Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51451 |
| ensemblid | ENSG00000205629.12 |
| hgncid | 17557 |
| symbol | LCMT1 |
| name | leucine carboxyl methyltransferase 1 |
| refseq_nuc | NM_016309.3 |
| refseq_prot | NP_057393.2 |
| ensembl_nuc | ENST00000399069.8 |
| ensembl_prot | ENSP00000382021.3 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 25111742 |
| end | 25178228 |
| strand | + |
| ver | v1.2 |
| region | chr16:25111742-25178228 |
| region5000 | chr16:25106742-25183228 |
| regionname0 | LCMT1_chr16_25111742_25178228 |
| regionname5000 | LCMT1_chr16_25106742_25183228 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 334 | 347 | 90 | 58 | 147 | 16 | 34 | 105 | LCMT1_chr16_25106742_25183228 | LCMT1 | copy fasta | chr16 | 25106742 | 25183228 |
| a0002 | 0/0 | 334 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | copy fasta | chr16 | 25106742 | 25183228 |
| chapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1005 | 347 | 90 | 58 | 147 | 16 | 34 | LCMT1_chr16_25106742_25183228 | LCMT1 | copy fasta | chr16 | 25106742 | 25183228 | |
| c0002 | 0/0 | 1005 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | copy fasta | chr16 | 25106742 | 25183228 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 348 | 328 | 73 | 55 | 148 | 16 | 34 | LCMT1_chr16_25106742_25183228 | LCMT1 | copy fasta | chr16 | 25106742 | 25183228 |
| t0002 | 0/0 | 348 | 9 | 8 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | copy fasta | chr16 | 25106742 | 25183228 |
| t0003 | 0/0 | 348 | 8 | 7 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | copy fasta | chr16 | 25106742 | 25183228 |
| t0004 | 0/0 | 348 | 2 | 2 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | copy fasta | chr16 | 25106742 | 25183228 |
| t0005 | 0/0 | 348 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | copy fasta | chr16 | 25106742 | 25183228 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0004 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0036 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0132 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1005 | 347 | 90 | 58 | 147 | 16 | 34 | LCMT1_chr16_25106742_25183228 | LCMT1 | copy fasta | chr16 | 25106742 | 25183228 | |
| a0002c0002 | 0/0 | 1005 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | copy fasta | chr16 | 25106742 | 25183228 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1352 | 327 | 73 | 55 | 147 | 16 | 34 | LCMT1_chr16_25106742_25183228 | LCMT1 | copy fasta | chr16 | 25106742 | 25183228 |
| a0001c0001t0002 | 0/0 | 1352 | 9 | 8 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | copy fasta | chr16 | 25106742 | 25183228 |
| a0001c0001t0003 | 0/0 | 1352 | 8 | 7 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | copy fasta | chr16 | 25106742 | 25183228 |
| a0001c0001t0004 | 0/0 | 1352 | 2 | 2 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | copy fasta | chr16 | 25106742 | 25183228 |
| a0001c0001t0005 | 0/0 | 1352 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | copy fasta | chr16 | 25106742 | 25183228 |
| a0002c0002t0001 | 0/0 | 1352 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | copy fasta | chr16 | 25106742 | 25183228 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0036 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0132 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0004g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0001c0001t0005g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0313 | EUR | GBR | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | GBR | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0216 | EUR | GBR | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0060 | EUR | GBR | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0259 | EUR | FIN | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0086 | EUR | FIN | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | CHS | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | CHS | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | CHS | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | CHS | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | CHS | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | CHS | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | CHS | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | CHS | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | CHS | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | PUR | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0210 | AMR | PUR | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0044 | AMR | PUR | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | CLM | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | CLM | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0082 | EUR | IBS | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0230 | EUR | IBS | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0131 | AFR | ACB | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PEL | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PEL | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01934 | hp2 | a0001 | c0001 | t0005 | g0027 | AMR | PEL | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0282 | AMR | PEL | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | PEL | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | KHV | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | KHV | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | KHV | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0094 | AFR | ACB | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | KHV | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | KHV | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | ACB | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | CDX | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | CDX | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | CDX | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | CDX | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0104 | AFR | ACB | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | ACB | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | ACB | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | PEL | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | PEL | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0334 | AFR | ACB | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0134 | AFR | GWD | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0315 | SAS | PJL | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0195 | AFR | GWD | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0080 | AFR | GWD | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0327 | SAS | PJL | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0015 | AFR | GWD | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | GWD | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0272 | SAS | PJL | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0218 | AFR | GWD | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | GWD | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0093 | AFR | GWD | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0090 | AFR | GWD | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0328 | AFR | GWD | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ESN | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | ESN | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | ESN | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0271 | SAS | PJL | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | MSL | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | MSL | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0133 | AFR | ESN | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | ESN | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | ESN | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | ESN | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0300 | AFR | ESN | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0016 | AFR | ESN | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | MSL | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0274 | SAS | PJL | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | MSL | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | MSL | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0292 | SAS | PJL | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0314 | SAS | PJL | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | ESN | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | MSL | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | MSL | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0269 | SAS | PJL | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0293 | SAS | STU | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | STU | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0275 | SAS | PJL | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0312 | SAS | PJL | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | BEB | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | BEB | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | BEB | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | BEB | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | BEB | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | BEB | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0284 | SAS | STU | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | STU | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0268 | SAS | STU | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | STU | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0264 | SAS | STU | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | STU | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | YRI | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | CHB | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | CHB | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | YRI | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | YRI | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | LWK | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | LWK | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | LWK | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | LWK | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA19082 | hp2 | a0002 | c0002 | t0001 | g0153 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | YRI | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | YRI | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | ASW | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ASW | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0286 | EUR | TSI | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0087 | EUR | TSI | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0085 | EUR | TSI | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0289 | EUR | TSI | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | CLM | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0103 | AFR | ACB | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | ACB | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0102 | AFR | ACB | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0333 | AFR | ACB | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0331 | AFR | USA | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0211 | AFR | USA | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0217 | AFR | USA | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | USA | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | LWK | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | LWK | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0036 | REF | REF | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0132 | REF | REF | LCMT1_chr16_25106742_25183228 | LCMT1 | chr16 | 25106742 | 25183228 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:25170756 | G | T | 1 | a0002 | 1 | NA19082.hp2 | missense_variant | MODERATE | c.835G>T | p.Val279Phe | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 9/11 | 977/1352 | 835/1005 | 279/334 | chr16 | 25170756 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:25178091 | C | G | 1 | a0001c0001t0002 | 9 | HG01243.hp2 HG01891.hp2 HG02258.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*68C>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 11/11 | 68 | chr16 | 25178091 | |||||
| chr16:25178113 | G | A | 2 | a0001c0001t0004a0001c0001t0005 | 3 | HG01934.hp2 HG02717.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*90G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 11/11 | 90 | chr16 | 25178113 | |||||
| chr16:25178218 | A | C | 2 | a0001c0001t0003a0001c0001t0005 | 9 | HG01175.hp2 HG01934.hp2 HG02055.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*195A>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 11/11 | 195 | chr16 | 25178218 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:25112298 | A | G | 2 | a0001c0001t0001g0333a0001c0001t0001g0334 | 2 | HG02451.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.113+302A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25112298 | ||||||
