Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 134829 |
| ensemblid | ENSG00000146352.13 |
| hgncid | 23046 |
| symbol | CLVS2 |
| name | clavesin 2 |
| refseq_nuc | NM_001010852.4 |
| refseq_prot | NP_001010852.2 |
| ensembl_nuc | ENST00000275162.10 |
| ensembl_prot | ENSP00000275162.4 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 122996235 |
| end | 123072925 |
| strand | + |
| ver | v1.2 |
| region | chr6:122996235-123072925 |
| region5000 | chr6:122991235-123077925 |
| regionname0 | CLVS2_chr6_122996235_123072925 |
| regionname5000 | CLVS2_chr6_122991235_123077925 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 327 | 335 | 92 | 59 | 136 | 12 | 34 | 112 | CLVS2_chr6_122991235_123077925 | CLVS2 | MTHLQ others(322): Show |
chr6 | 122991235 | 123077925 |
| a0002 | 0/0 | 327 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | MTHLQ others(322): Show |
chr6 | 122991235 | 123077925 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 981 | 329 | 87 | 59 | 136 | 12 | 33 | CLVS2_chr6_122991235_123077925 | CLVS2 | ATGAC others(976): Show |
chr6 | 122991235 | 123077925 | ||
| a0001c0002 | 0/0 | 981 | 5 | 5 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | ATGAC others(976): Show |
chr6 | 122991235 | 123077925 | ||
| a0001c0004 | 0/0 | 981 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | ATGAC others(976): Show |
chr6 | 122991235 | 123077925 | ||
| a0002c0003 | 0/0 | 981 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | ATGAC others(976): Show |
chr6 | 122991235 | 123077925 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 11219 | 44 | 6 | 6 | 28 | 1 | 3 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11214): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0002 | 0/0 | 11219 | 33 | 2 | 9 | 13 | 4 | 5 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11214): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0003 | 0/0 | 11219 | 28 | 4 | 11 | 8 | 1 | 4 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11214): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0004 | 0/0 | 11218 | 19 | 1 | 3 | 11 | 1 | 3 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11213): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0005 | 0/1 | 11219 | 17 | 2 | 4 | 8 | 0 | 2 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11214): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0006 | 0/0 | 11219 | 16 | 0 | 1 | 15 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11214): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0007 | 0/0 | 11223 | 10 | 0 | 1 | 8 | 1 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11218): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0008 | 0/0 | 11219 | 9 | 9 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11214): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0009 | 0/0 | 11227 | 7 | 1 | 0 | 1 | 0 | 5 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11222): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0010 | 0/0 | 11219 | 7 | 5 | 2 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11214): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0011 | 0/0 | 11219 | 7 | 0 | 0 | 7 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11214): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0012 | 0/0 | 11217 | 5 | 1 | 0 | 4 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11212): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0013 | 0/0 | 11219 | 5 | 0 | 0 | 4 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11214): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0014 | 0/0 | 11219 | 5 | 0 | 0 | 5 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11214): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0015 | 0/0 | 11218 | 4 | 4 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11213): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0016 | 0/0 | 11223 | 4 | 4 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11218): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0017 | 0/0 | 11221 | 4 | 4 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11216): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0018 | 0/0 | 11223 | 3 | 0 | 0 | 3 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11218): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0019 | 1/0 | 11219 | 3 | 0 | 2 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11214): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0020 | 0/0 | 11219 | 3 | 0 | 2 | 0 | 1 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11214): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0021 | 0/0 | 11225 | 3 | 0 | 3 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11220): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0022 | 0/0 | 11219 | 3 | 3 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11214): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0023 | 0/0 | 11219 | 3 | 0 | 2 | 0 | 1 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11214): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0025 | 0/0 | 11227 | 3 | 0 | 3 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11222): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0026 | 0/0 | 11219 | 3 | 3 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11214): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0027 | 0/0 | 11217 | 3 | 0 | 2 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11212): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0028 | 0/0 | 11217 | 2 | 2 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11212): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0030 | 0/0 | 11219 | 2 | 0 | 2 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11214): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0031 | 0/0 | 11219 | 2 | 0 | 0 | 2 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11214): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0032 | 0/0 | 11221 | 2 | 2 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11216): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0033 | 0/0 | 11219 | 2 | 0 | 0 | 2 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11214): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0034 | 0/0 | 11219 | 2 | 0 | 0 | 0 | 2 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11214): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0035 | 0/0 | 11221 | 2 | 2 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11216): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0036 | 0/0 | 11221 | 2 | 0 | 0 | 0 | 0 | 2 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11216): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0037 | 0/0 | 11218 | 2 | 0 | 0 | 2 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11213): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0038 | 0/0 | 11221 | 2 | 2 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11216): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0039 | 0/0 | 11219 | 2 | 0 | 0 | 2 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11214): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0040 | 0/0 | 11219 | 2 | 2 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11214): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0041 | 0/0 | 11227 | 2 | 2 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11222): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0042 | 0/0 | 11217 | 2 | 2 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11212): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0043 | 0/0 | 11217 | 2 | 0 | 0 | 2 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11212): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0044 | 0/0 | 11217 | 2 | 2 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11212): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0045 | 0/0 | 11228 | 2 | 2 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11223): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0046 | 0/0 | 11219 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11214): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0047 | 0/0 | 11219 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11214): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0048 | 0/0 | 11219 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11214): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0049 | 0/0 | 11218 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11213): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0050 | 0/0 | 11219 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11214): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0051 | 0/0 | 11219 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11214): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0052 | 0/0 | 11218 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11213): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0053 | 0/0 | 11219 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11214): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0054 | 0/0 | 11228 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11223): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0055 | 0/0 | 11219 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11214): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0056 | 0/0 | 11221 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11216): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0057 | 0/0 | 11221 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11216): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0058 | 0/0 | 11218 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11213): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0059 | 0/0 | 11218 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11213): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0060 | 0/0 | 11217 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11212): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0061 | 0/0 | 11219 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11214): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0062 | 0/0 | 11219 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11214): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0063 | 0/0 | 11219 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11214): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0064 | 0/0 | 11219 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11214): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0065 | 0/0 | 11201 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11196): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0066 | 0/0 | 11219 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11214): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0067 | 0/0 | 11219 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11214): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0068 | 0/0 | 11219 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11214): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0069 | 0/0 | 11227 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11222): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0070 | 0/0 | 11217 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11212): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0071 | 0/0 | 11223 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11218): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0072 | 0/0 | 11223 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11218): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0073 | 0/0 | 11221 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11216): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0074 | 0/0 | 11219 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11214): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0075 | 0/0 | 11218 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11213): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0077 | 0/0 | 11219 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11214): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0078 | 0/0 | 11219 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11214): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0079 | 0/0 | 11219 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11214): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0080 | 0/0 | 11219 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11214): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0081 | 0/0 | 11230 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11225): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0082 | 0/0 | 11221 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11216): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0083 | 0/0 | 11217 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11212): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0084 | 0/0 | 11221 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11216): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0085 | 0/0 | 11219 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11214): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0086 | 0/0 | 11221 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11216): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0087 | 0/0 | 11219 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11214): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0088 | 0/0 | 11217 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11212): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0089 | 0/0 | 11219 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11214): Show |
chr6 | 122991235 | 123077925 |
| a0001c0001t0090 | 0/0 | 11221 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11216): Show |
chr6 | 122991235 | 123077925 |
| a0001c0002t0024 | 0/0 | 11220 | 3 | 3 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11215): Show |
chr6 | 122991235 | 123077925 |
| a0001c0002t0029 | 0/0 | 11220 | 2 | 2 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11215): Show |
chr6 | 122991235 | 123077925 |
| a0001c0004t0076 | 0/0 | 11219 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11214): Show |
chr6 | 122991235 | 123077925 |
| a0002c0003t0005 | 0/0 | 11219 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | GTCCT others(11214): Show |
chr6 | 122991235 | 123077925 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0003g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0003g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0004g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0004g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0004g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0004g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0004g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0004g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0004g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0004g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0004g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0004g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0004g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0005g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0005g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0005g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0005g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0005g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0005g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0005g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0005g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0005g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0005g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0005g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0005g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0005g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0005g0282 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0006g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0006g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0006g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0006g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0006g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0006g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0006g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0006g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0006g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0006g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0006g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0006g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0006g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0006g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0007g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0007g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0007g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0007g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0007g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0007g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0007g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0007g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0008g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0008g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0008g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0008g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0009g0022 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0009g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0009g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0009g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0009g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0009g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0010g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0010g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0010g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0010g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0010g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0010g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0011g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0011g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0011g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0011g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0011g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0011g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0011g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0012g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0012g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0012g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0012g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0012g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0013g0005 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0013g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0013g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0014g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0014g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0014g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0014g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0014g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0015g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0015g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0015g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0015g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0016g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0016g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0016g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0017g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0017g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0017g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0017g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0018g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0019g0021 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0019g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0020g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0020g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0021g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0021g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0022g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0022g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0022g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0023g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0023g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0023g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0025g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0025g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0025g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0026g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0026g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0026g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0027g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0027g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0027g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0028g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0028g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0030g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0031g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0031g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0032g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0032g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0033g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0033g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0034g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0035g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0035g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0036g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0036g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0037g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0037g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0038g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0038g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0039g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0039g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0040g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0040g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0041g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0041g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0042g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0042g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0043g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0043g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0044g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0045g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0045g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0046g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0047g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0048g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0049g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0050g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0051g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0052g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0053g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0054g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0055g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0056g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0057g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0058g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0059g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0060g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0061g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0062g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0063g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0064g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0065g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0066g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0067g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0068g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0069g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0070g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0071g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0072g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0073g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0074g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0075g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0077g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0078g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0079g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0080g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0081g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0082g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0083g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0084g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0085g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0086g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0087g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0088g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0089g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0001t0090g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0002t0024g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0002t0024g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0002t0024g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0002t0029g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0002t0029g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0001c0004t0076g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| a0002c0003t0005g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0062 | EUR | GBR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG00099 | hp2 | a0001 | c0001 | t0020 | g0281 | EUR | GBR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0113 | EUR | GBR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0024 | EUR | GBR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0024 | EUR | FIN | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0103 | EUR | FIN | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0228 | EUR | FIN | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG00323 | hp2 | a0001 | c0001 | t0023 | g0097 | EUR | FIN | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG00408 | hp2 | a0001 | c0001 | t0004 | g0104 | EAS | CHS | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG00423 | hp2 | a0001 | c0001 | t0006 | g0237 | EAS | CHS | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG00438 | hp1 | a0001 | c0001 | t0039 | g0233 | EAS | CHS | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG00438 | hp2 | a0001 | c0001 | t0067 | g0038 | EAS | CHS | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | CHS | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG00621 | hp1 | a0001 | c0001 | t0013 | g0030 | EAS | CHS | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG00639 | hp1 | a0001 | c0001 | t0020 | g0031 