Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 29995 |
|---|---|
| ensemblid | ENSG00000071282.12 |
| hgncid | 6633 |
| symbol | LMCD1 |
| name | LIM and cysteine rich domains 1 |
| refseq_nuc | NM_014583.4 |
| refseq_prot | NP_055398.1 |
| ensembl_nuc | ENST00000157600.8 |
| ensembl_prot | ENSP00000157600.3 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 8501823 |
| end | 8574668 |
| strand | + |
| ver | v1.2 |
| region | chr3:8501823-8574668 |
| region5000 | chr3:8496823-8579668 |
| regionname0 | LMCD1_chr3_8501823_8574668 |
| regionname5000 | LMCD1_chr3_8496823_8579668 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 365 | 304 | 78 | 63 | 110 | 14 | 37 | 76 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0002 | 0/0 | 365 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0003 | 0/0 | 365 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0004 | 0/0 | 365 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0005 | 0/0 | 365 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0006 | 0/0 | 365 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0007 | 0/0 | 365 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0008 | 0/0 | 365 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0009 | 0/0 | 365 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0010 | 0/0 | 365 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 1098 | 266 | 67 | 56 | 102 | 13 | 27 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| c0002 | 0/1 | 1098 | 36 | 10 | 7 | 8 | 1 | 9 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| c0003 | 0/0 | 1098 | 2 | 0 | 1 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| c0004 | 0/0 | 1098 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| c0005 | 0/0 | 1098 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| c0006 | 0/0 | 1098 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| c0007 | 0/0 | 1098 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| c0008 | 0/0 | 1098 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| c0009 | 0/0 | 1098 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| c0010 | 0/0 | 1098 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| c0011 | 0/0 | 1098 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| c0012 | 0/0 | 1098 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| c0013 | 0/0 | 1098 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 7189 | 83 | 25 | 25 | 22 | 5 | 6 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| t0002 | 1/0 | 7187 | 71 | 17 | 14 | 26 | 2 | 11 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| t0003 | 0/1 | 7188 | 71 | 3 | 19 | 32 | 6 | 10 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| t0004 | 0/0 | 7187 | 13 | 7 | 0 | 0 | 0 | 6 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| t0005 | 0/0 | 7187 | 4 | 4 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| t0006 | 0/0 | 7189 | 4 | 0 | 0 | 4 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| t0007 | 0/0 | 7190 | 3 | 3 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| t0008 | 0/0 | 7187 | 3 | 3 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| t0009 | 0/0 | 7188 | 3 | 1 | 1 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| t0010 | 0/0 | 7186 | 3 | 0 | 0 | 3 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| t0011 | 0/0 | 7188 | 3 | 0 | 0 | 3 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| t0012 | 0/0 | 7172 | 2 | 2 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| t0013 | 0/0 | 7189 | 2 | 1 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| t0014 | 0/0 | 7187 | 2 | 2 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| t0015 | 0/0 | 7187 | 2 | 2 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| t0016 | 0/0 | 7186 | 2 | 0 | 0 | 2 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| t0017 | 0/0 | 7190 | 2 | 0 | 0 | 2 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| t0018 | 0/0 | 7188 | 2 | 0 | 0 | 2 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| t0019 | 0/0 | 7188 | 2 | 0 | 0 | 0 | 0 | 2 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| t0020 | 0/0 | 7187 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| t0021 | 0/0 | 7189 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| t0022 | 0/0 | 7190 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| t0023 | 0/0 | 7187 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| t0024 | 0/0 | 7189 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| t0025 | 0/0 | 7187 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| t0026 | 0/0 | 7188 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| t0027 | 0/0 | 7187 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| t0028 | 0/0 | 7189 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| t0029 | 0/0 | 7189 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| t0030 | 0/0 | 7187 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| t0031 | 0/0 | 7187 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| t0032 | 0/0 | 7188 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| t0033 | 0/0 | 7189 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| t0034 | 0/0 | 7190 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| t0035 | 0/0 | 7189 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| t0036 | 0/0 | 7189 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| t0037 | 0/0 | 7190 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| t0038 | 0/0 | 7189 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| t0039 | 0/0 | 7190 | 1 | 0 | 0 | 0 | 1 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| t0040 | 0/0 | 7189 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| t0041 | 0/0 | 7189 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| t0042 | 0/0 | 7189 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| t0043 | 0/0 | 7189 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| t0044 | 0/0 | 7186 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| t0045 | 0/0 | 7188 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| t0046 | 0/0 | 7188 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| t0047 | 0/0 | 7187 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| t0048 | 0/0 | 7188 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| t0049 | 0/0 | 7188 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| t0050 | 0/0 | 7187 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| t0051 | 0/0 | 7187 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| t0052 | 0/0 | 7187 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| t0053 | 0/0 | 7187 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| t0054 | 0/0 | 7188 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| t0055 | 0/0 | 7188 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| t0056 | 0/0 | 7188 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0005 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0009 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0273 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1098 | 266 | 67 | 56 | 102 | 13 | 27 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0002 | 0/1 | 1098 | 36 | 10 | 7 | 8 | 1 | 9 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0008 | 0/0 | 1098 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0013 | 0/0 | 1098 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0002c0003 | 0/0 | 1098 | 2 | 0 | 1 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0003c0012 | 0/0 | 1098 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0004c0004 | 0/0 | 1098 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0005c0006 | 0/0 | 1098 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0006c0010 | 0/0 | 1098 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0007c0007 | 0/0 | 1098 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0008c0009 | 0/0 | 1098 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0009c0005 | 0/0 | 1098 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0010c0011 | 0/0 | 1098 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 8286 | 66 | 21 | 18 | 20 | 5 | 2 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0001t0002 | 1/0 | 8284 | 64 | 14 | 13 | 25 | 2 | 9 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0001t0003 | 0/0 | 8285 | 64 | 3 | 19 | 29 | 5 | 8 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0001t0004 | 0/0 | 8284 | 10 | 5 | 0 | 0 | 0 | 5 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0001t0005 | 0/0 | 8284 | 3 | 3 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0001t0006 | 0/0 | 8286 | 4 | 0 | 0 | 4 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0001t0007 | 0/0 | 8287 | 3 | 3 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0001t0009 | 0/0 | 8285 | 3 | 1 | 1 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0001t0010 | 0/0 | 8283 | 3 | 0 | 0 | 3 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0001t0012 | 0/0 | 8269 | 2 | 2 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0001t0013 | 0/0 | 8286 | 2 | 1 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0001t0014 | 0/0 | 8284 | 2 | 2 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0001t0015 | 0/0 | 8284 | 2 | 2 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0001t0016 | 0/0 | 8283 | 2 | 0 | 0 | 2 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0001t0017 | 0/0 | 8287 | 2 | 0 | 0 | 2 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0001t0018 | 0/0 | 8285 | 2 | 0 | 0 | 2 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0001t0020 | 0/0 | 8284 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0001t0021 | 0/0 | 8286 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0001t0022 | 0/0 | 8287 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0001t0023 | 0/0 | 8284 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0001t0024 | 0/0 | 8286 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0001t0026 | 0/0 | 8285 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0001t0027 | 0/0 | 8284 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0001t0028 | 0/0 | 8286 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0001t0029 | 0/0 | 8286 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0001t0030 | 0/0 | 8284 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0001t0031 | 0/0 | 8284 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0001t0032 | 0/0 | 8285 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0001t0033 | 0/0 | 8286 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0001t0034 | 0/0 | 8287 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0001t0035 | 0/0 | 8286 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0001t0036 | 0/0 | 8286 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0001t0037 | 0/0 | 8287 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0001t0038 | 0/0 | 8286 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0001t0039 | 0/0 | 8287 | 1 | 0 | 0 | 0 | 1 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0001t0040 | 0/0 | 8286 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0001t0042 | 0/0 | 8286 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0001t0043 | 0/0 | 8286 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0001t0044 | 0/0 | 8283 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0001t0045 | 0/0 | 8285 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0001t0046 | 0/0 | 8285 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0001t0047 | 0/0 | 8284 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0001t0048 | 0/0 | 8285 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0001t0049 | 0/0 | 8285 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0001t0051 | 0/0 | 8284 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0001t0052 | 0/0 | 8284 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0001t0053 | 0/0 | 8284 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0001t0055 | 0/0 | 8285 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0002t0001 | 0/0 | 8286 | 11 | 2 | 6 | 0 | 0 | 3 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0002t0002 | 0/0 | 8284 | 4 | 1 | 1 | 0 | 0 | 2 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0002t0003 | 0/1 | 8285 | 6 | 0 | 0 | 2 | 1 | 2 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0002t0004 | 0/0 | 8284 | 3 | 2 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0002t0005 | 0/0 | 8284 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0002t0008 | 0/0 | 8284 | 3 | 3 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0002t0011 | 0/0 | 8285 | 3 | 0 | 0 | 3 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0002t0019 | 0/0 | 8285 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0002t0041 | 0/0 | 8286 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0002t0050 | 0/0 | 8284 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0002t0054 | 0/0 | 8285 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0002t0056 | 0/0 | 8285 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0008t0002 | 0/0 | 8284 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0001c0013t0019 | 0/0 | 8285 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0002c0003t0001 | 0/0 | 8286 | 2 | 0 | 1 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0003c0012t0001 | 0/0 | 8286 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0004c0004t0001 | 0/0 | 8286 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0005c0006t0001 | 0/0 | 8286 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0006c0010t0002 | 0/0 | 8284 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0007c0007t0025 | 0/0 | 8284 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0008c0009t0002 | 0/0 | 8284 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0009c0005t0003 | 0/0 | 8285 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| a0010c0011t0001 | 0/0 | 8286 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | copy fasta | chr3 | 8496823 | 8579668 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0009 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0005 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0003g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0004g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0004g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0004g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0004g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0004g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0004g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0005g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0005g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0005g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0006g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0006g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0006g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0006g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0007g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0007g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0007g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0009g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0009g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0009g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0010g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0010g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0010g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0012g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0012g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0013g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0013g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0014g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0014g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0015g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0015g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0016g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0016g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0017g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0017g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0018g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0018g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0020g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0021g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0022g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0023g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0024g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0026g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0027g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0028g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0029g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0030g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0031g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0032g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0033g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0034g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0035g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0036g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0037g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0038g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0039g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0040g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0042g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0043g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0044g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0045g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0046g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0047g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0048g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0049g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0051g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0052g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0053g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0001t0055g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0003g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0003g0273 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0003g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0004g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0004g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0004g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0005g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0008g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0008g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0008g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0011g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0011g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0011g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0019g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0041g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0050g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0054g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0002t0056g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0008t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0001c0013t0019g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0002c0003t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0002c0003t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0003c0012t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0004c0004t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0005c0006t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0006c0010t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0007c0007t0025g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0008c0009t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0009c0005t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| a0010c0011t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0261 | EUR | GBR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0280 | EUR | GBR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0189 | EUR | GBR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0036 | EUR | GBR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00323 | hp1 | a0001 | c0001 | t0039 | g0266 | EUR | FIN | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0046 | EUR | FIN | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00408 | hp1 | a0001 | c0001 | t0032 | g0110 | EAS | CHS | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00408 | hp2 | a0001 | c0002 | t0003 | g0139 | EAS | CHS | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00423 | hp1 | a0001 | c0002 | t0054 | g0213 | EAS | CHS | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | CHS | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | CHS | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0233 | EAS | CHS | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0106 | EAS | CHS | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | CHS | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00597 | hp1 | a0001 | c0002 | t0003 | g0095 | EAS | CHS | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00597 | hp2 | a0001 | c0001 | t0044 | g0249 | EAS | CHS | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00609 | hp1 | a0001 | c0001 | t0018 | g0122 | EAS | CHS | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | CHS | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0188 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0008 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0283 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0089 | EAS | CHS | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | CHS | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0269 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0148 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00738 | hp1 | a0001 | c0001 | t0055 | g0029 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0008 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0195 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0284 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0194 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0126 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01074 | hp2 | a0001 | c0001 | t0029 | g0285 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01081 | hp1 | a0001 | c0002 | t0002 | g0158 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01099 | hp1 | a0001 | c0001 | t0036 | g0250 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01106 | hp1 | a0002 | c0003 | t0001 | g0038 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0164 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01109 | hp2 | a0001 | c0001 | t0013 | g0292 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0115 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0289 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0245 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0116 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0193 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0034 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0113 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01192 | hp2 | a0001 | c0001 | t0049 | g0279 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0019 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | CLM | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0277 | AMR | CLM | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0300 | AMR | CLM | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | CLM | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0018 | AMR | CLM | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0275 | AMR | CLM | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | CLM | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0298 | AMR | CLM | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0050 | AMR | CLM | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01515 | hp1 | a0001 | c0002 | t0003 | g0278 | EUR | IBS | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0048 | EUR | IBS | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0005 | EUR | IBS | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0005 | EUR | IBS | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0295 | AFR | ACB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01884 | hp2 | a0001 | c0001 | t0052 | g0293 | AFR | ACB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0232 | AMR | PEL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0129 | AMR | PEL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0264 | AMR | PEL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0135 | AMR | PEL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0200 | AMR | PEL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0201 | AMR | PEL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01975 | hp2 | a0001 | c0001 | t0009 | g0084 | AMR | PEL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0112 | AMR | PEL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0251 | AMR | PEL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02015 | hp1 | a0001 | c0001 | t0051 | g0091 | EAS | KHV | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02015 | hp2 | a0001 | c0001 | t0030 | g0136 | EAS | KHV | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02055 | hp1 | a0001 | c0001 | t0014 | g0294 | AFR | ACB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | ACB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | KHV | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | KHV | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | KHV | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | KHV | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02080 | hp1 | a0001 | c0001 | t0038 | g0117 | EAS | KHV | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | KHV | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02129 | hp1 | a0001 | c0001 | t0009 | g0098 | EAS | KHV | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0114 | EAS | KHV | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0248 | EAS | KHV | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0100 | AFR | ACB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0031 | AMR | PEL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0192 | EAS | CDX | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | CDX | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02165 | hp1 | a0001 | c0001 | t0010 | g0101 | EAS | CDX | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02165 | hp2 | a0001 | c0001 | t0006 | g0076 | EAS | CDX | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0286 | AFR | ACB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02258 | hp1 | a0001 | c0002 | t0008 | g0161 | AFR | ACB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0178 | AFR | ACB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02280 | hp1 | a0001 | c0002 | t0008 | g0160 | AFR | ACB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02280 | hp2 | a0001 | c0002 | t0002 | g0157 | AFR | ACB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0142 | AMR | PEL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0028 | AMR | PEL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02451 | hp1 | a0001 | c0001 | t0047 | g0274 | AFR | ACB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02451 | hp2 | a0001 | c0002 | t0050 | g0159 | AFR | ACB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02523 | hp1 | a0001 | c0001 | t0017 | g0181 | EAS | KHV | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | KHV | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0242 | AFR | GWD | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02572 | hp2 | a0001 | c0001 | t0053 | g0268 | AFR | GWD | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0150 | SAS | PJL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0052 | SAS | PJL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02615 | hp1 | a0001 | c0001 | t0040 | g0169 | AFR | GWD | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02615 | hp2 | a0001 | c0001 | t0022 | g0305 | AFR | GWD | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02622 | hp1 | a0001 | c0001 | t0015 | g0222 | AFR | GWD | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0165 | AFR | GWD | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0297 | AFR | GWD | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0218 | SAS | PJL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0240 | SAS | PJL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0023 | SAS | PJL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02717 | hp1 | a0001 | c0001 | t0031 | g0066 | AFR | GWD | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02717 | hp2 | a0001 | c0001 | t0014 | g0184 | AFR | GWD | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0108 | SAS | PJL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02735 | hp2 | a0001 | c0002 | t0003 | g0174 | SAS | PJL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02818 | hp1 | a0001 | c0002 | t0005 | g0226 | AFR | GWD | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0224 | AFR | GWD | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0166 | AFR | GWD | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02886 | hp2 | a0001 | c0001 | t0005 | g0244 | AFR | GWD | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02895 | hp1 | a0001 | c0001 | t0009 | g0001 | AFR | GWD | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02895 | hp2 | a0001 | c0001 | t0015 | g0223 | AFR | GWD | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02896 | hp1 | a0006 | c0010 | t0002 | g0102 | AFR | GWD | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0267 | AFR | GWD | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02965 | hp1 | a0001 | c0002 | t0004 | g0177 | AFR | ESN | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02965 | hp2 | a0010 | c0011 | t0001 | g0256 | AFR | ESN | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0229 | AFR | ESN | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02976 | hp2 | a0001 | c0001 | t0034 | g0302 | AFR | ESN | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03017 | hp1 | a0001 | c0002 | t0003 | g0212 | SAS | PJL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0072 | SAS | PJL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03041 | hp1 | a0007 | c0007 | t0025 | g0167 | AFR | GWD | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0104 | AFR | MSL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03098 | hp2 | a0001 | c0001 | t0043 | g0012 | AFR | MSL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03130 | hp1 | a0001 | c0001 | t0012 | g0020 | AFR | ESN | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | ESN | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ESN | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0243 | AFR | ESN | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0296 | AFR | ESN | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0288 | AFR | ESN | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03209 | hp1 | a0001 | c0001 | t0007 | g0303 | AFR | MSL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0013 | AFR | MSL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03225 | hp1 | a0001 | c0001 | t0007 | g0301 | AFR | MSL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03225 | hp2 | a0001 | c0008 | t0002 | g0065 | AFR | MSL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0040 | SAS | PJL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0035 | SAS | PJL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | MSL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | MSL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03486 | hp1 | a0001 | c0001 | t0007 | g0230 | AFR | MSL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03491 | hp1 | a0001 | c0001 | t0004 | g0215 | SAS | PJL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03491 | hp2 | a0001 | c0001 | t0020 | g0022 | SAS | PJL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0128 | SAS | PJL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0214 | SAS | PJL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0179 | AFR | ESN | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | ESN | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0183 | AFR | GWD | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03579 | hp1 | a0001 | c0001 | t0013 | g0291 | AFR | MSL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0241 | AFR | MSL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0039 | SAS | PJL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03654 | hp2 | a0002 | c0003 | t0001 | g0231 | SAS | PJL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03669 | hp1 | a0001 | c0002 | t0019 | g0220 | SAS | PJL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03669 | hp2 | a0001 | c0013 | t0019 | g0119 | SAS | PJL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03688 | hp1 | a0001 | c0001 | t0035 | g0253 | SAS | STU | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0044 | SAS | STU | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03704 | hp1 | a0001 | c0002 | t0002 | g0239 | SAS | PJL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0024 | SAS | PJL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03710 | hp1 | a0001 | c0001 | t0004 | g0127 | SAS | PJL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03710 | hp2 | a0001 | c0002 | t0004 | g0068 | SAS | PJL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0132 | SAS | BEB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0021 | SAS | BEB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0252 | SAS | BEB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0216 | SAS | BEB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03927 | hp1 | a0001 | c0001 | t0004 | g0123 | SAS | BEB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0069 | SAS | BEB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0131 | SAS | STU | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG04115 | hp2 | a0001 | c0001 | t0045 | g0051 | SAS | STU | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0118 | SAS | STU | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0304 | SAS | STU | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18522 | hp1 | a0005 | c0006 | t0001 | g0225 | AFR | YRI | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0282 | AFR | YRI | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18612 | hp1 | a0001 | c0001 | t0023 | g0143 | EAS | CHB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18612 | hp2 | a0003 | c0012 | t0001 | g0082 | EAS | CHB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18747 | hp1 | a0008 | c0009 | t0002 | g0064 | EAS | CHB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | CHB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18939 | hp1 | a0001 | c0002 | t0011 | g0210 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18950 | hp2 | a0001 | c0002 | t0041 | g0258 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18956 | hp1 | a0001 | c0001 | t0017 | g0180 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0262 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18965 | hp1 | a0001 | c0001 | t0028 | g0147 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18965 | hp2 | a0001 | c0001 | t0010 | g0073 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18969 | hp2 | a0009 | c0005 | t0003 | g0092 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18974 | hp2 | a0001 | c0001 | t0027 | g0074 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18979 | hp1 | a0001 | c0001 | t0033 | g0109 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18981 | hp1 | a0001 | c0002 | t0011 | g0211 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18984 | hp2 | a0001 | c0002 | t0056 | g0219 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18990 | hp2 | a0001 | c0001 | t0024 | g0196 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18992 | hp1 | a0001 | c0001 | t0016 | g0151 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18992 | hp2 | a0001 | c0001 | t0006 | g0049 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0237 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18995 | hp2 | a0001 | c0001 | t0042 | g0175 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0234 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA18999 | hp2 | a0001 | c0001 | t0026 | g0057 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19005 | hp1 | a0001 | c0002 | t0011 | g0208 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19012 | hp2 | a0001 | c0001 | t0016 | g0199 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0099 | AFR | LWK | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | LWK | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | LWK | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0221 | AFR | LWK | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19057 | hp1 | a0001 | c0001 | t0037 | g0205 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19063 | hp1 | a0004 | c0004 | t0001 | g0097 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19063 | hp2 | a0001 | c0001 | t0006 | g0096 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0137 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19075 | hp1 | a0001 | c0001 | t0048 | g0078 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19080 | hp1 | a0001 | c0001 | t0010 | g0041 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19086 | hp1 | a0001 | c0001 | t0018 | g0202 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19087 | hp2 | a0001 | c0001 | t0006 | g0087 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0236 | EAS | JPT | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0227 | AFR | YRI | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA20129 | hp1 | a0001 | c0001 | t0021 | g0067 | AFR | ASW | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | ASW | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0270 | EUR | TSI | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0276 | EUR | TSI | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | GIH | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0055 | SAS | GIH | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02109 | hp1 | a0001 | c0002 | t0008 | g0156 | AFR | ACB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02109 | hp2 | a0001 | c0002 | t0004 | g0207 | AFR | ACB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0287 | AFR | ACB | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0281 | AFR | MSL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | MSL | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | USA | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| HG06807 | hp2 | a0001 | c0001 | t0012 | g0246 | AFR | USA | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA21309 | hp1 | a0001 | c0001 | t0046 | g0168 | AFR | LWK | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | LWK | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0003 | g0273 | REF | REF | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0009 | REF | REF | LMCD1_chr3_8496823_8579668 | LMCD1 | chr3 | 8496823 | 8579668 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:8537406
|
A | G | 1 | a0003 | 1 | NA18612.hp2 | missense_variant | MODERATE | c.353A>G | p.Tyr118Cys | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/6 | 469/8284 | 353/1098 | 118/365 | chr3 | 8537406 | ||
| chr3:8548610
|
G | A | 1 | a0004 | 1 | NA19063.hp1 | missense_variant | MODERATE | c.430G>A | p.Val144Met | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/6 | 546/8284 | 430/1098 | 144/365 | chr3 | 8548610 | ||
| chr3:8548781
|
C | T | 1 | a0005 | 1 | NA18522.hp1 | missense_variant | MODERATE | c.601C>T | p.Leu201Phe | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/6 | 717/8284 | 601/1098 | 201/365 | chr3 | 8548781 | ||
| chr3:8548854
|
C | T | 1 | a0010 | 1 | HG02965.hp2 | missense_variant | MODERATE | c.674C>T | p.Ala225Val | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/6 | 790/8284 | 674/1098 | 225/365 | chr3 | 8548854 | ||
| chr3:8565558
|
G | A | 1 | a0009 | 1 | NA18969.hp2 | missense_variant | MODERATE | c.850G>A | p.Asp284Asn | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 5/6 | 966/8284 | 850/1098 | 284/365 | chr3 | 8565558 | ||
| chr3:8565597
|
G | T | 1 | a0006 | 1 | HG02896.hp1 | missense_variant | MODERATE | c.889G>T | p.Gly297Cys | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 5/6 | 1005/8284 | 889/1098 | 297/365 | chr3 | 8565597 | ||
| chr3:8565621
|
C | T | 1 | a0002 | 2 | HG01106.hp1 HG03654.hp2 |
missense_variant | MODERATE | c.913C>T | p.Arg305Trp | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 5/6 | 1029/8284 | 913/1098 | 305/365 | chr3 | 8565621 | ||
| chr3:8567500
|
G | A | 1 | a0007 | 1 | HG03041.hp1 | missense_variant | MODERATE | c.1000G>A | p.Val334Ile | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 1116/8284 | 1000/1098 | 334/365 | chr3 | 8567500 | ||
| chr3:8567591
|
G | A | 1 | a0008 | 1 | NA18747.hp1 | missense_variant | MODERATE | c.1091G>A | p.Arg364His | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 1207/8284 | 1091/1098 | 364/365 | chr3 | 8567591 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:8537314
|
C | T | 1 | a0001c0013 | 1 | HG03669.hp2 | synonymous_variant | LOW | c.261C>T | p.Gly87Gly | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/6 | 377/8284 | 261/1098 | 87/365 | chr3 | 8537314 | ||
| chr3:8548627
|
T | C | 3 | a0001c0002a0005c0006a0009c0005 | 38 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(35): Show |
synonymous_variant | LOW | c.447T>C | p.Gly149Gly | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/6 | 563/8284 | 447/1098 | 149/365 | chr3 | 8548627 | ||
| chr3:8567538
|
G | A | 1 | a0001c0008 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.1038G>A | p.Ala346Ala | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 1154/8284 | 1038/1098 | 346/365 | chr3 | 8567538 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:8501842
|
G | T | 2 | a0001c0002t0011a0001c0002t0056 | 4 | NA18939.hp1 NA18981.hp1 NA18984.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-97G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/6 | 97 | chr3 | 8501842 | |||||
| chr3:8501915
|
G | A | 1 | a0001c0001t0020 | 1 | HG03491.hp2 | 5_prime_UTR_variant | MODIFIER | c.-24G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/6 | 24 | chr3 | 8501915 | |||||
| chr3:8567682
|
T | C | 4 | a0001c0001t0007a0001c0001t0012a0001c0001t0021others(1): Show | 7 | HG02615.hp2 HG03130.hp1 HG03209.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*84T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 84 | chr3 | 8567682 | |||||
| chr3:8567895
|
G | A | 1 | a0001c0001t0023 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*297G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 297 | chr3 | 8567895 | |||||
| chr3:8567939
|
C | T | 1 | a0001c0001t0055 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*341C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 341 | chr3 | 8567939 | |||||
| chr3:8567940
|
G | A | 1 | a0001c0002t0008 | 3 | HG02109.hp1 HG02258.hp1 HG02280.hp1 |
3_prime_UTR_variant | MODIFIER | c.*342G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 342 | chr3 | 8567940 | |||||
| chr3:8568085
|
A | G | 2 | a0001c0001t0007a0001c0001t0022 | 4 | HG02615.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*487A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 487 | chr3 | 8568085 | |||||
| chr3:8568270
|
G | A | 1 | a0001c0001t0024 | 1 | NA18990.hp2 | 3_prime_UTR_variant | MODIFIER | c.*672G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 672 | chr3 | 8568270 | |||||
| chr3:8568364
|
T | C | 1 | a0001c0001t0013 | 2 | HG01109.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*766T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 766 | chr3 | 8568364 | |||||
| chr3:8568425
|
T | C | 2 | a0001c0002t0008a0007c0007t0025 | 4 | HG02109.hp1 HG02258.hp1 HG02280.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*827T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 827 | chr3 | 8568425 | |||||
| chr3:8568548
|
T | C | 2 | a0001c0001t0026a0001c0001t0027 | 2 | NA18974.hp2 NA18999.hp2 |
3_prime_UTR_variant | MODIFIER | c.*950T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 950 | chr3 | 8568548 | |||||
| chr3:8568895
|
C | T | 23 | a0001c0001t0003a0001c0001t0004a0001c0001t0018others(20): Show | 105 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*1297C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 1297 | chr3 | 8568895 | |||||
| chr3:8569128
|
A | G | 1 | a0001c0002t0054 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1530A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 1530 | chr3 | 8569128 | |||||
| chr3:8569250
|
C | G | 25 | a0001c0001t0001a0001c0001t0006a0001c0001t0009others(22): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*1652C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 1652 | chr3 | 8569250 | |||||
| chr3:8569384
|
A | G | 24 | a0001c0001t0003a0001c0001t0004a0001c0001t0018others(21): Show | 106 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*1786A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 1786 | chr3 | 8569384 | |||||
| chr3:8569445
|
A | G | 1 | a0001c0001t0031 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1847A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 1847 | chr3 | 8569445 | |||||
| chr3:8569446
|
C | T | 1 | a0001c0001t0053 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1848C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 1848 | chr3 | 8569446 | |||||
| chr3:8569505
|
T | C | 1 | a0001c0001t0012 | 2 | HG03130.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1907T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 1907 | chr3 | 8569505 | |||||
| chr3:8569658
|
G | C | 22 | a0001c0001t0003a0001c0001t0004a0001c0001t0018others(19): Show | 104 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*2060G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 2060 | chr3 | 8569658 | |||||
| chr3:8569767
|
G | A | 2 | a0001c0001t0007a0001c0001t0022 | 4 | HG02615.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2169G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 2169 | chr3 | 8569767 | |||||
| chr3:8569980
|
C | CA | 23 | a0001c0001t0003a0001c0001t0004a0001c0001t0014others(20): Show | 106 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*2397dupA | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 2398 | INFO_REALIGN_3_PRIME | chr3 | 8569980 | ||||
| chr3:8569980
|
C | CAA | 3 | a0001c0001t0009a0001c0001t0012a0001c0001t0029 | 6 | HG01074.hp2 HG01975.hp2 HG02129.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2396_*2397dupAA | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 2398 | INFO_REALIGN_3_PRIME | chr3 | 8569980 | ||||
| chr3:8569980
|
C | CAAA | 26 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(23): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*2395_*2397dupAAA | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 2398 | INFO_REALIGN_3_PRIME | chr3 | 8569980 | ||||
| chr3:8570400
|
G | T | 52 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(49): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
3_prime_UTR_variant | MODIFIER | c.*2802G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 2802 | chr3 | 8570400 | |||||
| chr3:8570412
|
CA | C | 5 | a0001c0001t0004a0001c0001t0052a0001c0001t0053others(2): Show | 16 | HG01884.hp2 HG02109.hp2 HG02257.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2815delA | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 2815 | chr3 | 8570412 | |||||
| chr3:8570596
|
G | C | 56 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(53): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
3_prime_UTR_variant | MODIFIER | c.*2998G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 2998 | chr3 | 8570596 | |||||
| chr3:8570643
|
C | T | 1 | a0001c0001t0030 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3045C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 3045 | chr3 | 8570643 | |||||
| chr3:8570666
|
C | T | 1 | a0001c0001t0043 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3068C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 3068 | chr3 | 8570666 | |||||
| chr3:8570679
|
T | G | 1 | a0001c0001t0014 | 2 | HG02055.hp1 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3081T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 3081 | chr3 | 8570679 | |||||
| chr3:8570715
|
C | G | 1 | a0001c0001t0049 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3117C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 3117 | chr3 | 8570715 | |||||
| chr3:8570890
|
G | A | 51 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(48): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
3_prime_UTR_variant | MODIFIER | c.*3292G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 3292 | chr3 | 8570890 | |||||
| chr3:8571005
|
G | C | 1 | a0001c0001t0030 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3407G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 3407 | chr3 | 8571005 | |||||
| chr3:8571017
|
G | T | 24 | a0001c0001t0001a0001c0001t0006a0001c0001t0009others(21): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*3419G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 3419 | chr3 | 8571017 | |||||
| chr3:8571044
|
G | A | 1 | a0001c0002t0056 | 1 | NA18984.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3446G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 3446 | chr3 | 8571044 | |||||
| chr3:8571061
|
A | T | 1 | a0001c0001t0012 | 2 | HG03130.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3463A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 3463 | chr3 | 8571061 | |||||
| chr3:8571062
|
TGTCAGCA others(9): Show |
T | 1 | a0001c0001t0012 | 2 | HG03130.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3466_*3481delTCAG others(12): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 3466 | INFO_REALIGN_3_PRIME | chr3 | 8571062 | ||||
| chr3:8571079
|
G | C | 1 | a0001c0001t0012 | 2 | HG03130.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3481G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 3481 | chr3 | 8571079 | |||||
| chr3:8571247
|
A | G | 1 | a0001c0001t0042 | 1 | NA18995.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3649A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 3649 | chr3 | 8571247 | |||||
| chr3:8571515
|
G | C | 1 | a0001c0001t0017 | 2 | HG02523.hp1 NA18956.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3917G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 3917 | chr3 | 8571515 | |||||
| chr3:8571593
|
C | G | 53 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(50): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
3_prime_UTR_variant | MODIFIER | c.*3995C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 3995 | chr3 | 8571593 | |||||
| chr3:8571674
|
C | T | 1 | a0001c0002t0041 | 1 | NA18950.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4076C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 4076 | chr3 | 8571674 | |||||
| chr3:8571771
|
C | G | 2 | a0001c0001t0006a0001c0001t0044 | 5 | HG00597.hp2 HG02165.hp2 NA18992.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4173C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 4173 | chr3 | 8571771 | |||||
| chr3:8571782
|
T | G | 1 | a0001c0002t0050 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4184T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 4184 | chr3 | 8571782 | |||||
| chr3:8571810
|
G | A | 1 | a0001c0001t0014 | 2 | HG02055.hp1 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4212G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 4212 | chr3 | 8571810 | |||||
| chr3:8571813
|
A | C | 24 | a0001c0001t0003a0001c0001t0004a0001c0001t0018others(21): Show | 106 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*4215A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 4215 | chr3 | 8571813 | |||||
| chr3:8571820
|
A | G | 2 | a0001c0001t0006a0001c0001t0044 | 5 | HG00597.hp2 HG02165.hp2 NA18992.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4222A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 4222 | chr3 | 8571820 | |||||
| chr3:8571862
|
A | T | 1 | a0001c0001t0040 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4264A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 4264 | chr3 | 8571862 | |||||
| chr3:8571863
|
A | G | 3 | a0001c0001t0040a0001c0002t0008a0007c0007t0025 | 5 | HG02109.hp1 HG02258.hp1 HG02280.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4265A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 4265 | chr3 | 8571863 | |||||
| chr3:8571889
|
G | A | 25 | a0001c0001t0001a0001c0001t0006a0001c0001t0009others(22): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*4291G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 4291 | chr3 | 8571889 | |||||
| chr3:8571978
|
A | G | 2 | a0001c0001t0021a0001c0001t0029 | 2 | HG01074.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4380A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 4380 | chr3 | 8571978 | |||||
| chr3:8572158
|
A | G | 49 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(46): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
3_prime_UTR_variant | MODIFIER | c.*4560A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 4560 | chr3 | 8572158 | |||||
| chr3:8572453
|
T | G | 3 | a0001c0001t0007a0001c0001t0012a0001c0001t0022 | 6 | HG02615.hp2 HG03130.hp1 HG03209.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4855T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 4855 | chr3 | 8572453 | |||||
| chr3:8572537
|
T | C | 1 | a0001c0001t0035 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4939T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 4939 | chr3 | 8572537 | |||||
| chr3:8572649
|
T | C | 2 | a0001c0001t0021a0001c0001t0029 | 2 | HG01074.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5051T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 5051 | chr3 | 8572649 | |||||
| chr3:8572694
|
A | G | 1 | a0001c0001t0039 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5096A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 5096 | chr3 | 8572694 | |||||
| chr3:8572759
|
T | C | 25 | a0001c0001t0001a0001c0001t0006a0001c0001t0009others(22): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*5161T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 5161 | chr3 | 8572759 | |||||
| chr3:8572816
|
G | A | 1 | a0001c0001t0012 | 2 | HG03130.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5218G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 5218 | chr3 | 8572816 | |||||
| chr3:8572856
|
G | T | 20 | a0001c0001t0003a0001c0001t0004a0001c0001t0018others(17): Show | 102 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*5258G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 5258 | chr3 | 8572856 | |||||
| chr3:8573188
|
T | C | 1 | a0001c0001t0014 | 2 | HG02055.hp1 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5590T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 5590 | chr3 | 8573188 | |||||
| chr3:8573309
|
G | A | 23 | a0001c0001t0003a0001c0001t0004a0001c0001t0018others(20): Show | 105 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*5711G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 5711 | chr3 | 8573309 | |||||
| chr3:8573325
|
G | A | 1 | a0001c0001t0017 | 2 | HG02523.hp1 NA18956.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5727G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 5727 | chr3 | 8573325 | |||||
| chr3:8573372
|
T | C | 1 | a0001c0001t0022 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5774T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 5774 | chr3 | 8573372 | |||||
| chr3:8573376
|
T | C | 2 | a0001c0001t0005a0001c0002t0005 | 4 | HG02622.hp2 HG02818.hp1 HG02886.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5778T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 5778 | chr3 | 8573376 | |||||
| chr3:8573421
|
C | G | 1 | a0001c0001t0027 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5823C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 5823 | chr3 | 8573421 | |||||
| chr3:8573475
|
G | A | 1 | a0001c0001t0046 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5877G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 5877 | chr3 | 8573475 | |||||
| chr3:8573521
|
G | A | 24 | a0001c0001t0003a0001c0001t0004a0001c0001t0018others(21): Show | 106 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*5923G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 5923 | chr3 | 8573521 | |||||
| chr3:8573528
|
G | A | 1 | a0001c0001t0036 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5930G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 5930 | chr3 | 8573528 | |||||
| chr3:8573591
|
G | A | 49 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(46): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
3_prime_UTR_variant | MODIFIER | c.*5993G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 5993 | chr3 | 8573591 | |||||
| chr3:8573803
|
A | G | 49 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(46): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
3_prime_UTR_variant | MODIFIER | c.*6205A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 6205 | chr3 | 8573803 | |||||
| chr3:8573876
|
TA | T | 27 | a0001c0001t0001a0001c0001t0006a0001c0001t0009others(24): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*6292delA | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 6292 | INFO_REALIGN_3_PRIME | chr3 | 8573876 | ||||
| chr3:8573958
|
G | A | 1 | a0001c0001t0038 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6360G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 6360 | chr3 | 8573958 | |||||
| chr3:8574184
|
C | T | 1 | a0001c0001t0034 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6586C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 6586 | chr3 | 8574184 | |||||
| chr3:8574259
|
A | G | 3 | a0001c0001t0007a0001c0001t0021a0001c0001t0022 | 5 | HG02615.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6661A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 6661 | chr3 | 8574259 | |||||
| chr3:8574441
|
C | A | 1 | a0001c0001t0015 | 2 | HG02622.hp1 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6843C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 6843 | chr3 | 8574441 | |||||
| chr3:8574442
|
T | C | 50 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(47): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
3_prime_UTR_variant | MODIFIER | c.*6844T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 6844 | chr3 | 8574442 | |||||
