Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51185 |
| ensemblid | ENSG00000113851.16 |
| hgncid | 30185 |
| symbol | CRBN |
| name | cereblon |
| refseq_nuc | NM_016302.4 |
| refseq_prot | NP_057386.2 |
| ensembl_nuc | ENST00000231948.9 |
| ensembl_prot | ENSP00000231948.4 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 3150011 |
| end | 3179691 |
| strand | - |
| ver | v1.2 |
| region | chr3:3150011-3179691 |
| region5000 | chr3:3145011-3184691 |
| regionname0 | CRBN_chr3_3150011_3179691 |
| regionname5000 | CRBN_chr3_3145011_3184691 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 442 | 375 | 91 | 68 | 158 | 12 | 44 | 116 | CRBN_chr3_3145011_3184691 | CRBN | MAGEG others(437): Show |
chr3 | 3145011 | 3184691 |
| a0002 | 0/0 | 442 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | MAGEG others(437): Show |
chr3 | 3145011 | 3184691 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1326 | 231 | 84 | 55 | 50 | 10 | 30 | CRBN_chr3_3145011_3184691 | CRBN | ATGGC others(1321): Show |
chr3 | 3145011 | 3184691 | ||
| a0001c0002 | 0/0 | 1326 | 127 | 0 | 11 | 100 | 2 | 14 | CRBN_chr3_3145011_3184691 | CRBN | ATGGC others(1321): Show |
chr3 | 3145011 | 3184691 | ||
| a0001c0003 | 0/0 | 1326 | 9 | 1 | 0 | 8 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | ATGGC others(1321): Show |
chr3 | 3145011 | 3184691 | ||
| a0001c0004 | 0/0 | 1326 | 8 | 6 | 2 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | ATGGC others(1321): Show |
chr3 | 3145011 | 3184691 | ||
| a0002c0005 | 0/0 | 1326 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | ATGGC others(1321): Show |
chr3 | 3145011 | 3184691 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2186 | 19 | 8 | 4 | 4 | 0 | 3 | CRBN_chr3_3145011_3184691 | CRBN | AGACA others(2181): Show |
chr3 | 3145011 | 3184691 |
| a0001c0001t0002 | 0/1 | 2191 | 101 | 28 | 28 | 26 | 5 | 13 | CRBN_chr3_3145011_3184691 | CRBN | AGACA others(2186): Show |
chr3 | 3145011 | 3184691 |
| a0001c0001t0003 | 0/0 | 2187 | 42 | 9 | 14 | 11 | 2 | 6 | CRBN_chr3_3145011_3184691 | CRBN | AGACA others(2182): Show |
chr3 | 3145011 | 3184691 |
| a0001c0001t0004 | 1/0 | 2187 | 28 | 26 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | AGACA others(2182): Show |
chr3 | 3145011 | 3184691 |
| a0001c0001t0005 | 0/0 | 2191 | 19 | 5 | 2 | 9 | 1 | 2 | CRBN_chr3_3145011_3184691 | CRBN | AGACA others(2186): Show |
chr3 | 3145011 | 3184691 |
| a0001c0001t0006 | 0/0 | 2188 | 10 | 1 | 6 | 0 | 0 | 3 | CRBN_chr3_3145011_3184691 | CRBN | AGACA others(2183): Show |
chr3 | 3145011 | 3184691 |
| a0001c0001t0009 | 0/0 | 2186 | 4 | 3 | 0 | 0 | 1 | 0 | CRBN_chr3_3145011_3184691 | CRBN | AGACA others(2181): Show |
chr3 | 3145011 | 3184691 |
| a0001c0001t0010 | 0/0 | 2191 | 2 | 0 | 0 | 0 | 0 | 2 | CRBN_chr3_3145011_3184691 | CRBN | AGACA others(2186): Show |
chr3 | 3145011 | 3184691 |
| a0001c0001t0011 | 0/0 | 2219 | 2 | 2 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | AGACA others(2214): Show |
chr3 | 3145011 | 3184691 |
| a0001c0001t0012 | 0/0 | 2186 | 2 | 2 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | AGACA others(2181): Show |
chr3 | 3145011 | 3184691 |
| a0001c0001t0013 | 0/0 | 2200 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | AGACA others(2195): Show |
chr3 | 3145011 | 3184691 |
| a0001c0001t0014 | 0/0 | 2187 | 1 | 0 | 0 | 0 | 1 | 0 | CRBN_chr3_3145011_3184691 | CRBN | AGACA others(2182): Show |
chr3 | 3145011 | 3184691 |
| a0001c0002t0001 | 0/0 | 2186 | 123 | 0 | 10 | 98 | 2 | 13 | CRBN_chr3_3145011_3184691 | CRBN | AGACA others(2181): Show |
chr3 | 3145011 | 3184691 |
| a0001c0002t0002 | 0/0 | 2191 | 2 | 0 | 1 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | AGACA others(2186): Show |
chr3 | 3145011 | 3184691 |
| a0001c0002t0003 | 0/0 | 2187 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | AGACA others(2182): Show |
chr3 | 3145011 | 3184691 |
| a0001c0002t0015 | 0/0 | 2186 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | AGACA others(2181): Show |
chr3 | 3145011 | 3184691 |
| a0001c0003t0003 | 0/0 | 2187 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | AGACA others(2182): Show |
chr3 | 3145011 | 3184691 |
| a0001c0003t0007 | 0/0 | 2186 | 8 | 0 | 0 | 8 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | AGACA others(2181): Show |
chr3 | 3145011 | 3184691 |
| a0001c0004t0002 | 0/0 | 2191 | 4 | 4 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | AGACA others(2186): Show |
chr3 | 3145011 | 3184691 |
| a0001c0004t0008 | 0/0 | 2186 | 4 | 2 | 2 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | AGACA others(2181): Show |
chr3 | 3145011 | 3184691 |
| a0002c0005t0003 | 0/0 | 2187 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | AGACA others(2182): Show |
chr3 | 3145011 | 3184691 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0019 | 0/0 | 5 | 0 | 3 | 1 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0001g0021 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0002 | 0/0 | 23 | 1 | 7 | 12 | 1 | 2 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0005 | 0/0 | 9 | 3 | 2 | 1 | 1 | 2 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0006 | 0/0 | 9 | 1 | 5 | 2 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0020 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0022 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0025 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0028 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0029 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0047 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0052 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0158 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0003g0004 | 0/0 | 10 | 1 | 6 | 3 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0003g0015 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0003g0024 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0003g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0003g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0003g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0003g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0004g0009 | 1/0 | 7 | 5 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0004g0016 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0004g0017 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0004g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0004g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0004g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0004g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0004g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0004g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0004g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0005g0014 | 0/0 | 6 | 2 | 0 | 4 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0005g0023 | 0/0 | 4 | 2 | 0 | 0 | 0 | 2 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0005g0050 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0005g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0005g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0005g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0005g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0005g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0005g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0006g0007 | 0/0 | 8 | 0 | 5 | 0 | 0 | 3 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0006g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0006g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0009g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0009g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0009g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0009g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0010g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0011g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0012g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0013g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0001t0014g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0001 | 0/0 | 27 | 0 | 1 | 20 | 1 | 5 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0003 | 0/0 | 13 | 0 | 1 | 12 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0010 | 0/0 | 7 | 0 | 2 | 5 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0011 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0012 | 0/0 | 6 | 0 | 5 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0013 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0018 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0003g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0002t0015g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0003t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0003t0007g0008 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0003t0007g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0004t0002g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0004t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0004t0008g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0004t0008g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0004t0008g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0001c0004t0008g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| a0002c0005t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0109 | EUR | GBR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0149 | EUR | GBR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00140 | hp1 | a0001 | c0001 | t0014 | g0067 | EUR | GBR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | GBR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0064 | EUR | FIN | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00280 | hp2 | a0001 | c0001 | t0009 | g0140 | EUR | FIN | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0001 | EUR | FIN | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0047 | EUR | FIN | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | CHS | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | CHS | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00423 | hp2 | a0001 | c0001 | t0005 | g0138 | EAS | CHS | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | CHS | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | CHS | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | CHS | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | CHS | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | CHS | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0105 | EAS | CHS | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00609 | hp2 | a0001 | c0003 | t0007 | g0008 | EAS | CHS | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0052 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00642 | hp1 | a0001 | c0001 | t0006 | g0167 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0165 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | CHS | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0116 | EAS | CHS | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0153 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0068 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0010 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0010 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0143 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0155 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01106 | hp1 | a0001 | c0004 | t0008 | g0094 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01106 | hp2 | a0001 | c0001 | t0005 | g0168 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0031 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0150 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0034 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0024 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01175 | hp2 | a0001 | c0004 | t0008 | g0137 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0025 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0047 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01243 | hp2 | a0001 | c0001 | t0004 | g0009 | AMR | PUR | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01257 | hp1 | a0001 | c0001 | t0006 | g0007 | AMR | CLM | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0049 | AMR | CLM | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01258 | hp2 | a0001 | c0001 | t0006 | g0007 | AMR | CLM | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01261 | hp1 | a0001 | c0001 | t0005 | g0050 | AMR | CLM | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0012 | AMR | CLM | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0031 | AMR | CLM | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0049 | AMR | CLM | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0034 | AMR | CLM | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01361 | hp2 | a0001 | c0001 | t0006 | g0007 | AMR | CLM | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0024 | AMR | CLM | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0174 | EUR | IBS | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0065 | EUR | IBS | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0079 | AFR | ACB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0151 | AFR | ACB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0014 | AFR | ACB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01891 | hp2 | a0001 | c0001 | t0011 | g0035 | AFR | ACB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PEL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0055 | AMR | PEL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01943 | hp1 | a0001 | c0001 | t0006 | g0007 | AMR | PEL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PEL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0012 | AMR | PEL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01978 | hp2 | a0001 | c0001 | t0006 | g0007 | AMR | PEL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0012 | AMR | PEL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0052 | AMR | PEL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0152 | AMR | PEL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0071 | AMR | PEL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0027 | EAS | KHV | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0129 | EAS | KHV | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0075 | EAS | KHV | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0027 | EAS | KHV | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0081 | AFR | ACB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02056 | hp2 | a0001 | c0001 | t0005 | g0014 | EAS | KHV | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | KHV | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | KHV | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | KHV | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | KHV | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PEL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | CDX | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | CDX | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02165 | hp1 | a0001 | c0003 | t0007 | g0008 | EAS | CDX | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0027 | EAS | CDX | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02257 | hp1 | a0001 | c0001 | t0011 | g0035 | AFR | ACB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0009 | AFR | ACB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0083 | AFR | ACB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02258 | hp2 | a0001 | c0003 | t0003 | g0091 | AFR | ACB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02280 | hp2 | a0001 | c0001 | t0006 | g0060 | AFR | ACB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PEL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0012 | AMR | PEL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PEL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0012 | AMR | PEL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0023 | AFR | ACB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | KHV | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0111 | EAS | KHV | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02572 | hp2 | a0002 | c0005 | t0003 | g0076 | AFR | GWD | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02602 | hp1 | a0001 | c0001 | t0013 | g0131 | SAS | PJL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0028 | SAS | PJL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0016 | AFR | GWD | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02615 | hp2 | a0001 | c0001 | t0009 | g0142 | AFR | GWD | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0057 | AFR | GWD | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0166 | AFR | GWD | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | GWD | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02647 | hp2 | a0001 | c0001 | t0012 | g0046 | AFR | GWD | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0025 | SAS | PJL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02698 | hp2 | a0001 | c0001 | t0005 | g0023 | SAS | PJL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0087 | AFR | GWD | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02717 | hp2 | a0001 | c0004 | t0002 | g0026 | AFR | GWD | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | GWD | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02735 | hp1 | a0001 | c0001 | t0006 | g0007 | SAS | PJL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0169 | SAS | PJL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02738 | hp1 | a0001 | c0001 | t0006 | g0007 | SAS | PJL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | GWD | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02809 | hp2 | a0001 | c0004 | t0002 | g0026 | AFR | GWD | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0086 | AFR | GWD | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0148 | AFR | GWD | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | GWD | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02886 | hp2 | a0001 | c0001 | t0009 | g0141 | AFR | GWD | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0032 | AFR | GWD | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0016 | AFR | GWD | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02896 | hp1 | a0001 | c0001 | t0005 | g0170 | AFR | GWD | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0017 | AFR | GWD | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0032 | AFR | GWD | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0014 | AFR | GWD | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | ESN | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02922 | hp2 | a0001 | c0004 | t0008 | g0135 | AFR | ESN | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0036 | AFR | ESN | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0048 | AFR | ESN | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0080 | AFR | ESN | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0062 | AFR | ESN | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0114 | SAS | PJL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0058 | AFR | GWD | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | MSL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0139 | AFR | MSL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | ESN | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0069 | AFR | ESN | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ESN | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | ESN | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0144 | AFR | ESN | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | MSL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0030 | AFR | MSL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0023 | AFR | MSL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0089 | AFR | MSL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0063 | SAS | PJL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03239 | hp2 | a0001 | c0001 | t0005 | g0023 | SAS | PJL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | MSL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | MSL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03486 | hp1 | a0001 | c0001 | t0009 | g0059 | AFR | MSL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0016 | AFR | MSL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03491 | hp1 | a0001 | c0001 | t0010 | g0038 | SAS | PJL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0028 | SAS | PJL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0028 | SAS | PJL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0073 | SAS | PJL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03516 | hp1 | a0001 | c0004 | t0008 | g0136 | AFR | ESN | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0036 | AFR | ESN | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | MSL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0056 | SAS | PJL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0025 | SAS | PJL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0100 | SAS | STU | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | STU | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0112 | SAS | PJL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0085 | SAS | PJL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0074 | SAS | PJL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03831 | hp1 | a0001 | c0001 | t0006 | g0007 | SAS | BEB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | BEB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0124 | SAS | BEB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0119 | SAS | BEB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | BEB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG04115 | hp1 | a0001 | c0001 | t0010 | g0038 | SAS | STU | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0078 | SAS | STU | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0066 | SAS | BEB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0175 | SAS | STU | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0024 | SAS | STU | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0163 | SAS | STU | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG04204 | hp2 | a0001 | c0002 | t0003 | g0101 | SAS | STU | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | STU | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0070 | SAS | STU | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0146 | AFR | YRI | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0048 | AFR | YRI | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | CHB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | CHB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0090 | EAS | CHB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | CHB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0147 | AFR | YRI | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0016 | AFR | YRI | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18940 | hp1 | a0001 | c0003 | t0007 | g0054 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18949 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18952 | hp1 | a0001 | c0002 | t0002 | g0145 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0130 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18956 | hp2 | a0001 | c0001 | t0005 | g0051 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18961 | hp1 | a0001 | c0003 | t0007 | g0008 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0176 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18964 | hp1 | a0001 | c0001 | t0005 | g0173 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18965 | hp1 | a0001 | c0003 | t0007 | g0008 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18967 | hp2 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0127 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18969 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0121 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18972 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18974 | hp1 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0122 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18977 | hp1 | a0001 | c0001 | t0005 | g0014 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18978 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18986 | hp2 | a0001 | c0003 | t0007 | g0008 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0126 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19001 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19006 | hp1 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19006 | hp2 | a0001 | c0002 | t0001 | g0123 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19007 | hp2 | a0001 | c0001 | t0005 | g0014 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19010 | hp1 | a0001 | c0003 | t0007 | g0008 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19011 | hp2 | a0001 | c0001 | t0005 | g0092 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19012 | hp1 | a0001 | c0001 | t0005 | g0014 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19030 | hp1 | a0001 | c0001 | t0012 | g0046 | AFR | LWK | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0082 | AFR | LWK | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0172 | AFR | LWK | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | LWK | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19054 | hp2 | a0001 | c0003 | t0007 | g0008 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19055 | hp1 | a0001 | c0001 | t0005 | g0051 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19055 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19063 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0113 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19076 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19076 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19091 | hp1 | a0001 | c0002 | t0015 | g0117 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0160 | AFR | YRI | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | YRI | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ASW | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA20129 | hp2 | a0001 | c0004 | t0002 | g0026 | AFR | ASW | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA20752 | hp1 | a0001 | c0001 | t0005 | g0050 | EUR | TSI | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0005 | EUR | TSI | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | GIH | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | GIH | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01123 | hp1 | a0001 | c0002 | t0002 | g0108 | AMR | CLM | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0164 | AMR | CLM | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0030 | AFR | ACB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0161 | AFR | ACB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02559 | hp1 | a0001 | c0004 | t0002 | g0088 | AFR | ACB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0084 | AFR | ACB | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | MSL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0017 | AFR | MSL | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | USA | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0162 | AFR | USA | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0016 | AFR | USA | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | USA | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0171 | AFR | LWK | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0061 | AFR | LWK | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0158 | REF | REF | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0009 | REF | REF | CRBN_chr3_3145011_3184691 | CRBN | chr3 | 3145011 | 3184691 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:3174136 | C | G | 1 | a0002 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.300G>C | p.Gln100His | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 3/11 | 304/2187 | 300/1329 | 100/442 | chr3 | 3174136 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:3150985 | C | T | 1 | a0001c0003 | 9 | HG00609.hp2 HG02165.hp1 HG02258.hp2 others(6): Show |
synonymous_variant | LOW | c.1209G>A | p.Thr403Thr | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 11/11 | 1213/2187 | 1209/1329 | 403/442 | chr3 | 3150985 | |||
| chr3:3156234 | A | G | 1 | a0001c0002 | 127 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(124): Show |
synonymous_variant | LOW | c.735T>C | p.Tyr245Tyr | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 6/11 | 739/2187 | 735/1329 | 245/442 | chr3 | 3156234 | |||
| chr3:3174217 | G | A | 1 | a0001c0004 | 8 | HG01106.hp1 HG01175.hp2 HG02559.hp1 others(5): Show |
synonymous_variant | LOW | c.219C>T | p.His73His | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 3/11 | 223/2187 | 219/1329 | 73/442 | chr3 | 3174217 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:3150030 | TTTAC | T | 1 | a0001c0002t0001 | 7 | HG01934.hp2 NA18974.hp1 NA18977.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*831_*834delGTAA | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 11/11 | 831 | chr3 | 3150030 | ||||||
| chr3:3150092 | T | C | 20 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(17): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
3_prime_UTR_variant | MODIFIER | c.*773A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 11/11 | 773 | chr3 | 3150092 | ||||||
| chr3:3150129 | T | G | 1 | a0001c0001t0009 | 4 | HG00280.hp2 HG02615.hp2 HG02886.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*736A>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 11/11 | 736 | chr3 | 3150129 | ||||||
| chr3:3150149 | A | G | 3 | a0001c0001t0009 a0001c0001t0012 a0001c0004t0008 |
10 | HG00280.hp2 HG01106.hp1 HG01175.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*716T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 11/11 | 716 | chr3 | 3150149 | ||||||
| chr3:3150248 | A | G | 1 | a0001c0002t0015 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*617T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 11/11 | 617 | chr3 | 3150248 | ||||||
| chr3:3150272 | G | C | 1 | a0001c0001t0005 | 19 | HG00423.hp2 HG01106.hp2 HG01261.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*593C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 11/11 | 593 | chr3 | 3150272 | ||||||