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG00673 | hp2 | a0001 | c0001 | t0013 | g0030 | EAS | CHS | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG00733 | hp1 | a0001 | c0001 | t0004 | g0131 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0225 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG00735 | hp1 | a0001 | c0001 | t0027 | g0162 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0138 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG00738 | hp1 | a0001 | c0001 | t0019 | g0021 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0015 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0195 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG00741 | hp2 | a0001 | c0001 | t0010 | g0168 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG01070 | hp1 | a0001 | c0001 | t0023 | g0189 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG01070 | hp2 | a0001 | c0001 | t0030 | g0010 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG01071 | hp1 | a0001 | c0001 | t0030 | g0010 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG01071 | hp2 | a0001 | c0001 | t0059 | g0279 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG01099 | hp1 | a0001 | c0001 | t0007 | g0255 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG01099 | hp2 | a0002 | c0003 | t0005 | g0269 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG01106 | hp1 | a0001 | c0001 | t0062 | g0143 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG01106 | hp2 | a0001 | c0001 | t0027 | g0163 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG01109 | hp2 | a0001 | c0001 | t0025 | g0264 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0102 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG01167 | hp2 | a0001 | c0001 | t0025 | g0263 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0014 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG01168 | hp2 | a0001 | c0001 | t0025 | g0260 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0016 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG01192 | hp1 | a0001 | c0001 | t0006 | g0215 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0098 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG01243 | hp1 | a0001 | c0001 | t0010 | g0019 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | PUR | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | CLM | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0111 | AMR | CLM | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG01256 | hp1 | a0001 | c0001 | t0023 | g0186 | AMR | CLM | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0120 | AMR | CLM | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0121 | AMR | CLM | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG01258 | hp2 | a0001 | c0001 | t0005 | g0003 | AMR | CLM | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0110 | AMR | CLM | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0209 | AMR | CLM | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG01346 | hp1 | a0001 | c0001 | t0005 | g0280 | AMR | CLM | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG01346 | hp2 | a0001 | c0001 | t0074 | g0112 | AMR | CLM | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG01361 | hp1 | a0001 | c0001 | t0058 | g0278 | AMR | CLM | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0220 | AMR | CLM | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0096 | AMR | CLM | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG01496 | hp1 | a0001 | c0001 | t0075 | g0243 | AMR | CLM | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG01496 | hp2 | a0001 | c0001 | t0080 | g0200 | AMR | CLM | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG01515 | hp1 | a0001 | c0001 | t0034 | g0003 | EUR | IBS | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG01515 | hp2 | a0001 | c0001 | t0007 | g0250 | EUR | IBS | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0224 | EUR | IBS | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG01517 | hp2 | a0001 | c0001 | t0034 | g0003 | EUR | IBS | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG01884 | hp2 | a0001 | c0001 | t0016 | g0027 | AFR | ACB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG01891 | hp1 | a0001 | c0001 | t0032 | g0283 | AFR | ACB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG01891 | hp2 | a0001 | c0001 | t0081 | g0035 | AFR | ACB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0146 | AMR | PEL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG01934 | hp2 | a0001 | c0001 | t0005 | g0005 | AMR | PEL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0194 | AMR | PEL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG01975 | hp2 | a0001 | c0001 | t0021 | g0004 | AMR | PEL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG01978 | hp1 | a0001 | c0001 | t0021 | g0005 | AMR | PEL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0197 | AMR | PEL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02004 | hp1 | a0001 | c0001 | t0020 | g0031 | AMR | PEL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02027 | hp1 | a0001 | c0001 | t0005 | g0028 | EAS | KHV | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | KHV | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02055 | hp1 | a0001 | c0001 | t0008 | g0002 | AFR | ACB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0123 | AFR | ACB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02074 | hp1 | a0001 | c0001 | t0006 | g0211 | EAS | KHV | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02074 | hp2 | a0001 | c0001 | t0039 | g0232 | EAS | KHV | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02083 | hp1 | a0001 | c0001 | t0009 | g0022 | EAS | KHV | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02083 | hp2 | a0001 | c0001 | t0004 | g0133 | EAS | KHV | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02145 | hp1 | a0001 | c0001 | t0035 | g0266 | AFR | ACB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0101 | AFR | ACB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | CDX | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02155 | hp2 | a0001 | c0001 | t0064 | g0180 | EAS | CDX | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02257 | hp1 | a0001 | c0001 | t0086 | g0149 | AFR | ACB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02257 | hp2 | a0001 | c0001 | t0015 | g0174 | AFR | ACB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02258 | hp1 | a0001 | c0001 | t0060 | g0247 | AFR | ACB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02273 | hp1 | a0001 | c0001 | t0005 | g0267 | AMR | PEL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0218 | AMR | PEL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02280 | hp1 | a0001 | c0001 | t0035 | g0265 | AFR | ACB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02280 | hp2 | a0001 | c0001 | t0045 | g0172 | AFR | ACB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02300 | hp2 | a0001 | c0001 | t0021 | g0004 | AMR | PEL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02451 | hp1 | a0001 | c0001 | t0015 | g0173 | AFR | ACB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02451 | hp2 | a0001 | c0001 | t0008 | g0001 | AFR | ACB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02523 | hp1 | a0001 | c0001 | t0049 | g0169 | EAS | KHV | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02523 | hp2 | a0001 | c0001 | t0055 | g0217 | EAS | KHV | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0214 | SAS | PJL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02615 | hp1 | a0001 | c0001 | t0042 | g0191 | AFR | GWD | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02622 | hp1 | a0001 | c0001 | t0008 | g0045 | AFR | GWD | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02622 | hp2 | a0001 | c0001 | t0041 | g0261 | AFR | GWD | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02630 | hp1 | a0001 | c0001 | t0041 | g0262 | AFR | GWD | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02630 | hp2 | a0001 | c0001 | t0026 | g0151 | AFR | GWD | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02647 | hp1 | a0001 | c0001 | t0008 | g0002 | AFR | GWD | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02647 | hp2 | a0001 | c0001 | t0087 | g0148 | AFR | GWD | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02683 | hp1 | a0001 | c0001 | t0009 | g0037 | SAS | PJL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0119 | SAS | PJL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02698 | hp1 | a0001 | c0001 | t0069 | g0182 | SAS | PJL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02698 | hp2 | a0001 | c0001 | t0036 | g0089 | SAS | PJL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02717 | hp1 | a0001 | c0001 | t0044 | g0018 | AFR | GWD | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02717 | hp2 | a0001 | c0002 | t0024 | g0259 | AFR | GWD | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02723 | hp1 | a0001 | c0001 | t0010 | g0166 | AFR | GWD | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02723 | hp2 | a0001 | c0001 | t0052 | g0147 | AFR | GWD | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02735 | hp1 | a0001 | c0001 | t0004 | g0125 | SAS | PJL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02735 | hp2 | a0001 | c0001 | t0053 | g0088 | SAS | PJL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02809 | hp1 | a0001 | c0001 | t0057 | g0156 | AFR | GWD | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02818 | hp1 | a0001 | c0001 | t0082 | g0285 | AFR | GWD | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02818 | hp2 | a0001 | c0001 | t0008 | g0002 | AFR | GWD | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02895 | hp1 | a0001 | c0001 | t0028 | g0032 | AFR | GWD | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02895 | hp2 | a0001 | c0001 | t0016 | g0244 | AFR | GWD | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02896 | hp1 | a0001 | c0001 | t0026 | g0093 | AFR | GWD | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02896 | hp2 | a0001 | c0002 | t0024 | g0258 | AFR | GWD | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02897 | hp1 | a0001 | c0001 | t0028 | g0033 | AFR | GWD | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02897 | hp2 | a0001 | c0002 | t0024 | g0257 | AFR | GWD | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02922 | hp1 | a0001 | c0001 | t0010 | g0158 | AFR | ESN | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02922 | hp2 | a0001 | c0001 | t0017 | g0099 | AFR | ESN | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0122 | AFR | ESN | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02965 | hp2 | a0001 | c0001 | t0010 | g0164 | AFR | ESN | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02970 | hp1 | a0001 | c0001 | t0017 | g0154 | AFR | ESN | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02970 | hp2 | a0001 | c0001 | t0022 | g0118 | AFR | ESN | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02976 | hp1 | a0001 | c0001 | t0008 | g0043 | AFR | ESN | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02976 | hp2 | a0001 | c0001 | t0073 | g0246 | AFR | ESN | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0241 | SAS | PJL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG03017 | hp2 | a0001 | c0001 | t0066 | g0015 | SAS | PJL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG03041 | hp1 | a0001 | c0001 | t0040 | g0100 | AFR | GWD | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG03041 | hp2 | a0001 | c0001 | t0089 | g0160 | AFR | GWD | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG03098 | hp1 | a0001 | c0001 | t0088 | g0117 | AFR | MSL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG03098 | hp2 | a0001 | c0001 | t0038 | g0095 | AFR | MSL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG03130 | hp1 | a0001 | c0001 | t0022 | g0145 | AFR | ESN | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG03130 | hp2 | a0001 | c0001 | t0042 | g0284 | AFR | ESN | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG03139 | hp1 | a0001 | c0001 | t0017 | g0155 | AFR | ESN | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG03139 | hp2 | a0001 | c0001 | t0008 | g0001 | AFR | ESN | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG03209 | hp1 | a0001 | c0001 | t0010 | g0165 | AFR | MSL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0171 | AFR | MSL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG03225 | hp1 | a0001 | c0001 | t0044 | g0018 | AFR | MSL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG03225 | hp2 | a0001 | c0001 | t0038 | g0094 | AFR | MSL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG03239 | hp1 | a0001 | c0001 | t0068 | g0036 | SAS | PJL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0016 | SAS | PJL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG03486 | hp1 | a0001 | c0001 | t0047 | g0046 | AFR | MSL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0248 | AFR | MSL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG03490 | hp1 | a0001 | c0001 | t0009 | g0181 | SAS | PJL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG03490 | hp2 | a0001 | c0001 | t0004 | g0132 | SAS | PJL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG03492 | hp1 | a0001 | c0001 | t0009 | g0022 | SAS | PJL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG03516 | hp1 | a0001 | c0001 | t0017 | g0170 | AFR | ESN | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG03516 | hp2 | a0001 | c0001 | t0045 | g0177 | AFR | ESN | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0115 | AFR | GWD | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG03540 | hp2 | a0001 | c0001 | t0016 | g0153 | AFR | GWD | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG03579 | hp1 | a0001 | c0001 | t0015 | g0175 | AFR | MSL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0213 | SAS | PJL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG03654 | hp2 | a0001 | c0001 | t0063 | g0142 | SAS | PJL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG03704 | hp1 | a0001 | c0001 | t0027 | g0161 | SAS | PJL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0116 | SAS | BEB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG03831 | hp2 | a0001 | c0001 | t0005 | g0275 | SAS | BEB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0205 | SAS | BEB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0114 | SAS | BEB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG03927 | hp1 | a0001 | c0001 | t0036 | g0108 | SAS | BEB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG03927 | hp2 | a0001 | c0004 | t0076 | g0192 | SAS | BEB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG03942 | hp1 | a0001 | c0001 | t0013 | g0005 | SAS | BEB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG03942 | hp2 | a0001 | c0001 | t0009 | g0183 | SAS | BEB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG04115 | hp1 | a0001 | c0001 | t0004 | g0141 | SAS | STU | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0239 | SAS | STU | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG04184 | hp1 | a0001 | c0001 | t0077 | g0222 | SAS | BEB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG04184 | hp2 | a0001 | c0001 | t0005 | g0268 | SAS | BEB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG04204 | hp1 | a0001 | c0001 | t0070 | g0050 | SAS | STU | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG04204 | hp2 | a0001 | c0001 | t0009 | g0184 | SAS | STU | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18522 | hp1 | a0001 | c0001 | t0090 | g0286 | AFR | YRI | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18522 | hp2 | a0001 | c0001 | t0008 | g0001 | AFR | YRI | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18906 | hp1 | a0001 | c0001 | t0016 | g0027 | AFR | YRI | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0229 | AFR | YRI | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18942 | hp2 | a0001 | c0001 | t0014 | g0227 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18945 | hp2 | a0001 | c0001 | t0006 | g0008 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18947 | hp1 | a0001 | c0001 | t0013 | g0005 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18948 | hp1 | a0001 | c0001 | t0007 | g0254 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18950 | hp1 | a0001 | c0001 | t0018 | g0007 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18950 | hp2 | a0001 | c0001 | t0005 | g0272 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18951 | hp1 | a0001 | c0001 | t0007 | g0009 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18951 | hp2 | a0001 | c0001 | t0014 | g0196 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18952 | hp1 | a0001 | c0001 | t0011 | g0077 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18952 | hp2 | a0001 | c0001 | t0004 | g0134 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18953 | hp1 | a0001 | c0001 | t0004 | g0140 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18956 | hp1 | a0001 | c0001 | t0014 | g0201 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18956 | hp2 | a0001 | c0001 | t0007 | g0251 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0135 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18961 | hp2 | a0001 | c0001 | t0006 | g0242 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18962 | hp1 | a0001 | c0001 | t0011 | g0070 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18962 | hp2 | a0001 | c0001 | t0006 | g0193 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18963 | hp1 | a0001 | c0001 | t0011 | g0067 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18963 | hp2 | a0001 | c0001 | t0006 | g0008 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18967 | hp1 | a0001 | c0001 | t0048 | g0137 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18967 | hp2 | a0001 | c0001 | t0007 | g0252 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0139 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18970 | hp2 | a0001 | c0001 | t0004 | g0017 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18972 | hp1 | a0001 | c0001 | t0006 | g0204 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18972 | hp2 | a0001 | c0001 | t0043 | g0234 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18973 | hp1 | a0001 | c0001 | t0018 | g0007 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18974 | hp1 | a0001 | c0001 | t0012 | g0085 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18977 | hp2 | a0001 | c0001 | t0011 | g0069 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18980 | hp2 | a0001 | c0001 | t0007 | g0009 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18981 | hp1 | a0001 | c0001 | t0005 | g0270 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18985 | hp1 | a0001 | c0001 | t0031 | g0188 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18986 | hp1 | a0001 | c0001 | t0018 | g0007 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18988 | hp1 | a0001 | c0001 | t0065 | g0128 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18990 | hp2 | a0001 | c0001 | t0012 | g0056 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18991 | hp1 | a0001 | c0001 | t0007 | g0009 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18994 | hp1 | a0001 | c0001 | t0037 | g0129 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18994 | hp2 | a0001 | c0001 | t0033 | g0271 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18995 | hp1 | a0001 | c0001 | t0006 | g0238 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18995 | hp2 | a0001 | c0001 | t0004 | g0107 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18997 | hp1 | a0001 | c0001 | t0004 | g0127 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18997 | hp2 | a0001 | c0001 | t0007 | g0249 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18998 | hp1 | a0001 | c0001 | t0012 | g0059 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18998 | hp2 | a0001 | c0001 | t0046 | g0025 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18999 | hp1 | a0001 | c0001 | t0051 | g0057 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18999 | hp2 | a0001 | c0001 | t0043 | g0202 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA19006 | hp1 | a0001 | c0001 | t0014 | g0230 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA19006 | hp2 | a0001 | c0001 | t0005 | g0276 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA19007 | hp2 | a0001 | c0001 | t0037 | g0126 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA19009 | hp1 | a0001 | c0001 | t0006 | g0216 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA19010 | hp1 | a0001 | c0001 | t0050 | g0006 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA19010 | hp2 | a0001 | c0001 | t0006 | g0210 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA19011 | hp1 | a0001 | c0001 | t0014 | g0198 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA19012 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA19030 | hp1 | a0001 | c0001 | t0012 | g0058 | AFR | LWK | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA19030 | hp2 | a0001 | c0001 | t0072 | g0245 | AFR | LWK | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA19043 | hp1 | a0001 | c0002 | t0029 | g0041 | AFR | LWK | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0124 | AFR | LWK | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA19054 | hp1 | a0001 | c0001 | t0031 | g0187 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA19056 | hp1 | a0001 | c0001 | t0061 | g0028 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA19058 | hp1 | a0001 | c0001 | t0013 | g0274 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA19058 | hp2 | a0001 | c0001 | t0011 | g0086 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0106 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA19063 | hp1 | a0001 | c0001 | t0007 | g0256 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA19063 | hp2 | a0001 | c0001 | t0078 | g0223 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA19065 | hp1 | a0001 | c0001 | t0004 | g0017 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA19065 | hp2 | a0001 | c0001 | t0005 | g0029 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA19066 | hp2 | a0001 | c0001 | t0006 | g0008 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA19068 | hp2 | a0001 | c0001 | t0006 | g0208 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA19070 | hp1 | a0001 | c0001 | t0005 | g0029 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA19076 | hp1 | a0001 | c0001 | t0012 | g0051 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA19077 | hp2 | a0001 | c0001 | t0011 | g0064 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA19080 | hp1 | a0001 | c0001 | t0006 | g0026 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0109 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA19084 | hp1 | a0001 | c0001 | t0011 | g0012 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA19084 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA19085 | hp1 | a0001 | c0001 | t0033 | g0273 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA19085 | hp2 | a0001 | c0001 | t0006 | g0212 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA19087 | hp2 | a0001 | c0001 | t0004 | g0130 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA19240 | hp1 | a0001 | c0001 | t0056 | g0048 | AFR | YRI | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA19240 | hp2 | a0001 | c0001 | t0079 | g0159 | AFR | YRI | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA20129 | hp1 | a0001 | c0001 | t0008 | g0001 | AFR | ASW | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA20129 | hp2 | a0001 | c0001 | t0009 | g0185 | AFR | ASW | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0014 | AMR | CLM | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG01123 | hp2 | a0001 | c0001 | t0019 | g0190 | AMR | CLM | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02109 | hp1 | a0001 | c0001 | t0054 | g0044 | AFR | ACB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02109 | hp2 | a0001 | c0001 | t0071 | g0178 | AFR | ACB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02486 | hp1 | a0001 | c0001 | t0010 | g0019 | AFR | ACB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0003 | AFR | ACB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02559 | hp1 | a0001 | c0001 | t0026 | g0150 | AFR | ACB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG02559 | hp2 | a0001 | c0001 | t0084 | g0287 | AFR | ACB | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG03471 | hp1 | a0001 | c0001 | t0085 | g0152 | AFR | MSL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG03471 | hp2 | a0001 | c0001 | t0022 | g0144 | AFR | MSL | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG06807 | hp1 | a0001 | c0001 | t0015 | g0176 | AFR | USA | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| HG06807 | hp2 | a0001 | c0002 | t0029 | g0042 | AFR | USA | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA18955 | hp2 | a0001 | c0001 | t0006 | g0025 | EAS | JPT | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA20300 | hp1 | a0001 | c0001 | t0083 | g0157 | AFR | USA | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA21309 | hp1 | a0001 | c0001 | t0032 | g0277 | AFR | LWK | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| NA21309 | hp2 | a0001 | c0001 | t0040 | g0167 | AFR | LWK | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0005 | g0282 | REF | REF | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0019 | g0021 | REF | REF | CLVS2_chr6_122991235_123077925 | CLVS2 | chr6 | 122991235 | 123077925 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:123055859 | G | C | 1 | a0002 | 1 | HG01099.hp2 | missense_variant | MODERATE | c.729G>C | p.Glu243Asp | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/6 | 1800/11219 | 729/984 | 243/327 | chr6 | 123055859 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:123055943 | C | T | 1 | a0001c0004 | 1 | HG03927.hp2 | synonymous_variant | LOW | c.813C>T | p.Asp271Asp | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/6 | 1884/11219 | 813/984 | 271/327 | chr6 | 123055943 | |||
| chr6:123055961 | T | C | 1 | a0001c0002 | 5 | HG02717.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
synonymous_variant | LOW | c.831T>C | p.Asn277Asn | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/6 | 1902/11219 | 831/984 | 277/327 | chr6 | 123055961 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:122996283 | G | A | 21 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0009 others(18): Show |
91 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(88): Show |
5_prime_UTR_variant | MODIFIER | c.-1023G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 1/6 | 1495 | chr6 | 122996283 | ||||||
| chr6:122996286 | A | C | 76 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(73): Show |
291 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(288): Show |
5_prime_UTR_variant | MODIFIER | c.-1020A>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 1/6 | 1492 | chr6 | 122996286 | ||||||
| chr6:122996299 | C | T | 1 | a0001c0001t0090 | 1 | NA18522.hp1 | 5_prime_UTR_variant | MODIFIER | c.-1007C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 1/6 | 1479 | chr6 | 122996299 | ||||||