| chr3:8574461
|
G | T | 2 | a0001c0002t0019a0001c0013t0019 | 2 | HG03669.hp1 HG03669.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6863G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 6863 | chr3 | 8574461 | |||||
| chr3:8574577
|
C | T | 1 | a0001c0001t0018 | 2 | HG00609.hp1 NA19086.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6979C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 6/6 | 6979 | chr3 | 8574577 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:8502027
|
G | GT | 306 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(303): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.42+49dupT | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502027 | |||||
| chr3:8502032
|
C | G | 1 | a0001c0001t0001g0306 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.42+52C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502032 | ||||||
| chr3:8502071
|
A | C | 67 | a0001c0001t0001g0247a0001c0001t0001g0254a0001c0001t0001g0255others(64): Show | 69 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.42+91A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502071 | ||||||
| chr3:8502076
|
G | A | 7 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(4): Show | 7 | HG02145.hp2 HG02559.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.42+96G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502076 | ||||||
| chr3:8502177
|
T | C | 1 | a0001c0001t0001g0015 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.42+197T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502177 | ||||||
| chr3:8502206
|
G | T | 2 | a0001c0002t0002g0239a0001c0002t0002g0240 | 2 | HG02698.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.42+226G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502206 | ||||||
| chr3:8502269
|
ATATATAT others(111): Show |
A | 7 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(4): Show | 7 | HG02145.hp2 HG02559.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.42+316_42+433del | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502269 | |||||
| chr3:8502270
|
T | TATATATT others(82): Show |
6 | a0001c0001t0001g0235a0001c0001t0002g0238a0001c0001t0003g0233others(3): Show | 6 | HG00438.hp2 HG01243.hp2 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.42+296_42+297insTT others(87): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502270 | |||||
| chr3:8502278
|
A | ATATATAT others(54): Show |
1 | a0001c0001t0002g0232 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.42+298_42+299insTA others(59): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502278 | ||||||
| chr3:8502278
|
A | T | 6 | a0001c0001t0001g0235a0001c0001t0002g0238a0001c0001t0003g0233others(3): Show | 6 | HG00438.hp2 HG01243.hp2 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.42+298A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502278 | ||||||
| chr3:8502279
|
A | T | 6 | a0001c0001t0001g0235a0001c0001t0002g0238a0001c0001t0003g0233others(3): Show | 6 | HG00438.hp2 HG01243.hp2 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.42+299A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502279 | ||||||
| chr3:8502287
|
T | A | 2 | a0001c0002t0002g0239a0001c0002t0002g0240 | 2 | HG02698.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.42+307T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502287 | ||||||
| chr3:8502288
|
A | T | 8 | a0001c0001t0001g0235a0001c0001t0002g0232a0001c0001t0002g0238others(5): Show | 8 | HG00438.hp2 HG01243.hp2 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.42+308A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502288 | ||||||
| chr3:8502296
|
T | A | 1 | a0001c0001t0002g0232 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.42+316T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502296 | ||||||
| chr3:8502296
|
T | TTTTA | 6 | a0001c0001t0001g0235a0001c0001t0002g0238a0001c0001t0003g0233others(3): Show | 6 | HG00438.hp2 HG01243.hp2 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.42+317_42+318insTT others(2): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502296 | |||||
| chr3:8502296
|
TTATATAT others(11): Show |
T | 4 | a0001c0001t0001g0015a0001c0001t0001g0228a0001c0001t0005g0229others(1): Show | 4 | HG02976.hp1 HG03453.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.42+324_42+341delAA others(16): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502296 | |||||
| chr3:8502297
|
T | A | 3 | a0001c0001t0002g0232a0001c0002t0002g0239a0001c0002t0002g0240 | 3 | HG01928.hp1 HG02698.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.42+317T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502297 | ||||||
| chr3:8502297
|
TATATATA others(9): Show |
T | 3 | a0001c0002t0001g0227a0001c0002t0005g0226a0005c0006t0001g0225 | 3 | HG02818.hp1 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.42+325_42+340delAT others(14): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502297 | |||||
| chr3:8502305
|
A | T | 2 | a0001c0002t0002g0239a0001c0002t0002g0240 | 2 | HG02698.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.42+325A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502305 | ||||||
| chr3:8502306
|
T | A | 67 | a0001c0001t0001g0247a0001c0001t0001g0254a0001c0001t0001g0255others(64): Show | 69 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.42+326T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502306 | ||||||
| chr3:8502312
|
A | T | 95 | a0001c0001t0001g0209a0001c0001t0001g0217a0001c0001t0001g0235others(92): Show | 97 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.42+332A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502312 | ||||||
| chr3:8502313
|
A | AATATATA others(63): Show |
1 | a0001c0001t0002g0017 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.42+349_42+350insTA others(68): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502313 | |||||
| chr3:8502313
|
A | AATATATA others(65): Show |
1 | a0002c0003t0001g0231 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.42+349_42+350insTA others(70): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502313 | |||||
| chr3:8502313
|
A | AATATATA others(65): Show |
168 | a0001c0001t0001g0003a0001c0001t0001g0025a0001c0001t0001g0026others(165): Show | 171 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.42+349_42+350insTA others(70): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502313 | |||||
| chr3:8502313
|
A | AATATATA others(90): Show |
1 | a0001c0001t0003g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.42+349_42+350insTA others(95): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502313 | |||||
| chr3:8502313
|
A | AATATATA others(81): Show |
8 | a0001c0001t0002g0006a0001c0001t0002g0200a0001c0001t0002g0201others(5): Show | 9 | HG00438.hp1 HG00609.hp2 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.42+349_42+350insTA others(86): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502313 | |||||
| chr3:8502313
|
A | T | 7 | a0001c0001t0001g0235a0001c0001t0002g0232a0001c0001t0002g0238others(4): Show | 7 | HG00438.hp2 HG01243.hp2 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.42+333A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502313 | ||||||
| chr3:8502314
|
A | T | 1 | a0001c0001t0022g0305 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.42+334A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502314 | ||||||
| chr3:8502320
|
A | ATTATATA others(2): Show |
19 | a0001c0001t0001g0209a0001c0001t0001g0217a0001c0001t0001g0306others(16): Show | 19 | HG00423.hp1 HG02109.hp2 HG02622.hp1 others(16): Show |
intron_variant | MODIFIER | c.42+348_42+349insTT others(7): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502320 | |||||
| chr3:8502321
|
T | TTATATAT others(15): Show |
3 | a0001c0001t0001g0002a0001c0001t0003g0018a0001c0001t0003g0019 | 4 | HG01243.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.42+349_42+350insTA others(20): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502321 | |||||
| chr3:8502322
|
T | TATATAAA others(167): Show |
3 | a0001c0001t0002g0241a0001c0001t0002g0242a0001c0001t0002g0243 | 3 | HG02572.hp1 HG03139.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.42+347_42+348insAA others(172): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502322 | |||||
| chr3:8502322
|
T | TATATAAA others(171): Show |
1 | a0001c0001t0005g0244 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.42+347_42+348insAA others(176): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502322 | |||||
| chr3:8502322
|
T | TATATAAA others(194): Show |
1 | a0001c0002t0001g0245 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.42+347_42+348insAA others(199): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502322 | |||||
| chr3:8502322
|
T | TATATAAA others(169): Show |
49 | a0001c0001t0001g0247a0001c0001t0001g0254a0001c0001t0001g0255others(46): Show | 51 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.42+347_42+348insAA others(174): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502322 | |||||
| chr3:8502322
|
T | TATATAAA others(196): Show |
2 | a0001c0001t0002g0295a0001c0001t0002g0296 | 2 | HG01884.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.42+347_42+348insAA others(201): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502322 | |||||
| chr3:8502322
|
T | TATATATA others(144): Show |
1 | a0001c0002t0001g0297 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.42+350_42+351insAA others(149): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502322 | |||||
| chr3:8502322
|
T | TATATATA others(240): Show |
1 | a0001c0001t0001g0298 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.42+350_42+351insAA others(245): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502322 | |||||
| chr3:8502322
|
T | TATATATA others(194): Show |
2 | a0001c0001t0001g0299a0001c0001t0001g0300 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.42+350_42+351insAA others(199): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502322 | |||||
| chr3:8502322
|
T | TATATATA others(169): Show |
2 | a0001c0001t0007g0301a0001c0001t0022g0305 | 2 | HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.42+357_42+358insAA others(174): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502322 | |||||
| chr3:8502322
|
T | TATATATA others(169): Show |
1 | a0001c0001t0007g0303 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.42+357_42+358insAA others(174): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502322 | |||||
| chr3:8502322
|
T | TATATATA others(40): Show |
1 | a0001c0001t0012g0020 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.42+349_42+350insTA others(45): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502322 | |||||
| chr3:8502323
|
A | ATATATAT others(65): Show |
4 | a0001c0001t0024g0196a0001c0002t0001g0193a0001c0002t0001g0194others(1): Show | 4 | HG01069.hp1 HG01071.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.42+349_42+350insTA others(70): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502323 | |||||
| chr3:8502323
|
A | T | 7 | a0001c0001t0001g0015a0001c0001t0001g0228a0001c0001t0005g0229others(4): Show | 7 | HG02818.hp1 HG02976.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.42+343A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502323 | ||||||
| chr3:8502328
|
T | A | 2 | a0001c0001t0014g0294a0001c0001t0052g0293 | 2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.42+348T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502328 | ||||||
| chr3:8502328
|
T | G | 2 | a0001c0001t0005g0244a0001c0001t0012g0246 | 2 | HG02886.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.42+348T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502328 | ||||||
| chr3:8502328
|
T | TATAA | 8 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0003g0186others(5): Show | 8 | HG00140.hp1 HG00639.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.42+349_42+350insTA others(2): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502328 | |||||
| chr3:8502329
|
A | ATAAAATA others(29): Show |
1 | a0001c0001t0003g0198 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.42+349_42+350insTA others(34): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502329 | ||||||
| chr3:8502335
|
T | A | 1 | a0001c0001t0001g0016 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.42+355T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502335 | ||||||
| chr3:8502337
|
T | A | 2 | a0001c0001t0001g0016a0001c0001t0003g0198 | 2 | NA18943.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.42+357T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502337 | ||||||
| chr3:8502337
|
T | TAATATAT others(159): Show |
1 | a0001c0001t0034g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.42+357_42+358insAA others(164): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502337 | ||||||
| chr3:8502338
|
T | A | 12 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0003g0186others(9): Show | 12 | HG00140.hp1 HG00639.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.42+358T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502338 | ||||||
| chr3:8502339
|
A | ATATATAT others(194): Show |
2 | a0001c0001t0014g0294a0001c0001t0052g0293 | 2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.42+365_42+366insTT others(199): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502339 | |||||
| chr3:8502339
|
A | T | 1 | a0001c0001t0003g0198 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.42+359A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502339 | ||||||
| chr3:8502346
|
A | T | 11 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0003g0186others(8): Show | 11 | HG00140.hp1 HG00639.hp1 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.42+366A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502346 | ||||||
| chr3:8502347
|
A | T | 3 | a0001c0001t0001g0016a0001c0002t0001g0227a0001c0002t0005g0226 | 3 | HG02818.hp1 NA18984.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.42+367A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502347 | ||||||
| chr3:8502348
|
A | T | 2 | a0001c0002t0001g0227a0001c0002t0005g0226 | 2 | HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.42+368A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502348 | ||||||
| chr3:8502355
|
A | T | 8 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0003g0186others(5): Show | 8 | HG00140.hp1 HG00639.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.42+375A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502355 | ||||||
| chr3:8502362
|
T | TAAAATAT others(90): Show |
7 | a0001c0001t0001g0191a0001c0001t0003g0186a0001c0001t0003g0187others(4): Show | 7 | HG00140.hp1 HG00639.hp1 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.42+382_42+383insAA others(95): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502362 | ||||||
| chr3:8502362
|
T | TTATATAA others(45): Show |
1 | a0001c0002t0004g0207 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.42+397_42+398insAT others(50): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502362 | |||||
| chr3:8502362
|
T | TTATATAA others(120): Show |
2 | a0001c0002t0002g0239a0001c0002t0002g0240 | 2 | HG02698.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.42+424_42+425insAT others(125): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502362 | |||||
| chr3:8502362
|
T | TTATATAT others(97): Show |
17 | a0001c0001t0001g0209a0001c0001t0001g0217a0001c0001t0001g0306others(14): Show | 17 | HG00423.hp1 HG02622.hp1 HG02683.hp1 others(14): Show |
intron_variant | MODIFIER | c.42+388_42+389insTA others(102): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502362 | |||||
| chr3:8502362
|
T | TTATATAT others(122): Show |
1 | a0001c0001t0002g0224 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.42+388_42+389insTT others(127): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502362 | |||||
| chr3:8502363
|
T | A | 1 | a0001c0001t0001g0197 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.42+383T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502363 | ||||||
| chr3:8502365
|
T | A | 1 | a0001c0001t0001g0197 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.42+385T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502365 | ||||||
| chr3:8502368
|
A | ATTCATAT others(5): Show |
1 | a0001c0001t0001g0197 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.42+388_42+389insTT others(10): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502368 | ||||||
| chr3:8502369
|
A | T | 4 | a0001c0001t0001g0182a0001c0001t0001g0185a0001c0001t0003g0183others(1): Show | 4 | HG02486.hp1 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.42+389A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502369 | ||||||
| chr3:8502370
|
A | T | 1 | a0001c0001t0001g0197 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.42+390A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502370 | ||||||
| chr3:8502370
|
AAT | A | 4 | a0001c0001t0001g0228a0001c0001t0001g0247a0001c0001t0005g0229others(1): Show | 4 | HG02976.hp1 HG03453.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.42+398_42+399delTA | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502370 | |||||
| chr3:8502372
|
T | TATATATA others(194): Show |
1 | a0001c0002t0001g0304 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.42+424_42+425insAT others(199): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502372 | |||||
| chr3:8502397
|
A | T | 2 | a0001c0001t0001g0016a0001c0001t0001g0197 | 2 | NA18984.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.42+417A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502397 | ||||||
| chr3:8502408
|
T | A | 1 | a0001c0001t0001g0197 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.42+428T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502408 | ||||||
| chr3:8502410
|
T | A | 1 | a0001c0001t0001g0197 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.42+430T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502410 | ||||||
| chr3:8502411
|
A | T | 1 | a0001c0001t0001g0197 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.42+431A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502411 | ||||||
| chr3:8502413
|
A | C | 1 | a0001c0001t0001g0197 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.42+433A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502413 | ||||||
| chr3:8502569
|
T | TAC | 6 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0003g0023others(3): Show | 6 | HG02698.hp2 HG03491.hp2 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.42+626_42+627dupAC | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502569 | |||||
| chr3:8502569
|
TAC | T | 129 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0071others(126): Show | 133 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.42+626_42+627delAC | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502569 | |||||
| chr3:8502569
|
TACAC | T | 40 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0162others(37): Show | 40 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.42+624_42+627delAC others(2): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502569 | |||||
| chr3:8502569
|
TACACAC | T | 12 | a0001c0001t0001g0176a0001c0001t0001g0191a0001c0001t0002g0179others(9): Show | 12 | HG02155.hp1 HG02258.hp2 HG02523.hp1 others(9): Show |
intron_variant | MODIFIER | c.42+622_42+627delAC others(4): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502569 | |||||
| chr3:8502569
|
TACACACA others(11): Show |
T | 1 | a0001c0001t0005g0244 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.42+610_42+627delAC others(16): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502569 | |||||
| chr3:8502569
|
TACACACA others(13): Show |
T | 65 | a0001c0001t0001g0247a0001c0001t0001g0254a0001c0001t0001g0255others(62): Show | 67 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.42+608_42+627delAC others(18): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502569 | |||||
| chr3:8502606
|
A | G | 6 | a0001c0001t0001g0015a0001c0001t0001g0228a0001c0001t0005g0229others(3): Show | 6 | HG02818.hp1 HG02976.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.42+626A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502606 | ||||||
| chr3:8502606
|
ACG | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0003g0028 | 4 | HG01256.hp1 HG01934.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.42+628_42+629delGC | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8502606 | |||||
| chr3:8502608
|
G | A | 1 | a0001c0001t0034g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.42+628G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502608 | ||||||
| chr3:8502630
|
G | T | 1 | a0001c0001t0034g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.42+650G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502630 | ||||||
| chr3:8502734
|
T | C | 73 | a0001c0001t0001g0247a0001c0001t0001g0254a0001c0001t0001g0255others(70): Show | 75 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.42+754T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502734 | ||||||
| chr3:8502817
|
G | T | 69 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0130others(66): Show | 70 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.42+837G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502817 | ||||||
| chr3:8502850
|
G | A | 1 | a0001c0001t0007g0301 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.42+870G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502850 | ||||||
| chr3:8502876
|
G | A | 1 | a0001c0002t0008g0156 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.42+896G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502876 | ||||||
| chr3:8502902
|
C | T | 5 | a0001c0001t0002g0152a0001c0001t0002g0154a0001c0001t0002g0155others(2): Show | 5 | HG00673.hp2 NA18943.hp2 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.42+922C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502902 | ||||||
| chr3:8502992
|
C | G | 1 | a0005c0006t0001g0225 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.42+1012C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8502992 | ||||||
| chr3:8503061
|
C | G | 1 | a0001c0001t0002g0224 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.42+1081C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8503061 | ||||||
| chr3:8503214
|
A | G | 1 | a0001c0001t0034g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.42+1234A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8503214 | ||||||
| chr3:8503645
|
G | A | 4 | a0001c0001t0001g0182a0001c0001t0001g0185a0001c0001t0003g0183others(1): Show | 4 | HG02486.hp1 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.42+1665G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8503645 | ||||||
| chr3:8503777
|
C | G | 1 | a0001c0001t0002g0150 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.42+1797C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8503777 | ||||||
| chr3:8503792
|
C | A | 17 | a0001c0001t0001g0209a0001c0001t0001g0217a0001c0001t0001g0306others(14): Show | 17 | HG00423.hp1 HG02622.hp1 HG02683.hp1 others(14): Show |
intron_variant | MODIFIER | c.42+1812C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8503792 | ||||||
| chr3:8503843
|
T | C | 2 | a0001c0002t0002g0239a0001c0002t0002g0240 | 2 | HG02698.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.42+1863T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8503843 | ||||||
| chr3:8504081
|
A | G | 1 | a0001c0001t0003g0005 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.42+2101A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8504081 | ||||||
| chr3:8504114
|
T | A | 64 | a0001c0001t0001g0247a0001c0001t0001g0254a0001c0001t0001g0255others(61): Show | 66 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.42+2134T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8504114 | ||||||
| chr3:8504204
|
G | A | 2 | a0001c0001t0002g0224a0001c0002t0004g0207 | 2 | HG02109.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.42+2224G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8504204 | ||||||
| chr3:8504215
|
G | C | 8 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(5): Show | 8 | HG02145.hp2 HG02559.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.42+2235G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8504215 | ||||||
| chr3:8504255
|
T | G | 1 | a0001c0001t0002g0111 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.42+2275T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8504255 | ||||||
| chr3:8504325
|
G | A | 1 | a0001c0001t0003g0112 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.42+2345G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8504325 | ||||||
| chr3:8504416
|
G | A | 86 | a0001c0001t0001g0209a0001c0001t0001g0217a0001c0001t0001g0247others(83): Show | 88 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.42+2436G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8504416 | ||||||
| chr3:8504468
|
C | T | 1 | a0001c0001t0002g0179 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.42+2488C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8504468 | ||||||
| chr3:8504595
|
G | A | 1 | a0001c0001t0003g0233 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.42+2615G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8504595 | ||||||
| chr3:8504625
|
C | T | 3 | a0001c0001t0001g0191a0001c0001t0003g0192a0001c0001t0003g0198 | 3 | HG02155.hp1 NA18943.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.42+2645C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8504625 | ||||||
| chr3:8504639
|
C | T | 72 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(69): Show | 74 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.42+2659C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8504639 | ||||||
| chr3:8504663
|
A | C | 1 | a0001c0001t0003g0289 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.42+2683A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8504663 | ||||||
| chr3:8504897
|
G | A | 2 | a0001c0001t0003g0252a0001c0001t0035g0253 | 2 | HG03688.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.42+2917G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8504897 | ||||||
| chr3:8504929
|
C | T | 1 | a0001c0001t0002g0155 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.42+2949C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8504929 | ||||||
| chr3:8504935
|
C | G | 1 | a0001c0002t0004g0207 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.42+2955C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8504935 | ||||||
| chr3:8505276
|
A | C | 2 | a0001c0002t0002g0239a0001c0002t0002g0240 | 2 | HG02698.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.42+3296A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8505276 | ||||||
| chr3:8505306
|
G | A | 107 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(104): Show | 109 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.42+3326G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8505306 | ||||||
| chr3:8505401
|
G | A | 1 | a0001c0001t0002g0070 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.42+3421G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8505401 | ||||||
| chr3:8505677
|
G | C | 1 | a0001c0001t0012g0246 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.42+3697G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8505677 | ||||||
| chr3:8505706
|
T | C | 75 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(72): Show | 77 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.42+3726T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8505706 | ||||||
| chr3:8505733
|
C | A | 3 | a0001c0001t0002g0224a0001c0002t0002g0157a0001c0002t0004g0207 | 3 | HG02109.hp2 HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.42+3753C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8505733 | ||||||
| chr3:8505764
|
T | C | 10 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(7): Show | 10 | HG01081.hp1 HG02145.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.42+3784T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8505764 | ||||||
| chr3:8505765
|
T | C | 27 | a0001c0001t0001g0015a0001c0001t0001g0306a0001c0001t0002g0214others(24): Show | 27 | HG00423.hp1 HG01169.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.42+3785T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8505765 | ||||||
| chr3:8505917
|
T | C | 75 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(72): Show | 77 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.42+3937T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8505917 | ||||||
| chr3:8506055
|
C | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(74): Show | 79 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.42+4075C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8506055 | ||||||
| chr3:8506138
|
C | T | 75 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(72): Show | 77 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.42+4158C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8506138 | ||||||
| chr3:8506177
|
T | C | 107 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(104): Show | 109 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.42+4197T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8506177 | ||||||
| chr3:8506187
|
G | A | 3 | a0001c0001t0002g0179a0001c0002t0002g0158a0001c0002t0004g0177 | 3 | HG01081.hp1 HG02965.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.42+4207G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8506187 | ||||||