| chr3:3150322 | T | TATCTCAG others(25): Show |
1 | a0001c0001t0011 | 2 | HG01891.hp2 HG02257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*511_*542dupTTCCTT others(26): Show |
CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 11/11 | 542 | chr3 | 3150322 | ||||||
| chr3:3150352 | G | C | 1 | a0001c0001t0014 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*513C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 11/11 | 513 | chr3 | 3150352 | ||||||
| chr3:3150451 | A | G | 1 | a0001c0001t0010 | 2 | HG03491.hp1 HG04115.hp1 |
3_prime_UTR_variant | MODIFIER | c.*414T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 11/11 | 414 | chr3 | 3150451 | ||||||
| chr3:3150459 | G | A | 1 | a0001c0003t0007 | 8 | HG00609.hp2 HG02165.hp1 NA18940.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*406C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 11/11 | 406 | chr3 | 3150459 | ||||||
| chr3:3150518 | A | AT | 1 | a0001c0001t0006 | 10 | HG00642.hp1 HG01257.hp1 HG01258.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*346dupA | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 11/11 | 346 | chr3 | 3150518 | ||||||
| chr3:3150518 | AT | A | 8 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0012 others(5): Show |
162 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(159): Show |
3_prime_UTR_variant | MODIFIER | c.*346delA | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 11/11 | 346 | chr3 | 3150518 | ||||||
| chr3:3150712 | T | A | 1 | a0001c0001t0012 | 2 | HG02647.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*153A>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 11/11 | 153 | chr3 | 3150712 | ||||||
| chr3:3150776 | A | ACTTAGGT others(7): Show |
1 | a0001c0001t0013 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*75_*88dupGATACATA others(6): Show |
CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 11/11 | 88 | chr3 | 3150776 | ||||||
| chr3:3150840 | A | ATAAC | 5 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0010 others(2): Show |
127 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*21_*24dupGTTA | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 11/11 | 24 | chr3 | 3150840 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:3151219 | C | T | 79 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(76): Show |
175 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.1149-174G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3151219 | |||||||
| chr3:3151243 | T | G | 53 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(50): Show |
122 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.1149-198A>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3151243 | |||||||
| chr3:3151260 | G | A | 2 | a0001c0001t0002g0147 a0001c0001t0002g0148 |
2 | HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1149-215C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3151260 | |||||||
| chr3:3151304 | A | T | 162 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0037 others(159): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.1149-259T>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3151304 | |||||||
| chr3:3151336 | GACCACAT others(16): Show |
G | 2 | a0001c0001t0001g0102 a0001c0002t0001g0100 |
2 | HG03688.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1149-314_1149-292d others(25): Show |
CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3151336 | |||||||
| chr3:3151422 | A | G | 4 | a0001c0001t0002g0061 a0001c0001t0002g0165 a0001c0001t0002g0166 others(1): Show |
4 | HG00642.hp2 HG02622.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1149-377T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3151422 | |||||||
| chr3:3151449 | T | A | 1 | a0001c0002t0001g0175 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1149-404A>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3151449 | |||||||
| chr3:3151492 | G | A | 162 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0037 others(159): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.1149-447C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3151492 | |||||||
| chr3:3151502 | A | AAAAACTA others(1): Show |
91 | a0001c0001t0001g0037 a0001c0001t0002g0002 a0001c0001t0002g0005 others(88): Show |
187 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.1149-458_1149-457i others(10): Show |
CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3151502 | |||||||
| chr3:3151528 | G | A | 2 | a0001c0001t0002g0020 a0001c0001t0002g0156 |
6 | HG02071.hp1 NA18943.hp1 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.1149-483C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3151528 | |||||||
| chr3:3151555 | G | GGTATTTT others(4): Show |
1 | a0001c0001t0002g0153 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1149-521_1149-511d others(13): Show |
CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3151555 | |||||||
| chr3:3151704 | T | G | 163 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0037 others(160): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.1149-659A>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3151704 | |||||||
| chr3:3151781 | G | GGGAACTG others(1): Show |
3 | a0001c0001t0001g0037 a0001c0001t0003g0079 a0001c0001t0011g0035 |
5 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1148+667_1148+674d others(10): Show |
CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3151781 | |||||||
| chr3:3151827 | G | GCAAACAA others(1): Show |
136 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0037 others(133): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.1148+621_1148+628d others(10): Show |
CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3151827 | |||||||
| chr3:3151828 | C | CAAACAAA others(1): Show |
27 | a0001c0001t0002g0074 a0001c0001t0003g0004 a0001c0001t0003g0015 others(24): Show |
54 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.1148+627_1148+628i others(10): Show |
CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3151828 | |||||||
| chr3:3151915 | C | T | 1 | a0001c0002t0001g0113 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1148+541G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3151915 | |||||||
| chr3:3151938 | T | C | 3 | a0001c0001t0005g0023 a0001c0001t0005g0050 a0001c0001t0005g0168 |
7 | HG01106.hp2 HG01261.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1148+518A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3151938 | |||||||
| chr3:3151962 | G | T | 78 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(75): Show |
173 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.1148+494C>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3151962 | |||||||
| chr3:3151992 | A | G | 86 | a0001c0001t0001g0037 a0001c0001t0002g0002 a0001c0001t0002g0005 others(83): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.1148+464T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3151992 | |||||||
| chr3:3152016 | T | C | 1 | a0001c0001t0002g0154 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1148+440A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3152016 | |||||||
| chr3:3152104 | C | G | 1 | a0001c0001t0001g0102 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1148+352G>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3152104 | |||||||
| chr3:3152142 | T | A | 53 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(50): Show |
122 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.1148+314A>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3152142 | |||||||
| chr3:3152150 | A | ATTT | 73 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(70): Show |
168 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.1148+303_1148+305d others(5): Show |
CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3152150 | |||||||
| chr3:3152159 | T | TTTC | 8 | a0001c0001t0001g0037 a0001c0001t0002g0061 a0001c0001t0002g0165 others(5): Show |
10 | HG00642.hp2 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1148+296_1148+297i others(5): Show |
CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3152159 | |||||||
| chr3:3152165 | T | A | 4 | a0001c0001t0009g0059 a0001c0001t0009g0140 a0001c0001t0009g0141 others(1): Show |
4 | HG00280.hp2 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1148+291A>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3152165 | |||||||
| chr3:3152166 | A | AAT | 4 | a0001c0001t0009g0059 a0001c0001t0009g0140 a0001c0001t0009g0141 others(1): Show |
4 | HG00280.hp2 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1148+289_1148+290i others(4): Show |
CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3152166 | |||||||
| chr3:3152219 | T | C | 74 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0039 others(71): Show |
155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.1148+237A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3152219 | |||||||
| chr3:3152264 | T | A | 2 | a0001c0003t0007g0008 a0001c0003t0007g0054 |
8 | HG00609.hp2 HG02165.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.1148+192A>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3152264 | |||||||
| chr3:3152273 | A | C | 163 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0037 others(160): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.1148+183T>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3152273 | |||||||
| chr3:3152404 | C | T | 1 | a0001c0001t0006g0060 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1148+52G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3152404 | |||||||
| chr3:3152423 | G | GA | 80 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0037 others(77): Show |
163 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.1148+32dupT | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 10/10 | chr3 | 3152423 | |||||||
| chr3:3152641 | T | C | 5 | a0001c0002t0001g0042 a0001c0002t0001g0044 a0001c0002t0001g0055 others(2): Show |
7 | HG01934.hp2 NA18974.hp1 NA18977.hp2 others(4): Show |
intron_variant | MODIFIER | c.1017-54A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 9/10 | chr3 | 3152641 | |||||||
| chr3:3152651 | A | G | 1 | a0001c0002t0001g0118 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1017-64T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 9/10 | chr3 | 3152651 | |||||||
| chr3:3152685 | T | G | 8 | a0001c0001t0001g0037 a0001c0001t0002g0061 a0001c0001t0002g0165 others(5): Show |
10 | HG00642.hp2 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1017-98A>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 9/10 | chr3 | 3152685 | |||||||
| chr3:3152744 | T | C | 1 | a0001c0002t0001g0114 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1017-157A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 9/10 | chr3 | 3152744 | |||||||
| chr3:3152879 | A | G | 2 | a0001c0001t0001g0102 a0001c0001t0012g0046 |
3 | HG02647.hp2 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1017-292T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 9/10 | chr3 | 3152879 | |||||||
| chr3:3152894 | T | C | 1 | a0001c0002t0001g0010 | 7 | HG00741.hp2 HG01069.hp2 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.1017-307A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 9/10 | chr3 | 3152894 | |||||||
| chr3:3152903 | G | A | 161 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0037 others(158): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.1017-316C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 9/10 | chr3 | 3152903 | |||||||
| chr3:3153210 | G | A | 1 | a0001c0001t0006g0060 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1016+214C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 9/10 | chr3 | 3153210 | |||||||
| chr3:3153229 | T | A | 2 | a0001c0003t0007g0008 a0001c0003t0007g0054 |
8 | HG00609.hp2 HG02165.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.1016+195A>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 9/10 | chr3 | 3153229 | |||||||
| chr3:3153238 | T | C | 5 | a0001c0001t0002g0156 a0001c0002t0001g0013 a0001c0002t0001g0118 others(2): Show |
10 | HG02071.hp1 NA18612.hp1 NA18952.hp1 others(7): Show |
intron_variant | MODIFIER | c.1016+186A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 9/10 | chr3 | 3153238 | |||||||
| chr3:3153261 | A | G | 1 | a0001c0001t0004g0082 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1016+163T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 9/10 | chr3 | 3153261 | |||||||
| chr3:3153367 | A | G | 1 | a0001c0002t0001g0112 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1016+57T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 9/10 | chr3 | 3153367 | |||||||
| chr3:3153641 | T | C | 8 | a0001c0001t0001g0037 a0001c0001t0002g0061 a0001c0001t0002g0165 others(5): Show |
10 | HG00642.hp2 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.952-153A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 8/10 | chr3 | 3153641 | |||||||
| chr3:3153667 | G | A | 5 | a0001c0001t0004g0016 a0001c0001t0004g0017 a0001c0001t0004g0082 others(2): Show |
13 | HG02258.hp1 HG02559.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.952-179C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 8/10 | chr3 | 3153667 | |||||||
| chr3:3153685 | A | G | 25 | a0001c0001t0003g0004 a0001c0001t0003g0015 a0001c0001t0003g0024 others(22): Show |
51 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.952-197T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 8/10 | chr3 | 3153685 | |||||||
| chr3:3153812 | T | C | 2 | a0001c0003t0007g0008 a0001c0003t0007g0054 |
8 | HG00609.hp2 HG02165.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.951+148A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 8/10 | chr3 | 3153812 | |||||||
| chr3:3153819 | G | T | 1 | a0001c0001t0003g0033 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.951+141C>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 8/10 | chr3 | 3153819 | |||||||
| chr3:3153870 | C | G | 1 | a0001c0001t0001g0104 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.951+90G>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 8/10 | chr3 | 3153870 | |||||||
| chr3:3153890 | C | T | 25 | a0001c0001t0003g0004 a0001c0001t0003g0015 a0001c0001t0003g0024 others(22): Show |
51 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.951+70G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 8/10 | chr3 | 3153890 | |||||||
| chr3:3154166 | C | G | 55 | a0001c0001t0002g0156 a0001c0002t0001g0001 a0001c0002t0001g0003 others(52): Show |
127 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.836-91G>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 7/10 | chr3 | 3154166 | |||||||
| chr3:3154209 | C | T | 1 | a0001c0001t0002g0028 | 3 | HG02602.hp2 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.836-134G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 7/10 | chr3 | 3154209 | |||||||
| chr3:3154253 | A | G | 1 | a0001c0001t0006g0060 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.836-178T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 7/10 | chr3 | 3154253 | |||||||
| chr3:3154288 | A | G | 2 | a0001c0003t0007g0008 a0001c0003t0007g0054 |
8 | HG00609.hp2 HG02165.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.836-213T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 7/10 | chr3 | 3154288 | |||||||