| chr6:122996434 | C | G | 20 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0009 others(17): Show |
93 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(90): Show |
5_prime_UTR_variant | MODIFIER | c.-872C>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 1/6 | 1344 | chr6 | 122996434 | ||||||
| chr6:122996532 | A | G | 75 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(72): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(263): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-774A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 1/6 | chr6 | 122996532 | |||||||
| chr6:122996553 | G | T | 1 | a0001c0001t0089 | 1 | HG03041.hp2 | 5_prime_UTR_variant | MODIFIER | c.-753G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 1/6 | 1225 | chr6 | 122996553 | ||||||
| chr6:122996554 | C | T | 1 | a0001c0001t0089 | 1 | HG03041.hp2 | 5_prime_UTR_variant | MODIFIER | c.-752C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 1/6 | 1224 | chr6 | 122996554 | ||||||
| chr6:122996686 | C | T | 2 | a0001c0001t0087 a0001c0001t0088 |
2 | HG02647.hp2 HG03098.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-620C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 1/6 | chr6 | 122996686 | |||||||
| chr6:122996734 | T | A | 1 | a0001c0001t0047 | 1 | HG03486.hp1 | 5_prime_UTR_variant | MODIFIER | c.-572T>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 1/6 | 1044 | chr6 | 122996734 | ||||||
| chr6:122997224 | C | G | 1 | a0001c0001t0035 | 2 | HG02145.hp1 HG02280.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-554C>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/6 | chr6 | 122997224 | |||||||
| chr6:122997333 | C | T | 2 | a0001c0001t0027 a0001c0001t0086 |
4 | HG00735.hp1 HG01106.hp2 HG02257.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-445C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/6 | 445 | chr6 | 122997333 | ||||||
| chr6:123063978 | G | C | 80 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(77): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
3_prime_UTR_variant | MODIFIER | c.*217G>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 217 | chr6 | 123063978 | ||||||
| chr6:123064100 | C | T | 21 | a0001c0001t0009 a0001c0001t0012 a0001c0001t0025 others(18): Show |
41 | HG00735.hp1 HG01106.hp2 HG01109.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*339C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 339 | chr6 | 123064100 | ||||||
| chr6:123064129 | C | G | 3 | a0001c0001t0006 a0001c0001t0046 a0001c0001t0055 |
18 | HG00423.hp2 HG01192.hp1 HG02074.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*368C>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 368 | chr6 | 123064129 | ||||||
| chr6:123064160 | A | G | 1 | a0001c0001t0084 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*399A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 399 | chr6 | 123064160 | ||||||
| chr6:123064183 | CT | C | 2 | a0001c0002t0024 a0001c0002t0029 |
5 | HG02717.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*423delT | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 423 | chr6 | 123064183 | ||||||
| chr6:123064297 | G | A | 5 | a0001c0001t0016 a0001c0001t0017 a0001c0001t0057 others(2): Show |
11 | HG01884.hp2 HG02109.hp2 HG02809.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*536G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 536 | chr6 | 123064297 | ||||||
| chr6:123064318 | G | T | 2 | a0001c0001t0013 a0001c0001t0031 |
7 | HG00621.hp1 HG00673.hp2 HG03942.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*557G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 557 | chr6 | 123064318 | ||||||
| chr6:123064433 | C | T | 3 | a0001c0001t0045 a0001c0001t0054 a0001c0001t0081 |
4 | HG01891.hp2 HG02109.hp1 HG02280.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*672C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 672 | chr6 | 123064433 | ||||||
| chr6:123064670 | G | GTA | 9 | a0001c0001t0017 a0001c0001t0032 a0001c0001t0036 others(6): Show |
18 | HG01891.hp1 HG02698.hp2 HG02717.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*925_*926dupAT | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 927 | INFO_REALIGN_3_PRIME | chr6 | 123064670 | |||||
| chr6:123064670 | G | GTATA | 5 | a0001c0001t0016 a0001c0001t0045 a0001c0001t0054 others(2): Show |
9 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*923_*926dupATAT | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 927 | INFO_REALIGN_3_PRIME | chr6 | 123064670 | |||||
| chr6:123064676 | A | G | 1 | a0001c0001t0083 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*915A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 915 | chr6 | 123064676 | ||||||
| chr6:123064859 | C | T | 2 | a0001c0001t0007 a0001c0001t0018 |
13 | HG01099.hp1 HG01515.hp2 NA18948.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1098C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 1098 | chr6 | 123064859 | ||||||
| chr6:123064918 | T | G | 18 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0020 others(15): Show |
68 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*1157T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 1157 | chr6 | 123064918 | ||||||
| chr6:123065135 | C | T | 3 | a0001c0001t0007 a0001c0001t0018 a0001c0001t0073 |
14 | HG01099.hp1 HG01515.hp2 HG02976.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1374C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 1374 | chr6 | 123065135 | ||||||
| chr6:123065154 | A | G | 3 | a0001c0001t0045 a0001c0001t0054 a0001c0001t0081 |
4 | HG01891.hp2 HG02109.hp1 HG02280.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1393A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 1393 | chr6 | 123065154 | ||||||
| chr6:123065358 | T | C | 3 | a0001c0001t0045 a0001c0001t0054 a0001c0001t0081 |
4 | HG01891.hp2 HG02109.hp1 HG02280.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1597T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 1597 | chr6 | 123065358 | ||||||
| chr6:123065515 | A | T | 21 | a0001c0001t0009 a0001c0001t0012 a0001c0001t0025 others(18): Show |
41 | HG00735.hp1 HG01106.hp2 HG01109.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1754A>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 1754 | chr6 | 123065515 | ||||||
| chr6:123065531 | A | G | 1 | a0001c0001t0034 | 2 | HG01515.hp1 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1770A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 1770 | chr6 | 123065531 | ||||||
| chr6:123065958 | A | G | 1 | a0001c0001t0053 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2197A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 2197 | chr6 | 123065958 | ||||||
| chr6:123066221 | A | T | 1 | a0001c0001t0080 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2460A>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 2460 | chr6 | 123066221 | ||||||
| chr6:123066264 | A | T | 1 | a0001c0001t0081 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2503A>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 2503 | chr6 | 123066264 | ||||||
| chr6:123066340 | A | ACT | 19 | a0001c0001t0012 a0001c0001t0027 a0001c0001t0028 others(16): Show |
31 | HG00735.hp1 HG01106.hp2 HG02109.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*2595_*2596dupTC | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 2597 | INFO_REALIGN_3_PRIME | chr6 | 123066340 | |||||
| chr6:123066356 | T | TCTCATAC others(1): Show |
5 | a0001c0001t0009 a0001c0001t0025 a0001c0001t0041 others(2): Show |
14 | HG01109.hp2 HG01167.hp2 HG01168.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2596_*2597insTCAT others(4): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 2597 | INFO_REALIGN_3_PRIME | chr6 | 123066356 | |||||
| chr6:123066357 | C | CTCAT | 2 | a0001c0001t0007 a0001c0001t0018 |
13 | HG01099.hp1 HG01515.hp2 NA18948.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2596_*2597insTCAT | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 2597 | chr6 | 123066357 | ||||||
| chr6:123066359 | T | C | 7 | a0001c0001t0007 a0001c0001t0009 a0001c0001t0018 others(4): Show |
27 | HG01099.hp1 HG01109.hp2 HG01167.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*2598T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 2598 | chr6 | 123066359 | ||||||
| chr6:123066391 | C | T | 1 | a0001c0001t0030 | 2 | HG01070.hp2 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2630C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 2630 | chr6 | 123066391 | ||||||
| chr6:123066700 | A | G | 6 | a0001c0001t0035 a0001c0001t0056 a0001c0001t0082 others(3): Show |
7 | HG02145.hp1 HG02257.hp1 HG02280.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2939A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 2939 | chr6 | 123066700 | ||||||
| chr6:123066869 | G | A | 1 | a0001c0001t0061 | 1 | NA19056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3108G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 3108 | chr6 | 123066869 | ||||||
| chr6:123066874 | TACTC | T | 11 | a0001c0001t0012 a0001c0001t0027 a0001c0001t0028 others(8): Show |
21 | HG00735.hp1 HG01106.hp2 HG02258.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*3115_*3118delCTCA | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 3115 | INFO_REALIGN_3_PRIME | chr6 | 123066874 | |||||
| chr6:123066926 | T | C | 1 | a0001c0001t0088 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3165T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 3165 | chr6 | 123066926 | ||||||
| chr6:123066962 | G | A | 6 | a0001c0001t0035 a0001c0001t0056 a0001c0001t0082 others(3): Show |
7 | HG02145.hp1 HG02257.hp1 HG02280.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3201G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 3201 | chr6 | 123066962 | ||||||
| chr6:123067057 | A | G | 1 | a0001c0001t0079 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3296A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 3296 | chr6 | 123067057 | ||||||
| chr6:123067083 | T | C | 1 | a0001c0001t0050 | 1 | NA19010.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3322T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 3322 | chr6 | 123067083 | ||||||
| chr6:123067106 | T | C | 21 | a0001c0001t0009 a0001c0001t0012 a0001c0001t0025 others(18): Show |
41 | HG00735.hp1 HG01106.hp2 HG01109.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*3345T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 3345 | chr6 | 123067106 | ||||||
| chr6:123067173 | A | T | 1 | a0001c0001t0066 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3412A>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 3412 | chr6 | 123067173 | ||||||
| chr6:123067502 | C | T | 4 | a0001c0001t0009 a0001c0001t0025 a0001c0001t0041 others(1): Show |
13 | HG01109.hp2 HG01167.hp2 HG01168.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3741C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 3741 | chr6 | 123067502 | ||||||
| chr6:123067785 | A | G | 2 | a0001c0001t0037 a0001c0001t0065 |
3 | NA18988.hp1 NA18994.hp1 NA19007.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4024A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 4024 | chr6 | 123067785 | ||||||
| chr6:123067802 | T | C | 2 | a0001c0002t0024 a0001c0002t0029 |
5 | HG02717.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4041T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 4041 | chr6 | 123067802 | ||||||
| chr6:123067873 | A | G | 3 | a0001c0001t0045 a0001c0001t0054 a0001c0001t0081 |
4 | HG01891.hp2 HG02109.hp1 HG02280.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4112A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 4112 | chr6 | 123067873 | ||||||
| chr6:123068084 | C | T | 2 | a0001c0001t0007 a0001c0001t0018 |
13 | HG01099.hp1 HG01515.hp2 NA18948.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*4323C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 4323 | chr6 | 123068084 | ||||||
| chr6:123068123 | T | C | 3 | a0001c0001t0045 a0001c0001t0054 a0001c0001t0081 |
4 | HG01891.hp2 HG02109.hp1 HG02280.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4362T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 4362 | chr6 | 123068123 | ||||||
| chr6:123068127 | G | A | 1 | a0001c0004t0076 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4366G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 4366 | chr6 | 123068127 | ||||||
| chr6:123068141 | T | A | 3 | a0001c0001t0045 a0001c0001t0054 a0001c0001t0081 |
4 | HG01891.hp2 HG02109.hp1 HG02280.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4380T>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 4380 | chr6 | 123068141 | ||||||
| chr6:123068290 | A | G | 3 | a0001c0001t0045 a0001c0001t0054 a0001c0001t0081 |
4 | HG01891.hp2 HG02109.hp1 HG02280.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4529A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 4529 | chr6 | 123068290 | ||||||
| chr6:123068488 | G | A | 6 | a0001c0001t0035 a0001c0001t0056 a0001c0001t0082 others(3): Show |
7 | HG02145.hp1 HG02257.hp1 HG02280.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4727G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 4727 | chr6 | 123068488 | ||||||
| chr6:123068761 | C | T | 1 | a0001c0001t0059 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5000C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 5000 | chr6 | 123068761 | ||||||
| chr6:123068811 | TA | T | 7 | a0001c0001t0004 a0001c0001t0037 a0001c0001t0049 others(4): Show |
26 | HG00280.hp2 HG00408.hp2 HG00733.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*5052delA | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 5052 | INFO_REALIGN_3_PRIME | chr6 | 123068811 | |||||
| chr6:123068917 | T | C | 2 | a0001c0001t0010 a0001c0001t0079 |
8 | HG00741.hp2 HG01243.hp1 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5156T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 5156 | chr6 | 123068917 | ||||||
| chr6:123069006 | G | C | 1 | a0001c0001t0062 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5245G>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 5245 | chr6 | 123069006 | ||||||
| chr6:123069115 | G | A | 1 | a0001c0001t0077 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5354G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 5354 | chr6 | 123069115 | ||||||
| chr6:123069178 | T | G | 2 | a0001c0001t0007 a0001c0001t0018 |
13 | HG01099.hp1 HG01515.hp2 NA18948.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*5417T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 5417 | chr6 | 123069178 | ||||||
| chr6:123069273 | A | C | 1 | a0001c0001t0030 | 2 | HG01070.hp2 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5512A>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 5512 | chr6 | 123069273 | ||||||
| chr6:123069356 | TA | T | 2 | a0001c0001t0015 a0001c0001t0052 |
5 | HG02257.hp2 HG02451.hp1 HG02723.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5605delA | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 5605 | INFO_REALIGN_3_PRIME | chr6 | 123069356 | |||||
| chr6:123069385 | A | G | 1 | a0001c0001t0044 | 2 | HG02717.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5624A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 5624 | chr6 | 123069385 | ||||||
| chr6:123069522 | A | G | 2 | a0001c0002t0024 a0001c0002t0029 |
5 | HG02717.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5761A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 5761 | chr6 | 123069522 | ||||||
| chr6:123069554 | T | C | 80 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(77): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
3_prime_UTR_variant | MODIFIER | c.*5793T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 5793 | chr6 | 123069554 | ||||||
| chr6:123069721 | T | C | 2 | a0001c0001t0010 a0001c0001t0079 |
8 | HG00741.hp2 HG01243.hp1 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5960T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 5960 | chr6 | 123069721 | ||||||
| chr6:123070057 | T | C | 3 | a0001c0001t0045 a0001c0001t0054 a0001c0001t0081 |
4 | HG01891.hp2 HG02109.hp1 HG02280.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6296T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 6296 | chr6 | 123070057 | ||||||
| chr6:123070129 | A | G | 26 | a0001c0001t0007 a0001c0001t0009 a0001c0001t0012 others(23): Show |
58 | HG00735.hp1 HG01099.hp1 HG01106.hp2 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*6368A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 6368 | chr6 | 123070129 | ||||||
| chr6:123070153 | A | G | 1 | a0001c0001t0041 | 2 | HG02622.hp2 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6392A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 6392 | chr6 | 123070153 | ||||||
| chr6:123070311 | G | GTCATCC | 1 | a0001c0001t0021 | 3 | HG01975.hp2 HG01978.hp1 HG02300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6553_*6558dupATCC others(2): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 6559 | INFO_REALIGN_3_PRIME | chr6 | 123070311 | |||||
| chr6:123070393 | C | A | 2 | a0001c0001t0014 a0001c0001t0051 |
6 | NA18942.hp2 NA18951.hp2 NA18956.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6632C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 6632 | chr6 | 123070393 | ||||||
| chr6:123070415 | A | ATCT | 3 | a0001c0001t0045 a0001c0001t0054 a0001c0001t0081 |
4 | HG01891.hp2 HG02109.hp1 HG02280.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6660_*6662dupTTC | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 6663 | INFO_REALIGN_3_PRIME | chr6 | 123070415 | |||||
| chr6:123070547 | C | T | 1 | a0001c0001t0085 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6786C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 6786 | chr6 | 123070547 | ||||||
| chr6:123070605 | A | G | 26 | a0001c0001t0007 a0001c0001t0009 a0001c0001t0012 others(23): Show |
58 | HG00735.hp1 HG01099.hp1 HG01106.hp2 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*6844A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 6844 | chr6 | 123070605 | ||||||
| chr6:123070706 | G | T | 4 | a0001c0001t0012 a0001c0001t0043 a0001c0001t0068 others(1): Show |
9 | HG03239.hp1 HG04204.hp1 NA18972.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*6945G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 6945 | chr6 | 123070706 | ||||||
| chr6:123071152 | G | T | 2 | a0001c0001t0016 a0001c0001t0072 |
5 | HG01884.hp2 HG02895.hp2 HG03540.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*7391G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 7391 | chr6 | 123071152 | ||||||
| chr6:123071235 | G | A | 1 | a0001c0001t0063 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7474G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 7474 | chr6 | 123071235 | ||||||
| chr6:123071582 | AGGAAGTT others(10): Show |
A | 1 | a0001c0001t0065 | 1 | NA18988.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7822_*7838delGGAA others(13): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 7822 | chr6 | 123071582 | ||||||
| chr6:123071662 | G | C | 26 | a0001c0001t0007 a0001c0001t0009 a0001c0001t0012 others(23): Show |
58 | HG00735.hp1 HG01099.hp1 HG01106.hp2 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*7901G>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 7901 | chr6 | 123071662 | ||||||
| chr6:123071784 | A | T | 1 | a0001c0001t0064 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8023A>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 8023 | chr6 | 123071784 | ||||||
| chr6:123071789 | C | T | 1 | a0001c0001t0030 | 2 | HG01070.hp2 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8028C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 8028 | chr6 | 123071789 | ||||||
| chr6:123071864 | G | T | 1 | a0001c0001t0078 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8103G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 8103 | chr6 | 123071864 | ||||||
| chr6:123072052 | T | G | 3 | a0001c0001t0045 a0001c0001t0054 a0001c0001t0081 |
4 | HG01891.hp2 HG02109.hp1 HG02280.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*8291T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 8291 | chr6 | 123072052 | ||||||
| chr6:123072097 | G | A | 1 | a0001c0001t0072 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8336G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 8336 | chr6 | 123072097 | ||||||
| chr6:123072231 | A | G | 18 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(15): Show |
120 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*8470A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 8470 | chr6 | 123072231 | ||||||
| chr6:123072237 | T | G | 3 | a0001c0001t0045 a0001c0001t0054 a0001c0001t0081 |
4 | HG01891.hp2 HG02109.hp1 HG02280.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*8476T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 8476 | chr6 | 123072237 | ||||||
| chr6:123072555 | A | G | 2 | a0001c0001t0039 a0001c0001t0048 |
3 | HG00438.hp1 HG02074.hp2 NA18967.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8794A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 8794 | chr6 | 123072555 | ||||||
| chr6:123072607 | C | T | 2 | a0001c0001t0007 a0001c0001t0018 |
13 | HG01099.hp1 HG01515.hp2 NA18948.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*8846C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 8846 | chr6 | 123072607 | ||||||
| chr6:123072617 | G | A | 3 | a0001c0001t0045 a0001c0001t0054 a0001c0001t0081 |
4 | HG01891.hp2 HG02109.hp1 HG02280.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*8856G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 8856 | chr6 | 123072617 | ||||||
| chr6:123072778 | A | G | 2 | a0001c0002t0024 a0001c0002t0029 |
5 | HG02717.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*9017A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 9017 | chr6 | 123072778 | ||||||
| chr6:123072873 | T | G | 2 | a0001c0001t0045 a0001c0001t0054 |
3 | HG02109.hp1 HG02280.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9112T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 6/6 | 9112 | chr6 | 123072873 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:122996879 | G | C | 2 | a0001c0001t0028g0032 a0001c0001t0028g0033 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-560+133G>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 1/5 | chr6 | 122996879 | |||||||
| chr6:122996885 | C | T | 4 | a0001c0001t0042g0284 a0001c0001t0082g0285 a0001c0001t0084g0287 others(1): Show |
4 | HG02559.hp2 HG02818.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-560+139C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 1/5 | chr6 | 122996885 | |||||||
| chr6:122997156 | C | G | 119 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0026 others(116): Show |
134 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.-559-63C>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 1/5 | chr6 | 122997156 | |||||||
| chr6:122997164 | A | C | 2 | a0001c0001t0028g0032 a0001c0001t0028g0033 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-559-55A>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 1/5 | chr6 | 122997164 | |||||||
| chr6:122998237 | C | T | 57 | a0001c0001t0002g0253 a0001c0001t0005g0003 a0001c0001t0005g0004 others(54): Show |
69 | HG00099.hp2 HG00621.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.389+71C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 122998237 | |||||||
| chr6:122998319 | C | A | 1 | a0001c0001t0003g0034 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.389+153C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 122998319 | |||||||
| chr6:122998463 | G | A | 58 | a0001c0001t0002g0253 a0001c0001t0005g0003 a0001c0001t0005g0004 others(55): Show |
70 | HG00099.hp2 HG00621.hp1 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.389+297G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 122998463 | |||||||
| chr6:122998541 | C | T | 58 | a0001c0001t0002g0253 a0001c0001t0005g0003 a0001c0001t0005g0004 others(55): Show |
70 | HG00099.hp2 HG00621.hp1 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.389+375C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 122998541 | |||||||
| chr6:122998595 | C | T | 56 | a0001c0001t0002g0253 a0001c0001t0005g0003 a0001c0001t0005g0004 others(53): Show |
68 | HG00099.hp2 HG00621.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.389+429C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 122998595 | |||||||
| chr6:122998646 | C | T | 58 | a0001c0001t0002g0253 a0001c0001t0005g0003 a0001c0001t0005g0004 others(55): Show |
70 | HG00099.hp2 HG00621.hp1 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.389+480C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 122998646 | |||||||
| chr6:122998675 | G | A | 1 | a0001c0001t0081g0035 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.389+509G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 122998675 | |||||||
| chr6:122998761 | G | A | 58 | a0001c0001t0002g0253 a0001c0001t0005g0003 a0001c0001t0005g0004 others(55): Show |
70 | HG00099.hp2 HG00621.hp1 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.389+595G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 122998761 | |||||||
| chr6:122998892 | TGTCAGTT others(1): Show |
T | 58 | a0001c0001t0002g0253 a0001c0001t0005g0003 a0001c0001t0005g0004 others(55): Show |
70 | HG00099.hp2 HG00621.hp1 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.389+729_389+736del others(8): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 122998892 | ||||||
| chr6:122999042 | T | C | 1 | a0001c0004t0076g0192 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.389+876T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 122999042 | |||||||
| chr6:122999191 | T | G | 1 | a0001c0001t0006g0193 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.389+1025T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 122999191 | |||||||
| chr6:122999311 | T | C | 58 | a0001c0001t0002g0253 a0001c0001t0005g0003 a0001c0001t0005g0004 others(55): Show |
70 | HG00099.hp2 HG00621.hp1 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.389+1145T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 122999311 | |||||||
| chr6:122999422 | T | C | 56 | a0001c0001t0002g0253 a0001c0001t0005g0003 a0001c0001t0005g0004 others(53): Show |
68 | HG00099.hp2 HG00621.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.389+1256T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 122999422 | |||||||
| chr6:122999452 | A | G | 58 | a0001c0001t0002g0253 a0001c0001t0005g0003 a0001c0001t0005g0004 others(55): Show |
70 | HG00099.hp2 HG00621.hp1 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.389+1286A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 122999452 | |||||||
| chr6:122999467 | T | C | 2 | a0001c0001t0028g0032 a0001c0001t0028g0033 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.389+1301T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 122999467 | |||||||
| chr6:122999578 | C | A | 5 | a0001c0001t0005g0003 a0001c0001t0005g0248 a0001c0001t0023g0186 others(2): Show |
7 | HG01256.hp1 HG01258.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.389+1412C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 122999578 | |||||||
| chr6:122999633 | A | G | 55 | a0001c0001t0002g0253 a0001c0001t0005g0003 a0001c0001t0005g0004 others(52): Show |
