | T | C | 3 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0269 |
3 | HG02257.hp1 HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.228+4794T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23249190 | |||||||
| chr14:23249206 | T | A | 2 | a0001c0001t0002g0104 a0001c0001t0002g0105 |
2 | HG02004.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.228+4810T>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23249206 | |||||||
| chr14:23249214 | A | G | 3 | a0001c0001t0002g0009 a0001c0001t0002g0134 a0001c0001t0002g0135 |
5 | HG02109.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.228+4818A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23249214 | |||||||
| chr14:23249262 | C | G | 3 | a0001c0001t0002g0039 a0001c0001t0002g0078 a0001c0001t0002g0081 |
3 | HG02055.hp1 HG03195.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.228+4866C>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23249262 | |||||||
| chr14:23249340 | G | C | 2 | a0001c0001t0001g0296 a0001c0001t0001g0297 |
2 | HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.228+4944G>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23249340 | |||||||
| chr14:23249378 | A | G | 70 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0027 others(67): Show |
79 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.228+4982A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23249378 | |||||||
| chr14:23249401 | C | A | 1 | a0001c0001t0002g0163 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.228+5005C>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23249401 | |||||||
| chr14:23249459 | T | C | 112 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(109): Show |
128 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.228+5063T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23249459 | |||||||
| chr14:23249460 | G | C | 30 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(27): Show |
38 | HG00544.hp2 HG01243.hp2 HG01884.hp1 others(35): Show |
intron_variant | MODIFIER | c.228+5064G>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23249460 | |||||||
| chr14:23250004 | G | A | 2 | a0001c0001t0001g0296 a0001c0001t0001g0297 |
2 | HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.228+5608G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23250004 | |||||||
| chr14:23250037 | T | C | 5 | a0001c0001t0001g0032 a0001c0001t0001g0279 a0001c0001t0001g0280 others(2): Show |
6 | HG02486.hp2 HG02818.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.228+5641T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23250037 | |||||||
| chr14:23250174 | T | G | 1 | a0001c0001t0001g0199 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.228+5778T>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23250174 | |||||||
| chr14:23250185 | A | G | 2 | a0001c0001t0001g0296 a0001c0001t0001g0297 |
2 | HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.228+5789A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23250185 | |||||||
| chr14:23250352 | G | A | 2 | a0001c0001t0001g0045 a0001c0001t0001g0072 |
2 | HG02451.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.228+5956G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23250352 | |||||||
| chr14:23250353 | C | T | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.228+5957C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23250353 | |||||||
| chr14:23250439 | T | C | 197 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(194): Show |
230 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.228+6043T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23250439 | |||||||
| chr14:23250482 | C | CA | 95 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(92): Show |
110 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.228+6101dupA | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr14 | 23250482 | ||||||
| chr14:23250482 | C | CAA | 54 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(51): Show |
64 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.228+6100_228+6101d others(4): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr14 | 23250482 | ||||||
| chr14:23250482 | CA | C | 12 | a0001c0001t0001g0044 a0001c0001t0001g0060 a0001c0001t0001g0144 others(9): Show |
12 | HG01978.hp2 HG02055.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.228+6101delA | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr14 | 23250482 | ||||||
| chr14:23250541 | G | T | 67 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0027 others(64): Show |
76 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.228+6145G>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23250541 | |||||||
| chr14:23250544 | A | C | 124 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(121): Show |
143 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.228+6148A>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23250544 | |||||||
| chr14:23250702 | G | A | 7 | a0001c0001t0001g0032 a0001c0001t0001g0279 a0001c0001t0001g0280 others(4): Show |
8 | HG02486.hp2 HG02818.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.228+6306G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23250702 | |||||||
| chr14:23250737 | G | T | 1 | a0001c0001t0002g0069 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.228+6341G>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23250737 | |||||||
| chr14:23251041 | G | A | 1 | a0001c0001t0002g0138 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.228+6645G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23251041 | |||||||
| chr14:23251059 | T | G | 1 | a0001c0001t0001g0215 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.228+6663T>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23251059 | |||||||
| chr14:23251246 | C | G | 57 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(54): Show |
67 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.228+6850C>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23251246 | |||||||
| chr14:23251248 | ACAATT | A | 176 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(173): Show |
204 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.228+6874_228+6878d others(7): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr14 | 23251248 | ||||||
| chr14:23251531 | A | G | 133 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(130): Show |
152 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.229-7018A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23251531 | |||||||
| chr14:23251586 | C | T | 76 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0027 others(73): Show |
85 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.229-6963C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23251586 | |||||||
| chr14:23251628 | C | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0276 a0001c0001t0005g0011 |
4 | HG02280.hp2 HG02647.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.229-6921C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23251628 | |||||||
| chr14:23251642 | C | T | 9 | a0001c0001t0002g0061 a0001c0001t0002g0071 a0001c0001t0002g0088 others(6): Show |
9 | HG01261.hp2 HG02451.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.229-6907C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23251642 | |||||||
| chr14:23251644 | T | A | 2 | a0001c0001t0001g0296 a0001c0001t0001g0297 |
2 | HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.229-6905T>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23251644 | |||||||
| chr14:23251646 | C | T | 2 | a0001c0001t0001g0296 a0001c0001t0001g0297 |
2 | HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.229-6903C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23251646 | |||||||
| chr14:23251801 | T | C | 133 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(130): Show |
152 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.229-6748T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23251801 | |||||||
| chr14:23251814 | C | CAAAA | 71 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0027 others(68): Show |
80 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.229-6727_229-6724d others(6): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr14 | 23251814 | ||||||
| chr14:23251814 | C | CAAAAAAA others(3): Show |
9 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0168 others(6): Show |
9 | HG01975.hp2 HG03041.hp1 HG03453.hp1 others(6): Show |
intron_variant | MODIFIER | c.229-6733_229-6724d others(12): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr14 | 23251814 | ||||||
| chr14:23251814 | C | CAAAAAAA others(4): Show |
44 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(41): Show |
54 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.229-6734_229-6724d others(13): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr14 | 23251814 | ||||||
| chr14:23251814 | C | CAAAAAAA others(5): Show |
4 | a0001c0001t0001g0189 a0001c0001t0001g0198 a0001c0001t0001g0200 others(1): Show |
4 | HG00438.hp2 HG00738.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.229-6724_229-6723i others(14): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr14 | 23251814 | ||||||
| chr14:23251826 | G | A | 1 | a0001c0001t0001g0224 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.229-6723G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23251826 | |||||||
| chr14:23251847 | C | G | 76 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0027 others(73): Show |
85 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.229-6702C>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23251847 | |||||||
| chr14:23251849 | T | C | 55 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(52): Show |
