Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 160492 |
| ensemblid | ENSG00000152936.11 |
| hgncid | 26683 |
| symbol | LMNTD1 |
| name | lamin tail domain containing 1 |
| refseq_nuc | NM_001145728.2 |
| refseq_prot | NP_001139200.1 |
| ensembl_nuc | ENST00000458174.7 |
| ensembl_prot | ENSP00000407353.2 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 25476082 |
| end | 25553283 |
| strand | - |
| ver | v1.2 |
| region | chr12:25476082-25553283 |
| region5000 | chr12:25471082-25558283 |
| regionname0 | LMNTD1_chr12_25476082_25553283 |
| regionname5000 | LMNTD1_chr12_25471082_25558283 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 409 | 289 | 42 | 55 | 156 | 8 | 27 | 127 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | MKDTQ others(404): Show |
chr12 | 25471082 | 25558283 |
| a0002 | 1/0 | 409 | 87 | 36 | 18 | 13 | 4 | 15 | 6 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | MKDTQ others(404): Show |
chr12 | 25471082 | 25558283 |
| a0003 | 0/0 | 409 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | MKDTQ others(404): Show |
chr12 | 25471082 | 25558283 |
| a0004 | 0/0 | 409 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | MKDTQ others(404): Show |
chr12 | 25471082 | 25558283 |
| a0005 | 0/0 | 409 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | MKDTQ others(404): Show |
chr12 | 25471082 | 25558283 |
| a0006 | 0/0 | 409 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | MKDTQ others(404): Show |
chr12 | 25471082 | 25558283 |
| a0007 | 0/0 | 409 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | MKDTQ others(404): Show |
chr12 | 25471082 | 25558283 |
| a0008 | 0/0 | 409 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | MKDTQ others(404): Show |
chr12 | 25471082 | 25558283 |
| a0009 | 0/0 | 409 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | MKDTQ others(404): Show |
chr12 | 25471082 | 25558283 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1227 | 280 | 39 | 55 | 150 | 8 | 27 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | ATGAA others(1222): Show |
chr12 | 25471082 | 25558283 | ||
| a0001c0004 | 0/0 | 1227 | 5 | 0 | 0 | 5 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | ATGAA others(1222): Show |
chr12 | 25471082 | 25558283 | ||
| a0001c0007 | 0/0 | 1227 | 2 | 2 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | ATGAA others(1222): Show |
chr12 | 25471082 | 25558283 | ||
| a0001c0010 | 0/0 | 1227 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | ATGAA others(1222): Show |
chr12 | 25471082 | 25558283 | ||
| a0001c0015 | 0/0 | 1227 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | ATGAA others(1222): Show |
chr12 | 25471082 | 25558283 | ||
| a0002c0002 | 1/0 | 1227 | 78 | 34 | 15 | 12 | 2 | 14 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | ATGAA others(1222): Show |
chr12 | 25471082 | 25558283 | ||
| a0002c0003 | 0/0 | 1227 | 8 | 1 | 3 | 1 | 2 | 1 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | ATGAA others(1222): Show |
chr12 | 25471082 | 25558283 | ||
| a0002c0014 | 0/0 | 1227 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | ATGAA others(1222): Show |
chr12 | 25471082 | 25558283 | ||
| a0003c0005 | 0/0 | 1227 | 4 | 4 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | ATGAA others(1222): Show |
chr12 | 25471082 | 25558283 | ||
| a0004c0006 | 0/0 | 1227 | 3 | 0 | 2 | 0 | 0 | 1 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | ATGAA others(1222): Show |
chr12 | 25471082 | 25558283 | ||
| a0005c0008 | 0/0 | 1227 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | ATGAA others(1222): Show |
chr12 | 25471082 | 25558283 | ||
| a0006c0012 | 0/0 | 1227 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | ATGAA others(1222): Show |
chr12 | 25471082 | 25558283 | ||
| a0007c0011 | 0/0 | 1227 | 1 | 0 | 0 | 0 | 0 | 1 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | ATGAA others(1222): Show |
chr12 | 25471082 | 25558283 | ||
| a0008c0013 | 0/0 | 1227 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | ATGAA others(1222): Show |
chr12 | 25471082 | 25558283 | ||
| a0009c0009 | 0/0 | 1227 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | ATGAA others(1222): Show |
chr12 | 25471082 | 25558283 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1876 | 205 | 24 | 44 | 111 | 5 | 20 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | GTAGT others(1871): Show |
chr12 | 25471082 | 25558283 |
| a0001c0001t0002 | 0/0 | 1876 | 73 | 14 | 11 | 38 | 3 | 7 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | GTAGT others(1871): Show |
chr12 | 25471082 | 25558283 |
| a0001c0001t0003 | 0/0 | 1876 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | GTAGT others(1871): Show |
chr12 | 25471082 | 25558283 |
| a0001c0001t0004 | 0/0 | 1876 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | GTAGT others(1871): Show |
chr12 | 25471082 | 25558283 |
| a0001c0004t0001 | 0/0 | 1876 | 5 | 0 | 0 | 5 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | GTAGT others(1871): Show |
chr12 | 25471082 | 25558283 |
| a0001c0007t0003 | 0/0 | 1876 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | GTAGT others(1871): Show |
chr12 | 25471082 | 25558283 |
| a0001c0007t0004 | 0/0 | 1876 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | GTAGT others(1871): Show |
chr12 | 25471082 | 25558283 |
| a0001c0010t0001 | 0/0 | 1876 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | GTAGT others(1871): Show |
chr12 | 25471082 | 25558283 |
| a0001c0015t0001 | 0/0 | 1876 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | GTAGT others(1871): Show |
chr12 | 25471082 | 25558283 |
| a0002c0002t0001 | 0/0 | 1876 | 12 | 3 | 2 | 3 | 0 | 4 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | GTAGT others(1871): Show |
chr12 | 25471082 | 25558283 |
| a0002c0002t0002 | 1/0 | 1876 | 66 | 31 | 13 | 9 | 2 | 10 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | GTAGT others(1871): Show |
chr12 | 25471082 | 25558283 |
| a0002c0003t0002 | 0/0 | 1876 | 7 | 1 | 2 | 1 | 2 | 1 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | GTAGT others(1871): Show |
chr12 | 25471082 | 25558283 |
| a0002c0003t0005 | 0/0 | 1876 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | GTAGT others(1871): Show |
chr12 | 25471082 | 25558283 |
| a0002c0014t0001 | 0/0 | 1876 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | GTAGT others(1871): Show |
chr12 | 25471082 | 25558283 |
| a0003c0005t0001 | 0/0 | 1876 | 3 | 3 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | GTAGT others(1871): Show |
chr12 | 25471082 | 25558283 |
| a0003c0005t0003 | 0/0 | 1876 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | GTAGT others(1871): Show |
chr12 | 25471082 | 25558283 |
| a0004c0006t0001 | 0/0 | 1876 | 3 | 0 | 2 | 0 | 0 | 1 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | GTAGT others(1871): Show |
chr12 | 25471082 | 25558283 |
| a0005c0008t0001 | 0/0 | 1876 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | GTAGT others(1871): Show |
chr12 | 25471082 | 25558283 |
| a0006c0012t0001 | 0/0 | 1876 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | GTAGT others(1871): Show |
chr12 | 25471082 | 25558283 |
| a0007c0011t0002 | 0/0 | 1876 | 1 | 0 | 0 | 0 | 0 | 1 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | GTAGT others(1871): Show |
chr12 | 25471082 | 25558283 |
| a0008c0013t0003 | 0/0 | 1876 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | GTAGT others(1871): Show |
chr12 | 25471082 | 25558283 |
| a0009c0009t0001 | 0/0 | 1876 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | GTAGT others(1871): Show |
chr12 | 25471082 | 25558283 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0298 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0003g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0001t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0004t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0004t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0004t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0004t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0004t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0007t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0007t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0010t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0001c0015t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0001g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0012 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0127 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0003t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0003t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0003t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0003t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0003t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0003t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0003t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0003t0005g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0002c0014t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0003c0005t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0003c0005t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0003c0005t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0003c0005t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0004c0006t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0004c0006t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0004c0006t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0005c0008t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0006c0012t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0007c0011t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0008c0013t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| a0009c0009t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0010 | EUR | GBR | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0242 | EUR | GBR | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG00280 | hp1 | a0002 | c0002 | t0002 | g0118 | EUR | FIN | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0258 | EUR | FIN | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | CHS | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | CHS | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | CHS | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | CHS | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | CHS | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | CHS | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | CHS | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | CHS | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | PUR | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG00642 | hp1 | a0002 | c0003 | t0002 | g0030 | AMR | PUR | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | CHS | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG00735 | hp2 | a0002 | c0002 | t0002 | g0120 | AMR | PUR | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG00738 | hp1 | a0002 | c0002 | t0002 | g0139 | AMR | PUR | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0082 | AMR | PUR | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0344 | AMR | PUR | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG00741 | hp2 | a0002 | c0003 | t0005 | g0050 | AMR | PUR | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01069 | hp1 | a0002 | c0002 | t0002 | g0132 | AMR | PUR | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0301 | AMR | PUR | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | PUR | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0089 | AMR | PUR | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01081 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0072 | AMR | PUR | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01167 | hp1 | a0002 | c0002 | t0002 | g0005 | AMR | PUR | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0335 | AMR | PUR | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01169 | hp2 | a0002 | c0002 | t0002 | g0005 | AMR | PUR | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0117 | AMR | PUR | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01175 | hp2 | a0005 | c0008 | t0001 | g0240 | AMR | PUR | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01243 | hp1 | a0002 | c0002 | t0002 | g0045 | AMR | PUR | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | CLM | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01256 | hp1 | a0002 | c0002 | t0002 | g0012 | AMR | CLM | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0289 | AMR | CLM | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01257 | hp2 | a0004 | c0006 | t0001 | g0274 | AMR | CLM | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01258 | hp2 | a0004 | c0006 | t0001 | g0275 | AMR | CLM | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | CLM | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0086 | AMR | CLM | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0313 | AMR | CLM | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0103 | AMR | CLM | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0302 | AMR | CLM | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | CLM | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | CLM | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0064 | AMR | CLM | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0321 | AMR | CLM | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01496 | hp2 | a0002 | c0003 | t0002 | g0029 | AMR | CLM | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0080 | EUR | IBS | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0217 | EUR | IBS | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0226 | EUR | IBS | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01516 | hp2 | a0002 | c0003 | t0002 | g0031 | EUR | IBS | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0227 | EUR | IBS | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0081 | EUR | IBS | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | ACB | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01884 | hp2 | a0002 | c0002 | t0002 | g0051 | AFR | ACB | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ACB | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01891 | hp2 | a0006 | c0012 | t0001 | g0360 | AFR | ACB | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01928 | hp1 | a0002 | c0002 | t0002 | g0027 | AMR | PEL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0338 | AMR | PEL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0311 | AMR | PEL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01943 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PEL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01952 | hp2 | a0002 | c0002 | t0002 | g0028 | AMR | PEL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PEL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | PEL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01993 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0299 | AMR | PEL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0290 | AMR | PEL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02015 | hp1 | a0002 | c0003 | t0002 | g0059 | EAS | KHV | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02015 | hp2 | a0001 | c0004 | t0001 | g0164 | EAS | KHV | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | KHV | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02027 | hp2 | a0001 | c0004 | t0001 | g0166 | EAS | KHV | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0350 | EAS | KHV | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02040 | hp2 | a0002 | c0002 | t0002 | g0134 | EAS | KHV | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | KHV | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02056 | hp2 | a0002 | c0002 | t0002 | g0047 | EAS | KHV | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0022 | EAS | KHV | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02080 | hp2 | a0002 | c0002 | t0002 | g0144 | EAS | KHV | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | KHV | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0346 | EAS | KHV | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02129 | hp1 | a0002 | c0002 | t0002 | g0038 | EAS | KHV | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0022 | EAS | KHV | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02132 | hp1 | a0001 | c0001 | t0004 | g0239 | EAS | KHV | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | KHV | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0352 | EAS | KHV | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | KHV | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02148 | hp1 | a0002 | c0002 | t0002 | g0026 | AMR | PEL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | PEL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0054 | AFR | ACB | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | ACB | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02258 | hp2 | a0002 | c0002 | t0002 | g0008 | AFR | ACB | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02280 | hp1 | a0002 | c0002 | t0002 | g0002 | AFR | ACB | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | ACB | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0331 | AMR | PEL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0312 | AMR | PEL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02451 | hp1 | a0002 | c0002 | t0002 | g0035 | AFR | ACB | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | KHV | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02572 | hp1 | a0002 | c0002 | t0002 | g0140 | AFR | GWD | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0102 | AFR | GWD | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02602 | hp2 | a0002 | c0003 | t0002 | g0052 | SAS | PJL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02615 | hp2 | a0002 | c0002 | t0002 | g0044 | AFR | GWD | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | GWD | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02622 | hp2 | a0002 | c0002 | t0002 | g0007 | AFR | GWD | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02630 | hp1 | a0002 | c0002 | t0002 | g0002 | AFR | GWD | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02630 | hp2 | a0003 | c0005 | t0001 | g0155 | AFR | GWD | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02647 | hp1 | a0002 | c0002 | t0002 | g0125 | AFR | GWD | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | GWD | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02683 | hp2 | a0002 | c0002 | t0001 | g0219 | SAS | PJL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0136 | SAS | PJL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02717 | hp1 | a0002 | c0002 | t0002 | g0007 | AFR | GWD | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02723 | hp1 | a0002 | c0002 | t0002 | g0133 | AFR | GWD | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0062 | AFR | GWD | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0300 | SAS | PJL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0293 | SAS | PJL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0291 | SAS | PJL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02809 | hp1 | a0002 | c0002 | t0002 | g0008 | AFR | GWD | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | GWD | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02886 | hp1 | a0002 | c0002 | t0002 | g0130 | AFR | GWD | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02895 | hp1 | a0002 | c0002 | t0002 | g0053 | AFR | GWD | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0124 | AFR | GWD | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02897 | hp1 | a0002 | c0002 | t0002 | g0042 | AFR | GWD | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0123 | AFR | GWD | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02970 | hp1 | a0002 | c0002 | t0001 | g0180 | AFR | ESN | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02970 | hp2 | a0002 | c0002 | t0002 | g0138 | AFR | ESN | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02976 | hp1 | a0002 | c0002 | t0002 | g0056 | AFR | ESN | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | ESN | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0288 | SAS | PJL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG03041 | hp1 | a0002 | c0002 | t0002 | g0131 | AFR | GWD | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | GWD | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | MSL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG03098 | hp2 | a0002 | c0002 | t0002 | g0141 | AFR | MSL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG03130 | hp1 | a0003 | c0005 | t0003 | g0156 | AFR | ESN | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG03130 | hp2 | a0002 | c0002 | t0002 | g0126 | AFR | ESN | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ESN | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG03139 | hp2 | a0002 | c0002 | t0002 | g0128 | AFR | ESN | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ESN | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | ESN | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG03209 | hp1 | a0001 | c0007 | t0003 | g0171 | AFR | MSL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG03209 | hp2 | a0002 | c0002 | t0002 | g0057 | AFR | MSL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | MSL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG03225 | hp2 | a0002 | c0002 | t0001 | g0160 | AFR | MSL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0105 | SAS | PJL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG03239 | hp2 | a0002 | c0002 | t0002 | g0039 | SAS | PJL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG03453 | hp1 | a0003 | c0005 | t0001 | g0153 | AFR | MSL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | MSL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG03486 | hp1 | a0002 | c0002 | t0002 | g0034 | AFR | MSL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG03486 | hp2 | a0003 | c0005 | t0001 | g0154 | AFR | MSL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG03491 | hp1 | a0002 | c0002 | t0002 | g0041 | SAS | PJL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ESN | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0162 | AFR | ESN | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | MSL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG03579 | hp2 | a0002 | c0002 | t0002 | g0129 | AFR | MSL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG03654 | hp1 | a0002 | c0002 | t0002 | g0121 | SAS | PJL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG03669 | hp1 | a0004 | c0006 | t0001 | g0310 | SAS | PJL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0106 | SAS | PJL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0328 | SAS | PJL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | PJL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG03710 | hp2 | a0002 | c0002 | t0002 | g0004 | SAS | PJL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | BEB | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0314 | SAS | BEB | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG03834 | hp1 | a0002 | c0002 | t0002 | g0033 | SAS | BEB | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG03834 | hp2 | a0002 | c0002 | t0002 | g0119 | SAS | BEB | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | BEB | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0071 | SAS | BEB | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | BEB | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0107 | SAS | BEB | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG04115 | hp1 | a0002 | c0002 | t0002 | g0049 | SAS | STU | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0355 | SAS | STU | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | BEB | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0112 | SAS | BEB | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG04199 | hp1 | a0002 | c0002 | t0002 | g0058 | SAS | STU | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0238 | SAS | STU | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG04204 | hp1 | a0007 | c0011 | t0002 | g0076 | SAS | STU | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0280 | SAS | STU | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | STU | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG04228 | hp2 | a0002 | c0002 | t0002 | g0037 | SAS | STU | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18522 | hp1 | a0008 | c0013 | t0003 | g0170 | AFR | YRI | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0145 | AFR | YRI | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18747 | hp1 | a0001 | c0010 | t0001 | g0292 | EAS | CHB | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | CHB | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18906 | hp1 | a0002 | c0002 | t0002 | g0043 | AFR | YRI | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0143 | AFR | YRI | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0353 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18951 | hp1 | a0002 | c0002 | t0002 | g0048 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18952 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0345 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0276 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18985 | hp1 | a0002 | c0002 | t0002 | g0036 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0358 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19002 | hp1 | a0002 | c0002 | t0002 | g0040 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0354 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19012 | hp2 | a0001 | c0004 | t0001 | g0167 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | LWK | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19043 | hp2 | a0001 | c0015 | t0001 | g0172 | AFR | LWK | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19054 | hp1 | a0001 | c0004 | t0001 | g0165 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19058 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0356 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19063 | hp2 | a0001 | c0004 | t0001 | g0161 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0347 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19085 | hp1 | a0009 | c0009 | t0001 | g0359 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0357 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19240 | hp1 | a0002 | c0002 | t0002 | g0032 | AFR | YRI | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | YRI | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA20129 | hp1 | a0002 | c0002 | t0002 | g0122 | AFR | ASW | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | ASW | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA20752 | hp1 | a0002 | c0002 | t0002 | g0012 | EUR | TSI | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA20752 | hp2 | a0002 | c0003 | t0002 | g0061 | EUR | TSI | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0069 | SAS | GIH | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA20905 | hp2 | a0002 | c0002 | t0002 | g0004 | SAS | GIH | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0339 | AMR | CLM | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0111 | AMR | CLM | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0142 | AFR | ACB | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0088 | AFR | ACB | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02486 | hp2 | a0002 | c0002 | t0002 | g0137 | AFR | ACB | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02559 | hp1 | a0002 | c0014 | t0001 | g0169 | AFR | ACB | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0269 | AFR | ACB | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0135 | AFR | MSL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | MSL | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG06807 | hp1 | a0002 | c0002 | t0002 | g0055 | AFR | USA | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| HG06807 | hp2 | a0002 | c0002 | t0002 | g0002 | AFR | USA | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA20300 | hp1 | a0002 | c0003 | t0002 | g0060 | AFR | USA | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA20300 | hp2 | a0001 | c0007 | t0004 | g0173 | AFR | USA | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA21309 | hp1 | a0002 | c0002 | t0002 | g0046 | AFR | LWK | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | LWK | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0298 | REF | REF | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0002 | g0127 | REF | REF | LMNTD1_chr12_25471082_25558283 | LMNTD1 | chr12 | 25471082 | 25558283 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:25518821 | C | A | 1 | a0006 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.1163G>T | p.Arg388Leu | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/10 | 1408/1876 | 1163/1230 | 388/409 | chr12 | 25518821 | |||
| chr12:25518825 | T | A | 7 | a0001 a0004 a0005 others(4): Show |
296 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(293): Show |
missense_variant | MODERATE | c.1159A>T | p.Thr387Ser | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/10 | 1404/1876 | 1159/1230 | 387/409 | chr12 | 25518825 | |||
| chr12:25518924 | A | G | 1 | a0007 | 1 | HG04204.hp1 | missense_variant | MODERATE | c.1060T>C | p.Trp354Arg | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/10 | 1305/1876 | 1060/1230 | 354/409 | chr12 | 25518924 | |||
| chr12:25519943 | C | T | 1 | a0003 | 4 | HG02630.hp2 HG03130.hp1 HG03453.hp1 others(1): Show |
missense_variant | MODERATE | c.931G>A | p.Ala311Thr | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 7/10 | 1176/1876 | 931/1230 | 311/409 | chr12 | 25519943 | |||
| chr12:25519946 | T | C | 1 | a0003 | 4 | HG02630.hp2 HG03130.hp1 HG03453.hp1 others(1): Show |
missense_variant | MODERATE | c.928A>G | p.Thr310Ala | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 7/10 | 1173/1876 | 928/1230 | 310/409 | chr12 | 25519946 | |||
| chr12:25520011 | T | C | 1 | a0003 | 4 | HG02630.hp2 HG03130.hp1 HG03453.hp1 others(1): Show |
missense_variant | MODERATE | c.863A>G | p.Glu288Gly | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 7/10 | 1108/1876 | 863/1230 | 288/409 | chr12 | 25520011 | |||
| chr12:25520021 | C | T | 1 | a0003 | 4 | HG02630.hp2 HG03130.hp1 HG03453.hp1 others(1): Show |
missense_variant | MODERATE | c.853G>A | p.Ala285Thr | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 7/10 | 1098/1876 | 853/1230 | 285/409 | chr12 | 25520021 | |||
| chr12:25526203 | A | G | 1 | a0009 | 1 | NA19085.hp1 | missense_variant | MODERATE | c.694T>C | p.Ser232Pro | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/10 | 939/1876 | 694/1230 | 232/409 | chr12 | 25526203 | |||
| chr12:25526810 | A | G | 1 | a0008 | 1 | NA18522.hp1 | missense_variant | MODERATE | c.637T>C | p.Phe213Leu | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 5/10 | 882/1876 | 637/1230 | 213/409 | chr12 | 25526810 | |||
| chr12:25526896 | A | G | 1 | a0005 | 1 | HG01175.hp2 | missense_variant | MODERATE | c.551T>C | p.Ile184Thr | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 5/10 | 796/1876 | 551/1230 | 184/409 | chr12 | 25526896 | |||
| chr12:25549544 | C | T | 1 | a0004 | 3 | HG01257.hp2 HG01258.hp2 HG03669.hp1 |
missense_variant&splice_region_variant | MODERATE | c.92G>A | p.Arg31Lys | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 3/10 | 337/1876 | 92/1230 | 31/409 | chr12 | 25549544 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:25503772 | T | C | 1 | a0002c0003 | 8 | HG00642.hp1 HG00741.hp2 HG01496.hp2 others(5): Show |
synonymous_variant | LOW | c.1218A>G | p.Ser406Ser | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/10 | 1463/1876 | 1218/1230 | 406/409 | chr12 | 25503772 | |||
| chr12:25518868 | G | A | 1 | a0001c0015 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.1116C>T | p.His372His | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/10 | 1361/1876 | 1116/1230 | 372/409 | chr12 | 25518868 | |||
| chr12:25518937 | A | G | 1 | a0003c0005 | 4 | HG02630.hp2 HG03130.hp1 HG03453.hp1 others(1): Show |
synonymous_variant | LOW | c.1047T>C | p.Pro349Pro | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/10 | 1292/1876 | 1047/1230 | 349/409 | chr12 | 25518937 | |||
| chr12:25520067 | C | G | 1 | a0003c0005 | 4 | HG02630.hp2 HG03130.hp1 HG03453.hp1 others(1): Show |
synonymous_variant | LOW | c.807G>C | p.Ala269Ala | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 7/10 | 1052/1876 | 807/1230 | 269/409 | chr12 | 25520067 | |||
| chr12:25520067 | C | T | 1 | a0001c0010 | 1 | NA18747.hp1 | synonymous_variant | LOW | c.807G>A | p.Ala269Ala | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 7/10 | 1052/1876 | 807/1230 | 269/409 | chr12 | 25520067 | |||
| chr12:25526907 | G | A | 4 | a0001c0007 a0001c0015 a0002c0014 others(1): Show |
5 | HG02559.hp1 HG03209.hp1 NA18522.hp1 others(2): Show |
synonymous_variant | LOW | c.540C>T | p.Phe180Phe | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 5/10 | 785/1876 | 540/1230 | 180/409 | chr12 | 25526907 | |||
| chr12:25546502 | C | T | 1 | a0001c0004 | 5 | HG02015.hp2 HG02027.hp2 NA19012.hp2 others(2): Show |
synonymous_variant | LOW | c.363G>A | p.Gly121Gly | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/10 | 608/1876 | 363/1230 | 121/409 | chr12 | 25546502 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:25476131 | C | T | 2 | a0001c0001t0004 a0001c0007t0004 |
2 | HG02132.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*352G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 10/10 | 27629 | chr12 | 25476131 | ||||||
| chr12:25476357 | T | G | 4 | a0001c0001t0003 a0001c0007t0003 a0003c0005t0003 others(1): Show |
4 | HG02559.hp2 HG03130.hp1 HG03209.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*126A>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 10/10 | 27403 | chr12 | 25476357 | ||||||
| chr12:25476410 | T | C | 1 | a0002c0003t0005 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*73A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 10/10 | 27350 | chr12 | 25476410 | ||||||
| chr12:25553200 | G | A | 17 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(14): Show |
239 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(236): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-162C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 1/10 | chr12 | 25553200 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:25476479 | G | A | 2 | a0001c0001t0002g0078 a0001c0001t0002g0113 |
2 | NA18950.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.*23-19C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25476479 | |||||||
| chr12:25476522 | A | G | 5 | a0001c0004t0001g0161 a0001c0004t0001g0164 a0001c0004t0001g0165 others(2): Show |
5 | HG02015.hp2 HG02027.hp2 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.*23-62T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25476522 | |||||||
| chr12:25476587 | C | T | 2 | a0001c0001t0001g0299 a0001c0001t0001g0300 |
2 | HG01993.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.*23-127G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25476587 | |||||||
| chr12:25476691 | C | T | 1 | a0001c0001t0001g0024 | 2 | HG00408.hp2 HG00673.hp2 |
intron_variant | MODIFIER | c.*23-231G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25476691 | |||||||
| chr12:25476725 | C | T | 111 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0179 others(108): Show |
114 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.*23-265G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25476725 | |||||||
| chr12:25476800 | C | T | 1 | a0002c0002t0002g0036 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.*23-340G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25476800 | |||||||
| chr12:25476846 | C | A | 1 | a0001c0001t0001g0236 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.*23-386G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25476846 | |||||||
| chr12:25476890 | T | A | 1 | a0001c0001t0003g0269 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.*23-430A>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25476890 | |||||||
| chr12:25476950 | T | C | 1 | a0001c0001t0001g0248 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.*23-490A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25476950 | |||||||
| chr12:25477021 | C | G | 107 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0179 others(104): Show |
109 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.*23-561G>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25477021 | |||||||
| chr12:25477068 | C | T | 74 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(71): Show |
83 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.*23-608G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25477068 | |||||||
| chr12:25477195 | T | A | 1 | a0002c0002t0002g0037 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.*23-735A>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25477195 | |||||||
| chr12:25477229 | A | G | 7 | a0001c0001t0001g0163 a0001c0004t0001g0161 a0001c0004t0001g0164 others(4): Show |
7 | HG01255.hp2 HG02015.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.*23-769T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25477229 | |||||||
| chr12:25477243 | T | G | 299 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(296): Show |
317 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.*23-783A>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25477243 | |||||||
| chr12:25477314 | C | T | 1 | a0002c0002t0002g0134 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.*23-854G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25477314 | |||||||
| chr12:25477371 | AACATTG | A | 5 | a0001c0001t0001g0015 a0001c0001t0001g0157 a0001c0001t0001g0158 others(2): Show |
6 | HG02109.hp2 HG02451.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.*23-917_*23-912del others(6): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25477371 | |||||||
| chr12:25477407 | G | A | 3 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 |
3 | HG03139.hp1 HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.*23-947C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25477407 | |||||||
| chr12:25477411 | G | A | 1 | a0001c0001t0001g0277 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.*23-951C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25477411 | |||||||
| chr12:25477730 | A | G | 7 | a0001c0001t0001g0163 a0001c0004t0001g0161 a0001c0004t0001g0164 others(4): Show |
7 | HG01255.hp2 HG02015.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.*23-1270T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25477730 | |||||||
| chr12:25477893 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.*23-1433G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25477893 | |||||||
| chr12:25477939 | G | T | 2 | a0001c0001t0001g0351 a0009c0009t0001g0359 |
2 | NA18966.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.*23-1479C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25477939 | |||||||
| chr12:25477997 | G | A | 286 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(283): Show |
303 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.*23-1537C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25477997 | |||||||
| chr12:25478080 | C | T | 30 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0023 others(27): Show |
35 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.*23-1620G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25478080 | |||||||
| chr12:25478131 | T | C | 1 | a0002c0002t0002g0008 | 2 | HG02258.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.*23-1671A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25478131 | |||||||
| chr12:25478152 | C | T | 150 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0152 others(147): Show |
153 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.*23-1692G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25478152 | |||||||
| chr12:25478173 | C | T | 45 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0198 others(42): Show |
45 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.*23-1713G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25478173 | |||||||
| chr12:25478195 | C | G | 5 | a0001c0004t0001g0161 a0001c0004t0001g0164 a0001c0004t0001g0165 others(2): Show |
5 | HG02015.hp2 HG02027.hp2 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.*23-1735G>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25478195 | |||||||
| chr12:25478291 | G | T | 2 | a0001c0001t0001g0152 a0002c0002t0002g0051 |
2 | HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.*23-1831C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25478291 | |||||||
| chr12:25478345 | C | T | 7 | a0001c0001t0001g0163 a0001c0004t0001g0161 a0001c0004t0001g0164 others(4): Show |
7 | HG01255.hp2 HG02015.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.*23-1885G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25478345 | |||||||
| chr12:25478346 | A | G | 287 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(284): Show |
304 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.*23-1886T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25478346 | |||||||
| chr12:25478404 | G | T | 1 | a0001c0001t0001g0253 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.*23-1944C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25478404 | |||||||
| chr12:25478407 | G | A | 1 | a0001c0001t0001g0356 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.*23-1947C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25478407 | |||||||
| chr12:25478549 | C | A | 1 | a0002c0002t0002g0058 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.*23-2089G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25478549 | |||||||
| chr12:25478583 | G | A | 286 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(283): Show |
303 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.*23-2123C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25478583 | |||||||
| chr12:25478652 | G | C | 4 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(1): Show |
4 | HG02109.hp1 HG03139.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.*23-2192C>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25478652 | |||||||
| chr12:25478717 | C | T | 287 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(284): Show |
304 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.*23-2257G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25478717 | |||||||
| chr12:25478758 | T | C | 335 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(332): Show |
359 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.*23-2298A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25478758 | |||||||
| chr12:25478875 | T | A | 85 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(82): Show |
91 | HG00099.hp2 HG00438.hp1 HG00642.hp2 others(88): Show |
intron_variant | MODIFIER | c.*23-2415A>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25478875 | |||||||
| chr12:25478877 | A | AT | 25 | a0001c0001t0001g0021 a0001c0001t0001g0146 a0001c0001t0001g0183 others(22): Show |
26 | HG00099.hp2 HG00642.hp2 HG01175.hp2 others(23): Show |
intron_variant | MODIFIER | c.*23-2418dupA | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25478877 | |||||||
| chr12:25478932 | C | T | 4 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(1): Show |
4 | HG02109.hp1 HG03139.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.*23-2472G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25478932 | |||||||
| chr12:25479088 | T | C | 54 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(51): Show |
59 | HG00438.hp1 HG01074.hp1 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.*23-2628A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25479088 | |||||||
| chr12:25479205 | G | A | 1 | a0001c0001t0001g0346 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.*23-2745C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25479205 | |||||||