67 | HG00099.hp2 HG00621.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.389+1467A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 122999633 | |||||||
| chr6:122999653 | A | G | 1 | a0001c0001t0032g0283 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.389+1487A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 122999653 | |||||||
| chr6:122999668 | A | C | 7 | a0001c0001t0005g0280 a0001c0001t0019g0190 a0001c0001t0020g0031 others(4): Show |
8 | HG00099.hp2 HG00639.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.389+1502A>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 122999668 | |||||||
| chr6:122999820 | G | A | 1 | a0001c0001t0042g0284 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.389+1654G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 122999820 | |||||||
| chr6:122999929 | T | A | 1 | a0001c0001t0006g0193 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.389+1763T>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 122999929 | |||||||
| chr6:123000221 | G | A | 1 | a0001c0001t0068g0036 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.389+2055G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123000221 | |||||||
| chr6:123000265 | A | G | 47 | a0001c0001t0005g0003 a0001c0001t0005g0004 a0001c0001t0005g0005 others(44): Show |
55 | HG00099.hp2 HG00621.hp1 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.389+2099A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123000265 | |||||||
| chr6:123000518 | C | A | 1 | a0001c0001t0009g0037 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.389+2352C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123000518 | |||||||
| chr6:123000706 | C | G | 11 | a0001c0001t0002g0253 a0001c0001t0007g0009 a0001c0001t0007g0249 others(8): Show |
15 | HG01099.hp1 HG01515.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.389+2540C>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123000706 | |||||||
| chr6:123000815 | C | G | 1 | a0001c0001t0032g0277 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.389+2649C>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123000815 | |||||||
| chr6:123000900 | G | A | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(122): Show |
141 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.389+2734G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123000900 | |||||||
| chr6:123001245 | A | G | 1 | a0001c0001t0006g0242 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.389+3079A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123001245 | |||||||
| chr6:123001274 | G | A | 3 | a0001c0002t0024g0257 a0001c0002t0024g0258 a0001c0002t0024g0259 |
3 | HG02717.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.389+3108G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123001274 | |||||||
| chr6:123001635 | C | T | 7 | a0001c0001t0009g0022 a0001c0001t0009g0037 a0001c0001t0009g0181 others(4): Show |
8 | HG02083.hp1 HG02683.hp1 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.389+3469C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123001635 | |||||||
| chr6:123001848 | G | A | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(247): Show |
278 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.389+3682G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123001848 | |||||||
| chr6:123001870 | A | G | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(236): Show |
263 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.389+3704A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123001870 | |||||||
| chr6:123001982 | C | G | 3 | a0001c0001t0003g0020 a0001c0001t0003g0179 a0001c0001t0064g0180 |
4 | HG02155.hp2 NA18948.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.389+3816C>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123001982 | |||||||
| chr6:123002261 | G | A | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(236): Show |
263 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.389+4095G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123002261 | |||||||
| chr6:123002262 | C | T | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(236): Show |
263 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.389+4096C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123002262 | |||||||
| chr6:123002310 | T | C | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(236): Show |
263 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.389+4144T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123002310 | |||||||
| chr6:123002331 | T | C | 10 | a0001c0001t0002g0253 a0001c0001t0007g0009 a0001c0001t0007g0249 others(7): Show |
14 | HG01099.hp1 HG01515.hp2 NA18947.hp2 others(11): Show |
intron_variant | MODIFIER | c.389+4165T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123002331 | |||||||
| chr6:123002401 | G | A | 1 | a0001c0001t0026g0093 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.389+4235G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123002401 | |||||||
| chr6:123002586 | T | TAATAA | 4 | a0001c0001t0001g0013 a0001c0001t0026g0093 a0001c0001t0042g0191 others(1): Show |
5 | HG02109.hp2 HG02602.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.389+4449_389+4453d others(7): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 123002586 | ||||||
| chr6:123002586 | T | TAATAAAA others(3): Show |
55 | a0001c0001t0002g0171 a0001c0001t0002g0253 a0001c0001t0007g0009 others(52): Show |
62 | HG00735.hp1 HG00741.hp2 HG01099.hp1 others(59): Show |
intron_variant | MODIFIER | c.389+4444_389+4453d others(12): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 123002586 | ||||||
| chr6:123002586 | T | TAATAAAA others(8): Show |
174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(171): Show |
193 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.389+4439_389+4453d others(17): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 123002586 | ||||||
| chr6:123002586 | T | TAATAAAA others(13): Show |
15 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0002g0023 others(12): Show |
16 | HG00438.hp2 HG00673.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.389+4434_389+4453d others(22): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 123002586 | ||||||
| chr6:123002586 | T | TAATAAAA others(18): Show |
2 | a0001c0001t0002g0194 a0001c0001t0002g0195 |
2 | HG00741.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.389+4429_389+4453d others(27): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 123002586 | ||||||
| chr6:123002692 | A | G | 10 | a0001c0001t0002g0253 a0001c0001t0007g0009 a0001c0001t0007g0249 others(7): Show |
14 | HG01099.hp1 HG01515.hp2 NA18947.hp2 others(11): Show |
intron_variant | MODIFIER | c.389+4526A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123002692 | |||||||
| chr6:123002840 | C | T | 1 | a0001c0001t0002g0241 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.389+4674C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123002840 | |||||||
| chr6:123002851 | T | C | 260 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(257): Show |
288 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.389+4685T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123002851 | |||||||
| chr6:123002912 | G | C | 2 | a0001c0001t0028g0032 a0001c0001t0028g0033 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.389+4746G>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123002912 | |||||||
| chr6:123003168 | A | C | 1 | a0001c0001t0001g0090 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.389+5002A>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123003168 | |||||||
| chr6:123003405 | C | A | 1 | a0001c0001t0087g0148 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.389+5239C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123003405 | |||||||
| chr6:123003584 | A | T | 1 | a0001c0001t0006g0193 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.389+5418A>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123003584 | |||||||
| chr6:123003593 | T | TTTGG | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(236): Show |
263 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.389+5430_389+5431i others(6): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 123003593 | ||||||
| chr6:123003658 | G | T | 1 | a0001c0001t0084g0287 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.389+5492G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123003658 | |||||||
| chr6:123004070 | C | T | 1 | a0001c0001t0018g0007 | 3 | NA18950.hp1 NA18973.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.389+5904C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123004070 | |||||||
| chr6:123004640 | C | T | 1 | a0001c0001t0036g0089 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.390-6345C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123004640 | |||||||
| chr6:123004667 | C | G | 1 | a0001c0001t0002g0240 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.390-6318C>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123004667 | |||||||
| chr6:123004687 | T | G | 2 | a0001c0001t0038g0094 a0001c0001t0038g0095 |
2 | HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.390-6298T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123004687 | |||||||
| chr6:123004746 | C | G | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(138): Show |
158 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.390-6239C>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123004746 | |||||||
| chr6:123004892 | G | T | 10 | a0001c0001t0002g0253 a0001c0001t0007g0009 a0001c0001t0007g0249 others(7): Show |
14 | HG01099.hp1 HG01515.hp2 NA18947.hp2 others(11): Show |
intron_variant | MODIFIER | c.390-6093G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123004892 | |||||||
| chr6:123004934 | AAACAAAA others(9): Show |
A | 1 | a0001c0001t0082g0285 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.390-6048_390-6033d others(18): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 123004934 | ||||||
| chr6:123004950 | CA | C | 8 | a0001c0001t0025g0260 a0001c0001t0025g0263 a0001c0001t0025g0264 others(5): Show |
8 | HG01109.hp2 HG01167.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.390-6021delA | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 123004950 | ||||||
| chr6:123004950 | CAA | C | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(138): Show |
158 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.390-6022_390-6021d others(4): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 123004950 | ||||||
| chr6:123004950 | CAAA | C | 27 | a0001c0001t0002g0253 a0001c0001t0007g0009 a0001c0001t0007g0249 others(24): Show |
33 | HG00741.hp2 HG01099.hp1 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.390-6023_390-6021d others(5): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 123004950 | ||||||
| chr6:123004950 | CAAAA | C | 80 | a0001c0001t0002g0171 a0001c0001t0003g0014 a0001c0001t0003g0015 others(77): Show |
85 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.390-6024_390-6021d others(6): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 123004950 | ||||||
| chr6:123004952 | A | C | 1 | a0001c0001t0053g0088 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.390-6033A>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123004952 | |||||||
| chr6:123004954 | A | C | 2 | a0001c0001t0005g0276 a0001c0001t0082g0285 |
2 | HG02818.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.390-6031A>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123004954 | |||||||
| chr6:123004955 | A | C | 1 | a0001c0001t0023g0186 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.390-6030A>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123004955 | |||||||
| chr6:123004957 | A | C | 1 | a0001c0001t0005g0275 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.390-6028A>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123004957 | |||||||
| chr6:123004959 | A | C | 1 | a0001c0001t0002g0239 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.390-6026A>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123004959 | |||||||
| chr6:123004964 | A | C | 2 | a0001c0001t0001g0071 a0001c0001t0001g0080 |
2 | NA19007.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.390-6021A>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123004964 | |||||||
| chr6:123005113 | C | T | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(236): Show |
263 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.390-5872C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123005113 | |||||||
| chr6:123005130 | C | T | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(236): Show |
263 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.390-5855C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123005130 | |||||||
| chr6:123005422 | G | A | 4 | a0001c0001t0042g0284 a0001c0001t0082g0285 a0001c0001t0084g0287 others(1): Show |
4 | HG02559.hp2 HG02818.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.390-5563G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123005422 | |||||||
| chr6:123005577 | G | A | 5 | a0001c0001t0025g0260 a0001c0001t0025g0263 a0001c0001t0025g0264 others(2): Show |
5 | HG01109.hp2 HG01167.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.390-5408G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123005577 | |||||||
| chr6:123005611 | A | G | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(236): Show |
263 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.390-5374A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123005611 | |||||||
| chr6:123005921 | C | T | 1 | a0001c0001t0001g0040 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.390-5064C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123005921 | |||||||
| chr6:123005985 | C | T | 32 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(29): Show |
34 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.390-5000C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123005985 | |||||||
| chr6:123006068 | C | A | 5 | a0001c0001t0026g0150 a0001c0001t0026g0151 a0001c0001t0044g0018 others(2): Show |
6 | HG02257.hp1 HG02559.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.390-4917C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123006068 | |||||||
| chr6:123006110 | C | T | 1 | a0001c0001t0045g0177 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.390-4875C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123006110 | |||||||
| chr6:123006178 | G | A | 3 | a0001c0001t0016g0153 a0001c0001t0017g0154 a0001c0001t0071g0178 |
3 | HG02109.hp2 HG02970.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.390-4807G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123006178 | |||||||
| chr6:123006276 | G | C | 1 | a0001c0001t0006g0204 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.390-4709G>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123006276 | |||||||
| chr6:123006401 | C | A | 1 | a0001c0001t0004g0096 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.390-4584C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123006401 | |||||||
| chr6:123006537 | G | T | 11 | a0001c0001t0002g0253 a0001c0001t0007g0009 a0001c0001t0007g0249 others(8): Show |
15 | HG01099.hp1 HG01515.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.390-4448G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123006537 | |||||||
| chr6:123006555 | A | G | 238 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(235): Show |
262 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.390-4430A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123006555 | |||||||
| chr6:123006607 | G | T | 1 | a0001c0001t0006g0238 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.390-4378G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123006607 | |||||||
| chr6:123006659 | G | A | 1 | a0001c0001t0002g0205 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.390-4326G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123006659 | |||||||
| chr6:123006721 | G | C | 5 | a0001c0001t0026g0150 a0001c0001t0026g0151 a0001c0001t0044g0018 others(2): Show |
6 | HG02257.hp1 HG02559.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.390-4264G>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123006721 | |||||||
| chr6:123006808 | C | T | 2 | a0001c0001t0028g0032 a0001c0001t0028g0033 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.390-4177C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123006808 | |||||||
| chr6:123006910 | A | G | 1 | a0001c0001t0007g0256 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.390-4075A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123006910 | |||||||
| chr6:123006912 | G | A | 1 | a0001c0001t0003g0034 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.390-4073G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123006912 | |||||||
| chr6:123006922 | G | A | 7 | a0001c0001t0009g0022 a0001c0001t0009g0037 a0001c0001t0009g0181 others(4): Show |
8 | HG02083.hp1 HG02683.hp1 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.390-4063G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123006922 | |||||||
| chr6:123007001 | T | C | 2 | a0001c0001t0003g0014 a0001c0001t0003g0098 |
3 | HG01123.hp1 HG01168.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.390-3984T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123007001 | |||||||
| chr6:123007250 | G | A | 2 | a0001c0001t0002g0206 a0001c0001t0002g0207 |
2 | NA18969.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.390-3735G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123007250 | |||||||
| chr6:123007525 | A | G | 1 | a0001c0001t0006g0237 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.390-3460A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123007525 | |||||||
| chr6:123007546 | G | A | 2 | a0001c0001t0035g0265 a0001c0001t0035g0266 |
2 | HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.390-3439G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123007546 | |||||||
| chr6:123007993 | A | G | 1 | a0001c0001t0003g0146 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.390-2992A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123007993 | |||||||
| chr6:123008009 | A | C | 1 | a0001c0001t0002g0236 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.390-2976A>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123008009 | |||||||
| chr6:123008026 | T | G | 1 | a0001c0001t0006g0242 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.390-2959T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123008026 | |||||||
| chr6:123008110 | T | C | 1 | a0001c0001t0006g0208 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.390-2875T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123008110 | |||||||
| chr6:123008202 | C | T | 1 | a0001c0001t0042g0191 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.390-2783C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123008202 | |||||||
| chr6:123008214 | A | G | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(248): Show |
279 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.390-2771A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123008214 | |||||||
| chr6:123008307 | A | G | 2 | a0001c0001t0022g0144 a0001c0001t0022g0145 |
2 | HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.390-2678A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123008307 | |||||||
| chr6:123008377 | C | T | 2 | a0001c0001t0038g0094 a0001c0001t0038g0095 |
2 | HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.390-2608C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123008377 | |||||||
| chr6:123008558 | G | A | 10 | a0001c0001t0002g0253 a0001c0001t0007g0009 a0001c0001t0007g0249 others(7): Show |
14 | HG01099.hp1 HG01515.hp2 NA18947.hp2 others(11): Show |
intron_variant | MODIFIER | c.390-2427G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123008558 | |||||||
| chr6:123008563 | T | G | 1 | a0001c0001t0042g0191 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.390-2422T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123008563 | |||||||
| chr6:123008653 | C | A | 238 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(235): Show |
262 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.390-2332C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123008653 | |||||||
| chr6:123008685 | C | CT | 238 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(235): Show |
262 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.390-2289dupT | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 123008685 | ||||||
| chr6:123008838 | A | G | 2 | a0001c0001t0002g0171 a0001c0001t0017g0170 |
2 | HG03209.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.390-2147A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123008838 | |||||||
| chr6:123008886 | C | T | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(248): Show |
279 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.390-2099C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123008886 | |||||||
| chr6:123009281 | A | G | 10 | a0001c0001t0002g0253 a0001c0001t0007g0009 a0001c0001t0007g0249 others(7): Show |
14 | HG01099.hp1 HG01515.hp2 NA18947.hp2 others(11): Show |
intron_variant | MODIFIER | c.390-1704A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123009281 | |||||||
| chr6:123009355 | A | G | 2 | a0001c0001t0001g0039 a0001c0001t0001g0087 |
2 | HG02300.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.390-1630A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123009355 | |||||||
| chr6:123009523 | T | C | 1 | a0001c0001t0002g0209 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.390-1462T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123009523 | |||||||
| chr6:123009605 | C | A | 1 | a0001c0001t0002g0024 | 2 | HG00140.hp2 HG00280.hp1 |
intron_variant | MODIFIER | c.390-1380C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123009605 | |||||||
| chr6:123009727 | C | T | 241 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(238): Show |
265 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.390-1258C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123009727 | |||||||
| chr6:123010191 | C | A | 8 | a0001c0001t0016g0153 a0001c0001t0017g0099 a0001c0001t0017g0154 others(5): Show |
8 | HG02109.hp2 HG02809.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.390-794C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123010191 | |||||||
| chr6:123010336 | G | A | 2 | a0001c0002t0029g0041 a0001c0002t0029g0042 |
2 | HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.390-649G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123010336 | |||||||
| chr6:123010622 | C | T | 2 | a0001c0001t0028g0032 a0001c0001t0028g0033 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.390-363C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123010622 | |||||||
| chr6:123010670 | A | C | 1 | a0001c0001t0062g0143 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.390-315A>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123010670 | |||||||
| chr6:123010768 | G | A | 240 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(237): Show |
264 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.390-217G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123010768 | |||||||
| chr6:123010797 | T | TAAATTCG others(6): Show |
1 | a0001c0001t0071g0178 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.390-187_390-175dup others(13): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 123010797 | ||||||
| chr6:123010803 | C | T | 2 | a0001c0001t0001g0062 a0001c0001t0001g0063 |
2 | HG00099.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.390-182C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 2/5 | chr6 | 123010803 | |||||||
| chr6:123011706 | A | G | 1 | a0001c0001t0009g0185 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.564+547A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123011706 | |||||||
| chr6:123012080 | G | A | 8 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0008g0001 others(5): Show |
16 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.564+921G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123012080 | |||||||
| chr6:123012234 | C | A | 1 | a0001c0001t0004g0101 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.564+1075C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123012234 | |||||||
| chr6:123012442 | G | A | 4 | a0001c0001t0006g0008 a0001c0001t0006g0210 a0001c0001t0006g0211 others(1): Show |
6 | HG02074.hp1 NA18945.hp2 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.564+1283G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123012442 | |||||||
| chr6:123012485 | C | T | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(234): Show |
261 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.564+1326C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123012485 | |||||||
| chr6:123012649 | G | C | 2 | a0001c0001t0002g0213 a0001c0001t0002g0214 |
2 | HG02602.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.564+1490G>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123012649 | |||||||
| chr6:123012962 | T | G | 1 | a0001c0001t0071g0178 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.564+1803T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123012962 | |||||||
| chr6:123013092 | C | A | 4 | a0001c0001t0042g0284 a0001c0001t0082g0285 a0001c0001t0084g0287 others(1): Show |
4 | HG02559.hp2 HG02818.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.564+1933C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123013092 | |||||||
| chr6:123013130 | G | A | 1 | a0001c0001t0010g0158 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.564+1971G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123013130 | |||||||
| chr6:123013183 | C | T | 1 | a0001c0001t0011g0086 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.564+2024C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123013183 | |||||||
| chr6:123013191 | C | A | 1 | a0001c0001t0087g0148 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.564+2032C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123013191 | |||||||
| chr6:123013240 | T | A | 1 | a0001c0001t0042g0191 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.564+2081T>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123013240 | |||||||
| chr6:123013254 | A | C | 238 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(235): Show |
262 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.564+2095A>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123013254 | |||||||
| chr6:123013528 | A | C | 1 | a0001c0001t0067g0038 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.564+2369A>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123013528 | |||||||
| chr6:123013654 | AT | A | 10 | a0001c0001t0010g0019 a0001c0001t0010g0158 a0001c0001t0010g0164 others(7): Show |
11 | HG00741.hp2 HG01243.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.564+2502delT | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123013654 | ||||||
| chr6:123013683 | A | T | 2 | a0001c0001t0002g0206 a0001c0001t0002g0207 |
2 | NA18969.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.564+2524A>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123013683 | |||||||
| chr6:123013691 | G | T | 1 | a0001c0001t0007g0255 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.564+2532G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123013691 | |||||||