65 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.229-6700T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23251849 | |||||||
| chr14:23251892 | G | T | 1 | a0001c0001t0002g0094 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.229-6657G>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23251892 | |||||||
| chr14:23252091 | T | TG | 19 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0224 others(16): Show |
22 | HG00738.hp2 HG01109.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.229-6452dupG | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr14 | 23252091 | ||||||
| chr14:23252096 | G | C | 1 | a0001c0001t0001g0168 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.229-6453G>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23252096 | |||||||
| chr14:23252098 | C | G | 75 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0027 others(72): Show |
84 | HG00408.hp2 HG00597.hp2 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.229-6451C>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23252098 | |||||||
| chr14:23252171 | T | C | 8 | a0001c0001t0001g0044 a0001c0001t0001g0060 a0001c0001t0001g0144 others(5): Show |
8 | HG02257.hp2 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.229-6378T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23252171 | |||||||
| chr14:23252231 | A | G | 45 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(42): Show |
54 | HG00099.hp1 HG00544.hp2 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.229-6318A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23252231 | |||||||
| chr14:23252264 | A | G | 43 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(40): Show |
52 | HG00099.hp1 HG00544.hp2 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.229-6285A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23252264 | |||||||
| chr14:23252548 | G | A | 55 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(52): Show |
65 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.229-6001G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23252548 | |||||||
| chr14:23252671 | T | G | 54 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(51): Show |
60 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.229-5878T>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23252671 | |||||||
| chr14:23252693 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.229-5856C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23252693 | |||||||
| chr14:23252751 | C | G | 54 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(51): Show |
60 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.229-5798C>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23252751 | |||||||
| chr14:23252947 | T | C | 6 | a0001c0001t0001g0028 a0001c0001t0001g0224 a0001c0001t0001g0226 others(3): Show |
7 | NA18984.hp2 NA18985.hp2 NA18987.hp1 others(4): Show |
intron_variant | MODIFIER | c.229-5602T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23252947 | |||||||
| chr14:23252988 | T | A | 44 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(41): Show |
53 | HG00099.hp1 HG00544.hp2 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.229-5561T>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23252988 | |||||||
| chr14:23253017 | A | C | 2 | a0001c0001t0001g0296 a0001c0001t0001g0297 |
2 | HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.229-5532A>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23253017 | |||||||
| chr14:23253332 | A | T | 1 | a0001c0001t0001g0176 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.229-5217A>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23253332 | |||||||
| chr14:23253476 | T | C | 1 | a0001c0001t0001g0265 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.229-5073T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23253476 | |||||||
| chr14:23253515 | A | G | 2 | a0001c0001t0001g0296 a0001c0001t0001g0297 |
2 | HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.229-5034A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23253515 | |||||||
| chr14:23253518 | A | T | 1 | a0001c0001t0002g0068 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.229-5031A>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23253518 | |||||||
| chr14:23253519 | T | C | 2 | a0001c0001t0001g0277 a0001c0001t0001g0303 |
2 | HG01891.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.229-5030T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23253519 | |||||||
| chr14:23253562 | T | C | 57 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(54): Show |
67 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.229-4987T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23253562 | |||||||
| chr14:23253631 | T | C | 57 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(54): Show |
67 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.229-4918T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23253631 | |||||||
| chr14:23253751 | A | T | 1 | a0001c0001t0001g0292 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.229-4798A>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23253751 | |||||||
| chr14:23253765 | T | C | 2 | a0001c0001t0001g0296 a0001c0001t0001g0297 |
2 | HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.229-4784T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23253765 | |||||||
| chr14:23253864 | G | A | 1 | a0001c0001t0001g0303 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.229-4685G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23253864 | |||||||
| chr14:23253937 | T | C | 176 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(173): Show |
204 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.229-4612T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23253937 | |||||||
| chr14:23253938 | G | A | 2 | a0001c0001t0001g0168 a0001c0001t0001g0294 |
2 | HG01109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.229-4611G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23253938 | |||||||
| chr14:23254042 | G | A | 57 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(54): Show |
67 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.229-4507G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23254042 | |||||||
| chr14:23254068 | C | T | 3 | a0001c0001t0002g0008 a0001c0001t0002g0131 a0001c0001t0002g0141 |
5 | HG00642.hp2 HG00741.hp1 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.229-4481C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23254068 | |||||||
| chr14:23254100 | A | G | 132 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(129): Show |
151 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.229-4449A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23254100 | |||||||
| chr14:23254202 | T | G | 54 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(51): Show |
60 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.229-4347T>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23254202 | |||||||
| chr14:23254285 | TCAAAAAC others(4): Show |
T | 1 | a0001c0001t0001g0271 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.229-4258_229-4248d others(13): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr14 | 23254285 | ||||||
| chr14:23254286 | C | CAAA | 14 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0279 others(11): Show |
17 | HG00738.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.229-4260_229-4258d others(5): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr14 | 23254286 | ||||||
| chr14:23254286 | CA | C | 7 | a0001c0001t0001g0021 a0001c0001t0001g0034 a0001c0001t0001g0045 others(4): Show |
8 | HG01109.hp1 HG01884.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.229-4258delA | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr14 | 23254286 | ||||||
| chr14:23254288 | AAAAC | A | 57 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(54): Show |
67 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.229-4257_229-4254d others(6): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr14 | 23254288 | ||||||
| chr14:23254290 | AAC | A | 34 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0144 others(31): Show |
38 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.229-4257_229-4256d others(4): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr14 | 23254290 | ||||||
| chr14:23254291 | AC | A | 44 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0027 others(41): Show |
52 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.229-4257delC | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23254291 | |||||||
| chr14:23254292 | C | A | 11 | a0001c0001t0001g0044 a0001c0001t0001g0060 a0001c0001t0001g0146 others(8): Show |
11 | HG02257.hp2 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.229-4257C>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23254292 | |||||||
| chr14:23254297 | C | A | 59 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(56): Show |
65 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.229-4252C>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23254297 | |||||||
| chr14:23254299 | A | C | 1 | a0001c0001t0001g0294 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.229-4250A>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23254299 | |||||||
| chr14:23254302 | C | A | 58 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(55): Show |
64 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.229-4247C>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23254302 | |||||||
| chr14:23254307 | C | A | 55 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(52): Show |
61 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.229-4242C>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23254307 | |||||||