| chr12:25479217 | A | G | 2 | a0001c0001t0001g0152 a0002c0002t0002g0051 |
2 | HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.*23-2757T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25479217 | |||||||
| chr12:25479404 | T | G | 1 | a0001c0010t0001g0292 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.*23-2944A>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25479404 | |||||||
| chr12:25479623 | G | T | 1 | a0002c0002t0002g0008 | 2 | HG02258.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.*23-3163C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25479623 | |||||||
| chr12:25479654 | A | C | 1 | a0002c0002t0002g0033 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.*23-3194T>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25479654 | |||||||
| chr12:25479655 | C | T | 1 | a0001c0001t0002g0074 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.*23-3195G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25479655 | |||||||
| chr12:25479699 | C | T | 2 | a0001c0001t0001g0215 a0001c0001t0001g0273 |
2 | HG01081.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.*23-3239G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25479699 | |||||||
| chr12:25479727 | C | T | 51 | a0001c0001t0001g0305 a0001c0001t0002g0054 a0001c0001t0002g0135 others(48): Show |
59 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.*23-3267G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25479727 | |||||||
| chr12:25479775 | T | G | 286 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(283): Show |
303 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.*23-3315A>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25479775 | |||||||
| chr12:25479817 | A | G | 287 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(284): Show |
305 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.*23-3357T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25479817 | |||||||
| chr12:25479907 | G | A | 286 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(283): Show |
303 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.*23-3447C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25479907 | |||||||
| chr12:25479985 | C | T | 7 | a0001c0001t0001g0163 a0001c0004t0001g0161 a0001c0004t0001g0164 others(4): Show |
7 | HG01255.hp2 HG02015.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.*23-3525G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25479985 | |||||||
| chr12:25479986 | T | A | 51 | a0001c0001t0001g0305 a0001c0001t0002g0054 a0001c0001t0002g0135 others(48): Show |
59 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.*23-3526A>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25479986 | |||||||
| chr12:25480015 | G | A | 1 | a0003c0005t0001g0153 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.*23-3555C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25480015 | |||||||
| chr12:25480118 | C | A | 9 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0149 others(6): Show |
12 | NA18747.hp2 NA18952.hp1 NA18953.hp1 others(9): Show |
intron_variant | MODIFIER | c.*23-3658G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25480118 | |||||||
| chr12:25480143 | C | T | 5 | a0002c0002t0002g0012 a0002c0002t0002g0118 a0002c0002t0002g0119 others(2): Show |
6 | HG00280.hp1 HG00735.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.*23-3683G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25480143 | |||||||
| chr12:25480282 | A | T | 1 | a0001c0001t0001g0211 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.*23-3822T>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25480282 | |||||||
| chr12:25480479 | C | T | 1 | a0001c0001t0001g0301 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.*23-4019G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25480479 | |||||||
| chr12:25480596 | C | G | 1 | a0001c0001t0001g0213 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.*23-4136G>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25480596 | |||||||
| chr12:25480866 | C | A | 4 | a0001c0001t0001g0179 a0001c0001t0001g0233 a0001c0001t0001g0347 others(1): Show |
4 | HG02132.hp1 NA18955.hp2 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.*23-4406G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25480866 | |||||||
| chr12:25480947 | C | T | 8 | a0001c0001t0001g0216 a0001c0001t0001g0270 a0001c0001t0001g0271 others(5): Show |
8 | HG01169.hp1 HG01255.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.*23-4487G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25480947 | |||||||
| chr12:25481036 | AGTTATAC others(3520): Show |
A | 1 | a0001c0001t0002g0142 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.*23-8103_*23-4577d others(2): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25481036 | |||||||
| chr12:25481200 | ATCAAAGT others(4): Show |
A | 1 | a0002c0002t0002g0008 | 2 | HG02258.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.*23-4751_*23-4741d others(13): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25481200 | |||||||
| chr12:25481204 | A | C | 286 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(283): Show |
303 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.*23-4744T>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25481204 | |||||||
| chr12:25481206 | G | C | 1 | a0002c0002t0001g0160 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.*23-4746C>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25481206 | |||||||
| chr12:25481241 | C | A | 286 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(283): Show |
303 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.*23-4781G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25481241 | |||||||
| chr12:25481309 | C | T | 1 | a0002c0002t0001g0160 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.*23-4849G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25481309 | |||||||
| chr12:25481433 | G | A | 1 | a0001c0001t0002g0069 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.*23-4973C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25481433 | |||||||
| chr12:25481454 | A | G | 7 | a0001c0001t0001g0163 a0001c0004t0001g0161 a0001c0004t0001g0164 others(4): Show |
7 | HG01255.hp2 HG02015.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.*23-4994T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25481454 | |||||||
| chr12:25481741 | G | T | 142 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0152 others(139): Show |
145 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.*23-5281C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25481741 | |||||||
| chr12:25481829 | C | T | 1 | a0006c0012t0001g0360 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.*23-5369G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25481829 | |||||||
| chr12:25481865 | T | TCA | 96 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(93): Show |
105 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.*23-5407_*23-5406d others(4): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25481865 | |||||||
| chr12:25481865 | T | TCACA | 42 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0146 others(39): Show |
45 | HG00099.hp1 HG00639.hp1 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.*23-5409_*23-5406d others(6): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25481865 | |||||||
| chr12:25481865 | T | TCACACA | 23 | a0001c0001t0001g0163 a0001c0001t0001g0184 a0001c0001t0001g0201 others(20): Show |
23 | HG01255.hp2 HG01261.hp1 HG01952.hp2 others(20): Show |
intron_variant | MODIFIER | c.*23-5411_*23-5406d others(8): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25481865 | |||||||
| chr12:25481865 | T | TCACACAC others(3): Show |
2 | a0001c0001t0002g0117 a0002c0002t0002g0053 |
2 | HG01175.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.*23-5415_*23-5406d others(12): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25481865 | |||||||
| chr12:25481865 | TCA | T | 25 | a0001c0001t0001g0003 a0001c0001t0001g0177 a0001c0001t0001g0213 others(22): Show |
26 | HG00280.hp2 HG00738.hp1 HG01358.hp1 others(23): Show |
intron_variant | MODIFIER | c.*23-5407_*23-5406d others(4): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25481865 | |||||||
| chr12:25481865 | TCACA | T | 7 | a0001c0001t0001g0152 a0001c0001t0001g0316 a0001c0001t0001g0323 others(4): Show |
7 | HG01884.hp2 HG02083.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.*23-5409_*23-5406d others(6): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25481865 | |||||||
| chr12:25481865 | TCACACA | T | 31 | a0001c0001t0001g0185 a0001c0001t0001g0215 a0001c0001t0001g0264 others(28): Show |
32 | HG00423.hp1 HG00621.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.*23-5411_*23-5406d others(8): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25481865 | |||||||
| chr12:25481865 | TCACACAC others(1): Show |
T | 3 | a0001c0001t0002g0074 a0001c0001t0002g0078 a0001c0001t0002g0113 |
3 | NA18950.hp2 NA18969.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.*23-5413_*23-5406d others(10): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25481865 | |||||||
| chr12:25481865 | TCACACAC others(3): Show |
T | 1 | a0007c0011t0002g0076 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.*23-5415_*23-5406d others(12): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25481865 | |||||||
| chr12:25481865 | TCACACAC others(5): Show |
T | 1 | a0001c0001t0001g0151 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.*23-5417_*23-5406d others(14): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25481865 | |||||||
| chr12:25481865 | TCACACAC others(7): Show |
T | 1 | a0002c0002t0002g0057 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.*23-5419_*23-5406d others(16): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25481865 | |||||||
| chr12:25481865 | TCACACAC others(9): Show |
T | 2 | a0002c0002t0002g0034 a0002c0002t0002g0035 |
2 | HG02451.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.*23-5421_*23-5406d others(18): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25481865 | |||||||
| chr12:25481865 | TCACACAC others(11): Show |
T | 1 | a0001c0001t0001g0015 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.*23-5423_*23-5406d others(20): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25481865 | |||||||
| chr12:25481900 | CACACACA others(1): Show |
C | 2 | a0001c0001t0001g0309 a0002c0002t0002g0008 |
3 | HG00408.hp1 HG02258.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.*23-5448_*23-5441d others(10): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25481900 | |||||||
| chr12:25481908 | T | C | 6 | a0001c0001t0002g0063 a0001c0004t0001g0161 a0001c0004t0001g0164 others(3): Show |
6 | HG02015.hp2 HG02027.hp2 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.*23-5448A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25481908 | |||||||
| chr12:25481936 | C | T | 84 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(81): Show |
90 | HG00099.hp2 HG00438.hp1 HG00642.hp2 others(87): Show |
intron_variant | MODIFIER | c.*23-5476G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25481936 | |||||||
| chr12:25482043 | T | C | 1 | a0001c0001t0002g0099 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.*23-5583A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25482043 | |||||||
| chr12:25482244 | T | C | 52 | a0001c0001t0001g0236 a0001c0001t0001g0305 a0001c0001t0002g0054 others(49): Show |
60 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.*23-5784A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25482244 | |||||||
| chr12:25482494 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.*23-6034A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25482494 | |||||||
| chr12:25482556 | A | G | 1 | a0001c0001t0001g0015 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.*23-6096T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25482556 | |||||||
| chr12:25482606 | G | A | 2 | a0001c0001t0001g0151 a0001c0001t0002g0101 |
2 | HG00609.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.*23-6146C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25482606 | |||||||
| chr12:25482761 | G | A | 1 | a0001c0001t0002g0074 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.*23-6301C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25482761 | |||||||
| chr12:25482795 | G | A | 1 | a0002c0002t0002g0037 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.*23-6335C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25482795 | |||||||
| chr12:25482841 | C | T | 1 | a0002c0002t0001g0160 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.*23-6381G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25482841 | |||||||
| chr12:25482890 | G | A | 3 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 |
3 | HG03139.hp1 HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.*23-6430C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25482890 | |||||||
| chr12:25482895 | G | A | 285 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(282): Show |
302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.*23-6435C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25482895 | |||||||
| chr12:25483086 | C | T | 3 | a0001c0001t0001g0146 a0001c0001t0001g0183 a0001c0001t0001g0238 |
3 | HG02602.hp1 HG03017.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.*23-6626G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25483086 | |||||||
| chr12:25483150 | C | T | 1 | a0002c0002t0002g0038 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.*23-6690G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25483150 | |||||||
| chr12:25483226 | A | T | 5 | a0001c0004t0001g0161 a0001c0004t0001g0164 a0001c0004t0001g0165 others(2): Show |
5 | HG02015.hp2 HG02027.hp2 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.*23-6766T>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25483226 | |||||||
| chr12:25483275 | T | G | 1 | a0001c0001t0001g0258 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.*23-6815A>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25483275 | |||||||
| chr12:25483285 | G | A | 1 | a0001c0001t0002g0073 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.*23-6825C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25483285 | |||||||
| chr12:25483295 | G | A | 57 | a0001c0001t0001g0015 a0001c0001t0001g0157 a0001c0001t0001g0158 others(54): Show |
66 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.*23-6835C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25483295 | |||||||
| chr12:25483515 | T | C | 1 | a0001c0001t0002g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.*23-7055A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25483515 | |||||||
| chr12:25483600 | C | T | 285 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(282): Show |
302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.*23-7140G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25483600 | |||||||
| chr12:25483629 | G | A | 7 | a0001c0001t0001g0015 a0001c0001t0001g0157 a0001c0001t0001g0158 others(4): Show |
8 | HG02109.hp2 HG02451.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.*23-7169C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25483629 | |||||||
| chr12:25483638 | G | T | 4 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 others(1): Show |
4 | NA18961.hp2 NA18965.hp1 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.*23-7178C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25483638 | |||||||
| chr12:25483665 | A | G | 51 | a0001c0001t0001g0305 a0001c0001t0002g0054 a0001c0001t0002g0135 others(48): Show |
59 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.*23-7205T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25483665 | |||||||
| chr12:25483706 | A | G | 3 | a0001c0001t0001g0185 a0001c0001t0001g0264 a0001c0001t0001g0340 |
3 | NA18971.hp2 NA18983.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.*23-7246T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25483706 | |||||||
| chr12:25483759 | T | C | 333 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(330): Show |
357 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(354): Show |
intron_variant | MODIFIER | c.*23-7299A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25483759 | |||||||
| chr12:25483772 | CA | C | 136 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0023 others(133): Show |
144 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.*23-7313delT | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25483772 | |||||||
| chr12:25483772 | CAA | C | 188 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(185): Show |
202 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.*23-7314_*23-7313d others(4): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25483772 | |||||||
| chr12:25483784 | A | G | 51 | a0001c0001t0001g0305 a0001c0001t0002g0054 a0001c0001t0002g0135 others(48): Show |
59 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.*23-7324T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25483784 | |||||||
| chr12:25483840 | A | C | 1 | a0006c0012t0001g0360 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.*23-7380T>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25483840 | |||||||
| chr12:25483987 | C | T | 27 | a0001c0001t0001g0185 a0001c0001t0001g0264 a0001c0001t0001g0309 others(24): Show |
28 | HG00408.hp1 HG00423.hp1 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.*23-7527G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25483987 | |||||||
| chr12:25483988 | C | G | 2 | a0001c0004t0001g0165 a0001c0004t0001g0167 |
2 | NA19012.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.*23-7528G>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25483988 | |||||||
| chr12:25484091 | A | G | 51 | a0001c0001t0001g0305 a0001c0001t0002g0054 a0001c0001t0002g0135 others(48): Show |
59 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.*23-7631T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25484091 | |||||||
| chr12:25484204 | A | C | 1 | a0002c0002t0002g0008 | 2 | HG02258.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.*23-7744T>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25484204 | |||||||
| chr12:25484214 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.*23-7754G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25484214 | |||||||
| chr12:25484215 | G | C | 85 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(82): Show |
91 | HG00099.hp2 HG00438.hp1 HG00642.hp2 others(88): Show |
intron_variant | MODIFIER | c.*23-7755C>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25484215 | |||||||
| chr12:25484265 | G | A | 8 | a0001c0001t0001g0216 a0001c0001t0001g0270 a0001c0001t0001g0271 others(5): Show |
8 | HG01169.hp1 HG01255.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.*23-7805C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25484265 | |||||||
| chr12:25484317 | T | G | 2 | a0001c0001t0001g0163 a0002c0002t0001g0355 |
2 | HG01255.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.*23-7857A>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25484317 | |||||||
| chr12:25484391 | G | A | 54 | a0001c0001t0001g0305 a0001c0001t0002g0054 a0001c0001t0002g0135 others(51): Show |
62 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.*23-7931C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25484391 | |||||||
| chr12:25484466 | C | T | 1 | a0001c0001t0001g0326 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.*23-8006G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25484466 | |||||||
| chr12:25484468 | T | C | 51 | a0001c0001t0001g0305 a0001c0001t0002g0054 a0001c0001t0002g0135 others(48): Show |
59 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.*23-8008A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25484468 | |||||||
| chr12:25484471 | T | C | 51 | a0001c0001t0001g0305 a0001c0001t0002g0054 a0001c0001t0002g0135 others(48): Show |
59 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.*23-8011A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25484471 | |||||||
| chr12:25484505 | A | G | 1 | a0002c0002t0002g0004 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.*23-8045T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25484505 | |||||||
| chr12:25484527 | A | C | 1 | a0002c0002t0001g0290 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.*23-8067T>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25484527 | |||||||
| chr12:25484566 | C | T | 1 | a0001c0001t0002g0142 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.*23-8106G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25484566 | |||||||
| chr12:25484571 | G | A | 1 | a0001c0001t0002g0142 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.*23-8111C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25484571 | |||||||
| chr12:25484573 | A | G | 8 | a0001c0001t0001g0216 a0001c0001t0001g0270 a0001c0001t0001g0271 others(5): Show |
8 | HG01169.hp1 HG01255.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.*23-8113T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25484573 | |||||||
| chr12:25484584 | G | A | 1 | a0001c0001t0002g0142 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.*23-8124C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25484584 | |||||||
| chr12:25484593 | C | T | 1 | a0001c0001t0002g0142 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.*23-8133G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25484593 | |||||||
| chr12:25484598 | C | T | 1 | a0001c0001t0002g0142 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.*23-8138G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25484598 | |||||||
| chr12:25484661 | C | A | 1 | a0002c0002t0001g0276 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.*23-8201G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25484661 | |||||||
| chr12:25484751 | G | A | 4 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(1): Show |
4 | HG02109.hp1 HG03139.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.*23-8291C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25484751 | |||||||
| chr12:25484766 | C | G | 54 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(51): Show |
59 | HG00438.hp1 HG01074.hp1 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.*23-8306G>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25484766 | |||||||
| chr12:25484768 | T | C | 54 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(51): Show |
59 | HG00438.hp1 HG01074.hp1 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.*23-8308A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25484768 | |||||||
| chr12:25484774 | G | A | 102 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0179 others(99): Show |
104 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.*23-8314C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25484774 | |||||||
| chr12:25484827 | T | C | 286 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(283): Show |
303 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.*23-8367A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25484827 | |||||||
| chr12:25484893 | C | A | 8 | a0001c0001t0001g0216 a0001c0001t0001g0270 a0001c0001t0001g0271 others(5): Show |
8 | HG01169.hp1 HG01255.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.*23-8433G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25484893 | |||||||
| chr12:25485043 | T | C | 5 | a0001c0001t0002g0068 a0001c0001t0002g0083 a0001c0001t0002g0110 others(2): Show |
5 | HG01069.hp1 HG02040.hp2 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.*23-8583A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25485043 | |||||||
| chr12:25485079 | T | C | 51 | a0001c0001t0001g0305 a0001c0001t0002g0054 a0001c0001t0002g0135 others(48): Show |
59 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.*23-8619A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25485079 | |||||||
| chr12:25485222 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.*23-8762A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25485222 | |||||||
| chr12:25485270 | T | C | 85 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(82): Show |
91 | HG00099.hp2 HG00438.hp1 HG00642.hp2 others(88): Show |
intron_variant | MODIFIER | c.*23-8810A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25485270 | |||||||
| chr12:25485326 | T | C | 1 | a0001c0001t0002g0063 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.*23-8866A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25485326 | |||||||
| chr12:25485349 | GTTGT | G | 10 | a0002c0002t0002g0007 a0002c0002t0002g0053 a0002c0003t0002g0029 others(7): Show |
11 | HG00642.hp1 HG00741.hp2 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.*23-8893_*23-8890d others(6): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25485349 | |||||||
| chr12:25485391 | G | A | 149 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0152 others(146): Show |
152 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.*23-8931C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25485391 | |||||||
| chr12:25485430 | G | A | 89 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(86): Show |
95 | HG00099.hp2 HG00438.hp1 HG00642.hp2 others(92): Show |
intron_variant | MODIFIER | c.*23-8970C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25485430 | |||||||
| chr12:25485438 | T | C | 4 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0277 others(1): Show |
6 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(3): Show |
intron_variant | MODIFIER | c.*23-8978A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25485438 | |||||||
| chr12:25485458 | T | C | 296 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(293): Show |
314 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.*23-8998A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25485458 | |||||||
| chr12:25485557 | G | A | 1 | a0006c0012t0001g0360 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.*23-9097C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25485557 | |||||||
| chr12:25485652 | A | G | 51 | a0001c0001t0001g0305 a0001c0001t0002g0054 a0001c0001t0002g0135 others(48): Show |
59 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.*23-9192T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25485652 | |||||||
| chr12:25485669 | A | T | 1 | a0002c0002t0002g0039 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.*23-9209T>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25485669 | |||||||
| chr12:25485745 | C | A | 2 | a0001c0001t0001g0163 a0002c0002t0001g0355 |
2 | HG01255.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.*23-9285G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25485745 | |||||||
| chr12:25485842 | T | G | 30 | a0001c0001t0001g0021 a0001c0001t0001g0146 a0001c0001t0001g0183 others(27): Show |
31 | HG00099.hp2 HG00642.hp2 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.*23-9382A>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25485842 | |||||||
| chr12:25485883 | G | A | 2 | a0001c0001t0002g0104 a0001c0001t0002g0114 |
2 | NA18962.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.*23-9423C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25485883 | |||||||
| chr12:25485993 | T | C | 51 | a0001c0001t0001g0305 a0001c0001t0002g0054 a0001c0001t0002g0135 others(48): Show |
59 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.*23-9533A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25485993 | |||||||
| chr12:25486062 | T | C | 3 | a0001c0001t0001g0250 a0001c0001t0001g0324 a0001c0001t0001g0329 |
3 | NA18945.hp2 NA18981.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.*23-9602A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25486062 | |||||||
| chr12:25486140 | A | G | 3 | a0001c0001t0001g0152 a0001c0001t0002g0062 a0002c0002t0002g0051 |
3 | HG01884.hp2 HG02723.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.*23-9680T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25486140 | |||||||
| chr12:25486180 | A | C | 1 | a0001c0001t0001g0151 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.*23-9720T>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25486180 | |||||||
| chr12:25486207 | G | C | 123 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0152 others(120): Show |
125 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.*23-9747C>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25486207 | |||||||
| chr12:25486233 | G | A | 3 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0005c0008t0001g0240 |
3 | HG01175.hp2 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.*23-9773C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25486233 | |||||||
| chr12:25486258 | C | G | 1 | a0001c0001t0001g0283 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.*23-9798G>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25486258 | |||||||
| chr12:25486271 | G | A | 51 | a0001c0001t0001g0305 a0001c0001t0002g0054 a0001c0001t0002g0135 others(48): Show |
59 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.*23-9811C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25486271 | |||||||
| chr12:25486412 | G | A | 100 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0163 others(97): Show |
102 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.*23-9952C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25486412 | |||||||
| chr12:25486417 | G | T | 1 | a0006c0012t0001g0360 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.*23-9957C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25486417 | |||||||
| chr12:25486497 | T | A | 1 | a0001c0001t0001g0021 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.*23-10037A>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25486497 | |||||||
| chr12:25486511 | A | C | 1 | a0001c0001t0002g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.*23-10051T>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25486511 | |||||||
| chr12:25486535 | T | C | 286 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(283): Show |
303 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.*23-10075A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25486535 | |||||||
| chr12:25486626 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.*23-10166T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25486626 | |||||||
| chr12:25486650 | A | G | 8 | a0001c0001t0001g0216 a0001c0001t0001g0270 a0001c0001t0001g0271 others(5): Show |
8 | HG01169.hp1 HG01255.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.*23-10190T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25486650 | |||||||
| chr12:25486700 | A | T | 51 | a0001c0001t0001g0305 a0001c0001t0002g0054 a0001c0001t0002g0135 others(48): Show |
59 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.*23-10240T>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25486700 | |||||||
| chr12:25486711 | T | C | 4 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(1): Show |
4 | HG02109.hp1 HG03139.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.*23-10251A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25486711 | |||||||
| chr12:25486739 | T | C | 1 | a0002c0002t0002g0008 | 2 | HG02258.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.*23-10279A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25486739 | |||||||
| chr12:25486829 | C | G | 151 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0152 others(148): Show |
154 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.*23-10369G>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25486829 | |||||||
| chr12:25486854 | C | T | 3 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 |
3 | HG03139.hp1 HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.*23-10394G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25486854 | |||||||
| chr12:25486891 | G | C | 1 | a0001c0001t0001g0238 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.*23-10431C>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25486891 | |||||||
| chr12:25486926 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.*23-10466A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25486926 | |||||||
| chr12:25486999 | C | T | 286 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(283): Show |
303 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.*23-10539G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25486999 | |||||||
| chr12:25487053 | A | C | 51 | a0001c0001t0001g0305 a0001c0001t0002g0054 a0001c0001t0002g0135 others(48): Show |
59 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.*23-10593T>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25487053 | |||||||
| chr12:25487065 | A | G | 7 | a0001c0001t0001g0163 a0001c0004t0001g0161 a0001c0004t0001g0164 others(4): Show |
7 | HG01255.hp2 HG02015.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.*23-10605T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25487065 | |||||||
| chr12:25487076 | G | A | 2 | a0002c0002t0002g0056 a0002c0002t0002g0133 |
2 | HG02723.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.*23-10616C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25487076 | |||||||
| chr12:25487079 | G | A | 2 | a0002c0002t0002g0056 a0002c0002t0002g0133 |
2 | HG02723.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.*23-10619C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25487079 | |||||||
| chr12:25487080 | T | C | 2 | a0002c0002t0002g0056 a0002c0002t0002g0133 |
2 | HG02723.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.*23-10620A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25487080 | |||||||
| chr12:25487167 | G | T | 51 | a0001c0001t0001g0305 a0001c0001t0002g0054 a0001c0001t0002g0135 others(48): Show |
59 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.*23-10707C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25487167 | |||||||
| chr12:25487246 | C | A | 3 | a0001c0007t0003g0171 a0003c0005t0003g0156 a0008c0013t0003g0170 |
3 | HG03130.hp1 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.*23-10786G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25487246 | |||||||
| chr12:25487268 | G | T | 286 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(283): Show |
303 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.*23-10808C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25487268 | |||||||
| chr12:25487277 | T | G | 84 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(81): Show |
90 | HG00099.hp2 HG00438.hp1 HG00642.hp2 others(87): Show |
intron_variant | MODIFIER | c.*23-10817A>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25487277 | |||||||
| chr12:25487320 | A | T | 1 | a0001c0001t0001g0021 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.*23-10860T>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25487320 | |||||||
| chr12:25487396 | C | T | 7 | a0001c0001t0001g0216 a0001c0001t0001g0270 a0001c0001t0001g0271 others(4): Show |
7 | HG01169.hp1 HG01255.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.*23-10936G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25487396 | |||||||
| chr12:25487481 | T | G | 1 | a0001c0001t0002g0142 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.*23-11021A>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25487481 | |||||||
| chr12:25487492 | T | A | 3 | a0001c0001t0001g0249 a0001c0001t0001g0348 a0001c0001t0001g0354 |
3 | NA18939.hp1 NA18964.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.*23-11032A>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25487492 | |||||||
| chr12:25487493 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.*23-11033G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25487493 | |||||||
| chr12:25487494 | T | G | 1 | a0001c0001t0001g0151 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.*23-11034A>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25487494 | |||||||
| chr12:25487505 | T | C | 1 | a0001c0001t0001g0237 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.*23-11045A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25487505 | |||||||
| chr12:25487518 | A | C | 1 | a0001c0001t0001g0237 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.*23-11058T>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25487518 | |||||||
| chr12:25487525 | T | C | 1 | a0006c0012t0001g0360 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.*23-11065A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25487525 | |||||||
| chr12:25487536 | G | A | 1 | a0002c0002t0002g0026 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.*23-11076C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25487536 | |||||||
| chr12:25487567 | A | G | 1 | a0001c0001t0001g0237 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.*23-11107T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25487567 | |||||||
| chr12:25487569 | A | G | 5 | a0001c0001t0001g0237 a0002c0002t0001g0290 a0002c0002t0002g0001 others(2): Show |
7 | HG01081.hp1 HG01928.hp1 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.*23-11109T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25487569 | |||||||
| chr12:25487596 | T | A | 286 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(283): Show |
303 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.*23-11136A>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25487596 | |||||||
| chr12:25487618 | A | C | 2 | a0001c0001t0001g0237 a0001c0001t0002g0062 |
2 | HG02723.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.*23-11158T>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25487618 | |||||||
| chr12:25487692 | G | T | 2 | a0001c0001t0002g0080 a0001c0001t0002g0081 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.*23-11232C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25487692 | |||||||
| chr12:25487711 | C | T | 150 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0152 others(147): Show |
153 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.*23-11251G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25487711 | |||||||
| chr12:25487796 | C | T | 1 | a0002c0002t0002g0008 | 2 | HG02258.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.*23-11336G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25487796 | |||||||
| chr12:25487810 | G | GCT | 286 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(283): Show |
303 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.*23-11352_*23-1135 others(6): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25487810 | |||||||
| chr12:25487861 | G | A | 1 | a0002c0002t0002g0055 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.*23-11401C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25487861 | |||||||
| chr12:25487904 | C | T | 1 | a0001c0001t0001g0285 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.*23-11444G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25487904 | |||||||
| chr12:25487922 | G | T | 3 | a0001c0001t0001g0152 a0001c0001t0002g0062 a0002c0002t0002g0051 |
3 | HG01884.hp2 HG02723.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.*23-11462C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25487922 | |||||||
| chr12:25487937 | C | G | 84 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(81): Show |
90 | HG00099.hp2 HG00438.hp1 HG00642.hp2 others(87): Show |
intron_variant | MODIFIER | c.*23-11477G>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25487937 | |||||||
| chr12:25487959 | C | T | 1 | a0002c0002t0002g0055 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.*23-11499G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25487959 | |||||||
| chr12:25487973 | T | C | 86 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(83): Show |
92 | HG00099.hp2 HG00438.hp1 HG00642.hp2 others(89): Show |
intron_variant | MODIFIER | c.*23-11513A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25487973 | |||||||
| chr12:25487974 | G | A | 1 | a0002c0002t0002g0055 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.*23-11514C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25487974 | |||||||
| chr12:25487981 | G | A | 1 | a0002c0002t0002g0055 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.*23-11521C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25487981 | |||||||
| chr12:25487992 | C | T | 200 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0152 others(197): Show |
211 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.*23-11532G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25487992 | |||||||
| chr12:25487993 | G | A | 2 | a0001c0001t0001g0215 a0001c0001t0001g0273 |
2 | HG01081.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.*23-11533C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25487993 | |||||||
| chr12:25487993 | G | T | 1 | a0002c0002t0002g0055 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.*23-11533C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25487993 | |||||||
| chr12:25487999 | T | G | 1 | a0001c0001t0001g0151 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.*23-11539A>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25487999 | |||||||
| chr12:25488000 | C | G | 1 | a0002c0002t0002g0007 | 2 | HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.*23-11540G>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25488000 | |||||||
| chr12:25488002 | A | G | 1 | a0002c0002t0002g0055 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.*23-11542T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25488002 | |||||||
| chr12:25488030 | G | A | 1 | a0001c0001t0002g0117 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.*23-11570C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25488030 | |||||||
| chr12:25488054 | C | T | 1 | a0002c0002t0002g0055 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.*23-11594G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25488054 | |||||||
| chr12:25488056 | G | T | 1 | a0001c0001t0001g0253 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.*23-11596C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25488056 | |||||||
| chr12:25488100 | A | G | 1 | a0002c0002t0002g0055 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.*23-11640T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25488100 | |||||||
| chr12:25488104 | G | A | 1 | a0002c0002t0002g0055 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.*23-11644C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25488104 | |||||||
| chr12:25488123 | T | G | 1 | a0002c0002t0002g0055 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.*23-11663A>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25488123 | |||||||
| chr12:25488146 | A | G | 1 | a0002c0002t0002g0055 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.*23-11686T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25488146 | |||||||
| chr12:25488171 | C | T | 1 | a0002c0002t0002g0055 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.*23-11711G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25488171 | |||||||
| chr12:25488199 | G | A | 1 | a0002c0002t0002g0055 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.*23-11739C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25488199 | |||||||
| chr12:25488232 | C | G | 2 | a0002c0002t0001g0289 a0002c0002t0002g0028 |
2 | HG01257.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.*23-11772G>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25488232 | |||||||
| chr12:25488234 | C | A | 88 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(85): Show |
94 | HG00099.hp2 HG00438.hp1 HG00642.hp2 others(91): Show |
intron_variant | MODIFIER | c.*23-11774G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25488234 | |||||||
| chr12:25488328 | A | G | 1 | a0002c0002t0002g0055 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.*23-11868T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25488328 | |||||||
| chr12:25488366 | G | A | 3 | a0001c0007t0003g0171 a0003c0005t0003g0156 a0008c0013t0003g0170 |
3 | HG03130.hp1 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.*23-11906C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25488366 | |||||||
| chr12:25488400 | T | C | 103 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0179 others(100): Show |
105 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.*23-11940A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25488400 | |||||||