| chr3:8506296
|
T | G | 1 | a0001c0001t0001g0030 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.42+4316T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8506296 | ||||||
| chr3:8506362
|
T | A | 75 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(72): Show | 77 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.42+4382T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8506362 | ||||||
| chr3:8506369
|
C | A | 1 | a0001c0001t0003g0186 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.42+4389C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8506369 | ||||||
| chr3:8506546
|
A | T | 15 | a0001c0001t0001g0306a0001c0001t0002g0214a0001c0001t0003g0221others(12): Show | 15 | HG00423.hp1 HG02735.hp2 HG03017.hp1 others(12): Show |
intron_variant | MODIFIER | c.42+4566A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8506546 | ||||||
| chr3:8506843
|
G | A | 9 | a0001c0001t0031g0066a0001c0002t0001g0227a0001c0002t0001g0245others(6): Show | 9 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.42+4863G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8506843 | ||||||
| chr3:8506914
|
G | A | 15 | a0001c0001t0001g0306a0001c0001t0002g0214a0001c0001t0003g0221others(12): Show | 15 | HG00423.hp1 HG02735.hp2 HG03017.hp1 others(12): Show |
intron_variant | MODIFIER | c.42+4934G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8506914 | ||||||
| chr3:8507141
|
G | T | 98 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(95): Show | 100 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.42+5161G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8507141 | ||||||
| chr3:8507145
|
A | G | 1 | a0001c0001t0002g0238 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.42+5165A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8507145 | ||||||
| chr3:8507164
|
G | A | 98 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(95): Show | 100 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.42+5184G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8507164 | ||||||
| chr3:8507199
|
T | C | 100 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(97): Show | 102 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.42+5219T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8507199 | ||||||
| chr3:8507233
|
G | A | 2 | a0001c0002t0002g0239a0001c0002t0002g0240 | 2 | HG02698.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.42+5253G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8507233 | ||||||
| chr3:8507512
|
C | G | 2 | a0001c0001t0032g0110a0001c0001t0033g0109 | 2 | HG00408.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.42+5532C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8507512 | ||||||
| chr3:8507645
|
T | C | 1 | a0001c0001t0003g0031 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.42+5665T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8507645 | ||||||
| chr3:8507736
|
C | T | 75 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(72): Show | 77 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.42+5756C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8507736 | ||||||
| chr3:8507782
|
G | C | 1 | a0001c0001t0002g0113 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.42+5802G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8507782 | ||||||
| chr3:8507798
|
A | T | 2 | a0001c0001t0004g0178a0001c0001t0005g0229 | 2 | HG02258.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.42+5818A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8507798 | ||||||
| chr3:8507904
|
A | G | 21 | a0001c0001t0001g0002a0001c0001t0002g0006a0001c0001t0002g0054others(18): Show | 23 | HG00438.hp1 HG00609.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.42+5924A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8507904 | ||||||
| chr3:8507979
|
C | T | 114 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(111): Show | 116 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.42+5999C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8507979 | ||||||
| chr3:8507982
|
G | C | 1 | a0001c0001t0001g0306 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.42+6002G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8507982 | ||||||
| chr3:8508223
|
G | A | 4 | a0001c0001t0001g0182a0001c0001t0001g0185a0001c0001t0003g0183others(1): Show | 4 | HG02486.hp1 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.42+6243G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8508223 | ||||||
| chr3:8508264
|
A | G | 2 | a0001c0002t0002g0239a0001c0002t0002g0240 | 2 | HG02698.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.42+6284A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8508264 | ||||||
| chr3:8508275
|
C | T | 1 | a0001c0001t0002g0238 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.42+6295C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8508275 | ||||||
| chr3:8508329
|
C | T | 75 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(72): Show | 77 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.42+6349C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8508329 | ||||||
| chr3:8508677
|
C | A | 92 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(89): Show | 94 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.42+6697C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8508677 | ||||||
| chr3:8508717
|
C | G | 3 | a0001c0001t0002g0224a0001c0002t0002g0157a0001c0002t0004g0207 | 3 | HG02109.hp2 HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.42+6737C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8508717 | ||||||
| chr3:8508923
|
C | T | 1 | a0001c0001t0003g0283 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.42+6943C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8508923 | ||||||
| chr3:8509094
|
A | G | 2 | a0001c0001t0002g0281a0001c0001t0002g0282 | 2 | HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.42+7114A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8509094 | ||||||
| chr3:8509159
|
G | A | 2 | a0001c0001t0021g0067a0001c0001t0034g0302 | 2 | HG02976.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.42+7179G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8509159 | ||||||
| chr3:8509189
|
G | A | 1 | a0001c0002t0002g0157 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.42+7209G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8509189 | ||||||
| chr3:8509216
|
T | G | 1 | a0001c0001t0003g0114 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.42+7236T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8509216 | ||||||
| chr3:8509426
|
A | G | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(228): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.42+7446A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8509426 | ||||||
| chr3:8509471
|
C | T | 24 | a0001c0001t0001g0306a0001c0001t0002g0214a0001c0001t0002g0224others(21): Show | 24 | HG00423.hp1 HG02109.hp2 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.42+7491C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8509471 | ||||||
| chr3:8509648
|
G | A | 1 | a0001c0001t0021g0067 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.42+7668G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8509648 | ||||||
| chr3:8509681
|
A | C | 2 | a0001c0001t0021g0067a0001c0001t0034g0302 | 2 | HG02976.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.42+7701A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8509681 | ||||||
| chr3:8509851
|
C | T | 1 | a0001c0001t0036g0250 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.42+7871C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8509851 | ||||||
| chr3:8509963
|
A | G | 24 | a0001c0001t0001g0306a0001c0001t0002g0214a0001c0001t0002g0224others(21): Show | 24 | HG00423.hp1 HG02109.hp2 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.42+7983A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8509963 | ||||||
| chr3:8510059
|
T | C | 22 | a0001c0001t0001g0306a0001c0001t0002g0214a0001c0001t0002g0224others(19): Show | 22 | HG00423.hp1 HG02109.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.42+8079T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8510059 | ||||||
| chr3:8510164
|
C | A | 1 | a0001c0001t0002g0032 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.42+8184C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8510164 | ||||||
| chr3:8510193
|
C | T | 7 | a0001c0001t0001g0280a0001c0001t0003g0277a0001c0001t0049g0279others(4): Show | 8 | HG00099.hp2 HG00642.hp1 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.42+8213C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8510193 | ||||||
| chr3:8510349
|
A | G | 1 | a0001c0001t0003g0276 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.42+8369A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8510349 | ||||||
| chr3:8510352
|
G | C | 23 | a0001c0001t0001g0306a0001c0001t0002g0214a0001c0001t0002g0224others(20): Show | 23 | HG00423.hp1 HG02109.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.42+8372G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8510352 | ||||||
| chr3:8510539
|
T | G | 2 | a0001c0001t0001g0016a0001c0001t0001g0197 | 2 | NA18984.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.42+8559T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8510539 | ||||||
| chr3:8510571
|
C | T | 1 | a0001c0002t0001g0227 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.42+8591C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8510571 | ||||||
| chr3:8510754
|
A | G | 1 | a0001c0001t0046g0168 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.42+8774A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8510754 | ||||||
| chr3:8510866
|
A | G | 1 | a0001c0001t0006g0096 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.42+8886A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8510866 | ||||||
| chr3:8510953
|
C | T | 2 | a0001c0002t0002g0239a0001c0002t0002g0240 | 2 | HG02698.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.42+8973C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8510953 | ||||||
| chr3:8511076
|
C | T | 2 | a0001c0001t0004g0178a0001c0001t0005g0229 | 2 | HG02258.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.42+9096C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8511076 | ||||||
| chr3:8511401
|
T | C | 94 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(91): Show | 96 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.42+9421T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8511401 | ||||||
| chr3:8511455
|
T | C | 6 | a0001c0002t0001g0227a0001c0002t0005g0226a0001c0002t0008g0156others(3): Show | 6 | HG02109.hp1 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.42+9475T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8511455 | ||||||
| chr3:8511552
|
G | A | 94 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(91): Show | 96 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.42+9572G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8511552 | ||||||
| chr3:8511681
|
A | G | 1 | a0001c0001t0002g0243 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.42+9701A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8511681 | ||||||
| chr3:8511932
|
T | C | 1 | a0001c0002t0001g0245 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.42+9952T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8511932 | ||||||
| chr3:8511977
|
T | C | 1 | a0001c0001t0001g0071 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.42+9997T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8511977 | ||||||
| chr3:8512305
|
C | G | 14 | a0001c0001t0001g0306a0001c0001t0002g0214a0001c0001t0003g0221others(11): Show | 14 | HG00423.hp1 HG02258.hp2 HG02735.hp2 others(11): Show |
intron_variant | MODIFIER | c.42+10325C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8512305 | ||||||
| chr3:8512345
|
C | T | 3 | a0001c0001t0002g0224a0001c0002t0002g0157a0001c0002t0004g0207 | 3 | HG02109.hp2 HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.42+10365C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8512345 | ||||||
| chr3:8512366
|
A | G | 12 | a0001c0001t0001g0306a0001c0001t0002g0214a0001c0001t0003g0221others(9): Show | 12 | HG00423.hp1 HG02735.hp2 HG03017.hp1 others(9): Show |
intron_variant | MODIFIER | c.42+10386A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8512366 | ||||||
| chr3:8512600
|
G | A | 17 | a0001c0001t0001g0306a0001c0001t0002g0214a0001c0001t0002g0224others(14): Show | 17 | HG00423.hp1 HG02109.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.42+10620G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8512600 | ||||||
| chr3:8512617
|
C | T | 67 | a0001c0001t0001g0209a0001c0001t0001g0247a0001c0001t0001g0254others(64): Show | 69 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.42+10637C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8512617 | ||||||
| chr3:8512840
|
A | G | 1 | a0007c0007t0025g0167 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.42+10860A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8512840 | ||||||
| chr3:8512948
|
T | C | 11 | a0001c0001t0001g0306a0001c0001t0002g0214a0001c0001t0003g0221others(8): Show | 11 | HG00423.hp1 HG02735.hp2 HG03017.hp1 others(8): Show |
intron_variant | MODIFIER | c.42+10968T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8512948 | ||||||
| chr3:8513024
|
A | G | 297 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(294): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.42+11044A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8513024 | ||||||
| chr3:8513603
|
T | C | 1 | a0001c0001t0003g0018 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.42+11623T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8513603 | ||||||
| chr3:8513821
|
A | C | 68 | a0001c0001t0001g0209a0001c0001t0001g0247a0001c0001t0001g0254others(65): Show | 70 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.42+11841A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8513821 | ||||||
| chr3:8514104
|
G | GATAC | 4 | a0001c0001t0002g0152a0001c0001t0015g0222a0001c0001t0015g0223others(1): Show | 4 | HG00673.hp2 HG02622.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.42+12144_42+12147d others(6): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8514104 | |||||
| chr3:8514211
|
C | T | 3 | a0001c0001t0002g0224a0001c0002t0002g0157a0001c0002t0004g0207 | 3 | HG02109.hp2 HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.42+12231C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8514211 | ||||||
| chr3:8514302
|
C | A | 12 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(9): Show | 12 | HG01081.hp1 HG02145.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.42+12322C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8514302 | ||||||
| chr3:8514391
|
A | G | 2 | a0001c0002t0002g0239a0001c0002t0002g0240 | 2 | HG02698.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.42+12411A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8514391 | ||||||
| chr3:8514511
|
G | A | 1 | a0001c0001t0042g0175 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.42+12531G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8514511 | ||||||
| chr3:8514567
|
T | G | 1 | a0001c0001t0004g0072 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.42+12587T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8514567 | ||||||
| chr3:8514625
|
G | A | 1 | a0001c0001t0021g0067 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.42+12645G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8514625 | ||||||
| chr3:8514694
|
A | T | 2 | a0001c0001t0004g0178a0001c0001t0005g0229 | 2 | HG02258.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.42+12714A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8514694 | ||||||
| chr3:8514754
|
G | A | 6 | a0001c0002t0001g0227a0001c0002t0005g0226a0001c0002t0008g0156others(3): Show | 6 | HG02109.hp1 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.42+12774G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8514754 | ||||||
| chr3:8514764
|
C | T | 1 | a0001c0001t0003g0275 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.42+12784C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8514764 | ||||||
| chr3:8514931
|
A | G | 76 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(73): Show | 78 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.42+12951A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8514931 | ||||||
| chr3:8514963
|
C | T | 6 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(3): Show | 6 | HG02145.hp2 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.42+12983C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8514963 | ||||||
| chr3:8514985
|
T | G | 47 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0306others(44): Show | 49 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.42+13005T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8514985 | ||||||
| chr3:8514987
|
C | T | 1 | a0001c0001t0003g0198 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.42+13007C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8514987 | ||||||
| chr3:8515067
|
G | A | 1 | a0001c0001t0002g0056 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.42+13087G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8515067 | ||||||
| chr3:8515098
|
A | C | 81 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(78): Show | 83 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.42+13118A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8515098 | ||||||
| chr3:8515146
|
G | A | 14 | a0001c0001t0001g0306a0001c0001t0002g0214a0001c0001t0002g0224others(11): Show | 14 | HG00423.hp1 HG02280.hp2 HG02735.hp2 others(11): Show |
intron_variant | MODIFIER | c.42+13166G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8515146 | ||||||
| chr3:8515199
|
T | C | 3 | a0001c0001t0002g0224a0001c0002t0002g0157a0001c0002t0004g0207 | 3 | HG02109.hp2 HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.42+13219T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8515199 | ||||||
| chr3:8515223
|
T | C | 95 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(92): Show | 97 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.42+13243T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8515223 | ||||||
| chr3:8515431
|
C | A | 85 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(82): Show | 87 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.42+13451C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8515431 | ||||||
| chr3:8515547
|
A | G | 3 | a0001c0001t0001g0185a0001c0001t0004g0178a0001c0002t0004g0207 | 3 | HG02109.hp2 HG02258.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.42+13567A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8515547 | ||||||
| chr3:8515873
|
T | C | 95 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(92): Show | 97 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.42+13893T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8515873 | ||||||
| chr3:8516002
|
C | T | 106 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(103): Show | 108 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.42+14022C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8516002 | ||||||
| chr3:8516160
|
A | G | 67 | a0001c0001t0001g0053a0001c0001t0001g0170a0001c0001t0001g0209others(64): Show | 69 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.42+14180A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8516160 | ||||||
| chr3:8516189
|
T | A | 97 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(94): Show | 99 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.42+14209T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8516189 | ||||||
| chr3:8516306
|
A | G | 42 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(39): Show | 42 | HG00423.hp1 HG01069.hp1 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.42+14326A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8516306 | ||||||
| chr3:8516310
|
G | A | 57 | a0001c0001t0001g0053a0001c0001t0001g0209a0001c0001t0001g0247others(54): Show | 59 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.42+14330G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8516310 | ||||||
| chr3:8516400
|
A | G | 9 | a0001c0002t0001g0227a0001c0002t0001g0245a0001c0002t0002g0157others(6): Show | 9 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.42+14420A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8516400 | ||||||
| chr3:8516428
|
C | G | 14 | a0001c0001t0001g0170a0001c0001t0001g0182a0001c0001t0001g0185others(11): Show | 14 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.42+14448C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8516428 | ||||||
| chr3:8516429
|
TG | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0027 | 3 | HG01256.hp1 HG01934.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.42+14451delG | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8516429 | |||||
| chr3:8516508
|
T | C | 14 | a0001c0001t0001g0170a0001c0001t0001g0182a0001c0001t0001g0185others(11): Show | 14 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.42+14528T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8516508 | ||||||
| chr3:8516527
|
C | T | 14 | a0001c0001t0001g0170a0001c0001t0001g0182a0001c0001t0001g0185others(11): Show | 14 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.42+14547C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8516527 | ||||||
| chr3:8516614
|
G | A | 14 | a0001c0001t0001g0170a0001c0001t0001g0182a0001c0001t0001g0185others(11): Show | 14 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.42+14634G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8516614 | ||||||
| chr3:8516699
|
A | G | 14 | a0001c0001t0001g0170a0001c0001t0001g0182a0001c0001t0001g0185others(11): Show | 14 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.42+14719A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8516699 | ||||||
| chr3:8516829
|
T | C | 57 | a0001c0001t0001g0053a0001c0001t0001g0209a0001c0001t0001g0247others(54): Show | 59 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.42+14849T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8516829 | ||||||
| chr3:8516918
|
T | G | 14 | a0001c0001t0001g0170a0001c0001t0001g0182a0001c0001t0001g0185others(11): Show | 14 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.42+14938T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8516918 | ||||||
| chr3:8516968
|
G | A | 1 | a0001c0002t0002g0157 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.42+14988G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8516968 | ||||||
| chr3:8517054
|
C | T | 1 | a0001c0001t0002g0052 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.42+15074C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8517054 | ||||||
| chr3:8517137
|
G | A | 14 | a0001c0001t0001g0170a0001c0001t0001g0182a0001c0001t0001g0185others(11): Show | 14 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.42+15157G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8517137 | ||||||
| chr3:8517150
|
G | A | 14 | a0001c0001t0001g0170a0001c0001t0001g0182a0001c0001t0001g0185others(11): Show | 14 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.42+15170G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8517150 | ||||||
| chr3:8517155
|
A | T | 3 | a0001c0001t0003g0275a0001c0001t0003g0283a0001c0001t0047g0274 | 3 | HG00642.hp2 HG01346.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.42+15175A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8517155 | ||||||
| chr3:8517368
|
T | C | 1 | a0001c0001t0002g0033 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.43-15369T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8517368 | ||||||
| chr3:8517370
|
G | A | 3 | a0001c0001t0001g0257a0001c0002t0002g0158a0010c0011t0001g0256 | 3 | HG01081.hp1 HG02965.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.43-15367G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8517370 | ||||||
| chr3:8517477
|
C | T | 14 | a0001c0001t0001g0170a0001c0001t0001g0182a0001c0001t0001g0185others(11): Show | 14 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.43-15260C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8517477 | ||||||
| chr3:8517528
|
T | C | 2 | a0001c0001t0002g0238a0001c0001t0003g0234 | 2 | HG02056.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.43-15209T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8517528 | ||||||
| chr3:8517604
|
C | T | 6 | a0001c0001t0001g0280a0001c0001t0049g0279a0001c0002t0001g0008others(3): Show | 7 | HG00099.hp2 HG00642.hp1 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.43-15133C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8517604 | ||||||
| chr3:8517833
|
T | G | 1 | a0001c0001t0038g0117 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.43-14904T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8517833 | ||||||
| chr3:8517959
|
T | C | 14 | a0001c0001t0001g0170a0001c0001t0001g0182a0001c0001t0001g0185others(11): Show | 14 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.43-14778T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8517959 | ||||||
| chr3:8518052
|
GA | G | 14 | a0001c0001t0001g0170a0001c0001t0001g0182a0001c0001t0001g0185others(11): Show | 14 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.43-14674delA | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8518052 | |||||
| chr3:8518132
|
G | T | 1 | a0001c0001t0003g0221 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.43-14605G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8518132 | ||||||
| chr3:8518167
|
C | A | 14 | a0001c0001t0001g0170a0001c0001t0001g0182a0001c0001t0001g0185others(11): Show | 14 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.43-14570C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8518167 | ||||||
| chr3:8518170
|
A | G | 57 | a0001c0001t0001g0053a0001c0001t0001g0209a0001c0001t0001g0247others(54): Show | 59 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.43-14567A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8518170 | ||||||
| chr3:8518368
|
G | A | 76 | a0001c0001t0001g0053a0001c0001t0001g0170a0001c0001t0001g0182others(73): Show | 78 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.43-14369G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8518368 | ||||||
| chr3:8518452
|
T | C | 14 | a0001c0001t0001g0170a0001c0001t0001g0182a0001c0001t0001g0185others(11): Show | 14 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.43-14285T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8518452 | ||||||
| chr3:8518482
|
C | T | 1 | a0005c0006t0001g0225 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.43-14255C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8518482 | ||||||
| chr3:8518610
|
A | G | 7 | a0001c0002t0001g0227a0001c0002t0001g0245a0001c0002t0002g0157others(4): Show | 7 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.43-14127A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8518610 | ||||||
| chr3:8518637
|
C | T | 2 | a0001c0002t0002g0239a0001c0002t0002g0240 | 2 | HG02698.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.43-14100C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8518637 | ||||||
| chr3:8518724
|
A | C | 14 | a0001c0001t0001g0170a0001c0001t0001g0182a0001c0001t0001g0185others(11): Show | 14 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.43-14013A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8518724 | ||||||
| chr3:8518761
|
A | C | 14 | a0001c0001t0001g0306a0001c0001t0002g0214a0001c0001t0004g0215others(11): Show | 14 | HG00423.hp1 HG01069.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.43-13976A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8518761 | ||||||
| chr3:8518783
|
G | A | 1 | a0001c0001t0001g0306 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.43-13954G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8518783 | ||||||
| chr3:8519007
|
A | T | 1 | a0001c0002t0001g0216 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.43-13730A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8519007 | ||||||
| chr3:8519096
|
G | C | 27 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(24): Show | 27 | HG00423.hp1 HG01069.hp1 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.43-13641G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8519096 | ||||||
| chr3:8519125
|
C | T | 1 | a0001c0001t0001g0280 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.43-13612C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8519125 | ||||||
| chr3:8519195
|
A | G | 12 | a0001c0001t0001g0140a0001c0001t0001g0144a0001c0001t0001g0197others(9): Show | 12 | HG00735.hp2 HG02074.hp2 HG02293.hp1 others(9): Show |
intron_variant | MODIFIER | c.43-13542A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8519195 | ||||||
| chr3:8519371
|
A | T | 1 | a0001c0001t0004g0178 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.43-13366A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8519371 | ||||||
| chr3:8519409
|
T | C | 1 | a0001c0001t0010g0073 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.43-13328T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8519409 | ||||||
| chr3:8519454
|
C | T | 14 | a0001c0001t0001g0170a0001c0001t0001g0182a0001c0001t0001g0185others(11): Show | 14 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.43-13283C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8519454 | ||||||
| chr3:8519585
|