| chr14:23254312 | C | A | 3 | a0001c0001t0001g0144 a0001c0001t0001g0249 a0001c0001t0001g0258 |
3 | HG01258.hp2 HG02622.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.229-4237C>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23254312 | |||||||
| chr14:23254317 | C | A | 17 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0279 others(14): Show |
20 | HG00738.hp2 HG01433.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.229-4232C>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23254317 | |||||||
| chr14:23254319 | A | AC | 17 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0279 others(14): Show |
20 | HG00738.hp2 HG01433.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.229-4230_229-4229i others(3): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23254319 | |||||||
| chr14:23254338 | AAAAACT | A | 74 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0014 others(71): Show |
87 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.229-4198_229-4193d others(8): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr14 | 23254338 | ||||||
| chr14:23254344 | T | A | 100 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(97): Show |
115 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(112): Show |
intron_variant | MODIFIER | c.229-4205T>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23254344 | |||||||
| chr14:23254585 | C | T | 44 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(41): Show |
53 | HG00099.hp1 HG00544.hp2 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.229-3964C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23254585 | |||||||
| chr14:23254838 | T | C | 75 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0027 others(72): Show |
84 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.229-3711T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23254838 | |||||||
| chr14:23255046 | GGA | G | 14 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0279 others(11): Show |
17 | HG00738.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.229-3493_229-3492d others(4): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr14 | 23255046 | ||||||
| chr14:23255303 | A | G | 1 | a0001c0001t0001g0023 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.229-3246A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23255303 | |||||||
| chr14:23255554 | T | G | 44 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(41): Show |
53 | HG00099.hp1 HG00544.hp2 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.229-2995T>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23255554 | |||||||
| chr14:23255765 | C | T | 1 | a0001c0001t0002g0167 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.229-2784C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23255765 | |||||||
| chr14:23255908 | A | T | 1 | a0001c0001t0002g0108 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.229-2641A>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23255908 | |||||||
| chr14:23255938 | G | T | 176 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(173): Show |
204 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.229-2611G>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23255938 | |||||||
| chr14:23255989 | TTGGAATG others(5): Show |
T | 1 | a0001c0001t0001g0224 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.229-2558_229-2547d others(14): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr14 | 23255989 | ||||||
| chr14:23256030 | T | C | 183 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(180): Show |
211 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.229-2519T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23256030 | |||||||
| chr14:23256081 | G | T | 1 | a0001c0001t0001g0160 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.229-2468G>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23256081 | |||||||
| chr14:23256251 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.229-2298C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23256251 | |||||||
| chr14:23256369 | C | T | 1 | a0001c0001t0002g0130 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.229-2180C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23256369 | |||||||
| chr14:23256376 | A | AT | 173 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(170): Show |
201 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.229-2160dupT | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr14 | 23256376 | ||||||
| chr14:23256485 | C | T | 9 | a0001c0001t0001g0044 a0001c0001t0001g0060 a0001c0001t0001g0144 others(6): Show |
9 | HG02257.hp2 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.229-2064C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23256485 | |||||||
| chr14:23256594 | A | G | 1 | a0001c0001t0001g0168 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.229-1955A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23256594 | |||||||
| chr14:23256664 | G | A | 1 | a0001c0001t0001g0204 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.229-1885G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23256664 | |||||||
| chr14:23256694 | A | C | 2 | a0001c0001t0001g0298 a0001c0001t0001g0300 |
2 | HG02717.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.229-1855A>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23256694 | |||||||
| chr14:23256821 | A | G | 55 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(52): Show |
65 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.229-1728A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23256821 | |||||||
| chr14:23256877 | G | A | 57 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(54): Show |
67 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.229-1672G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23256877 | |||||||
| chr14:23256957 | A | T | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.229-1592A>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23256957 | |||||||
| chr14:23256988 | A | G | 1 | a0001c0001t0001g0188 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.229-1561A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23256988 | |||||||
| chr14:23257014 | G | A | 1 | a0001c0001t0002g0109 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.229-1535G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23257014 | |||||||
| chr14:23257024 | A | G | 132 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(129): Show |
151 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.229-1525A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23257024 | |||||||
| chr14:23257107 | C | T | 44 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(41): Show |
53 | HG00099.hp1 HG00544.hp2 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.229-1442C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23257107 | |||||||
| chr14:23257121 | C | T | 44 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(41): Show |
53 | HG00099.hp1 HG00544.hp2 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.229-1428C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23257121 | |||||||
| chr14:23257132 | G | A | 2 | a0001c0001t0001g0277 a0001c0001t0001g0303 |
2 | HG01891.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.229-1417G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23257132 | |||||||
| chr14:23257156 | C | A | 130 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(127): Show |
149 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.229-1393C>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23257156 | |||||||
| chr14:23257158 | C | A | 132 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(129): Show |
151 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.229-1391C>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23257158 | |||||||
| chr14:23257160 | C | A | 174 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(171): Show |
202 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.229-1389C>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23257160 | |||||||
| chr14:23257162 | A | AT | 130 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(127): Show |
149 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.229-1387_229-1386i others(3): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23257162 | |||||||
| chr14:23257162 | A | C | 3 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0269 |
3 | HG02257.hp1 HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.229-1387A>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23257162 | |||||||
| chr14:23257164 | A | C | 3 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0269 |
3 | HG02257.hp1 HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.229-1385A>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23257164 | |||||||
| chr14:23257164 | A | T | 27 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0029 others(24): Show |
34 | HG00099.hp1 HG00544.hp2 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.229-1385A>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23257164 | |||||||
| chr14:23257169 | T | A | 14 | a0001c0001t0001g0021 a0001c0001t0001g0045 a0001c0001t0001g0046 others(11): Show |
15 | HG01109.hp1 HG02257.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.229-1380T>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23257169 | |||||||
| chr14:23257199 | T | C | 1 | a0001c0001t0002g0095 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.229-1350T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23257199 | |||||||
| chr14:23257326 | G | A | 132 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(129): Show |