| chr16:25112324 | G | A | 1 | a0001c0001t0001g0013 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.113+328G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25112324 | ||||||
| chr16:25112561 | G | A | 12 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0018others(9): Show | 12 | HG02280.hp1 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.113+565G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25112561 | ||||||
| chr16:25112759 | C | T | 1 | a0001c0001t0001g0012 | 2 | HG01884.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.113+763C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25112759 | ||||||
| chr16:25112808 | C | G | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(205): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.113+812C>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25112808 | ||||||
| chr16:25112815 | G | A | 1 | a0001c0001t0001g0026 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.113+819G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25112815 | ||||||
| chr16:25113047 | C | T | 1 | a0001c0001t0001g0025 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.113+1051C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25113047 | ||||||
| chr16:25113127 | C | T | 1 | a0001c0001t0001g0332 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.113+1131C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25113127 | ||||||
| chr16:25113133 | T | G | 1 | a0001c0001t0001g0135 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.113+1137T>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25113133 | ||||||
| chr16:25113140 | C | CA | 268 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(265): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.113+1164dupA | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 25113140 | |||||
| chr16:25113140 | C | CAA | 49 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(46): Show | 52 | HG00544.hp1 HG00609.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.113+1163_113+1164d others(4): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 25113140 | |||||
| chr16:25113192 | T | C | 1 | a0001c0001t0001g0014 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.113+1196T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25113192 | ||||||
| chr16:25113200 | G | C | 1 | a0001c0001t0001g0174 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.113+1204G>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25113200 | ||||||
| chr16:25113526 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.113+1530A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25113526 | ||||||
| chr16:25113558 | G | A | 1 | a0001c0001t0001g0008 | 2 | HG01074.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.113+1562G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25113558 | ||||||
| chr16:25113692 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.113+1696C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25113692 | ||||||
| chr16:25113792 | T | A | 1 | a0001c0001t0001g0175 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.113+1796T>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25113792 | ||||||
| chr16:25113834 | C | T | 1 | a0001c0001t0001g0327 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.113+1838C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25113834 | ||||||
| chr16:25113879 | G | A | 3 | a0001c0001t0001g0019a0001c0001t0004g0015a0001c0001t0004g0016 | 3 | HG02717.hp1 HG02965.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.113+1883G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25113879 | ||||||
| chr16:25113946 | A | G | 6 | a0001c0001t0001g0321a0001c0001t0001g0322a0001c0001t0001g0323others(3): Show | 6 | HG00673.hp1 HG02027.hp2 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.113+1950A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25113946 | ||||||
| chr16:25113952 | A | C | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0025 | 3 | HG02451.hp2 HG02897.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.113+1956A>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25113952 | ||||||
| chr16:25114156 | G | A | 330 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(327): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.113+2160G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25114156 | ||||||
| chr16:25114437 | T | C | 114 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(111): Show | 119 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.113+2441T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25114437 | ||||||
| chr16:25114461 | C | T | 5 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(2): Show | 5 | HG02280.hp1 HG02630.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.113+2465C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25114461 | ||||||
| chr16:25114548 | A | G | 2 | a0001c0001t0001g0172a0001c0001t0001g0173 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.113+2552A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25114548 | ||||||
| chr16:25114737 | T | C | 10 | a0001c0001t0001g0002a0001c0001t0001g0136a0001c0001t0001g0175others(7): Show | 12 | HG01192.hp2 HG01257.hp2 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.113+2741T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25114737 | ||||||
| chr16:25114830 | C | T | 1 | a0001c0001t0001g0320 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.113+2834C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25114830 | ||||||
| chr16:25115036 | G | C | 1 | a0001c0001t0001g0025 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.113+3040G>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25115036 | ||||||
| chr16:25115306 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.113+3310C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25115306 | ||||||
| chr16:25115347 | G | T | 1 | a0001c0001t0001g0319 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.113+3351G>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25115347 | ||||||
| chr16:25115442 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.113+3446G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25115442 | ||||||
| chr16:25115462 | C | A | 5 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(2): Show | 5 | HG02280.hp1 HG02630.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.113+3466C>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25115462 | ||||||
| chr16:25115467 | A | G | 3 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126 | 3 | HG00408.hp2 HG02074.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.113+3471A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25115467 | ||||||