C | T | 14 | a0001c0001t0001g0170a0001c0001t0001g0182a0001c0001t0001g0185others(11): Show | 14 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.43-13152C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8519585 | ||||||
| chr3:8519740
|
G | A | 1 | a0001c0001t0001g0209 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.43-12997G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8519740 | ||||||
| chr3:8519741
|
C | CA | 8 | a0001c0001t0001g0026a0001c0001t0001g0140a0001c0001t0001g0162others(5): Show | 8 | HG00639.hp2 HG02615.hp1 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.43-12983dupA | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8519741 | |||||
| chr3:8519741
|
CA | C | 25 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(22): Show | 25 | HG00423.hp1 HG01069.hp1 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.43-12983delA | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8519741 | |||||
| chr3:8519750
|
A | G | 2 | a0001c0001t0003g0188a0001c0001t0003g0189 | 2 | HG00140.hp1 HG00639.hp1 |
intron_variant | MODIFIER | c.43-12987A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8519750 | ||||||
| chr3:8519753
|
AAG | A | 12 | a0001c0001t0001g0170a0001c0001t0001g0182a0001c0001t0001g0185others(9): Show | 12 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.43-12982_43-12981d others(4): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8519753 | |||||
| chr3:8519852
|
TTTACCAT others(6): Show |
T | 1 | a0001c0002t0003g0174 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.43-12883_43-12871d others(15): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8519852 | |||||
| chr3:8519907
|
C | CGTGTGTG others(1): Show |
3 | a0001c0001t0001g0185a0001c0001t0003g0183a0001c0001t0014g0184 | 3 | HG02647.hp1 HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.43-12826_43-12819d others(10): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8519907 | |||||
| chr3:8519917
|
T | TGTGTGTG others(3): Show |
2 | a0001c0001t0001g0170a0001c0001t0001g0182 | 2 | HG02486.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.43-12819_43-12818i others(12): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8519917 | |||||
| chr3:8519917
|
T | TGTGTGTG others(5): Show |
2 | a0001c0002t0002g0239a0001c0002t0002g0240 | 2 | HG02698.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.43-12819_43-12818i others(14): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8519917 | |||||
| chr3:8519917
|
T | TGTGTGTG others(7): Show |
7 | a0001c0002t0001g0227a0001c0002t0001g0245a0001c0002t0002g0157others(4): Show | 7 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.43-12819_43-12818i others(16): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8519917 | |||||
| chr3:8519925
|
A | AGT | 15 | a0001c0001t0001g0306a0001c0001t0002g0214a0001c0001t0004g0215others(12): Show | 15 | HG00423.hp1 HG01069.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.43-12793_43-12792d others(4): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8519925 | |||||
| chr3:8519925
|
A | AGTGT | 5 | a0001c0001t0001g0290a0001c0001t0002g0241a0001c0001t0002g0242others(2): Show | 5 | HG02572.hp1 HG03139.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.43-12795_43-12792d others(6): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8519925 | |||||
| chr3:8519925
|
A | T | 7 | a0001c0002t0001g0227a0001c0002t0001g0245a0001c0002t0002g0157others(4): Show | 7 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.43-12812A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8519925 | ||||||
| chr3:8519927
|
T | A | 7 | a0001c0001t0001g0170a0001c0001t0001g0182a0001c0001t0001g0185others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.43-12810T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8519927 | ||||||
| chr3:8519929
|
T | A | 5 | a0001c0001t0001g0170a0001c0001t0001g0182a0001c0001t0001g0185others(2): Show | 5 | HG02486.hp1 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.43-12808T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8519929 | ||||||
| chr3:8519966
|
T | A | 14 | a0001c0001t0001g0170a0001c0001t0001g0182a0001c0001t0001g0185others(11): Show | 14 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.43-12771T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8519966 | ||||||
| chr3:8520046
|
T | C | 61 | a0001c0001t0001g0015a0001c0001t0001g0053a0001c0001t0001g0071others(58): Show | 63 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.43-12691T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8520046 | ||||||
| chr3:8520260
|
A | G | 1 | a0001c0001t0002g0203 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.43-12477A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8520260 | ||||||
| chr3:8520324
|
T | C | 15 | a0001c0001t0001g0170a0001c0001t0001g0182a0001c0001t0001g0185others(12): Show | 15 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.43-12413T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8520324 | ||||||
| chr3:8520360
|
A | G | 14 | a0001c0001t0001g0170a0001c0001t0001g0182a0001c0001t0001g0185others(11): Show | 14 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.43-12377A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8520360 | ||||||
| chr3:8520606
|
G | C | 14 | a0001c0001t0001g0170a0001c0001t0001g0182a0001c0001t0001g0185others(11): Show | 14 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.43-12131G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8520606 | ||||||
| chr3:8520837
|
T | A | 14 | a0001c0001t0001g0170a0001c0001t0001g0182a0001c0001t0001g0185others(11): Show | 14 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.43-11900T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8520837 | ||||||
| chr3:8520951
|
A | G | 64 | a0001c0001t0001g0053a0001c0001t0001g0209a0001c0001t0001g0247others(61): Show | 66 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.43-11786A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8520951 | ||||||
| chr3:8521058
|
G | A | 2 | a0001c0001t0003g0248a0001c0001t0044g0249 | 2 | HG00597.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.43-11679G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8521058 | ||||||
| chr3:8521081
|
C | T | 1 | a0001c0001t0003g0114 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.43-11656C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8521081 | ||||||
| chr3:8521370
|
T | G | 1 | a0001c0002t0019g0220 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.43-11367T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8521370 | ||||||
| chr3:8521458
|
C | A | 24 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(21): Show | 24 | HG00423.hp1 HG01069.hp1 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.43-11279C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8521458 | ||||||
| chr3:8521462
|
C | T | 1 | a0001c0001t0004g0288 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.43-11275C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8521462 | ||||||
| chr3:8521514
|
G | A | 4 | a0001c0002t0001g0193a0001c0002t0001g0194a0001c0002t0001g0195others(1): Show | 4 | HG01069.hp1 HG01071.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.43-11223G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8521514 | ||||||
| chr3:8521558
|
C | A | 2 | a0001c0002t0001g0069a0001c0002t0003g0174 | 2 | HG02735.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.43-11179C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8521558 | ||||||
| chr3:8521582
|
T | C | 1 | a0001c0001t0034g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.43-11155T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8521582 | ||||||
| chr3:8521715
|
T | A | 14 | a0001c0001t0001g0170a0001c0001t0001g0182a0001c0001t0001g0185others(11): Show | 14 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.43-11022T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8521715 | ||||||
| chr3:8521743
|
T | C | 14 | a0001c0001t0001g0170a0001c0001t0001g0182a0001c0001t0001g0185others(11): Show | 14 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.43-10994T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8521743 | ||||||
| chr3:8521755
|
C | A | 1 | a0001c0002t0002g0157 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.43-10982C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8521755 | ||||||
| chr3:8521769
|
A | C | 59 | a0001c0001t0001g0053a0001c0001t0001g0209a0001c0001t0001g0247others(56): Show | 61 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.43-10968A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8521769 | ||||||
| chr3:8521791
|
G | A | 107 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(104): Show | 109 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.43-10946G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8521791 | ||||||
| chr3:8521825
|
G | A | 1 | a0001c0001t0004g0178 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.43-10912G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8521825 | ||||||
| chr3:8521891
|
G | T | 14 | a0001c0001t0001g0170a0001c0001t0001g0182a0001c0001t0001g0185others(11): Show | 14 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.43-10846G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8521891 | ||||||
| chr3:8521898
|
GT | G | 4 | a0001c0001t0001g0228a0001c0001t0004g0178a0001c0001t0021g0067others(1): Show | 4 | HG02258.hp2 HG02615.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.43-10831delT | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8521898 | |||||
| chr3:8521977
|
A | G | 9 | a0001c0002t0001g0227a0001c0002t0001g0245a0001c0002t0002g0157others(6): Show | 9 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.43-10760A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8521977 | ||||||
| chr3:8521987
|
A | G | 14 | a0001c0001t0001g0170a0001c0001t0001g0182a0001c0001t0001g0185others(11): Show | 14 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.43-10750A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8521987 | ||||||
| chr3:8522071
|
G | A | 1 | a0001c0001t0001g0075 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.43-10666G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8522071 | ||||||
| chr3:8522396
|
C | G | 9 | a0001c0002t0001g0227a0001c0002t0001g0245a0001c0002t0002g0157others(6): Show | 9 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.43-10341C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8522396 | ||||||
| chr3:8522439
|
G | A | 9 | a0001c0002t0001g0227a0001c0002t0001g0245a0001c0002t0002g0157others(6): Show | 9 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.43-10298G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8522439 | ||||||
| chr3:8522749
|
G | A | 1 | a0001c0001t0034g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.43-9988G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8522749 | ||||||
| chr3:8522809
|
TTTAAAAA | T | 6 | a0001c0002t0001g0227a0001c0002t0001g0245a0001c0002t0005g0226others(3): Show | 6 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.43-9915_43-9909del others(7): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8522809 | |||||
| chr3:8522964
|
C | T | 14 | a0001c0001t0001g0306a0001c0001t0002g0214a0001c0001t0004g0215others(11): Show | 14 | HG00423.hp1 HG01069.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.43-9773C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8522964 | ||||||
| chr3:8523011
|
A | G | 1 | a0001c0001t0002g0111 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.43-9726A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8523011 | ||||||
| chr3:8523253
|
T | C | 61 | a0001c0001t0001g0053a0001c0001t0001g0209a0001c0001t0001g0247others(58): Show | 63 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.43-9484T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8523253 | ||||||
| chr3:8523577
|
A | G | 61 | a0001c0001t0001g0053a0001c0001t0001g0209a0001c0001t0001g0247others(58): Show | 63 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.43-9160A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8523577 | ||||||
| chr3:8523835
|
A | C | 25 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(22): Show | 25 | HG00423.hp1 HG01069.hp1 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.43-8902A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8523835 | ||||||
| chr3:8524018
|
A | G | 1 | a0001c0001t0003g0050 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.43-8719A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8524018 | ||||||
| chr3:8524074
|
T | G | 1 | a0001c0001t0002g0179 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.43-8663T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8524074 | ||||||
| chr3:8524200
|
G | GA | 8 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0254others(5): Show | 8 | HG02055.hp1 HG02055.hp2 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.43-8517dupA | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8524200 | |||||
| chr3:8524201
|
A | G | 1 | a0001c0001t0007g0301 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.43-8536A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8524201 | ||||||
| chr3:8524465
|
A | G | 1 | a0001c0001t0004g0288 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.43-8272A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8524465 | ||||||
| chr3:8524602
|
A | G | 1 | a0001c0001t0012g0020 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.43-8135A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8524602 | ||||||
| chr3:8524681
|
A | G | 75 | a0001c0001t0001g0053a0001c0001t0001g0170a0001c0001t0001g0182others(72): Show | 77 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.43-8056A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8524681 | ||||||
| chr3:8524687
|
C | CTGTTGT | 75 | a0001c0001t0001g0053a0001c0001t0001g0170a0001c0001t0001g0182others(72): Show | 77 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.43-8038_43-8033dup others(6): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8524687 | |||||
| chr3:8524925
|
G | T | 75 | a0001c0001t0001g0053a0001c0001t0001g0170a0001c0001t0001g0182others(72): Show | 77 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.43-7812G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8524925 | ||||||
| chr3:8524969
|
G | A | 12 | a0001c0002t0001g0227a0001c0002t0001g0245a0001c0002t0002g0157others(9): Show | 12 | HG01081.hp1 HG01169.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.43-7768G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8524969 | ||||||
| chr3:8525075
|
A | T | 75 | a0001c0001t0001g0053a0001c0001t0001g0170a0001c0001t0001g0182others(72): Show | 77 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.43-7662A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8525075 | ||||||
| chr3:8525159
|
T | C | 75 | a0001c0001t0001g0053a0001c0001t0001g0170a0001c0001t0001g0182others(72): Show | 77 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.43-7578T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8525159 | ||||||
| chr3:8525165
|
C | G | 1 | a0007c0007t0025g0167 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.43-7572C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8525165 | ||||||
| chr3:8525569
|
T | G | 78 | a0001c0001t0001g0053a0001c0001t0001g0170a0001c0001t0001g0182others(75): Show | 80 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.43-7168T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8525569 | ||||||
| chr3:8525754
|
C | T | 1 | a0001c0001t0003g0005 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.43-6983C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8525754 | ||||||
| chr3:8525874
|
T | G | 77 | a0001c0001t0001g0053a0001c0001t0001g0170a0001c0001t0001g0182others(74): Show | 79 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.43-6863T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8525874 | ||||||
| chr3:8526189
|
A | G | 1 | a0001c0001t0003g0237 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.43-6548A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8526189 | ||||||
| chr3:8526250
|
G | A | 5 | a0001c0001t0001g0170a0001c0001t0001g0182a0001c0001t0001g0185others(2): Show | 5 | HG02486.hp1 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.43-6487G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8526250 | ||||||
| chr3:8526257
|
G | A | 1 | a0001c0001t0003g0252 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.43-6480G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8526257 | ||||||
| chr3:8526495
|
CAGTT | C | 76 | a0001c0001t0001g0053a0001c0001t0001g0170a0001c0001t0001g0182others(73): Show | 78 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.43-6236_43-6233del others(4): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8526495 | |||||
| chr3:8526640
|
T | C | 1 | a0001c0001t0002g0203 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.43-6097T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8526640 | ||||||
| chr3:8526782
|
A | G | 77 | a0001c0001t0001g0053a0001c0001t0001g0170a0001c0001t0001g0182others(74): Show | 79 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.43-5955A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8526782 | ||||||
| chr3:8526940
|
G | A | 10 | a0001c0001t0001g0247a0001c0001t0001g0259a0001c0001t0001g0260others(7): Show | 12 | HG00099.hp2 HG00642.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.43-5797G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8526940 | ||||||
| chr3:8527236
|
C | A | 8 | a0001c0001t0001g0016a0001c0001t0001g0075a0001c0001t0001g0176others(5): Show | 8 | HG00544.hp2 HG02165.hp2 NA18977.hp1 others(5): Show |
intron_variant | MODIFIER | c.43-5501C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8527236 | ||||||
| chr3:8527270
|
T | C | 76 | a0001c0001t0001g0053a0001c0001t0001g0170a0001c0001t0001g0182others(73): Show | 78 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.43-5467T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8527270 | ||||||
| chr3:8527284
|
C | G | 7 | a0001c0002t0001g0227a0001c0002t0001g0245a0001c0002t0002g0157others(4): Show | 7 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.43-5453C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8527284 | ||||||
| chr3:8527291
|
T | C | 76 | a0001c0001t0001g0053a0001c0001t0001g0170a0001c0001t0001g0182others(73): Show | 78 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.43-5446T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8527291 | ||||||
| chr3:8527376
|
G | C | 5 | a0001c0001t0001g0170a0001c0001t0001g0182a0001c0001t0001g0185others(2): Show | 5 | HG02486.hp1 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.43-5361G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8527376 | ||||||
| chr3:8527436
|
G | T | 2 | a0001c0001t0002g0152a0001c0001t0016g0151 | 2 | HG00673.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.43-5301G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8527436 | ||||||
| chr3:8527446
|
G | A | 4 | a0001c0002t0002g0158a0001c0002t0004g0177a0001c0002t0004g0207others(1): Show | 4 | HG01081.hp1 HG02109.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.43-5291G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8527446 | ||||||
| chr3:8527508
|
A | G | 76 | a0001c0001t0001g0053a0001c0001t0001g0170a0001c0001t0001g0182others(73): Show | 78 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.43-5229A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8527508 | ||||||
| chr3:8527523
|
T | C | 108 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(105): Show | 110 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.43-5214T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8527523 | ||||||
| chr3:8527649
|
T | C | 4 | a0001c0001t0003g0023a0001c0001t0003g0024a0001c0001t0003g0040others(1): Show | 4 | HG01255.hp2 HG02698.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.43-5088T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8527649 | ||||||
| chr3:8527675
|
C | T | 3 | a0001c0002t0002g0157a0001c0002t0002g0239a0001c0002t0002g0240 | 3 | HG02280.hp2 HG02698.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.43-5062C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8527675 | ||||||
| chr3:8527711
|
C | T | 6 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(3): Show | 6 | HG02145.hp2 HG02559.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.43-5026C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8527711 | ||||||
| chr3:8527798
|
T | C | 301 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(298): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.43-4939T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8527798 | ||||||
| chr3:8527888
|
G | C | 1 | a0002c0003t0001g0231 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.43-4849G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8527888 | ||||||
| chr3:8527905
|
T | C | 1 | a0001c0001t0009g0098 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.43-4832T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8527905 | ||||||
| chr3:8527939
|
A | G | 15 | a0001c0001t0001g0306a0001c0001t0026g0057a0001c0001t0027g0074others(12): Show | 15 | HG00423.hp1 HG01069.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.43-4798A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8527939 | ||||||
| chr3:8528107
|
G | A | 20 | a0001c0001t0001g0209a0001c0001t0001g0261a0001c0001t0001g0263others(17): Show | 20 | HG00099.hp1 HG00642.hp2 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.43-4630G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8528107 | ||||||
| chr3:8528315
|
A | G | 1 | a0002c0003t0001g0231 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.43-4422A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8528315 | ||||||
| chr3:8528352
|
G | GT | 33 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(30): Show | 33 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.43-4376dupT | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8528352 | |||||
| chr3:8528352
|
GT | G | 76 | a0001c0001t0001g0002a0001c0001t0001g0053a0001c0001t0001g0170others(73): Show | 79 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.43-4376delT | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 8528352 | |||||
| chr3:8528359
|
T | G | 2 | a0001c0001t0010g0041a0001c0001t0010g0073 | 2 | NA18965.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.43-4378T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8528359 | ||||||
| chr3:8528374
|
C | T | 76 | a0001c0001t0001g0002a0001c0001t0001g0053a0001c0001t0001g0170others(73): Show | 79 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.43-4363C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8528374 | ||||||
| chr3:8528386
|
G | A | 1 | a0001c0002t0002g0157 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.43-4351G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8528386 | ||||||
| chr3:8528704
|
G | A | 76 | a0001c0001t0001g0002a0001c0001t0001g0053a0001c0001t0001g0170others(73): Show | 79 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.43-4033G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8528704 | ||||||
| chr3:8528740
|
C | T | 76 | a0001c0001t0001g0002a0001c0001t0001g0053a0001c0001t0001g0170others(73): Show | 79 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.43-3997C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8528740 | ||||||
| chr3:8528760
|
C | T | 1 | a0001c0001t0001g0306 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.43-3977C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8528760 | ||||||
| chr3:8528856
|
G | C | 1 | a0001c0001t0031g0066 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.43-3881G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8528856 | ||||||
| chr3:8528991
|
G | T | 5 | a0001c0001t0001g0170a0001c0001t0001g0182a0001c0001t0001g0185others(2): Show | 5 | HG02486.hp1 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.43-3746G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8528991 | ||||||
| chr3:8529188
|
A | G | 76 | a0001c0001t0001g0002a0001c0001t0001g0053a0001c0001t0001g0170others(73): Show | 79 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.43-3549A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8529188 | ||||||
| chr3:8529309
|
G | A | 2 | a0001c0001t0014g0294a0001c0001t0052g0293 | 2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.43-3428G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8529309 | ||||||
| chr3:8529424
|
G | A | 57 | a0001c0001t0001g0002a0001c0001t0001g0053a0001c0001t0001g0209others(54): Show | 60 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.43-3313G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8529424 | ||||||
| chr3:8529451
|
G | A | 1 | a0001c0001t0003g0058 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.43-3286G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8529451 | ||||||
| chr3:8529471
|
G | GA | 93 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(90): Show | 96 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.43-3266_43-3265ins others(1): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8529471 | ||||||
| chr3:8529499
|
C | T | 1 | a0001c0002t0002g0157 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.43-3238C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8529499 | ||||||
| chr3:8529532
|
C | T | 1 | a0001c0001t0004g0288 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.43-3205C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8529532 | ||||||
| chr3:8529535
|
C | T | 1 | a0001c0001t0003g0221 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.43-3202C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8529535 | ||||||
| chr3:8529548
|
G | A | 2 | a0001c0002t0002g0239a0001c0002t0002g0240 | 2 | HG02698.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.43-3189G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8529548 | ||||||
| chr3:8529802
|
C | A | 1 | a0001c0002t0004g0207 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.43-2935C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8529802 | ||||||
| chr3:8529965
|
C | T | 6 | a0001c0002t0001g0245a0001c0002t0002g0157a0001c0002t0005g0226others(3): Show | 6 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.43-2772C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8529965 | ||||||
| chr3:8530124
|
A | C | 1 | a0001c0001t0001g0254 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.43-2613A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8530124 | ||||||
| chr3:8530246
|
G | C | 1 | a0001c0001t0003g0289 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.43-2491G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8530246 | ||||||
| chr3:8530402
|
C | G | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(92): Show | 98 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.43-2335C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8530402 | ||||||
| chr3:8530687
|
G | A | 101 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(98): Show | 104 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.43-2050G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8530687 | ||||||
| chr3:8531086
|
G | T | 1 | a0001c0001t0001g0093 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.43-1651G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8531086 | ||||||
| chr3:8531150
|
A | G | 4 | a0001c0002t0002g0158a0001c0002t0004g0177a0001c0002t0004g0207others(1): Show | 4 | HG01081.hp1 HG02109.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.43-1587A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8531150 | ||||||
| chr3:8531343
|
C | T | 16 | a0001c0001t0001g0306a0001c0001t0026g0057a0001c0001t0027g0074others(13): Show | 16 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.43-1394C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8531343 | ||||||
| chr3:8531409
|
T | C | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(255): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.43-1328T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8531409 | ||||||
| chr3:8531482
|
C | T | 2 | a0001c0001t0003g0188a0001c0001t0003g0189 | 2 | HG00140.hp1 HG00639.hp1 |
intron_variant | MODIFIER | c.43-1255C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8531482 | ||||||
| chr3:8531578
|
T | C | 1 | a0001c0001t0002g0121 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.43-1159T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8531578 | ||||||
| chr3:8531957
|
T | G | 2 | a0001c0002t0002g0239a0001c0002t0002g0240 | 2 | HG02698.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.43-780T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8531957 | ||||||
| chr3:8532296
|
G | A | 1 | a0001c0001t0018g0122 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.43-441G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8532296 | ||||||
| chr3:8532320
|
C | T | 1 | a0001c0001t0001g0075 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.43-417C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8532320 | ||||||
| chr3:8532360
|
C | G | 1 | a0001c0001t0003g0135 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.43-377C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8532360 | ||||||
| chr3:8532406
|
G | A | 3 | a0001c0001t0010g0041a0001c0001t0010g0073a0005c0006t0001g0225 | 3 | NA18522.hp1 NA18965.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.43-331G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8532406 | ||||||
| chr3:8532444
|