| chr12:25488482 | G | A | 1 | a0001c0001t0003g0269 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.*23-12022C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25488482 | |||||||
| chr12:25488561 | C | G | 1 | a0002c0002t0002g0051 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.*23-12101G>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25488561 | |||||||
| chr12:25488573 | T | C | 7 | a0001c0001t0001g0163 a0001c0004t0001g0161 a0001c0004t0001g0164 others(4): Show |
7 | HG01255.hp2 HG02015.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.*23-12113A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25488573 | |||||||
| chr12:25488584 | T | C | 1 | a0001c0001t0001g0297 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.*23-12124A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25488584 | |||||||
| chr12:25488585 | C | G | 1 | a0001c0001t0001g0262 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.*23-12125G>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25488585 | |||||||
| chr12:25488585 | C | T | 1 | a0001c0001t0001g0297 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.*23-12125G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25488585 | |||||||
| chr12:25488608 | C | T | 3 | a0001c0001t0001g0152 a0001c0001t0002g0062 a0002c0002t0002g0051 |
3 | HG01884.hp2 HG02723.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.*23-12148G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25488608 | |||||||
| chr12:25488609 | G | A | 7 | a0001c0001t0001g0163 a0001c0004t0001g0161 a0001c0004t0001g0164 others(4): Show |
7 | HG01255.hp2 HG02015.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.*23-12149C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25488609 | |||||||
| chr12:25488708 | T | C | 1 | a0006c0012t0001g0360 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.*23-12248A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25488708 | |||||||
| chr12:25488832 | G | C | 1 | a0002c0002t0002g0055 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.*23-12372C>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25488832 | |||||||
| chr12:25488894 | G | A | 1 | a0008c0013t0003g0170 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.*23-12434C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25488894 | |||||||
| chr12:25488919 | T | A | 1 | a0002c0002t0002g0122 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.*23-12459A>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25488919 | |||||||
| chr12:25488940 | G | A | 2 | a0001c0001t0001g0152 a0002c0002t0002g0051 |
2 | HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.*23-12480C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25488940 | |||||||
| chr12:25488944 | G | A | 5 | a0001c0001t0002g0068 a0001c0001t0002g0083 a0001c0001t0002g0110 others(2): Show |
5 | HG01069.hp1 HG02040.hp2 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.*23-12484C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25488944 | |||||||
| chr12:25488960 | C | A | 54 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(51): Show |
59 | HG00438.hp1 HG01074.hp1 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.*23-12500G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25488960 | |||||||
| chr12:25488996 | C | T | 1 | a0001c0001t0001g0315 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.*23-12536G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25488996 | |||||||
| chr12:25489017 | A | C | 1 | a0001c0001t0001g0185 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.*23-12557T>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25489017 | |||||||
| chr12:25489064 | G | A | 1 | a0001c0001t0001g0314 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.*23-12604C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25489064 | |||||||
| chr12:25489098 | T | C | 326 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(323): Show |
349 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(346): Show |
intron_variant | MODIFIER | c.*23-12638A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25489098 | |||||||
| chr12:25489150 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.*23-12690G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25489150 | |||||||
| chr12:25489171 | C | T | 1 | a0001c0015t0001g0172 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.*23-12711G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25489171 | |||||||
| chr12:25489226 | A | C | 8 | a0002c0002t0001g0022 a0002c0002t0001g0219 a0002c0002t0001g0289 others(5): Show |
9 | HG01257.hp1 HG01952.hp2 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.*23-12766T>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25489226 | |||||||
| chr12:25489235 | T | C | 64 | a0001c0001t0001g0151 a0001c0001t0001g0216 a0001c0001t0001g0250 others(61): Show |
73 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(70): Show |
intron_variant | MODIFIER | c.*23-12775A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25489235 | |||||||
| chr12:25489276 | T | C | 1 | a0007c0011t0002g0076 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.*23-12816A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25489276 | |||||||
| chr12:25489278 | A | C | 1 | a0007c0011t0002g0076 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.*23-12818T>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25489278 | |||||||
| chr12:25489326 | G | C | 60 | a0001c0001t0001g0151 a0001c0001t0001g0216 a0001c0001t0001g0270 others(57): Show |
69 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.*23-12866C>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25489326 | |||||||
| chr12:25489369 | C | T | 1 | a0002c0002t0002g0055 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.*23-12909G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25489369 | |||||||
| chr12:25489385 | G | A | 1 | a0001c0001t0001g0346 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.*23-12925C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25489385 | |||||||
| chr12:25489423 | G | T | 60 | a0001c0001t0001g0151 a0001c0001t0001g0216 a0001c0001t0001g0270 others(57): Show |
69 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.*23-12963C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25489423 | |||||||
| chr12:25489475 | C | A | 60 | a0001c0001t0001g0151 a0001c0001t0001g0216 a0001c0001t0001g0270 others(57): Show |
69 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.*23-13015G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25489475 | |||||||
| chr12:25489482 | T | C | 60 | a0001c0001t0001g0151 a0001c0001t0001g0216 a0001c0001t0001g0270 others(57): Show |
69 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.*23-13022A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25489482 | |||||||
| chr12:25489507 | G | A | 211 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0151 others(208): Show |
223 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.*23-13047C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25489507 | |||||||
| chr12:25489511 | A | G | 60 | a0001c0001t0001g0151 a0001c0001t0001g0216 a0001c0001t0001g0270 others(57): Show |
69 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.*23-13051T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25489511 | |||||||
| chr12:25489551 | T | C | 326 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(323): Show |
349 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(346): Show |
intron_variant | MODIFIER | c.*23-13091A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25489551 | |||||||
| chr12:25489582 | A | C | 60 | a0001c0001t0001g0151 a0001c0001t0001g0216 a0001c0001t0001g0270 others(57): Show |
69 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.*23-13122T>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25489582 | |||||||
| chr12:25489600 | C | T | 60 | a0001c0001t0001g0151 a0001c0001t0001g0216 a0001c0001t0001g0270 others(57): Show |
69 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.*23-13140G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25489600 | |||||||
| chr12:25489601 | G | A | 1 | a0001c0001t0001g0279 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.*23-13141C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25489601 | |||||||
| chr12:25489611 | G | A | 147 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0152 others(144): Show |
150 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.*23-13151C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25489611 | |||||||
| chr12:25489680 | T | C | 60 | a0001c0001t0001g0151 a0001c0001t0001g0216 a0001c0001t0001g0270 others(57): Show |
69 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.*23-13220A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25489680 | |||||||
| chr12:25489695 | T | A | 60 | a0001c0001t0001g0151 a0001c0001t0001g0216 a0001c0001t0001g0270 others(57): Show |
69 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.*23-13235A>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25489695 | |||||||
| chr12:25489718 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.*23-13258C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25489718 | |||||||
| chr12:25489730 | C | G | 1 | a0001c0001t0001g0217 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.*23-13270G>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25489730 | |||||||
| chr12:25490016 | T | A | 1 | a0001c0001t0001g0297 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.*23-13556A>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25490016 | |||||||
| chr12:25490077 | G | A | 1 | a0001c0001t0002g0112 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.*23-13617C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25490077 | |||||||
| chr12:25490156 | TC | T | 8 | a0001c0001t0001g0216 a0001c0001t0001g0270 a0001c0001t0001g0271 others(5): Show |
8 | HG01169.hp1 HG01255.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.*22+13581delG | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25490156 | |||||||
| chr12:25490176 | A | C | 60 | a0001c0001t0001g0151 a0001c0001t0001g0216 a0001c0001t0001g0270 others(57): Show |
69 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.*22+13562T>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25490176 | |||||||
| chr12:25490209 | G | A | 334 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(331): Show |
358 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(355): Show |
intron_variant | MODIFIER | c.*22+13529C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25490209 | |||||||
| chr12:25490272 | C | T | 3 | a0001c0001t0001g0152 a0001c0001t0002g0062 a0002c0002t0002g0051 |
3 | HG01884.hp2 HG02723.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.*22+13466G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25490272 | |||||||
| chr12:25490316 | TA | T | 147 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0152 others(144): Show |
150 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.*22+13421delT | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25490316 | |||||||
| chr12:25490382 | C | T | 30 | a0001c0001t0001g0185 a0001c0001t0001g0264 a0001c0001t0001g0309 others(27): Show |
31 | HG00408.hp1 HG00423.hp1 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.*22+13356G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25490382 | |||||||
| chr12:25490407 | A | G | 2 | a0001c0001t0001g0348 a0001c0001t0001g0354 |
2 | NA18939.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.*22+13331T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25490407 | |||||||
| chr12:25490552 | C | T | 60 | a0001c0001t0001g0151 a0001c0001t0001g0216 a0001c0001t0001g0270 others(57): Show |
69 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.*22+13186G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25490552 | |||||||
| chr12:25490553 | G | A | 1 | a0002c0002t0001g0162 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.*22+13185C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25490553 | |||||||
| chr12:25490586 | A | G | 1 | a0001c0001t0001g0285 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.*22+13152T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25490586 | |||||||
| chr12:25490638 | G | C | 179 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(176): Show |
198 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.*22+13100C>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25490638 | |||||||
| chr12:25490656 | G | T | 126 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(123): Show |
137 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.*22+13082C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25490656 | |||||||
| chr12:25490862 | T | G | 1 | a0001c0001t0001g0254 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.*22+12876A>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25490862 | |||||||
| chr12:25490991 | T | C | 60 | a0001c0001t0001g0151 a0001c0001t0001g0216 a0001c0001t0001g0270 others(57): Show |
69 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.*22+12747A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25490991 | |||||||
| chr12:25491017 | T | C | 60 | a0001c0001t0001g0151 a0001c0001t0001g0216 a0001c0001t0001g0270 others(57): Show |
69 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.*22+12721A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25491017 | |||||||
| chr12:25491112 | A | G | 1 | a0002c0002t0002g0126 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.*22+12626T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25491112 | |||||||
| chr12:25491180 | A | G | 1 | a0001c0001t0001g0255 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.*22+12558T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25491180 | |||||||
| chr12:25491430 | C | T | 30 | a0001c0001t0001g0185 a0001c0001t0001g0264 a0001c0001t0001g0309 others(27): Show |
31 | HG00408.hp1 HG00423.hp1 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.*22+12308G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25491430 | |||||||
| chr12:25491460 | C | T | 60 | a0001c0001t0001g0151 a0001c0001t0001g0216 a0001c0001t0001g0270 others(57): Show |
69 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.*22+12278G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25491460 | |||||||
| chr12:25491575 | A | G | 8 | a0001c0001t0001g0216 a0001c0001t0001g0270 a0001c0001t0001g0271 others(5): Show |
8 | HG01169.hp1 HG01255.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.*22+12163T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25491575 | |||||||
| chr12:25491655 | T | A | 59 | a0001c0001t0001g0151 a0001c0001t0001g0216 a0001c0001t0001g0270 others(56): Show |
67 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.*22+12083A>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25491655 | |||||||
| chr12:25491719 | C | A | 4 | a0001c0001t0001g0015 a0001c0001t0001g0157 a0001c0001t0001g0158 others(1): Show |
5 | HG02109.hp2 HG02615.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.*22+12019G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25491719 | |||||||
| chr12:25491723 | G | A | 334 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(331): Show |
358 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(355): Show |
intron_variant | MODIFIER | c.*22+12015C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25491723 | |||||||
| chr12:25491801 | G | A | 2 | a0001c0001t0001g0152 a0002c0002t0002g0051 |
2 | HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.*22+11937C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25491801 | |||||||
| chr12:25491801 | G | C | 1 | a0002c0002t0002g0055 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.*22+11937C>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25491801 | |||||||
| chr12:25492074 | T | C | 1 | a0001c0007t0003g0171 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.*22+11664A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25492074 | |||||||
| chr12:25492089 | C | T | 30 | a0001c0001t0001g0185 a0001c0001t0001g0264 a0001c0001t0001g0309 others(27): Show |
31 | HG00408.hp1 HG00423.hp1 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.*22+11649G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25492089 | |||||||
| chr12:25492136 | C | G | 118 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(115): Show |
129 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.*22+11602G>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25492136 | |||||||
| chr12:25492149 | A | G | 60 | a0001c0001t0001g0151 a0001c0001t0001g0216 a0001c0001t0001g0270 others(57): Show |
69 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.*22+11589T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25492149 | |||||||
| chr12:25492169 | A | G | 2 | a0002c0002t0001g0289 a0002c0002t0002g0028 |
2 | HG01257.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.*22+11569T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25492169 | |||||||
| chr12:25492430 | A | T | 60 | a0001c0001t0001g0151 a0001c0001t0001g0216 a0001c0001t0001g0270 others(57): Show |
69 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.*22+11308T>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25492430 | |||||||
| chr12:25492729 | C | T | 1 | a0001c0001t0001g0321 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.*22+11009G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25492729 | |||||||
| chr12:25492883 | T | C | 60 | a0001c0001t0001g0151 a0001c0001t0001g0216 a0001c0001t0001g0270 others(57): Show |
69 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.*22+10855A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25492883 | |||||||
| chr12:25493218 | T | G | 59 | a0001c0001t0001g0151 a0001c0001t0001g0216 a0001c0001t0001g0270 others(56): Show |
67 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.*22+10520A>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25493218 | |||||||
| chr12:25493245 | T | C | 60 | a0001c0001t0001g0151 a0001c0001t0001g0216 a0001c0001t0001g0270 others(57): Show |
69 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.*22+10493A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25493245 | |||||||
| chr12:25493350 | T | C | 88 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(85): Show |
94 | HG00099.hp2 HG00438.hp1 HG00642.hp2 others(91): Show |
intron_variant | MODIFIER | c.*22+10388A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25493350 | |||||||
| chr12:25493383 | A | C | 2 | a0001c0001t0001g0163 a0002c0002t0001g0355 |
2 | HG01255.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.*22+10355T>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25493383 | |||||||
| chr12:25493398 | T | C | 60 | a0001c0001t0001g0151 a0001c0001t0001g0216 a0001c0001t0001g0270 others(57): Show |
69 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.*22+10340A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25493398 | |||||||
| chr12:25493452 | T | C | 12 | a0001c0001t0001g0178 a0001c0001t0001g0206 a0001c0001t0001g0207 others(9): Show |
12 | HG00438.hp1 HG01943.hp2 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.*22+10286A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25493452 | |||||||
| chr12:25493495 | A | G | 1 | a0002c0003t0002g0060 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.*22+10243T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25493495 | |||||||
| chr12:25493510 | T | C | 1 | a0002c0002t0002g0132 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.*22+10228A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25493510 | |||||||
| chr12:25493575 | T | C | 30 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0023 others(27): Show |
35 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.*22+10163A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25493575 | |||||||
| chr12:25493588 | C | G | 1 | a0001c0001t0001g0282 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.*22+10150G>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25493588 | |||||||
| chr12:25493649 | C | T | 51 | a0001c0001t0001g0151 a0001c0001t0001g0305 a0001c0001t0002g0054 others(48): Show |
59 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.*22+10089G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25493649 | |||||||
| chr12:25493828 | T | C | 5 | a0001c0004t0001g0161 a0001c0004t0001g0164 a0001c0004t0001g0165 others(2): Show |
5 | HG02015.hp2 HG02027.hp2 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.*22+9910A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25493828 | |||||||
| chr12:25493905 | T | C | 102 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0179 others(99): Show |
104 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.*22+9833A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25493905 | |||||||
| chr12:25493924 | A | G | 60 | a0001c0001t0001g0151 a0001c0001t0001g0216 a0001c0001t0001g0270 others(57): Show |
69 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.*22+9814T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25493924 | |||||||
| chr12:25494117 | T | C | 61 | a0001c0001t0001g0151 a0001c0001t0001g0216 a0001c0001t0001g0270 others(58): Show |
70 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(67): Show |
intron_variant | MODIFIER | c.*22+9621A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25494117 | |||||||
| chr12:25494301 | GAAACTTT others(7570): Show |
G | 2 | a0001c0001t0001g0218 a0001c0001t0001g0286 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.*22+1860_*22+9436d others(2): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25494301 | |||||||
| chr12:25494445 | T | G | 1 | a0002c0002t0002g0008 | 2 | HG02258.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.*22+9293A>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25494445 | |||||||
| chr12:25494459 | C | A | 2 | a0002c0002t0002g0141 a0003c0005t0001g0155 |
2 | HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.*22+9279G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25494459 | |||||||
| chr12:25494765 | T | C | 61 | a0001c0001t0001g0151 a0001c0001t0001g0216 a0001c0001t0001g0236 others(58): Show |
70 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(67): Show |
intron_variant | MODIFIER | c.*22+8973A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25494765 | |||||||
| chr12:25494920 | G | A | 1 | a0002c0002t0001g0160 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.*22+8818C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25494920 | |||||||
| chr12:25495114 | G | C | 1 | a0002c0002t0002g0041 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.*22+8624C>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25495114 | |||||||
| chr12:25495196 | T | C | 30 | a0001c0001t0001g0185 a0001c0001t0001g0264 a0001c0001t0001g0309 others(27): Show |
31 | HG00408.hp1 HG00423.hp1 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.*22+8542A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25495196 | |||||||
| chr12:25495249 | C | CGCGTGTG others(1): Show |
9 | a0001c0001t0001g0261 a0001c0001t0002g0009 a0001c0001t0002g0010 others(6): Show |
11 | HG00099.hp1 HG00639.hp1 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.*22+8488_*22+8489i others(10): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25495249 | |||||||
| chr12:25495249 | C | CGT | 41 | a0001c0001t0001g0185 a0001c0001t0001g0236 a0001c0001t0001g0264 others(38): Show |
45 | HG00280.hp1 HG00408.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.*22+8487_*22+8488d others(4): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25495249 | |||||||
| chr12:25495249 | C | CGTGT | 58 | a0001c0001t0001g0146 a0001c0001t0001g0151 a0001c0001t0001g0258 others(55): Show |
63 | HG00280.hp2 HG00423.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.*22+8485_*22+8488d others(6): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25495249 | |||||||
| chr12:25495249 | C | CGTGTGT | 34 | a0001c0001t0001g0024 a0001c0001t0001g0175 a0001c0001t0001g0176 others(31): Show |
34 | HG00673.hp2 HG00738.hp1 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.*22+8483_*22+8488d others(8): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25495249 | |||||||
| chr12:25495249 | C | CGTGTGTG others(1): Show |
88 | a0001c0001t0001g0025 a0001c0001t0001g0148 a0001c0001t0001g0152 others(85): Show |
88 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.*22+8481_*22+8488d others(10): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25495249 | |||||||
| chr12:25495249 | C | CGTGTGTG others(3): Show |
40 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(37): Show |
43 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.*22+8479_*22+8488d others(12): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25495249 | |||||||
| chr12:25495249 | C | CGTGTGTG others(5): Show |
4 | a0001c0001t0001g0023 a0001c0001t0001g0220 a0001c0001t0001g0232 others(1): Show |
4 | HG01934.hp2 HG02293.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.*22+8477_*22+8488d others(14): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25495249 | |||||||
| chr12:25495249 | C | CGTGTGTG others(11): Show |
1 | a0001c0001t0001g0311 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.*22+8471_*22+8488d others(20): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25495249 | |||||||
| chr12:25495249 | CGT | C | 11 | a0001c0001t0001g0015 a0001c0001t0001g0157 a0001c0001t0001g0158 others(8): Show |
12 | HG01496.hp2 HG02040.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.*22+8487_*22+8488d others(4): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25495249 | |||||||
| chr12:25495256 | G | GTGTGTGT others(1): Show |
7 | a0001c0001t0001g0018 a0001c0001t0001g0174 a0001c0001t0001g0195 others(4): Show |
8 | HG02148.hp2 NA18945.hp1 NA18948.hp1 others(5): Show |
intron_variant | MODIFIER | c.*22+8481_*22+8482i others(10): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25495256 | |||||||
| chr12:25495258 | G | GTGTGTA | 50 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(47): Show |
54 | HG00438.hp1 HG01074.hp1 HG01081.hp2 others(51): Show |
intron_variant | MODIFIER | c.*22+8479_*22+8480i others(8): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25495258 | |||||||
| chr12:25495394 | G | T | 115 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(112): Show |
126 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.*22+8344C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25495394 | |||||||
| chr12:25495566 | T | C | 2 | a0002c0002t0002g0056 a0002c0002t0002g0133 |
2 | HG02723.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.*22+8172A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25495566 | |||||||
| chr12:25495742 | A | G | 53 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(50): Show |
58 | HG00438.hp1 HG01074.hp1 HG01081.hp2 others(55): Show |
intron_variant | MODIFIER | c.*22+7996T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25495742 | |||||||
| chr12:25495910 | A | G | 1 | a0002c0003t0005g0050 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.*22+7828T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25495910 | |||||||
| chr12:25496071 | T | C | 1 | a0002c0002t0001g0162 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.*22+7667A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25496071 | |||||||
| chr12:25496423 | G | A | 178 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(175): Show |
198 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.*22+7315C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25496423 | |||||||
| chr12:25496572 | C | T | 5 | a0001c0004t0001g0161 a0001c0004t0001g0164 a0001c0004t0001g0165 others(2): Show |
5 | HG02015.hp2 HG02027.hp2 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.*22+7166G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25496572 | |||||||
| chr12:25496619 | G | A | 1 | a0001c0001t0002g0063 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.*22+7119C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25496619 | |||||||
| chr12:25496676 | A | AT | 5 | a0001c0004t0001g0161 a0001c0004t0001g0164 a0001c0004t0001g0165 others(2): Show |
5 | HG02015.hp2 HG02027.hp2 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.*22+7061dupA | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25496676 | |||||||
| chr12:25496697 | A | C | 1 | a0002c0002t0002g0008 | 2 | HG02258.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.*22+7041T>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25496697 | |||||||
| chr12:25496789 | A | G | 61 | a0001c0001t0001g0151 a0001c0001t0001g0216 a0001c0001t0001g0236 others(58): Show |
70 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(67): Show |
intron_variant | MODIFIER | c.*22+6949T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25496789 | |||||||
| chr12:25496859 | A | T | 7 | a0001c0001t0001g0163 a0001c0004t0001g0161 a0001c0004t0001g0164 others(4): Show |
7 | HG01255.hp2 HG02015.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.*22+6879T>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25496859 | |||||||
| chr12:25496927 | A | AT | 7 | a0001c0001t0001g0163 a0001c0004t0001g0161 a0001c0004t0001g0164 others(4): Show |
7 | HG01255.hp2 HG02015.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.*22+6810dupA | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25496927 | |||||||
| chr12:25497047 | T | A | 2 | a0001c0001t0001g0228 a0001c0001t0002g0143 |
2 | HG01891.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.*22+6691A>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25497047 | |||||||
| chr12:25497317 | G | A | 8 | a0001c0001t0001g0216 a0001c0001t0001g0270 a0001c0001t0001g0271 others(5): Show |
8 | HG01169.hp1 HG01255.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.*22+6421C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25497317 | |||||||
| chr12:25497381 | C | T | 1 | a0001c0001t0001g0341 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.*22+6357G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25497381 | |||||||
| chr12:25497577 | C | T | 1 | a0002c0002t0002g0008 | 2 | HG02258.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.*22+6161G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25497577 | |||||||
| chr12:25497668 | G | C | 1 | a0001c0001t0001g0003 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.*22+6070C>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25497668 | |||||||
| chr12:25497698 | T | G | 3 | a0001c0001t0001g0152 a0001c0001t0002g0062 a0002c0002t0002g0051 |
3 | HG01884.hp2 HG02723.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.*22+6040A>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25497698 | |||||||
| chr12:25497797 | GA | G | 59 | a0001c0001t0001g0151 a0001c0001t0001g0216 a0001c0001t0001g0270 others(56): Show |
68 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(65): Show |
intron_variant | MODIFIER | c.*22+5940delT | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25497797 | |||||||
| chr12:25497925 | A | G | 1 | a0001c0001t0001g0018 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.*22+5813T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25497925 | |||||||
| chr12:25497933 | G | C | 2 | a0001c0001t0001g0303 a0001c0001t0001g0350 |
2 | HG02040.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.*22+5805C>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25497933 | |||||||
| chr12:25497992 | C | T | 116 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(113): Show |
127 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.*22+5746G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25497992 | |||||||
| chr12:25498284 | T | C | 59 | a0001c0001t0001g0151 a0001c0001t0001g0216 a0001c0001t0001g0270 others(56): Show |
67 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.*22+5454A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25498284 | |||||||
| chr12:25498298 | C | A | 1 | a0001c0001t0002g0105 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.*22+5440G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25498298 | |||||||
| chr12:25498355 | T | C | 60 | a0001c0001t0001g0151 a0001c0001t0001g0216 a0001c0001t0001g0270 others(57): Show |
69 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.*22+5383A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25498355 | |||||||
| chr12:25498413 | G | A | 3 | a0002c0003t0002g0029 a0002c0003t0002g0030 a0002c0003t0002g0031 |
3 | HG00642.hp1 HG01496.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.*22+5325C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25498413 | |||||||
| chr12:25498537 | G | A | 1 | a0002c0002t0002g0134 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.*22+5201C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25498537 | |||||||
| chr12:25498660 | C | T | 1 | a0006c0012t0001g0360 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.*22+5078G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25498660 | |||||||
| chr12:25498761 | A | AT | 5 | a0001c0001t0002g0068 a0001c0001t0002g0083 a0001c0001t0002g0110 others(2): Show |
5 | HG01069.hp1 HG02040.hp2 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.*22+4976dupA | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25498761 | |||||||
| chr12:25498823 | G | A | 1 | a0001c0001t0001g0206 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.*22+4915C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25498823 | |||||||
| chr12:25498965 | A | G | 60 | a0001c0001t0001g0151 a0001c0001t0001g0216 a0001c0001t0001g0270 others(57): Show |
69 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.*22+4773T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25498965 | |||||||
| chr12:25498983 | T | C | 1 | a0002c0002t0002g0008 | 2 | HG02258.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.*22+4755A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25498983 | |||||||
| chr12:25499048 | C | T | 3 | a0001c0001t0001g0163 a0002c0002t0001g0355 a0006c0012t0001g0360 |
3 | HG01255.hp2 HG01891.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.*22+4690G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25499048 | |||||||
| chr12:25499073 | C | A | 3 | a0001c0001t0001g0152 a0001c0001t0002g0062 a0002c0002t0002g0051 |
3 | HG01884.hp2 HG02723.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.*22+4665G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25499073 | |||||||
| chr12:25499254 | T | TTTTTTTT others(183): Show |
4 | a0001c0004t0001g0161 a0001c0004t0001g0164 a0001c0004t0001g0165 others(1): Show |
4 | HG02015.hp2 NA19012.hp2 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.*22+4483_*22+4484i others(192): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25499254 | |||||||
| chr12:25499254 | T | TTTTTTTT others(184): Show |
1 | a0001c0004t0001g0166 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.*22+4483_*22+4484i others(193): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25499254 | |||||||
| chr12:25499259 | T | A | 5 | a0001c0004t0001g0161 a0001c0004t0001g0164 a0001c0004t0001g0165 others(2): Show |
5 | HG02015.hp2 HG02027.hp2 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.*22+4479A>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25499259 | |||||||
| chr12:25499263 | A | G | 5 | a0001c0004t0001g0161 a0001c0004t0001g0164 a0001c0004t0001g0165 others(2): Show |
5 | HG02015.hp2 HG02027.hp2 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.*22+4475T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25499263 | |||||||
| chr12:25499265 | A | G | 5 | a0001c0004t0001g0161 a0001c0004t0001g0164 a0001c0004t0001g0165 others(2): Show |
5 | HG02015.hp2 HG02027.hp2 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.*22+4473T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25499265 | |||||||
| chr12:25499273 | T | C | 5 | a0001c0004t0001g0161 a0001c0004t0001g0164 a0001c0004t0001g0165 others(2): Show |
5 | HG02015.hp2 HG02027.hp2 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.*22+4465A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25499273 | |||||||
| chr12:25499274 | A | G | 5 | a0001c0004t0001g0161 a0001c0004t0001g0164 a0001c0004t0001g0165 others(2): Show |
5 | HG02015.hp2 HG02027.hp2 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.*22+4464T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25499274 | |||||||
| chr12:25499276 | G | T | 5 | a0001c0004t0001g0161 a0001c0004t0001g0164 a0001c0004t0001g0165 others(2): Show |
5 | HG02015.hp2 HG02027.hp2 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.*22+4462C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25499276 | |||||||
| chr12:25499279 | T | A | 5 | a0001c0004t0001g0161 a0001c0004t0001g0164 a0001c0004t0001g0165 others(2): Show |
5 | HG02015.hp2 HG02027.hp2 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.*22+4459A>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25499279 | |||||||
| chr12:25499280 | C | G | 5 | a0001c0004t0001g0161 a0001c0004t0001g0164 a0001c0004t0001g0165 others(2): Show |
5 | HG02015.hp2 HG02027.hp2 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.*22+4458G>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25499280 | |||||||
| chr12:25499283 | A | G | 5 | a0001c0004t0001g0161 a0001c0004t0001g0164 a0001c0004t0001g0165 others(2): Show |
5 | HG02015.hp2 HG02027.hp2 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.*22+4455T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25499283 | |||||||
| chr12:25499286 | C | A | 5 | a0001c0004t0001g0161 a0001c0004t0001g0164 a0001c0004t0001g0165 others(2): Show |
5 | HG02015.hp2 HG02027.hp2 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.*22+4452G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25499286 | |||||||
| chr12:25499293 | T | C | 5 | a0001c0004t0001g0161 a0001c0004t0001g0164 a0001c0004t0001g0165 others(2): Show |
5 | HG02015.hp2 HG02027.hp2 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.*22+4445A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25499293 | |||||||
| chr12:25499296 | A | T | 5 | a0001c0004t0001g0161 a0001c0004t0001g0164 a0001c0004t0001g0165 others(2): Show |
5 | HG02015.hp2 HG02027.hp2 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.*22+4442T>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25499296 | |||||||
| chr12:25499298 | T | TCCTGACC others(10): Show |
5 | a0001c0004t0001g0161 a0001c0004t0001g0164 a0001c0004t0001g0165 others(2): Show |
5 | HG02015.hp2 HG02027.hp2 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.*22+4439_*22+4440i others(19): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25499298 | |||||||
| chr12:25499302 | A | G | 5 | a0001c0004t0001g0161 a0001c0004t0001g0164 a0001c0004t0001g0165 others(2): Show |
5 | HG02015.hp2 HG02027.hp2 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.*22+4436T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25499302 | |||||||
| chr12:25499321 | T | C | 5 | a0001c0004t0001g0161 a0001c0004t0001g0164 a0001c0004t0001g0165 others(2): Show |
5 | HG02015.hp2 HG02027.hp2 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.*22+4417A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25499321 | |||||||
| chr12:25499415 | T | C | 1 | a0001c0001t0001g0303 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.*22+4323A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25499415 | |||||||
| chr12:25499508 | T | C | 116 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(113): Show |
127 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.*22+4230A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25499508 | |||||||
| chr12:25499526 | A | G | 5 | a0001c0004t0001g0161 a0001c0004t0001g0164 a0001c0004t0001g0165 others(2): Show |
5 | HG02015.hp2 HG02027.hp2 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.*22+4212T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25499526 | |||||||
| chr12:25499736 | G | GA | 40 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0023 others(37): Show |
46 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.*22+4001dupT | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25499736 | |||||||
| chr12:25499745 | A | C | 60 | a0001c0001t0001g0151 a0001c0001t0001g0216 a0001c0001t0001g0236 others(57): Show |
68 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(65): Show |
intron_variant | MODIFIER | c.*22+3993T>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25499745 | |||||||
| chr12:25499862 | G | A | 1 | a0001c0001t0002g0115 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.*22+3876C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25499862 | |||||||
| chr12:25499868 | C | T | 1 | a0002c0002t0002g0055 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.*22+3870G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25499868 | |||||||
| chr12:25500139 | G | A | 4 | a0001c0001t0002g0096 a0001c0001t0002g0097 a0001c0001t0002g0098 others(1): Show |
4 | NA19000.hp2 NA19057.hp1 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.*22+3599C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25500139 | |||||||
| chr12:25500181 | A | C | 1 | a0001c0001t0002g0073 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.*22+3557T>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25500181 | |||||||
| chr12:25500403 | T | C | 4 | a0002c0003t0002g0052 a0002c0003t0002g0059 a0002c0003t0002g0060 others(1): Show |
4 | HG02015.hp1 HG02602.hp2 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.*22+3335A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25500403 | |||||||
| chr12:25500621 | A | G | 60 | a0001c0001t0001g0151 a0001c0001t0001g0216 a0001c0001t0001g0236 others(57): Show |
68 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(65): Show |
intron_variant | MODIFIER | c.*22+3117T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25500621 | |||||||
| chr12:25500834 | AC | A | 5 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(2): Show |
5 | HG02109.hp1 HG03139.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.*22+2903delG | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25500834 | |||||||
| chr12:25500869 | T | C | 2 | a0001c0001t0001g0215 a0001c0001t0001g0273 |
2 | HG01081.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.*22+2869A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25500869 | |||||||
| chr12:25500930 | C | T | 350 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(347): Show |
376 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(373): Show |
intron_variant | MODIFIER | c.*22+2808G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25500930 | |||||||
| chr12:25500943 | A | G | 1 | a0002c0002t0002g0040 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.*22+2795T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25500943 | |||||||
| chr12:25500960 | G | A | 1 | a0001c0007t0004g0173 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.*22+2778C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25500960 | |||||||
| chr12:25500981 | C | CTGTT | 4 | a0001c0001t0002g0054 a0001c0001t0002g0135 a0002c0002t0001g0180 others(1): Show |
4 | HG02257.hp1 HG02970.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.*22+2753_*22+2756d others(6): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25500981 | |||||||
| chr12:25500981 | CTGTT | C | 115 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(112): Show |
126 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.*22+2753_*22+2756d others(6): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25500981 | |||||||
| chr12:25501115 | G | A | 1 | a0001c0001t0001g0147 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.*22+2623C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25501115 | |||||||
| chr12:25501206 | C | G | 61 | a0001c0001t0001g0151 a0001c0001t0001g0216 a0001c0001t0001g0236 others(58): Show |
70 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(67): Show |
intron_variant | MODIFIER | c.*22+2532G>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25501206 | |||||||
| chr12:25501222 | C | T | 1 | a0001c0001t0001g0178 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.*22+2516G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25501222 | |||||||