| chr3:3154379 | TAAAG | T | 69 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0039 others(66): Show |
150 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.836-308_836-305del others(4): Show |
CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 7/10 | chr3 | 3154379 | |||||||
| chr3:3154518 | T | C | 1 | a0001c0001t0002g0143 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.835+229A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 7/10 | chr3 | 3154518 | |||||||
| chr3:3154558 | G | C | 1 | a0001c0001t0002g0061 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.835+189C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 7/10 | chr3 | 3154558 | |||||||
| chr3:3154589 | AT | A | 162 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0037 others(159): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.835+157delA | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 7/10 | chr3 | 3154589 | |||||||
| chr3:3154726 | C | G | 1 | a0001c0003t0003g0091 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.835+21G>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 7/10 | chr3 | 3154726 | |||||||
| chr3:3154969 | A | G | 1 | a0001c0002t0001g0110 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.751-138T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 6/10 | chr3 | 3154969 | |||||||
| chr3:3155152 | C | T | 162 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0037 others(159): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.751-321G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 6/10 | chr3 | 3155152 | |||||||
| chr3:3155315 | G | C | 1 | a0001c0001t0003g0033 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.751-484C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 6/10 | chr3 | 3155315 | |||||||
| chr3:3155329 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.751-498A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 6/10 | chr3 | 3155329 | |||||||
| chr3:3155351 | T | G | 95 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0039 others(92): Show |
201 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.751-520A>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 6/10 | chr3 | 3155351 | |||||||
| chr3:3155378 | T | C | 4 | a0001c0001t0001g0037 a0001c0001t0003g0079 a0001c0001t0003g0139 others(1): Show |
6 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.751-547A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 6/10 | chr3 | 3155378 | |||||||
| chr3:3155445 | T | C | 1 | a0001c0001t0002g0049 | 2 | HG01257.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.751-614A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 6/10 | chr3 | 3155445 | |||||||
| chr3:3155447 | G | A | 3 | a0001c0001t0001g0037 a0001c0001t0003g0079 a0001c0001t0011g0035 |
5 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.751-616C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 6/10 | chr3 | 3155447 | |||||||
| chr3:3155461 | C | A | 1 | a0001c0001t0002g0146 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.751-630G>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 6/10 | chr3 | 3155461 | |||||||
| chr3:3155675 | G | A | 1 | a0001c0001t0003g0062 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.750+544C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 6/10 | chr3 | 3155675 | |||||||
| chr3:3155677 | C | T | 1 | a0001c0002t0001g0090 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.750+542G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 6/10 | chr3 | 3155677 | |||||||
| chr3:3155810 | C | CT | 96 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0039 others(93): Show |
202 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.750+408dupA | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 6/10 | chr3 | 3155810 | |||||||
| chr3:3155820 | C | T | 161 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0037 others(158): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.750+399G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 6/10 | chr3 | 3155820 | |||||||
| chr3:3155956 | G | A | 1 | a0001c0001t0003g0062 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.750+263C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 6/10 | chr3 | 3155956 | |||||||
| chr3:3156064 | A | C | 10 | a0001c0001t0003g0139 a0001c0001t0009g0059 a0001c0001t0009g0140 others(7): Show |
11 | HG00280.hp2 HG01106.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.750+155T>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 6/10 | chr3 | 3156064 | |||||||
| chr3:3156116 | A | G | 1 | a0001c0001t0009g0140 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.750+103T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 6/10 | chr3 | 3156116 | |||||||
| chr3:3156132 | T | C | 1 | a0001c0001t0003g0068 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.750+87A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 6/10 | chr3 | 3156132 | |||||||
| chr3:3156187 | T | C | 163 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0037 others(160): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.750+32A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 6/10 | chr3 | 3156187 | |||||||
| chr3:3156426 | G | T | 4 | a0001c0001t0009g0059 a0001c0001t0009g0140 a0001c0001t0009g0141 others(1): Show |
4 | HG00280.hp2 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.688-145C>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3156426 | |||||||
| chr3:3156474 | T | C | 1 | a0001c0003t0003g0091 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.688-193A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3156474 | |||||||
| chr3:3156537 | A | G | 2 | a0001c0003t0007g0008 a0001c0003t0007g0054 |
8 | HG00609.hp2 HG02165.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.688-256T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3156537 | |||||||
| chr3:3156696 | G | T | 92 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(89): Show |
191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.688-415C>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3156696 | |||||||
| chr3:3156829 | C | T | 65 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(62): Show |
138 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.688-548G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3156829 | |||||||
| chr3:3157125 | A | G | 2 | a0001c0003t0007g0008 a0001c0003t0007g0054 |
8 | HG00609.hp2 HG02165.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.688-844T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3157125 | |||||||
| chr3:3157164 | T | C | 1 | a0001c0001t0002g0157 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.688-883A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3157164 | |||||||
| chr3:3157262 | A | G | 9 | a0001c0002t0001g0011 a0001c0002t0001g0013 a0001c0002t0001g0027 others(6): Show |
22 | HG00438.hp2 HG02015.hp1 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.688-981T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3157262 | |||||||
| chr3:3157486 | T | G | 67 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(64): Show |
143 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.688-1205A>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3157486 | |||||||
| chr3:3157555 | G | C | 1 | a0001c0004t0008g0137 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.688-1274C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3157555 | |||||||
| chr3:3157586 | C | G | 1 | a0001c0004t0008g0136 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.688-1305G>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3157586 | |||||||
| chr3:3157594 | A | T | 171 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0037 others(168): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.688-1313T>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3157594 | |||||||
| chr3:3157610 | C | T | 3 | a0001c0001t0003g0004 a0001c0001t0003g0071 a0001c0001t0003g0075 |
12 | HG00597.hp2 HG00733.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.688-1329G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3157610 | |||||||
| chr3:3157780 | T | G | 1 | a0001c0002t0001g0027 | 3 | HG02015.hp1 HG02040.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.688-1499A>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3157780 | |||||||
| chr3:3157813 | G | C | 2 | a0001c0004t0008g0094 a0001c0004t0008g0137 |
2 | HG01106.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.688-1532C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3157813 | |||||||
| chr3:3157834 | A | C | 161 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0037 others(158): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.688-1553T>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3157834 | |||||||
| chr3:3157890 | T | C | 1 | a0001c0002t0001g0116 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.688-1609A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3157890 | |||||||
| chr3:3157951 | A | C | 120 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0039 others(117): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.688-1670T>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3157951 | |||||||
| chr3:3158035 | A | G | 69 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0037 others(66): Show |
151 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.688-1754T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3158035 | |||||||
| chr3:3158107 | G | A | 89 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(86): Show |
188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.688-1826C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3158107 | |||||||
| chr3:3158116 | A | G | 1 | a0001c0001t0003g0071 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.688-1835T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3158116 | |||||||
| chr3:3158231 | A | G | 1 | a0001c0002t0001g0175 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.688-1950T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3158231 | |||||||
| chr3:3158329 | C | T | 25 | a0001c0001t0003g0004 a0001c0001t0003g0015 a0001c0001t0003g0024 others(22): Show |
52 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.688-2048G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3158329 | |||||||
| chr3:3158357 | A | C | 2 | a0001c0003t0007g0008 a0001c0003t0007g0054 |
8 | HG00609.hp2 HG02165.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.688-2076T>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3158357 | |||||||
| chr3:3158406 | G | C | 3 | a0001c0001t0002g0061 a0001c0001t0002g0165 a0001c0001t0002g0166 |
3 | HG00642.hp2 HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.688-2125C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3158406 | |||||||
| chr3:3158433 | T | C | 1 | a0001c0002t0001g0116 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.688-2152A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3158433 | |||||||
| chr3:3158532 | T | C | 3 | a0001c0001t0001g0037 a0001c0001t0003g0079 a0001c0001t0011g0035 |
5 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.688-2251A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3158532 | |||||||
| chr3:3158844 | G | A | 1 | a0001c0002t0001g0106 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.688-2563C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3158844 | |||||||
| chr3:3159007 | G | T | 161 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0037 others(158): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.688-2726C>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3159007 | |||||||
| chr3:3159008 | A | C | 161 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0037 others(158): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.688-2727T>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3159008 | |||||||
| chr3:3159095 | C | G | 1 | a0001c0001t0001g0098 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.688-2814G>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3159095 | |||||||
| chr3:3159164 | C | T | 3 | a0001c0001t0005g0168 a0001c0004t0002g0026 a0001c0004t0002g0088 |
5 | HG01106.hp2 HG02559.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.688-2883G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3159164 | |||||||
| chr3:3159165 | G | A | 1 | a0001c0001t0001g0102 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.688-2884C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3159165 | |||||||
| chr3:3159191 | T | C | 1 | a0001c0003t0003g0091 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.688-2910A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3159191 | |||||||
| chr3:3159279 | C | G | 163 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0037 others(160): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.688-2998G>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3159279 | |||||||
| chr3:3159536 | G | A | 3 | a0001c0001t0001g0037 a0001c0001t0003g0079 a0001c0001t0011g0035 |
5 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.688-3255C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3159536 | |||||||
| chr3:3159621 | A | G | 1 | a0001c0001t0003g0070 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.688-3340T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3159621 | |||||||
| chr3:3159748 | T | C | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
100 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.688-3467A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3159748 | |||||||
| chr3:3159852 | A | C | 1 | a0001c0001t0002g0160 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.688-3571T>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3159852 | |||||||
| chr3:3159957 | G | T | 47 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(44): Show |
102 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.688-3676C>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3159957 | |||||||
| chr3:3160058 | G | T | 1 | a0001c0001t0005g0168 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.688-3777C>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3160058 | |||||||
| chr3:3160096 | G | C | 51 | a0001c0001t0002g0061 a0001c0001t0002g0074 a0001c0001t0002g0169 others(48): Show |
95 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.688-3815C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3160096 | |||||||
| chr3:3160595 | T | C | 27 | a0001c0001t0002g0061 a0001c0001t0002g0074 a0001c0001t0003g0004 others(24): Show |
54 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.688-4314A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3160595 | |||||||
| chr3:3160608 | A | G | 46 | a0001c0001t0002g0006 a0001c0001t0002g0022 a0001c0001t0002g0028 others(43): Show |
98 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.688-4327T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3160608 | |||||||
| chr3:3160631 | T | C | 1 | a0001c0002t0001g0122 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.688-4350A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3160631 | |||||||
| chr3:3160662 | A | G | 1 | a0001c0001t0003g0069 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.688-4381T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3160662 | |||||||