G | A | 1 | a0001c0001t0003g0277 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.43-293G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8532444 | ||||||
| chr3:8532549
|
C | G | 1 | a0001c0001t0004g0288 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.43-188C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8532549 | ||||||
| chr3:8532686
|
C | T | 1 | a0001c0001t0002g0032 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.43-51C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 1/5 | chr3 | 8532686 | ||||||
| chr3:8532927
|
G | C | 5 | a0001c0001t0001g0170a0001c0001t0001g0182a0001c0001t0001g0185others(2): Show | 5 | HG02486.hp1 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.131+102G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8532927 | ||||||
| chr3:8533166
|
G | T | 1 | a0001c0001t0001g0265 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.131+341G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8533166 | ||||||
| chr3:8533397
|
A | G | 1 | a0001c0001t0002g0179 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.131+572A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8533397 | ||||||
| chr3:8533436
|
T | A | 1 | a0001c0001t0003g0277 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.131+611T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8533436 | ||||||
| chr3:8533560
|
G | A | 2 | a0001c0001t0026g0057a0001c0001t0027g0074 | 2 | NA18974.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.131+735G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8533560 | ||||||
| chr3:8533725
|
C | T | 44 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(41): Show | 45 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.131+900C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8533725 | ||||||
| chr3:8533812
|
A | G | 4 | a0001c0002t0002g0158a0001c0002t0004g0177a0001c0002t0004g0207others(1): Show | 4 | HG01081.hp1 HG02109.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.131+987A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8533812 | ||||||
| chr3:8533821
|
T | A | 1 | a0001c0008t0002g0065 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.131+996T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8533821 | ||||||
| chr3:8533867
|
A | G | 69 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(66): Show | 71 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.131+1042A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8533867 | ||||||
| chr3:8533918
|
G | A | 1 | a0001c0001t0004g0178 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.131+1093G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8533918 | ||||||
| chr3:8534159
|
G | A | 23 | a0001c0001t0001g0306a0001c0002t0001g0008a0001c0002t0001g0069others(20): Show | 24 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(21): Show |
intron_variant | MODIFIER | c.131+1334G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8534159 | ||||||
| chr3:8534208
|
C | G | 1 | a0001c0001t0002g0164 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.131+1383C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8534208 | ||||||
| chr3:8534369
|
C | A | 1 | a0001c0001t0004g0123 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.131+1544C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8534369 | ||||||
| chr3:8534715
|
T | C | 30 | a0001c0001t0001g0306a0001c0002t0001g0008a0001c0002t0001g0069others(27): Show | 31 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.131+1890T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8534715 | ||||||
| chr3:8534754
|
G | A | 1 | a0001c0002t0002g0158 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.131+1929G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8534754 | ||||||
| chr3:8534754
|
G | T | 1 | a0001c0001t0048g0078 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.131+1929G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8534754 | ||||||
| chr3:8535323
|
A | AT | 10 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(7): Show | 10 | HG01109.hp2 HG02145.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.132-1854dupT | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 8535323 | |||||
| chr3:8535374
|
G | A | 37 | a0001c0001t0001g0306a0001c0001t0002g0179a0001c0002t0001g0008others(34): Show | 38 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.132-1811G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8535374 | ||||||
| chr3:8535551
|
G | A | 37 | a0001c0001t0001g0306a0001c0001t0002g0179a0001c0002t0001g0008others(34): Show | 38 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.132-1634G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8535551 | ||||||
| chr3:8535616
|
A | G | 3 | a0001c0001t0003g0040a0001c0001t0003g0277a0001c0001t0049g0279 | 3 | HG01192.hp2 HG01255.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.132-1569A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8535616 | ||||||
| chr3:8535662
|
A | C | 1 | a0001c0001t0051g0091 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.132-1523A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8535662 | ||||||
| chr3:8536128
|
C | T | 1 | a0001c0001t0001g0093 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.132-1057C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8536128 | ||||||
| chr3:8536157
|
G | C | 10 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(7): Show | 10 | HG01109.hp2 HG02145.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.132-1028G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8536157 | ||||||
| chr3:8536286
|
G | A | 7 | a0001c0002t0001g0227a0001c0002t0001g0245a0001c0002t0002g0157others(4): Show | 7 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.132-899G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8536286 | ||||||
| chr3:8536293
|
G | A | 1 | a0001c0001t0002g0044 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.132-892G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8536293 | ||||||
| chr3:8536399
|
G | A | 1 | a0001c0001t0006g0076 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.132-786G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8536399 | ||||||
| chr3:8536505
|
C | G | 100 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(97): Show | 103 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.132-680C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8536505 | ||||||
| chr3:8536566
|
C | T | 1 | a0001c0001t0003g0264 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.132-619C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8536566 | ||||||
| chr3:8536582
|
A | G | 6 | a0001c0001t0001g0134a0001c0001t0002g0062a0001c0001t0003g0063others(3): Show | 6 | NA18747.hp1 NA18970.hp1 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.132-603A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8536582 | ||||||
| chr3:8536608
|
C | T | 4 | a0001c0002t0001g0008a0001c0002t0001g0304a0001c0002t0003g0273others(1): Show | 5 | HG00642.hp1 HG00741.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.132-577C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8536608 | ||||||
| chr3:8536798
|
G | T | 1 | a0001c0008t0002g0065 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.132-387G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8536798 | ||||||
| chr3:8536911
|
G | A | 39 | a0001c0001t0001g0306a0001c0001t0002g0179a0001c0001t0013g0291others(36): Show | 40 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.132-274G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8536911 | ||||||
| chr3:8536975
|
C | G | 1 | a0001c0001t0003g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.132-210C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8536975 | ||||||
| chr3:8537062
|
C | T | 39 | a0001c0001t0001g0306a0001c0001t0002g0179a0001c0001t0013g0291others(36): Show | 40 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.132-123C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 2/5 | chr3 | 8537062 | ||||||
| chr3:8537450
|
C | T | 1 | a0001c0001t0003g0236 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.387+10C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8537450 | ||||||
| chr3:8537604
|
G | A | 37 | a0001c0001t0001g0306a0001c0001t0002g0179a0001c0002t0001g0008others(34): Show | 38 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.387+164G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8537604 | ||||||
| chr3:8537656
|
G | T | 49 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0025others(46): Show | 51 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.387+216G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8537656 | ||||||
| chr3:8537996
|
G | A | 8 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(5): Show | 8 | HG02145.hp2 HG02559.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.387+556G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8537996 | ||||||
| chr3:8538044
|
G | A | 1 | a0001c0001t0003g0283 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.387+604G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8538044 | ||||||
| chr3:8538164
|
G | A | 62 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(59): Show | 64 | HG00099.hp1 HG00323.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.387+724G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8538164 | ||||||
| chr3:8538166
|
G | C | 1 | a0001c0001t0004g0013 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.387+726G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8538166 | ||||||
| chr3:8538266
|
C | T | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(96): Show | 102 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.387+826C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8538266 | ||||||
| chr3:8538286
|
G | A | 1 | a0001c0002t0004g0068 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.387+846G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8538286 | ||||||
| chr3:8538351
|
A | G | 37 | a0001c0001t0001g0306a0001c0001t0002g0179a0001c0002t0001g0008others(34): Show | 38 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.387+911A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8538351 | ||||||
| chr3:8538375
|
T | A | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(96): Show | 102 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.387+935T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8538375 | ||||||
| chr3:8538405
|
T | C | 31 | a0001c0001t0001g0306a0001c0002t0001g0008a0001c0002t0001g0069others(28): Show | 32 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.387+965T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8538405 | ||||||
| chr3:8538531
|
C | T | 2 | a0001c0001t0017g0180a0001c0001t0017g0181 | 2 | HG02523.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.387+1091C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8538531 | ||||||
| chr3:8538551
|
C | G | 52 | a0001c0001t0001g0002a0001c0001t0001g0053a0001c0001t0001g0209others(49): Show | 54 | HG00099.hp1 HG00323.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.387+1111C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8538551 | ||||||
| chr3:8538614
|
C | T | 37 | a0001c0001t0001g0306a0001c0001t0002g0179a0001c0002t0001g0008others(34): Show | 38 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.387+1174C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8538614 | ||||||
| chr3:8538707
|
T | C | 1 | a0001c0001t0001g0093 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.387+1267T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8538707 | ||||||
| chr3:8538795
|
AC | A | 37 | a0001c0001t0001g0306a0001c0001t0002g0179a0001c0002t0001g0008others(34): Show | 38 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.387+1358delC | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8538795 | |||||
| chr3:8538800
|
G | T | 37 | a0001c0001t0001g0306a0001c0001t0002g0179a0001c0002t0001g0008others(34): Show | 38 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.387+1360G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8538800 | ||||||
| chr3:8539093
|
G | A | 1 | a0001c0008t0002g0065 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.387+1653G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8539093 | ||||||
| chr3:8539246
|
GAA | G | 6 | a0001c0001t0003g0023a0001c0001t0003g0024a0001c0001t0003g0040others(3): Show | 6 | HG01192.hp2 HG01255.hp2 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.387+1809_387+1810d others(4): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8539246 | |||||
| chr3:8539459
|
C | A | 7 | a0001c0002t0001g0227a0001c0002t0001g0245a0001c0002t0002g0157others(4): Show | 7 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.387+2019C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8539459 | ||||||
| chr3:8539477
|
G | A | 1 | a0001c0001t0001g0191 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.387+2037G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8539477 | ||||||
| chr3:8539512
|
G | T | 4 | a0001c0002t0002g0158a0001c0002t0004g0177a0001c0002t0004g0207others(1): Show | 4 | HG01081.hp1 HG02109.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.387+2072G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8539512 | ||||||
| chr3:8539656
|
G | A | 4 | a0001c0002t0002g0158a0001c0002t0004g0177a0001c0002t0004g0207others(1): Show | 4 | HG01081.hp1 HG02109.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.387+2216G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8539656 | ||||||
| chr3:8539795
|
T | TTTA | 60 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0045others(57): Show | 61 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.387+2397_387+2399d others(5): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8539795 | |||||
| chr3:8539795
|
T | TTTATTA | 4 | a0001c0001t0001g0124a0001c0001t0015g0222a0001c0001t0018g0122others(1): Show | 4 | HG00323.hp1 HG00609.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.387+2394_387+2399d others(8): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8539795 | |||||
| chr3:8539795
|
TTTA | T | 94 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(91): Show | 96 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.387+2397_387+2399d others(5): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8539795 | |||||
| chr3:8539795
|
TTTATTA | T | 9 | a0001c0001t0001g0075a0001c0001t0001g0170a0001c0001t0001g0182others(6): Show | 9 | HG01255.hp2 HG02486.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.387+2394_387+2399d others(8): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8539795 | |||||
| chr3:8539795
|
TTTATTAT others(2): Show |
T | 4 | a0001c0002t0002g0158a0001c0002t0004g0177a0001c0002t0004g0207others(1): Show | 4 | HG01081.hp1 HG02109.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.387+2391_387+2399d others(11): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8539795 | |||||
| chr3:8539795
|
TTTATTAT others(8): Show |
T | 1 | a0001c0001t0001g0015 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.387+2385_387+2399d others(17): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8539795 | |||||
| chr3:8539910
|
G | GTGTGCTG others(45): Show |
13 | a0001c0002t0001g0008a0001c0002t0001g0069a0001c0002t0001g0304others(10): Show | 14 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(11): Show |
intron_variant | MODIFIER | c.387+2470_387+2471i others(54): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8539910 | ||||||
| chr3:8539911
|
C | T | 81 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(78): Show | 83 | HG00099.hp1 HG00323.hp1 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.387+2471C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8539911 | ||||||
| chr3:8539911
|
C | TGTGCTGC others(45): Show |
5 | a0001c0002t0001g0216a0001c0002t0003g0212a0001c0002t0004g0068others(2): Show | 5 | HG03017.hp1 HG03669.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.387+2470_387+2471i others(54): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8539911 | ||||||
| chr3:8539934
|
A | G | 2 | a0001c0001t0001g0093a0001c0001t0003g0004 | 3 | NA18953.hp2 NA18971.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.387+2494A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8539934 | ||||||
| chr3:8539971
|
C | G | 4 | a0001c0002t0002g0158a0001c0002t0004g0177a0001c0002t0004g0207others(1): Show | 4 | HG01081.hp1 HG02109.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.387+2531C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8539971 | ||||||
| chr3:8539972
|
A | AG | 31 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0053others(28): Show | 31 | HG00639.hp2 HG00642.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.387+2534dupG | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8539972 | |||||
| chr3:8540043
|
A | G | 2 | a0001c0001t0002g0141a0001c0001t0028g0147 | 2 | NA18950.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.387+2603A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8540043 | ||||||
| chr3:8540571
|
A | T | 1 | a0001c0002t0011g0211 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.387+3131A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8540571 | ||||||
| chr3:8540590
|
G | A | 1 | a0001c0001t0001g0079 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.387+3150G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8540590 | ||||||
| chr3:8540682
|
G | A | 4 | a0001c0002t0002g0158a0001c0002t0004g0177a0001c0002t0004g0207others(1): Show | 4 | HG01081.hp1 HG02109.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.387+3242G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8540682 | ||||||
| chr3:8540737
|
G | A | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(107): Show | 113 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.387+3297G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8540737 | ||||||
| chr3:8540786
|
G | A | 53 | a0001c0001t0001g0002a0001c0001t0001g0053a0001c0001t0001g0209others(50): Show | 55 | HG00099.hp1 HG00323.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.387+3346G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8540786 | ||||||
| chr3:8540816
|
C | T | 1 | a0001c0001t0002g0270 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.387+3376C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8540816 | ||||||
| chr3:8540977
|
T | C | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(96): Show | 102 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.387+3537T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8540977 | ||||||
| chr3:8541102
|
C | G | 10 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(7): Show | 10 | HG01109.hp2 HG02145.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.387+3662C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8541102 | ||||||
| chr3:8541144
|
T | G | 1 | a0001c0001t0002g0048 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.387+3704T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8541144 | ||||||
| chr3:8541298
|
C | G | 1 | a0001c0002t0004g0207 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.387+3858C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8541298 | ||||||
| chr3:8541365
|
C | A | 52 | a0001c0001t0001g0002a0001c0001t0001g0053a0001c0001t0001g0209others(49): Show | 54 | HG00099.hp1 HG00323.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.387+3925C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8541365 | ||||||
| chr3:8541378
|
C | G | 1 | a0001c0002t0004g0207 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.387+3938C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8541378 | ||||||
| chr3:8541473
|
C | T | 5 | a0001c0001t0001g0170a0001c0001t0001g0182a0001c0001t0001g0185others(2): Show | 5 | HG02486.hp1 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.387+4033C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8541473 | ||||||
| chr3:8541582
|
A | G | 1 | a0001c0001t0006g0087 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.387+4142A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8541582 | ||||||
| chr3:8541610
|
C | T | 1 | a0001c0002t0005g0226 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.387+4170C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8541610 | ||||||
| chr3:8541874
|
G | A | 1 | a0001c0001t0003g0248 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.387+4434G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8541874 | ||||||
| chr3:8542002
|
C | CT | 45 | a0001c0001t0001g0053a0001c0001t0001g0086a0001c0001t0001g0272others(42): Show | 46 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.387+4586dupT | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8542002 | |||||
| chr3:8542002
|
C | CTT | 49 | a0001c0001t0001g0002a0001c0001t0001g0209a0001c0001t0001g0247others(46): Show | 51 | HG00099.hp1 HG00323.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.387+4585_387+4586d others(4): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8542002 | |||||
| chr3:8542002
|
C | CTTT | 19 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(16): Show | 19 | HG00735.hp1 HG01109.hp2 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.387+4584_387+4586d others(5): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8542002 | |||||
| chr3:8542205
|
T | C | 2 | a0001c0002t0002g0239a0001c0002t0002g0240 | 2 | HG02698.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.387+4765T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8542205 | ||||||
| chr3:8542551
|
C | G | 1 | a0005c0006t0001g0225 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.387+5111C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8542551 | ||||||
| chr3:8542606
|
C | A | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(95): Show | 101 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.387+5166C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8542606 | ||||||
| chr3:8542835
|
C | G | 1 | a0001c0001t0001g0014 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.387+5395C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8542835 | ||||||
| chr3:8542837
|
T | G | 1 | a0001c0002t0001g0227 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.387+5397T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8542837 | ||||||
| chr3:8542960
|
G | T | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(96): Show | 102 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.387+5520G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8542960 | ||||||
| chr3:8543023
|
G | T | 1 | a0001c0001t0002g0111 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.388-5545G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8543023 | ||||||
| chr3:8543072
|
A | G | 1 | a0001c0001t0001g0133 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.388-5496A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8543072 | ||||||
| chr3:8543080
|
A | G | 2 | a0001c0001t0003g0183a0001c0001t0014g0184 | 2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.388-5488A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8543080 | ||||||
| chr3:8543180
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.388-5388G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8543180 | ||||||
| chr3:8543313
|
G | C | 100 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(97): Show | 103 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.388-5255G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8543313 | ||||||
| chr3:8543315
|
G | A | 1 | a0001c0001t0006g0076 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.388-5253G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8543315 | ||||||
| chr3:8543377
|
CTGATAGA others(12): Show |
C | 52 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(49): Show | 54 | HG00099.hp1 HG00597.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.388-5170_388-5152d others(21): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8543377 | |||||
| chr3:8543378
|
TGATAGAT others(16): Show |
T | 23 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0299others(20): Show | 24 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.388-5170_388-5148d others(25): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8543378 | |||||
| chr3:8543378
|
TGATAGAT others(20): Show |
T | 2 | a0001c0001t0003g0252a0001c0002t0001g0193 | 2 | HG01175.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.388-5170_388-5144d others(29): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8543378 | |||||
| chr3:8543378
|
TGATAGAT others(24): Show |
T | 1 | a0001c0001t0036g0250 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.388-5170_388-5140d others(33): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8543378 | |||||
| chr3:8543378
|
TGATAGAT others(28): Show |
T | 3 | a0001c0002t0001g0069a0001c0002t0001g0227a0001c0002t0005g0226 | 3 | HG02818.hp1 HG03927.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.388-5170_388-5136d others(37): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8543378 | |||||
| chr3:8543378
|
TGATAGAT others(32): Show |
T | 4 | a0001c0002t0002g0157a0001c0002t0008g0156a0001c0002t0008g0160others(1): Show | 4 | HG02109.hp1 HG02258.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.388-5170_388-5132d others(41): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8543378 | |||||
| chr3:8543382
|
AGATAGAT others(8): Show |
A | 8 | a0001c0001t0001g0014a0001c0001t0001g0254a0001c0001t0001g0255others(5): Show | 8 | HG01169.hp1 HG02055.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.388-5170_388-5156d others(17): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8543382 | |||||
| chr3:8543386
|
AGATAGAT others(4): Show |
A | 4 | a0001c0001t0003g0248a0001c0001t0012g0246a0001c0001t0039g0266others(1): Show | 4 | HG00323.hp1 HG01515.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.388-5170_388-5160d others(13): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8543386 | |||||
| chr3:8543397
|
T | TAGATA | 3 | a0001c0001t0002g0270a0001c0001t0003g0198a0001c0001t0031g0066 | 3 | HG02717.hp1 NA18943.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.388-5171_388-5170i others(7): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8543397 | ||||||
| chr3:8543397
|
T | TGATA | 33 | a0001c0001t0001g0003a0001c0001t0001g0025a0001c0001t0001g0027others(30): Show | 34 | HG00673.hp2 HG01081.hp2 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.388-5128_388-5125d others(6): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8543397 | |||||
| chr3:8543397
|
T | TGATAGAT others(1): Show |
22 | a0001c0001t0001g0036a0001c0001t0001g0124a0001c0001t0002g0047others(19): Show | 22 | HG00140.hp2 HG01074.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.388-5132_388-5125d others(10): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8543397 | |||||
| chr3:8543397
|
T | TGATAGAT others(5): Show |
7 | a0001c0001t0001g0085a0001c0001t0001g0133a0001c0001t0003g0276others(4): Show | 7 | HG00408.hp1 HG01975.hp2 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.388-5136_388-5125d others(14): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8543397 | |||||
| chr3:8543397
|
TGATA | T | 22 | a0001c0001t0001g0030a0001c0001t0001g0125a0001c0001t0001g0197others(19): Show | 23 | HG00544.hp1 HG01192.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.388-5128_388-5125d others(6): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8543397 | |||||
| chr3:8543397
|
TGATAGAT others(1): Show |
T | 5 | a0001c0001t0001g0107a0001c0001t0002g0148a0001c0001t0003g0005others(2): Show | 6 | HG00735.hp2 HG01516.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.388-5132_388-5125d others(10): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8543397 | |||||
| chr3:8543424
|
T | C | 1 | a0001c0001t0039g0266 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.388-5144T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8543424 | ||||||
| chr3:8543440
|
T | C | 7 | a0001c0001t0001g0014a0001c0001t0001g0185a0001c0001t0002g0270others(4): Show | 7 | HG00323.hp1 HG02647.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.388-5128T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8543440 | ||||||
| chr3:8543440
|
T | TAGATAGA others(1): Show |
4 | a0001c0001t0001g0170a0001c0001t0002g0033a0001c0001t0003g0183others(1): Show | 4 | HG01433.hp2 HG02976.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.388-5125_388-5124i others(10): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8543440 | |||||
| chr3:8543440
|
T | TAGATAGA others(5): Show |
3 | a0001c0001t0001g0081a0001c0001t0001g0130a0001c0001t0037g0205 | 3 | NA19057.hp1 NA19057.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.388-5125_388-5124i others(14): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8543440 | |||||
| chr3:8543440
|
T | TAGATAGA others(9): Show |
3 | a0001c0001t0001g0079a0001c0001t0001g0083a0003c0012t0001g0082 | 3 | HG02132.hp1 NA18612.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.388-5125_388-5124i others(18): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8543440 | |||||
| chr3:8543440
|
T | TAGATAGA others(17): Show |
1 | a0001c0001t0001g0182 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.388-5125_388-5124i others(26): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8543440 | |||||
| chr3:8543444
|
C | T | 35 | a0001c0001t0002g0179a0001c0001t0002g0201a0001c0001t0003g0267others(32): Show | 36 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.388-5124C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8543444 | ||||||