| chr12:25501436 | G | T | 51 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(48): Show |
56 | HG00438.hp1 HG01074.hp1 HG01943.hp2 others(53): Show |
intron_variant | MODIFIER | c.*22+2302C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25501436 | |||||||
| chr12:25501511 | A | C | 5 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(2): Show |
5 | HG02109.hp1 HG03139.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.*22+2227T>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25501511 | |||||||
| chr12:25501520 | T | C | 1 | a0002c0002t0002g0055 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.*22+2218A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25501520 | |||||||
| chr12:25501730 | T | C | 1 | a0001c0001t0001g0264 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.*22+2008A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25501730 | |||||||
| chr12:25501926 | G | A | 2 | a0001c0001t0001g0327 a0001c0001t0001g0333 |
2 | NA18950.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.*22+1812C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25501926 | |||||||
| chr12:25501972 | G | T | 2 | a0002c0002t0002g0056 a0002c0002t0002g0133 |
2 | HG02723.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.*22+1766C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25501972 | |||||||
| chr12:25502043 | T | A | 114 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(111): Show |
120 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.*22+1695A>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25502043 | |||||||
| chr12:25502043 | T | C | 1 | a0006c0012t0001g0360 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.*22+1695A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25502043 | |||||||
| chr12:25502186 | G | A | 1 | a0002c0002t0002g0008 | 2 | HG02258.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.*22+1552C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25502186 | |||||||
| chr12:25502219 | T | A | 52 | a0001c0001t0001g0236 a0001c0001t0002g0054 a0001c0001t0002g0135 others(49): Show |
61 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(58): Show |
intron_variant | MODIFIER | c.*22+1519A>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25502219 | |||||||
| chr12:25502235 | T | C | 84 | a0001c0001t0001g0179 a0001c0001t0001g0182 a0001c0001t0001g0184 others(81): Show |
87 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.*22+1503A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25502235 | |||||||
| chr12:25502381 | C | G | 1 | a0002c0002t0002g0043 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.*22+1357G>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25502381 | |||||||
| chr12:25502538 | G | A | 1 | a0001c0001t0002g0107 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.*22+1200C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25502538 | |||||||
| chr12:25502588 | C | T | 31 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0023 others(28): Show |
36 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.*22+1150G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25502588 | |||||||
| chr12:25502714 | C | T | 50 | a0001c0001t0002g0054 a0001c0001t0002g0135 a0002c0002t0001g0022 others(47): Show |
58 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.*22+1024G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25502714 | |||||||
| chr12:25502726 | A | C | 168 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(165): Show |
179 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.*22+1012T>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25502726 | |||||||
| chr12:25502727 | G | A | 9 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0321 others(6): Show |
9 | HG00741.hp1 HG01123.hp1 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.*22+1011C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25502727 | |||||||
| chr12:25502741 | T | C | 2 | a0001c0001t0001g0163 a0002c0002t0001g0355 |
2 | HG01255.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.*22+997A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25502741 | |||||||
| chr12:25502876 | T | G | 3 | a0001c0001t0001g0186 a0001c0007t0003g0171 a0008c0013t0003g0170 |
3 | HG03209.hp1 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.*22+862A>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25502876 | |||||||
| chr12:25502944 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.*22+794T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25502944 | |||||||
| chr12:25503411 | T | C | 1 | a0001c0001t0002g0070 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.*22+327A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25503411 | |||||||
| chr12:25503498 | T | A | 3 | a0001c0001t0002g0068 a0001c0001t0002g0083 a0001c0001t0002g0110 |
3 | NA18975.hp1 NA19085.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.*22+240A>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25503498 | |||||||
| chr12:25503564 | T | C | 51 | a0001c0001t0002g0054 a0001c0001t0002g0135 a0002c0002t0001g0022 others(48): Show |
60 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.*22+174A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25503564 | |||||||
| chr12:25503585 | C | G | 1 | a0002c0002t0002g0051 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.*22+153G>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 9/9 | chr12 | 25503585 | |||||||
| chr12:25503809 | T | TA | 5 | a0001c0001t0001g0179 a0001c0001t0001g0233 a0001c0001t0001g0347 others(2): Show |
5 | HG02132.hp1 HG02572.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.1190-10dupT | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25503809 | |||||||
| chr12:25503893 | T | C | 1 | a0002c0002t0002g0139 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1190-93A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25503893 | |||||||
| chr12:25503986 | C | T | 14 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(11): Show |
14 | HG01169.hp1 HG01255.hp1 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.1190-186G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25503986 | |||||||
| chr12:25504012 | C | T | 3 | a0002c0003t0002g0029 a0002c0003t0002g0030 a0002c0003t0002g0031 |
3 | HG00642.hp1 HG01496.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.1190-212G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25504012 | |||||||
| chr12:25504247 | A | G | 85 | a0001c0001t0001g0179 a0001c0001t0001g0182 a0001c0001t0001g0184 others(82): Show |
88 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.1190-447T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25504247 | |||||||
| chr12:25504335 | G | A | 2 | a0002c0002t0002g0055 a0002c0002t0002g0056 |
2 | HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1190-535C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25504335 | |||||||
| chr12:25504541 | AT | A | 82 | a0001c0001t0001g0179 a0001c0001t0001g0182 a0001c0001t0001g0184 others(79): Show |
85 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.1190-742delA | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25504541 | |||||||
| chr12:25504555 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1190-755G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25504555 | |||||||
| chr12:25504586 | T | C | 221 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(218): Show |
241 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(238): Show |
intron_variant | MODIFIER | c.1190-786A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25504586 | |||||||
| chr12:25504605 | C | T | 1 | a0001c0015t0001g0172 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1190-805G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25504605 | |||||||
| chr12:25505090 | C | T | 55 | a0001c0001t0001g0152 a0001c0001t0002g0054 a0001c0001t0002g0062 others(52): Show |
64 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.1190-1290G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25505090 | |||||||
| chr12:25505140 | C | G | 1 | a0001c0001t0001g0152 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1190-1340G>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25505140 | |||||||
| chr12:25505172 | A | G | 1 | a0002c0002t0002g0008 | 2 | HG02258.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1190-1372T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25505172 | |||||||
| chr12:25505193 | GT | G | 51 | a0001c0001t0002g0054 a0001c0001t0002g0135 a0002c0002t0001g0022 others(48): Show |
60 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.1190-1394delA | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25505193 | |||||||
| chr12:25505239 | A | G | 55 | a0001c0001t0001g0152 a0001c0001t0002g0054 a0001c0001t0002g0062 others(52): Show |
64 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.1190-1439T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25505239 | |||||||
| chr12:25505288 | G | A | 2 | a0002c0002t0002g0012 a0002c0002t0002g0120 |
3 | HG00735.hp2 HG01256.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1190-1488C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25505288 | |||||||
| chr12:25505321 | T | G | 4 | a0002c0002t0002g0141 a0003c0005t0001g0153 a0003c0005t0001g0154 others(1): Show |
4 | HG02630.hp2 HG03098.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1190-1521A>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25505321 | |||||||
| chr12:25505327 | C | T | 53 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(50): Show |
58 | HG00438.hp1 HG01074.hp1 HG01943.hp2 others(55): Show |
intron_variant | MODIFIER | c.1190-1527G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25505327 | |||||||
| chr12:25505606 | T | C | 53 | a0001c0001t0001g0152 a0001c0001t0002g0054 a0001c0001t0002g0062 others(50): Show |
62 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.1190-1806A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25505606 | |||||||
| chr12:25505642 | C | CTAATT | 55 | a0001c0001t0001g0152 a0001c0001t0002g0054 a0001c0001t0002g0062 others(52): Show |
64 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.1190-1843_1190-184 others(9): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25505642 | |||||||
| chr12:25505742 | G | A | 1 | a0002c0002t0001g0162 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1190-1942C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25505742 | |||||||
| chr12:25505829 | T | C | 1 | a0001c0015t0001g0172 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1190-2029A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25505829 | |||||||
| chr12:25506166 | C | T | 1 | a0006c0012t0001g0360 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1190-2366G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25506166 | |||||||
| chr12:25506281 | G | A | 55 | a0001c0001t0001g0152 a0001c0001t0002g0054 a0001c0001t0002g0062 others(52): Show |
64 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.1190-2481C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25506281 | |||||||
| chr12:25506536 | G | C | 1 | a0001c0001t0002g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1190-2736C>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25506536 | |||||||
| chr12:25506582 | T | C | 1 | a0002c0002t0002g0128 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1190-2782A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25506582 | |||||||
| chr12:25506585 | A | G | 1 | a0001c0001t0002g0135 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1190-2785T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25506585 | |||||||
| chr12:25506603 | G | A | 1 | a0001c0001t0002g0088 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1190-2803C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25506603 | |||||||
| chr12:25506612 | A | G | 2 | a0002c0002t0002g0055 a0002c0002t0002g0056 |
2 | HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1190-2812T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25506612 | |||||||
| chr12:25506639 | G | A | 2 | a0001c0001t0001g0152 a0001c0001t0002g0062 |
2 | HG02723.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1190-2839C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25506639 | |||||||
| chr12:25506738 | T | C | 198 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(195): Show |
213 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(210): Show |
intron_variant | MODIFIER | c.1190-2938A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25506738 | |||||||
| chr12:25506744 | T | C | 2 | a0002c0002t0002g0055 a0002c0002t0002g0056 |
2 | HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1190-2944A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25506744 | |||||||
| chr12:25506758 | T | C | 53 | a0001c0001t0001g0152 a0001c0001t0002g0054 a0001c0001t0002g0062 others(50): Show |
62 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.1190-2958A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25506758 | |||||||
| chr12:25506863 | A | T | 2 | a0002c0002t0002g0055 a0002c0002t0002g0056 |
2 | HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1190-3063T>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25506863 | |||||||
| chr12:25506941 | G | A | 3 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 |
3 | HG03139.hp1 HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1190-3141C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25506941 | |||||||
| chr12:25507123 | A | G | 1 | a0002c0002t0002g0008 | 2 | HG02258.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1190-3323T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25507123 | |||||||
| chr12:25507128 | G | A | 1 | a0006c0012t0001g0360 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1190-3328C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25507128 | |||||||
| chr12:25507255 | A | G | 2 | a0001c0001t0001g0345 a0001c0001t0001g0358 |
2 | NA18953.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.1190-3455T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25507255 | |||||||
| chr12:25507289 | C | A | 55 | a0001c0001t0001g0152 a0001c0001t0002g0054 a0001c0001t0002g0062 others(52): Show |
64 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.1190-3489G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25507289 | |||||||
| chr12:25507389 | A | G | 1 | a0002c0002t0002g0004 | 2 | HG03710.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1190-3589T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25507389 | |||||||
| chr12:25507427 | T | A | 55 | a0001c0001t0001g0152 a0001c0001t0002g0054 a0001c0001t0002g0062 others(52): Show |
64 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.1190-3627A>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25507427 | |||||||
| chr12:25507450 | C | G | 1 | a0001c0001t0001g0216 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1190-3650G>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25507450 | |||||||
| chr12:25507644 | C | T | 2 | a0002c0002t0002g0055 a0002c0002t0002g0056 |
2 | HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1190-3844G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25507644 | |||||||
| chr12:25507645 | A | G | 221 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(218): Show |
241 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(238): Show |
intron_variant | MODIFIER | c.1190-3845T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25507645 | |||||||
| chr12:25507746 | A | T | 2 | a0002c0002t0002g0055 a0002c0002t0002g0056 |
2 | HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1190-3946T>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25507746 | |||||||
| chr12:25507882 | A | G | 2 | a0002c0002t0002g0055 a0002c0002t0002g0056 |
2 | HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1190-4082T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25507882 | |||||||
| chr12:25507902 | C | T | 10 | a0001c0001t0001g0216 a0001c0001t0001g0236 a0001c0001t0001g0270 others(7): Show |
10 | HG01169.hp1 HG01255.hp1 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.1190-4102G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25507902 | |||||||
| chr12:25507914 | A | G | 9 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0064 others(6): Show |
11 | HG00099.hp1 HG00639.hp1 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.1190-4114T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25507914 | |||||||
| chr12:25507962 | T | C | 1 | a0001c0001t0001g0230 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1190-4162A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25507962 | |||||||
| chr12:25508011 | G | A | 2 | a0002c0002t0002g0034 a0002c0002t0002g0035 |
2 | HG02451.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1190-4211C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25508011 | |||||||
| chr12:25508084 | T | C | 2 | a0002c0002t0002g0055 a0002c0002t0002g0056 |
2 | HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1190-4284A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25508084 | |||||||
| chr12:25508100 | C | A | 31 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0023 others(28): Show |
36 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.1190-4300G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25508100 | |||||||
| chr12:25508111 | G | GTTCA | 222 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(219): Show |
242 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(239): Show |
intron_variant | MODIFIER | c.1190-4312_1190-431 others(8): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25508111 | |||||||
| chr12:25508223 | T | G | 1 | a0001c0001t0001g0206 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1190-4423A>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25508223 | |||||||
| chr12:25508226 | A | G | 1 | a0002c0002t0002g0008 | 2 | HG02258.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1190-4426T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25508226 | |||||||
| chr12:25508353 | G | T | 86 | a0001c0001t0001g0179 a0001c0001t0001g0182 a0001c0001t0001g0184 others(83): Show |
89 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.1190-4553C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25508353 | |||||||
| chr12:25508396 | G | C | 1 | a0002c0002t0001g0288 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1190-4596C>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25508396 | |||||||
| chr12:25508467 | C | A | 1 | a0001c0001t0002g0071 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1190-4667G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25508467 | |||||||
| chr12:25508488 | T | C | 1 | a0001c0001t0002g0106 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1190-4688A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25508488 | |||||||
| chr12:25508629 | A | G | 2 | a0002c0002t0002g0055 a0002c0002t0002g0056 |
2 | HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1190-4829T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25508629 | |||||||
| chr12:25508832 | T | G | 50 | a0001c0001t0002g0054 a0001c0001t0002g0135 a0002c0002t0001g0022 others(47): Show |
58 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.1190-5032A>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25508832 | |||||||
| chr12:25508859 | C | T | 2 | a0001c0001t0001g0152 a0001c0001t0002g0062 |
2 | HG02723.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1190-5059G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25508859 | |||||||
| chr12:25508902 | T | TCTC | 55 | a0001c0001t0001g0152 a0001c0001t0002g0054 a0001c0001t0002g0062 others(52): Show |
64 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.1190-5105_1190-510 others(7): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25508902 | |||||||
| chr12:25508939 | T | A | 1 | a0003c0005t0003g0156 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1190-5139A>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25508939 | |||||||
| chr12:25508944 | T | C | 2 | a0002c0002t0002g0055 a0002c0002t0002g0056 |
2 | HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1190-5144A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25508944 | |||||||
| chr12:25508952 | G | A | 53 | a0001c0001t0002g0054 a0001c0001t0002g0135 a0002c0002t0001g0022 others(50): Show |
62 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.1190-5152C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25508952 | |||||||
| chr12:25509074 | T | C | 1 | a0002c0002t0002g0144 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1190-5274A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25509074 | |||||||
| chr12:25509077 | G | T | 2 | a0002c0002t0002g0055 a0002c0002t0002g0056 |
2 | HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1190-5277C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25509077 | |||||||
| chr12:25509091 | T | C | 1 | a0002c0002t0002g0039 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1190-5291A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25509091 | |||||||
| chr12:25509210 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1190-5410G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25509210 | |||||||
| chr12:25509327 | C | T | 1 | a0001c0001t0001g0237 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1190-5527G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25509327 | |||||||
| chr12:25509344 | G | A | 3 | a0001c0001t0002g0068 a0001c0001t0002g0083 a0001c0001t0002g0110 |
3 | NA18975.hp1 NA19085.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1190-5544C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25509344 | |||||||
| chr12:25509360 | G | A | 1 | a0001c0001t0001g0302 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1190-5560C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25509360 | |||||||
| chr12:25509608 | T | C | 2 | a0001c0001t0001g0322 a0001c0001t0001g0356 |
2 | NA18951.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.1190-5808A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25509608 | |||||||
| chr12:25509616 | C | A | 1 | a0001c0001t0001g0163 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1190-5816G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25509616 | |||||||
| chr12:25509625 | C | T | 1 | a0001c0001t0002g0099 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1190-5825G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25509625 | |||||||
| chr12:25509626 | G | C | 2 | a0002c0002t0002g0055 a0002c0002t0002g0056 |
2 | HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1190-5826C>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25509626 | |||||||
| chr12:25509742 | G | C | 1 | a0001c0001t0002g0079 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1190-5942C>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25509742 | |||||||
| chr12:25509776 | C | A | 1 | a0001c0001t0001g0248 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1190-5976G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25509776 | |||||||
| chr12:25509792 | G | A | 1 | a0002c0002t0002g0008 | 2 | HG02258.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1190-5992C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25509792 | |||||||
| chr12:25510082 | G | A | 1 | a0002c0002t0002g0055 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1190-6282C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25510082 | |||||||
| chr12:25510097 | A | G | 2 | a0001c0007t0004g0173 a0003c0005t0003g0156 |
2 | HG03130.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1190-6297T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25510097 | |||||||
| chr12:25510137 | T | A | 1 | a0002c0002t0002g0122 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1190-6337A>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25510137 | |||||||
| chr12:25510141 | T | A | 1 | a0001c0001t0002g0069 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1190-6341A>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25510141 | |||||||
| chr12:25510241 | G | GT | 9 | a0001c0001t0001g0152 a0001c0001t0001g0220 a0002c0002t0001g0219 others(6): Show |
9 | HG02148.hp1 HG02630.hp2 HG02683.hp2 others(6): Show |
intron_variant | MODIFIER | c.1190-6442dupA | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25510241 | |||||||
| chr12:25510252 | T | C | 14 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(11): Show |
14 | HG01169.hp1 HG01255.hp1 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.1190-6452A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25510252 | |||||||
| chr12:25510291 | T | G | 2 | a0002c0002t0002g0055 a0002c0002t0002g0056 |
2 | HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1190-6491A>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25510291 | |||||||
| chr12:25510300 | T | A | 2 | a0001c0001t0001g0152 a0001c0001t0002g0062 |
2 | HG02723.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1190-6500A>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25510300 | |||||||
| chr12:25510368 | A | C | 1 | a0001c0004t0001g0165 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1190-6568T>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25510368 | |||||||
| chr12:25510413 | T | C | 3 | a0002c0003t0002g0029 a0002c0003t0002g0030 a0002c0003t0002g0031 |
3 | HG00642.hp1 HG01496.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.1190-6613A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25510413 | |||||||
| chr12:25510690 | T | C | 1 | a0002c0002t0002g0138 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1190-6890A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25510690 | |||||||
| chr12:25510774 | G | C | 2 | a0002c0002t0002g0055 a0002c0002t0002g0056 |
2 | HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1190-6974C>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25510774 | |||||||
| chr12:25510831 | T | C | 2 | a0002c0002t0002g0055 a0002c0002t0002g0056 |
2 | HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1190-7031A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25510831 | |||||||
| chr12:25510947 | T | C | 1 | a0002c0002t0002g0139 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1190-7147A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25510947 | |||||||
| chr12:25510964 | A | G | 51 | a0001c0001t0002g0054 a0001c0001t0002g0135 a0002c0002t0001g0022 others(48): Show |
60 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.1190-7164T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25510964 | |||||||
| chr12:25511008 | G | A | 2 | a0002c0002t0002g0055 a0002c0002t0002g0056 |
2 | HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1190-7208C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25511008 | |||||||
| chr12:25511011 | G | T | 166 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(163): Show |
177 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.1190-7211C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25511011 | |||||||
| chr12:25511043 | T | G | 53 | a0001c0001t0001g0179 a0001c0001t0001g0182 a0001c0001t0001g0184 others(50): Show |
55 | HG00099.hp1 HG00280.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.1190-7243A>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25511043 | |||||||
| chr12:25511058 | G | T | 1 | a0002c0002t0002g0008 | 2 | HG02258.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1190-7258C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25511058 | |||||||
| chr12:25511062 | T | C | 1 | a0001c0001t0002g0136 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1190-7262A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25511062 | |||||||
| chr12:25511211 | A | T | 53 | a0001c0001t0001g0152 a0001c0001t0002g0054 a0001c0001t0002g0062 others(50): Show |
62 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.1190-7411T>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25511211 | |||||||
| chr12:25511361 | G | A | 222 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(219): Show |
242 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(239): Show |
intron_variant | MODIFIER | c.1189+7434C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25511361 | |||||||
| chr12:25511380 | C | T | 2 | a0002c0002t0002g0055 a0002c0002t0002g0056 |
2 | HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1189+7415G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25511380 | |||||||
| chr12:25511567 | G | A | 1 | a0006c0012t0001g0360 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1189+7228C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25511567 | |||||||
| chr12:25511704 | G | C | 335 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(332): Show |
359 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.1189+7091C>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25511704 | |||||||
| chr12:25511746 | G | T | 1 | a0003c0005t0003g0156 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1189+7049C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25511746 | |||||||
| chr12:25511821 | G | A | 58 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(55): Show |
63 | HG00438.hp1 HG01074.hp1 HG01081.hp2 others(60): Show |
intron_variant | MODIFIER | c.1189+6974C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25511821 | |||||||
| chr12:25511834 | G | C | 2 | a0002c0002t0002g0055 a0002c0002t0002g0056 |
2 | HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1189+6961C>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25511834 | |||||||
| chr12:25511919 | C | T | 75 | a0001c0001t0001g0021 a0001c0001t0001g0146 a0001c0001t0001g0148 others(72): Show |
76 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.1189+6876G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25511919 | |||||||
| chr12:25511920 | C | T | 1 | a0001c0001t0001g0281 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1189+6875G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25511920 | |||||||
| chr12:25511922 | C | T | 1 | a0001c0001t0001g0178 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1189+6873G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25511922 | |||||||
| chr12:25512004 | G | A | 1 | a0006c0012t0001g0360 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1189+6791C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25512004 | |||||||
| chr12:25512093 | G | A | 50 | a0001c0001t0002g0054 a0001c0001t0002g0135 a0002c0002t0001g0022 others(47): Show |
58 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.1189+6702C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25512093 | |||||||
| chr12:25512190 | A | G | 1 | a0001c0001t0001g0357 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1189+6605T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25512190 | |||||||
| chr12:25512207 | A | G | 1 | a0001c0001t0002g0064 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1189+6588T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25512207 | |||||||
| chr12:25512254 | A | G | 2 | a0002c0002t0002g0055 a0002c0002t0002g0056 |
2 | HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1189+6541T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25512254 | |||||||
| chr12:25512417 | G | C | 30 | a0001c0001t0001g0185 a0001c0001t0001g0264 a0001c0001t0001g0309 others(27): Show |
31 | HG00408.hp1 HG00423.hp1 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.1189+6378C>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25512417 | |||||||
| chr12:25512473 | G | A | 2 | a0002c0002t0002g0033 a0002c0002t0002g0046 |
2 | HG03834.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1189+6322C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25512473 | |||||||
| chr12:25512704 | G | A | 1 | a0001c0001t0002g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1189+6091C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25512704 | |||||||
| chr12:25512755 | C | T | 1 | a0002c0002t0002g0008 | 2 | HG02258.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1189+6040G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25512755 | |||||||
| chr12:25512786 | G | T | 2 | a0002c0002t0002g0055 a0002c0002t0002g0056 |
2 | HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1189+6009C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25512786 | |||||||
| chr12:25512816 | G | A | 2 | a0002c0002t0002g0055 a0002c0002t0002g0056 |
2 | HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1189+5979C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25512816 | |||||||
| chr12:25512852 | AT | A | 74 | a0001c0001t0001g0021 a0001c0001t0001g0148 a0001c0001t0001g0150 others(71): Show |
75 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.1189+5942delA | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25512852 | |||||||
| chr12:25512862 | T | A | 1 | a0001c0001t0001g0146 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1189+5933A>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25512862 | |||||||
| chr12:25512863 | A | T | 1 | a0001c0001t0001g0146 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1189+5932T>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25512863 | |||||||
| chr12:25512864 | T | G | 1 | a0001c0001t0001g0146 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1189+5931A>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25512864 | |||||||
| chr12:25512864 | T | TG | 22 | a0001c0001t0001g0147 a0001c0001t0001g0163 a0001c0001t0001g0175 others(19): Show |
22 | HG01169.hp1 HG01255.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.1189+5930dupC | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25512864 | |||||||
| chr12:25512868 | G | GA | 55 | a0001c0001t0001g0152 a0001c0001t0002g0054 a0001c0001t0002g0062 others(52): Show |
64 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.1189+5926_1189+592 others(5): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25512868 | |||||||
| chr12:25512906 | A | T | 2 | a0002c0002t0002g0055 a0002c0002t0002g0056 |
2 | HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1189+5889T>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25512906 | |||||||
| chr12:25513053 | T | C | 2 | a0002c0002t0002g0055 a0002c0002t0002g0056 |
2 | HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1189+5742A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25513053 | |||||||
| chr12:25513079 | G | C | 2 | a0002c0002t0002g0055 a0002c0002t0002g0056 |
2 | HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1189+5716C>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25513079 | |||||||
| chr12:25513099 | A | G | 175 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(172): Show |
186 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.1189+5696T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25513099 | |||||||
| chr12:25513129 | C | T | 1 | a0001c0001t0002g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1189+5666G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25513129 | |||||||
| chr12:25513177 | C | A | 2 | a0002c0002t0002g0055 a0002c0002t0002g0056 |
2 | HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1189+5618G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25513177 | |||||||
| chr12:25513321 | T | C | 52 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(49): Show |
57 | HG00438.hp1 HG01074.hp1 HG01943.hp2 others(54): Show |
intron_variant | MODIFIER | c.1189+5474A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25513321 | |||||||
| chr12:25513326 | C | A | 1 | a0001c0001t0001g0328 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1189+5469G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25513326 | |||||||
| chr12:25513349 | A | G | 55 | a0001c0001t0001g0152 a0001c0001t0002g0054 a0001c0001t0002g0062 others(52): Show |
64 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.1189+5446T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25513349 | |||||||
| chr12:25513375 | A | G | 55 | a0001c0001t0001g0152 a0001c0001t0002g0054 a0001c0001t0002g0062 others(52): Show |
64 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.1189+5420T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25513375 | |||||||
| chr12:25513590 | C | T | 55 | a0001c0001t0001g0152 a0001c0001t0002g0054 a0001c0001t0002g0062 others(52): Show |
64 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.1189+5205G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25513590 | |||||||
| chr12:25513632 | C | T | 55 | a0001c0001t0001g0152 a0001c0001t0002g0054 a0001c0001t0002g0062 others(52): Show |
64 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.1189+5163G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25513632 | |||||||
| chr12:25513648 | G | A | 55 | a0001c0001t0001g0152 a0001c0001t0002g0054 a0001c0001t0002g0062 others(52): Show |
64 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.1189+5147C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25513648 | |||||||
| chr12:25513758 | A | G | 1 | a0006c0012t0001g0360 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1189+5037T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25513758 | |||||||
| chr12:25513783 | GAGAT | G | 53 | a0001c0001t0001g0152 a0001c0001t0002g0054 a0001c0001t0002g0062 others(50): Show |
62 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.1189+5008_1189+501 others(8): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25513783 | |||||||
| chr12:25513787 | T | C | 32 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0023 others(29): Show |
37 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.1189+5008A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25513787 | |||||||
| chr12:25513840 | G | C | 1 | a0001c0004t0001g0166 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1189+4955C>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25513840 | |||||||
| chr12:25513858 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1189+4937C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25513858 | |||||||
| chr12:25513974 | A | ACTTT | 53 | a0001c0001t0001g0152 a0001c0001t0002g0054 a0001c0001t0002g0062 others(50): Show |
62 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.1189+4820_1189+482 others(8): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25513974 | |||||||
| chr12:25513983 | A | G | 53 | a0001c0001t0001g0152 a0001c0001t0002g0054 a0001c0001t0002g0062 others(50): Show |
62 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.1189+4812T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25513983 | |||||||
| chr12:25514143 | C | G | 54 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(51): Show |
59 | HG00438.hp1 HG01074.hp1 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.1189+4652G>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25514143 | |||||||
| chr12:25514148 | C | A | 1 | a0003c0005t0003g0156 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1189+4647G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25514148 | |||||||
| chr12:25514204 | G | A | 55 | a0001c0001t0001g0151 a0001c0001t0002g0054 a0001c0001t0002g0062 others(52): Show |
64 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.1189+4591C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25514204 | |||||||
| chr12:25514208 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1189+4587G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25514208 | |||||||
| chr12:25514274 | C | G | 52 | a0001c0001t0002g0054 a0001c0001t0002g0135 a0002c0002t0001g0022 others(49): Show |
61 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(58): Show |
intron_variant | MODIFIER | c.1189+4521G>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25514274 | |||||||
| chr12:25514307 | C | G | 60 | a0001c0001t0001g0015 a0001c0001t0001g0157 a0001c0001t0001g0158 others(57): Show |
70 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(67): Show |
intron_variant | MODIFIER | c.1189+4488G>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25514307 | |||||||
| chr12:25514307 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1189+4488G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25514307 | |||||||
| chr12:25514390 | A | T | 9 | a0001c0001t0001g0015 a0001c0001t0001g0157 a0001c0001t0001g0158 others(6): Show |
11 | HG02109.hp2 HG02258.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1189+4405T>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25514390 | |||||||
| chr12:25514401 | T | G | 9 | a0001c0001t0001g0015 a0001c0001t0001g0157 a0001c0001t0001g0158 others(6): Show |
11 | HG02109.hp2 HG02258.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1189+4394A>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25514401 | |||||||
| chr12:25514422 | T | C | 74 | a0001c0001t0001g0015 a0001c0001t0001g0157 a0001c0001t0001g0158 others(71): Show |
78 | HG00099.hp1 HG00280.hp2 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.1189+4373A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25514422 | |||||||
| chr12:25514477 | C | G | 24 | a0001c0001t0001g0015 a0001c0001t0001g0157 a0001c0001t0001g0158 others(21): Show |
25 | HG01891.hp1 HG02109.hp1 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1189+4318G>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25514477 | |||||||
| chr12:25514481 | G | A | 6 | a0001c0001t0001g0163 a0001c0004t0001g0161 a0001c0004t0001g0164 others(3): Show |
6 | HG01255.hp2 HG02015.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.1189+4314C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25514481 | |||||||
| chr12:25514481 | G | C | 9 | a0001c0001t0001g0185 a0001c0001t0001g0248 a0001c0001t0001g0264 others(6): Show |
9 | HG00408.hp1 HG02132.hp2 NA18939.hp2 others(6): Show |
intron_variant | MODIFIER | c.1189+4314C>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25514481 | |||||||
| chr12:25514528 | A | G | 334 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(331): Show |
359 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.1189+4267T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25514528 | |||||||
| chr12:25514533 | A | G | 332 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(329): Show |
357 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(354): Show |
intron_variant | MODIFIER | c.1189+4262T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25514533 | |||||||
| chr12:25514559 | CA | C | 234 | a0001c0001t0001g0021 a0001c0001t0001g0146 a0001c0001t0001g0148 others(231): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.1189+4235delT | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25514559 | |||||||
| chr12:25514559 | CAA | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(93): Show |
109 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.1189+4234_1189+423 others(6): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25514559 | |||||||
| chr12:25514715 | A | C | 279 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(276): Show |
294 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(291): Show |
intron_variant | MODIFIER | c.1189+4080T>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25514715 | |||||||
| chr12:25514747 | C | T | 280 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(277): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.1189+4048G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25514747 | |||||||
| chr12:25514759 | G | A | 280 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(277): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.1189+4036C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25514759 | |||||||
| chr12:25514980 | C | T | 5 | a0001c0004t0001g0161 a0001c0004t0001g0164 a0001c0004t0001g0165 others(2): Show |
5 | HG02015.hp2 HG02027.hp2 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.1189+3815G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25514980 | |||||||
| chr12:25515188 | A | AT | 276 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(273): Show |
292 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(289): Show |
intron_variant | MODIFIER | c.1189+3606dupA | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25515188 | |||||||
| chr12:25515241 | T | C | 281 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(278): Show |
298 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.1189+3554A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25515241 | |||||||