151 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.229-1223G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23257326 | |||||||
| chr14:23257345 | A | G | 1 | a0001c0001t0001g0265 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.229-1204A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23257345 | |||||||
| chr14:23257383 | GT | G | 75 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0027 others(72): Show |
84 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.229-1163delT | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr14 | 23257383 | ||||||
| chr14:23257417 | A | G | 55 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(52): Show |
65 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.229-1132A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23257417 | |||||||
| chr14:23257525 | T | G | 1 | a0001c0001t0001g0291 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.229-1024T>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23257525 | |||||||
| chr14:23257552 | G | A | 57 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(54): Show |
67 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.229-997G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23257552 | |||||||
| chr14:23257605 | G | A | 55 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(52): Show |
65 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.229-944G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23257605 | |||||||
| chr14:23257625 | A | C | 44 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(41): Show |
53 | HG00099.hp1 HG00544.hp2 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.229-924A>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23257625 | |||||||
| chr14:23258068 | G | T | 55 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(52): Show |
65 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.229-481G>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23258068 | |||||||
| chr14:23258128 | C | T | 132 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(129): Show |
151 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.229-421C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23258128 | |||||||
| chr14:23258263 | A | C | 1 | a0001c0001t0001g0150 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.229-286A>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23258263 | |||||||
| chr14:23258276 | T | C | 2 | a0001c0001t0001g0234 a0001c0001t0004g0236 |
2 | HG00280.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.229-273T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23258276 | |||||||
| chr14:23258338 | C | CA | 104 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(101): Show |
121 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.229-193dupA | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr14 | 23258338 | ||||||
| chr14:23258338 | C | CAA | 70 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0021 others(67): Show |
81 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.229-194_229-193dup others(2): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr14 | 23258338 | ||||||
| chr14:23258358 | A | G | 2 | a0001c0001t0001g0296 a0001c0001t0001g0297 |
2 | HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.229-191A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23258358 | |||||||
| chr14:23258400 | T | C | 2 | a0001c0001t0001g0296 a0001c0001t0001g0297 |
2 | HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.229-149T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 4/14 | chr14 | 23258400 | |||||||
| chr14:23258693 | CTT | C | 169 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(166): Show |
195 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.344+47_344+48delTT | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr14 | 23258693 | ||||||
| chr14:23258693 | CTTT | C | 6 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0160 others(3): Show |
8 | HG02015.hp1 HG02109.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.344+46_344+48delTT others(1): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr14 | 23258693 | ||||||
| chr14:23258710 | T | C | 132 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(129): Show |
151 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.344+46T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 5/14 | chr14 | 23258710 | |||||||
| chr14:23258736 | T | G | 1 | a0001c0001t0001g0224 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.344+72T>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 5/14 | chr14 | 23258736 | |||||||
| chr14:23258820 | A | AT | 4 | a0001c0001t0001g0262 a0001c0001t0001g0277 a0001c0001t0001g0303 others(1): Show |
4 | HG01891.hp1 HG02258.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.344+162dupT | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr14 | 23258820 | ||||||
| chr14:23258905 | A | G | 176 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(173): Show |
204 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.344+241A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 5/14 | chr14 | 23258905 | |||||||
| chr14:23259002 | C | T | 45 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(42): Show |
51 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.344+338C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 5/14 | chr14 | 23259002 | |||||||
| chr14:23259065 | A | G | 5 | a0001c0001t0002g0039 a0001c0001t0002g0078 a0001c0001t0002g0079 others(2): Show |
5 | HG02055.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.344+401A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 5/14 | chr14 | 23259065 | |||||||
| chr14:23259121 | G | C | 4 | a0001c0001t0001g0262 a0001c0001t0001g0277 a0001c0001t0001g0303 others(1): Show |
4 | HG01891.hp1 HG02258.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.344+457G>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 5/14 | chr14 | 23259121 | |||||||
| chr14:23259163 | C | T | 45 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(42): Show |
51 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.344+499C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 5/14 | chr14 | 23259163 | |||||||
| chr14:23259202 | CA | C | 130 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(127): Show |
149 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.344+547delA | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr14 | 23259202 | ||||||
| chr14:23259264 | T | C | 1 | a0001c0001t0001g0289 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.344+600T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 5/14 | chr14 | 23259264 | |||||||
| chr14:23259363 | A | AT | 68 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0021 others(65): Show |
76 | HG00099.hp1 HG00673.hp2 HG00741.hp2 others(73): Show |
intron_variant | MODIFIER | c.345-505dupT | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr14 | 23259363 | ||||||
| chr14:23259394 | C | T | 1 | a0001c0001t0001g0294 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.345-490C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 5/14 | chr14 | 23259394 | |||||||
| chr14:23259404 | C | A | 3 | a0001c0001t0002g0110 a0001c0001t0002g0139 a0001c0001t0002g0140 |
3 | NA18959.hp2 NA18999.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.345-480C>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 5/14 | chr14 | 23259404 | |||||||
| chr14:23259423 | C | CT | 58 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(55): Show |
68 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.345-452dupT | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr14 | 23259423 | ||||||
| chr14:23259444 | G | GT | 60 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(57): Show |
66 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.345-432dupT | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr14 | 23259444 | ||||||
| chr14:23259452 | T | TTG | 12 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0279 others(9): Show |
15 | HG00738.hp2 HG01884.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.345-432_345-431ins others(2): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 5/14 | chr14 | 23259452 | |||||||
| chr14:23259453 | G | GT | 9 | a0001c0001t0001g0086 a0001c0001t0001g0127 a0001c0001t0001g0272 others(6): Show |
9 | HG00544.hp2 HG00642.hp2 HG04199.hp2 others(6): Show |
intron_variant | MODIFIER | c.345-419dupT | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr14 | 23259453 | ||||||
| chr14:23259453 | G | T | 15 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0224 others(12): Show |
18 | HG00738.hp2 HG01884.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.345-431G>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 5/14 | chr14 | 23259453 | |||||||
| chr14:23259503 | G | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0276 a0001c0001t0005g0011 |
4 | HG02280.hp2 HG02647.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.345-381G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 5/14 | chr14 | 23259503 | |||||||
| chr14:23259536 | A | T | 1 | a0001c0001t0001g0224 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.345-348A>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 5/14 | chr14 | 23259536 | |||||||
| chr14:23259557 | A | G | 44 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(41): Show |
53 | HG00099.hp1 HG00544.hp2 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.345-327A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 5/14 | chr14 | 23259557 | |||||||
| chr14:23259581 | G | A | 27 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0029 others(24): Show |