| chr3:8543492
|
C | CAGAT | 4 | a0001c0001t0001g0105a0001c0001t0002g0118a0001c0001t0003g0028others(1): Show | 4 | HG02300.hp1 HG02300.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.388-5063_388-5060d others(6): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8543492 | |||||
| chr3:8543518
|
T | C | 2 | a0001c0001t0009g0098a0001c0001t0010g0101 | 2 | HG02129.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.388-5050T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8543518 | ||||||
| chr3:8543551
|
C | T | 100 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(97): Show | 103 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.388-5017C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8543551 | ||||||
| chr3:8543639
|
C | T | 4 | a0001c0002t0002g0158a0001c0002t0004g0177a0001c0002t0004g0207others(1): Show | 4 | HG01081.hp1 HG02109.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.388-4929C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8543639 | ||||||
| chr3:8543682
|
T | C | 1 | a0006c0010t0002g0102 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.388-4886T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8543682 | ||||||
| chr3:8543785
|
G | A | 54 | a0001c0001t0001g0002a0001c0001t0001g0053a0001c0001t0001g0209others(51): Show | 56 | HG00099.hp1 HG00323.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.388-4783G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8543785 | ||||||
| chr3:8544139
|
TTC | T | 8 | a0001c0002t0001g0227a0001c0002t0001g0245a0001c0002t0002g0157others(5): Show | 8 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.388-4419_388-4418d others(4): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8544139 | |||||
| chr3:8544221
|
A | G | 92 | a0001c0001t0001g0002a0001c0001t0001g0053a0001c0001t0001g0209others(89): Show | 95 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.388-4347A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8544221 | ||||||
| chr3:8544283
|
T | C | 92 | a0001c0001t0001g0002a0001c0001t0001g0053a0001c0001t0001g0209others(89): Show | 95 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.388-4285T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8544283 | ||||||
| chr3:8544493
|
G | A | 91 | a0001c0001t0001g0002a0001c0001t0001g0053a0001c0001t0001g0209others(88): Show | 94 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.388-4075G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8544493 | ||||||
| chr3:8544673
|
G | C | 1 | a0001c0002t0001g0245 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.388-3895G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8544673 | ||||||
| chr3:8544755
|
G | A | 91 | a0001c0001t0001g0002a0001c0001t0001g0053a0001c0001t0001g0209others(88): Show | 94 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.388-3813G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8544755 | ||||||
| chr3:8544779
|
C | A | 91 | a0001c0001t0001g0002a0001c0001t0001g0053a0001c0001t0001g0209others(88): Show | 94 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.388-3789C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8544779 | ||||||
| chr3:8544816
|
A | G | 92 | a0001c0001t0001g0002a0001c0001t0001g0053a0001c0001t0001g0209others(89): Show | 95 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.388-3752A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8544816 | ||||||
| chr3:8544851
|
A | C | 1 | a0001c0001t0002g0104 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.388-3717A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8544851 | ||||||
| chr3:8544954
|
G | A | 1 | a0001c0001t0002g0059 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.388-3614G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8544954 | ||||||
| chr3:8545025
|
C | T | 1 | a0001c0001t0003g0094 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.388-3543C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8545025 | ||||||
| chr3:8545105
|
G | A | 1 | a0001c0001t0002g0155 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.388-3463G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8545105 | ||||||
| chr3:8545246
|
G | T | 1 | a0001c0001t0046g0168 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.388-3322G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8545246 | ||||||
| chr3:8545416
|
A | C | 1 | a0002c0003t0001g0231 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.388-3152A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8545416 | ||||||
| chr3:8545488
|
C | T | 4 | a0001c0002t0002g0158a0001c0002t0004g0177a0001c0002t0004g0207others(1): Show | 4 | HG01081.hp1 HG02109.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.388-3080C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8545488 | ||||||
| chr3:8545495
|
T | C | 9 | a0001c0002t0001g0227a0001c0002t0001g0245a0001c0002t0002g0157others(6): Show | 9 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.388-3073T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8545495 | ||||||
| chr3:8545578
|
G | C | 1 | a0001c0001t0002g0179 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.388-2990G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8545578 | ||||||
| chr3:8545622
|
A | C | 1 | a0001c0001t0003g0189 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.388-2946A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8545622 | ||||||
| chr3:8545721
|
A | C | 1 | a0001c0001t0001g0016 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.388-2847A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8545721 | ||||||
| chr3:8545864
|
G | A | 2 | a0001c0001t0002g0113a0001c0001t0002g0232 | 2 | HG01192.hp1 HG01928.hp1 |
intron_variant | MODIFIER | c.388-2704G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8545864 | ||||||
| chr3:8545930
|
C | T | 4 | a0001c0001t0003g0089a0001c0001t0006g0049a0001c0001t0006g0087others(1): Show | 4 | HG00673.hp1 NA18992.hp2 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.388-2638C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8545930 | ||||||
| chr3:8545956
|
G | A | 53 | a0001c0001t0001g0002a0001c0001t0001g0053a0001c0001t0001g0209others(50): Show | 55 | HG00099.hp1 HG00323.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.388-2612G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8545956 | ||||||
| chr3:8545976
|
A | C | 1 | a0001c0001t0001g0015 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.388-2592A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8545976 | ||||||
| chr3:8545984
|
G | A | 22 | a0001c0002t0001g0008a0001c0002t0001g0069a0001c0002t0001g0193others(19): Show | 23 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.388-2584G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8545984 | ||||||
| chr3:8545999
|
C | T | 1 | a0001c0001t0001g0261 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.388-2569C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8545999 | ||||||
| chr3:8546004
|
A | C | 1 | a0001c0001t0003g0004 | 2 | NA18953.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.388-2564A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8546004 | ||||||
| chr3:8546071
|
T | C | 1 | a0005c0006t0001g0225 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.388-2497T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8546071 | ||||||
| chr3:8546119
|
C | G | 2 | a0001c0002t0002g0239a0001c0002t0002g0240 | 2 | HG02698.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.388-2449C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8546119 | ||||||
| chr3:8546155
|
A | C | 1 | a0001c0001t0046g0168 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.388-2413A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8546155 | ||||||
| chr3:8546425
|
A | G | 37 | a0001c0002t0001g0008a0001c0002t0001g0069a0001c0002t0001g0193others(34): Show | 38 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.388-2143A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8546425 | ||||||
| chr3:8546487
|
A | G | 37 | a0001c0002t0001g0008a0001c0002t0001g0069a0001c0002t0001g0193others(34): Show | 38 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.388-2081A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8546487 | ||||||
| chr3:8546588
|
T | C | 37 | a0001c0002t0001g0008a0001c0002t0001g0069a0001c0002t0001g0193others(34): Show | 38 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.388-1980T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8546588 | ||||||
| chr3:8546663
|
G | GT | 37 | a0001c0002t0001g0008a0001c0002t0001g0069a0001c0002t0001g0193others(34): Show | 38 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.388-1903dupT | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8546663 | |||||
| chr3:8546807
|
G | A | 1 | a0001c0008t0002g0065 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.388-1761G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8546807 | ||||||
| chr3:8546817
|
C | T | 37 | a0001c0002t0001g0008a0001c0002t0001g0069a0001c0002t0001g0193others(34): Show | 38 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.388-1751C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8546817 | ||||||
| chr3:8546818
|
G | A | 1 | a0001c0001t0003g0187 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.388-1750G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8546818 | ||||||
| chr3:8547107
|
C | T | 4 | a0001c0002t0001g0193a0001c0002t0001g0194a0001c0002t0001g0195others(1): Show | 4 | HG01069.hp1 HG01071.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.388-1461C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8547107 | ||||||
| chr3:8547113
|
T | C | 1 | a0001c0002t0011g0211 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.388-1455T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8547113 | ||||||
| chr3:8547163
|
C | G | 37 | a0001c0002t0001g0008a0001c0002t0001g0069a0001c0002t0001g0193others(34): Show | 38 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.388-1405C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8547163 | ||||||
| chr3:8547364
|
C | T | 37 | a0001c0002t0001g0008a0001c0002t0001g0069a0001c0002t0001g0193others(34): Show | 38 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.388-1204C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8547364 | ||||||
| chr3:8547380
|
T | A | 1 | a0001c0001t0001g0228 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.388-1188T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8547380 | ||||||
| chr3:8547401
|
G | A | 5 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(2): Show | 5 | HG02145.hp2 HG02559.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.388-1167G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8547401 | ||||||
| chr3:8547510
|
C | G | 1 | a0001c0001t0004g0287 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.388-1058C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8547510 | ||||||
| chr3:8547688
|
C | A | 37 | a0001c0002t0001g0008a0001c0002t0001g0069a0001c0002t0001g0193others(34): Show | 38 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.388-880C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8547688 | ||||||
| chr3:8547696
|
T | C | 37 | a0001c0002t0001g0008a0001c0002t0001g0069a0001c0002t0001g0193others(34): Show | 38 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.388-872T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8547696 | ||||||
| chr3:8547699
|
C | T | 37 | a0001c0002t0001g0008a0001c0002t0001g0069a0001c0002t0001g0193others(34): Show | 38 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.388-869C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8547699 | ||||||
| chr3:8547736
|
CA | C | 37 | a0001c0002t0001g0008a0001c0002t0001g0069a0001c0002t0001g0193others(34): Show | 38 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.388-825delA | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8547736 | |||||
| chr3:8547746
|
A | AGCCGGGC | 292 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(289): Show | 299 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.388-820_388-819ins others(7): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8547746 | |||||
| chr3:8547849
|
G | A | 1 | a0001c0002t0001g0245 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.388-719G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8547849 | ||||||
| chr3:8547872
|
C | T | 47 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(44): Show | 48 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.388-696C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8547872 | ||||||
| chr3:8547885
|
C | CA | 37 | a0001c0002t0001g0008a0001c0002t0001g0069a0001c0002t0001g0193others(34): Show | 38 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.388-673dupA | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8547885 | |||||
| chr3:8547894
|
A | G | 1 | a0001c0001t0001g0254 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.388-674A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8547894 | ||||||
| chr3:8547964
|
T | C | 4 | a0001c0001t0003g0267a0001c0001t0014g0294a0001c0001t0052g0293others(1): Show | 4 | HG01884.hp2 HG02055.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.388-604T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8547964 | ||||||
| chr3:8548167
|
G | A | 1 | a0001c0001t0002g0146 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.388-401G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8548167 | ||||||
| chr3:8548196
|
G | A | 1 | a0001c0001t0003g0267 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.388-372G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8548196 | ||||||
| chr3:8548220
|
T | C | 100 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(97): Show | 103 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.388-348T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8548220 | ||||||
| chr3:8548263
|
T | C | 1 | a0001c0001t0036g0250 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.388-305T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8548263 | ||||||
| chr3:8548271
|
C | T | 37 | a0001c0002t0001g0008a0001c0002t0001g0069a0001c0002t0001g0193others(34): Show | 38 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.388-297C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | chr3 | 8548271 | ||||||
| chr3:8548329
|
G | GT | 9 | a0001c0002t0001g0227a0001c0002t0001g0245a0001c0002t0002g0157others(6): Show | 9 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.388-233dupT | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 8548329 | |||||
| chr3:8548925
|
A | C | 1 | a0001c0001t0003g0131 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.723+22A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8548925 | ||||||
| chr3:8549120
|
G | A | 1 | a0001c0001t0004g0178 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.723+217G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8549120 | ||||||
| chr3:8549268
|
G | A | 31 | a0001c0001t0001g0053a0001c0001t0001g0209a0001c0001t0001g0247others(28): Show | 32 | HG00597.hp2 HG00738.hp2 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.723+365G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8549268 | ||||||
| chr3:8549298
|
A | C | 37 | a0001c0002t0001g0008a0001c0002t0001g0069a0001c0002t0001g0193others(34): Show | 38 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.723+395A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8549298 | ||||||
| chr3:8549489
|
A | T | 37 | a0001c0002t0001g0008a0001c0002t0001g0069a0001c0002t0001g0193others(34): Show | 38 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.723+586A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8549489 | ||||||
| chr3:8549664
|
T | G | 35 | a0001c0002t0001g0008a0001c0002t0001g0069a0001c0002t0001g0193others(32): Show | 36 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.723+761T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8549664 | ||||||
| chr3:8549724
|
G | T | 1 | a0001c0001t0005g0229 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.723+821G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8549724 | ||||||
| chr3:8549764
|
T | A | 1 | a0001c0001t0002g0224 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.723+861T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8549764 | ||||||
| chr3:8549783
|
G | A | 22 | a0001c0002t0001g0008a0001c0002t0001g0069a0001c0002t0001g0193others(19): Show | 23 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.723+880G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8549783 | ||||||
| chr3:8549790
|
C | G | 35 | a0001c0002t0001g0008a0001c0002t0001g0069a0001c0002t0001g0193others(32): Show | 36 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.723+887C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8549790 | ||||||
| chr3:8549882
|
C | T | 1 | a0001c0001t0001g0027 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.723+979C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8549882 | ||||||
| chr3:8549889
|
G | A | 9 | a0001c0002t0001g0227a0001c0002t0001g0245a0001c0002t0002g0157others(6): Show | 9 | HG01169.hp1 HG02109.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.723+986G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8549889 | ||||||
| chr3:8549899
|
C | T | 1 | a0001c0002t0050g0159 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.723+996C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8549899 | ||||||
| chr3:8550228
|
T | C | 35 | a0001c0002t0001g0008a0001c0002t0001g0069a0001c0002t0001g0193others(32): Show | 36 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.723+1325T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8550228 | ||||||
| chr3:8550245
|
C | A | 4 | a0001c0001t0001g0014a0001c0001t0002g0281a0001c0001t0002g0282others(1): Show | 4 | HG02717.hp1 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.723+1342C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8550245 | ||||||
| chr3:8550258
|
T | G | 12 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(9): Show | 12 | HG01109.hp2 HG02145.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.723+1355T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8550258 | ||||||
| chr3:8550289
|
G | C | 12 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(9): Show | 12 | HG01109.hp2 HG02145.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.723+1386G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8550289 | ||||||
| chr3:8550430
|
C | T | 1 | a0005c0006t0001g0225 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.723+1527C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8550430 | ||||||
| chr3:8550431
|
A | G | 259 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(256): Show | 265 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(262): Show |
intron_variant | MODIFIER | c.723+1528A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8550431 | ||||||
| chr3:8550665
|
T | C | 34 | a0001c0001t0001g0053a0001c0001t0001g0209a0001c0001t0001g0247others(31): Show | 35 | HG00597.hp2 HG00738.hp2 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.723+1762T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8550665 | ||||||
| chr3:8550727
|
CT | C | 92 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(89): Show | 94 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.723+1828delT | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 8550727 | |||||
| chr3:8550731
|
T | C | 1 | a0001c0001t0001g0209 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.723+1828T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8550731 | ||||||
| chr3:8550887
|
G | A | 81 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(78): Show | 83 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.723+1984G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8550887 | ||||||
| chr3:8551117
|
T | C | 81 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(78): Show | 83 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.723+2214T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8551117 | ||||||
| chr3:8551248
|
T | C | 38 | a0001c0001t0001g0107a0001c0002t0001g0008a0001c0002t0001g0069others(35): Show | 39 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.723+2345T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8551248 | ||||||
| chr3:8551352
|
G | A | 37 | a0001c0002t0001g0008a0001c0002t0001g0069a0001c0002t0001g0193others(34): Show | 38 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.723+2449G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8551352 | ||||||
| chr3:8551359
|
A | C | 1 | a0001c0001t0002g0055 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.723+2456A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8551359 | ||||||
| chr3:8551575
|
G | A | 4 | a0001c0001t0002g0150a0001c0001t0002g0251a0001c0001t0003g0018others(1): Show | 4 | HG01243.hp1 HG01258.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.723+2672G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8551575 | ||||||
| chr3:8551755
|
G | A | 1 | a0001c0001t0002g0070 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.723+2852G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8551755 | ||||||
| chr3:8551799
|
C | T | 33 | a0001c0001t0001g0053a0001c0001t0001g0209a0001c0001t0001g0247others(30): Show | 34 | HG00597.hp2 HG00738.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.723+2896C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8551799 | ||||||
| chr3:8552004
|
G | A | 1 | a0001c0001t0001g0015 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.723+3101G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8552004 | ||||||
| chr3:8552313
|
G | A | 10 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(7): Show | 10 | HG02145.hp2 HG02559.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.723+3410G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8552313 | ||||||
| chr3:8552509
|
C | T | 4 | a0001c0002t0002g0158a0001c0002t0004g0177a0001c0002t0004g0207others(1): Show | 4 | HG01081.hp1 HG02109.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.723+3606C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8552509 | ||||||
| chr3:8552524
|
G | C | 2 | a0001c0001t0002g0055a0001c0001t0002g0108 | 2 | HG02735.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.723+3621G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8552524 | ||||||
| chr3:8552563
|
G | A | 1 | a0001c0002t0001g0069 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.723+3660G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8552563 | ||||||
| chr3:8552726
|
T | C | 1 | a0001c0001t0003g0153 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.723+3823T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8552726 | ||||||
| chr3:8552815
|
C | T | 12 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(9): Show | 12 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.723+3912C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8552815 | ||||||
| chr3:8552914
|
G | A | 14 | a0001c0001t0001g0140a0001c0001t0001g0144a0001c0001t0001g0191others(11): Show | 14 | HG00735.hp2 HG02074.hp1 HG02293.hp1 others(11): Show |
intron_variant | MODIFIER | c.723+4011G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8552914 | ||||||
| chr3:8553105
|
C | T | 1 | a0001c0002t0001g0227 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.723+4202C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8553105 | ||||||
| chr3:8553125
|
A | C | 12 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(9): Show | 12 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.723+4222A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8553125 | ||||||
| chr3:8553163
|
C | G | 12 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(9): Show | 12 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.723+4260C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8553163 | ||||||
| chr3:8553311
|
C | T | 30 | a0001c0001t0002g0179a0001c0001t0003g0221a0001c0001t0031g0066others(27): Show | 31 | HG00408.hp2 HG00423.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.723+4408C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8553311 | ||||||
| chr3:8553357
|
T | C | 1 | a0001c0001t0039g0266 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.723+4454T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8553357 | ||||||
| chr3:8553377
|
A | T | 80 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(77): Show | 82 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.723+4474A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8553377 | ||||||
| chr3:8553404
|
G | T | 1 | a0001c0002t0041g0258 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.723+4501G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8553404 | ||||||
| chr3:8553442
|
G | A | 5 | a0001c0001t0002g0152a0001c0001t0002g0154a0001c0001t0002g0155others(2): Show | 5 | HG00673.hp2 NA18943.hp2 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.723+4539G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8553442 | ||||||
| chr3:8553472
|
C | A | 2 | a0001c0001t0002g0044a0001c0001t0002g0047 | 2 | HG01255.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.723+4569C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8553472 | ||||||
| chr3:8553560
|
A | T | 12 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(9): Show | 12 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.723+4657A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8553560 | ||||||
| chr3:8553585
|
A | C | 1 | a0001c0002t0041g0258 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.723+4682A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8553585 | ||||||
| chr3:8553639
|
C | A | 12 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(9): Show | 12 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.723+4736C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8553639 | ||||||
| chr3:8553650
|
G | A | 2 | a0001c0001t0026g0057a0001c0001t0027g0074 | 2 | NA18974.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.723+4747G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8553650 | ||||||
| chr3:8553851
|
A | G | 12 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(9): Show | 12 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.723+4948A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8553851 | ||||||
| chr3:8554011
|
G | A | 1 | a0001c0001t0007g0303 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.723+5108G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8554011 | ||||||
| chr3:8554043
|
C | T | 1 | a0001c0001t0003g0042 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.723+5140C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8554043 | ||||||
| chr3:8554096
|
G | A | 7 | a0001c0002t0003g0095a0001c0002t0003g0139a0001c0002t0011g0208others(4): Show | 7 | HG00408.hp2 HG00597.hp1 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.723+5193G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8554096 | ||||||
| chr3:8554305
|
C | T | 1 | a0001c0001t0003g0138 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.723+5402C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8554305 | ||||||
| chr3:8554364
|
C | T | 2 | a0001c0002t0001g0245a0005c0006t0001g0225 | 2 | HG01169.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.723+5461C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8554364 | ||||||
| chr3:8554401
|
G | A | 13 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(10): Show | 13 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.723+5498G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8554401 | ||||||
| chr3:8554624
|
A | G | 13 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(10): Show | 13 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.723+5721A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8554624 | ||||||
| chr3:8554682
|
C | T | 13 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(10): Show | 13 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.723+5779C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8554682 | ||||||
| chr3:8554714
|
C | T | 1 | a0001c0001t0003g0192 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.723+5811C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8554714 | ||||||
| chr3:8554772
|
G | A | 1 | a0001c0001t0022g0305 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.723+5869G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8554772 | ||||||
| chr3:8554910
|
A | T | 2 | a0001c0002t0002g0239a0001c0002t0002g0240 | 2 | HG02698.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.723+6007A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8554910 | ||||||
| chr3:8554912
|
C | T | 1 | a0001c0001t0002g0172 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.723+6009C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8554912 | ||||||
| chr3:8554943
|
G | C | 1 | a0001c0001t0034g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.723+6040G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8554943 | ||||||
| chr3:8555071
|
C | T | 4 | a0001c0001t0001g0263a0001c0001t0001g0265a0001c0001t0003g0262others(1): Show | 4 | NA18956.hp2 NA18965.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.723+6168C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8555071 | ||||||
| chr3:8555073
|
C | T | 13 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(10): Show | 13 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.723+6170C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8555073 | ||||||