| chr12:25515250 | C | T | 23 | a0002c0002t0001g0288 a0002c0002t0002g0001 a0002c0002t0002g0004 others(20): Show |
28 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.1189+3545G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25515250 | |||||||
| chr12:25515408 | T | G | 2 | a0001c0001t0002g0054 a0001c0001t0002g0135 |
2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1189+3387A>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25515408 | |||||||
| chr12:25515417 | T | C | 1 | a0001c0001t0001g0342 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1189+3378A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25515417 | |||||||
| chr12:25515430 | T | C | 281 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(278): Show |
298 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.1189+3365A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25515430 | |||||||
| chr12:25515446 | AAT | A | 6 | a0002c0002t0002g0005 a0002c0002t0002g0042 a0002c0002t0002g0043 others(3): Show |
7 | HG01167.hp1 HG01169.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1189+3347_1189+334 others(6): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25515446 | |||||||
| chr12:25515455 | A | G | 281 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(278): Show |
298 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.1189+3340T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25515455 | |||||||
| chr12:25515535 | T | A | 1 | a0002c0002t0002g0141 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1189+3260A>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25515535 | |||||||
| chr12:25515623 | A | C | 2 | a0002c0002t0002g0130 a0002c0002t0002g0131 |
2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1189+3172T>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25515623 | |||||||
| chr12:25515661 | G | A | 1 | a0001c0001t0001g0222 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1189+3134C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25515661 | |||||||
| chr12:25515701 | G | A | 281 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(278): Show |
298 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.1189+3094C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25515701 | |||||||
| chr12:25515760 | G | C | 281 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(278): Show |
298 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.1189+3035C>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25515760 | |||||||
| chr12:25515770 | A | G | 281 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(278): Show |
298 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.1189+3025T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25515770 | |||||||
| chr12:25515783 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1189+3012C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25515783 | |||||||
| chr12:25515785 | C | G | 1 | a0002c0002t0002g0129 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1189+3010G>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25515785 | |||||||
| chr12:25515844 | T | C | 3 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0010t0001g0292 |
5 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(2): Show |
intron_variant | MODIFIER | c.1189+2951A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25515844 | |||||||
| chr12:25515894 | A | G | 4 | a0003c0005t0001g0153 a0003c0005t0001g0154 a0003c0005t0001g0155 others(1): Show |
4 | HG02630.hp2 HG03130.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1189+2901T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25515894 | |||||||
| chr12:25515897 | A | G | 4 | a0003c0005t0001g0153 a0003c0005t0001g0154 a0003c0005t0001g0155 others(1): Show |
4 | HG02630.hp2 HG03130.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1189+2898T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25515897 | |||||||
| chr12:25515936 | G | C | 4 | a0003c0005t0001g0153 a0003c0005t0001g0154 a0003c0005t0001g0155 others(1): Show |
4 | HG02630.hp2 HG03130.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1189+2859C>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25515936 | |||||||
| chr12:25515939 | TG | T | 281 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(278): Show |
298 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.1189+2855delC | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25515939 | |||||||
| chr12:25515963 | T | TAA | 281 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(278): Show |
298 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.1189+2831_1189+283 others(6): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25515963 | |||||||
| chr12:25516085 | T | C | 51 | a0001c0001t0001g0015 a0001c0001t0001g0151 a0001c0001t0001g0152 others(48): Show |
53 | HG00423.hp1 HG00621.hp1 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.1189+2710A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25516085 | |||||||
| chr12:25516165 | G | A | 281 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(278): Show |
298 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.1189+2630C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25516165 | |||||||
| chr12:25516226 | C | G | 281 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(278): Show |
298 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.1189+2569G>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25516226 | |||||||
| chr12:25516252 | G | A | 230 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(227): Show |
245 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.1189+2543C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25516252 | |||||||
| chr12:25516266 | T | G | 281 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(278): Show |
298 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.1189+2529A>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25516266 | |||||||
| chr12:25516318 | A | G | 4 | a0003c0005t0001g0153 a0003c0005t0001g0154 a0003c0005t0001g0155 others(1): Show |
4 | HG02630.hp2 HG03130.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1189+2477T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25516318 | |||||||
| chr12:25516364 | A | G | 1 | a0001c0001t0001g0295 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1189+2431T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25516364 | |||||||
| chr12:25516365 | G | A | 1 | a0001c0001t0001g0277 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1189+2430C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25516365 | |||||||
| chr12:25516368 | A | G | 281 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(278): Show |
298 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.1189+2427T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25516368 | |||||||
| chr12:25516422 | T | A | 230 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(227): Show |
245 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.1189+2373A>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25516422 | |||||||
| chr12:25516423 | C | G | 230 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(227): Show |
245 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.1189+2372G>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25516423 | |||||||
| chr12:25516456 | TA | T | 3 | a0001c0001t0001g0215 a0001c0001t0001g0273 a0002c0002t0001g0180 |
3 | HG01081.hp2 HG01106.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1189+2338delT | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25516456 | |||||||
| chr12:25516560 | T | C | 281 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(278): Show |
298 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.1189+2235A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25516560 | |||||||
| chr12:25516585 | T | A | 4 | a0001c0001t0001g0018 a0001c0001t0001g0174 a0001c0001t0001g0211 others(1): Show |
5 | NA18945.hp1 NA18948.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.1189+2210A>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25516585 | |||||||
| chr12:25516692 | T | C | 50 | a0001c0001t0001g0015 a0001c0001t0001g0151 a0001c0001t0001g0152 others(47): Show |
52 | HG00423.hp1 HG00621.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.1189+2103A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25516692 | |||||||
| chr12:25516824 | C | T | 281 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(278): Show |
298 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.1189+1971G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25516824 | |||||||
| chr12:25516894 | G | A | 281 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(278): Show |
298 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.1189+1901C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25516894 | |||||||
| chr12:25516929 | T | A | 1 | a0001c0001t0002g0136 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1189+1866A>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25516929 | |||||||
| chr12:25516974 | C | A | 2 | a0001c0001t0001g0322 a0001c0001t0001g0356 |
2 | NA18951.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.1189+1821G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25516974 | |||||||
| chr12:25517066 | T | C | 2 | a0002c0002t0002g0033 a0002c0002t0002g0046 |
2 | HG03834.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1189+1729A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25517066 | |||||||
| chr12:25517086 | AGGAACAC others(464): Show |
A | 279 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(276): Show |
296 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(293): Show |
intron_variant | MODIFIER | c.1189+1238_1189+170 others(4): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25517086 | |||||||
| chr12:25517087 | GGAACACT others(463): Show |
G | 2 | a0001c0001t0001g0245 a0001c0001t0002g0071 |
2 | HG01261.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1189+1238_1189+170 others(4): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25517087 | |||||||
| chr12:25517561 | G | T | 2 | a0001c0001t0001g0245 a0001c0001t0002g0071 |
2 | HG01261.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1189+1234C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25517561 | |||||||
| chr12:25517562 | T | G | 2 | a0001c0001t0001g0245 a0001c0001t0002g0071 |
2 | HG01261.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1189+1233A>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25517562 | |||||||
| chr12:25517616 | G | C | 1 | a0001c0001t0001g0158 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1189+1179C>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25517616 | |||||||
| chr12:25517632 | T | C | 281 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(278): Show |
298 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.1189+1163A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25517632 | |||||||
| chr12:25517640 | T | C | 1 | a0001c0001t0001g0251 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1189+1155A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25517640 | |||||||
| chr12:25517707 | GAAT | G | 41 | a0002c0002t0001g0288 a0002c0002t0002g0001 a0002c0002t0002g0002 others(38): Show |
49 | HG00738.hp1 HG00741.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.1189+1085_1189+108 others(7): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25517707 | |||||||
| chr12:25517707 | GAATAAT | G | 12 | a0002c0002t0001g0160 a0002c0002t0002g0005 a0002c0002t0002g0042 others(9): Show |
13 | HG01167.hp1 HG01169.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.1189+1082_1189+108 others(10): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25517707 | |||||||
| chr12:25517707 | GAATAATA others(2): Show |
G | 19 | a0002c0002t0001g0022 a0002c0002t0001g0162 a0002c0002t0001g0219 others(16): Show |
21 | HG00280.hp1 HG00735.hp2 HG01256.hp1 others(18): Show |
intron_variant | MODIFIER | c.1189+1079_1189+108 others(13): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25517707 | |||||||
| chr12:25517707 | GAATAATA others(5): Show |
G | 1 | a0002c0002t0002g0130 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1189+1076_1189+108 others(16): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25517707 | |||||||
| chr12:25517707 | GAATAATA others(14): Show |
G | 281 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(278): Show |
298 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.1189+1067_1189+108 others(25): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25517707 | |||||||
| chr12:25517767 | A | AAAAAAAG | 230 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(227): Show |
245 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.1189+1027_1189+102 others(11): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25517767 | |||||||
| chr12:25517767 | A | AAAAAG | 50 | a0001c0001t0001g0015 a0001c0001t0001g0151 a0001c0001t0001g0152 others(47): Show |
52 | HG00423.hp1 HG00621.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.1189+1027_1189+102 others(9): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25517767 | |||||||
| chr12:25517831 | G | A | 281 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(278): Show |
298 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.1189+964C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25517831 | |||||||
| chr12:25517971 | T | C | 281 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(278): Show |
298 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.1189+824A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25517971 | |||||||
| chr12:25518059 | A | T | 281 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(278): Show |
298 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.1189+736T>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25518059 | |||||||
| chr12:25518132 | C | T | 281 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(278): Show |
298 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.1189+663G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25518132 | |||||||
| chr12:25518192 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1189+603G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25518192 | |||||||
| chr12:25518363 | A | C | 230 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(227): Show |
245 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.1189+432T>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25518363 | |||||||
| chr12:25518496 | GT | G | 280 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(277): Show |
297 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(294): Show |
intron_variant | MODIFIER | c.1189+298delA | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25518496 | |||||||
| chr12:25518521 | A | G | 4 | a0003c0005t0001g0153 a0003c0005t0001g0154 a0003c0005t0001g0155 others(1): Show |
4 | HG02630.hp2 HG03130.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1189+274T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25518521 | |||||||
| chr12:25518576 | T | C | 6 | a0001c0001t0001g0163 a0001c0004t0001g0161 a0001c0004t0001g0164 others(3): Show |
6 | HG01255.hp2 HG02015.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.1189+219A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 8/9 | chr12 | 25518576 | |||||||
| chr12:25519293 | A | C | 280 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(277): Show |
297 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(294): Show |
intron_variant | MODIFIER | c.1017-326T>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 7/9 | chr12 | 25519293 | |||||||
| chr12:25519320 | G | C | 281 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(278): Show |
298 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.1017-353C>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 7/9 | chr12 | 25519320 | |||||||
| chr12:25519348 | T | C | 1 | a0001c0001t0001g0163 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1017-381A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 7/9 | chr12 | 25519348 | |||||||
| chr12:25519366 | C | T | 280 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(277): Show |
297 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(294): Show |
intron_variant | MODIFIER | c.1017-399G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 7/9 | chr12 | 25519366 | |||||||
| chr12:25519374 | A | AAGGTC | 280 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(277): Show |
297 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(294): Show |
intron_variant | MODIFIER | c.1017-408_1017-407i others(7): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 7/9 | chr12 | 25519374 | |||||||
| chr12:25519413 | C | T | 275 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(272): Show |
291 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(288): Show |
intron_variant | MODIFIER | c.1016+445G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 7/9 | chr12 | 25519413 | |||||||
| chr12:25519436 | A | G | 1 | a0002c0002t0002g0133 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1016+422T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 7/9 | chr12 | 25519436 | |||||||
| chr12:25519515 | A | G | 204 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(201): Show |
217 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.1016+343T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 7/9 | chr12 | 25519515 | |||||||
| chr12:25519542 | G | C | 203 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(200): Show |
216 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.1016+316C>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 7/9 | chr12 | 25519542 | |||||||
| chr12:25519583 | G | T | 204 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(201): Show |
217 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.1016+275C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 7/9 | chr12 | 25519583 | |||||||
| chr12:25519584 | T | TTAAAAAA others(10): Show |
2 | a0001c0001t0001g0231 a0001c0001t0001g0236 |
2 | HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1016+273_1016+274i others(19): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 7/9 | chr12 | 25519584 | |||||||
| chr12:25519585 | C | A | 2 | a0001c0001t0001g0231 a0001c0001t0001g0236 |
2 | HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1016+273G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 7/9 | chr12 | 25519585 | |||||||
| chr12:25519585 | C | T | 202 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(199): Show |
215 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.1016+273G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 7/9 | chr12 | 25519585 | |||||||
| chr12:25519586 | T | A | 2 | a0001c0001t0001g0231 a0001c0001t0001g0236 |
2 | HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1016+272A>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 7/9 | chr12 | 25519586 | |||||||
| chr12:25519586 | T | TA | 26 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0023 others(23): Show |
31 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.1016+271_1016+272i others(3): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 7/9 | chr12 | 25519586 | |||||||
| chr12:25519586 | T | TAAAAAAA others(2): Show |
6 | a0001c0001t0001g0321 a0001c0001t0001g0331 a0001c0001t0001g0335 others(3): Show |
6 | HG00741.hp1 HG01123.hp1 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.1016+271_1016+272i others(11): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 7/9 | chr12 | 25519586 | |||||||
| chr12:25519586 | T | TAAAAAAA others(3): Show |
3 | a0001c0001t0001g0327 a0001c0001t0001g0332 a0001c0001t0001g0333 |
3 | HG00621.hp2 NA18950.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.1016+271_1016+272i others(12): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 7/9 | chr12 | 25519586 | |||||||
| chr12:25519586 | T | TAAAAAAA others(6): Show |
3 | a0001c0001t0001g0190 a0001c0001t0001g0204 a0001c0001t0001g0207 |
3 | NA18969.hp1 NA19011.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1016+271_1016+272i others(15): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 7/9 | chr12 | 25519586 | |||||||
| chr12:25519586 | T | TAAAAAAA others(7): Show |
33 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(30): Show |
37 | HG00597.hp1 HG01074.hp1 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.1016+271_1016+272i others(16): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 7/9 | chr12 | 25519586 | |||||||
| chr12:25519586 | T | TAAAAAAA others(8): Show |
16 | a0001c0001t0001g0147 a0001c0001t0001g0182 a0001c0001t0001g0201 others(13): Show |
16 | HG00280.hp2 HG00438.hp1 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.1016+271_1016+272i others(17): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 7/9 | chr12 | 25519586 | |||||||
| chr12:25519586 | T | TAAAAAAA others(9): Show |
19 | a0001c0001t0001g0018 a0001c0001t0001g0174 a0001c0001t0001g0178 others(16): Show |
20 | HG01070.hp1 HG01433.hp1 HG01516.hp1 others(17): Show |
intron_variant | MODIFIER | c.1016+271_1016+272i others(18): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 7/9 | chr12 | 25519586 | |||||||
| chr12:25519586 | T | TAAAAAAA others(10): Show |
49 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0183 others(46): Show |
49 | HG00099.hp2 HG00408.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.1016+271_1016+272i others(19): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 7/9 | chr12 | 25519586 | |||||||
| chr12:25519586 | T | TAAAAAAA others(11): Show |
25 | a0001c0001t0001g0146 a0001c0001t0001g0148 a0001c0001t0001g0216 others(22): Show |
26 | HG00423.hp2 HG00642.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.1016+271_1016+272i others(20): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 7/9 | chr12 | 25519586 | |||||||
| chr12:25519586 | T | TAAAAAAA others(12): Show |
5 | a0001c0001t0001g0299 a0001c0001t0001g0347 a0001c0001t0002g0014 others(2): Show |
6 | HG01993.hp2 HG02257.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1016+271_1016+272i others(21): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 7/9 | chr12 | 25519586 | |||||||
| chr12:25519586 | T | TAAAAAAA others(13): Show |
5 | a0001c0001t0001g0021 a0001c0001t0001g0232 a0001c0001t0001g0237 others(2): Show |
6 | HG01256.hp2 HG01258.hp1 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.1016+271_1016+272i others(22): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 7/9 | chr12 | 25519586 | |||||||
| chr12:25519586 | T | TAAAAAAA others(14): Show |
1 | a0001c0001t0001g0228 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1016+271_1016+272i others(23): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 7/9 | chr12 | 25519586 | |||||||
| chr12:25519586 | T | TAAAAAAA others(15): Show |
1 | a0001c0001t0001g0342 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1016+271_1016+272i others(24): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 7/9 | chr12 | 25519586 | |||||||
| chr12:25519586 | T | TTAAAAAA others(9): Show |
2 | a0001c0001t0001g0257 a0001c0001t0001g0268 |
2 | HG03704.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1016+271_1016+272i others(18): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 7/9 | chr12 | 25519586 | |||||||
| chr12:25519586 | T | TTAAAAAA others(10): Show |
2 | a0001c0001t0001g0270 a0001c0001t0001g0305 |
2 | HG02622.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1016+271_1016+272i others(19): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 7/9 | chr12 | 25519586 | |||||||
| chr12:25519586 | T | TTTAAAAA others(9): Show |
2 | a0001c0001t0001g0271 a0001c0001t0001g0272 |
2 | HG01169.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1016+271_1016+272i others(18): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 7/9 | chr12 | 25519586 | |||||||
| chr12:25519587 | C | A | 204 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(201): Show |
217 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.1016+271G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 7/9 | chr12 | 25519587 | |||||||
| chr12:25519587 | C | CA | 7 | a0001c0001t0001g0015 a0001c0001t0001g0157 a0001c0001t0001g0158 others(4): Show |
8 | HG02109.hp2 HG02615.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.1016+270dupT | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 7/9 | chr12 | 25519587 | |||||||
| chr12:25519587 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0002g0080 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1016+261_1016+270d others(12): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 7/9 | chr12 | 25519587 | |||||||
| chr12:25519587 | C | CAAAAAAA others(4): Show |
36 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(33): Show |
39 | HG00099.hp1 HG00609.hp1 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1016+260_1016+270d others(13): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 7/9 | chr12 | 25519587 | |||||||
| chr12:25519587 | C | CAAAAAAA others(5): Show |
19 | a0001c0001t0001g0152 a0001c0001t0002g0065 a0001c0001t0002g0066 others(16): Show |
19 | HG00423.hp1 HG00621.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.1016+259_1016+270d others(14): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 7/9 | chr12 | 25519587 | |||||||
| chr12:25519587 | C | CAAAAAAA others(6): Show |
9 | a0001c0001t0002g0067 a0001c0001t0002g0072 a0001c0001t0002g0088 others(6): Show |
9 | HG01106.hp1 HG02056.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1016+258_1016+270d others(15): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 7/9 | chr12 | 25519587 | |||||||
| chr12:25519587 | C | CAAAAAAA others(7): Show |
1 | a0001c0004t0001g0166 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1016+257_1016+270d others(16): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 7/9 | chr12 | 25519587 | |||||||
| chr12:25519587 | C | CAAAAAAA others(8): Show |
2 | a0001c0004t0001g0164 a0001c0007t0003g0171 |
2 | HG02015.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1016+256_1016+270d others(17): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 7/9 | chr12 | 25519587 | |||||||
| chr12:25519615 | T | C | 1 | a0001c0001t0002g0114 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1016+243A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 7/9 | chr12 | 25519615 | |||||||
| chr12:25519620 | A | G | 1 | a0001c0001t0001g0301 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1016+238T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 7/9 | chr12 | 25519620 | |||||||
| chr12:25519651 | G | A | 53 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(50): Show |
58 | HG00438.hp1 HG00597.hp1 HG01074.hp1 others(55): Show |
intron_variant | MODIFIER | c.1016+207C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 7/9 | chr12 | 25519651 | |||||||
| chr12:25519674 | T | C | 2 | a0002c0002t0002g0055 a0002c0002t0002g0056 |
2 | HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1016+184A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 7/9 | chr12 | 25519674 | |||||||
| chr12:25519766 | C | T | 4 | a0003c0005t0001g0153 a0003c0005t0001g0154 a0003c0005t0001g0155 others(1): Show |
4 | HG02630.hp2 HG03130.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1016+92G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 7/9 | chr12 | 25519766 | |||||||
| chr12:25519768 | C | T | 4 | a0003c0005t0001g0153 a0003c0005t0001g0154 a0003c0005t0001g0155 others(1): Show |
4 | HG02630.hp2 HG03130.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1016+90G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 7/9 | chr12 | 25519768 | |||||||
| chr12:25519803 | T | C | 4 | a0003c0005t0001g0153 a0003c0005t0001g0154 a0003c0005t0001g0155 others(1): Show |
4 | HG02630.hp2 HG03130.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1016+55A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 7/9 | chr12 | 25519803 | |||||||
| chr12:25520084 | A | G | 1 | a0001c0001t0001g0203 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.799-9T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25520084 | |||||||
| chr12:25520139 | G | GAT | 37 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0019 others(34): Show |
42 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.799-66_799-65dupAT | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25520139 | |||||||
| chr12:25520139 | G | GATAT | 39 | a0001c0001t0001g0146 a0001c0001t0001g0150 a0001c0001t0001g0152 others(36): Show |
39 | HG00738.hp2 HG01074.hp2 HG01123.hp2 others(36): Show |
intron_variant | MODIFIER | c.799-68_799-65dupAT others(2): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25520139 | |||||||
| chr12:25520139 | G | GATATAT | 23 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0182 others(20): Show |
24 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.799-65_799-64insAT others(4): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25520139 | |||||||
| chr12:25520139 | G | GATATATA others(1): Show |
15 | a0001c0001t0001g0179 a0001c0001t0001g0189 a0001c0001t0001g0230 others(12): Show |
15 | HG00280.hp2 HG01433.hp2 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.799-65_799-64insAT others(6): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25520139 | |||||||
| chr12:25520139 | G | GATATATA others(3): Show |
8 | a0001c0001t0001g0188 a0001c0001t0001g0231 a0001c0001t0002g0009 others(5): Show |
9 | HG01069.hp2 HG01071.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.799-65_799-64insAT others(8): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25520139 | |||||||
| chr12:25520139 | G | GATATATA others(5): Show |
6 | a0001c0001t0001g0234 a0001c0001t0001g0247 a0001c0001t0001g0262 others(3): Show |
6 | HG00733.hp1 HG01952.hp1 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.799-65_799-64insAT others(10): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25520139 | |||||||
| chr12:25520139 | G | GATATATA others(7): Show |
2 | a0001c0001t0002g0096 a0001c0001t0002g0116 |
2 | NA19000.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.799-65_799-64insAT others(12): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25520139 | |||||||
| chr12:25520139 | GATATAC | G | 5 | a0001c0001t0001g0015 a0001c0001t0001g0157 a0001c0001t0001g0158 others(2): Show |
6 | HG01891.hp2 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.799-70_799-65delGT others(4): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25520139 | |||||||
| chr12:25520139 | GATATACA others(1): Show |
G | 8 | a0001c0001t0001g0183 a0001c0001t0001g0215 a0001c0001t0001g0273 others(5): Show |
8 | HG01081.hp2 HG01106.hp2 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.799-72_799-65delAT others(6): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25520139 | |||||||
| chr12:25520139 | GATATACA others(3): Show |
G | 3 | a0001c0007t0003g0171 a0002c0014t0001g0169 a0008c0013t0003g0170 |
3 | HG02559.hp1 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.799-74_799-65delAT others(8): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25520139 | |||||||
| chr12:25520139 | GATATACA others(5): Show |
G | 1 | a0001c0015t0001g0172 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.799-76_799-65delAT others(10): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25520139 | |||||||
| chr12:25520139 | GATATACA others(7): Show |
G | 2 | a0001c0001t0001g0018 a0001c0001t0001g0174 |
3 | NA18948.hp1 NA18971.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.799-78_799-65delAT others(12): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25520139 | |||||||
| chr12:25520139 | GATATACA others(9): Show |
G | 4 | a0003c0005t0001g0153 a0003c0005t0001g0154 a0003c0005t0001g0155 others(1): Show |
4 | HG02630.hp2 HG03130.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.799-80_799-65delAT others(14): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25520139 | |||||||
| chr12:25520139 | GATATACA others(11): Show |
G | 1 | a0001c0001t0002g0136 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.799-82_799-65delAT others(16): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25520139 | |||||||
| chr12:25520139 | GATATACA others(17): Show |
G | 1 | a0001c0001t0001g0341 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.799-88_799-65delAT others(22): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25520139 | |||||||
| chr12:25520141 | T | G | 1 | a0001c0001t0001g0287 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.799-66A>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25520141 | |||||||
| chr12:25520141 | TATAC | T | 38 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0024 others(35): Show |
42 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.799-70_799-67delGT others(2): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25520141 | |||||||
| chr12:25520143 | TAC | T | 47 | a0001c0001t0001g0020 a0001c0001t0001g0185 a0001c0001t0001g0199 others(44): Show |
48 | HG00408.hp1 HG00423.hp2 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.799-70_799-69delGT | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25520143 | |||||||
| chr12:25520145 | C | CAT | 22 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0135 others(19): Show |
26 | HG00280.hp1 HG00735.hp2 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.799-72_799-71dupAT | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25520145 | |||||||
| chr12:25520145 | C | CATAT | 6 | a0002c0002t0001g0288 a0002c0002t0001g0289 a0002c0002t0002g0032 others(3): Show |
6 | HG01257.hp1 HG02040.hp2 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.799-74_799-71dupAT others(2): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25520145 | |||||||
| chr12:25520145 | C | CATATAT | 8 | a0002c0002t0001g0219 a0002c0002t0001g0291 a0002c0002t0002g0007 others(5): Show |
9 | HG00741.hp2 HG02486.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.799-76_799-71dupAT others(4): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25520145 | |||||||
| chr12:25520145 | C | CATATATA others(1): Show |
8 | a0002c0002t0001g0355 a0002c0002t0002g0001 a0002c0002t0002g0006 others(5): Show |
9 | HG01081.hp1 HG01243.hp1 HG02015.hp1 others(6): Show |
intron_variant | MODIFIER | c.799-78_799-71dupAT others(6): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25520145 | |||||||
| chr12:25520145 | C | CATATATA others(3): Show |
8 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0002c0002t0001g0290 others(5): Show |
8 | HG01496.hp2 HG02004.hp2 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.799-80_799-71dupAT others(8): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25520145 | |||||||
| chr12:25520145 | C | CATATATA others(5): Show |
8 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0005 others(5): Show |
9 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.799-82_799-71dupAT others(10): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25520145 | |||||||
| chr12:25520145 | C | CATATATA others(7): Show |
6 | a0002c0002t0002g0004 a0002c0002t0002g0026 a0002c0002t0002g0036 others(3): Show |
6 | HG01516.hp2 HG02148.hp1 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.799-84_799-71dupAT others(12): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25520145 | |||||||
| chr12:25520145 | C | CATATATA others(9): Show |
3 | a0002c0002t0002g0001 a0002c0002t0002g0038 a0002c0002t0002g0058 |
3 | HG01993.hp1 HG02129.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.799-86_799-71dupAT others(14): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25520145 | |||||||
| chr12:25520145 | C | CATATATA others(13): Show |
1 | a0002c0002t0002g0039 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.799-90_799-71dupAT others(18): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25520145 | |||||||
| chr12:25520145 | C | T | 166 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(163): Show |
174 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.799-70G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25520145 | |||||||
| chr12:25520159 | T | G | 4 | a0003c0005t0001g0153 a0003c0005t0001g0154 a0003c0005t0001g0155 others(1): Show |
4 | HG02630.hp2 HG03130.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.799-84A>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25520159 | |||||||
| chr12:25520160 | A | G | 5 | a0001c0004t0001g0161 a0001c0004t0001g0164 a0001c0004t0001g0165 others(2): Show |
5 | HG02015.hp2 HG02027.hp2 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.799-85T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25520160 | |||||||
| chr12:25520167 | T | C | 4 | a0003c0005t0001g0153 a0003c0005t0001g0154 a0003c0005t0001g0155 others(1): Show |
4 | HG02630.hp2 HG03130.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.799-92A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25520167 | |||||||
| chr12:25520170 | A | G | 5 | a0001c0007t0003g0171 a0001c0007t0004g0173 a0001c0015t0001g0172 others(2): Show |
5 | HG02559.hp1 HG03209.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.799-95T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25520170 | |||||||
| chr12:25520173 | T | G | 4 | a0003c0005t0001g0153 a0003c0005t0001g0154 a0003c0005t0001g0155 others(1): Show |
4 | HG02630.hp2 HG03130.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.799-98A>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25520173 | |||||||
| chr12:25520177 | G | T | 2 | a0001c0001t0002g0074 a0001c0001t0003g0269 |
2 | HG02559.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.799-102C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25520177 | |||||||
| chr12:25520200 | C | A | 4 | a0003c0005t0001g0153 a0003c0005t0001g0154 a0003c0005t0001g0155 others(1): Show |
4 | HG02630.hp2 HG03130.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.799-125G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25520200 | |||||||
| chr12:25520471 | A | G | 15 | a0001c0001t0001g0163 a0001c0004t0001g0161 a0001c0004t0001g0164 others(12): Show |
15 | HG01255.hp2 HG02015.hp2 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.799-396T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25520471 | |||||||
| chr12:25520490 | GTGTC | G | 10 | a0001c0001t0001g0163 a0001c0004t0001g0161 a0001c0004t0001g0164 others(7): Show |
10 | HG01255.hp2 HG02015.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.799-419_799-416del others(4): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25520490 | |||||||
| chr12:25520566 | T | G | 4 | a0001c0001t0001g0015 a0001c0001t0001g0157 a0001c0001t0001g0158 others(1): Show |
5 | HG02109.hp2 HG02451.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.799-491A>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25520566 | |||||||
| chr12:25520619 | T | A | 10 | a0001c0001t0001g0163 a0001c0004t0001g0161 a0001c0004t0001g0164 others(7): Show |
10 | HG01255.hp2 HG02015.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.799-544A>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25520619 | |||||||
| chr12:25520662 | T | C | 1 | a0001c0001t0001g0231 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.799-587A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25520662 | |||||||
| chr12:25520693 | T | C | 2 | a0001c0001t0001g0184 a0001c0001t0001g0246 |
2 | NA18957.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.799-618A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25520693 | |||||||
| chr12:25520719 | G | A | 49 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(46): Show |
54 | HG00438.hp1 HG00597.hp1 HG01074.hp1 others(51): Show |
intron_variant | MODIFIER | c.799-644C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25520719 | |||||||
| chr12:25520748 | T | TCTACTTT others(324): Show |
1 | a0001c0001t0001g0342 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.799-674_799-673ins others(331): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25520748 | |||||||
| chr12:25520779 | T | C | 10 | a0001c0001t0001g0163 a0001c0004t0001g0161 a0001c0004t0001g0164 others(7): Show |
10 | HG01255.hp2 HG02015.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.799-704A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25520779 | |||||||
| chr12:25520866 | T | C | 1 | a0006c0012t0001g0360 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.799-791A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25520866 | |||||||
| chr12:25520887 | T | C | 110 | a0001c0001t0001g0021 a0001c0001t0001g0146 a0001c0001t0001g0148 others(107): Show |
111 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.799-812A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25520887 | |||||||
| chr12:25520981 | G | A | 274 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(271): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(286): Show |
intron_variant | MODIFIER | c.799-906C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25520981 | |||||||
| chr12:25521096 | G | C | 10 | a0001c0001t0001g0163 a0001c0004t0001g0161 a0001c0004t0001g0164 others(7): Show |
10 | HG01255.hp2 HG02015.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.799-1021C>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25521096 | |||||||
| chr12:25521138 | CT | C | 205 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(202): Show |
216 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.799-1064delA | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25521138 | |||||||
| chr12:25521142 | T | C | 1 | a0001c0001t0002g0105 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.799-1067A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25521142 | |||||||
| chr12:25521219 | A | G | 1 | a0001c0001t0001g0297 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.799-1144T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25521219 | |||||||
| chr12:25521291 | C | G | 10 | a0001c0001t0001g0163 a0001c0004t0001g0161 a0001c0004t0001g0164 others(7): Show |
10 | HG01255.hp2 HG02015.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.799-1216G>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25521291 | |||||||
| chr12:25521333 | A | G | 10 | a0001c0001t0001g0163 a0001c0004t0001g0161 a0001c0004t0001g0164 others(7): Show |
10 | HG01255.hp2 HG02015.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.799-1258T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25521333 | |||||||
| chr12:25521358 | C | T | 1 | a0001c0001t0001g0337 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.799-1283G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25521358 | |||||||
| chr12:25521369 | T | C | 10 | a0001c0001t0001g0163 a0001c0004t0001g0161 a0001c0004t0001g0164 others(7): Show |
10 | HG01255.hp2 HG02015.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.799-1294A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25521369 | |||||||
| chr12:25521422 | AT | A | 10 | a0001c0001t0001g0163 a0001c0004t0001g0161 a0001c0004t0001g0164 others(7): Show |
10 | HG01255.hp2 HG02015.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.799-1348delA | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25521422 | |||||||
| chr12:25521463 | C | T | 11 | a0001c0001t0001g0163 a0001c0001t0001g0313 a0001c0004t0001g0161 others(8): Show |
11 | HG01255.hp2 HG01358.hp1 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.799-1388G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25521463 | |||||||
| chr12:25521472 | G | A | 1 | a0001c0001t0002g0100 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.799-1397C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25521472 | |||||||
| chr12:25521552 | G | A | 10 | a0001c0001t0001g0163 a0001c0004t0001g0161 a0001c0004t0001g0164 others(7): Show |
10 | HG01255.hp2 HG02015.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.799-1477C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25521552 | |||||||
| chr12:25521628 | T | C | 10 | a0001c0001t0001g0163 a0001c0004t0001g0161 a0001c0004t0001g0164 others(7): Show |
10 | HG01255.hp2 HG02015.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.799-1553A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25521628 | |||||||
| chr12:25521681 | A | T | 10 | a0001c0001t0001g0163 a0001c0004t0001g0161 a0001c0004t0001g0164 others(7): Show |