| chr3:3160669 | T | C | 1 | a0001c0001t0002g0151 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.688-4388A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3160669 | |||||||
| chr3:3160961 | A | G | 1 | a0001c0001t0002g0144 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.688-4680T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3160961 | |||||||
| chr3:3160998 | C | T | 2 | a0001c0002t0001g0096 a0001c0002t0001g0110 |
2 | NA18944.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.688-4717G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3160998 | |||||||
| chr3:3161081 | T | G | 2 | a0001c0004t0008g0094 a0001c0004t0008g0137 |
2 | HG01106.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.688-4800A>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3161081 | |||||||
| chr3:3161151 | C | T | 1 | a0001c0002t0001g0103 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.688-4870G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3161151 | |||||||
| chr3:3161430 | CAAT | C | 3 | a0001c0001t0001g0037 a0001c0001t0003g0079 a0001c0001t0011g0035 |
5 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.688-5152_688-5150d others(5): Show |
CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3161430 | |||||||
| chr3:3161462 | T | C | 1 | a0001c0004t0008g0136 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.688-5181A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3161462 | |||||||
| chr3:3161474 | C | T | 6 | a0001c0001t0003g0139 a0001c0001t0012g0046 a0001c0004t0008g0094 others(3): Show |
7 | HG01106.hp1 HG01175.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.688-5193G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3161474 | |||||||
| chr3:3161656 | G | T | 1 | a0001c0002t0001g0027 | 3 | HG02015.hp1 HG02040.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.688-5375C>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3161656 | |||||||
| chr3:3161693 | T | C | 1 | a0001c0001t0004g0036 | 2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.688-5412A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3161693 | |||||||
| chr3:3161773 | T | G | 4 | a0001c0001t0009g0059 a0001c0001t0009g0140 a0001c0001t0009g0141 others(1): Show |
4 | HG00280.hp2 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.688-5492A>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3161773 | |||||||
| chr3:3161789 | G | C | 2 | a0001c0003t0007g0008 a0001c0003t0007g0054 |
8 | HG00609.hp2 HG02165.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.688-5508C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3161789 | |||||||
| chr3:3161820 | A | G | 68 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0037 others(65): Show |
150 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.688-5539T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3161820 | |||||||
| chr3:3161922 | A | G | 1 | a0001c0001t0004g0080 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.688-5641T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3161922 | |||||||
| chr3:3162079 | G | A | 1 | a0001c0002t0001g0107 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.687+5555C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3162079 | |||||||
| chr3:3162086 | G | A | 1 | a0001c0004t0008g0136 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.687+5548C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3162086 | |||||||
| chr3:3162123 | G | A | 2 | a0001c0001t0004g0080 a0001c0001t0004g0081 |
2 | HG02055.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.687+5511C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3162123 | |||||||
| chr3:3162154 | G | T | 1 | a0001c0003t0003g0091 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.687+5480C>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3162154 | |||||||
| chr3:3162196 | A | G | 1 | a0001c0001t0010g0038 | 2 | HG03491.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.687+5438T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3162196 | |||||||
| chr3:3162200 | T | C | 1 | a0001c0001t0003g0063 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.687+5434A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3162200 | |||||||
| chr3:3162242 | A | G | 1 | a0001c0003t0003g0091 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.687+5392T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3162242 | |||||||
| chr3:3162316 | C | T | 25 | a0001c0001t0003g0004 a0001c0001t0003g0015 a0001c0001t0003g0024 others(22): Show |
52 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.687+5318G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3162316 | |||||||
| chr3:3162347 | G | A | 3 | a0001c0001t0001g0037 a0001c0001t0003g0079 a0001c0001t0011g0035 |
5 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.687+5287C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3162347 | |||||||
| chr3:3162353 | C | G | 1 | a0001c0003t0003g0091 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.687+5281G>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3162353 | |||||||
| chr3:3162405 | G | A | 163 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0037 others(160): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.687+5229C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3162405 | |||||||
| chr3:3162408 | G | A | 1 | a0001c0002t0001g0123 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.687+5226C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3162408 | |||||||
| chr3:3162614 | T | A | 163 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0037 others(160): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.687+5020A>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3162614 | |||||||
| chr3:3162645 | C | T | 2 | a0001c0002t0001g0109 a0001c0002t0002g0108 |
2 | HG00099.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.687+4989G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3162645 | |||||||
| chr3:3162660 | T | C | 3 | a0001c0001t0001g0037 a0001c0001t0003g0079 a0001c0001t0011g0035 |
5 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.687+4974A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3162660 | |||||||
| chr3:3162694 | ACTTTAAG others(2): Show |
A | 4 | a0001c0001t0009g0059 a0001c0001t0009g0140 a0001c0001t0009g0141 others(1): Show |
4 | HG00280.hp2 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.687+4931_687+4939d others(11): Show |
CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3162694 | |||||||
| chr3:3162709 | T | G | 4 | a0001c0001t0009g0059 a0001c0001t0009g0140 a0001c0001t0009g0141 others(1): Show |
4 | HG00280.hp2 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.687+4925A>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3162709 | |||||||
| chr3:3162755 | G | C | 1 | a0001c0002t0001g0116 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.687+4879C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3162755 | |||||||
| chr3:3162791 | T | C | 8 | a0001c0002t0001g0011 a0001c0002t0001g0013 a0001c0002t0001g0027 others(5): Show |
21 | HG00438.hp2 HG02015.hp1 HG02040.hp2 others(18): Show |
intron_variant | MODIFIER | c.687+4843A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3162791 | |||||||
| chr3:3162928 | C | A | 1 | a0001c0001t0002g0047 | 2 | HG00323.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.687+4706G>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3162928 | |||||||
| chr3:3163016 | T | C | 147 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0039 others(144): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.687+4618A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3163016 | |||||||
| chr3:3163049 | G | A | 165 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0037 others(162): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.687+4585C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3163049 | |||||||
| chr3:3163071 | G | A | 1 | a0001c0001t0002g0148 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.687+4563C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3163071 | |||||||
| chr3:3163120 | T | C | 146 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0039 others(143): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.687+4514A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3163120 | |||||||
| chr3:3163122 | G | C | 1 | a0001c0003t0003g0091 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.687+4512C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3163122 | |||||||
| chr3:3163205 | T | C | 161 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0039 others(158): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.687+4429A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3163205 | |||||||
| chr3:3163238 | C | T | 1 | a0001c0001t0004g0030 | 2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.687+4396G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3163238 | |||||||
| chr3:3163258 | T | G | 1 | a0001c0001t0013g0131 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.687+4376A>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3163258 | |||||||
| chr3:3163274 | C | G | 1 | a0001c0001t0004g0030 | 2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.687+4360G>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3163274 | |||||||
| chr3:3163385 | C | T | 8 | a0001c0002t0001g0018 a0001c0002t0001g0041 a0001c0002t0001g0043 others(5): Show |
15 | HG00408.hp1 HG02080.hp1 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.687+4249G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3163385 | |||||||
| chr3:3163455 | C | CA | 64 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0039 others(61): Show |
144 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.687+4178dupT | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3163455 | |||||||
| chr3:3163458 | T | G | 64 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0039 others(61): Show |
144 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.687+4176A>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3163458 | |||||||
| chr3:3163662 | C | T | 1 | a0001c0001t0003g0065 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.687+3972G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3163662 | |||||||
| chr3:3163748 | G | C | 45 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(42): Show |
104 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.687+3886C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3163748 | |||||||
| chr3:3163771 | A | T | 1 | a0001c0001t0005g0051 | 2 | NA18956.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.687+3863T>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3163771 | |||||||
| chr3:3163831 | A | C | 35 | a0001c0001t0002g0074 a0001c0001t0002g0169 a0001c0001t0003g0004 others(32): Show |
71 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.687+3803T>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3163831 | |||||||
| chr3:3163832 | A | C | 1 | a0001c0001t0003g0072 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.687+3802T>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3163832 | |||||||
| chr3:3163840 | A | G | 159 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0039 others(156): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.687+3794T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3163840 | |||||||
| chr3:3163849 | T | C | 13 | a0001c0001t0003g0139 a0001c0001t0009g0059 a0001c0001t0009g0140 others(10): Show |
20 | HG00280.hp2 HG00609.hp2 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.687+3785A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3163849 | |||||||
| chr3:3163867 | C | G | 1 | a0001c0001t0006g0167 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.687+3767G>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3163867 | |||||||
| chr3:3164155 | C | T | 1 | a0001c0001t0002g0048 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.687+3479G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3164155 | |||||||
| chr3:3164235 | C | A | 2 | a0001c0001t0003g0139 a0001c0001t0012g0046 |
3 | HG02647.hp2 HG03098.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.687+3399G>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3164235 | |||||||
| chr3:3164401 | C | A | 1 | a0001c0001t0002g0029 | 3 | HG03098.hp1 HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.687+3233G>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3164401 | |||||||
| chr3:3164409 | C | T | 2 | a0001c0001t0002g0143 a0001c0001t0002g0151 |
2 | HG01074.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.687+3225G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3164409 | |||||||
| chr3:3164464 | G | C | 2 | a0001c0003t0007g0008 a0001c0003t0007g0054 |
8 | HG00609.hp2 HG02165.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.687+3170C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3164464 | |||||||
| chr3:3164478 | G | A | 2 | a0001c0001t0002g0161 a0001c0001t0002g0162 |
2 | HG02109.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.687+3156C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3164478 | |||||||
| chr3:3164511 | G | C | 2 | a0001c0001t0003g0139 a0001c0001t0012g0046 |
3 | HG02647.hp2 HG03098.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.687+3123C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3164511 | |||||||
| chr3:3164552 | G | C | 1 | a0001c0002t0001g0095 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.687+3082C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3164552 | |||||||
| chr3:3164597 | C | T | 40 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(37): Show |
96 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.687+3037G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3164597 | |||||||
| chr3:3164829 | C | T | 2 | a0001c0003t0007g0008 a0001c0003t0007g0054 |
8 | HG00609.hp2 HG02165.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.687+2805G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3164829 | |||||||
| chr3:3164872 | C | G | 1 | a0001c0001t0002g0047 | 2 | HG00323.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.687+2762G>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3164872 | |||||||
| chr3:3164929 | G | C | 1 | a0001c0002t0001g0085 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.687+2705C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3164929 | |||||||
| chr3:3164968 | C | T | 1 | a0001c0001t0004g0030 | 2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.687+2666G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3164968 | |||||||
| chr3:3165022 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.687+2612G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3165022 | |||||||
| chr3:3165075 | C | A | 1 | a0001c0002t0001g0119 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.687+2559G>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3165075 | |||||||
| chr3:3165086 | G | A | 1 | a0001c0001t0004g0030 | 2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.687+2548C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3165086 | |||||||
| chr3:3165149 | C | T | 1 | a0001c0001t0004g0030 | 2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.687+2485G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3165149 | |||||||