| chr6:123013723 | A | G | 1 | a0001c0001t0052g0147 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.564+2564A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123013723 | |||||||
| chr6:123013738 | T | C | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(248): Show |
279 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.564+2579T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123013738 | |||||||
| chr6:123013767 | G | C | 13 | a0001c0001t0006g0008 a0001c0001t0006g0025 a0001c0001t0006g0193 others(10): Show |
15 | HG01192.hp1 HG02074.hp1 HG02523.hp2 others(12): Show |
intron_variant | MODIFIER | c.564+2608G>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123013767 | |||||||
| chr6:123013817 | C | G | 1 | a0001c0002t0024g0259 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.564+2658C>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123013817 | |||||||
| chr6:123013817 | C | T | 4 | a0001c0001t0016g0027 a0001c0001t0016g0244 a0001c0001t0072g0245 others(1): Show |
5 | HG01884.hp2 HG02895.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.564+2658C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123013817 | |||||||
| chr6:123014040 | T | G | 238 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(235): Show |
262 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.564+2881T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123014040 | |||||||
| chr6:123014123 | C | T | 58 | a0001c0001t0001g0061 a0001c0001t0003g0014 a0001c0001t0003g0015 others(55): Show |
62 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.564+2964C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123014123 | |||||||
| chr6:123014318 | C | A | 1 | a0001c0004t0076g0192 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.564+3159C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123014318 | |||||||
| chr6:123014320 | C | T | 238 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(235): Show |
262 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.564+3161C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123014320 | |||||||
| chr6:123014335 | CT | C | 238 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(235): Show |
262 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.564+3185delT | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123014335 | ||||||
| chr6:123014549 | C | T | 1 | a0001c0001t0005g0275 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.564+3390C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123014549 | |||||||
| chr6:123014626 | G | A | 2 | a0001c0001t0028g0032 a0001c0001t0028g0033 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.564+3467G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123014626 | |||||||
| chr6:123014632 | A | G | 1 | a0001c0001t0063g0142 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.564+3473A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123014632 | |||||||
| chr6:123014887 | C | A | 2 | a0001c0001t0031g0187 a0001c0001t0031g0188 |
2 | NA18985.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.564+3728C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123014887 | |||||||
| chr6:123014994 | G | C | 238 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(235): Show |
262 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.564+3835G>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123014994 | |||||||
| chr6:123015027 | T | G | 1 | a0001c0001t0032g0283 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.564+3868T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123015027 | |||||||
| chr6:123015035 | AG | A | 238 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(235): Show |
262 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.564+3877delG | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123015035 | |||||||
| chr6:123015046 | T | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(137): Show |
157 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.564+3887T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123015046 | |||||||
| chr6:123015515 | C | T | 2 | a0001c0001t0028g0032 a0001c0001t0028g0033 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.564+4356C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123015515 | |||||||
| chr6:123015604 | C | A | 1 | a0001c0001t0079g0159 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.564+4445C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123015604 | |||||||
| chr6:123015710 | G | A | 2 | a0001c0001t0004g0102 a0001c0001t0004g0103 |
2 | HG00280.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.564+4551G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123015710 | |||||||
| chr6:123015848 | G | A | 1 | a0001c0001t0008g0043 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.564+4689G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123015848 | |||||||
| chr6:123015905 | G | C | 2 | a0001c0001t0031g0187 a0001c0001t0031g0188 |
2 | NA18985.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.564+4746G>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123015905 | |||||||
| chr6:123015996 | G | A | 1 | a0001c0001t0004g0104 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.564+4837G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123015996 | |||||||
| chr6:123016021 | C | CT | 76 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0011 others(73): Show |
93 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.564+4889dupT | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123016021 | ||||||
| chr6:123016021 | C | CTT | 76 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0049 others(73): Show |
83 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.564+4888_564+4889d others(4): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123016021 | ||||||
| chr6:123016021 | C | CTTT | 24 | a0001c0001t0001g0055 a0001c0001t0001g0090 a0001c0001t0002g0195 others(21): Show |
25 | HG00323.hp1 HG00438.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.564+4887_564+4889d others(5): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123016021 | ||||||
| chr6:123016021 | C | CTTTT | 6 | a0001c0001t0001g0060 a0001c0001t0002g0235 a0001c0001t0006g0204 others(3): Show |
6 | NA18953.hp2 NA18972.hp1 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.564+4886_564+4889d others(6): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123016021 | ||||||
| chr6:123016021 | CT | C | 14 | a0001c0001t0003g0020 a0001c0001t0003g0135 a0001c0001t0003g0136 others(11): Show |
15 | HG00735.hp1 HG00735.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.564+4889delT | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123016021 | ||||||
| chr6:123016021 | CTT | C | 56 | a0001c0001t0001g0061 a0001c0001t0003g0014 a0001c0001t0003g0015 others(53): Show |
61 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.564+4888_564+4889d others(4): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123016021 | ||||||
| chr6:123016021 | CTTT | C | 11 | a0001c0001t0003g0105 a0001c0001t0003g0146 a0001c0001t0004g0106 others(8): Show |
11 | HG01934.hp1 HG02647.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.564+4887_564+4889d others(5): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123016021 | ||||||
| chr6:123016021 | CTTTTT | C | 10 | a0001c0001t0002g0253 a0001c0001t0007g0009 a0001c0001t0007g0249 others(7): Show |
14 | HG01099.hp1 HG01515.hp2 NA18947.hp2 others(11): Show |
intron_variant | MODIFIER | c.564+4885_564+4889d others(7): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123016021 | ||||||
| chr6:123016113 | G | A | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(120): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.564+4954G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123016113 | |||||||
| chr6:123016152 | C | A | 4 | a0001c0001t0042g0284 a0001c0001t0082g0285 a0001c0001t0084g0287 others(1): Show |
4 | HG02559.hp2 HG02818.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.564+4993C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123016152 | |||||||
| chr6:123016158 | A | G | 2 | a0001c0001t0038g0094 a0001c0001t0038g0095 |
2 | HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.564+4999A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123016158 | |||||||
| chr6:123016237 | C | T | 1 | a0001c0002t0029g0042 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.564+5078C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123016237 | |||||||
| chr6:123016339 | T | TG | 9 | a0001c0001t0002g0205 a0001c0001t0026g0150 a0001c0001t0026g0151 others(6): Show |
10 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.564+5187dupG | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123016339 | ||||||
| chr6:123016339 | T | TGG | 221 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(218): Show |
248 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.564+5186_564+5187d others(4): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123016339 | ||||||
| chr6:123016339 | T | TTG | 5 | a0001c0001t0042g0284 a0001c0001t0045g0177 a0001c0001t0082g0285 others(2): Show |
5 | HG02559.hp2 HG02818.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.564+5180_564+5181i others(4): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123016339 | |||||||
| chr6:123016340 | G | A | 2 | a0001c0001t0084g0287 a0001c0001t0090g0286 |
2 | HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.564+5181G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123016340 | |||||||
| chr6:123016340 | G | T | 1 | a0001c0001t0042g0191 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.564+5181G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123016340 | |||||||
| chr6:123016453 | T | A | 1 | a0001c0001t0073g0246 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.564+5294T>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123016453 | |||||||
| chr6:123016625 | G | C | 1 | a0001c0001t0023g0097 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.564+5466G>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123016625 | |||||||
| chr6:123016653 | C | T | 2 | a0001c0001t0002g0206 a0001c0001t0002g0207 |
2 | NA18969.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.564+5494C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123016653 | |||||||
| chr6:123016669 | A | C | 5 | a0001c0001t0002g0171 a0001c0001t0026g0093 a0001c0001t0027g0161 others(2): Show |
5 | HG00735.hp1 HG01106.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.564+5510A>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123016669 | |||||||
| chr6:123017088 | A | ATG | 13 | a0001c0001t0002g0171 a0001c0001t0002g0253 a0001c0001t0005g0029 others(10): Show |
18 | HG01099.hp1 HG02896.hp2 HG02897.hp2 others(15): Show |
intron_variant | MODIFIER | c.564+5956_564+5957d others(4): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123017088 | ||||||
| chr6:123017088 | ATG | A | 94 | a0001c0001t0001g0061 a0001c0001t0003g0014 a0001c0001t0003g0015 others(91): Show |
100 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.564+5956_564+5957d others(4): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123017088 | ||||||
| chr6:123017088 | ATGTG | A | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(135): Show |
156 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.564+5954_564+5957d others(6): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123017088 | ||||||
| chr6:123017133 | G | A | 1 | a0001c0001t0004g0101 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.564+5974G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123017133 | |||||||
| chr6:123017147 | G | T | 1 | a0001c0001t0053g0088 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.564+5988G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123017147 | |||||||
| chr6:123017208 | T | C | 1 | a0001c0001t0026g0093 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.564+6049T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123017208 | |||||||
| chr6:123017228 | T | C | 5 | a0001c0001t0002g0171 a0001c0001t0026g0093 a0001c0001t0027g0161 others(2): Show |
5 | HG00735.hp1 HG01106.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.564+6069T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123017228 | |||||||
| chr6:123017354 | C | G | 5 | a0001c0001t0002g0171 a0001c0001t0026g0093 a0001c0001t0027g0161 others(2): Show |
5 | HG00735.hp1 HG01106.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.564+6195C>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123017354 | |||||||
| chr6:123017369 | T | C | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(128): Show |
147 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.564+6210T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123017369 | |||||||
| chr6:123017788 | T | C | 1 | a0001c0001t0042g0191 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.564+6629T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123017788 | |||||||
| chr6:123017920 | T | G | 15 | a0001c0001t0002g0171 a0001c0001t0002g0253 a0001c0001t0007g0009 others(12): Show |
19 | HG00735.hp1 HG01099.hp1 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.564+6761T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123017920 | |||||||
| chr6:123017945 | T | A | 1 | a0001c0001t0060g0247 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.564+6786T>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123017945 | |||||||
| chr6:123018118 | T | C | 2 | a0001c0001t0038g0094 a0001c0001t0038g0095 |
2 | HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.564+6959T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123018118 | |||||||
| chr6:123018262 | G | T | 2 | a0001c0001t0001g0078 a0001c0001t0011g0077 |
2 | HG00408.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.564+7103G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123018262 | |||||||
| chr6:123018273 | G | C | 1 | a0001c0001t0010g0168 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.564+7114G>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123018273 | |||||||
| chr6:123018276 | T | A | 1 | a0001c0001t0042g0191 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.564+7117T>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123018276 | |||||||
| chr6:123018384 | G | A | 4 | a0001c0001t0042g0284 a0001c0001t0082g0285 a0001c0001t0084g0287 others(1): Show |
4 | HG02559.hp2 HG02818.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.564+7225G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123018384 | |||||||
| chr6:123018465 | A | G | 94 | a0001c0001t0001g0061 a0001c0001t0003g0014 a0001c0001t0003g0015 others(91): Show |
101 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.564+7306A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123018465 | |||||||
| chr6:123018469 | C | T | 94 | a0001c0001t0001g0061 a0001c0001t0003g0014 a0001c0001t0003g0015 others(91): Show |
101 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.564+7310C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123018469 | |||||||
| chr6:123018668 | C | CT | 35 | a0001c0001t0005g0003 a0001c0001t0005g0004 a0001c0001t0005g0005 others(32): Show |
43 | HG00099.hp2 HG00323.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.564+7526dupT | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123018668 | ||||||
| chr6:123018668 | CT | C | 94 | a0001c0001t0001g0061 a0001c0001t0002g0171 a0001c0001t0003g0014 others(91): Show |
102 | HG00140.hp1 HG00280.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.564+7526delT | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123018668 | ||||||
| chr6:123018668 | CTT | C | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(138): Show |
157 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.564+7525_564+7526d others(4): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123018668 | ||||||
| chr6:123018684 | T | A | 15 | a0001c0001t0002g0171 a0001c0001t0002g0206 a0001c0001t0002g0219 others(12): Show |
19 | HG01099.hp1 HG01515.hp2 HG03209.hp2 others(16): Show |
intron_variant | MODIFIER | c.564+7525T>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123018684 | |||||||
| chr6:123018685 | T | A | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(215): Show |
245 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.564+7526T>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123018685 | |||||||
| chr6:123019203 | G | A | 2 | a0001c0001t0036g0089 a0001c0001t0036g0108 |
2 | HG02698.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.564+8044G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123019203 | |||||||
| chr6:123019212 | A | G | 297 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(294): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.564+8053A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123019212 | |||||||
| chr6:123019531 | T | G | 1 | a0001c0001t0035g0265 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.564+8372T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123019531 | |||||||
| chr6:123019688 | G | A | 2 | a0001c0001t0028g0032 a0001c0001t0028g0033 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.564+8529G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123019688 | |||||||
| chr6:123019733 | G | C | 2 | a0001c0001t0022g0144 a0001c0001t0022g0145 |
2 | HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.564+8574G>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123019733 | |||||||
| chr6:123019969 | CT | C | 292 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(289): Show |
328 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.564+8820delT | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123019969 | ||||||
| chr6:123020247 | AT | A | 4 | a0001c0001t0003g0105 a0001c0001t0003g0109 a0001c0001t0003g0135 others(1): Show |
4 | NA18961.hp1 NA18977.hp1 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.564+9090delT | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123020247 | ||||||
| chr6:123020361 | C | A | 2 | a0001c0001t0036g0089 a0001c0001t0036g0108 |
2 | HG02698.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.564+9202C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123020361 | |||||||
| chr6:123020375 | T | A | 2 | a0001c0001t0028g0032 a0001c0001t0028g0033 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.564+9216T>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123020375 | |||||||
| chr6:123020547 | A | G | 2 | a0001c0001t0028g0032 a0001c0001t0028g0033 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.564+9388A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123020547 | |||||||
| chr6:123020558 | C | A | 1 | a0001c0001t0001g0079 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.564+9399C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123020558 | |||||||
| chr6:123020860 | T | G | 1 | a0001c0001t0042g0191 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.564+9701T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123020860 | |||||||
| chr6:123020946 | G | A | 1 | a0001c0001t0005g0270 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.564+9787G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123020946 | |||||||
| chr6:123021051 | T | TG | 98 | a0001c0001t0001g0061 a0001c0001t0002g0253 a0001c0001t0003g0014 others(95): Show |
109 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.564+9900dupG | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123021051 | ||||||
| chr6:123021060 | T | G | 96 | a0001c0001t0001g0061 a0001c0001t0003g0014 a0001c0001t0003g0015 others(93): Show |
103 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.564+9901T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123021060 | |||||||
| chr6:123021061 | A | G | 3 | a0001c0001t0004g0134 a0001c0001t0022g0144 a0001c0001t0022g0145 |
3 | HG03130.hp1 HG03471.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.564+9902A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123021061 | |||||||
| chr6:123021550 | G | A | 4 | a0001c0001t0016g0027 a0001c0001t0016g0244 a0001c0001t0072g0245 others(1): Show |
5 | HG01884.hp2 HG02895.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.564+10391G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123021550 | |||||||
| chr6:123021569 | T | C | 15 | a0001c0001t0002g0171 a0001c0001t0002g0253 a0001c0001t0007g0009 others(12): Show |
19 | HG00735.hp1 HG01099.hp1 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.564+10410T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123021569 | |||||||
| chr6:123021591 | G | A | 249 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(246): Show |
277 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.564+10432G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123021591 | |||||||
| chr6:123021729 | C | T | 1 | a0001c0001t0027g0163 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.564+10570C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123021729 | |||||||
| chr6:123021848 | A | AT | 5 | a0001c0001t0026g0150 a0001c0001t0026g0151 a0001c0001t0044g0018 others(2): Show |
6 | HG02257.hp1 HG02559.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.564+10698dupT | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123021848 | ||||||
| chr6:123021891 | C | A | 2 | a0001c0001t0006g0216 a0001c0001t0006g0238 |
2 | NA18995.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.564+10732C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123021891 | |||||||
| chr6:123022052 | T | G | 2 | a0001c0001t0028g0032 a0001c0001t0028g0033 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.564+10893T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123022052 | |||||||
| chr6:123022053 | G | A | 2 | a0001c0001t0001g0066 a0001c0001t0001g0068 |
2 | HG01433.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.564+10894G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123022053 | |||||||
| chr6:123022121 | C | T | 3 | a0001c0001t0016g0027 a0001c0001t0016g0244 a0001c0001t0072g0245 |
4 | HG01884.hp2 HG02895.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.564+10962C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123022121 | |||||||
| chr6:123022203 | C | T | 2 | a0001c0001t0022g0144 a0001c0001t0022g0145 |
2 | HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.564+11044C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123022203 | |||||||
| chr6:123022316 | C | T | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(248): Show |
279 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.564+11157C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123022316 | |||||||
| chr6:123022458 | G | C | 2 | a0001c0001t0028g0032 a0001c0001t0028g0033 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.564+11299G>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123022458 | |||||||
| chr6:123022607 | C | T | 1 | a0001c0001t0017g0170 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.564+11448C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123022607 | |||||||
| chr6:123022845 | A | G | 249 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(246): Show |
277 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.564+11686A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123022845 | |||||||
| chr6:123022861 | C | T | 1 | a0001c0001t0004g0133 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.564+11702C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123022861 | |||||||
| chr6:123022949 | G | A | 96 | a0001c0001t0001g0061 a0001c0001t0003g0014 a0001c0001t0003g0015 others(93): Show |
103 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.564+11790G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123022949 | |||||||
| chr6:123023124 | C | T | 249 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(246): Show |
277 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.564+11965C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123023124 | |||||||
| chr6:123023254 | G | C | 1 | a0001c0001t0002g0218 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.564+12095G>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123023254 | |||||||
| chr6:123023374 | T | C | 1 | a0001c0001t0002g0226 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.564+12215T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123023374 | |||||||
| chr6:123023526 | A | T | 1 | a0001c0001t0009g0183 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.564+12367A>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123023526 | |||||||
| chr6:123023647 | C | T | 249 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(246): Show |
277 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.564+12488C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123023647 | |||||||
| chr6:123023850 | C | A | 1 | a0001c0001t0037g0126 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.564+12691C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123023850 | |||||||
| chr6:123023875 | C | A | 5 | a0001c0001t0002g0171 a0001c0001t0026g0093 a0001c0001t0027g0161 others(2): Show |
5 | HG00735.hp1 HG01106.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.564+12716C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123023875 | |||||||
| chr6:123023909 | TAC | T | 10 | a0001c0001t0002g0253 a0001c0001t0007g0009 a0001c0001t0007g0249 others(7): Show |
14 | HG01099.hp1 HG01515.hp2 NA18947.hp2 others(11): Show |
intron_variant | MODIFIER | c.564+12752_564+1275 others(6): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123023909 | ||||||
| chr6:123023945 | A | G | 1 | a0001c0001t0003g0124 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.564+12786A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123023945 | |||||||
| chr6:123024034 | C | G | 1 | a0001c0001t0080g0200 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.564+12875C>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123024034 | |||||||
| chr6:123024083 | C | G | 4 | a0001c0001t0002g0199 a0001c0001t0002g0203 a0001c0001t0039g0232 others(1): Show |
4 | HG00438.hp1 HG02074.hp2 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.564+12924C>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123024083 | |||||||
| chr6:123024216 | C | T | 10 | a0001c0001t0002g0253 a0001c0001t0007g0009 a0001c0001t0007g0249 others(7): Show |
14 | HG01099.hp1 HG01515.hp2 NA18947.hp2 others(11): Show |
intron_variant | MODIFIER | c.564+13057C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123024216 | |||||||
| chr6:123024235 | A | G | 1 | a0001c0001t0087g0148 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.564+13076A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123024235 | |||||||
| chr6:123024450 | A | G | 4 | a0001c0001t0016g0027 a0001c0001t0016g0244 a0001c0001t0072g0245 others(1): Show |
5 | HG01884.hp2 HG02895.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.564+13291A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123024450 | |||||||
| chr6:123024766 | A | G | 1 | a0001c0001t0042g0284 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.564+13607A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123024766 | |||||||
| chr6:123024832 | G | A | 2 | a0001c0001t0028g0032 a0001c0001t0028g0033 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.564+13673G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123024832 | |||||||