| chr16:25115497 | A | G | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0025 | 3 | HG02451.hp2 HG02897.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.113+3501A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25115497 | ||||||
| chr16:25115504 | T | C | 1 | a0001c0001t0001g0187 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.113+3508T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25115504 | ||||||
| chr16:25115585 | A | C | 1 | a0001c0001t0001g0017 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.113+3589A>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25115585 | ||||||
| chr16:25115693 | T | C | 4 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(1): Show | 4 | HG02280.hp1 HG02630.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.113+3697T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25115693 | ||||||
| chr16:25115738 | C | T | 2 | a0001c0001t0001g0030a0001c0001t0001g0123 | 2 | HG02922.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.113+3742C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25115738 | ||||||
| chr16:25115770 | C | T | 4 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318others(1): Show | 4 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(1): Show |
intron_variant | MODIFIER | c.113+3774C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25115770 | ||||||
| chr16:25116073 | G | C | 29 | a0001c0001t0001g0135a0001c0001t0001g0188a0001c0001t0001g0189others(26): Show | 29 | HG01175.hp2 HG02145.hp1 HG02257.hp1 others(26): Show |
intron_variant | MODIFIER | c.113+4077G>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25116073 | ||||||
| chr16:25116109 | T | C | 5 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(2): Show | 5 | HG02280.hp1 HG02630.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.113+4113T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25116109 | ||||||
| chr16:25116120 | G | A | 109 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(106): Show | 114 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.113+4124G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25116120 | ||||||
| chr16:25116242 | C | T | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0025 | 3 | HG02451.hp2 HG02897.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.113+4246C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25116242 | ||||||
| chr16:25116324 | A | G | 9 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(6): Show | 9 | HG00099.hp1 HG00735.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.113+4328A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25116324 | ||||||
| chr16:25116414 | C | T | 3 | a0001c0001t0001g0313a0001c0001t0001g0314a0001c0001t0001g0315 | 3 | HG00099.hp1 HG02602.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.113+4418C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25116414 | ||||||
| chr16:25116454 | G | A | 5 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(2): Show | 5 | HG02280.hp1 HG02630.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.113+4458G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25116454 | ||||||
| chr16:25116692 | G | A | 1 | a0001c0001t0005g0027 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.113+4696G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25116692 | ||||||
| chr16:25116717 | C | CA | 7 | a0001c0001t0001g0032a0001c0001t0001g0137a0001c0001t0001g0214others(4): Show | 7 | HG01891.hp2 HG02717.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.113+4739dupA | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 25116717 | |||||
| chr16:25116719 | A | C | 1 | a0001c0001t0001g0121 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.113+4723A>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25116719 | ||||||
| chr16:25116772 | A | C | 1 | a0001c0001t0001g0311 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.113+4776A>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25116772 | ||||||
| chr16:25116782 | A | C | 1 | a0001c0001t0001g0120 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.113+4786A>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25116782 | ||||||
| chr16:25116854 | G | A | 12 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(9): Show | 12 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.113+4858G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25116854 | ||||||
| chr16:25116974 | G | A | 2 | a0001c0001t0001g0033a0001c0001t0001g0034 | 2 | NA18989.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.113+4978G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25116974 | ||||||
| chr16:25117058 | C | T | 6 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(3): Show | 6 | HG02280.hp1 HG02630.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.113+5062C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25117058 | ||||||
| chr16:25117070 | C | G | 4 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0004g0015others(1): Show | 4 | HG02717.hp1 HG02965.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.113+5074C>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25117070 | ||||||
| chr16:25117156 | G | A | 5 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(2): Show | 5 | HG02280.hp1 HG02630.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.113+5160G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25117156 | ||||||
| chr16:25117377 | T | C | 12 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0018others(9): Show | 12 | HG02280.hp1 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.113+5381T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25117377 | ||||||
| chr16:25117425 | G | A | 30 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0138others(27): Show | 32 | HG01884.hp1 HG01891.hp1 HG02071.hp2 others(29): Show |
intron_variant | MODIFIER | c.113+5429G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25117425 | ||||||
| chr16:25117498 | C | T | 1 | a0001c0001t0001g0023 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.113+5502C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25117498 | ||||||
| chr16:25117528 | A | C | 5 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(2): Show | 5 | HG02280.hp1 HG02630.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.113+5532A>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25117528 | ||||||
| chr16:25117593 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.113+5597C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25117593 | ||||||