34 | HG00099.hp1 HG00544.hp2 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.345-303G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 5/14 | chr14 | 23259581 | |||||||
| chr14:23259979 | T | C | 74 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0027 others(71): Show |
83 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.405+35T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 6/14 | chr14 | 23259979 | |||||||
| chr14:23260085 | A | G | 2 | a0001c0001t0002g0065 a0001c0001t0002g0069 |
2 | NA18612.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.405+141A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 6/14 | chr14 | 23260085 | |||||||
| chr14:23260096 | A | C | 45 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(42): Show |
54 | HG00099.hp1 HG00544.hp2 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.405+152A>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 6/14 | chr14 | 23260096 | |||||||
| chr14:23260193 | A | G | 131 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(128): Show |
150 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.405+249A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 6/14 | chr14 | 23260193 | |||||||
| chr14:23260268 | C | CCTT | 45 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(42): Show |
54 | HG00099.hp1 HG00544.hp2 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.405+326_405+328dup others(3): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr14 | 23260268 | ||||||
| chr14:23260345 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.406-314A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 6/14 | chr14 | 23260345 | |||||||
| chr14:23260398 | T | C | 1 | a0001c0001t0001g0224 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.406-261T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 6/14 | chr14 | 23260398 | |||||||
| chr14:23260399 | C | T | 1 | a0001c0001t0001g0224 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.406-260C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 6/14 | chr14 | 23260399 | |||||||
| chr14:23260400 | T | C | 1 | a0001c0001t0001g0224 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.406-259T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 6/14 | chr14 | 23260400 | |||||||
| chr14:23260406 | C | A | 1 | a0001c0001t0001g0224 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.406-253C>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 6/14 | chr14 | 23260406 | |||||||
| chr14:23260434 | T | A | 1 | a0001c0001t0001g0224 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.406-225T>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 6/14 | chr14 | 23260434 | |||||||
| chr14:23260541 | G | A | 131 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(128): Show |
150 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.406-118G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 6/14 | chr14 | 23260541 | |||||||
| chr14:23260580 | T | A | 5 | a0001c0001t0001g0185 a0001c0001t0001g0201 a0001c0001t0001g0202 others(2): Show |
5 | HG02040.hp2 HG02071.hp1 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.406-79T>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 6/14 | chr14 | 23260580 | |||||||
| chr14:23260639 | C | G | 1 | a0001c0001t0002g0124 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.406-20C>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 6/14 | chr14 | 23260639 | |||||||
| chr14:23260650 | C | T | 2 | a0001c0001t0001g0296 a0001c0001t0001g0297 |
2 | HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.406-9C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 6/14 | chr14 | 23260650 | |||||||
| chr14:23260753 | G | A | 1 | a0001c0001t0002g0136 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.434+66G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 7/14 | chr14 | 23260753 | |||||||
| chr14:23260766 | TGAGA | T | 14 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0279 others(11): Show |
17 | HG00738.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.434+86_434+89delGA others(2): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr14 | 23260766 | ||||||
| chr14:23260808 | C | T | 13 | a0001c0001t0002g0061 a0001c0001t0002g0071 a0001c0001t0002g0088 others(10): Show |
16 | HG01069.hp1 HG01192.hp1 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.434+121C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 7/14 | chr14 | 23260808 | |||||||
| chr14:23260887 | C | A | 131 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(128): Show |
150 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.434+200C>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 7/14 | chr14 | 23260887 | |||||||
| chr14:23261100 | A | G | 131 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(128): Show |
150 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.434+413A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 7/14 | chr14 | 23261100 | |||||||
| chr14:23261149 | T | C | 1 | a0001c0001t0001g0132 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.434+462T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 7/14 | chr14 | 23261149 | |||||||
| chr14:23261166 | A | G | 55 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(52): Show |
65 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.434+479A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 7/14 | chr14 | 23261166 | |||||||
| chr14:23261472 | C | T | 2 | a0001c0001t0002g0097 a0001c0001t0002g0138 |
2 | HG02027.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.434+785C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 7/14 | chr14 | 23261472 | |||||||
| chr14:23261515 | C | T | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.434+828C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 7/14 | chr14 | 23261515 | |||||||
| chr14:23261517 | C | CTGTGAAG others(11): Show |
1 | a0001c0001t0002g0143 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.434+833_434+850dup others(18): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr14 | 23261517 | ||||||
| chr14:23261571 | A | T | 1 | a0001c0001t0001g0176 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.434+884A>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 7/14 | chr14 | 23261571 | |||||||
| chr14:23261601 | C | T | 1 | a0001c0001t0002g0154 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.434+914C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 7/14 | chr14 | 23261601 | |||||||
| chr14:23261680 | G | A | 3 | a0001c0001t0002g0062 a0001c0001t0002g0111 a0001c0001t0002g0143 |
3 | NA18939.hp1 NA18977.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.435-985G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 7/14 | chr14 | 23261680 | |||||||
| chr14:23261704 | G | A | 55 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(52): Show |
65 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.435-961G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 7/14 | chr14 | 23261704 | |||||||
| chr14:23261755 | A | G | 2 | a0001c0001t0001g0175 a0001c0001t0001g0182 |
2 | HG01106.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.435-910A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 7/14 | chr14 | 23261755 | |||||||
| chr14:23261817 | T | C | 12 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0279 others(9): Show |
15 | HG00738.hp2 HG01884.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.435-848T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 7/14 | chr14 | 23261817 | |||||||
| chr14:23261916 | C | T | 1 | a0001c0001t0002g0123 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.435-749C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 7/14 | chr14 | 23261916 | |||||||
| chr14:23261965 | C | T | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.435-700C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 7/14 | chr14 | 23261965 | |||||||
| chr14:23261968 | A | AAAAC | 132 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(129): Show |
151 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.435-689_435-686dup others(4): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr14 | 23261968 | ||||||
| chr14:23261980 | A | C | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.435-685A>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 7/14 | chr14 | 23261980 | |||||||
| chr14:23262009 | A | C | 3 | a0001c0001t0001g0262 a0001c0001t0001g0287 a0001c0001t0001g0288 |
3 | HG01884.hp2 HG02055.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.435-656A>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 7/14 | chr14 | 23262009 | |||||||
| chr14:23262016 | C | T | 131 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(128): Show |
150 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.435-649C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 7/14 | chr14 | 23262016 | |||||||
| chr14:23262071 | C | T | 42 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0021 others(39): Show |
50 | HG00099.hp1 HG00544.hp2 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.435-594C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 7/14 | chr14 | 23262071 | |||||||
| chr14:23262105 | T | C | 1 | a0001c0001t0001g0303 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.435-560T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 7/14 | chr14 | 23262105 | |||||||
| chr14:23262178 | C | A | 19 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0029 others(16): Show |
26 | HG00099.hp1 HG00544.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.435-487C>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 7/14 | chr14 | 23262178 | |||||||
| chr14:23262502 | T | G | 7 | a0001c0001t0001g0044 a0001c0001t0001g0060 a0001c0001t0001g0144 others(4): Show |