| chr6:123024870 | C | T | 1 | a0001c0001t0087g0148 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.564+13711C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123024870 | |||||||
| chr6:123024958 | T | G | 2 | a0001c0001t0028g0032 a0001c0001t0028g0033 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.564+13799T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123024958 | |||||||
| chr6:123024968 | C | A | 249 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(246): Show |
277 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.564+13809C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123024968 | |||||||
| chr6:123024971 | C | T | 249 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(246): Show |
277 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.564+13812C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123024971 | |||||||
| chr6:123025217 | G | T | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(120): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.564+14058G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123025217 | |||||||
| chr6:123025538 | G | A | 1 | a0001c0001t0005g0275 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.564+14379G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123025538 | |||||||
| chr6:123025627 | C | G | 6 | a0001c0001t0038g0094 a0001c0001t0038g0095 a0001c0001t0042g0284 others(3): Show |
6 | HG02559.hp2 HG02818.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.564+14468C>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123025627 | |||||||
| chr6:123025774 | C | T | 59 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(56): Show |
63 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.564+14615C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123025774 | |||||||
| chr6:123025777 | C | G | 96 | a0001c0001t0001g0061 a0001c0001t0003g0014 a0001c0001t0003g0015 others(93): Show |
103 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.564+14618C>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123025777 | |||||||
| chr6:123026055 | A | T | 249 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(246): Show |
277 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.564+14896A>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123026055 | |||||||
| chr6:123026056 | A | G | 1 | a0001c0001t0004g0140 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.564+14897A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123026056 | |||||||
| chr6:123026125 | A | C | 1 | a0001c0001t0014g0198 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.564+14966A>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123026125 | |||||||
| chr6:123026421 | T | G | 1 | a0001c0001t0010g0168 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.564+15262T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123026421 | |||||||
| chr6:123026513 | G | A | 2 | a0001c0001t0028g0032 a0001c0001t0028g0033 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.564+15354G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123026513 | |||||||
| chr6:123026817 | T | C | 9 | a0001c0001t0016g0153 a0001c0001t0017g0099 a0001c0001t0017g0154 others(6): Show |
9 | HG02109.hp2 HG02809.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.564+15658T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123026817 | |||||||
| chr6:123027002 | T | C | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(230): Show |
257 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.564+15843T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123027002 | |||||||
| chr6:123027016 | C | T | 1 | a0001c0001t0042g0191 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.564+15857C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123027016 | |||||||
| chr6:123027077 | T | G | 1 | a0001c0001t0045g0172 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.564+15918T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123027077 | |||||||
| chr6:123027132 | A | G | 2 | a0001c0001t0030g0010 a0001c0001t0053g0088 |
3 | HG01070.hp2 HG01071.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.564+15973A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123027132 | |||||||
| chr6:123027199 | A | G | 2 | a0001c0001t0003g0122 a0001c0001t0003g0123 |
2 | HG02055.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.564+16040A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123027199 | |||||||
| chr6:123027434 | G | A | 6 | a0001c0001t0038g0094 a0001c0001t0038g0095 a0001c0001t0042g0284 others(3): Show |
6 | HG02559.hp2 HG02818.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.564+16275G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123027434 | |||||||
| chr6:123027913 | A | G | 1 | a0001c0001t0008g0045 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.564+16754A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123027913 | |||||||
| chr6:123028243 | T | TA | 255 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(252): Show |
283 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.564+17086dupA | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123028243 | ||||||
| chr6:123028365 | G | T | 2 | a0001c0001t0028g0032 a0001c0001t0028g0033 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.564+17206G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123028365 | |||||||
| chr6:123028419 | G | A | 1 | a0001c0001t0048g0137 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.564+17260G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123028419 | |||||||
| chr6:123028422 | G | C | 1 | a0001c0001t0087g0148 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.564+17263G>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123028422 | |||||||
| chr6:123028458 | G | A | 6 | a0001c0001t0014g0196 a0001c0001t0014g0198 a0001c0001t0014g0201 others(3): Show |
6 | NA18942.hp2 NA18951.hp2 NA18956.hp1 others(3): Show |
intron_variant | MODIFIER | c.564+17299G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123028458 | |||||||
| chr6:123028694 | T | A | 1 | a0001c0001t0001g0052 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.564+17535T>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123028694 | |||||||
| chr6:123029233 | G | A | 1 | a0001c0001t0002g0220 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.564+18074G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123029233 | |||||||
| chr6:123029306 | G | A | 2 | a0001c0001t0028g0032 a0001c0001t0028g0033 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.564+18147G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123029306 | |||||||
| chr6:123029375 | T | A | 2 | a0001c0001t0028g0032 a0001c0001t0028g0033 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.564+18216T>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123029375 | |||||||
| chr6:123029413 | T | C | 4 | a0001c0001t0042g0284 a0001c0001t0082g0285 a0001c0001t0084g0287 others(1): Show |
4 | HG02559.hp2 HG02818.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.564+18254T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123029413 | |||||||
| chr6:123029459 | T | C | 5 | a0001c0001t0026g0150 a0001c0001t0026g0151 a0001c0001t0044g0018 others(2): Show |
6 | HG02257.hp1 HG02559.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.564+18300T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123029459 | |||||||
| chr6:123029545 | C | T | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(249): Show |
280 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.564+18386C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123029545 | |||||||
| chr6:123029590 | G | A | 2 | a0001c0001t0028g0032 a0001c0001t0028g0033 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.564+18431G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123029590 | |||||||
| chr6:123029984 | C | T | 1 | a0001c0001t0056g0048 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.565-18638C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123029984 | |||||||
| chr6:123029989 | A | C | 1 | a0001c0001t0087g0148 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.565-18633A>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123029989 | |||||||
| chr6:123030053 | G | A | 5 | a0001c0001t0002g0171 a0001c0001t0026g0093 a0001c0001t0027g0161 others(2): Show |
5 | HG00735.hp1 HG01106.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.565-18569G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123030053 | |||||||
| chr6:123030144 | A | G | 15 | a0001c0001t0002g0171 a0001c0001t0002g0253 a0001c0001t0007g0009 others(12): Show |
19 | HG00735.hp1 HG01099.hp1 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.565-18478A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123030144 | |||||||
| chr6:123030151 | A | T | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(249): Show |
280 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.565-18471A>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123030151 | |||||||
| chr6:123030585 | C | A | 1 | a0001c0001t0003g0111 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.565-18037C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123030585 | |||||||
| chr6:123030818 | A | AAT | 15 | a0001c0001t0002g0171 a0001c0001t0002g0253 a0001c0001t0007g0009 others(12): Show |
19 | HG00735.hp1 HG01099.hp1 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.565-17788_565-1778 others(6): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123030818 | ||||||
| chr6:123030837 | A | AAT | 95 | a0001c0001t0001g0061 a0001c0001t0003g0014 a0001c0001t0003g0015 others(92): Show |
102 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.565-17773_565-1777 others(6): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123030837 | ||||||
| chr6:123030837 | A | T | 1 | a0001c0001t0082g0285 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.565-17785A>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123030837 | |||||||
| chr6:123030968 | T | C | 7 | a0001c0001t0015g0173 a0001c0001t0015g0174 a0001c0001t0015g0175 others(4): Show |
7 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.565-17654T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123030968 | |||||||
| chr6:123030982 | G | A | 2 | a0001c0001t0038g0094 a0001c0001t0038g0095 |
2 | HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.565-17640G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123030982 | |||||||
| chr6:123031056 | C | T | 1 | a0001c0001t0003g0016 | 2 | HG01175.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.565-17566C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123031056 | |||||||
| chr6:123031104 | T | A | 15 | a0001c0001t0002g0171 a0001c0001t0002g0253 a0001c0001t0007g0009 others(12): Show |
19 | HG00735.hp1 HG01099.hp1 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.565-17518T>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123031104 | |||||||
| chr6:123031139 | T | G | 1 | a0001c0001t0004g0130 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.565-17483T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123031139 | |||||||
| chr6:123031255 | G | A | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(109): Show |
128 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.565-17367G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123031255 | |||||||
| chr6:123031326 | G | A | 10 | a0001c0001t0010g0019 a0001c0001t0010g0158 a0001c0001t0010g0164 others(7): Show |
11 | HG00741.hp2 HG01243.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.565-17296G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123031326 | |||||||
| chr6:123031393 | C | G | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(247): Show |
278 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.565-17229C>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123031393 | |||||||
| chr6:123031447 | G | A | 1 | a0001c0001t0026g0150 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.565-17175G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123031447 | |||||||
| chr6:123031507 | T | C | 1 | a0001c0001t0004g0101 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.565-17115T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123031507 | |||||||
| chr6:123031652 | T | C | 2 | a0001c0001t0011g0069 a0001c0001t0011g0086 |
2 | NA18977.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.565-16970T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123031652 | |||||||
| chr6:123031709 | C | T | 1 | a0001c0001t0002g0225 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.565-16913C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123031709 | |||||||
| chr6:123031715 | C | A | 1 | a0001c0004t0076g0192 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.565-16907C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123031715 | |||||||
| chr6:123031832 | G | A | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(247): Show |
278 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.565-16790G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123031832 | |||||||
| chr6:123031957 | G | C | 2 | a0001c0001t0028g0032 a0001c0001t0028g0033 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.565-16665G>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123031957 | |||||||
| chr6:123031979 | T | G | 1 | a0001c0001t0001g0091 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.565-16643T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123031979 | |||||||
| chr6:123032202 | C | T | 1 | a0001c0001t0002g0231 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.565-16420C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123032202 | |||||||
| chr6:123032248 | A | T | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(137): Show |
157 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.565-16374A>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123032248 | |||||||
| chr6:123032262 | G | A | 1 | a0001c0001t0070g0050 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.565-16360G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123032262 | |||||||
| chr6:123032306 | A | C | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(247): Show |
278 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.565-16316A>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123032306 | |||||||
| chr6:123032360 | T | A | 2 | a0001c0001t0028g0032 a0001c0001t0028g0033 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.565-16262T>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123032360 | |||||||
| chr6:123032630 | T | C | 1 | a0001c0001t0005g0268 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.565-15992T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123032630 | |||||||
| chr6:123032778 | C | T | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(231): Show |
258 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.565-15844C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123032778 | |||||||
| chr6:123032841 | C | T | 2 | a0001c0001t0028g0032 a0001c0001t0028g0033 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.565-15781C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123032841 | |||||||
| chr6:123032873 | G | A | 1 | a0001c0001t0081g0035 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.565-15749G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123032873 | |||||||
| chr6:123032916 | A | T | 13 | a0001c0001t0010g0019 a0001c0001t0010g0158 a0001c0001t0010g0164 others(10): Show |
14 | HG00741.hp2 HG01243.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.565-15706A>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123032916 | |||||||
| chr6:123032937 | T | A | 1 | a0001c0001t0001g0011 | 2 | NA18988.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.565-15685T>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123032937 | |||||||
| chr6:123033391 | C | T | 93 | a0001c0001t0001g0061 a0001c0001t0003g0014 a0001c0001t0003g0015 others(90): Show |
99 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.565-15231C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123033391 | |||||||
| chr6:123033561 | T | G | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(231): Show |
258 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.565-15061T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123033561 | |||||||
| chr6:123033645 | A | G | 2 | a0001c0001t0028g0032 a0001c0001t0028g0033 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.565-14977A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123033645 | |||||||
| chr6:123033703 | T | A | 1 | a0001c0001t0042g0191 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.565-14919T>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123033703 | |||||||
| chr6:123033873 | A | G | 2 | a0001c0001t0004g0106 a0001c0001t0004g0107 |
2 | NA18995.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.565-14749A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123033873 | |||||||
| chr6:123033909 | G | A | 2 | a0001c0001t0028g0032 a0001c0001t0028g0033 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.565-14713G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123033909 | |||||||
| chr6:123034217 | C | T | 4 | a0001c0001t0016g0027 a0001c0001t0016g0244 a0001c0001t0072g0245 others(1): Show |
5 | HG01884.hp2 HG02895.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.565-14405C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123034217 | |||||||
| chr6:123034321 | T | C | 1 | a0001c0001t0035g0266 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.565-14301T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123034321 | |||||||
| chr6:123034358 | A | G | 1 | a0001c0001t0035g0266 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.565-14264A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123034358 | |||||||
| chr6:123034391 | T | C | 1 | a0001c0001t0074g0112 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.565-14231T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123034391 | |||||||
| chr6:123034408 | C | T | 5 | a0001c0001t0025g0260 a0001c0001t0025g0263 a0001c0001t0025g0264 others(2): Show |
5 | HG01109.hp2 HG01167.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.565-14214C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123034408 | |||||||
| chr6:123034672 | T | C | 1 | a0001c0001t0002g0171 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.565-13950T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123034672 | |||||||
| chr6:123034752 | C | T | 2 | a0001c0001t0003g0111 a0001c0001t0063g0142 |
2 | HG01255.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.565-13870C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123034752 | |||||||
| chr6:123034965 | A | G | 1 | a0001c0001t0005g0280 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.565-13657A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123034965 | |||||||
| chr6:123035124 | T | C | 2 | a0001c0001t0028g0032 a0001c0001t0028g0033 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.565-13498T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123035124 | |||||||
| chr6:123035235 | G | A | 235 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(232): Show |
259 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.565-13387G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123035235 | |||||||
| chr6:123035335 | C | T | 2 | a0001c0001t0028g0032 a0001c0001t0028g0033 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.565-13287C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123035335 | |||||||
| chr6:123035347 | C | A | 1 | a0001c0001t0002g0171 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.565-13275C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123035347 | |||||||
| chr6:123035441 | G | A | 1 | a0001c0001t0002g0024 | 2 | HG00140.hp2 HG00280.hp1 |
intron_variant | MODIFIER | c.565-13181G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123035441 | |||||||
| chr6:123035902 | C | G | 2 | a0001c0001t0028g0032 a0001c0001t0028g0033 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.565-12720C>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123035902 | |||||||
| chr6:123035903 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.565-12719A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123035903 | |||||||
| chr6:123035980 | G | A | 4 | a0001c0001t0016g0027 a0001c0001t0016g0244 a0001c0001t0072g0245 others(1): Show |
5 | HG01884.hp2 HG02895.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.565-12642G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123035980 | |||||||
| chr6:123036292 | A | C | 4 | a0001c0001t0042g0284 a0001c0001t0082g0285 a0001c0001t0084g0287 others(1): Show |
4 | HG02559.hp2 HG02818.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.565-12330A>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123036292 | |||||||
| chr6:123036570 | CT | C | 8 | a0001c0001t0002g0253 a0001c0001t0007g0009 a0001c0001t0007g0249 others(5): Show |
12 | NA18947.hp2 NA18948.hp1 NA18950.hp1 others(9): Show |
intron_variant | MODIFIER | c.565-12051delT | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123036570 | |||||||
| chr6:123036647 | G | A | 7 | a0001c0001t0009g0022 a0001c0001t0009g0037 a0001c0001t0009g0181 others(4): Show |
8 | HG02083.hp1 HG02683.hp1 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.565-11975G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123036647 | |||||||
| chr6:123036652 | A | G | 1 | a0001c0001t0042g0191 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.565-11970A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123036652 | |||||||
| chr6:123036778 | G | T | 2 | a0001c0001t0025g0260 a0001c0001t0025g0263 |
2 | HG01167.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.565-11844G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123036778 | |||||||
| chr6:123036866 | G | A | 2 | a0001c0001t0004g0106 a0001c0001t0004g0107 |
2 | NA18995.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.565-11756G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123036866 | |||||||
| chr6:123037104 | C | T | 4 | a0001c0001t0042g0284 a0001c0001t0082g0285 a0001c0001t0084g0287 others(1): Show |
4 | HG02559.hp2 HG02818.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.565-11518C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123037104 | |||||||
| chr6:123037235 | G | C | 1 | a0001c0001t0027g0161 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.565-11387G>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123037235 | |||||||
| chr6:123037438 | A | G | 2 | a0001c0001t0002g0205 a0001c0001t0002g0228 |
2 | HG00323.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.565-11184A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123037438 | |||||||
| chr6:123038357 | G | C | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(249): Show |
280 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.565-10265G>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123038357 | |||||||
| chr6:123038490 | G | T | 1 | a0001c0001t0042g0191 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.565-10132G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123038490 | |||||||
| chr6:123038662 | A | G | 1 | a0001c0001t0005g0248 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.565-9960A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123038662 | |||||||
| chr6:123038670 | C | G | 1 | a0001c0001t0011g0069 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.565-9952C>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123038670 | |||||||
| chr6:123038914 | G | A | 1 | a0001c0001t0002g0221 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.565-9708G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123038914 | |||||||
| chr6:123038991 | T | C | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(120): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.565-9631T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123038991 | |||||||
| chr6:123039015 | C | A | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(137): Show |
157 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.565-9607C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123039015 | |||||||
| chr6:123039305 | C | A | 1 | a0001c0001t0007g0252 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.565-9317C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123039305 | |||||||
| chr6:123039890 | C | T | 2 | a0001c0001t0028g0032 a0001c0001t0028g0033 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.565-8732C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123039890 | |||||||
| chr6:123039921 | G | A | 1 | a0001c0001t0003g0110 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.565-8701G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123039921 | |||||||
| chr6:123039952 | T | C | 2 | a0001c0001t0011g0064 a0001c0001t0011g0070 |
2 | NA18962.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.565-8670T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123039952 | |||||||
| chr6:123040060 | G | T | 2 | a0001c0001t0003g0120 a0001c0001t0003g0121 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.565-8562G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123040060 | |||||||
| chr6:123040092 | G | A | 10 | a0001c0001t0010g0019 a0001c0001t0010g0158 a0001c0001t0010g0164 others(7): Show |
11 | HG00741.hp2 HG01243.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.565-8530G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123040092 | |||||||
| chr6:123040160 | G | T | 59 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(56): Show |
63 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.565-8462G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123040160 | |||||||
| chr6:123040174 | T | C | 1 | a0001c0001t0012g0058 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.565-8448T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123040174 | |||||||
| chr6:123040234 | G | A | 1 | a0001c0001t0009g0037 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.565-8388G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123040234 | |||||||
| chr6:123040603 | G | A | 1 | a0001c0001t0043g0234 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.565-8019G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123040603 | |||||||
| chr6:123040693 | G | A | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(120): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.565-7929G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123040693 | |||||||
| chr6:123040717 | G | A | 1 | a0001c0001t0004g0104 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.565-7905G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123040717 | |||||||
| chr6:123040769 | A | AAAAAG | 18 | a0001c0001t0001g0075 a0001c0001t0003g0113 a0001c0001t0006g0193 others(15): Show |
18 | HG00140.hp1 HG00735.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.565-7820_565-7816d others(7): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123040769 | ||||||
| chr6:123040769 | A | AAAAAGAA others(3): Show |
22 | a0001c0001t0001g0011 a0001c0001t0001g0074 a0001c0001t0002g0171 others(19): Show |
25 | HG00609.hp1 HG00733.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.565-7825_565-7816d others(12): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123040769 | ||||||
| chr6:123040769 | A | AAAAAGAA others(8): Show |
88 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(85): Show |