| chr16:25117625 | G | T | 1 | a0001c0001t0001g0019 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.113+5629G>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25117625 | ||||||
| chr16:25117669 | A | C | 1 | a0001c0001t0001g0019 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.113+5673A>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25117669 | ||||||
| chr16:25117725 | C | T | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0025 | 3 | HG02451.hp2 HG02897.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.113+5729C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25117725 | ||||||
| chr16:25117822 | G | A | 92 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0013others(89): Show | 95 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.113+5826G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25117822 | ||||||
| chr16:25117830 | C | T | 9 | a0001c0001t0001g0137a0001c0001t0001g0166a0001c0001t0001g0304others(6): Show | 9 | NA18947.hp1 NA18991.hp2 NA19000.hp2 others(6): Show |
intron_variant | MODIFIER | c.113+5834C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25117830 | ||||||
| chr16:25117851 | C | CA | 6 | a0001c0001t0001g0035a0001c0001t0001g0120a0001c0001t0001g0138others(3): Show | 6 | HG02293.hp2 HG03704.hp2 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.113+5872dupA | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 25117851 | |||||
| chr16:25117851 | CA | C | 13 | a0001c0001t0001g0006a0001c0001t0001g0115a0001c0001t0001g0116others(10): Show | 14 | HG01069.hp2 HG01070.hp2 HG02165.hp1 others(11): Show |
intron_variant | MODIFIER | c.113+5872delA | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 25117851 | |||||
| chr16:25117868 | A | AT | 4 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(1): Show | 4 | HG02280.hp1 HG02630.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.113+5875dupT | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 25117868 | |||||
| chr16:25117920 | C | G | 2 | a0001c0001t0004g0015a0001c0001t0004g0016 | 2 | HG02717.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.113+5924C>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25117920 | ||||||
| chr16:25117969 | T | C | 64 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(61): Show | 67 | HG00621.hp2 HG00741.hp1 HG01069.hp1 others(64): Show |
intron_variant | MODIFIER | c.113+5973T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25117969 | ||||||
| chr16:25118083 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.113+6087G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25118083 | ||||||
| chr16:25118083 | G | C | 12 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0018others(9): Show | 12 | HG02280.hp1 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.113+6087G>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25118083 | ||||||
| chr16:25118110 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.113+6114A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25118110 | ||||||
| chr16:25118156 | G | T | 1 | a0001c0001t0001g0025 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.113+6160G>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25118156 | ||||||
| chr16:25118160 | C | T | 1 | a0001c0001t0001g0295 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.113+6164C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25118160 | ||||||
| chr16:25118249 | A | T | 1 | a0001c0001t0001g0025 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.113+6253A>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25118249 | ||||||
| chr16:25118440 | G | A | 110 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(107): Show | 115 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.113+6444G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25118440 | ||||||
| chr16:25118450 | G | C | 5 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(2): Show | 5 | HG02280.hp1 HG02630.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.113+6454G>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25118450 | ||||||
| chr16:25118507 | T | C | 5 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(2): Show | 5 | HG02280.hp1 HG02630.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.113+6511T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25118507 | ||||||
| chr16:25118584 | C | T | 110 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(107): Show | 115 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.113+6588C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25118584 | ||||||
| chr16:25118999 | T | C | 3 | a0001c0001t0001g0214a0001c0001t0001g0221a0001c0001t0001g0311 | 3 | NA18942.hp2 NA18995.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.113+7003T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25118999 | ||||||
| chr16:25119024 | G | A | 3 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0191 | 3 | HG02723.hp1 NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.113+7028G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25119024 | ||||||
| chr16:25119214 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.113+7218A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25119214 | ||||||
| chr16:25119295 | G | A | 1 | a0001c0001t0001g0036 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.113+7299G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25119295 | ||||||
| chr16:25119522 | A | G | 10 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(7): Show | 10 | HG00621.hp1 HG02080.hp1 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.113+7526A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25119522 | ||||||
| chr16:25119713 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.113+7717C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25119713 | ||||||
| chr16:25119759 | C | T | 2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | HG02280.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.113+7763C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25119759 | ||||||
| chr16:25119898 | T | TG | 3 | a0001c0001t0003g0102a0001c0001t0003g0103a0001c0001t0003g0104 | 3 | HG02109.hp1 HG02257.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.113+7903dupG | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 25119898 | |||||
| chr16:25119988 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.113+7992G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25119988 | ||||||
| chr16:25120004 | C | T | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | NA18948.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.113+8008C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25120004 | ||||||