10 | HG01255.hp2 HG02015.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.799-1606T>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25521681 | |||||||
| chr12:25521733 | C | CTG | 4 | a0003c0005t0001g0153 a0003c0005t0001g0154 a0003c0005t0001g0155 others(1): Show |
4 | HG02630.hp2 HG03130.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.799-1660_799-1659d others(4): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25521733 | |||||||
| chr12:25521749 | A | G | 10 | a0001c0001t0001g0163 a0001c0004t0001g0161 a0001c0004t0001g0164 others(7): Show |
10 | HG01255.hp2 HG02015.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.799-1674T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25521749 | |||||||
| chr12:25521787 | G | A | 10 | a0001c0001t0001g0163 a0001c0004t0001g0161 a0001c0004t0001g0164 others(7): Show |
10 | HG01255.hp2 HG02015.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.799-1712C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25521787 | |||||||
| chr12:25521808 | T | C | 1 | a0001c0001t0001g0295 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.799-1733A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25521808 | |||||||
| chr12:25521944 | A | C | 10 | a0001c0001t0001g0163 a0001c0004t0001g0161 a0001c0004t0001g0164 others(7): Show |
10 | HG01255.hp2 HG02015.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.799-1869T>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25521944 | |||||||
| chr12:25521983 | C | T | 10 | a0001c0001t0001g0163 a0001c0004t0001g0161 a0001c0004t0001g0164 others(7): Show |
10 | HG01255.hp2 HG02015.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.799-1908G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25521983 | |||||||
| chr12:25522060 | G | C | 10 | a0001c0001t0001g0163 a0001c0004t0001g0161 a0001c0004t0001g0164 others(7): Show |
10 | HG01255.hp2 HG02015.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.799-1985C>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25522060 | |||||||
| chr12:25522117 | G | T | 11 | a0001c0001t0001g0163 a0001c0004t0001g0161 a0001c0004t0001g0164 others(8): Show |
12 | HG01255.hp2 HG02015.hp2 HG02027.hp2 others(9): Show |
intron_variant | MODIFIER | c.799-2042C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25522117 | |||||||
| chr12:25522160 | T | C | 10 | a0001c0001t0001g0163 a0001c0004t0001g0161 a0001c0004t0001g0164 others(7): Show |
10 | HG01255.hp2 HG02015.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.799-2085A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25522160 | |||||||
| chr12:25522186 | T | A | 10 | a0001c0001t0001g0163 a0001c0004t0001g0161 a0001c0004t0001g0164 others(7): Show |
10 | HG01255.hp2 HG02015.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.799-2111A>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25522186 | |||||||
| chr12:25522192 | C | CA | 33 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0023 others(30): Show |
38 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.799-2118dupT | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25522192 | |||||||
| chr12:25522192 | C | CT | 4 | a0003c0005t0001g0153 a0003c0005t0001g0154 a0003c0005t0001g0155 others(1): Show |
4 | HG02630.hp2 HG03130.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.799-2118_799-2117i others(3): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25522192 | |||||||
| chr12:25522193 | A | T | 6 | a0001c0001t0001g0163 a0001c0004t0001g0161 a0001c0004t0001g0164 others(3): Show |
6 | HG01255.hp2 HG02015.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.799-2118T>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25522193 | |||||||
| chr12:25522262 | A | G | 1 | a0001c0001t0001g0321 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.799-2187T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25522262 | |||||||
| chr12:25522311 | G | A | 10 | a0001c0001t0001g0163 a0001c0004t0001g0161 a0001c0004t0001g0164 others(7): Show |
10 | HG01255.hp2 HG02015.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.799-2236C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25522311 | |||||||
| chr12:25522312 | T | G | 10 | a0001c0001t0001g0163 a0001c0004t0001g0161 a0001c0004t0001g0164 others(7): Show |
10 | HG01255.hp2 HG02015.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.799-2237A>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25522312 | |||||||
| chr12:25522372 | G | A | 10 | a0001c0001t0001g0163 a0001c0004t0001g0161 a0001c0004t0001g0164 others(7): Show |
10 | HG01255.hp2 HG02015.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.799-2297C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25522372 | |||||||
| chr12:25522426 | T | G | 1 | a0002c0002t0002g0006 | 2 | NA18952.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.799-2351A>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25522426 | |||||||
| chr12:25522430 | G | A | 1 | a0001c0015t0001g0172 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.799-2355C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25522430 | |||||||
| chr12:25522638 | G | A | 10 | a0001c0001t0001g0163 a0001c0004t0001g0161 a0001c0004t0001g0164 others(7): Show |
10 | HG01255.hp2 HG02015.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.799-2563C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25522638 | |||||||
| chr12:25522652 | T | C | 1 | a0002c0002t0002g0008 | 2 | HG02258.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.799-2577A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25522652 | |||||||
| chr12:25522768 | C | A | 259 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(256): Show |
273 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(270): Show |
intron_variant | MODIFIER | c.799-2693G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25522768 | |||||||
| chr12:25522787 | AAGGTCCA others(1): Show |
A | 5 | a0001c0001t0001g0015 a0001c0001t0001g0157 a0001c0001t0001g0158 others(2): Show |
6 | HG02109.hp2 HG02451.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.799-2720_799-2713d others(10): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25522787 | |||||||
| chr12:25522840 | T | C | 10 | a0001c0001t0001g0163 a0001c0004t0001g0161 a0001c0004t0001g0164 others(7): Show |
10 | HG01255.hp2 HG02015.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.799-2765A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25522840 | |||||||
| chr12:25522848 | G | A | 10 | a0001c0001t0001g0163 a0001c0004t0001g0161 a0001c0004t0001g0164 others(7): Show |
10 | HG01255.hp2 HG02015.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.799-2773C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25522848 | |||||||
| chr12:25522983 | T | C | 110 | a0001c0001t0001g0021 a0001c0001t0001g0146 a0001c0001t0001g0148 others(107): Show |
111 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.799-2908A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25522983 | |||||||
| chr12:25523278 | C | T | 10 | a0001c0001t0001g0163 a0001c0004t0001g0161 a0001c0004t0001g0164 others(7): Show |
10 | HG01255.hp2 HG02015.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.798+2821G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25523278 | |||||||
| chr12:25523318 | C | T | 1 | a0001c0001t0001g0279 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.798+2781G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25523318 | |||||||
| chr12:25523326 | T | C | 345 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(342): Show |
371 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(368): Show |
intron_variant | MODIFIER | c.798+2773A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25523326 | |||||||
| chr12:25523605 | T | C | 1 | a0001c0001t0002g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.798+2494A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25523605 | |||||||
| chr12:25523613 | C | T | 10 | a0001c0001t0001g0163 a0001c0004t0001g0161 a0001c0004t0001g0164 others(7): Show |
10 | HG01255.hp2 HG02015.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.798+2486G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25523613 | |||||||
| chr12:25523642 | G | T | 10 | a0001c0001t0001g0163 a0001c0004t0001g0161 a0001c0004t0001g0164 others(7): Show |
10 | HG01255.hp2 HG02015.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.798+2457C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25523642 | |||||||
| chr12:25523816 | T | TA | 21 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0151 others(18): Show |
24 | HG01255.hp1 HG01884.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.798+2282dupT | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25523816 | |||||||
| chr12:25523816 | TA | T | 14 | a0001c0001t0001g0146 a0001c0001t0001g0163 a0001c0001t0001g0182 others(11): Show |
14 | HG01169.hp1 HG01255.hp2 HG01975.hp2 others(11): Show |
intron_variant | MODIFIER | c.798+2282delT | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25523816 | |||||||
| chr12:25523896 | G | A | 2 | a0001c0001t0002g0062 a0006c0012t0001g0360 |
2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.798+2203C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25523896 | |||||||
| chr12:25523897 | C | T | 267 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(264): Show |
282 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.798+2202G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25523897 | |||||||
| chr12:25523906 | A | C | 5 | a0001c0001t0001g0015 a0001c0001t0001g0157 a0001c0001t0001g0158 others(2): Show |
6 | HG02109.hp2 HG02451.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.798+2193T>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25523906 | |||||||
| chr12:25523919 | C | T | 1 | a0001c0001t0002g0090 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.798+2180G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25523919 | |||||||
| chr12:25523987 | A | G | 1 | a0002c0002t0002g0053 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.798+2112T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25523987 | |||||||
| chr12:25523999 | A | G | 267 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(264): Show |
282 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.798+2100T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25523999 | |||||||
| chr12:25524071 | G | A | 1 | a0002c0002t0001g0162 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.798+2028C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25524071 | |||||||
| chr12:25524106 | C | T | 261 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(258): Show |
275 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.798+1993G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25524106 | |||||||
| chr12:25524177 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.798+1922G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25524177 | |||||||
| chr12:25524215 | C | A | 1 | a0001c0001t0002g0054 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.798+1884G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25524215 | |||||||
| chr12:25524245 | C | G | 1 | a0002c0002t0002g0125 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.798+1854G>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25524245 | |||||||
| chr12:25524596 | A | G | 1 | a0002c0002t0002g0144 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.798+1503T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25524596 | |||||||
| chr12:25524657 | T | TAAGAATG others(308): Show |
3 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 |
3 | HG03139.hp1 HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.798+1441_798+1442i others(317): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25524657 | |||||||
| chr12:25524657 | T | TAAGAATG others(314): Show |
1 | a0001c0001t0001g0186 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.798+1441_798+1442i others(323): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25524657 | |||||||
| chr12:25524743 | T | C | 65 | a0001c0001t0001g0152 a0001c0001t0002g0009 a0001c0001t0002g0010 others(62): Show |
68 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.798+1356A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25524743 | |||||||
| chr12:25524828 | C | T | 65 | a0001c0001t0001g0152 a0001c0001t0002g0009 a0001c0001t0002g0010 others(62): Show |
68 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.798+1271G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25524828 | |||||||
| chr12:25524841 | A | T | 1 | a0008c0013t0003g0170 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.798+1258T>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25524841 | |||||||
| chr12:25524988 | A | G | 1 | a0001c0001t0002g0085 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.798+1111T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25524988 | |||||||
| chr12:25524991 | T | C | 1 | a0001c0001t0002g0085 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.798+1108A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25524991 | |||||||
| chr12:25524993 | A | C | 1 | a0001c0001t0002g0085 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.798+1106T>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25524993 | |||||||
| chr12:25524996 | T | A | 65 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0002g0009 others(62): Show |
68 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.798+1103A>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25524996 | |||||||
| chr12:25525001 | G | A | 1 | a0001c0001t0002g0085 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.798+1098C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25525001 | |||||||
| chr12:25525007 | A | T | 1 | a0001c0001t0002g0085 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.798+1092T>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25525007 | |||||||
| chr12:25525015 | C | G | 1 | a0001c0001t0002g0085 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.798+1084G>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25525015 | |||||||
| chr12:25525016 | A | G | 1 | a0001c0001t0002g0085 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.798+1083T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25525016 | |||||||
| chr12:25525017 | G | C | 1 | a0001c0001t0002g0085 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.798+1082C>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25525017 | |||||||
| chr12:25525018 | A | T | 1 | a0001c0001t0002g0085 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.798+1081T>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25525018 | |||||||
| chr12:25525019 | G | A | 1 | a0001c0001t0002g0085 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.798+1080C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25525019 | |||||||
| chr12:25525023 | G | T | 1 | a0001c0001t0002g0085 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.798+1076C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25525023 | |||||||
| chr12:25525030 | G | T | 1 | a0001c0001t0002g0085 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.798+1069C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25525030 | |||||||
| chr12:25525031 | T | A | 1 | a0001c0001t0002g0085 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.798+1068A>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25525031 | |||||||
| chr12:25525032 | T | G | 1 | a0001c0001t0002g0085 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.798+1067A>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25525032 | |||||||
| chr12:25525034 | A | G | 1 | a0001c0001t0002g0085 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.798+1065T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25525034 | |||||||
| chr12:25525042 | T | A | 1 | a0001c0001t0002g0085 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.798+1057A>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25525042 | |||||||
| chr12:25525043 | G | C | 1 | a0001c0001t0002g0085 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.798+1056C>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25525043 | |||||||
| chr12:25525049 | A | C | 1 | a0001c0001t0002g0085 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.798+1050T>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25525049 | |||||||
| chr12:25525050 | G | T | 1 | a0001c0001t0002g0085 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.798+1049C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25525050 | |||||||
| chr12:25525055 | A | T | 1 | a0001c0001t0002g0085 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.798+1044T>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25525055 | |||||||
| chr12:25525056 | T | G | 1 | a0001c0001t0002g0085 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.798+1043A>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25525056 | |||||||
| chr12:25525135 | C | A | 66 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0002g0009 others(63): Show |
69 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.798+964G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25525135 | |||||||
| chr12:25525176 | T | A | 66 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0002g0009 others(63): Show |
69 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.798+923A>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25525176 | |||||||
| chr12:25525186 | C | T | 1 | a0001c0001t0001g0303 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.798+913G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25525186 | |||||||
| chr12:25525210 | T | C | 1 | a0001c0001t0001g0248 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.798+889A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25525210 | |||||||
| chr12:25525247 | G | A | 3 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 |
3 | HG01169.hp1 HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.798+852C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25525247 | |||||||
| chr12:25525476 | G | A | 1 | a0001c0001t0002g0114 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.798+623C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25525476 | |||||||
| chr12:25525500 | C | T | 5 | a0001c0001t0001g0015 a0001c0001t0001g0157 a0001c0001t0001g0158 others(2): Show |
6 | HG02109.hp2 HG02451.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.798+599G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25525500 | |||||||
| chr12:25525534 | C | T | 1 | a0001c0001t0001g0278 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.798+565G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25525534 | |||||||
| chr12:25525551 | G | A | 4 | a0002c0002t0002g0032 a0002c0002t0002g0034 a0002c0002t0002g0035 others(1): Show |
4 | HG02451.hp1 HG03209.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.798+548C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25525551 | |||||||
| chr12:25525604 | C | T | 1 | a0001c0001t0001g0206 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.798+495G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25525604 | |||||||
| chr12:25525705 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.798+394C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25525705 | |||||||
| chr12:25525758 | G | C | 279 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(276): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.798+341C>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25525758 | |||||||
| chr12:25525860 | A | T | 2 | a0001c0001t0001g0215 a0001c0001t0001g0273 |
2 | HG01081.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.798+239T>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25525860 | |||||||
| chr12:25525907 | G | T | 65 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0002g0009 others(62): Show |
68 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.798+192C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25525907 | |||||||
| chr12:25525947 | C | T | 213 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(210): Show |
226 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.798+152G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25525947 | |||||||
| chr12:25525976 | A | T | 3 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0006c0012t0001g0360 |
3 | HG01891.hp2 HG02258.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.798+123T>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25525976 | |||||||
| chr12:25526061 | T | TA | 68 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0334 others(65): Show |
71 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.798+37dupT | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25526061 | |||||||
| chr12:25526070 | A | C | 5 | a0001c0001t0001g0015 a0001c0001t0001g0157 a0001c0001t0001g0158 others(2): Show |
6 | HG02109.hp2 HG02451.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.798+29T>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25526070 | |||||||
| chr12:25526079 | G | T | 2 | a0001c0007t0003g0171 a0002c0014t0001g0169 |
2 | HG02559.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.798+20C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 6/9 | chr12 | 25526079 | |||||||
| chr12:25526400 | C | A | 63 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(60): Show |
66 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.679-182G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 5/9 | chr12 | 25526400 | |||||||
| chr12:25526436 | T | C | 285 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(282): Show |
301 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(298): Show |
intron_variant | MODIFIER | c.679-218A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 5/9 | chr12 | 25526436 | |||||||
| chr12:25526623 | G | A | 3 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0006c0012t0001g0360 |
3 | HG01891.hp2 HG02258.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.678+146C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 5/9 | chr12 | 25526623 | |||||||
| chr12:25526971 | C | T | 1 | a0003c0005t0003g0156 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.492-16G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25526971 | |||||||
| chr12:25526998 | G | A | 278 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(275): Show |
294 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(291): Show |
intron_variant | MODIFIER | c.492-43C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25526998 | |||||||
| chr12:25527210 | A | G | 4 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(1): Show |
4 | HG03139.hp1 HG03195.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.492-255T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527210 | |||||||
| chr12:25527233 | T | G | 279 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(276): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.492-278A>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527233 | |||||||
| chr12:25527320 | ATTTAC | A | 66 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0002g0009 others(63): Show |
69 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.492-370_492-366del others(5): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527320 | |||||||
| chr12:25527332 | T | G | 1 | a0002c0002t0002g0045 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.492-377A>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527332 | |||||||
| chr12:25527385 | A | C | 4 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(1): Show |
4 | HG03139.hp1 HG03195.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.492-430T>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527385 | |||||||
| chr12:25527444 | A | G | 4 | a0001c0001t0001g0303 a0001c0001t0001g0305 a0001c0001t0001g0347 others(1): Show |
4 | HG02040.hp1 NA18999.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.492-489T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527444 | |||||||
| chr12:25527458 | G | A | 64 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(61): Show |
67 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.492-503C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527458 | |||||||
| chr12:25527537 | G | A | 202 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(199): Show |
214 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.492-582C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527537 | |||||||
| chr12:25527591 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.492-636C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527591 | |||||||
| chr12:25527624 | C | G | 67 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0002g0009 others(64): Show |
70 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.492-669G>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527624 | |||||||
| chr12:25527635 | T | A | 67 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0002g0009 others(64): Show |
70 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.492-680A>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527635 | |||||||
| chr12:25527640 | C | CTA | 9 | a0001c0001t0001g0183 a0001c0001t0001g0238 a0001c0001t0001g0241 others(6): Show |
9 | HG00423.hp2 HG02109.hp1 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.492-687_492-686dup others(2): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527640 | |||||||
| chr12:25527640 | C | CTATA | 15 | a0001c0001t0001g0148 a0001c0001t0001g0184 a0001c0001t0001g0216 others(12): Show |
15 | HG00099.hp2 HG00609.hp2 HG00621.hp2 others(12): Show |
intron_variant | MODIFIER | c.492-689_492-686dup others(4): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527640 | |||||||
| chr12:25527640 | C | CTATATA | 14 | a0001c0001t0001g0149 a0001c0001t0001g0179 a0001c0001t0001g0235 others(11): Show |
14 | HG00280.hp1 HG01167.hp2 HG01978.hp2 others(11): Show |
intron_variant | MODIFIER | c.492-691_492-686dup others(6): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527640 | |||||||
| chr12:25527640 | C | CTATATAT others(1): Show |
23 | a0001c0001t0001g0228 a0001c0001t0001g0254 a0001c0001t0001g0257 others(20): Show |
24 | HG00280.hp2 HG01070.hp1 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.492-693_492-686dup others(8): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527640 | |||||||
| chr12:25527640 | C | CTATATAT others(3): Show |
6 | a0001c0001t0001g0224 a0001c0001t0001g0243 a0001c0001t0001g0255 others(3): Show |
6 | HG00642.hp2 HG00735.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.492-695_492-686dup others(10): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527640 | |||||||
| chr12:25527640 | C | CTATATAT others(5): Show |
12 | a0001c0001t0001g0182 a0001c0001t0001g0223 a0001c0001t0001g0244 others(9): Show |
12 | HG00741.hp1 HG01243.hp2 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.492-697_492-686dup others(12): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527640 | |||||||
| chr12:25527640 | C | CTATATAT others(7): Show |
3 | a0001c0001t0001g0185 a0001c0001t0001g0271 a0003c0005t0001g0155 |
3 | HG02630.hp2 HG02647.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.492-699_492-686dup others(14): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527640 | |||||||
| chr12:25527640 | C | CTATATAT others(9): Show |
2 | a0001c0001t0001g0256 a0001c0001t0001g0272 |
2 | HG01169.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.492-701_492-686dup others(16): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527640 | |||||||
| chr12:25527640 | C | CTATATAT others(11): Show |
1 | a0001c0001t0001g0357 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.492-703_492-686dup others(18): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527640 | |||||||
| chr12:25527640 | C | CTATATAT others(25): Show |
1 | a0001c0001t0001g0245 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.492-717_492-686dup others(32): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527640 | |||||||
| chr12:25527640 | CTA | C | 11 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0136 others(8): Show |
11 | HG00642.hp1 HG01069.hp1 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.492-687_492-686del others(2): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527640 | |||||||
| chr12:25527640 | CTATA | C | 6 | a0002c0002t0002g0032 a0002c0002t0002g0046 a0002c0002t0002g0053 others(3): Show |
6 | HG01496.hp2 HG02015.hp1 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.492-689_492-686del others(4): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527640 | |||||||
| chr12:25527640 | CTATATAT others(3): Show |
C | 1 | a0002c0002t0002g0033 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.492-695_492-686del others(10): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527640 | |||||||
| chr12:25527640 | CTATATAT others(7): Show |
C | 1 | a0001c0001t0001g0151 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.492-699_492-686del others(14): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527640 | |||||||
| chr12:25527640 | CTATATAT others(13): Show |
C | 1 | a0006c0012t0001g0360 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.492-705_492-686del others(20): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527640 | |||||||
| chr12:25527640 | CTATATAT others(15): Show |
C | 1 | a0001c0001t0002g0054 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.492-707_492-686del others(22): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527640 | |||||||
| chr12:25527640 | CTATATAT others(17): Show |
C | 1 | a0001c0001t0001g0152 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.492-709_492-686del others(24): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527640 | |||||||
| chr12:25527648 | A | ATATTATA others(52): Show |
1 | a0002c0002t0002g0056 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.492-694_492-693ins others(59): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527648 | |||||||
| chr12:25527651 | TATATATA others(29): Show |
T | 5 | a0001c0004t0001g0161 a0001c0004t0001g0164 a0001c0004t0001g0165 others(2): Show |
5 | HG02015.hp2 HG02027.hp2 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.492-732_492-697del others(36): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527651 | |||||||
| chr12:25527652 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.492-697T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527652 | |||||||
| chr12:25527653 | TATATATA others(25): Show |
T | 1 | a0001c0001t0001g0163 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.492-730_492-699del others(32): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527653 | |||||||
| chr12:25527653 | TATATATA others(29): Show |
T | 63 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(60): Show |
66 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.492-734_492-699del others(36): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527653 | |||||||
| chr12:25527659 | TATATATA others(23): Show |
T | 1 | a0009c0009t0001g0359 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.492-734_492-705del others(30): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527659 | |||||||
| chr12:25527661 | TATATATA others(21): Show |
T | 2 | a0001c0001t0001g0220 a0001c0001t0001g0221 |
2 | NA18983.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.492-734_492-707del others(28): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527661 | |||||||
| chr12:25527663 | TATATATA others(15): Show |
T | 7 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0218 others(4): Show |
9 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(6): Show |
intron_variant | MODIFIER | c.492-730_492-709del others(22): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527663 | |||||||
| chr12:25527663 | TATATATA others(19): Show |
T | 1 | a0001c0001t0001g0150 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.492-734_492-709del others(26): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527663 | |||||||
| chr12:25527665 | TATATATA others(13): Show |
T | 1 | a0002c0002t0001g0022 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.492-730_492-711del others(20): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527665 | |||||||
| chr12:25527665 | TATATATA others(15): Show |
T | 26 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0023 others(23): Show |
28 | HG00733.hp2 HG01257.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.492-732_492-711del others(22): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527665 | |||||||
| chr12:25527665 | TATATATA others(19): Show |
T | 1 | a0001c0001t0001g0285 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.492-736_492-711del others(26): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527665 | |||||||
| chr12:25527667 | TATATATA others(13): Show |
T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0280 |
2 | HG04204.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.492-732_492-713del others(20): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527667 | |||||||
| chr12:25527667 | TATATATA others(17): Show |
T | 1 | a0001c0001t0001g0287 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.492-736_492-713del others(24): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527667 | |||||||
| chr12:25527669 | TATATATA others(9): Show |
T | 1 | a0001c0001t0001g0208 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.492-730_492-715del others(16): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527669 | |||||||
| chr12:25527669 | TATATATA others(11): Show |
T | 4 | a0001c0001t0001g0147 a0001c0001t0001g0190 a0001c0001t0001g0211 others(1): Show |
4 | NA18969.hp1 NA19006.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.492-732_492-715del others(18): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527669 | |||||||
| chr12:25527669 | TATATATA others(13): Show |
T | 1 | a0002c0002t0001g0180 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.492-734_492-715del others(20): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527669 | |||||||
| chr12:25527669 | TATATATA others(15): Show |
T | 1 | a0001c0001t0001g0186 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.492-736_492-715del others(22): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527669 | |||||||
| chr12:25527671 | TATATATA others(9): Show |
T | 41 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(38): Show |
46 | HG00438.hp1 HG00597.hp1 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.492-732_492-717del others(16): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527671 | |||||||
| chr12:25527673 | TATATATA others(5): Show |
T | 1 | a0002c0002t0001g0160 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.492-730_492-719del others(12): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527673 | |||||||
| chr12:25527673 | TATATATA others(7): Show |
T | 2 | a0001c0001t0001g0181 a0001c0001t0001g0296 |
2 | NA18990.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.492-732_492-719del others(14): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527673 | |||||||
| chr12:25527673 | TATATATA others(9): Show |
T | 1 | a0001c0001t0001g0213 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.492-734_492-719del others(16): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527673 | |||||||
| chr12:25527673 | TATATATA others(11): Show |
T | 3 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 |
3 | HG03139.hp1 HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.492-736_492-719del others(18): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527673 | |||||||
| chr12:25527673 | TATATATA others(15): Show |
T | 2 | a0001c0001t0001g0305 a0001c0001t0001g0347 |
2 | NA19057.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.492-740_492-719del others(22): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527673 | |||||||
| chr12:25527675 | T | C | 4 | a0001c0001t0001g0151 a0002c0002t0002g0051 a0002c0003t0002g0030 others(1): Show |
4 | HG00642.hp1 HG01516.hp2 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.492-720A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527675 | |||||||
| chr12:25527675 | TATATATA others(1): Show |
T | 3 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0005c0008t0001g0240 |
3 | HG01175.hp2 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.492-728_492-721del others(8): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527675 | |||||||
| chr12:25527677 | T | C | 10 | a0001c0001t0001g0151 a0002c0002t0002g0004 a0002c0002t0002g0027 others(7): Show |
10 | HG00642.hp1 HG01496.hp2 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.492-722A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527677 | |||||||
| chr12:25527677 | T | TACACAC | 3 | a0002c0002t0002g0001 a0002c0002t0002g0026 a0002c0002t0002g0040 |
4 | HG01081.hp1 HG01993.hp1 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.492-723_492-722ins others(6): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527677 | |||||||
| chr12:25527677 | T | TACACACA others(3): Show |
1 | a0002c0002t0002g0037 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.492-723_492-722ins others(10): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527677 | |||||||
| chr12:25527677 | TATATACA others(9): Show |
T | 2 | a0001c0001t0001g0215 a0001c0001t0001g0273 |
2 | HG01081.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.492-738_492-723del others(16): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527677 | |||||||
| chr12:25527679 | T | C | 22 | a0001c0001t0001g0151 a0001c0001t0002g0054 a0002c0002t0002g0001 others(19): Show |
25 | HG00642.hp1 HG00741.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.492-724A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527679 | |||||||
| chr12:25527679 | T | TACAC | 3 | a0002c0002t0002g0005 a0002c0002t0002g0038 a0002c0002t0002g0043 |
4 | HG01167.hp1 HG01169.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.492-725_492-724ins others(4): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527679 | |||||||
| chr12:25527679 | T | TACACACA others(1): Show |
3 | a0002c0002t0002g0007 a0002c0002t0002g0036 a0002c0002t0002g0047 |
4 | HG02056.hp2 HG02622.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.492-725_492-724ins others(8): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527679 | |||||||
| chr12:25527679 | TATAC | T | 2 | a0002c0002t0002g0008 a0002c0002t0002g0141 |
3 | HG02258.hp2 HG02809.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.492-728_492-725del others(4): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527679 | |||||||
| chr12:25527679 | TATACACA others(5): Show |
T | 2 | a0001c0001t0001g0353 a0001c0001t0003g0269 |
2 | HG02559.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.492-736_492-725del others(12): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527679 | |||||||
| chr12:25527679 | TATACACA others(17): Show |
T | 4 | a0001c0001t0001g0015 a0001c0001t0001g0157 a0001c0001t0001g0158 others(1): Show |
4 | HG02451.hp2 HG02615.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.492-748_492-725del others(24): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527679 | |||||||
| chr12:25527681 | T | C | 37 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0002g0054 others(34): Show |
42 | HG00642.hp1 HG00741.hp2 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.492-726A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527681 | |||||||
| chr12:25527681 | T | TACACACA others(5): Show |
1 | a0002c0002t0002g0041 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.492-738_492-727dup others(12): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527681 | |||||||
| chr12:25527681 | T | TATACAC | 3 | a0001c0001t0002g0013 a0001c0001t0002g0145 a0002c0002t0002g0002 |
4 | HG01884.hp1 HG02280.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.492-727_492-726ins others(6): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527681 | |||||||
| chr12:25527681 | T | TATACACA others(5): Show |
1 | a0002c0002t0002g0048 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.492-727_492-726ins others(12): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527681 | |||||||
| chr12:25527681 | T | TATATATA others(9): Show |
1 | a0002c0002t0002g0144 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.492-727_492-726ins others(16): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527681 | |||||||
| chr12:25527681 | TAC | T | 6 | a0001c0001t0001g0021 a0001c0001t0001g0222 a0001c0001t0001g0253 others(3): Show |
7 | HG01256.hp2 HG01258.hp1 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.492-728_492-727del others(2): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527681 | |||||||
| chr12:25527681 | TACAC | T | 5 | a0001c0001t0001g0236 a0001c0001t0001g0247 a0001c0001t0001g0323 others(2): Show |
5 | HG00673.hp1 HG00733.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.492-730_492-727del others(4): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527681 | |||||||
| chr12:25527681 | TACACAC | T | 4 | a0001c0001t0001g0231 a0001c0001t0001g0300 a0001c0001t0001g0321 others(1): Show |
4 | HG01496.hp1 HG02735.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.492-732_492-727del others(6): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527681 | |||||||
| chr12:25527681 | TACACACA others(3): Show |
T | 2 | a0001c0001t0001g0348 a0002c0002t0001g0162 |
2 | HG03516.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.492-736_492-727del others(10): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527681 | |||||||
| chr12:25527681 | TACACACA others(15): Show |
T | 1 | a0001c0001t0001g0015 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.492-748_492-727del others(22): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527681 | |||||||
| chr12:25527683 | C | T | 94 | a0001c0001t0001g0146 a0001c0001t0001g0148 a0001c0001t0001g0149 others(91): Show |
95 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.492-728G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527683 | |||||||
| chr12:25527685 | C | T | 89 | a0001c0001t0001g0021 a0001c0001t0001g0146 a0001c0001t0001g0148 others(86): Show |
90 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.492-730G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527685 | |||||||
| chr12:25527687 | C | T | 94 | a0001c0001t0001g0021 a0001c0001t0001g0146 a0001c0001t0001g0148 others(91): Show |
95 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.492-732G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527687 | |||||||
| chr12:25527689 | C | T | 89 | a0001c0001t0001g0021 a0001c0001t0001g0146 a0001c0001t0001g0148 others(86): Show |
90 | HG00280.hp2 HG00423.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.492-734G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527689 | |||||||
| chr12:25527691 | C | T | 62 | a0001c0001t0001g0149 a0001c0001t0001g0179 a0001c0001t0001g0182 others(59): Show |
62 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.492-736G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527691 | |||||||
| chr12:25527693 | C | T | 13 | a0001c0001t0001g0149 a0001c0001t0001g0152 a0001c0001t0001g0230 others(10): Show |
13 | HG01496.hp1 HG01934.hp2 HG01993.hp2 others(10): Show |
intron_variant | MODIFIER | c.492-738G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527693 | |||||||
| chr12:25527695 | C | T | 9 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 others(6): Show |
9 | HG01496.hp1 HG01934.hp2 HG01993.hp2 others(6): Show |
intron_variant | MODIFIER | c.492-740G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527695 | |||||||
| chr12:25527697 | C | T | 1 | a0002c0002t0001g0162 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.492-742G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527697 | |||||||
| chr12:25527699 | C | T | 1 | a0002c0002t0001g0162 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.492-744G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527699 | |||||||
| chr12:25527701 | C | T | 1 | a0002c0002t0001g0162 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.492-746G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527701 | |||||||
| chr12:25527707 | C | T | 66 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0002g0009 others(63): Show |