7 | HG02257.hp2 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.435-163T>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 7/14 | chr14 | 23262502 | |||||||
| chr14:23262536 | T | C | 47 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(44): Show |
56 | HG00099.hp1 HG00544.hp2 HG01109.hp1 others(53): Show |
intron_variant | MODIFIER | c.435-129T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 7/14 | chr14 | 23262536 | |||||||
| chr14:23262646 | C | CT | 51 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(48): Show |
57 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.435-10dupT | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr14 | 23262646 | ||||||
| chr14:23262656 | C | T | 1 | a0001c0001t0002g0067 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.435-9C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 7/14 | chr14 | 23262656 | |||||||
| chr14:23262759 | T | C | 1 | a0001c0001t0002g0112 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.481+48T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 8/14 | chr14 | 23262759 | |||||||
| chr14:23262882 | A | G | 178 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(175): Show |
206 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.482-46A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 8/14 | chr14 | 23262882 | |||||||
| chr14:23262883 | T | C | 178 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(175): Show |
206 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.482-45T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 8/14 | chr14 | 23262883 | |||||||
| chr14:23263073 | T | A | 1 | a0001c0001t0002g0067 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.524+103T>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 9/14 | chr14 | 23263073 | |||||||
| chr14:23263073 | T | C | 1 | a0001c0001t0001g0277 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.524+103T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 9/14 | chr14 | 23263073 | |||||||
| chr14:23263091 | G | GT | 125 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(122): Show |
144 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.524+132dupT | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr14 | 23263091 | ||||||
| chr14:23263270 | C | T | 130 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(127): Show |
149 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.524+300C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 9/14 | chr14 | 23263270 | |||||||
| chr14:23263296 | T | C | 128 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(125): Show |
147 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.524+326T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 9/14 | chr14 | 23263296 | |||||||
| chr14:23263313 | G | C | 1 | a0001c0001t0001g0210 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.524+343G>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 9/14 | chr14 | 23263313 | |||||||
| chr14:23263413 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.524+443C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 9/14 | chr14 | 23263413 | |||||||
| chr14:23263529 | G | A | 128 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(125): Show |
147 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.524+559G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 9/14 | chr14 | 23263529 | |||||||
| chr14:23263576 | G | A | 1 | a0001c0001t0002g0018 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.525-598G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 9/14 | chr14 | 23263576 | |||||||
| chr14:23263589 | C | T | 2 | a0001c0001t0002g0121 a0001c0001t0002g0154 |
2 | HG01256.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.525-585C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 9/14 | chr14 | 23263589 | |||||||
| chr14:23263700 | T | C | 1 | a0001c0001t0002g0067 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.525-474T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 9/14 | chr14 | 23263700 | |||||||
| chr14:23263701 | C | T | 1 | a0001c0001t0002g0067 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.525-473C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 9/14 | chr14 | 23263701 | |||||||
| chr14:23263729 | A | G | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.525-445A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 9/14 | chr14 | 23263729 | |||||||
| chr14:23263749 | C | A | 2 | a0001c0001t0001g0298 a0001c0001t0001g0300 |
2 | HG02717.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.525-425C>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 9/14 | chr14 | 23263749 | |||||||
| chr14:23263753 | C | A | 3 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0277 |
3 | HG02258.hp1 HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.525-421C>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 9/14 | chr14 | 23263753 | |||||||
| chr14:23263754 | A | C | 55 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(52): Show |
64 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.525-420A>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 9/14 | chr14 | 23263754 | |||||||
| chr14:23263755 | A | C | 1 | a0001c0001t0001g0033 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.525-419A>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 9/14 | chr14 | 23263755 | |||||||
| chr14:23263853 | T | C | 59 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(56): Show |
65 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.525-321T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 9/14 | chr14 | 23263853 | |||||||
| chr14:23263905 | T | A | 53 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(50): Show |
59 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.525-269T>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 9/14 | chr14 | 23263905 | |||||||
| chr14:23263950 | T | C | 1 | a0001c0001t0002g0113 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.525-224T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 9/14 | chr14 | 23263950 | |||||||
| chr14:23263961 | G | C | 1 | a0001c0001t0001g0303 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.525-213G>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 9/14 | chr14 | 23263961 | |||||||
| chr14:23263996 | G | A | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.525-178G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 9/14 | chr14 | 23263996 | |||||||
| chr14:23264316 | A | T | 1 | a0001c0001t0001g0253 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.585+82A>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 10/14 | chr14 | 23264316 | |||||||
| chr14:23264503 | A | G | 1 | a0001c0001t0002g0135 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.586-120A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 10/14 | chr14 | 23264503 | |||||||
| chr14:23264509 | C | T | 4 | a0001c0001t0001g0150 a0001c0001t0001g0296 a0001c0001t0001g0297 others(1): Show |
4 | HG01891.hp1 HG02922.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.586-114C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 10/14 | chr14 | 23264509 | |||||||
| chr14:23264516 | C | T | 105 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(102): Show |
120 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.586-107C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 10/14 | chr14 | 23264516 | |||||||
| chr14:23264584 | G | A | 1 | a0001c0001t0001g0171 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.586-39G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 10/14 | chr14 | 23264584 | |||||||
| chr14:23264682 | G | A | 2 | a0001c0001t0001g0012 a0001c0001t0001g0278 |
4 | NA18961.hp1 NA19009.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.634+11G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | chr14 | 23264682 | |||||||
| chr14:23264723 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.634+52C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | chr14 | 23264723 | |||||||
| chr14:23264754 | A | G | 1 | a0001c0001t0008g0206 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.634+83A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | chr14 | 23264754 | |||||||
| chr14:23264766 | C | T | 5 | a0001c0001t0002g0039 a0001c0001t0002g0078 a0001c0001t0002g0079 others(2): Show |
5 | HG02055.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.634+95C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | chr14 | 23264766 | |||||||
| chr14:23264769 | GT | G | 104 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(101): Show |
119 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.634+107delT | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr14 | 23264769 | ||||||
| chr14:23264795 | T | C | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.634+124T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | chr14 | 23264795 | |||||||
| chr14:23264814 | C | A | 19 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0045 others(16): Show |
21 | HG01109.hp1 HG02257.hp1 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.634+143C>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | chr14 | 23264814 | |||||||
| chr14:23264818 | G | A | 1 | a0001c0001t0002g0128 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.634+147G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | chr14 | 23264818 | |||||||
| chr14:23264818 | G | GT | 7 | a0001c0001t0002g0019 a0001c0001t0002g0052 a0001c0001t0002g0057 others(4): Show |
8 | HG01346.hp2 NA18961.hp2 NA18963.hp2 others(5): Show |
intron_variant | MODIFIER | c.634+164dupT | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr14 | 23264818 | ||||||