| chr16:25120117 | A | C | 4 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(1): Show | 4 | HG02280.hp1 HG02630.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.113+8121A>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25120117 | ||||||
| chr16:25120125 | A | C | 2 | a0001c0001t0001g0136a0001c0001t0001g0186 | 2 | HG02135.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.113+8129A>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25120125 | ||||||
| chr16:25120160 | A | G | 4 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0004g0015others(1): Show | 4 | HG02717.hp1 HG02965.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.113+8164A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25120160 | ||||||
| chr16:25120172 | A | T | 2 | a0001c0001t0001g0271a0001c0001t0001g0272 | 2 | HG02738.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.113+8176A>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25120172 | ||||||
| chr16:25120220 | G | GT | 4 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0025others(1): Show | 4 | HG02451.hp2 HG02897.hp1 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.113+8231dupT | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 25120220 | |||||
| chr16:25120227 | TG | T | 5 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(2): Show | 5 | HG02280.hp1 HG02630.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.113+8232delG | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25120227 | ||||||
| chr16:25120228 | G | GT | 4 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0004g0015others(1): Show | 4 | HG02717.hp1 HG02965.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.113+8236dupT | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 25120228 | |||||
| chr16:25120228 | G | T | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0025 | 3 | HG02451.hp2 HG02897.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.113+8232G>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25120228 | ||||||
| chr16:25120310 | G | A | 1 | a0001c0001t0001g0037 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.114-8165G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25120310 | ||||||
| chr16:25120399 | C | T | 5 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(2): Show | 5 | HG02280.hp1 HG02630.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.114-8076C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25120399 | ||||||
| chr16:25120411 | ATTTCTTT others(3): Show |
A | 1 | a0001c0001t0001g0038 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.114-8054_114-8045d others(12): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 25120411 | |||||
| chr16:25120452 | T | C | 1 | a0001c0001t0001g0219 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.114-8023T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25120452 | ||||||
| chr16:25120479 | C | T | 3 | a0001c0001t0001g0215a0001c0001t0001g0268a0001c0001t0001g0269 | 3 | HG03669.hp2 HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.114-7996C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25120479 | ||||||
| chr16:25120527 | C | T | 1 | a0001c0001t0001g0024 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.114-7948C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25120527 | ||||||
| chr16:25120591 | C | T | 1 | a0001c0001t0001g0267 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.114-7884C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25120591 | ||||||
| chr16:25120640 | T | G | 330 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(327): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.114-7835T>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25120640 | ||||||
| chr16:25120733 | T | G | 1 | a0001c0001t0001g0277 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.114-7742T>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25120733 | ||||||
| chr16:25120736 | TTTGTTTT others(9): Show |
T | 1 | a0001c0001t0001g0024 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.114-7736_114-7721d others(18): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 25120736 | |||||
| chr16:25120739 | G | T | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0099 | 3 | HG00735.hp1 HG02451.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.114-7736G>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25120739 | ||||||
| chr16:25120740 | T | G | 1 | a0001c0001t0001g0175 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.114-7735T>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25120740 | ||||||
| chr16:25120741 | T | G | 1 | a0001c0001t0001g0304 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.114-7734T>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25120741 | ||||||
| chr16:25120746 | T | TG | 4 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0004g0015others(1): Show | 4 | HG02717.hp1 HG02965.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.114-7729_114-7728i others(3): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25120746 | ||||||
| chr16:25120752 | G | T | 12 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0018others(9): Show | 12 | HG02280.hp1 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.114-7723G>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25120752 | ||||||
| chr16:25120754 | T | G | 4 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0004g0015others(1): Show | 4 | HG02717.hp1 HG02965.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.114-7721T>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25120754 | ||||||
| chr16:25120817 | A | G | 5 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(2): Show | 5 | HG02280.hp1 HG02630.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.114-7658A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25120817 | ||||||
| chr16:25120896 | G | A | 1 | a0001c0001t0001g0019 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.114-7579G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25120896 | ||||||
| chr16:25120904 | A | G | 2 | a0001c0001t0001g0163a0001c0001t0001g0164 | 2 | HG00544.hp1 HG00609.hp1 |
intron_variant | MODIFIER | c.114-7571A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25120904 | ||||||
| chr16:25120915 | A | AT | 5 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(2): Show | 5 | HG02280.hp1 HG02630.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.114-7556dupT | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 25120915 | |||||