69 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.492-752G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527707 | |||||||
| chr12:25527709 | C | T | 67 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0002g0009 others(64): Show |
70 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.492-754G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527709 | |||||||
| chr12:25527711 | C | T | 67 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0002g0009 others(64): Show |
70 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.492-756G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527711 | |||||||
| chr12:25527719 | C | T | 67 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0002g0009 others(64): Show |
70 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.492-764G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527719 | |||||||
| chr12:25527721 | T | C | 3 | a0001c0001t0001g0163 a0001c0001t0001g0184 a0001c0001t0001g0246 |
3 | HG01255.hp2 NA18957.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.492-766A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527721 | |||||||
| chr12:25527723 | T | C | 5 | a0002c0002t0002g0012 a0002c0002t0002g0118 a0002c0002t0002g0119 others(2): Show |
6 | HG00280.hp1 HG00735.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.492-768A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527723 | |||||||
| chr12:25527725 | C | T | 67 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0002g0009 others(64): Show |
70 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.492-770G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527725 | |||||||
| chr12:25527819 | C | G | 1 | a0001c0001t0001g0152 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.492-864G>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527819 | |||||||
| chr12:25527860 | T | A | 64 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(61): Show |
67 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.492-905A>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25527860 | |||||||
| chr12:25528126 | T | A | 1 | a0001c0001t0001g0247 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.492-1171A>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25528126 | |||||||
| chr12:25528147 | C | T | 2 | a0002c0002t0002g0132 a0002c0002t0002g0144 |
2 | HG01069.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.492-1192G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25528147 | |||||||
| chr12:25528148 | G | T | 68 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0002g0009 others(65): Show |
71 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.492-1193C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25528148 | |||||||
| chr12:25528161 | A | G | 68 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0002g0009 others(65): Show |
71 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.492-1206T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25528161 | |||||||
| chr12:25528249 | G | C | 68 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0002g0009 others(65): Show |
71 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.492-1294C>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25528249 | |||||||
| chr12:25528349 | C | T | 68 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0002g0009 others(65): Show |
71 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.492-1394G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25528349 | |||||||
| chr12:25528352 | C | T | 63 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(60): Show |
66 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.492-1397G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25528352 | |||||||
| chr12:25528452 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.492-1497C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25528452 | |||||||
| chr12:25528633 | A | G | 78 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0163 others(75): Show |
81 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.492-1678T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25528633 | |||||||
| chr12:25528645 | C | T | 6 | a0001c0001t0001g0163 a0001c0004t0001g0161 a0001c0004t0001g0164 others(3): Show |
6 | HG01255.hp2 HG02015.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.492-1690G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25528645 | |||||||
| chr12:25528667 | A | G | 78 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0163 others(75): Show |
81 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.492-1712T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25528667 | |||||||
| chr12:25528671 | T | G | 207 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(204): Show |
219 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.492-1716A>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25528671 | |||||||
| chr12:25528684 | C | A | 1 | a0001c0004t0001g0161 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.492-1729G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25528684 | |||||||
| chr12:25528686 | T | C | 289 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(286): Show |
305 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(302): Show |
intron_variant | MODIFIER | c.492-1731A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25528686 | |||||||
| chr12:25528789 | A | G | 78 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0163 others(75): Show |
81 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.492-1834T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25528789 | |||||||
| chr12:25528958 | G | T | 1 | a0001c0001t0001g0152 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.492-2003C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25528958 | |||||||
| chr12:25528984 | C | T | 5 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0142 others(2): Show |
7 | HG01884.hp1 HG02109.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.492-2029G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25528984 | |||||||
| chr12:25529028 | A | G | 78 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0163 others(75): Show |
81 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.492-2073T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25529028 | |||||||
| chr12:25529077 | A | G | 1 | a0002c0003t0005g0050 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.492-2122T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25529077 | |||||||
| chr12:25529097 | T | C | 39 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0023 others(36): Show |
45 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.492-2142A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25529097 | |||||||
| chr12:25529106 | C | A | 2 | a0001c0001t0001g0151 a0002c0002t0001g0160 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.492-2151G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25529106 | |||||||
| chr12:25529348 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.492-2393C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25529348 | |||||||
| chr12:25529372 | G | A | 217 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(214): Show |
230 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.492-2417C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25529372 | |||||||
| chr12:25529407 | A | G | 1 | a0006c0012t0001g0360 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.492-2452T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25529407 | |||||||
| chr12:25529408 | G | T | 1 | a0006c0012t0001g0360 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.492-2453C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25529408 | |||||||
| chr12:25529412 | C | T | 207 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(204): Show |
220 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.492-2457G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25529412 | |||||||
| chr12:25529415 | C | A | 1 | a0006c0012t0001g0360 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.492-2460G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25529415 | |||||||
| chr12:25529560 | G | A | 1 | a0002c0002t0002g0008 | 2 | HG02258.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.492-2605C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25529560 | |||||||
| chr12:25529716 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.492-2761A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25529716 | |||||||
| chr12:25529904 | T | G | 280 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(277): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.492-2949A>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25529904 | |||||||
| chr12:25529981 | C | T | 1 | a0001c0001t0002g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.492-3026G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25529981 | |||||||
| chr12:25530112 | C | T | 6 | a0001c0001t0001g0163 a0001c0004t0001g0161 a0001c0004t0001g0164 others(3): Show |
6 | HG01255.hp2 HG02015.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.492-3157G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25530112 | |||||||
| chr12:25530136 | T | C | 1 | a0001c0001t0002g0087 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.492-3181A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25530136 | |||||||
| chr12:25530197 | T | G | 9 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0002g0062 others(6): Show |
9 | HG01891.hp2 HG02258.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.492-3242A>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25530197 | |||||||
| chr12:25530413 | A | G | 1 | a0001c0001t0001g0248 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.492-3458T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25530413 | |||||||
| chr12:25530416 | C | A | 8 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0002c0002t0001g0160 others(5): Show |
8 | HG01891.hp2 HG02258.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.492-3461G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25530416 | |||||||
| chr12:25530502 | G | C | 67 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0002g0009 others(64): Show |
70 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.492-3547C>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25530502 | |||||||
| chr12:25530562 | A | G | 213 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(210): Show |
225 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.492-3607T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25530562 | |||||||
| chr12:25530752 | A | G | 1 | a0008c0013t0003g0170 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.492-3797T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25530752 | |||||||
| chr12:25530813 | G | A | 2 | a0002c0002t0002g0055 a0002c0002t0002g0056 |
2 | HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.492-3858C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25530813 | |||||||
| chr12:25530904 | T | A | 5 | a0001c0004t0001g0161 a0001c0004t0001g0164 a0001c0004t0001g0165 others(2): Show |
5 | HG02015.hp2 HG02027.hp2 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.492-3949A>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25530904 | |||||||
| chr12:25531468 | T | A | 5 | a0001c0004t0001g0161 a0001c0004t0001g0164 a0001c0004t0001g0165 others(2): Show |
5 | HG02015.hp2 HG02027.hp2 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.492-4513A>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25531468 | |||||||
| chr12:25531574 | G | A | 5 | a0001c0001t0001g0015 a0001c0001t0001g0157 a0001c0001t0001g0158 others(2): Show |
6 | HG02109.hp2 HG02451.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.492-4619C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25531574 | |||||||
| chr12:25531662 | T | G | 1 | a0002c0002t0001g0160 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.492-4707A>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25531662 | |||||||
| chr12:25531731 | T | C | 1 | a0002c0002t0001g0160 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.492-4776A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25531731 | |||||||
| chr12:25531799 | C | T | 289 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(286): Show |
306 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(303): Show |
intron_variant | MODIFIER | c.492-4844G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25531799 | |||||||
| chr12:25531839 | A | G | 11 | a0001c0001t0001g0178 a0001c0001t0001g0206 a0001c0001t0001g0207 others(8): Show |
11 | HG00438.hp1 HG01943.hp2 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.492-4884T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25531839 | |||||||
| chr12:25531937 | C | T | 2 | a0002c0002t0002g0130 a0002c0002t0002g0131 |
2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.492-4982G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25531937 | |||||||
| chr12:25531946 | A | AT | 58 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(55): Show |
61 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.492-4992dupA | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25531946 | |||||||
| chr12:25531962 | G | T | 4 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0002c0002t0001g0160 others(1): Show |
4 | HG01891.hp2 HG02258.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.492-5007C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25531962 | |||||||
| chr12:25532087 | C | A | 8 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0002c0002t0001g0160 others(5): Show |
8 | HG01891.hp2 HG02258.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.492-5132G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25532087 | |||||||
| chr12:25532104 | G | T | 1 | a0001c0001t0001g0157 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.492-5149C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25532104 | |||||||
| chr12:25532140 | T | A | 5 | a0001c0007t0003g0171 a0001c0007t0004g0173 a0001c0015t0001g0172 others(2): Show |
5 | HG02559.hp1 HG03209.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.492-5185A>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25532140 | |||||||
| chr12:25532154 | G | A | 4 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0186 others(1): Show |
6 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(3): Show |
intron_variant | MODIFIER | c.492-5199C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25532154 | |||||||
| chr12:25532443 | C | T | 1 | a0002c0002t0002g0122 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.492-5488G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25532443 | |||||||
| chr12:25532483 | C | T | 12 | a0001c0001t0001g0181 a0001c0001t0001g0187 a0001c0001t0001g0189 others(9): Show |
12 | HG00597.hp1 HG01952.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.492-5528G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25532483 | |||||||
| chr12:25532493 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.492-5538G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25532493 | |||||||
| chr12:25532541 | G | A | 4 | a0003c0005t0001g0153 a0003c0005t0001g0154 a0003c0005t0001g0155 others(1): Show |
4 | HG02630.hp2 HG03130.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.492-5586C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25532541 | |||||||
| chr12:25532603 | C | G | 5 | a0002c0002t0002g0012 a0002c0002t0002g0118 a0002c0002t0002g0119 others(2): Show |
6 | HG00280.hp1 HG00735.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.492-5648G>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25532603 | |||||||
| chr12:25532618 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.492-5663C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25532618 | |||||||
| chr12:25532778 | T | A | 1 | a0006c0012t0001g0360 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.492-5823A>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25532778 | |||||||
| chr12:25532874 | GA | G | 4 | a0003c0005t0001g0153 a0003c0005t0001g0154 a0003c0005t0001g0155 others(1): Show |
4 | HG02630.hp2 HG03130.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.492-5920delT | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25532874 | |||||||
| chr12:25532897 | T | G | 2 | a0002c0002t0001g0219 a0002c0002t0001g0291 |
2 | HG02683.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.492-5942A>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25532897 | |||||||
| chr12:25532958 | C | A | 1 | a0002c0002t0002g0051 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.492-6003G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25532958 | |||||||
| chr12:25533172 | C | T | 2 | a0002c0002t0002g0055 a0002c0002t0002g0056 |
2 | HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.492-6217G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25533172 | |||||||
| chr12:25533193 | G | A | 1 | a0002c0002t0002g0041 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.492-6238C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25533193 | |||||||
| chr12:25533292 | C | T | 1 | a0001c0001t0002g0106 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.492-6337G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25533292 | |||||||
| chr12:25533501 | GT | G | 226 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(223): Show |
239 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.492-6547delA | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25533501 | |||||||
| chr12:25533506 | T | C | 226 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(223): Show |
239 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.492-6551A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25533506 | |||||||
| chr12:25533528 | A | T | 2 | a0001c0001t0002g0013 a0001c0001t0002g0145 |
3 | HG01884.hp1 HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.492-6573T>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25533528 | |||||||
| chr12:25533694 | T | C | 3 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0002c0002t0001g0160 |
3 | HG02258.hp1 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.492-6739A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25533694 | |||||||
| chr12:25533710 | C | T | 1 | a0001c0001t0001g0277 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.492-6755G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25533710 | |||||||
| chr12:25533837 | T | C | 11 | a0001c0001t0001g0178 a0001c0001t0001g0206 a0001c0001t0001g0207 others(8): Show |
11 | HG00438.hp1 HG01943.hp2 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.492-6882A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25533837 | |||||||
| chr12:25533848 | A | G | 1 | a0002c0002t0002g0008 | 2 | HG02258.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.492-6893T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25533848 | |||||||
| chr12:25533918 | C | T | 1 | a0003c0005t0003g0156 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.492-6963G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25533918 | |||||||
| chr12:25534049 | G | T | 1 | a0001c0001t0001g0151 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.492-7094C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25534049 | |||||||
| chr12:25534161 | G | A | 36 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0023 others(33): Show |
42 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.492-7206C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25534161 | |||||||
| chr12:25534191 | T | C | 4 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0002c0002t0001g0160 others(1): Show |
4 | HG01891.hp2 HG02258.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.492-7236A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25534191 | |||||||
| chr12:25534227 | T | C | 5 | a0002c0002t0002g0005 a0002c0002t0002g0042 a0002c0002t0002g0043 others(2): Show |
6 | HG01167.hp1 HG01169.hp2 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.492-7272A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25534227 | |||||||
| chr12:25534281 | A | G | 58 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(55): Show |
61 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.492-7326T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25534281 | |||||||
| chr12:25534441 | C | T | 5 | a0001c0001t0001g0015 a0001c0001t0001g0157 a0001c0001t0001g0158 others(2): Show |
6 | HG02109.hp2 HG02451.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.492-7486G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25534441 | |||||||
| chr12:25534516 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.492-7561C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25534516 | |||||||
| chr12:25534574 | C | T | 276 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(273): Show |
292 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(289): Show |
intron_variant | MODIFIER | c.492-7619G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25534574 | |||||||
| chr12:25534740 | G | A | 3 | a0001c0001t0001g0215 a0001c0001t0001g0273 a0002c0002t0001g0180 |
3 | HG01081.hp2 HG01106.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.492-7785C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25534740 | |||||||
| chr12:25534862 | G | A | 1 | a0002c0002t0001g0160 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.492-7907C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25534862 | |||||||
| chr12:25534902 | G | C | 1 | a0001c0001t0001g0352 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.492-7947C>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25534902 | |||||||
| chr12:25535069 | AT | A | 5 | a0001c0004t0001g0161 a0001c0004t0001g0164 a0001c0004t0001g0165 others(2): Show |
5 | HG02015.hp2 HG02027.hp2 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.492-8115delA | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25535069 | |||||||
| chr12:25535264 | C | A | 1 | a0001c0001t0002g0136 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.492-8309G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25535264 | |||||||
| chr12:25535302 | CAG | C | 4 | a0003c0005t0001g0153 a0003c0005t0001g0154 a0003c0005t0001g0155 others(1): Show |
4 | HG02630.hp2 HG03130.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.492-8349_492-8348d others(4): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25535302 | |||||||
| chr12:25535307 | C | G | 1 | a0001c0001t0002g0054 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.492-8352G>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25535307 | |||||||
| chr12:25535412 | G | A | 213 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(210): Show |
225 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.492-8457C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25535412 | |||||||
| chr12:25535413 | T | TA | 218 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(215): Show |
231 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.492-8459dupT | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25535413 | |||||||
| chr12:25535513 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.492-8558C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25535513 | |||||||
| chr12:25535567 | A | G | 226 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(223): Show |
239 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.492-8612T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25535567 | |||||||
| chr12:25535794 | C | A | 3 | a0001c0001t0002g0088 a0001c0001t0002g0089 a0001c0001t0002g0105 |
3 | HG01074.hp2 HG02486.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.492-8839G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25535794 | |||||||
| chr12:25535834 | T | C | 4 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 others(1): Show |
4 | NA18961.hp1 NA18965.hp1 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.492-8879A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25535834 | |||||||
| chr12:25535986 | G | T | 39 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0023 others(36): Show |
45 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.492-9031C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25535986 | |||||||
| chr12:25535995 | T | TAA | 226 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(223): Show |
239 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.492-9042_492-9041d others(4): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25535995 | |||||||
| chr12:25536382 | C | T | 1 | a0001c0001t0002g0072 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.492-9427G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25536382 | |||||||
| chr12:25536774 | G | A | 8 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0002c0002t0001g0160 others(5): Show |
8 | HG01891.hp2 HG02258.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.491+9600C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25536774 | |||||||
| chr12:25536783 | G | C | 9 | a0001c0001t0002g0011 a0001c0001t0002g0070 a0001c0001t0002g0090 others(6): Show |
10 | HG02027.hp1 HG02056.hp1 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.491+9591C>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25536783 | |||||||
| chr12:25536870 | G | A | 55 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(52): Show |
55 | HG00408.hp1 HG00423.hp2 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.491+9504C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25536870 | |||||||
| chr12:25536875 | G | T | 4 | a0001c0001t0001g0297 a0001c0001t0001g0318 a0001c0001t0001g0319 others(1): Show |
4 | HG00609.hp2 NA18959.hp1 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.491+9499C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25536875 | |||||||
| chr12:25536879 | G | A | 109 | a0001c0001t0001g0021 a0001c0001t0001g0146 a0001c0001t0001g0148 others(106): Show |
110 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.491+9495C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25536879 | |||||||
| chr12:25536895 | C | T | 3 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0002c0002t0001g0160 |
3 | HG02258.hp1 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.491+9479G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25536895 | |||||||
| chr12:25537007 | G | C | 6 | a0001c0001t0001g0163 a0001c0004t0001g0161 a0001c0004t0001g0164 others(3): Show |
6 | HG01255.hp2 HG02015.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.491+9367C>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25537007 | |||||||
| chr12:25537033 | G | A | 219 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(216): Show |
232 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.491+9341C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25537033 | |||||||
| chr12:25537036 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.491+9338C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25537036 | |||||||
| chr12:25537037 | A | C | 227 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(224): Show |
240 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.491+9337T>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25537037 | |||||||
| chr12:25537042 | C | T | 1 | a0006c0012t0001g0360 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.491+9332G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25537042 | |||||||
| chr12:25537072 | G | T | 2 | a0002c0002t0001g0022 a0002c0002t0001g0276 |
3 | HG02080.hp1 HG02129.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.491+9302C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25537072 | |||||||
| chr12:25537139 | G | C | 2 | a0003c0005t0001g0154 a0003c0005t0001g0155 |
2 | HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.491+9235C>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25537139 | |||||||
| chr12:25537145 | G | T | 213 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(210): Show |
225 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.491+9229C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25537145 | |||||||
| chr12:25537197 | T | G | 227 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(224): Show |
240 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.491+9177A>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25537197 | |||||||
| chr12:25537208 | A | C | 213 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(210): Show |
225 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.491+9166T>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25537208 | |||||||
| chr12:25537228 | G | T | 5 | a0001c0001t0001g0015 a0001c0001t0001g0157 a0001c0001t0001g0158 others(2): Show |
6 | HG02109.hp2 HG02451.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.491+9146C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25537228 | |||||||
| chr12:25537262 | C | T | 213 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(210): Show |
225 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.491+9112G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25537262 | |||||||
| chr12:25537377 | G | A | 4 | a0001c0001t0001g0018 a0001c0001t0001g0174 a0001c0001t0001g0211 others(1): Show |
5 | NA18945.hp1 NA18948.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.491+8997C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25537377 | |||||||
| chr12:25537421 | C | T | 1 | a0002c0002t0001g0355 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.491+8953G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25537421 | |||||||
| chr12:25537480 | C | T | 1 | a0002c0002t0001g0160 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.491+8894G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25537480 | |||||||
| chr12:25537509 | G | T | 207 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(204): Show |
219 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.491+8865C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25537509 | |||||||
| chr12:25537519 | G | T | 226 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(223): Show |
239 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.491+8855C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25537519 | |||||||
| chr12:25537568 | T | A | 1 | a0002c0002t0001g0162 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.491+8806A>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25537568 | |||||||
| chr12:25537633 | G | C | 213 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(210): Show |
225 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.491+8741C>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25537633 | |||||||
| chr12:25537668 | C | G | 8 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0002c0002t0001g0160 others(5): Show |
8 | HG01891.hp2 HG02258.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.491+8706G>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25537668 | |||||||
| chr12:25537704 | C | T | 1 | a0001c0001t0001g0178 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.491+8670G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25537704 | |||||||
| chr12:25537705 | A | G | 1 | a0001c0001t0001g0178 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.491+8669T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25537705 | |||||||
| chr12:25537756 | C | A | 1 | a0002c0002t0002g0140 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.491+8618G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25537756 | |||||||
| chr12:25537814 | G | C | 3 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 |
3 | HG01169.hp1 HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.491+8560C>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25537814 | |||||||
| chr12:25537863 | C | T | 5 | a0001c0001t0001g0015 a0001c0001t0001g0157 a0001c0001t0001g0158 others(2): Show |
6 | HG02109.hp2 HG02451.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.491+8511G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25537863 | |||||||
| chr12:25537887 | T | C | 66 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0002g0009 others(63): Show |
69 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.491+8487A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25537887 | |||||||
| chr12:25537916 | C | T | 1 | a0002c0002t0002g0055 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.491+8458G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25537916 | |||||||
| chr12:25538093 | C | T | 2 | a0001c0004t0001g0161 a0001c0004t0001g0164 |
2 | HG02015.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.491+8281G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25538093 | |||||||
| chr12:25538135 | G | T | 227 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(224): Show |
240 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.491+8239C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25538135 | |||||||
| chr12:25538170 | T | C | 1 | a0001c0001t0001g0308 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.491+8204A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25538170 | |||||||
| chr12:25538195 | A | C | 58 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(55): Show |
61 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.491+8179T>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25538195 | |||||||
| chr12:25538197 | C | T | 1 | a0003c0005t0001g0153 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.491+8177G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25538197 | |||||||
| chr12:25538198 | A | G | 226 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(223): Show |
239 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.491+8176T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25538198 | |||||||
| chr12:25538223 | C | T | 7 | a0001c0001t0001g0163 a0001c0004t0001g0161 a0001c0004t0001g0164 others(4): Show |
7 | HG01255.hp2 HG02015.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.491+8151G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25538223 | |||||||
| chr12:25538237 | T | A | 1 | a0001c0001t0002g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.491+8137A>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25538237 | |||||||
| chr12:25538246 | C | A | 227 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(224): Show |
240 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.491+8128G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25538246 | |||||||
| chr12:25538330 | C | T | 1 | a0006c0012t0001g0360 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.491+8044G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25538330 | |||||||
| chr12:25538395 | T | C | 227 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(224): Show |
240 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.491+7979A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25538395 | |||||||
| chr12:25538402 | G | C | 1 | a0002c0002t0002g0049 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.491+7972C>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25538402 | |||||||
| chr12:25538411 | C | A | 1 | a0001c0001t0001g0251 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.491+7963G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25538411 | |||||||
| chr12:25538462 | C | A | 1 | a0001c0001t0001g0358 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.491+7912G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25538462 | |||||||
| chr12:25538508 | T | C | 1 | a0002c0002t0002g0051 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.491+7866A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25538508 | |||||||
| chr12:25538658 | A | G | 227 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(224): Show |
240 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.491+7716T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25538658 | |||||||
| chr12:25538747 | C | A | 3 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0002c0002t0001g0160 |
3 | HG02258.hp1 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.491+7627G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25538747 | |||||||
| chr12:25538755 | C | T | 286 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(283): Show |
302 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(299): Show |
intron_variant | MODIFIER | c.491+7619G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25538755 | |||||||
| chr12:25538802 | C | T | 1 | a0001c0001t0002g0101 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.491+7572G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25538802 | |||||||
| chr12:25538804 | T | C | 207 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(204): Show |
219 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.491+7570A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25538804 | |||||||
| chr12:25538933 | G | A | 2 | a0001c0001t0001g0351 a0009c0009t0001g0359 |
2 | NA18966.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.491+7441C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25538933 | |||||||
| chr12:25538993 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.491+7381C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25538993 | |||||||
| chr12:25538997 | T | A | 6 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.491+7377A>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25538997 | |||||||
| chr12:25539052 | A | G | 1 | a0002c0002t0002g0129 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.491+7322T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25539052 | |||||||
| chr12:25539104 | A | G | 229 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(226): Show |
243 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(240): Show |
intron_variant | MODIFIER | c.491+7270T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25539104 | |||||||
| chr12:25539165 | C | T | 1 | a0001c0001t0002g0071 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.491+7209G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25539165 | |||||||
| chr12:25539187 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.491+7187A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25539187 | |||||||
| chr12:25539211 | G | C | 2 | a0001c0001t0001g0257 a0001c0001t0001g0268 |
2 | HG03704.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.491+7163C>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25539211 | |||||||
| chr12:25539220 | G | A | 55 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(52): Show |
60 | HG00438.hp1 HG00597.hp1 HG01074.hp1 others(57): Show |
intron_variant | MODIFIER | c.491+7154C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25539220 | |||||||
| chr12:25539248 | C | T | 8 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0002c0002t0001g0160 others(5): Show |
8 | HG01891.hp2 HG02258.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.491+7126G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25539248 | |||||||
| chr12:25539251 | C | G | 4 | a0001c0001t0002g0096 a0001c0001t0002g0097 a0001c0001t0002g0098 others(1): Show |
4 | NA19000.hp2 NA19057.hp1 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.491+7123G>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25539251 | |||||||
| chr12:25539340 | G | C | 1 | a0002c0014t0001g0169 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.491+7034C>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25539340 | |||||||
| chr12:25539369 | A | C | 1 | a0001c0001t0002g0054 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.491+7005T>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25539369 | |||||||
| chr12:25539408 | G | A | 2 | a0001c0001t0001g0151 a0002c0002t0001g0160 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.491+6966C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25539408 | |||||||
| chr12:25539487 | C | T | 207 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(204): Show |
219 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.491+6887G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25539487 | |||||||
| chr12:25539562 | C | T | 4 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0311 others(1): Show |
4 | HG01934.hp1 HG02258.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.491+6812G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25539562 | |||||||
| chr12:25539592 | T | G | 1 | a0001c0001t0001g0268 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.491+6782A>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25539592 | |||||||
| chr12:25539640 | T | C | 1 | a0002c0002t0002g0141 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.491+6734A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25539640 | |||||||
| chr12:25539671 | A | G | 227 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(224): Show |
240 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.491+6703T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25539671 | |||||||
| chr12:25539686 | C | T | 6 | a0001c0001t0001g0163 a0001c0004t0001g0161 a0001c0004t0001g0164 others(3): Show |
6 | HG01255.hp2 HG02015.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.491+6688G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25539686 | |||||||
| chr12:25539757 | A | C | 1 | a0001c0001t0002g0070 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.491+6617T>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25539757 | |||||||
| chr12:25539764 | T | C | 230 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(227): Show |
243 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(240): Show |
intron_variant | MODIFIER | c.491+6610A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25539764 | |||||||
| chr12:25539771 | T | A | 4 | a0001c0001t0002g0096 a0001c0001t0002g0097 a0001c0001t0002g0098 others(1): Show |
4 | NA19000.hp2 NA19057.hp1 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.491+6603A>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25539771 | |||||||
| chr12:25539790 | G | A | 4 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0260 others(1): Show |
4 | HG00280.hp2 HG01433.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.491+6584C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25539790 | |||||||
| chr12:25539823 | G | A | 40 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0023 others(37): Show |
46 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.491+6551C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25539823 | |||||||
| chr12:25539857 | A | T | 1 | a0002c0002t0002g0008 | 2 | HG02258.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.491+6517T>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25539857 | |||||||
| chr12:25539869 | G | A | 54 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(51): Show |
59 | HG00438.hp1 HG00597.hp1 HG01074.hp1 others(56): Show |
intron_variant | MODIFIER | c.491+6505C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25539869 | |||||||
| chr12:25539894 | T | C | 1 | a0001c0001t0001g0352 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.491+6480A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25539894 | |||||||
| chr12:25539912 | G | A | 5 | a0001c0001t0001g0015 a0001c0001t0001g0157 a0001c0001t0001g0158 others(2): Show |
6 | HG02109.hp2 HG02451.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.491+6462C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25539912 | |||||||
| chr12:25539953 | A | G | 1 | a0001c0001t0002g0069 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.491+6421T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25539953 | |||||||
| chr12:25539963 | T | C | 1 | a0001c0001t0001g0179 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.491+6411A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25539963 | |||||||
| chr12:25540003 | C | T | 4 | a0003c0005t0001g0153 a0003c0005t0001g0154 a0003c0005t0001g0155 others(1): Show |
4 | HG02630.hp2 HG03130.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.491+6371G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25540003 | |||||||
| chr12:25540033 | T | C | 1 | a0001c0001t0002g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.491+6341A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25540033 | |||||||