| chr14:23264818 | GT | G | 99 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0014 others(96): Show |
115 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.634+164delT | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr14 | 23264818 | ||||||
| chr14:23264818 | GTT | G | 5 | a0001c0001t0001g0186 a0001c0001t0003g0006 a0001c0001t0003g0020 others(2): Show |
8 | HG01069.hp1 HG01192.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.634+163_634+164del others(2): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr14 | 23264818 | ||||||
| chr14:23264823 | T | A | 105 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(102): Show |
120 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.634+152T>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | chr14 | 23264823 | |||||||
| chr14:23264828 | T | A | 105 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(102): Show |
120 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.634+157T>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | chr14 | 23264828 | |||||||
| chr14:23264925 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.634+254G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | chr14 | 23264925 | |||||||
| chr14:23264958 | A | G | 2 | a0001c0001t0001g0028 a0001c0001t0001g0245 |
3 | NA18984.hp2 NA18998.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.634+287A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | chr14 | 23264958 | |||||||
| chr14:23265063 | C | T | 5 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0272 others(2): Show |
9 | HG00544.hp2 NA18747.hp1 NA18961.hp1 others(6): Show |
intron_variant | MODIFIER | c.634+392C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | chr14 | 23265063 | |||||||
| chr14:23265116 | C | A | 1 | a0001c0001t0002g0115 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.634+445C>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | chr14 | 23265116 | |||||||
| chr14:23265184 | G | A | 76 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0014 others(73): Show |
90 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.634+513G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | chr14 | 23265184 | |||||||
| chr14:23265310 | G | T | 1 | a0001c0001t0001g0277 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.634+639G>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | chr14 | 23265310 | |||||||
| chr14:23265459 | G | A | 182 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(179): Show |
211 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.634+788G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | chr14 | 23265459 | |||||||
| chr14:23265750 | T | C | 1 | a0001c0001t0002g0116 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.634+1079T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | chr14 | 23265750 | |||||||
| chr14:23265843 | T | C | 19 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0045 others(16): Show |
21 | HG01109.hp1 HG02257.hp1 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.634+1172T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | chr14 | 23265843 | |||||||
| chr14:23266070 | A | G | 4 | a0001c0001t0001g0150 a0001c0001t0001g0296 a0001c0001t0001g0297 others(1): Show |
4 | HG01891.hp1 HG02922.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.634+1399A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | chr14 | 23266070 | |||||||
| chr14:23266107 | T | C | 107 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(104): Show |
122 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.634+1436T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | chr14 | 23266107 | |||||||
| chr14:23266145 | G | A | 1 | a0001c0001t0001g0249 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.634+1474G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | chr14 | 23266145 | |||||||
| chr14:23266299 | A | G | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.634+1628A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | chr14 | 23266299 | |||||||
| chr14:23266302 | G | GGTTGTTT others(8): Show |
1 | a0001c0001t0002g0118 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.634+1638_634+1652d others(17): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr14 | 23266302 | ||||||
| chr14:23266362 | T | G | 1 | a0001c0001t0001g0268 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.634+1691T>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | chr14 | 23266362 | |||||||
| chr14:23266364 | T | C | 1 | a0001c0001t0003g0137 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.634+1693T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | chr14 | 23266364 | |||||||
| chr14:23266404 | G | GT | 21 | a0001c0001t0001g0032 a0001c0001t0001g0165 a0001c0001t0001g0277 others(18): Show |
22 | HG00544.hp1 HG01243.hp1 HG01346.hp2 others(19): Show |
intron_variant | MODIFIER | c.634+1757dupT | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr14 | 23266404 | ||||||
| chr14:23266404 | G | GTT | 22 | a0001c0001t0001g0014 a0001c0001t0001g0029 a0001c0001t0001g0031 others(19): Show |
26 | HG00099.hp1 HG00738.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.634+1756_634+1757d others(4): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr14 | 23266404 | ||||||
| chr14:23266404 | G | GTTT | 45 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0027 others(42): Show |
53 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.634+1755_634+1757d others(5): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr14 | 23266404 | ||||||
| chr14:23266404 | G | GTTTT | 27 | a0001c0001t0001g0021 a0001c0001t0001g0046 a0001c0001t0001g0060 others(24): Show |
28 | HG00639.hp1 HG01099.hp1 HG02056.hp2 others(25): Show |
intron_variant | MODIFIER | c.634+1754_634+1757d others(6): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr14 | 23266404 | ||||||
| chr14:23266404 | G | GTTTTT | 10 | a0001c0001t0001g0082 a0001c0001t0001g0151 a0001c0001t0001g0243 others(7): Show |
10 | HG01109.hp1 HG01891.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.634+1753_634+1757d others(7): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr14 | 23266404 | ||||||
| chr14:23266404 | GT | G | 32 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0015 others(29): Show |
42 | HG00408.hp1 HG00438.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.634+1757delT | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr14 | 23266404 | ||||||
| chr14:23266404 | GTTTTTTT others(3): Show |
G | 2 | a0001c0001t0001g0281 a0001c0001t0001g0282 |
2 | HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.634+1748_634+1757d others(12): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr14 | 23266404 | ||||||
| chr14:23266406 | T | G | 7 | a0001c0001t0002g0058 a0001c0001t0002g0059 a0001c0001t0002g0070 others(4): Show |
7 | HG00609.hp2 HG02071.hp2 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.634+1735T>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | chr14 | 23266406 | |||||||
| chr14:23266412 | T | TG | 58 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0016 others(55): Show |
69 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.634+1741_634+1742i others(3): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | chr14 | 23266412 | |||||||
| chr14:23266418 | T | TTG | 5 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0272 others(2): Show |
9 | HG00544.hp2 NA18747.hp1 NA18961.hp1 others(6): Show |
intron_variant | MODIFIER | c.634+1748_634+1749i others(4): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr14 | 23266418 | ||||||
| chr14:23266437 | G | A | 2 | a0001c0001t0001g0291 a0001c0001t0001g0292 |
2 | HG02559.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.634+1766G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | chr14 | 23266437 | |||||||
| chr14:23266691 | G | A | 60 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0016 others(57): Show |
71 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.634+2020G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | chr14 | 23266691 | |||||||
| chr14:23266693 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.634+2022G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | chr14 | 23266693 | |||||||
| chr14:23266739 | T | A | 1 | a0001c0001t0002g0052 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.634+2068T>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | chr14 | 23266739 | |||||||
| chr14:23266752 | A | G | 2 | a0001c0001t0001g0212 a0001c0001t0001g0217 |
2 | HG00673.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.634+2081A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | chr14 | 23266752 | |||||||
| chr14:23267125 | C | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0267 a0001c0001t0005g0011 |
4 | HG02647.hp2 HG02976.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.635-1799C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | chr14 | 23267125 | |||||||
| chr14:23267230 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.635-1694C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | chr14 | 23267230 | |||||||
| chr14:23267436 | T | A | 1 | a0001c0001t0002g0091 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.635-1488T>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | chr14 | 23267436 | |||||||
| chr14:23267573 | C | T | 3 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0294 |
3 | HG01109.hp2 HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.635-1351C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | chr14 | 23267573 | |||||||
| chr14:23267588 | C | T | 87 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(84): Show |