| chr3:8555097
|
T | C | 1 | a0001c0001t0012g0246 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.723+6194T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8555097 | ||||||
| chr3:8555164
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.723+6261C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8555164 | ||||||
| chr3:8555193
|
C | T | 3 | a0001c0001t0005g0165a0001c0001t0005g0229a0001c0001t0005g0244 | 3 | HG02622.hp2 HG02886.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.723+6290C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8555193 | ||||||
| chr3:8555419
|
A | G | 2 | a0001c0001t0029g0285a0001c0002t0041g0258 | 2 | HG01074.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.723+6516A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8555419 | ||||||
| chr3:8555495
|
C | A | 1 | a0001c0001t0001g0002 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.723+6592C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8555495 | ||||||
| chr3:8555624
|
CT | C | 13 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(10): Show | 13 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.723+6730delT | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 8555624 | |||||
| chr3:8555712
|
C | A | 4 | a0001c0002t0002g0158a0001c0002t0004g0177a0001c0002t0004g0207others(1): Show | 4 | HG01081.hp1 HG02109.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.723+6809C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8555712 | ||||||
| chr3:8555716
|
C | CT | 45 | a0001c0001t0001g0015a0001c0001t0001g0103a0001c0001t0001g0130others(42): Show | 46 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.723+6837dupT | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 8555716 | |||||
| chr3:8555716
|
C | CTT | 9 | a0001c0001t0001g0170a0001c0001t0001g0182a0001c0001t0001g0185others(6): Show | 9 | HG01169.hp1 HG02486.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.723+6836_723+6837d others(4): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 8555716 | |||||
| chr3:8555716
|
C | CTTT | 42 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(39): Show | 43 | HG00597.hp2 HG01069.hp2 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.723+6835_723+6837d others(5): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 8555716 | |||||
| chr3:8555716
|
CT | C | 8 | a0001c0001t0001g0299a0001c0001t0003g0129a0001c0001t0003g0284others(5): Show | 8 | HG00609.hp1 HG01070.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.723+6837delT | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 8555716 | |||||
| chr3:8555743
|
G | C | 1 | a0001c0001t0043g0012 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.723+6840G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8555743 | ||||||
| chr3:8555775
|
G | C | 1 | a0001c0001t0055g0029 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.723+6872G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8555775 | ||||||
| chr3:8555849
|
C | T | 1 | a0001c0001t0034g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.723+6946C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8555849 | ||||||
| chr3:8555926
|
A | G | 4 | a0001c0002t0002g0158a0001c0002t0004g0177a0001c0002t0004g0207others(1): Show | 4 | HG01081.hp1 HG02109.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.723+7023A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8555926 | ||||||
| chr3:8555998
|
G | A | 1 | a0001c0001t0002g0104 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.723+7095G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8555998 | ||||||
| chr3:8556085
|
G | T | 73 | a0001c0001t0001g0053a0001c0001t0001g0103a0001c0001t0001g0170others(70): Show | 74 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.723+7182G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8556085 | ||||||
| chr3:8556361
|
A | G | 1 | a0001c0001t0004g0288 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.723+7458A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8556361 | ||||||
| chr3:8556480
|
A | C | 2 | a0001c0001t0017g0180a0001c0001t0017g0181 | 2 | HG02523.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.723+7577A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8556480 | ||||||
| chr3:8556481
|
A | G | 1 | a0001c0001t0004g0288 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.723+7578A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8556481 | ||||||
| chr3:8556550
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.723+7647G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8556550 | ||||||
| chr3:8556624
|
C | T | 2 | a0001c0002t0001g0245a0005c0006t0001g0225 | 2 | HG01169.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.723+7721C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8556624 | ||||||
| chr3:8556644
|
A | G | 78 | a0001c0001t0001g0053a0001c0001t0001g0103a0001c0001t0001g0170others(75): Show | 80 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.723+7741A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8556644 | ||||||
| chr3:8556984
|
G | C | 78 | a0001c0001t0001g0053a0001c0001t0001g0103a0001c0001t0001g0170others(75): Show | 80 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.723+8081G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8556984 | ||||||
| chr3:8557004
|
C | T | 13 | a0001c0001t0001g0026a0001c0001t0001g0290a0001c0001t0002g0099others(10): Show | 13 | HG01884.hp1 HG02145.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.723+8101C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8557004 | ||||||
| chr3:8557251
|
A | G | 1 | a0001c0001t0003g0218 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.724-8181A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8557251 | ||||||
| chr3:8557597
|
C | A | 7 | a0001c0001t0001g0228a0001c0001t0004g0178a0001c0001t0021g0067others(4): Show | 7 | HG01169.hp1 HG02258.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.724-7835C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8557597 | ||||||
| chr3:8557603
|
A | C | 2 | a0001c0001t0002g0152a0001c0001t0016g0151 | 2 | HG00673.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.724-7829A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8557603 | ||||||
| chr3:8557737
|
G | A | 2 | a0001c0001t0026g0057a0001c0001t0027g0074 | 2 | NA18974.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.724-7695G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8557737 | ||||||
| chr3:8557827
|
G | C | 24 | a0001c0001t0001g0053a0001c0001t0001g0209a0001c0001t0001g0247others(21): Show | 25 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.724-7605G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8557827 | ||||||
| chr3:8558038
|
G | C | 71 | a0001c0001t0001g0217a0001c0001t0001g0280a0001c0001t0002g0006others(68): Show | 72 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.724-7394G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8558038 | ||||||
| chr3:8558228
|
G | A | 1 | a0001c0002t0001g0069 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.724-7204G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8558228 | ||||||
| chr3:8558247
|
C | T | 1 | a0001c0001t0002g0118 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.724-7185C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8558247 | ||||||
| chr3:8558324
|
T | C | 60 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(57): Show | 62 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.724-7108T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8558324 | ||||||
| chr3:8558329
|
G | T | 2 | a0001c0001t0034g0302a0001c0001t0040g0169 | 2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.724-7103G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8558329 | ||||||
| chr3:8558540
|
G | A | 1 | a0001c0001t0002g0214 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.724-6892G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8558540 | ||||||
| chr3:8558707
|
T | C | 1 | a0001c0001t0042g0175 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.724-6725T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8558707 | ||||||
| chr3:8558823
|
T | C | 5 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(2): Show | 5 | HG02145.hp2 HG02559.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.724-6609T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8558823 | ||||||
| chr3:8558950
|
C | T | 55 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(52): Show | 57 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.724-6482C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8558950 | ||||||
| chr3:8558982
|
C | T | 1 | a0001c0001t0002g0270 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.724-6450C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8558982 | ||||||
| chr3:8559021
|
A | AC | 55 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(52): Show | 57 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.724-6410dupC | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 8559021 | |||||
| chr3:8559059
|
G | A | 22 | a0001c0001t0001g0014a0001c0001t0001g0103a0001c0001t0001g0290others(19): Show | 22 | HG01069.hp1 HG01071.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.724-6373G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8559059 | ||||||
| chr3:8559062
|
C | CCTCCA | 4 | a0001c0001t0001g0228a0001c0001t0017g0180a0001c0001t0017g0181others(1): Show | 4 | HG02523.hp1 HG03453.hp1 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.724-6369_724-6365d others(7): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 8559062 | |||||
| chr3:8559285
|
G | C | 19 | a0001c0001t0001g0014a0001c0001t0001g0290a0001c0001t0002g0179others(16): Show | 19 | HG01069.hp1 HG01071.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.724-6147G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8559285 | ||||||
| chr3:8559353
|
C | T | 4 | a0001c0001t0004g0288a0001c0001t0014g0294a0001c0001t0052g0293others(1): Show | 4 | HG01884.hp2 HG02055.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.724-6079C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8559353 | ||||||
| chr3:8559394
|
A | G | 2 | a0001c0002t0004g0177a0001c0002t0050g0159 | 2 | HG02451.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.724-6038A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8559394 | ||||||
| chr3:8559422
|
C | CCACAATC others(697): Show |
7 | a0001c0001t0001g0170a0001c0001t0001g0182a0001c0001t0001g0185others(4): Show | 7 | HG02486.hp1 HG02523.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.724-5785_724-5784i others(706): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 8559422 | |||||
| chr3:8559574
|
T | G | 3 | a0001c0001t0001g0103a0001c0001t0003g0183a0001c0001t0014g0184 | 3 | HG02717.hp2 HG03041.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.724-5858T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8559574 | ||||||
| chr3:8559648
|
A | G | 100 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(97): Show | 102 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.724-5784A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8559648 | ||||||
| chr3:8559677
|
C | T | 1 | a0001c0001t0002g0238 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.724-5755C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8559677 | ||||||
| chr3:8559723
|
A | G | 1 | a0001c0001t0036g0250 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.724-5709A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8559723 | ||||||
| chr3:8559793
|
C | A | 1 | a0001c0001t0001g0247 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.724-5639C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8559793 | ||||||
| chr3:8559878
|
T | C | 19 | a0001c0001t0001g0014a0001c0001t0001g0290a0001c0001t0002g0179others(16): Show | 19 | HG01069.hp1 HG01071.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.724-5554T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8559878 | ||||||
| chr3:8559927
|
T | C | 36 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0053others(33): Show | 36 | HG01106.hp1 HG01109.hp2 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.724-5505T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8559927 | ||||||
| chr3:8560060
|
A | G | 1 | a0001c0001t0002g0214 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.724-5372A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8560060 | ||||||
| chr3:8560078
|
A | AATTAGAA others(697): Show |
1 | a0001c0001t0035g0253 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.724-5304_724-5303i others(706): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 8560078 | |||||
| chr3:8560078
|
A | AATTAGAA others(697): Show |
3 | a0001c0001t0001g0263a0001c0001t0001g0265a0001c0001t0028g0147 | 3 | NA18965.hp1 NA18969.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.724-5304_724-5303i others(706): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 8560078 | |||||
| chr3:8560078
|
A | AATTAGAA others(697): Show |
28 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0053others(25): Show | 28 | HG01106.hp1 HG01109.hp2 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.724-5304_724-5303i others(706): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 8560078 | |||||
| chr3:8560078
|
A | G | 68 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(65): Show | 70 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.724-5354A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8560078 | ||||||
| chr3:8560126
|
G | T | 5 | a0001c0001t0001g0130a0001c0001t0001g0140a0001c0001t0001g0191others(2): Show | 5 | NA18979.hp2 NA18994.hp1 NA19068.hp1 others(2): Show |
intron_variant | MODIFIER | c.724-5306G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8560126 | ||||||
| chr3:8560190
|
C | A | 122 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(119): Show | 124 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.724-5242C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8560190 | ||||||
| chr3:8560490
|
G | A | 2 | a0001c0001t0001g0228a0001c0001t0021g0067 | 2 | HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.724-4942G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8560490 | ||||||
| chr3:8560758
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.724-4674C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8560758 | ||||||
| chr3:8560790
|
G | C | 58 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(55): Show | 60 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.724-4642G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8560790 | ||||||
| chr3:8561026
|
T | C | 1 | a0001c0001t0003g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.724-4406T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8561026 | ||||||
| chr3:8561215
|
C | T | 1 | a0001c0001t0004g0178 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.724-4217C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8561215 | ||||||
| chr3:8561253
|
A | G | 32 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0053others(29): Show | 32 | HG01106.hp1 HG01109.hp2 HG02055.hp2 others(29): Show |
intron_variant | MODIFIER | c.724-4179A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8561253 | ||||||
| chr3:8561346
|
A | G | 3 | a0001c0001t0003g0040a0001c0001t0003g0277a0001c0001t0049g0279 | 3 | HG01192.hp2 HG01255.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.724-4086A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8561346 | ||||||
| chr3:8561356
|
A | G | 1 | a0001c0001t0036g0250 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.724-4076A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8561356 | ||||||
| chr3:8561381
|
GT | G | 9 | a0001c0001t0001g0228a0001c0001t0002g0115a0001c0001t0003g0031others(6): Show | 9 | HG01167.hp1 HG01928.hp2 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.724-4034delT | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 8561381 | |||||
| chr3:8561381
|
GTT | G | 111 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(108): Show | 113 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.724-4035_724-4034d others(4): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 8561381 | |||||
| chr3:8561389
|
T | G | 5 | a0001c0001t0003g0264a0001c0001t0003g0275a0001c0001t0003g0283others(2): Show | 5 | HG00642.hp2 HG00738.hp1 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.724-4043T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8561389 | ||||||
| chr3:8561412
|
A | T | 2 | a0001c0001t0034g0302a0001c0001t0040g0169 | 2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.724-4020A>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8561412 | ||||||
| chr3:8561544
|
C | T | 1 | a0001c0001t0003g0112 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.724-3888C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8561544 | ||||||
| chr3:8561545
|
G | A | 1 | a0006c0010t0002g0102 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.724-3887G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8561545 | ||||||
| chr3:8561557
|
T | C | 237 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(234): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.724-3875T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8561557 | ||||||
| chr3:8561573
|
C | T | 1 | a0001c0008t0002g0065 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.724-3859C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8561573 | ||||||
| chr3:8561674
|
C | T | 1 | a0001c0001t0012g0246 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.724-3758C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8561674 | ||||||
| chr3:8561708
|
A | G | 3 | a0001c0001t0001g0263a0001c0001t0001g0265a0001c0001t0028g0147 | 3 | NA18965.hp1 NA18969.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.724-3724A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8561708 | ||||||
| chr3:8561797
|
C | A | 121 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(118): Show | 123 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.724-3635C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8561797 | ||||||
| chr3:8561871
|
C | CATT | 121 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(118): Show | 123 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.724-3559_724-3558i others(5): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 8561871 | |||||
| chr3:8561986
|
G | A | 2 | a0001c0001t0003g0269a0001c0001t0003g0284 | 2 | HG00735.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.724-3446G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8561986 | ||||||
| chr3:8561988
|
T | G | 1 | a0001c0001t0002g0034 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.724-3444T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8561988 | ||||||
| chr3:8562193
|
A | G | 3 | a0001c0001t0001g0170a0001c0001t0001g0182a0001c0001t0001g0185 | 3 | HG02486.hp1 HG02647.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.724-3239A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8562193 | ||||||
| chr3:8562250
|
T | C | 45 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0053others(42): Show | 45 | HG01106.hp1 HG01109.hp2 HG01884.hp2 others(42): Show |
intron_variant | MODIFIER | c.724-3182T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8562250 | ||||||
| chr3:8562330
|
A | C | 1 | a0001c0001t0002g0204 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.724-3102A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8562330 | ||||||
| chr3:8562393
|
T | A | 102 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(99): Show | 104 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.724-3039T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8562393 | ||||||
| chr3:8562496
|
C | T | 1 | a0001c0002t0001g0245 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.724-2936C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8562496 | ||||||
| chr3:8562683
|
C | A | 1 | a0001c0002t0001g0216 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.724-2749C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8562683 | ||||||
| chr3:8562768
|
A | G | 32 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0053others(29): Show | 32 | HG01106.hp1 HG01109.hp2 HG02055.hp2 others(29): Show |
intron_variant | MODIFIER | c.724-2664A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8562768 | ||||||
| chr3:8562898
|
G | C | 2 | a0001c0001t0001g0228a0001c0001t0021g0067 | 2 | HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.724-2534G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8562898 | ||||||
| chr3:8562964
|
G | T | 2 | a0001c0001t0017g0180a0001c0001t0017g0181 | 2 | HG02523.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.724-2468G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8562964 | ||||||
| chr3:8563033
|
T | C | 1 | a0001c0001t0002g0224 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.724-2399T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8563033 | ||||||
| chr3:8563278
|
T | C | 1 | a0001c0001t0051g0091 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.724-2154T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8563278 | ||||||
| chr3:8563289
|
C | G | 2 | a0001c0001t0034g0302a0001c0001t0040g0169 | 2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.724-2143C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8563289 | ||||||
| chr3:8563381
|
C | G | 121 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(118): Show | 123 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.724-2051C>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8563381 | ||||||
| chr3:8563459
|
G | A | 117 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(114): Show | 119 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.724-1973G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8563459 | ||||||
| chr3:8563608
|
G | T | 1 | a0001c0001t0002g0166 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.724-1824G>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8563608 | ||||||
| chr3:8563613
|
G | A | 1 | a0001c0001t0002g0232 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.724-1819G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8563613 | ||||||
| chr3:8563645
|
T | C | 1 | a0003c0012t0001g0082 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.724-1787T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8563645 | ||||||
| chr3:8563683
|
A | G | 1 | a0010c0011t0001g0256 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.724-1749A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8563683 | ||||||
| chr3:8563711
|
C | A | 3 | a0001c0001t0001g0170a0001c0001t0001g0182a0001c0001t0001g0185 | 3 | HG02486.hp1 HG02647.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.724-1721C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8563711 | ||||||
| chr3:8563884
|
A | G | 56 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(53): Show | 58 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.724-1548A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8563884 | ||||||
| chr3:8563885
|
C | T | 1 | a0001c0001t0001g0085 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.724-1547C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8563885 | ||||||
| chr3:8564027
|
G | A | 3 | a0001c0001t0001g0170a0001c0001t0001g0182a0001c0001t0001g0185 | 3 | HG02486.hp1 HG02647.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.724-1405G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8564027 | ||||||
| chr3:8564214
|
T | A | 1 | a0001c0001t0002g0034 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.724-1218T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8564214 | ||||||
| chr3:8564216
|
C | A | 5 | a0001c0001t0001g0170a0001c0001t0001g0182a0001c0001t0001g0185others(2): Show | 5 | HG02486.hp1 HG02647.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.724-1216C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8564216 | ||||||
| chr3:8564262
|
A | ATAT | 3 | a0001c0001t0001g0010a0001c0001t0014g0294a0001c0001t0052g0293 | 3 | HG01884.hp2 HG02055.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.724-1153_724-1151d others(5): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 8564262 | |||||
| chr3:8564533
|
A | G | 1 | a0001c0001t0001g0043 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.724-899A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8564533 | ||||||
| chr3:8564667
|
A | C | 121 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(118): Show | 123 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.724-765A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8564667 | ||||||
| chr3:8564673
|
A | G | 1 | a0001c0001t0004g0178 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.724-759A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8564673 | ||||||
| chr3:8564745
|
T | G | 3 | a0001c0001t0004g0178a0001c0001t0034g0302a0001c0001t0040g0169 | 3 | HG02258.hp2 HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.724-687T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8564745 | ||||||
| chr3:8565153
|
A | G | 60 | a0001c0001t0001g0014a0001c0001t0001g0026a0001c0001t0001g0093others(57): Show | 61 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.724-279A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8565153 | ||||||
| chr3:8565245
|
G | A | 2 | a0001c0001t0021g0067a0001c0001t0040g0169 | 2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.724-187G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8565245 | ||||||
| chr3:8565307
|
C | T | 1 | a0001c0001t0002g0242 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.724-125C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 4/5 | chr3 | 8565307 | ||||||
| chr3:8565681
|
T | C | 1 | a0006c0010t0002g0102 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.939+34T>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 5/5 | chr3 | 8565681 | ||||||
| chr3:8565847
|
G | C | 142 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(139): Show | 146 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.939+200G>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 5/5 | chr3 | 8565847 | ||||||
| chr3:8565953
|
T | A | 1 | a0001c0001t0003g0046 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.939+306T>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 5/5 | chr3 | 8565953 | ||||||
| chr3:8565968
|
T | G | 1 | a0001c0001t0034g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.939+321T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 5/5 | chr3 | 8565968 | ||||||
| chr3:8566266
|
GTAACTC | G | 14 | a0001c0001t0001g0016a0001c0001t0001g0079a0001c0001t0001g0081others(11): Show | 14 | HG00597.hp2 HG02080.hp1 HG02132.hp1 others(11): Show |
intron_variant | MODIFIER | c.939+623_939+628del others(6): Show |
LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 8566266 | |||||
| chr3:8566331
|
C | A | 1 | a0001c0001t0001g0036 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.939+684C>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 5/5 | chr3 | 8566331 | ||||||
| chr3:8566561
|
T | G | 5 | a0001c0001t0012g0020a0001c0001t0012g0246a0001c0001t0014g0184others(2): Show | 5 | HG01074.hp2 HG02055.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.940-879T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 5/5 | chr3 | 8566561 | ||||||
| chr3:8566652
|
A | G | 1 | a0001c0001t0034g0302 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.940-788A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 5/5 | chr3 | 8566652 | ||||||
| chr3:8566743
|
A | C | 5 | a0001c0001t0007g0230a0001c0001t0007g0301a0001c0001t0007g0303others(2): Show | 5 | HG02615.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.940-697A>C | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 5/5 | chr3 | 8566743 | ||||||
| chr3:8566817
|
T | G | 2 | a0001c0001t0003g0188a0001c0001t0003g0189 | 2 | HG00140.hp1 HG00639.hp1 |
intron_variant | MODIFIER | c.940-623T>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 5/5 | chr3 | 8566817 | ||||||
| chr3:8567023
|
G | A | 1 | a0001c0001t0029g0285 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.940-417G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 5/5 | chr3 | 8567023 | ||||||
| chr3:8567220
|
A | AT | 7 | a0001c0001t0007g0230a0001c0001t0007g0301a0001c0001t0007g0303others(4): Show | 7 | HG02615.hp2 HG03130.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.940-212dupT | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 8567220 | |||||
| chr3:8567234
|
G | A | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(214): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.940-206G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 5/5 | chr3 | 8567234 | ||||||
| chr3:8567385
|
G | A | 96 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0007others(93): Show | 99 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.940-55G>A | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 5/5 | chr3 | 8567385 | ||||||
| chr3:8567395
|
A | G | 7 | a0001c0001t0007g0230a0001c0001t0007g0301a0001c0001t0007g0303others(4): Show | 7 | HG02615.hp2 HG03130.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.940-45A>G | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 5/5 | chr3 | 8567395 | ||||||
| chr3:8567430
|
C | T | 1 | a0001c0001t0003g0058 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.940-10C>T | LMCD1 | ENSG00000071282.12 | transcript | ENST00000157600.8 | protein_coding | 5/5 | chr3 | 8567430 |