| chr12:25540034 | G | A | 1 | a0001c0001t0002g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.491+6340C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25540034 | |||||||
| chr12:25540104 | G | A | 227 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(224): Show |
240 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.491+6270C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25540104 | |||||||
| chr12:25540129 | C | T | 1 | a0001c0001t0002g0063 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.491+6245G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25540129 | |||||||
| chr12:25540156 | A | G | 4 | a0003c0005t0001g0153 a0003c0005t0001g0154 a0003c0005t0001g0155 others(1): Show |
4 | HG02630.hp2 HG03130.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.491+6218T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25540156 | |||||||
| chr12:25540265 | A | G | 1 | a0001c0001t0002g0054 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.491+6109T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25540265 | |||||||
| chr12:25540290 | C | G | 1 | a0002c0002t0002g0033 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.491+6084G>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25540290 | |||||||
| chr12:25540344 | G | A | 50 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(47): Show |
55 | HG00438.hp1 HG00597.hp1 HG01074.hp1 others(52): Show |
intron_variant | MODIFIER | c.491+6030C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25540344 | |||||||
| chr12:25540365 | G | A | 347 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(344): Show |
373 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(370): Show |
intron_variant | MODIFIER | c.491+6009C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25540365 | |||||||
| chr12:25540395 | T | C | 50 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(47): Show |
55 | HG00438.hp1 HG00597.hp1 HG01074.hp1 others(52): Show |
intron_variant | MODIFIER | c.491+5979A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25540395 | |||||||
| chr12:25540423 | A | C | 1 | a0001c0001t0001g0213 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.491+5951T>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25540423 | |||||||
| chr12:25540439 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.491+5935C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25540439 | |||||||
| chr12:25540527 | C | G | 1 | a0001c0007t0004g0173 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.491+5847G>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25540527 | |||||||
| chr12:25540561 | T | C | 2 | a0003c0005t0001g0154 a0003c0005t0001g0155 |
2 | HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.491+5813A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25540561 | |||||||
| chr12:25540582 | G | A | 59 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(56): Show |
62 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.491+5792C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25540582 | |||||||
| chr12:25540612 | C | A | 1 | a0001c0001t0002g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.491+5762G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25540612 | |||||||
| chr12:25540634 | A | C | 3 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0002c0002t0001g0160 |
3 | HG02258.hp1 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.491+5740T>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25540634 | |||||||
| chr12:25540679 | C | T | 58 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(55): Show |
61 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.491+5695G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25540679 | |||||||
| chr12:25540690 | G | A | 7 | a0001c0001t0001g0015 a0001c0001t0001g0157 a0001c0001t0001g0158 others(4): Show |
9 | HG02056.hp2 HG02109.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.491+5684C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25540690 | |||||||
| chr12:25540781 | A | C | 1 | a0002c0002t0001g0160 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.491+5593T>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25540781 | |||||||
| chr12:25540801 | T | C | 216 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(213): Show |
229 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.491+5573A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25540801 | |||||||
| chr12:25540802 | G | A | 5 | a0001c0001t0001g0015 a0001c0001t0001g0157 a0001c0001t0001g0158 others(2): Show |
6 | HG02109.hp2 HG02451.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.491+5572C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25540802 | |||||||
| chr12:25540813 | A | T | 1 | a0003c0005t0001g0153 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.491+5561T>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25540813 | |||||||
| chr12:25540819 | A | G | 1 | a0001c0001t0001g0317 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.491+5555T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25540819 | |||||||
| chr12:25540830 | T | C | 214 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(211): Show |
226 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.491+5544A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25540830 | |||||||
| chr12:25540939 | A | G | 3 | a0001c0001t0001g0215 a0001c0001t0001g0273 a0002c0002t0001g0180 |
3 | HG01081.hp2 HG01106.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.491+5435T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25540939 | |||||||
| chr12:25540942 | G | A | 286 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(283): Show |
302 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(299): Show |
intron_variant | MODIFIER | c.491+5432C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25540942 | |||||||
| chr12:25540959 | G | A | 1 | a0001c0001t0001g0212 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.491+5415C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25540959 | |||||||
| chr12:25540979 | G | T | 5 | a0001c0001t0001g0216 a0001c0001t0001g0270 a0001c0001t0001g0271 others(2): Show |
5 | HG01169.hp1 HG01255.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.491+5395C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25540979 | |||||||
| chr12:25540991 | A | G | 4 | a0003c0005t0001g0153 a0003c0005t0001g0154 a0003c0005t0001g0155 others(1): Show |
4 | HG02630.hp2 HG03130.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.491+5383T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25540991 | |||||||
| chr12:25541055 | C | T | 1 | a0001c0001t0002g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.491+5319G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25541055 | |||||||
| chr12:25541117 | G | C | 1 | a0001c0001t0001g0213 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.491+5257C>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25541117 | |||||||
| chr12:25541131 | T | C | 213 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(210): Show |
226 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.491+5243A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25541131 | |||||||
| chr12:25541140 | G | T | 1 | a0001c0001t0002g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.491+5234C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25541140 | |||||||
| chr12:25541148 | T | C | 1 | a0001c0010t0001g0292 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.491+5226A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25541148 | |||||||
| chr12:25541164 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.491+5210G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25541164 | |||||||
| chr12:25541185 | C | G | 2 | a0002c0002t0002g0055 a0002c0002t0002g0056 |
2 | HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.491+5189G>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25541185 | |||||||
| chr12:25541198 | C | A | 9 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0002g0062 others(6): Show |
9 | HG01891.hp2 HG02258.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.491+5176G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25541198 | |||||||
| chr12:25541217 | A | T | 1 | a0001c0001t0002g0105 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.491+5157T>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25541217 | |||||||
| chr12:25541238 | T | C | 1 | a0001c0001t0001g0313 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.491+5136A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25541238 | |||||||
| chr12:25541264 | A | G | 219 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(216): Show |
232 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.491+5110T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25541264 | |||||||
| chr12:25541269 | T | G | 219 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(216): Show |
232 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.491+5105A>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25541269 | |||||||
| chr12:25541330 | T | C | 1 | a0002c0002t0002g0048 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.491+5044A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25541330 | |||||||
| chr12:25541440 | T | C | 2 | a0001c0001t0001g0214 a0001c0001t0001g0267 |
2 | HG00438.hp1 NA18940.hp1 |
intron_variant | MODIFIER | c.491+4934A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25541440 | |||||||
| chr12:25541485 | T | A | 1 | a0001c0007t0004g0173 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.491+4889A>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25541485 | |||||||
| chr12:25541496 | T | G | 3 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0002c0002t0001g0160 |
3 | HG02258.hp1 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.491+4878A>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25541496 | |||||||
| chr12:25541510 | C | A | 58 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(55): Show |
61 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.491+4864G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25541510 | |||||||
| chr12:25541593 | T | C | 332 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(329): Show |
356 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(353): Show |
intron_variant | MODIFIER | c.491+4781A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25541593 | |||||||
| chr12:25541662 | C | A | 1 | a0001c0001t0002g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.491+4712G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25541662 | |||||||
| chr12:25541706 | A | C | 2 | a0003c0005t0001g0154 a0003c0005t0001g0155 |
2 | HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.491+4668T>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25541706 | |||||||
| chr12:25541882 | A | G | 2 | a0001c0001t0002g0068 a0001c0001t0002g0104 |
2 | NA18975.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.491+4492T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25541882 | |||||||
| chr12:25541999 | C | A | 287 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(284): Show |
303 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.491+4375G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25541999 | |||||||
| chr12:25542015 | C | T | 1 | a0001c0001t0001g0179 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.491+4359G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25542015 | |||||||
| chr12:25542252 | G | C | 1 | a0002c0002t0002g0139 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.491+4122C>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25542252 | |||||||
| chr12:25542270 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.491+4104C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25542270 | |||||||
| chr12:25542271 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.491+4103A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25542271 | |||||||
| chr12:25542284 | C | T | 2 | a0002c0002t0002g0055 a0002c0002t0002g0056 |
2 | HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.491+4090G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25542284 | |||||||
| chr12:25542341 | A | T | 1 | a0003c0005t0001g0153 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.491+4033T>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25542341 | |||||||
| chr12:25542355 | G | A | 227 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(224): Show |
240 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.491+4019C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25542355 | |||||||
| chr12:25542360 | G | T | 1 | a0001c0001t0001g0151 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.491+4014C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25542360 | |||||||
| chr12:25542363 | C | T | 1 | a0001c0001t0001g0178 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.491+4011G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25542363 | |||||||
| chr12:25542375 | G | A | 4 | a0003c0005t0001g0153 a0003c0005t0001g0154 a0003c0005t0001g0155 others(1): Show |
4 | HG02630.hp2 HG03130.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.491+3999C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25542375 | |||||||
| chr12:25542526 | T | A | 228 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(225): Show |
242 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.491+3848A>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25542526 | |||||||
| chr12:25542572 | G | A | 1 | a0002c0002t0002g0137 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.491+3802C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25542572 | |||||||
| chr12:25542751 | G | GAA | 225 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(222): Show |
239 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.491+3621_491+3622d others(4): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25542751 | |||||||
| chr12:25542918 | C | G | 1 | a0001c0001t0002g0054 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.491+3456G>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25542918 | |||||||
| chr12:25542965 | A | G | 5 | a0001c0001t0001g0015 a0001c0001t0001g0157 a0001c0001t0001g0158 others(2): Show |
6 | HG02109.hp2 HG02451.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.491+3409T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25542965 | |||||||
| chr12:25543041 | C | G | 5 | a0001c0001t0001g0015 a0001c0001t0001g0157 a0001c0001t0001g0158 others(2): Show |
6 | HG02109.hp2 HG02451.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.491+3333G>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25543041 | |||||||
| chr12:25543096 | A | T | 5 | a0001c0001t0001g0015 a0001c0001t0001g0157 a0001c0001t0001g0158 others(2): Show |
6 | HG02109.hp2 HG02451.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.491+3278T>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25543096 | |||||||
| chr12:25543144 | C | A | 288 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(285): Show |
305 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(302): Show |
intron_variant | MODIFIER | c.491+3230G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25543144 | |||||||
| chr12:25543284 | C | T | 219 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(216): Show |
232 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.491+3090G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25543284 | |||||||
| chr12:25543479 | T | C | 1 | a0002c0002t0002g0049 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.491+2895A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25543479 | |||||||
| chr12:25543512 | A | G | 1 | a0002c0002t0001g0276 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.491+2862T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25543512 | |||||||
| chr12:25543626 | T | C | 58 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(55): Show |
61 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.491+2748A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25543626 | |||||||
| chr12:25543628 | C | T | 2 | a0001c0001t0001g0222 a0001c0001t0001g0223 |
2 | NA18965.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.491+2746G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25543628 | |||||||
| chr12:25543634 | G | GT | 50 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(47): Show |
55 | HG00438.hp1 HG00597.hp1 HG01074.hp1 others(52): Show |
intron_variant | MODIFIER | c.491+2739dupA | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25543634 | |||||||
| chr12:25543638 | T | G | 1 | a0001c0001t0002g0117 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.491+2736A>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25543638 | |||||||
| chr12:25543672 | C | T | 1 | a0001c0001t0001g0295 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.491+2702G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25543672 | |||||||
| chr12:25543741 | T | C | 8 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0002c0002t0001g0160 others(5): Show |
8 | HG01891.hp2 HG02258.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.491+2633A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25543741 | |||||||
| chr12:25543749 | C | T | 4 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0002c0002t0001g0160 others(1): Show |
4 | HG01891.hp2 HG02258.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.491+2625G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25543749 | |||||||
| chr12:25543908 | G | T | 208 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(205): Show |
220 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.491+2466C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25543908 | |||||||
| chr12:25543916 | T | A | 1 | a0002c0002t0002g0008 | 2 | HG02258.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.491+2458A>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25543916 | |||||||
| chr12:25544104 | C | T | 228 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(225): Show |
241 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.491+2270G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25544104 | |||||||
| chr12:25544106 | T | C | 1 | a0001c0001t0001g0268 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.491+2268A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25544106 | |||||||
| chr12:25544124 | G | A | 1 | a0001c0001t0001g0314 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.491+2250C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25544124 | |||||||
| chr12:25544367 | C | CTGATA | 287 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(284): Show |
303 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.491+2006_491+2007i others(7): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25544367 | |||||||
| chr12:25544372 | T | C | 58 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(55): Show |
61 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.491+2002A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25544372 | |||||||
| chr12:25544389 | T | A | 1 | a0001c0001t0002g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.491+1985A>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25544389 | |||||||
| chr12:25544465 | G | A | 5 | a0001c0007t0003g0171 a0001c0007t0004g0173 a0001c0015t0001g0172 others(2): Show |
5 | HG02559.hp1 HG03209.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.491+1909C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25544465 | |||||||
| chr12:25544568 | T | C | 5 | a0001c0001t0001g0015 a0001c0001t0001g0157 a0001c0001t0001g0158 others(2): Show |
6 | HG02109.hp2 HG02451.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.491+1806A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25544568 | |||||||
| chr12:25544718 | G | A | 5 | a0001c0001t0001g0216 a0001c0001t0001g0270 a0001c0001t0001g0271 others(2): Show |
5 | HG01169.hp1 HG01255.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.491+1656C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25544718 | |||||||
| chr12:25544972 | T | C | 1 | a0002c0003t0002g0052 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.491+1402A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25544972 | |||||||
| chr12:25544978 | T | C | 2 | a0002c0002t0002g0138 a0002c0002t0002g0139 |
2 | HG00738.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.491+1396A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25544978 | |||||||
| chr12:25545189 | A | C | 1 | a0002c0002t0001g0160 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.491+1185T>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25545189 | |||||||
| chr12:25545249 | G | A | 2 | a0001c0001t0002g0099 a0001c0001t0002g0100 |
2 | HG00621.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.491+1125C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25545249 | |||||||
| chr12:25545359 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.491+1015A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25545359 | |||||||
| chr12:25546002 | G | A | 2 | a0001c0001t0001g0293 a0001c0001t0001g0314 |
2 | HG02738.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.491+372C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25546002 | |||||||
| chr12:25546099 | A | G | 5 | a0001c0001t0001g0015 a0001c0001t0001g0157 a0001c0001t0001g0158 others(2): Show |
6 | HG02109.hp2 HG02451.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.491+275T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25546099 | |||||||
| chr12:25546266 | G | A | 3 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0002c0002t0001g0160 |
3 | HG02258.hp1 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.491+108C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25546266 | |||||||
| chr12:25546322 | T | C | 1 | a0001c0001t0002g0101 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.491+52A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 4/9 | chr12 | 25546322 | |||||||
| chr12:25546589 | A | G | 286 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(283): Show |
303 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.311-35T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 3/9 | chr12 | 25546589 | |||||||
| chr12:25546609 | T | C | 2 | a0002c0002t0002g0055 a0002c0002t0002g0056 |
2 | HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.311-55A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 3/9 | chr12 | 25546609 | |||||||
| chr12:25546686 | A | G | 5 | a0001c0001t0001g0015 a0001c0001t0001g0157 a0001c0001t0001g0158 others(2): Show |
6 | HG02109.hp2 HG02451.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.311-132T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 3/9 | chr12 | 25546686 | |||||||
| chr12:25546698 | T | C | 1 | a0002c0002t0002g0140 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.311-144A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 3/9 | chr12 | 25546698 | |||||||
| chr12:25546861 | C | A | 227 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(224): Show |
241 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.311-307G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 3/9 | chr12 | 25546861 | |||||||
| chr12:25547137 | G | C | 207 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(204): Show |
219 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.311-583C>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 3/9 | chr12 | 25547137 | |||||||
| chr12:25547160 | A | G | 3 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0002g0067 |
3 | NA19001.hp1 NA19007.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.311-606T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 3/9 | chr12 | 25547160 | |||||||
| chr12:25547182 | AT | A | 58 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(55): Show |
61 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.311-629delA | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 3/9 | chr12 | 25547182 | |||||||
| chr12:25547318 | C | G | 1 | a0002c0002t0002g0032 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.311-764G>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 3/9 | chr12 | 25547318 | |||||||
| chr12:25547331 | GTT | G | 4 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0002c0002t0001g0160 others(1): Show |
4 | HG01891.hp2 HG02258.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.311-779_311-778del others(2): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 3/9 | chr12 | 25547331 | |||||||
| chr12:25547501 | C | T | 2 | a0001c0001t0001g0226 a0001c0001t0001g0227 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.311-947G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 3/9 | chr12 | 25547501 | |||||||
| chr12:25547532 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.311-978G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 3/9 | chr12 | 25547532 | |||||||
| chr12:25547579 | G | T | 1 | a0002c0002t0001g0160 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.311-1025C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 3/9 | chr12 | 25547579 | |||||||
| chr12:25547611 | C | A | 58 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(55): Show |
61 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.311-1057G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 3/9 | chr12 | 25547611 | |||||||
| chr12:25547632 | C | T | 67 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0002g0009 others(64): Show |
71 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.311-1078G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 3/9 | chr12 | 25547632 | |||||||
| chr12:25547636 | GA | G | 7 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(4): Show |
7 | NA18961.hp1 NA18965.hp1 NA18973.hp2 others(4): Show |
intron_variant | MODIFIER | c.311-1083delT | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 3/9 | chr12 | 25547636 | |||||||
| chr12:25548204 | GA | G | 9 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0002c0002t0001g0160 others(6): Show |
10 | HG01891.hp2 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.310+1121delT | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 3/9 | chr12 | 25548204 | |||||||
| chr12:25548229 | G | A | 58 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(55): Show |
61 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.310+1097C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 3/9 | chr12 | 25548229 | |||||||
| chr12:25548231 | C | G | 1 | a0002c0014t0001g0169 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.310+1095G>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 3/9 | chr12 | 25548231 | |||||||
| chr12:25548244 | A | T | 3 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 |
3 | HG03139.hp1 HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.310+1082T>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 3/9 | chr12 | 25548244 | |||||||
| chr12:25548289 | ATAGATGA others(4): Show |
A | 11 | a0002c0002t0002g0007 a0002c0002t0002g0051 a0002c0002t0002g0053 others(8): Show |
12 | HG00642.hp1 HG00741.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.310+1026_310+1036d others(13): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 3/9 | chr12 | 25548289 | |||||||
| chr12:25548364 | C | G | 4 | a0001c0001t0001g0015 a0001c0001t0001g0157 a0001c0001t0001g0158 others(1): Show |
5 | HG02109.hp2 HG02451.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.310+962G>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 3/9 | chr12 | 25548364 | |||||||
| chr12:25548467 | A | C | 229 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(226): Show |
243 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(240): Show |
intron_variant | MODIFIER | c.310+859T>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 3/9 | chr12 | 25548467 | |||||||
| chr12:25548564 | T | C | 1 | a0002c0002t0001g0162 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.310+762A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 3/9 | chr12 | 25548564 | |||||||
| chr12:25548670 | A | T | 5 | a0002c0002t0002g0012 a0002c0002t0002g0118 a0002c0002t0002g0119 others(2): Show |
6 | HG00280.hp1 HG00735.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.310+656T>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 3/9 | chr12 | 25548670 | |||||||
| chr12:25548688 | C | G | 3 | a0001c0001t0002g0054 a0002c0002t0002g0055 a0002c0002t0002g0056 |
3 | HG02257.hp1 HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.310+638G>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 3/9 | chr12 | 25548688 | |||||||
| chr12:25548698 | C | T | 285 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(282): Show |
302 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(299): Show |
intron_variant | MODIFIER | c.310+628G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 3/9 | chr12 | 25548698 | |||||||
| chr12:25549031 | C | A | 1 | a0006c0012t0001g0360 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.310+295G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 3/9 | chr12 | 25549031 | |||||||
| chr12:25549034 | T | C | 5 | a0001c0004t0001g0161 a0001c0004t0001g0164 a0001c0004t0001g0165 others(2): Show |
5 | HG02015.hp2 HG02027.hp2 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.310+292A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 3/9 | chr12 | 25549034 | |||||||
| chr12:25549080 | T | G | 1 | a0001c0001t0001g0152 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.310+246A>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 3/9 | chr12 | 25549080 | |||||||
| chr12:25549081 | A | T | 1 | a0001c0001t0001g0152 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.310+245T>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 3/9 | chr12 | 25549081 | |||||||
| chr12:25549082 | A | T | 1 | a0001c0001t0001g0152 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.310+244T>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 3/9 | chr12 | 25549082 | |||||||
| chr12:25549083 | C | G | 1 | a0001c0001t0001g0152 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.310+243G>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 3/9 | chr12 | 25549083 | |||||||
| chr12:25549249 | T | A | 4 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0002c0002t0001g0160 others(1): Show |
4 | HG01891.hp2 HG02258.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.310+77A>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 3/9 | chr12 | 25549249 | |||||||
| chr12:25549270 | A | G | 1 | a0001c0001t0001g0174 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.310+56T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 3/9 | chr12 | 25549270 | |||||||
| chr12:25549588 | T | C | 4 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0002c0002t0001g0160 others(1): Show |
4 | HG01891.hp2 HG02258.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.90-42A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 2/9 | chr12 | 25549588 | |||||||
| chr12:25549610 | A | C | 58 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(55): Show |
61 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.90-64T>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 2/9 | chr12 | 25549610 | |||||||
| chr12:25549692 | T | G | 9 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0002c0002t0001g0160 others(6): Show |
10 | HG01891.hp2 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.90-146A>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 2/9 | chr12 | 25549692 | |||||||
| chr12:25549733 | A | T | 289 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(286): Show |
306 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(303): Show |
intron_variant | MODIFIER | c.90-187T>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 2/9 | chr12 | 25549733 | |||||||
| chr12:25549740 | A | G | 5 | a0002c0002t0002g0008 a0003c0005t0001g0153 a0003c0005t0001g0154 others(2): Show |
6 | HG02258.hp2 HG02630.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.90-194T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 2/9 | chr12 | 25549740 | |||||||
| chr12:25549746 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.90-200A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 2/9 | chr12 | 25549746 | |||||||
| chr12:25549805 | G | C | 2 | a0001c0001t0001g0215 a0001c0001t0001g0273 |
2 | HG01081.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.90-259C>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 2/9 | chr12 | 25549805 | |||||||
| chr12:25549837 | C | T | 1 | a0001c0001t0002g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.90-291G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 2/9 | chr12 | 25549837 | |||||||
| chr12:25549878 | T | C | 2 | a0001c0001t0001g0215 a0001c0001t0001g0273 |
2 | HG01081.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.90-332A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 2/9 | chr12 | 25549878 | |||||||
| chr12:25549887 | C | T | 1 | a0001c0001t0002g0103 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.90-341G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 2/9 | chr12 | 25549887 | |||||||
| chr12:25550032 | C | T | 5 | a0001c0007t0003g0171 a0001c0007t0004g0173 a0001c0015t0001g0172 others(2): Show |
5 | HG02559.hp1 HG03209.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.90-486G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 2/9 | chr12 | 25550032 | |||||||
| chr12:25550130 | G | A | 1 | a0002c0002t0002g0028 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.90-584C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 2/9 | chr12 | 25550130 | |||||||
| chr12:25550210 | C | CT | 288 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(285): Show |
305 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(302): Show |
intron_variant | MODIFIER | c.90-665dupA | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 2/9 | chr12 | 25550210 | |||||||
| chr12:25550263 | G | A | 1 | a0002c0002t0002g0053 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.90-717C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 2/9 | chr12 | 25550263 | |||||||
| chr12:25550271 | G | A | 1 | a0002c0002t0002g0008 | 2 | HG02258.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.90-725C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 2/9 | chr12 | 25550271 | |||||||
| chr12:25550394 | G | A | 1 | a0002c0002t0002g0008 | 2 | HG02258.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.90-848C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 2/9 | chr12 | 25550394 | |||||||
| chr12:25550455 | C | T | 1 | a0001c0001t0002g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.90-909G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 2/9 | chr12 | 25550455 | |||||||
| chr12:25550502 | C | T | 57 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(54): Show |
60 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.90-956G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 2/9 | chr12 | 25550502 | |||||||
| chr12:25550508 | C | T | 2 | a0001c0001t0001g0220 a0001c0001t0001g0221 |
2 | NA18983.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.90-962G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 2/9 | chr12 | 25550508 | |||||||
| chr12:25550537 | A | G | 37 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0023 others(34): Show |
43 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.90-991T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 2/9 | chr12 | 25550537 | |||||||
| chr12:25550605 | A | C | 5 | a0002c0002t0002g0008 a0003c0005t0001g0153 a0003c0005t0001g0154 others(2): Show |
6 | HG02258.hp2 HG02630.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.90-1059T>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 2/9 | chr12 | 25550605 | |||||||
| chr12:25550609 | G | A | 228 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(225): Show |
242 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.90-1063C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 2/9 | chr12 | 25550609 | |||||||
| chr12:25550779 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.90-1233G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 2/9 | chr12 | 25550779 | |||||||
| chr12:25550780 | T | G | 1 | a0001c0001t0001g0159 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.90-1234A>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 2/9 | chr12 | 25550780 | |||||||
| chr12:25550808 | C | G | 1 | a0001c0001t0001g0309 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.90-1262G>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 2/9 | chr12 | 25550808 | |||||||
| chr12:25551019 | G | T | 1 | a0002c0002t0001g0160 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.90-1473C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 2/9 | chr12 | 25551019 | |||||||
| chr12:25551159 | C | T | 59 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(56): Show |
62 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.90-1613G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 2/9 | chr12 | 25551159 | |||||||
| chr12:25551257 | A | G | 9 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0002c0002t0001g0160 others(6): Show |
10 | HG01891.hp2 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.89+1614T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 2/9 | chr12 | 25551257 | |||||||
| chr12:25551383 | T | TTTTTC | 63 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(60): Show |
66 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.89+1483_89+1487dup others(5): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 2/9 | chr12 | 25551383 | |||||||
| chr12:25551415 | G | T | 1 | a0001c0001t0001g0216 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.89+1456C>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 2/9 | chr12 | 25551415 | |||||||
| chr12:25551838 | G | C | 289 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(286): Show |
306 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(303): Show |
intron_variant | MODIFIER | c.89+1033C>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 2/9 | chr12 | 25551838 | |||||||
| chr12:25551959 | A | G | 207 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(204): Show |
219 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.89+912T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 2/9 | chr12 | 25551959 | |||||||
| chr12:25552117 | G | A | 1 | a0001c0001t0002g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.89+754C>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 2/9 | chr12 | 25552117 | |||||||
| chr12:25552283 | T | C | 2 | a0001c0001t0001g0353 a0001c0001t0001g0354 |
2 | NA18939.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.89+588A>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 2/9 | chr12 | 25552283 | |||||||
| chr12:25552384 | C | T | 3 | a0002c0003t0002g0029 a0002c0003t0002g0030 a0002c0003t0002g0031 |
3 | HG00642.hp1 HG01496.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.89+487G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 2/9 | chr12 | 25552384 | |||||||
| chr12:25552387 | C | T | 207 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(204): Show |
219 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.89+484G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 2/9 | chr12 | 25552387 | |||||||
| chr12:25552466 | C | T | 227 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(224): Show |
240 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.89+405G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 2/9 | chr12 | 25552466 | |||||||
| chr12:25552516 | A | C | 5 | a0001c0001t0001g0015 a0001c0001t0001g0157 a0001c0001t0001g0158 others(2): Show |
6 | HG02109.hp2 HG02451.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.89+355T>G | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 2/9 | chr12 | 25552516 | |||||||
| chr12:25552581 | G | GA | 11 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0142 others(8): Show |
13 | HG01884.hp1 HG02015.hp1 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.89+289dupT | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 2/9 | chr12 | 25552581 | |||||||
| chr12:25552581 | G | GAAA | 8 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0002g0145 others(5): Show |
8 | HG01891.hp2 HG02258.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.89+287_89+289dupTT others(1): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 2/9 | chr12 | 25552581 | |||||||
| chr12:25552581 | G | GAAAA | 7 | a0001c0001t0001g0015 a0001c0001t0001g0157 a0001c0001t0001g0158 others(4): Show |
9 | HG02109.hp2 HG02258.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.89+286_89+289dupTT others(2): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 2/9 | chr12 | 25552581 | |||||||
| chr12:25552581 | G | GAAAAA | 7 | a0001c0001t0001g0163 a0001c0001t0002g0062 a0001c0004t0001g0164 others(4): Show |
7 | HG01255.hp2 HG02015.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.89+285_89+289dupTT others(3): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 2/9 | chr12 | 25552581 | |||||||
| chr12:25552581 | G | GAAAAAA | 52 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(49): Show |
55 | HG00438.hp1 HG00597.hp1 HG01074.hp1 others(52): Show |
intron_variant | MODIFIER | c.89+284_89+289dupTT others(4): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 2/9 | chr12 | 25552581 | |||||||
| chr12:25552581 | G | GAAAAAAA | 63 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(60): Show |
68 | HG00099.hp2 HG00280.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.89+283_89+289dupTT others(5): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 2/9 | chr12 | 25552581 | |||||||
| chr12:25552581 | G | GAAAAAAA others(1): Show |
39 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(36): Show |
43 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.89+282_89+289dupTT others(6): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 2/9 | chr12 | 25552581 | |||||||
| chr12:25552581 | G | GAAAAAAA others(2): Show |
88 | a0001c0001t0001g0309 a0001c0001t0001g0311 a0001c0001t0001g0312 others(85): Show |
91 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.89+281_89+289dupTT others(7): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 2/9 | chr12 | 25552581 | |||||||
| chr12:25552581 | G | GAAAAAAA others(3): Show |
19 | a0001c0001t0001g0356 a0001c0001t0001g0357 a0001c0001t0001g0358 others(16): Show |
19 | HG01123.hp2 HG01358.hp2 HG02132.hp2 others(16): Show |
intron_variant | MODIFIER | c.89+280_89+289dupTT others(8): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 2/9 | chr12 | 25552581 | |||||||
| chr12:25552581 | G | GAAAAAAA others(4): Show |
1 | a0001c0001t0002g0117 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.89+279_89+289dupTT others(9): Show |
LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 2/9 | chr12 | 25552581 | |||||||
| chr12:25552602 | C | G | 327 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(324): Show |
350 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(347): Show |
intron_variant | MODIFIER | c.89+269G>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 2/9 | chr12 | 25552602 | |||||||
| chr12:25552653 | A | G | 1 | a0001c0001t0001g0147 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.89+218T>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 2/9 | chr12 | 25552653 | |||||||
| chr12:25552689 | C | A | 226 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(223): Show |
239 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.89+182G>T | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 2/9 | chr12 | 25552689 | |||||||
| chr12:25552765 | C | G | 4 | a0002c0002t0002g0001 a0002c0002t0002g0026 a0002c0002t0002g0027 others(1): Show |
6 | HG01081.hp1 HG01928.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.89+106G>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 2/9 | chr12 | 25552765 | |||||||
| chr12:25552823 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.89+48G>A | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 2/9 | chr12 | 25552823 | |||||||
| chr12:25552991 | T | G | 1 | a0006c0012t0001g0360 | 1 | HG01891.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.-30-2A>C | LMNTD1 | ENSG00000152936.11 | transcript | ENST00000458174.7 | protein_coding | 1/9 | chr12 | 25552991 |