| chr16:25120922 | A | AT | 22 | a0001c0001t0001g0036a0001c0001t0001g0095a0001c0001t0001g0096others(19): Show | 22 | HG00597.hp1 HG01106.hp1 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.114-7535dupT | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 25120922 | |||||
| chr16:25120922 | AT | A | 7 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0018others(4): Show | 7 | HG01433.hp2 HG02451.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.114-7535delT | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 25120922 | |||||
| chr16:25121000 | A | G | 1 | a0001c0001t0001g0264 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.114-7475A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25121000 | ||||||
| chr16:25121007 | C | T | 2 | a0001c0001t0003g0093a0001c0001t0003g0094 | 2 | HG02055.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.114-7468C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25121007 | ||||||
| chr16:25121086 | A | T | 3 | a0001c0001t0001g0006a0001c0001t0001g0118a0001c0001t0001g0119 | 4 | NA18983.hp1 NA19010.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.114-7389A>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25121086 | ||||||
| chr16:25121154 | G | A | 7 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0194others(4): Show | 7 | HG02145.hp1 HG02622.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.114-7321G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25121154 | ||||||
| chr16:25121203 | G | GGATCACG others(9): Show |
5 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(2): Show | 5 | HG02280.hp1 HG02630.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.114-7269_114-7268i others(18): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 25121203 | |||||
| chr16:25121312 | A | G | 5 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(2): Show | 5 | HG02280.hp1 HG02630.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.114-7163A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25121312 | ||||||
| chr16:25121425 | G | T | 1 | a0001c0001t0001g0092 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.114-7050G>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25121425 | ||||||
| chr16:25121443 | T | C | 1 | a0001c0001t0001g0019 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.114-7032T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25121443 | ||||||
| chr16:25121499 | C | G | 5 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(2): Show | 5 | HG02280.hp1 HG02630.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.114-6976C>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25121499 | ||||||
| chr16:25121652 | A | G | 333 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(330): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.114-6823A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25121652 | ||||||
| chr16:25122095 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.114-6380G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25122095 | ||||||
| chr16:25122176 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.114-6299G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25122176 | ||||||
| chr16:25122298 | CTGA | C | 330 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(327): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.114-6160_114-6158d others(5): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 25122298 | |||||
| chr16:25122305 | T | C | 1 | a0001c0001t0001g0007 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.114-6170T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25122305 | ||||||
| chr16:25122353 | T | C | 6 | a0001c0001t0001g0176a0001c0001t0001g0224a0001c0001t0001g0225others(3): Show | 6 | HG01070.hp1 HG01255.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.114-6122T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25122353 | ||||||
| chr16:25122434 | G | A | 108 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(105): Show | 112 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.114-6041G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25122434 | ||||||
| chr16:25122476 | GT | G | 12 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0018others(9): Show | 12 | HG02280.hp1 HG02451.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.114-5992delT | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 25122476 | |||||
| chr16:25122483 | T | A | 1 | a0001c0001t0001g0296 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.114-5992T>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25122483 | ||||||
| chr16:25122611 | G | A | 1 | a0001c0001t0001g0019 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.114-5864G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25122611 | ||||||
| chr16:25122626 | G | A | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | NA18948.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.114-5849G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25122626 | ||||||
| chr16:25122712 | C | A | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0025 | 3 | HG02451.hp2 HG02897.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.114-5763C>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25122712 | ||||||
| chr16:25122713 | G | A | 1 | a0001c0001t0001g0036 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.114-5762G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25122713 | ||||||
| chr16:25122744 | G | A | 1 | a0001c0001t0001g0025 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.114-5731G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25122744 | ||||||
| chr16:25122977 | G | A | 5 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(2): Show | 5 | HG02280.hp1 HG02630.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.114-5498G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25122977 | ||||||
| chr16:25122981 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.114-5494C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25122981 | ||||||
| chr16:25122994 | C | T | 108 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(105): Show | 113 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.114-5481C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25122994 | ||||||
| chr16:25123089 | C | T | 109 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(106): Show | 114 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.114-5386C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25123089 | ||||||
| chr16:25123223 | C | CT | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(191): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.114-5233dupT | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 25123223 | |||||