101 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.565-7830_565-7816d others(17): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123040769 | ||||||
| chr6:123040769 | A | AAAAAGAA others(13): Show |
15 | a0001c0001t0001g0040 a0001c0001t0001g0055 a0001c0001t0001g0062 others(12): Show |
16 | HG00099.hp1 HG00673.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.565-7835_565-7816d others(22): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123040769 | ||||||
| chr6:123040769 | A | AAAAAGAA others(18): Show |
2 | a0001c0001t0002g0195 a0001c0001t0012g0056 |
2 | HG00741.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.565-7840_565-7816d others(27): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123040769 | ||||||
| chr6:123040769 | A | AAAAAGAA others(23): Show |
7 | a0001c0001t0001g0084 a0001c0001t0002g0229 a0001c0001t0012g0051 others(4): Show |
7 | NA18906.hp2 NA18972.hp2 NA18998.hp1 others(4): Show |
intron_variant | MODIFIER | c.565-7845_565-7816d others(32): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123040769 | ||||||
| chr6:123040769 | A | AAAAAGAA others(28): Show |
3 | a0001c0001t0001g0071 a0001c0001t0001g0080 a0001c0001t0070g0050 |
3 | HG04204.hp1 NA19007.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.565-7850_565-7816d others(37): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123040769 | ||||||
| chr6:123040769 | A | AAAAAGAA others(33): Show |
1 | a0001c0001t0068g0036 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.565-7816_565-7815i others(42): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123040769 | ||||||
| chr6:123040769 | AAAAAG | A | 4 | a0001c0001t0005g0268 a0001c0001t0016g0027 a0001c0001t0016g0244 others(1): Show |
5 | HG01884.hp2 HG02895.hp2 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.565-7820_565-7816d others(7): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123040769 | ||||||
| chr6:123040961 | C | A | 3 | a0001c0001t0027g0161 a0001c0001t0027g0162 a0001c0001t0027g0163 |
3 | HG00735.hp1 HG01106.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.565-7661C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123040961 | |||||||
| chr6:123041047 | C | A | 1 | a0001c0001t0042g0284 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.565-7575C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123041047 | |||||||
| chr6:123041091 | G | T | 4 | a0001c0001t0042g0284 a0001c0001t0082g0285 a0001c0001t0084g0287 others(1): Show |
4 | HG02559.hp2 HG02818.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.565-7531G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123041091 | |||||||
| chr6:123041366 | T | G | 5 | a0001c0001t0002g0023 a0001c0001t0002g0194 a0001c0001t0002g0195 others(2): Show |
6 | HG00741.hp1 HG01243.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.565-7256T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123041366 | |||||||
| chr6:123041440 | A | G | 9 | a0001c0001t0010g0019 a0001c0001t0010g0158 a0001c0001t0010g0164 others(6): Show |
10 | HG00741.hp2 HG01243.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.565-7182A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123041440 | |||||||
| chr6:123041446 | G | T | 94 | a0001c0001t0001g0061 a0001c0001t0003g0014 a0001c0001t0003g0015 others(91): Show |
101 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.565-7176G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123041446 | |||||||
| chr6:123041531 | T | G | 1 | a0001c0001t0002g0218 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.565-7091T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123041531 | |||||||
| chr6:123041577 | A | G | 4 | a0001c0001t0016g0027 a0001c0001t0016g0244 a0001c0001t0072g0245 others(1): Show |
5 | HG01884.hp2 HG02895.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.565-7045A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123041577 | |||||||
| chr6:123041732 | A | T | 3 | a0001c0001t0017g0155 a0001c0001t0040g0100 a0001c0001t0083g0157 |
3 | HG03041.hp1 HG03139.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.565-6890A>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123041732 | |||||||
| chr6:123041817 | A | G | 1 | a0001c0001t0017g0154 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.565-6805A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123041817 | |||||||
| chr6:123041830 | T | C | 2 | a0001c0001t0028g0032 a0001c0001t0028g0033 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.565-6792T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123041830 | |||||||
| chr6:123041911 | G | A | 1 | a0001c0001t0017g0099 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.565-6711G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123041911 | |||||||
| chr6:123041949 | A | G | 1 | a0001c0001t0003g0119 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.565-6673A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123041949 | |||||||
| chr6:123041956 | A | G | 1 | a0001c0001t0025g0264 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.565-6666A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123041956 | |||||||
| chr6:123042130 | C | T | 1 | a0001c0001t0005g0280 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.565-6492C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123042130 | |||||||
| chr6:123042346 | T | C | 2 | a0001c0001t0028g0032 a0001c0001t0028g0033 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.565-6276T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123042346 | |||||||
| chr6:123042398 | A | G | 13 | a0001c0001t0010g0019 a0001c0001t0010g0158 a0001c0001t0010g0164 others(10): Show |
14 | HG00741.hp2 HG01243.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.565-6224A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123042398 | |||||||
| chr6:123042780 | C | T | 1 | a0001c0001t0042g0191 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.565-5842C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123042780 | |||||||
| chr6:123043001 | C | A | 3 | a0001c0001t0025g0264 a0001c0001t0041g0261 a0001c0001t0041g0262 |
3 | HG01109.hp2 HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.565-5621C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123043001 | |||||||
| chr6:123043113 | T | C | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(146): Show |
167 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.565-5509T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123043113 | |||||||
| chr6:123043147 | C | T | 1 | a0001c0001t0039g0233 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.565-5475C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123043147 | |||||||
| chr6:123043403 | A | G | 6 | a0001c0001t0002g0171 a0001c0001t0027g0161 a0001c0001t0027g0162 others(3): Show |
6 | HG00735.hp1 HG01106.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.565-5219A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123043403 | |||||||
| chr6:123043642 | A | C | 1 | a0001c0001t0042g0191 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.565-4980A>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123043642 | |||||||
| chr6:123043702 | T | G | 3 | a0001c0001t0082g0285 a0001c0001t0084g0287 a0001c0001t0090g0286 |
3 | HG02559.hp2 HG02818.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.565-4920T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123043702 | |||||||
| chr6:123043825 | G | T | 7 | a0001c0001t0004g0017 a0001c0001t0004g0104 a0001c0001t0004g0106 others(4): Show |
8 | HG00408.hp2 NA18952.hp2 NA18969.hp2 others(5): Show |
intron_variant | MODIFIER | c.565-4797G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123043825 | |||||||
| chr6:123043873 | G | A | 5 | a0001c0001t0025g0260 a0001c0001t0025g0263 a0001c0001t0025g0264 others(2): Show |
5 | HG01109.hp2 HG01167.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.565-4749G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123043873 | |||||||
| chr6:123043946 | A | T | 1 | a0001c0001t0002g0224 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.565-4676A>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123043946 | |||||||
| chr6:123043984 | A | G | 10 | a0001c0001t0002g0253 a0001c0001t0007g0009 a0001c0001t0007g0249 others(7): Show |
14 | HG01099.hp1 HG01515.hp2 NA18947.hp2 others(11): Show |
intron_variant | MODIFIER | c.565-4638A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123043984 | |||||||
| chr6:123044064 | C | T | 3 | a0001c0001t0027g0161 a0001c0001t0027g0162 a0001c0001t0027g0163 |
3 | HG00735.hp1 HG01106.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.565-4558C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123044064 | |||||||
| chr6:123044403 | G | A | 5 | a0001c0001t0025g0260 a0001c0001t0025g0263 a0001c0001t0025g0264 others(2): Show |
5 | HG01109.hp2 HG01167.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.565-4219G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123044403 | |||||||
| chr6:123044667 | GTAAATCT others(15): Show |
G | 2 | a0001c0001t0001g0061 a0001c0001t0003g0034 |
2 | HG00544.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.565-3954_565-3933d others(24): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123044667 | |||||||
| chr6:123044690 | G | A | 2 | a0001c0001t0001g0061 a0001c0001t0003g0034 |
2 | HG00544.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.565-3932G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123044690 | |||||||
| chr6:123044691 | G | C | 2 | a0001c0001t0001g0061 a0001c0001t0003g0034 |
2 | HG00544.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.565-3931G>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123044691 | |||||||
| chr6:123044696 | G | A | 2 | a0001c0001t0001g0061 a0001c0001t0003g0034 |
2 | HG00544.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.565-3926G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123044696 | |||||||
| chr6:123045142 | G | GAC | 11 | a0001c0001t0001g0052 a0001c0001t0001g0084 a0001c0001t0002g0224 others(8): Show |
11 | HG01517.hp1 HG02257.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.565-3455_565-3454d others(4): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123045142 | ||||||
| chr6:123045142 | G | GACAC | 7 | a0001c0001t0016g0027 a0001c0001t0016g0244 a0001c0001t0035g0265 others(4): Show |
8 | HG01884.hp2 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.565-3457_565-3454d others(6): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123045142 | ||||||
| chr6:123045142 | G | GACACAC | 5 | a0001c0002t0024g0257 a0001c0002t0024g0258 a0001c0002t0024g0259 others(2): Show |
5 | HG02717.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.565-3459_565-3454d others(8): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123045142 | ||||||
| chr6:123045142 | GAC | G | 15 | a0001c0001t0002g0253 a0001c0001t0007g0009 a0001c0001t0007g0249 others(12): Show |
19 | HG01099.hp1 HG01109.hp2 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.565-3455_565-3454d others(4): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123045142 | ||||||
| chr6:123045271 | C | T | 2 | a0001c0002t0024g0257 a0001c0002t0024g0258 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.565-3351C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123045271 | |||||||
| chr6:123045304 | A | T | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(185): Show |
211 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.565-3318A>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123045304 | |||||||
| chr6:123045339 | G | A | 8 | a0001c0001t0035g0265 a0001c0001t0035g0266 a0001c0001t0056g0048 others(5): Show |
8 | HG02145.hp1 HG02280.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.565-3283G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123045339 | |||||||
| chr6:123045588 | C | T | 1 | a0001c0001t0001g0076 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.565-3034C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123045588 | |||||||
| chr6:123046480 | T | G | 3 | a0001c0001t0045g0172 a0001c0001t0045g0177 a0001c0001t0054g0044 |
3 | HG02109.hp1 HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.565-2142T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123046480 | |||||||
| chr6:123046490 | T | C | 66 | a0001c0001t0001g0061 a0001c0001t0001g0079 a0001c0001t0003g0014 others(63): Show |
70 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.565-2132T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123046490 | |||||||
| chr6:123046573 | C | T | 9 | a0001c0001t0009g0022 a0001c0001t0009g0037 a0001c0001t0009g0181 others(6): Show |
11 | HG01891.hp2 HG02083.hp1 HG02683.hp1 others(8): Show |
intron_variant | MODIFIER | c.565-2049C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123046573 | |||||||
| chr6:123046658 | CA | C | 19 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0073 others(16): Show |
19 | HG01109.hp2 HG01167.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.565-1949delA | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123046658 | ||||||
| chr6:123046658 | CAA | C | 235 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(232): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.565-1950_565-1949d others(4): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123046658 | ||||||
| chr6:123046671 | A | T | 2 | a0001c0001t0002g0213 a0001c0001t0002g0214 |
2 | HG02602.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.565-1951A>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123046671 | |||||||
| chr6:123046674 | T | A | 1 | a0001c0001t0026g0150 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.565-1948T>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123046674 | |||||||
| chr6:123046729 | A | C | 35 | a0001c0001t0010g0019 a0001c0001t0010g0158 a0001c0001t0010g0164 others(32): Show |
37 | HG00741.hp2 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.565-1893A>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123046729 | |||||||
| chr6:123046866 | G | A | 5 | a0001c0002t0024g0257 a0001c0002t0024g0258 a0001c0002t0024g0259 others(2): Show |
5 | HG02717.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.565-1756G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123046866 | |||||||
| chr6:123046878 | T | C | 1 | a0001c0001t0003g0020 | 2 | NA19009.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.565-1744T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123046878 | |||||||
| chr6:123047051 | G | T | 1 | a0001c0001t0016g0153 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.565-1571G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123047051 | |||||||
| chr6:123047141 | G | C | 5 | a0001c0002t0024g0257 a0001c0002t0024g0258 a0001c0002t0024g0259 others(2): Show |
5 | HG02717.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.565-1481G>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123047141 | |||||||
| chr6:123047250 | T | C | 1 | a0001c0001t0040g0167 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.565-1372T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123047250 | |||||||
| chr6:123047263 | T | G | 40 | a0001c0001t0010g0019 a0001c0001t0010g0158 a0001c0001t0010g0164 others(37): Show |
42 | HG00741.hp2 HG01243.hp1 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.565-1359T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123047263 | |||||||
| chr6:123047300 | T | C | 10 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0040 others(7): Show |
12 | HG00423.hp1 HG00438.hp2 HG00621.hp2 others(9): Show |
intron_variant | MODIFIER | c.565-1322T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123047300 | |||||||
| chr6:123047362 | A | T | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(111): Show |
130 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.565-1260A>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123047362 | |||||||
| chr6:123047365 | T | C | 40 | a0001c0001t0010g0019 a0001c0001t0010g0158 a0001c0001t0010g0164 others(37): Show |
42 | HG00741.hp2 HG01243.hp1 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.565-1257T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123047365 | |||||||
| chr6:123047475 | A | G | 7 | a0001c0001t0035g0265 a0001c0001t0035g0266 a0001c0001t0056g0048 others(4): Show |
7 | HG02145.hp1 HG02257.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.565-1147A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123047475 | |||||||
| chr6:123047535 | T | A | 1 | a0001c0001t0042g0191 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.565-1087T>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123047535 | |||||||
| chr6:123047703 | C | T | 40 | a0001c0001t0010g0019 a0001c0001t0010g0158 a0001c0001t0010g0164 others(37): Show |
42 | HG00741.hp2 HG01243.hp1 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.565-919C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123047703 | |||||||
| chr6:123047745 | G | GT | 67 | a0001c0001t0001g0061 a0001c0001t0001g0079 a0001c0001t0002g0197 others(64): Show |
71 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.565-867dupT | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123047745 | ||||||
| chr6:123047891 | C | G | 4 | a0001c0001t0002g0253 a0001c0001t0007g0249 a0001c0001t0007g0254 others(1): Show |
4 | NA18947.hp2 NA18948.hp1 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.565-731C>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123047891 | |||||||
| chr6:123048026 | T | TCCTTAAG others(18): Show |
1 | a0001c0001t0004g0141 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.565-595_565-571dup others(25): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123048026 | ||||||
| chr6:123048209 | T | G | 5 | a0001c0001t0025g0260 a0001c0001t0025g0263 a0001c0001t0025g0264 others(2): Show |
5 | HG01109.hp2 HG01167.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.565-413T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123048209 | |||||||
| chr6:123048271 | A | T | 5 | a0001c0001t0025g0260 a0001c0001t0025g0263 a0001c0001t0025g0264 others(2): Show |
5 | HG01109.hp2 HG01167.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.565-351A>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123048271 | |||||||
| chr6:123048353 | T | G | 5 | a0001c0001t0015g0173 a0001c0001t0015g0174 a0001c0001t0015g0175 others(2): Show |
5 | HG02257.hp2 HG02451.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.565-269T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123048353 | |||||||
| chr6:123048403 | C | A | 65 | a0001c0001t0001g0061 a0001c0001t0003g0014 a0001c0001t0003g0015 others(62): Show |
69 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.565-219C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123048403 | |||||||
| chr6:123048465 | G | A | 40 | a0001c0001t0010g0019 a0001c0001t0010g0158 a0001c0001t0010g0164 others(37): Show |
42 | HG00741.hp2 HG01243.hp1 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.565-157G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123048465 | |||||||
| chr6:123048543 | G | A | 40 | a0001c0001t0010g0019 a0001c0001t0010g0158 a0001c0001t0010g0164 others(37): Show |
42 | HG00741.hp2 HG01243.hp1 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.565-79G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | chr6 | 123048543 | |||||||
| chr6:123048561 | CCTAAA | C | 40 | a0001c0001t0010g0019 a0001c0001t0010g0158 a0001c0001t0010g0164 others(37): Show |
42 | HG00741.hp2 HG01243.hp1 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.565-59_565-55delTA others(3): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 123048561 | ||||||
| chr6:123048765 | T | C | 292 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(289): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.675+33T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123048765 | |||||||
| chr6:123048788 | T | TGCATAAT others(15): Show |
1 | a0001c0001t0004g0127 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.675+59_675+80dupAT others(20): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr6 | 123048788 | ||||||
| chr6:123048800 | A | G | 1 | a0001c0001t0010g0166 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.675+68A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123048800 | |||||||
| chr6:123048867 | G | T | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(111): Show |
130 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.675+135G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123048867 | |||||||
| chr6:123049026 | T | C | 3 | a0001c0002t0024g0259 a0001c0002t0029g0041 a0001c0002t0029g0042 |
3 | HG02717.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.675+294T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123049026 | |||||||
| chr6:123049074 | T | A | 1 | a0001c0001t0002g0240 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.675+342T>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123049074 | |||||||
| chr6:123049121 | G | A | 1 | a0001c0001t0003g0138 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.675+389G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123049121 | |||||||
| chr6:123049403 | A | C | 40 | a0001c0001t0010g0019 a0001c0001t0010g0158 a0001c0001t0010g0164 others(37): Show |
42 | HG00741.hp2 HG01243.hp1 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.675+671A>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123049403 | |||||||
| chr6:123049478 | G | T | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(111): Show |
130 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.675+746G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123049478 | |||||||
| chr6:123049532 | C | T | 1 | a0001c0001t0003g0124 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.675+800C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123049532 | |||||||
| chr6:123049562 | A | G | 1 | a0001c0001t0045g0172 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.675+830A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123049562 | |||||||
| chr6:123049674 | A | G | 40 | a0001c0001t0010g0019 a0001c0001t0010g0158 a0001c0001t0010g0164 others(37): Show |
42 | HG00741.hp2 HG01243.hp1 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.675+942A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123049674 | |||||||
| chr6:123049684 | C | T | 2 | a0001c0001t0001g0047 a0001c0001t0001g0049 |
2 | HG01175.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.675+952C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123049684 | |||||||
| chr6:123049701 | C | T | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(111): Show |
130 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.675+969C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123049701 | |||||||
| chr6:123049732 | T | C | 5 | a0001c0001t0025g0260 a0001c0001t0025g0263 a0001c0001t0025g0264 others(2): Show |
5 | HG01109.hp2 HG01167.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.675+1000T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123049732 | |||||||
| chr6:123049789 | G | T | 1 | a0001c0001t0001g0083 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.675+1057G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123049789 | |||||||
| chr6:123049804 | T | TG | 12 | a0001c0001t0003g0020 a0001c0001t0003g0114 a0001c0001t0003g0120 others(9): Show |
13 | HG00408.hp2 HG01256.hp2 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.675+1078dupG | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr6 | 123049804 | ||||||
| chr6:123049804 | T | TGG | 42 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0016 others(39): Show |
45 | HG00099.hp2 HG00140.hp1 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.675+1077_675+1078d others(4): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr6 | 123049804 | ||||||
| chr6:123049804 | T | TGGG | 21 | a0001c0001t0001g0061 a0001c0001t0001g0079 a0001c0001t0003g0098 others(18): Show |
21 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(18): Show |
intron_variant | MODIFIER | c.675+1076_675+1078d others(5): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr6 | 123049804 | ||||||
| chr6:123049807 | G | GGA | 8 | a0001c0001t0012g0051 a0001c0001t0012g0056 a0001c0001t0012g0058 others(5): Show |
8 | HG03239.hp1 HG04204.hp1 NA18972.hp2 others(5): Show |
intron_variant | MODIFIER | c.675+1076_675+1077i others(4): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr6 | 123049807 | ||||||
| chr6:123049809 | GGC | G | 40 | a0001c0001t0010g0019 a0001c0001t0010g0158 a0001c0001t0010g0164 others(37): Show |
42 | HG00741.hp2 HG01243.hp1 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.675+1079_675+1080d others(4): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr6 | 123049809 | ||||||
| chr6:123049810 | G | C | 122 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(119): Show |
142 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.675+1078G>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123049810 | |||||||
| chr6:123049810 | GC | G | 3 | a0001c0001t0045g0172 a0001c0001t0045g0177 a0001c0001t0054g0044 |
3 | HG02109.hp1 HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.675+1079delC | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123049810 | |||||||
| chr6:123049811 | C | G | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(217): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.675+1079C>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123049811 | |||||||
| chr6:123049852 | A | T | 5 | a0001c0001t0025g0260 a0001c0001t0025g0263 a0001c0001t0025g0264 others(2): Show |
5 | HG01109.hp2 HG01167.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.675+1120A>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123049852 | |||||||
| chr6:123049886 | A | G | 1 | a0001c0001t0026g0150 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.675+1154A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123049886 | |||||||
| chr6:123049958 | G | T | 1 | a0001c0001t0002g0240 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.675+1226G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123049958 | |||||||
| chr6:123049972 | C | T | 1 | a0001c0001t0003g0114 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.675+1240C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123049972 | |||||||
| chr6:123049976 | T | C | 45 | a0001c0001t0010g0019 a0001c0001t0010g0158 a0001c0001t0010g0164 others(42): Show |
47 | HG00741.hp2 HG01109.hp2 HG01167.hp2 others(44): Show |
intron_variant | MODIFIER | c.675+1244T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123049976 | |||||||
| chr6:123050007 | T | C | 106 | a0001c0001t0001g0061 a0001c0001t0001g0079 a0001c0001t0003g0014 others(103): Show |
112 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.675+1275T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123050007 | |||||||
| chr6:123050154 | G | A | 45 | a0001c0001t0010g0019 a0001c0001t0010g0158 a0001c0001t0010g0164 others(42): Show |
47 | HG00741.hp2 HG01109.hp2 HG01167.hp2 others(44): Show |
intron_variant | MODIFIER | c.675+1422G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123050154 | |||||||
| chr6:123050445 | T | C | 1 | a0001c0001t0057g0156 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.675+1713T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123050445 | |||||||