| chr3:3165198 | G | A | 2 | a0001c0001t0001g0037 a0001c0001t0011g0035 |
4 | HG01891.hp2 HG02257.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.687+2436C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3165198 | |||||||
| chr3:3165327 | G | C | 1 | a0001c0001t0003g0139 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.687+2307C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3165327 | |||||||
| chr3:3165363 | G | A | 1 | a0001c0001t0002g0160 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.687+2271C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3165363 | |||||||
| chr3:3165366 | G | A | 1 | a0001c0002t0001g0120 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.687+2268C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3165366 | |||||||
| chr3:3165422 | G | A | 161 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0039 others(158): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.687+2212C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3165422 | |||||||
| chr3:3165423 | T | C | 2 | a0001c0003t0007g0008 a0001c0003t0007g0054 |
8 | HG00609.hp2 HG02165.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.687+2211A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3165423 | |||||||
| chr3:3165670 | T | C | 1 | a0001c0002t0001g0099 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.687+1964A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3165670 | |||||||
| chr3:3165674 | G | C | 1 | a0001c0001t0004g0030 | 2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.687+1960C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3165674 | |||||||
| chr3:3165759 | C | T | 1 | a0001c0003t0007g0054 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.687+1875G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3165759 | |||||||
| chr3:3165775 | C | A | 1 | a0001c0001t0003g0066 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.687+1859G>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3165775 | |||||||
| chr3:3165791 | T | C | 4 | a0001c0001t0009g0059 a0001c0001t0009g0140 a0001c0001t0009g0141 others(1): Show |
4 | HG00280.hp2 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.687+1843A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3165791 | |||||||
| chr3:3165830 | C | G | 1 | a0001c0001t0003g0072 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.687+1804G>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3165830 | |||||||
| chr3:3165977 | A | C | 2 | a0001c0001t0004g0030 a0001c0001t0004g0058 |
3 | HG02109.hp1 HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.687+1657T>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3165977 | |||||||
| chr3:3166037 | G | C | 4 | a0001c0001t0003g0032 a0001c0001t0003g0033 a0001c0001t0003g0069 others(1): Show |
6 | HG02572.hp2 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.687+1597C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3166037 | |||||||
| chr3:3166037 | G | T | 1 | a0001c0001t0006g0060 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.687+1597C>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3166037 | |||||||
| chr3:3166054 | G | A | 1 | a0001c0001t0004g0083 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.687+1580C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3166054 | |||||||
| chr3:3166070 | T | C | 145 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0039 others(142): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.687+1564A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3166070 | |||||||
| chr3:3166081 | G | C | 4 | a0001c0001t0003g0032 a0001c0001t0003g0033 a0001c0001t0003g0069 others(1): Show |
6 | HG02572.hp2 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.687+1553C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3166081 | |||||||
| chr3:3166098 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.687+1536G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3166098 | |||||||
| chr3:3166164 | CAT | C | 70 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0039 others(67): Show |
160 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.687+1468_687+1469d others(4): Show |
CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3166164 | |||||||
| chr3:3166325 | G | A | 1 | a0001c0001t0002g0087 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.687+1309C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3166325 | |||||||
| chr3:3166467 | C | T | 2 | a0001c0003t0007g0008 a0001c0003t0007g0054 |
8 | HG00609.hp2 HG02165.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.687+1167G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3166467 | |||||||
| chr3:3166487 | C | A | 2 | a0001c0001t0004g0030 a0001c0001t0004g0058 |
3 | HG02109.hp1 HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.687+1147G>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3166487 | |||||||
| chr3:3166558 | G | C | 1 | a0001c0001t0004g0030 | 2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.687+1076C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3166558 | |||||||
| chr3:3166730 | A | G | 173 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0037 others(170): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.687+904T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3166730 | |||||||
| chr3:3166765 | A | C | 1 | a0001c0001t0002g0144 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.687+869T>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3166765 | |||||||
| chr3:3166790 | A | G | 5 | a0001c0001t0002g0005 a0001c0001t0002g0143 a0001c0001t0002g0151 others(2): Show |
13 | HG01074.hp2 HG01109.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.687+844T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3166790 | |||||||
| chr3:3166914 | G | C | 3 | a0001c0003t0003g0091 a0001c0004t0002g0026 a0001c0004t0002g0088 |
5 | HG02258.hp2 HG02559.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.687+720C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3166914 | |||||||
| chr3:3166935 | TA | T | 61 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0098 others(58): Show |
139 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.687+698delT | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3166935 | |||||||
| chr3:3166955 | G | A | 1 | a0001c0002t0001g0121 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.687+679C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3166955 | |||||||
| chr3:3167031 | T | C | 1 | a0001c0001t0004g0030 | 2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.687+603A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3167031 | |||||||
| chr3:3167047 | C | T | 38 | a0001c0001t0002g0074 a0001c0001t0002g0169 a0001c0001t0003g0004 others(35): Show |
75 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.687+587G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3167047 | |||||||
| chr3:3167048 | G | A | 60 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0039 others(57): Show |
139 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.687+586C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3167048 | |||||||
| chr3:3167050 | G | A | 1 | a0001c0002t0001g0043 | 2 | NA18967.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.687+584C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3167050 | |||||||
| chr3:3167078 | T | C | 161 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0039 others(158): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.687+556A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3167078 | |||||||
| chr3:3167365 | C | T | 1 | a0001c0003t0003g0091 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.687+269G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3167365 | |||||||
| chr3:3167373 | T | A | 4 | a0001c0002t0001g0003 a0001c0002t0001g0097 a0001c0002t0001g0122 others(1): Show |
16 | HG00423.hp1 HG00544.hp1 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.687+261A>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3167373 | |||||||
| chr3:3167388 | G | A | 1 | a0001c0002t0001g0124 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.687+246C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3167388 | |||||||
| chr3:3167558 | G | T | 19 | a0001c0001t0003g0004 a0001c0001t0003g0024 a0001c0001t0003g0031 others(16): Show |
41 | HG00140.hp1 HG00280.hp1 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.687+76C>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3167558 | |||||||
| chr3:3167578 | G | GA | 3 | a0001c0001t0002g0163 a0001c0001t0003g0015 a0001c0001t0003g0077 |
7 | HG00438.hp1 HG02155.hp2 HG04204.hp1 others(4): Show |
intron_variant | MODIFIER | c.687+55dupT | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 5/10 | chr3 | 3167578 | |||||||
| chr3:3167834 | T | C | 3 | a0001c0003t0003g0091 a0001c0004t0002g0026 a0001c0004t0002g0088 |
5 | HG02258.hp2 HG02559.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.528-41A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3167834 | |||||||
| chr3:3167971 | A | T | 80 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(77): Show |
173 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.528-178T>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3167971 | |||||||
| chr3:3168109 | C | A | 10 | a0001c0001t0002g0169 a0001c0001t0005g0014 a0001c0001t0005g0023 others(7): Show |
20 | HG00423.hp2 HG01106.hp2 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.528-316G>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3168109 | |||||||
| chr3:3168153 | A | G | 1 | a0001c0002t0001g0012 | 6 | HG01261.hp2 HG01975.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.528-360T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3168153 | |||||||
| chr3:3168156 | C | A | 1 | a0001c0001t0004g0030 | 2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.528-363G>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3168156 | |||||||
| chr3:3168158 | C | T | 1 | a0001c0001t0004g0030 | 2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.528-365G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3168158 | |||||||
| chr3:3168159 | C | T | 1 | a0001c0001t0004g0030 | 2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.528-366G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3168159 | |||||||
| chr3:3168161 | A | G | 1 | a0001c0001t0004g0030 | 2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.528-368T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3168161 | |||||||
| chr3:3168224 | CATCTA | C | 3 | a0001c0001t0001g0037 a0001c0001t0003g0079 a0001c0001t0011g0035 |
5 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.528-436_528-432del others(5): Show |
CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3168224 | |||||||
| chr3:3168225 | A | T | 1 | a0001c0001t0006g0060 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.528-432T>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3168225 | |||||||
| chr3:3168348 | T | G | 67 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0039 others(64): Show |
147 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.528-555A>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3168348 | |||||||
| chr3:3168489 | G | A | 1 | a0001c0001t0002g0162 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.528-696C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3168489 | |||||||
| chr3:3168500 | G | A | 2 | a0001c0001t0004g0080 a0001c0001t0004g0081 |
2 | HG02055.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.528-707C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3168500 | |||||||
| chr3:3168521 | T | C | 1 | a0001c0002t0001g0044 | 2 | NA19005.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.528-728A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3168521 | |||||||
| chr3:3168625 | T | C | 3 | a0001c0001t0001g0037 a0001c0001t0003g0079 a0001c0001t0011g0035 |
5 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.528-832A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3168625 | |||||||
| chr3:3168652 | T | G | 45 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(42): Show |
104 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.528-859A>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3168652 | |||||||
| chr3:3168892 | TC | T | 2 | a0001c0004t0002g0026 a0001c0004t0002g0088 |
4 | HG02559.hp1 HG02717.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.528-1100delG | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3168892 | |||||||
| chr3:3168921 | T | C | 2 | a0001c0001t0002g0161 a0001c0001t0002g0162 |
2 | HG02109.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.528-1128A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3168921 | |||||||
| chr3:3168928 | A | C | 1 | a0001c0001t0001g0021 | 4 | HG00597.hp1 HG02738.hp2 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.528-1135T>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3168928 | |||||||
| chr3:3169015 | T | C | 2 | a0001c0003t0007g0008 a0001c0003t0007g0054 |
8 | HG00609.hp2 HG02165.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.528-1222A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3169015 | |||||||
| chr3:3169059 | T | C | 1 | a0001c0001t0004g0030 | 2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.528-1266A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3169059 | |||||||
| chr3:3169093 | C | G | 1 | a0001c0001t0012g0046 | 2 | HG02647.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.528-1300G>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3169093 | |||||||
| chr3:3169103 | A | T | 2 | a0001c0002t0001g0041 a0001c0002t0001g0103 |
3 | NA18998.hp1 NA19011.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.528-1310T>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3169103 | |||||||
| chr3:3169140 | C | T | 1 | a0001c0001t0003g0066 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.528-1347G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3169140 | |||||||
| chr3:3169157 | T | C | 13 | a0001c0001t0002g0029 a0001c0001t0002g0147 a0001c0001t0002g0148 others(10): Show |
16 | HG00280.hp2 HG01106.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.528-1364A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3169157 | |||||||
| chr3:3169189 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.528-1396A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3169189 | |||||||
| chr3:3169210 | T | G | 2 | a0001c0001t0002g0147 a0001c0001t0002g0148 |
2 | HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.528-1417A>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3169210 | |||||||
| chr3:3169233 | A | G | 1 | a0001c0001t0009g0140 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.528-1440T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3169233 | |||||||
| chr3:3169368 | A | G | 1 | a0001c0001t0002g0163 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.528-1575T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3169368 | |||||||
| chr3:3169474 | A | ATAG | 147 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0039 others(144): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.528-1684_528-1682d others(5): Show |
CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3169474 | |||||||
| chr3:3169535 | T | G | 1 | a0001c0001t0004g0030 | 2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.528-1742A>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3169535 | |||||||
| chr3:3169650 | T | C | 1 | a0001c0001t0004g0030 | 2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.528-1857A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3169650 | |||||||
| chr3:3169685 | A | C | 10 | a0001c0001t0002g0169 a0001c0001t0005g0014 a0001c0001t0005g0023 others(7): Show |
20 | HG00423.hp2 HG01106.hp2 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.528-1892T>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3169685 | |||||||
| chr3:3169788 | A | T | 42 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(39): Show |
99 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.528-1995T>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3169788 | |||||||
| chr3:3169831 | T | C | 42 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(39): Show |
99 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.528-2038A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3169831 | |||||||
| chr3:3169871 | C | G | 23 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0020 others(20): Show |
64 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.528-2078G>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3169871 | |||||||
| chr3:3169888 | G | A | 2 | a0001c0004t0002g0026 a0001c0004t0002g0088 |
4 | HG02559.hp1 HG02717.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.528-2095C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3169888 | |||||||
| chr3:3169896 | T | TA | 146 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0039 others(143): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.528-2104dupT | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3169896 | |||||||
| chr3:3169936 | C | G | 45 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(42): Show |
102 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.528-2143G>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3169936 | |||||||
| chr3:3170102 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.528-2309G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3170102 | |||||||
| chr3:3170307 | G | A | 1 | a0001c0003t0003g0091 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.527+2469C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3170307 | |||||||
| chr3:3170322 | A | C | 2 | a0001c0002t0001g0100 a0001c0002t0003g0101 |
2 | HG03688.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.527+2454T>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3170322 | |||||||
| chr3:3170454 | C | G | 3 | a0001c0001t0001g0037 a0001c0001t0003g0079 a0001c0001t0011g0035 |
5 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.527+2322G>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3170454 | |||||||
| chr3:3170570 | T | C | 1 | a0001c0001t0002g0163 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.527+2206A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3170570 | |||||||
| chr3:3170582 | C | T | 1 | a0001c0002t0001g0099 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.527+2194G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3170582 | |||||||
| chr3:3170609 | T | C | 1 | a0001c0002t0001g0126 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.527+2167A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3170609 | |||||||
| chr3:3170745 | A | G | 10 | a0001c0001t0003g0139 a0001c0001t0009g0059 a0001c0001t0009g0140 others(7): Show |
11 | HG00280.hp2 HG01106.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.527+2031T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3170745 | |||||||
| chr3:3170816 | T | C | 1 | a0001c0002t0001g0127 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.527+1960A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3170816 | |||||||
| chr3:3170931 | T | A | 165 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0037 others(162): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.527+1845A>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3170931 | |||||||
| chr3:3170946 | C | T | 1 | a0001c0001t0002g0150 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.527+1830G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3170946 | |||||||
| chr3:3170962 | T | C | 146 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0039 others(143): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.527+1814A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3170962 | |||||||
| chr3:3170976 | T | C | 146 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0039 others(143): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.527+1800A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3170976 | |||||||
| chr3:3171052 | G | A | 1 | a0001c0004t0008g0137 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.527+1724C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3171052 | |||||||
| chr3:3171070 | A | G | 147 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0039 others(144): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.527+1706T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3171070 | |||||||
| chr3:3171215 | T | C | 15 | a0001c0001t0003g0139 a0001c0001t0004g0084 a0001c0001t0009g0059 others(12): Show |
24 | HG00280.hp2 HG00609.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.527+1561A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3171215 | |||||||
| chr3:3171302 | T | C | 1 | a0001c0001t0002g0166 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.527+1474A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3171302 | |||||||
| chr3:3171578 | A | G | 164 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0037 others(161): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.527+1198T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3171578 | |||||||
| chr3:3171586 | T | G | 11 | a0001c0001t0002g0169 a0001c0001t0003g0062 a0001c0001t0005g0014 others(8): Show |
21 | HG00423.hp2 HG01106.hp2 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.527+1190A>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3171586 | |||||||
| chr3:3171618 | A | T | 2 | a0001c0003t0007g0008 a0001c0003t0007g0054 |
8 | HG00609.hp2 HG02165.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.527+1158T>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3171618 | |||||||
| chr3:3171857 | G | C | 1 | a0001c0001t0004g0017 | 5 | HG02647.hp1 HG02723.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.527+919C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3171857 | |||||||
| chr3:3171997 | G | A | 165 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0037 others(162): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.527+779C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3171997 | |||||||
| chr3:3172005 | G | A | 39 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(36): Show |
96 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.527+771C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3172005 | |||||||
| chr3:3172037 | T | C | 1 | a0001c0002t0001g0128 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.527+739A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3172037 | |||||||
| chr3:3172091 | G | A | 24 | a0001c0001t0002g0074 a0001c0001t0003g0004 a0001c0001t0003g0015 others(21): Show |
50 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.527+685C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3172091 | |||||||
| chr3:3172103 | C | A | 1 | a0001c0002t0001g0129 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.527+673G>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3172103 | |||||||
| chr3:3172127 | T | A | 79 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(76): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.527+649A>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3172127 | |||||||
| chr3:3172146 | T | C | 1 | a0001c0001t0002g0164 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.527+630A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3172146 | |||||||
| chr3:3172653 | A | G | 1 | a0001c0001t0002g0149 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.527+123T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3172653 | |||||||
| chr3:3172704 | A | G | 1 | a0001c0002t0001g0040 | 2 | NA18970.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.527+72T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3172704 | |||||||
| chr3:3172770 | T | G | 1 | a0001c0002t0001g0130 | 1 | NA18953.hp2 | splice_region_variant&intron_variant | LOW | c.527+6A>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 4/10 | chr3 | 3172770 | |||||||
| chr3:3173052 | T | TTTTA | 8 | a0001c0003t0007g0008 a0001c0003t0007g0054 a0001c0004t0002g0026 others(5): Show |
16 | HG00609.hp2 HG01106.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.378-131_378-128dup others(4): Show |
CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 3/10 | chr3 | 3173052 | |||||||
| chr3:3173088 | C | T | 48 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(45): Show |
112 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.378-163G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 3/10 | chr3 | 3173088 | |||||||
| chr3:3173184 | A | C | 1 | a0001c0001t0003g0065 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.378-259T>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 3/10 | chr3 | 3173184 | |||||||
| chr3:3173247 | G | A | 6 | a0001c0004t0002g0026 a0001c0004t0002g0088 a0001c0004t0008g0094 others(3): Show |
8 | HG01106.hp1 HG01175.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.378-322C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 3/10 | chr3 | 3173247 | |||||||
| chr3:3173403 | T | G | 2 | a0001c0002t0001g0045 a0001c0002t0001g0132 |
3 | NA18947.hp2 NA19006.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.378-478A>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 3/10 | chr3 | 3173403 | |||||||
| chr3:3173571 | G | A | 2 | a0001c0003t0007g0008 a0001c0003t0007g0054 |
8 | HG00609.hp2 HG02165.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.377+488C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 3/10 | chr3 | 3173571 | |||||||
| chr3:3173843 | T | C | 1 | a0001c0001t0013g0131 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.377+216A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 3/10 | chr3 | 3173843 | |||||||
| chr3:3173924 | C | T | 2 | a0001c0001t0001g0039 a0001c0001t0001g0098 |
3 | HG02055.hp2 HG02486.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.377+135G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 3/10 | chr3 | 3173924 | |||||||
| chr3:3173955 | C | G | 1 | a0001c0001t0003g0064 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.377+104G>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 3/10 | chr3 | 3173955 | |||||||
| chr3:3173993 | C | A | 1 | a0001c0001t0003g0062 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.377+66G>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 3/10 | chr3 | 3173993 | |||||||
| chr3:3174032 | T | G | 1 | a0001c0002t0001g0132 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.377+27A>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 3/10 | chr3 | 3174032 | |||||||
| chr3:3174047 | C | G | 1 | a0001c0001t0001g0134 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.377+12G>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 3/10 | chr3 | 3174047 | |||||||
| chr3:3174270 | A | G | 161 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0039 others(158): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.175-9T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 2/10 | chr3 | 3174270 | |||||||
| chr3:3174302 | T | C | 1 | a0001c0002t0001g0133 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.175-41A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 2/10 | chr3 | 3174302 | |||||||
| chr3:3174372 | G | A | 5 | a0001c0001t0003g0139 a0001c0001t0009g0140 a0001c0001t0009g0141 others(2): Show |
6 | HG00280.hp2 HG02615.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.175-111C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 2/10 | chr3 | 3174372 | |||||||
| chr3:3174594 | T | C | 1 | a0001c0001t0003g0075 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.175-333A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 2/10 | chr3 | 3174594 | |||||||
| chr3:3174635 | A | C | 4 | a0001c0004t0008g0094 a0001c0004t0008g0135 a0001c0004t0008g0136 others(1): Show |
4 | HG01106.hp1 HG01175.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.175-374T>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 2/10 | chr3 | 3174635 | |||||||
| chr3:3174684 | TAATA | T | 80 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(77): Show |
173 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.175-427_175-424del others(4): Show |
CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 2/10 | chr3 | 3174684 | |||||||
| chr3:3174732 | C | T | 1 | a0001c0002t0001g0027 | 3 | HG02015.hp1 HG02040.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.174+431G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 2/10 | chr3 | 3174732 | |||||||
| chr3:3174791 | T | C | 80 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(77): Show |
173 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.174+372A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 2/10 | chr3 | 3174791 | |||||||
| chr3:3174876 | T | C | 1 | a0001c0001t0001g0134 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.174+287A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 2/10 | chr3 | 3174876 | |||||||
| chr3:3174913 | G | T | 1 | a0002c0005t0003g0076 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.174+250C>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 2/10 | chr3 | 3174913 | |||||||
| chr3:3174938 | C | T | 81 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(78): Show |
175 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.174+225G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 2/10 | chr3 | 3174938 | |||||||
| chr3:3175030 | T | A | 80 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(77): Show |
173 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.174+133A>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 2/10 | chr3 | 3175030 | |||||||
| chr3:3175032 | G | T | 80 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(77): Show |
173 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.174+131C>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 2/10 | chr3 | 3175032 | |||||||
| chr3:3175033 | C | T | 80 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(77): Show |
173 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.174+130G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 2/10 | chr3 | 3175033 | |||||||
| chr3:3175037 | T | TGAGG | 80 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(77): Show |
173 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.174+125_174+126ins others(4): Show |
CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 2/10 | chr3 | 3175037 | |||||||
| chr3:3175039 | G | C | 80 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(77): Show |