100 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.635-1336C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | chr14 | 23267588 | |||||||
| chr14:23267744 | T | G | 60 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0016 others(57): Show |
71 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.635-1180T>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | chr14 | 23267744 | |||||||
| chr14:23267870 | A | G | 1 | a0001c0001t0002g0096 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.635-1054A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | chr14 | 23267870 | |||||||
| chr14:23268062 | A | T | 1 | a0001c0001t0001g0228 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.635-862A>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | chr14 | 23268062 | |||||||
| chr14:23268070 | G | A | 1 | a0001c0001t0002g0092 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.635-854G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | chr14 | 23268070 | |||||||
| chr14:23268192 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.635-732G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | chr14 | 23268192 | |||||||
| chr14:23268313 | T | C | 107 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(104): Show |
122 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.635-611T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | chr14 | 23268313 | |||||||
| chr14:23268566 | CATTTTTG others(19): Show |
C | 4 | a0001c0001t0001g0150 a0001c0001t0001g0296 a0001c0001t0001g0297 others(1): Show |
4 | HG01891.hp1 HG02922.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.635-323_635-298del others(26): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr14 | 23268566 | ||||||
| chr14:23268584 | T | G | 1 | a0001c0001t0001g0292 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.635-340T>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | chr14 | 23268584 | |||||||
| chr14:23268736 | G | T | 1 | a0001c0001t0001g0147 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.635-188G>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 11/14 | chr14 | 23268736 | |||||||
| chr14:23269326 | C | A | 1 | a0001c0001t0002g0041 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.674+363C>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 12/14 | chr14 | 23269326 | |||||||
| chr14:23269339 | C | A | 1 | a0001c0001t0001g0221 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.674+376C>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 12/14 | chr14 | 23269339 | |||||||
| chr14:23269407 | G | C | 1 | a0001c0001t0002g0037 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.674+444G>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 12/14 | chr14 | 23269407 | |||||||
| chr14:23269412 | A | C | 1 | a0001c0001t0002g0109 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.674+449A>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 12/14 | chr14 | 23269412 | |||||||
| chr14:23269475 | TAATCCTA others(13): Show |
T | 1 | a0001c0001t0002g0118 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.675-387_675-368del others(20): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 12/14 | chr14 | 23269475 | |||||||
| chr14:23269481 | T | C | 4 | a0001c0001t0002g0017 a0001c0001t0002g0048 a0001c0001t0002g0077 others(1): Show |
4 | NA18957.hp2 NA19057.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.675-382T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 12/14 | chr14 | 23269481 | |||||||
| chr14:23269623 | G | T | 3 | a0001c0001t0002g0110 a0001c0001t0002g0139 a0001c0001t0002g0140 |
3 | NA18959.hp2 NA18999.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.675-240G>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 12/14 | chr14 | 23269623 | |||||||
| chr14:23269725 | G | GA | 19 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0045 others(16): Show |
21 | HG01109.hp1 HG02257.hp1 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.675-132dupA | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr14 | 23269725 | ||||||
| chr14:23269749 | C | T | 1 | a0001c0001t0002g0064 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.675-114C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 12/14 | chr14 | 23269749 | |||||||
| chr14:23269784 | G | T | 1 | a0001c0001t0002g0143 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.675-79G>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 12/14 | chr14 | 23269784 | |||||||
| chr14:23270062 | A | G | 1 | a0001c0001t0001g0168 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.772+102A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 13/14 | chr14 | 23270062 | |||||||
| chr14:23270435 | C | T | 2 | a0001c0001t0002g0121 a0001c0001t0002g0154 |
2 | HG01256.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.773-165C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 13/14 | chr14 | 23270435 | |||||||
| chr14:23270829 | A | T | 1 | a0001c0001t0001g0290 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.834+168A>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 14/14 | chr14 | 23270829 | |||||||
| chr14:23271029 | T | C | 86 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0012 others(83): Show |
104 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.834+368T>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 14/14 | chr14 | 23271029 | |||||||
| chr14:23271090 | C | T | 3 | a0001c0001t0001g0127 a0001c0001t0001g0291 a0001c0001t0001g0292 |
3 | HG02559.hp1 HG03017.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.834+429C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 14/14 | chr14 | 23271090 | |||||||
| chr14:23271375 | G | A | 44 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(41): Show |
50 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.834+714G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 14/14 | chr14 | 23271375 | |||||||
| chr14:23271490 | T | A | 1 | a0001c0001t0001g0277 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.834+829T>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 14/14 | chr14 | 23271490 | |||||||
| chr14:23271501 | GT | G | 142 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(139): Show |
167 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.834+848delT | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr14 | 23271501 | ||||||
| chr14:23271681 | G | C | 2 | a0001c0001t0001g0258 a0001c0001t0001g0259 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.834+1020G>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 14/14 | chr14 | 23271681 | |||||||
| chr14:23271697 | C | T | 4 | a0001c0001t0001g0150 a0001c0001t0001g0296 a0001c0001t0001g0297 others(1): Show |
4 | HG01891.hp1 HG02922.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.834+1036C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 14/14 | chr14 | 23271697 | |||||||
| chr14:23271778 | C | T | 77 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0012 others(74): Show |
95 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.835-1045C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 14/14 | chr14 | 23271778 | |||||||
| chr14:23272053 | A | G | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.835-770A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 14/14 | chr14 | 23272053 | |||||||
| chr14:23272120 | A | ATTTTTTG others(33): Show |
1 | a0001c0001t0001g0240 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.835-701_835-662dup others(40): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr14 | 23272120 | ||||||
| chr14:23272187 | G | GCGGGCGG others(23): Show |
1 | a0001c0001t0001g0240 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.835-634_835-605dup others(30): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr14 | 23272187 | ||||||
| chr14:23272227 | C | T | 6 | a0001c0001t0002g0037 a0001c0001t0002g0039 a0001c0001t0002g0078 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.835-596C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 14/14 | chr14 | 23272227 | |||||||
| chr14:23272354 | A | C | 1 | a0001c0001t0002g0037 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.835-469A>C | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 14/14 | chr14 | 23272354 | |||||||
| chr14:23272355 | G | A | 14 | a0001c0001t0001g0021 a0001c0001t0001g0045 a0001c0001t0001g0046 others(11): Show |
15 | HG01109.hp1 HG02280.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.835-468G>A | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 14/14 | chr14 | 23272355 | |||||||
| chr14:23272367 | C | T | 6 | a0001c0001t0002g0037 a0001c0001t0002g0039 a0001c0001t0002g0078 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.835-456C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 14/14 | chr14 | 23272367 | |||||||
| chr14:23272380 | C | G | 97 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0012 others(94): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.835-443C>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 14/14 | chr14 | 23272380 | |||||||
| chr14:23272426 | C | CAACA | 3 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0294 |
3 | HG01109.hp2 HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.835-375_835-372dup others(4): Show |
RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr14 | 23272426 | ||||||
| chr14:23272450 | A | G | 1 | a0001c0001t0002g0018 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.835-373A>G | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 14/14 | chr14 | 23272450 | |||||||
| chr14:23272733 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.835-90C>T | RNF212B | ENSG00000215277.9 | transcript | ENST00000430154.7 | protein_coding | 14/14 | chr14 | 23272733 |