| chr6:123050679 | G | C | 2 | a0001c0001t0028g0032 a0001c0001t0028g0033 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.675+1947G>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123050679 | |||||||
| chr6:123050705 | C | T | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(260): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.675+1973C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123050705 | |||||||
| chr6:123050714 | A | G | 116 | a0001c0001t0001g0061 a0001c0001t0001g0079 a0001c0001t0002g0253 others(113): Show |
126 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.675+1982A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123050714 | |||||||
| chr6:123050725 | C | A | 1 | a0001c0001t0001g0065 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.675+1993C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123050725 | |||||||
| chr6:123050981 | G | A | 2 | a0001c0001t0001g0062 a0001c0001t0001g0063 |
2 | HG00099.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.675+2249G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123050981 | |||||||
| chr6:123051055 | T | C | 1 | a0001c0001t0048g0137 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.675+2323T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123051055 | |||||||
| chr6:123051126 | TACTC | T | 4 | a0001c0001t0016g0027 a0001c0001t0016g0244 a0001c0001t0072g0245 others(1): Show |
5 | HG01884.hp2 HG02895.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.675+2397_675+2400d others(6): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr6 | 123051126 | ||||||
| chr6:123051174 | G | A | 40 | a0001c0001t0010g0019 a0001c0001t0010g0158 a0001c0001t0010g0164 others(37): Show |
42 | HG00741.hp2 HG01243.hp1 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.675+2442G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123051174 | |||||||
| chr6:123051196 | A | G | 40 | a0001c0001t0010g0019 a0001c0001t0010g0158 a0001c0001t0010g0164 others(37): Show |
42 | HG00741.hp2 HG01243.hp1 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.675+2464A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123051196 | |||||||
| chr6:123051336 | C | T | 1 | a0001c0001t0002g0024 | 2 | HG00140.hp2 HG00280.hp1 |
intron_variant | MODIFIER | c.675+2604C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123051336 | |||||||
| chr6:123051391 | A | G | 8 | a0001c0001t0010g0019 a0001c0001t0010g0158 a0001c0001t0010g0164 others(5): Show |
9 | HG00741.hp2 HG01243.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.675+2659A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123051391 | |||||||
| chr6:123051601 | T | C | 1 | a0001c0001t0001g0082 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.675+2869T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123051601 | |||||||
| chr6:123051885 | A | G | 18 | a0001c0001t0002g0253 a0001c0001t0007g0009 a0001c0001t0007g0249 others(15): Show |
23 | HG01099.hp1 HG01515.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.675+3153A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123051885 | |||||||
| chr6:123051948 | T | G | 25 | a0001c0001t0012g0051 a0001c0001t0012g0056 a0001c0001t0012g0058 others(22): Show |
26 | HG00735.hp1 HG01106.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.675+3216T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123051948 | |||||||
| chr6:123052102 | T | TA | 109 | a0001c0001t0001g0061 a0001c0001t0001g0079 a0001c0001t0002g0253 others(106): Show |
119 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.675+3371dupA | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr6 | 123052102 | ||||||
| chr6:123052169 | A | G | 1 | a0001c0001t0015g0176 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.675+3437A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123052169 | |||||||
| chr6:123052179 | A | G | 2 | a0001c0001t0022g0144 a0001c0001t0022g0145 |
2 | HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.675+3447A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123052179 | |||||||
| chr6:123052376 | T | G | 51 | a0001c0001t0003g0122 a0001c0001t0003g0123 a0001c0001t0009g0022 others(48): Show |
54 | HG00741.hp2 HG01109.hp2 HG01167.hp2 others(51): Show |
intron_variant | MODIFIER | c.676-3430T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123052376 | |||||||
| chr6:123052665 | T | G | 1 | a0001c0001t0006g0211 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.676-3141T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123052665 | |||||||
| chr6:123052729 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.676-3077G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123052729 | |||||||
| chr6:123052736 | TAGTGA | T | 25 | a0001c0001t0012g0051 a0001c0001t0012g0056 a0001c0001t0012g0058 others(22): Show |
26 | HG00735.hp1 HG01106.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.676-3069_676-3065d others(7): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123052736 | |||||||
| chr6:123052745 | C | T | 25 | a0001c0001t0012g0051 a0001c0001t0012g0056 a0001c0001t0012g0058 others(22): Show |
26 | HG00735.hp1 HG01106.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.676-3061C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123052745 | |||||||
| chr6:123052748 | TAACTGAT others(324): Show |
T | 25 | a0001c0001t0012g0051 a0001c0001t0012g0056 a0001c0001t0012g0058 others(22): Show |
26 | HG00735.hp1 HG01106.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.676-3057_676-2727d others(2): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123052748 | |||||||
| chr6:123052800 | A | G | 24 | a0001c0001t0009g0022 a0001c0001t0009g0037 a0001c0001t0009g0181 others(21): Show |
26 | HG01884.hp2 HG01891.hp1 HG02083.hp1 others(23): Show |
intron_variant | MODIFIER | c.676-3006A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123052800 | |||||||
| chr6:123053069 | A | C | 5 | a0001c0001t0015g0173 a0001c0001t0015g0174 a0001c0001t0015g0175 others(2): Show |
5 | HG02257.hp2 HG02451.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.676-2737A>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123053069 | |||||||
| chr6:123053174 | G | A | 2 | a0001c0001t0004g0127 a0001c0001t0004g0140 |
2 | NA18953.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.676-2632G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123053174 | |||||||
| chr6:123053397 | C | A | 1 | a0001c0001t0002g0213 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.676-2409C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123053397 | |||||||
| chr6:123053416 | A | G | 1 | a0001c0001t0038g0095 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.676-2390A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123053416 | |||||||
| chr6:123053537 | C | G | 1 | a0001c0001t0006g0210 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.676-2269C>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123053537 | |||||||
| chr6:123053543 | G | T | 2 | a0001c0001t0041g0261 a0001c0001t0041g0262 |
2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.676-2263G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123053543 | |||||||
| chr6:123053880 | G | C | 3 | a0001c0001t0003g0115 a0001c0001t0003g0122 a0001c0001t0003g0123 |
3 | HG02055.hp2 HG02965.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.676-1926G>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123053880 | |||||||
| chr6:123054083 | G | A | 1 | a0001c0001t0014g0227 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.676-1723G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123054083 | |||||||
| chr6:123054111 | G | A | 4 | a0001c0001t0003g0105 a0001c0001t0003g0109 a0001c0001t0003g0135 others(1): Show |
4 | NA18961.hp1 NA18977.hp1 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.676-1695G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123054111 | |||||||
| chr6:123054139 | TGAA | T | 10 | a0001c0001t0002g0253 a0001c0001t0007g0009 a0001c0001t0007g0249 others(7): Show |
14 | HG01099.hp1 HG01515.hp2 NA18947.hp2 others(11): Show |
intron_variant | MODIFIER | c.676-1661_676-1659d others(5): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr6 | 123054139 | ||||||
| chr6:123054257 | C | A | 1 | a0001c0001t0081g0035 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.676-1549C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123054257 | |||||||
| chr6:123054539 | T | C | 1 | a0001c0001t0003g0124 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.676-1267T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123054539 | |||||||
| chr6:123054823 | G | GT | 24 | a0001c0001t0012g0051 a0001c0001t0012g0056 a0001c0001t0012g0058 others(21): Show |
25 | HG00735.hp1 HG01106.hp2 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.676-970dupT | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr6 | 123054823 | ||||||
| chr6:123054913 | T | C | 2 | a0001c0001t0002g0225 a0001c0001t0002g0239 |
2 | HG00733.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.676-893T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123054913 | |||||||
| chr6:123055101 | A | G | 1 | a0001c0001t0006g0210 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.676-705A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123055101 | |||||||
| chr6:123055302 | G | A | 1 | a0001c0001t0012g0056 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.676-504G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123055302 | |||||||
| chr6:123055319 | AT | A | 229 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(226): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.676-482delT | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr6 | 123055319 | ||||||
| chr6:123055541 | T | C | 4 | a0001c0001t0082g0285 a0001c0001t0084g0287 a0001c0001t0086g0149 others(1): Show |
4 | HG02257.hp1 HG02559.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.676-265T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123055541 | |||||||
| chr6:123055577 | C | T | 1 | a0001c0001t0087g0148 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.676-229C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123055577 | |||||||
| chr6:123055661 | C | A | 2 | a0001c0001t0002g0205 a0001c0001t0002g0228 |
2 | HG00323.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.676-145C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123055661 | |||||||
| chr6:123055798 | A | G | 1 | a0001c0001t0002g0024 | 2 | HG00140.hp2 HG00280.hp1 |
splice_region_variant&intron_variant | LOW | c.676-8A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 4/5 | chr6 | 123055798 | |||||||
| chr6:123056137 | A | C | 229 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(226): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.896+111A>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123056137 | |||||||
| chr6:123056372 | C | A | 2 | a0001c0001t0003g0113 a0001c0001t0062g0143 |
2 | HG00140.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.896+346C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123056372 | |||||||
| chr6:123056372 | C | G | 1 | a0001c0001t0071g0178 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.896+346C>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123056372 | |||||||
| chr6:123056438 | G | A | 31 | a0001c0001t0009g0022 a0001c0001t0009g0037 a0001c0001t0009g0181 others(28): Show |
33 | HG00735.hp1 HG01106.hp2 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.896+412G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123056438 | |||||||
| chr6:123056655 | G | T | 1 | a0001c0001t0003g0116 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.896+629G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123056655 | |||||||
| chr6:123056665 | G | A | 1 | a0001c0001t0081g0035 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.896+639G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123056665 | |||||||
| chr6:123056700 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.896+674G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123056700 | |||||||
| chr6:123056989 | A | G | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(223): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.896+963A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123056989 | |||||||
| chr6:123057038 | A | G | 1 | a0001c0001t0004g0101 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.896+1012A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123057038 | |||||||
| chr6:123057071 | A | G | 6 | a0001c0001t0003g0119 a0001c0001t0003g0120 a0001c0001t0003g0121 others(3): Show |
7 | HG00639.hp1 HG00735.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.896+1045A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123057071 | |||||||
| chr6:123057099 | C | T | 5 | a0001c0001t0015g0173 a0001c0001t0015g0174 a0001c0001t0015g0175 others(2): Show |
5 | HG02257.hp2 HG02451.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.896+1073C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123057099 | |||||||
| chr6:123057163 | G | A | 266 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(263): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.896+1137G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123057163 | |||||||
| chr6:123057261 | A | G | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(222): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.896+1235A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123057261 | |||||||
| chr6:123057334 | CT | C | 24 | a0001c0001t0005g0003 a0001c0001t0005g0004 a0001c0001t0005g0005 others(21): Show |
30 | HG01070.hp1 HG01099.hp2 HG01256.hp1 others(27): Show |
intron_variant | MODIFIER | c.896+1339delT | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr6 | 123057334 | ||||||
| chr6:123057334 | CTTT | C | 11 | a0001c0001t0007g0009 a0001c0001t0007g0249 a0001c0001t0007g0250 others(8): Show |
15 | HG01099.hp1 HG01515.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.896+1337_896+1339d others(5): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr6 | 123057334 | ||||||
| chr6:123057334 | CTTTTT | C | 23 | a0001c0001t0009g0022 a0001c0001t0009g0037 a0001c0001t0009g0181 others(20): Show |
25 | HG01109.hp2 HG01167.hp2 HG02083.hp1 others(22): Show |
intron_variant | MODIFIER | c.896+1335_896+1339d others(7): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr6 | 123057334 | ||||||
| chr6:123057334 | CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0004g0141 a0001c0001t0074g0112 |
2 | HG01346.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.896+1330_896+1339d others(12): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr6 | 123057334 | ||||||
| chr6:123057334 | CTTTTTTT others(4): Show |
C | 65 | a0001c0001t0001g0060 a0001c0001t0001g0079 a0001c0001t0001g0084 others(62): Show |
70 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.896+1329_896+1339d others(13): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr6 | 123057334 | ||||||
| chr6:123057334 | CTTTTTTT others(5): Show |
C | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(145): Show |
166 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.896+1328_896+1339d others(14): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr6 | 123057334 | ||||||
| chr6:123057334 | CTTTTTTT others(6): Show |
C | 7 | a0001c0001t0001g0065 a0001c0001t0006g0193 a0001c0001t0011g0064 others(4): Show |
7 | HG02647.hp2 HG02897.hp2 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.896+1327_896+1339d others(15): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr6 | 123057334 | ||||||
| chr6:123057410 | G | A | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(250): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.896+1384G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123057410 | |||||||
| chr6:123057596 | G | A | 2 | a0001c0001t0028g0032 a0001c0001t0028g0033 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.896+1570G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123057596 | |||||||
| chr6:123057783 | T | G | 9 | a0001c0001t0007g0009 a0001c0001t0007g0249 a0001c0001t0007g0250 others(6): Show |
13 | HG01099.hp1 HG01515.hp2 NA18948.hp1 others(10): Show |
intron_variant | MODIFIER | c.896+1757T>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123057783 | |||||||
| chr6:123057841 | C | G | 7 | a0001c0001t0010g0019 a0001c0001t0010g0158 a0001c0001t0010g0164 others(4): Show |
8 | HG00741.hp2 HG01243.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.896+1815C>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123057841 | |||||||
| chr6:123057911 | T | A | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(222): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.896+1885T>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123057911 | |||||||
| chr6:123058145 | C | CT | 9 | a0001c0001t0007g0009 a0001c0001t0007g0249 a0001c0001t0007g0250 others(6): Show |
13 | HG01099.hp1 HG01515.hp2 NA18948.hp1 others(10): Show |
intron_variant | MODIFIER | c.896+2127dupT | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr6 | 123058145 | ||||||
| chr6:123058209 | C | T | 1 | a0001c0001t0063g0142 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.896+2183C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123058209 | |||||||
| chr6:123058210 | G | A | 1 | a0001c0001t0052g0147 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.896+2184G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123058210 | |||||||
| chr6:123058233 | A | G | 3 | a0001c0001t0012g0051 a0001c0001t0012g0059 a0001c0001t0043g0202 |
3 | NA18998.hp1 NA18999.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.896+2207A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123058233 | |||||||
| chr6:123058280 | C | T | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(212): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.896+2254C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123058280 | |||||||
| chr6:123058631 | C | G | 3 | a0001c0001t0006g0025 a0001c0001t0006g0242 a0001c0001t0046g0025 |
3 | NA18955.hp2 NA18961.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.896+2605C>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123058631 | |||||||
| chr6:123058664 | T | A | 4 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0225 others(1): Show |
4 | HG00733.hp2 HG02602.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.896+2638T>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123058664 | |||||||
| chr6:123058756 | A | G | 1 | a0001c0001t0081g0035 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.896+2730A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123058756 | |||||||
| chr6:123058992 | A | G | 1 | a0001c0001t0081g0035 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.896+2966A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123058992 | |||||||
| chr6:123059108 | T | C | 3 | a0001c0001t0045g0172 a0001c0001t0045g0177 a0001c0001t0054g0044 |
3 | HG02109.hp1 HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.896+3082T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123059108 | |||||||
| chr6:123059135 | C | T | 1 | a0001c0001t0059g0279 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.896+3109C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123059135 | |||||||
| chr6:123059202 | AAG | A | 9 | a0001c0001t0007g0009 a0001c0001t0007g0249 a0001c0001t0007g0250 others(6): Show |
13 | HG01099.hp1 HG01515.hp2 NA18948.hp1 others(10): Show |
intron_variant | MODIFIER | c.896+3179_896+3180d others(4): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr6 | 123059202 | ||||||
| chr6:123059214 | A | G | 20 | a0001c0001t0012g0051 a0001c0001t0012g0056 a0001c0001t0012g0058 others(17): Show |
21 | HG00735.hp1 HG01106.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.896+3188A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123059214 | |||||||
| chr6:123059222 | C | T | 1 | a0002c0003t0005g0269 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.896+3196C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123059222 | |||||||
| chr6:123059652 | G | A | 1 | a0001c0001t0083g0157 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.896+3626G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123059652 | |||||||
| chr6:123059814 | G | T | 6 | a0001c0001t0006g0008 a0001c0001t0006g0193 a0001c0001t0006g0210 others(3): Show |
8 | HG00423.hp2 HG02074.hp1 NA18945.hp2 others(5): Show |
intron_variant | MODIFIER | c.896+3788G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123059814 | |||||||
| chr6:123059825 | C | A | 2 | a0001c0001t0001g0075 a0001c0001t0002g0253 |
2 | NA18947.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.896+3799C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123059825 | |||||||
| chr6:123059892 | G | A | 1 | a0001c0001t0081g0035 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.897-3782G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123059892 | |||||||
| chr6:123060125 | T | A | 1 | a0001c0001t0001g0062 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.897-3549T>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123060125 | |||||||
| chr6:123060417 | C | G | 7 | a0001c0001t0035g0265 a0001c0001t0035g0266 a0001c0001t0056g0048 others(4): Show |
7 | HG02145.hp1 HG02257.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.897-3257C>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123060417 | |||||||
| chr6:123060598 | C | T | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(110): Show |
129 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.897-3076C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123060598 | |||||||
| chr6:123060674 | A | C | 4 | a0001c0001t0045g0172 a0001c0001t0045g0177 a0001c0001t0054g0044 others(1): Show |
4 | HG01891.hp2 HG02109.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.897-3000A>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123060674 | |||||||
| chr6:123060699 | C | T | 2 | a0001c0001t0038g0094 a0001c0001t0038g0095 |
2 | HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.897-2975C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123060699 | |||||||
| chr6:123060713 | G | A | 1 | a0001c0001t0025g0264 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.897-2961G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123060713 | |||||||
| chr6:123060797 | G | A | 12 | a0001c0001t0009g0022 a0001c0001t0009g0037 a0001c0001t0009g0181 others(9): Show |
13 | HG01109.hp2 HG01167.hp2 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.897-2877G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123060797 | |||||||
| chr6:123060873 | C | T | 1 | a0001c0001t0038g0095 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.897-2801C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123060873 | |||||||
| chr6:123061192 | T | C | 1 | a0001c0001t0002g0253 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.897-2482T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123061192 | |||||||
| chr6:123061219 | C | T | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(211): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.897-2455C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123061219 | |||||||
| chr6:123061246 | G | A | 2 | a0001c0001t0041g0261 a0001c0001t0041g0262 |
2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.897-2428G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123061246 | |||||||
| chr6:123061262 | A | G | 1 | a0001c0001t0042g0191 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.897-2412A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123061262 | |||||||
| chr6:123061311 | C | T | 1 | a0001c0001t0060g0247 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.897-2363C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123061311 | |||||||
| chr6:123061312 | G | GA | 9 | a0001c0001t0004g0017 a0001c0001t0004g0130 a0001c0001t0004g0134 others(6): Show |
10 | HG01891.hp2 HG02109.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.897-2351dupA | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr6 | 123061312 | ||||||
| chr6:123061312 | GA | G | 17 | a0001c0001t0002g0219 a0001c0001t0002g0226 a0001c0001t0002g0235 others(14): Show |
18 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.897-2351delA | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr6 | 123061312 | ||||||
| chr6:123061324 | C | A | 4 | a0001c0001t0045g0172 a0001c0001t0045g0177 a0001c0001t0054g0044 others(1): Show |
4 | HG01891.hp2 HG02109.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.897-2350C>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123061324 | |||||||
| chr6:123061441 | C | G | 1 | a0001c0001t0081g0035 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.897-2233C>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123061441 | |||||||
| chr6:123061799 | T | C | 9 | a0001c0001t0012g0051 a0001c0001t0012g0056 a0001c0001t0012g0058 others(6): Show |
9 | HG03239.hp1 HG04204.hp1 NA18972.hp2 others(6): Show |
intron_variant | MODIFIER | c.897-1875T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123061799 | |||||||
| chr6:123061868 | T | TATATA | 52 | a0001c0001t0007g0009 a0001c0001t0007g0249 a0001c0001t0007g0250 others(49): Show |
58 | HG00735.hp1 HG01099.hp1 HG01106.hp2 others(55): Show |
intron_variant | MODIFIER | c.897-1805_897-1801d others(7): Show |
CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr6 | 123061868 | ||||||
| chr6:123061922 | A | G | 1 | a0001c0001t0006g0237 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.897-1752A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123061922 | |||||||
| chr6:123062081 | T | C | 1 | a0001c0001t0081g0035 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.897-1593T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123062081 | |||||||
| chr6:123062107 | G | A | 1 | a0001c0001t0074g0112 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.897-1567G>A | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123062107 | |||||||
| chr6:123062503 | C | G | 1 | a0001c0001t0062g0143 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.897-1171C>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123062503 | |||||||
| chr6:123062551 | A | G | 2 | a0001c0001t0001g0071 a0001c0001t0001g0080 |
2 | NA19007.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.897-1123A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123062551 | |||||||
| chr6:123062564 | C | T | 1 | a0001c0001t0081g0035 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.897-1110C>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123062564 | |||||||
| chr6:123062618 | A | G | 9 | a0001c0001t0007g0009 a0001c0001t0007g0249 a0001c0001t0007g0250 others(6): Show |
13 | HG01099.hp1 HG01515.hp2 NA18948.hp1 others(10): Show |
intron_variant | MODIFIER | c.897-1056A>G | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123062618 | |||||||
| chr6:123062750 | G | T | 12 | a0001c0001t0009g0022 a0001c0001t0009g0037 a0001c0001t0009g0181 others(9): Show |
13 | HG01109.hp2 HG01167.hp2 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.897-924G>T | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123062750 | |||||||
| chr6:123063010 | T | C | 9 | a0001c0001t0007g0009 a0001c0001t0007g0249 a0001c0001t0007g0250 others(6): Show |
13 | HG01099.hp1 HG01515.hp2 NA18948.hp1 others(10): Show |
intron_variant | MODIFIER | c.897-664T>C | CLVS2 | ENSG00000146352.13 | transcript | ENST00000275162.10 | protein_coding | 5/5 | chr6 | 123063010 |