173 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.174+124C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 2/10 | chr3 | 3175039 | |||||||
| chr3:3175040 | C | T | 80 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(77): Show |
173 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.174+123G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 2/10 | chr3 | 3175040 | |||||||
| chr3:3175041 | C | A | 80 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(77): Show |
173 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.174+122G>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 2/10 | chr3 | 3175041 | |||||||
| chr3:3175292 | GA | G | 7 | a0001c0001t0002g0147 a0001c0001t0002g0148 a0001c0001t0012g0046 others(4): Show |
16 | HG00609.hp2 HG02165.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.68-24delT | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3175292 | |||||||
| chr3:3175301 | A | C | 1 | a0001c0001t0005g0050 | 2 | HG01261.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.68-32T>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3175301 | |||||||
| chr3:3175351 | G | A | 10 | a0001c0001t0002g0169 a0001c0001t0005g0014 a0001c0001t0005g0023 others(7): Show |
20 | HG00423.hp2 HG01106.hp2 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.68-82C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3175351 | |||||||
| chr3:3175444 | AT | A | 159 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0039 others(156): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.68-176delA | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3175444 | |||||||
| chr3:3175780 | C | A | 1 | a0001c0001t0004g0030 | 2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.68-511G>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3175780 | |||||||
| chr3:3175788 | G | C | 14 | a0001c0001t0003g0139 a0001c0001t0009g0059 a0001c0001t0009g0140 others(11): Show |
23 | HG00280.hp2 HG00609.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.68-519C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3175788 | |||||||
| chr3:3175887 | CT | C | 2 | a0001c0001t0003g0139 a0001c0001t0012g0046 |
3 | HG02647.hp2 HG03098.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.68-619delA | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3175887 | |||||||
| chr3:3175993 | C | A | 77 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(74): Show |
168 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.68-724G>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3175993 | |||||||
| chr3:3175998 | G | C | 3 | a0001c0001t0009g0140 a0001c0001t0009g0141 a0001c0001t0009g0142 |
3 | HG00280.hp2 HG02615.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.68-729C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3175998 | |||||||
| chr3:3176006 | C | T | 3 | a0001c0001t0001g0037 a0001c0001t0003g0079 a0001c0001t0011g0035 |
5 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-737G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3176006 | |||||||
| chr3:3176065 | G | C | 1 | a0002c0005t0003g0076 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.68-796C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3176065 | |||||||
| chr3:3176089 | C | T | 1 | a0001c0001t0003g0031 | 2 | HG01109.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.68-820G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3176089 | |||||||
| chr3:3176244 | A | C | 67 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0039 others(64): Show |
147 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.68-975T>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3176244 | |||||||
| chr3:3176321 | A | T | 1 | a0001c0002t0001g0097 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.68-1052T>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3176321 | |||||||
| chr3:3176345 | A | C | 1 | a0001c0002t0001g0096 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.68-1076T>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3176345 | |||||||
| chr3:3176382 | G | A | 1 | a0001c0001t0002g0052 | 2 | HG00639.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.68-1113C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3176382 | |||||||
| chr3:3176412 | GACA | G | 3 | a0001c0001t0009g0140 a0001c0001t0009g0141 a0001c0001t0009g0142 |
3 | HG00280.hp2 HG02615.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.68-1146_68-1144del others(3): Show |
CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3176412 | |||||||
| chr3:3176558 | C | A | 2 | a0001c0004t0002g0026 a0001c0004t0002g0088 |
4 | HG02559.hp1 HG02717.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-1289G>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3176558 | |||||||
| chr3:3176593 | G | A | 2 | a0001c0001t0003g0139 a0001c0001t0012g0046 |
3 | HG02647.hp2 HG03098.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.68-1324C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3176593 | |||||||
| chr3:3176607 | G | A | 1 | a0001c0001t0003g0139 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.68-1338C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3176607 | |||||||
| chr3:3176715 | G | A | 2 | a0001c0001t0003g0015 a0001c0001t0003g0077 |
6 | HG00438.hp1 HG02155.hp2 NA19056.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-1446C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3176715 | |||||||
| chr3:3176799 | A | C | 1 | a0001c0001t0004g0030 | 2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.68-1530T>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3176799 | |||||||
| chr3:3176853 | C | T | 2 | a0001c0003t0007g0008 a0001c0003t0007g0054 |
8 | HG00609.hp2 HG02165.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.68-1584G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3176853 | |||||||
| chr3:3177007 | G | C | 1 | a0001c0001t0002g0171 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.68-1738C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3177007 | |||||||
| chr3:3177009 | G | T | 1 | a0001c0001t0002g0144 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.68-1740C>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3177009 | |||||||
| chr3:3177147 | G | GA | 28 | a0001c0001t0002g0061 a0001c0001t0002g0074 a0001c0001t0002g0172 others(25): Show |
54 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.68-1879dupT | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3177147 | |||||||
| chr3:3177501 | T | C | 2 | a0001c0003t0007g0008 a0001c0003t0007g0054 |
8 | HG00609.hp2 HG02165.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+2120A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3177501 | |||||||
| chr3:3177644 | T | C | 1 | a0001c0001t0004g0030 | 2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.67+1977A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3177644 | |||||||
| chr3:3177732 | T | C | 1 | a0001c0001t0003g0078 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.67+1889A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3177732 | |||||||
| chr3:3177737 | T | C | 8 | a0001c0001t0004g0016 a0001c0001t0004g0017 a0001c0001t0004g0058 others(5): Show |
16 | HG02055.hp1 HG02258.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.67+1884A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3177737 | |||||||
| chr3:3177793 | A | G | 5 | a0001c0001t0001g0037 a0001c0001t0003g0079 a0001c0001t0011g0035 others(2): Show |
9 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.67+1828T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3177793 | |||||||
| chr3:3177827 | T | C | 3 | a0001c0001t0009g0140 a0001c0001t0009g0141 a0001c0001t0009g0142 |
3 | HG00280.hp2 HG02615.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.67+1794A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3177827 | |||||||
| chr3:3177981 | C | T | 164 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0037 others(161): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.67+1640G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3177981 | |||||||
| chr3:3178016 | AC | A | 54 | a0001c0001t0005g0138 a0001c0002t0001g0001 a0001c0002t0001g0003 others(51): Show |
124 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.67+1604delG | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3178016 | |||||||
| chr3:3178017 | C | CA | 26 | a0001c0001t0002g0061 a0001c0001t0002g0074 a0001c0001t0002g0146 others(23): Show |
51 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.67+1603dupT | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3178017 | |||||||
| chr3:3178017 | CA | C | 3 | a0001c0001t0009g0141 a0001c0003t0007g0008 a0001c0003t0007g0054 |
9 | HG00609.hp2 HG02165.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.67+1603delT | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3178017 | |||||||
| chr3:3178019 | A | C | 1 | a0001c0002t0001g0095 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.67+1602T>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3178019 | |||||||
| chr3:3178027 | A | C | 1 | a0001c0003t0003g0091 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.67+1594T>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3178027 | |||||||
| chr3:3178048 | C | T | 1 | a0001c0001t0002g0143 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.67+1573G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3178048 | |||||||
| chr3:3178058 | C | G | 1 | a0001c0004t0008g0094 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.67+1563G>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3178058 | |||||||
| chr3:3178094 | G | A | 1 | a0001c0001t0001g0021 | 4 | HG00597.hp1 HG02738.hp2 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+1527C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3178094 | |||||||
| chr3:3178202 | T | C | 6 | a0001c0001t0004g0016 a0001c0001t0004g0017 a0001c0001t0004g0058 others(3): Show |
14 | HG02258.hp1 HG02559.hp2 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.67+1419A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3178202 | |||||||
| chr3:3178394 | T | C | 1 | a0001c0001t0005g0173 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.67+1227A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3178394 | |||||||
| chr3:3178450 | A | AC | 30 | a0001c0001t0002g0061 a0001c0001t0002g0074 a0001c0001t0003g0004 others(27): Show |
57 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.67+1170dupG | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3178450 | |||||||
| chr3:3178540 | T | C | 1 | a0001c0001t0001g0037 | 2 | HG03130.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.67+1081A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3178540 | |||||||
| chr3:3178705 | C | A | 1 | a0001c0001t0004g0030 | 2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.67+916G>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3178705 | |||||||
| chr3:3178714 | A | T | 1 | a0001c0001t0009g0059 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.67+907T>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3178714 | |||||||
| chr3:3178720 | C | A | 1 | a0001c0001t0004g0030 | 2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.67+901G>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3178720 | |||||||
| chr3:3178734 | T | G | 29 | a0001c0001t0002g0061 a0001c0001t0002g0074 a0001c0001t0003g0004 others(26): Show |
55 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.67+887A>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3178734 | |||||||
| chr3:3178750 | G | A | 1 | a0001c0001t0002g0174 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.67+871C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3178750 | |||||||
| chr3:3178789 | G | C | 24 | a0001c0001t0002g0074 a0001c0001t0003g0004 a0001c0001t0003g0015 others(21): Show |
50 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.67+832C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3178789 | |||||||
| chr3:3178804 | A | G | 1 | a0001c0002t0001g0093 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.67+817T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3178804 | |||||||
| chr3:3178805 | T | C | 53 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(50): Show |
120 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.67+816A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3178805 | |||||||
| chr3:3178887 | A | C | 161 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0039 others(158): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.67+734T>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3178887 | |||||||
| chr3:3178887 | A | T | 1 | a0001c0001t0005g0092 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.67+734T>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3178887 | |||||||
| chr3:3178950 | G | C | 128 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0039 others(125): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.67+671C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3178950 | |||||||
| chr3:3179045 | G | C | 2 | a0001c0003t0007g0008 a0001c0003t0007g0054 |
8 | HG00609.hp2 HG02165.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+576C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3179045 | |||||||
| chr3:3179067 | G | T | 1 | a0001c0002t0001g0090 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.67+554C>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3179067 | |||||||
| chr3:3179201 | T | C | 1 | a0001c0002t0001g0175 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.67+420A>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3179201 | |||||||
| chr3:3179318 | G | C | 1 | a0001c0002t0001g0176 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.67+303C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3179318 | |||||||
| chr3:3179339 | CT | C | 3 | a0001c0001t0002g0089 a0001c0004t0002g0026 a0001c0004t0002g0088 |
5 | HG02559.hp1 HG02717.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+281delA | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3179339 | |||||||
| chr3:3179343 | G | C | 1 | a0001c0001t0002g0053 | 2 | HG02135.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.67+278C>G | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3179343 | |||||||
| chr3:3179376 | G | A | 123 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0039 others(120): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.67+245C>T | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3179376 | |||||||
| chr3:3179414 | A | G | 1 | a0001c0001t0004g0057 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.67+207T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3179414 | |||||||
| chr3:3179443 | A | G | 1 | a0001c0002t0001g0056 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.67+178T>C | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3179443 | |||||||
| chr3:3179527 | C | T | 1 | a0001c0002t0001g0055 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.67+94G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3179527 | |||||||
| chr3:3179544 | C | T | 2 | a0001c0003t0007g0008 a0001c0003t0007g0054 |
8 | HG00609.hp2 HG02165.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+77G>A | CRBN | ENSG00000113851.16 | transcript | ENST00000231948.9 | protein_coding | 1/10 | chr3 | 3179544 |