| chr16:25123223 | C | CTT | 14 | a0001c0001t0001g0122a0001c0001t0001g0154a0001c0001t0001g0155others(11): Show | 14 | HG01175.hp2 HG01261.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.114-5234_114-5233d others(4): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 25123223 | |||||
| chr16:25123252 | T | A | 1 | a0001c0001t0001g0180 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.114-5223T>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25123252 | ||||||
| chr16:25123311 | A | T | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0025 | 3 | HG02451.hp2 HG02897.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.114-5164A>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25123311 | ||||||
| chr16:25123346 | T | C | 4 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0004g0015others(1): Show | 4 | HG02717.hp1 HG02965.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.114-5129T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25123346 | ||||||
| chr16:25123490 | G | T | 5 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(2): Show | 5 | HG02280.hp1 HG02630.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.114-4985G>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25123490 | ||||||
| chr16:25123504 | C | T | 1 | a0001c0001t0001g0292 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.114-4971C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25123504 | ||||||
| chr16:25123586 | C | T | 109 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(106): Show | 114 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.114-4889C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25123586 | ||||||
| chr16:25123600 | C | CT | 17 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0018others(14): Show | 18 | HG00621.hp1 HG01256.hp1 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.114-4850dupT | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 25123600 | |||||
| chr16:25123600 | CT | C | 184 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(181): Show | 194 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(191): Show |
intron_variant | MODIFIER | c.114-4850delT | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 25123600 | |||||
| chr16:25123600 | CTT | C | 12 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(9): Show | 12 | HG00140.hp1 HG02055.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.114-4851_114-4850d others(4): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 25123600 | |||||
| chr16:25123600 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0024 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.114-4862_114-4850d others(15): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 25123600 | |||||
| chr16:25123676 | T | C | 330 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(327): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.114-4799T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25123676 | ||||||
| chr16:25123711 | G | A | 1 | a0001c0001t0003g0093 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.114-4764G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25123711 | ||||||
| chr16:25123768 | C | T | 1 | a0001c0001t0001g0291 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.114-4707C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25123768 | ||||||
| chr16:25123769 | G | A | 5 | a0001c0001t0001g0038a0001c0001t0001g0043a0001c0001t0002g0039others(2): Show | 5 | HG01167.hp1 HG01243.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.114-4706G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25123769 | ||||||
| chr16:25123801 | G | GT | 4 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0004g0015others(1): Show | 4 | HG02717.hp1 HG02965.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.114-4671dupT | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 25123801 | |||||
| chr16:25123842 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.114-4633C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25123842 | ||||||
| chr16:25123932 | T | C | 1 | a0001c0001t0001g0035 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.114-4543T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25123932 | ||||||
| chr16:25124049 | T | A | 1 | a0001c0001t0001g0045 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.114-4426T>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25124049 | ||||||
| chr16:25124309 | C | G | 1 | a0001c0001t0001g0222 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.114-4166C>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25124309 | ||||||
| chr16:25124353 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.114-4122G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25124353 | ||||||
| chr16:25124357 | A | T | 1 | a0001c0001t0002g0080 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.114-4118A>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25124357 | ||||||
| chr16:25124557 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.114-3918C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25124557 | ||||||
| chr16:25124718 | G | T | 1 | a0001c0001t0001g0259 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.114-3757G>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25124718 | ||||||
| chr16:25124721 | C | G | 2 | a0001c0001t0001g0162a0001c0001t0001g0258 | 2 | HG00597.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.114-3754C>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25124721 | ||||||
| chr16:25124927 | A | T | 1 | a0001c0001t0001g0334 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.114-3548A>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25124927 | ||||||
| chr16:25125031 | A | C | 126 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(123): Show | 133 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.114-3444A>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25125031 | ||||||
| chr16:25125167 | T | A | 2 | a0001c0001t0001g0231a0001c0001t0001g0273 | 2 | HG01256.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.114-3308T>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25125167 | ||||||
| chr16:25125171 | C | T | 5 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG02145.hp2 HG02897.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.114-3304C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25125171 | ||||||
| chr16:25125277 | A | G | 32 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0024others(29): Show | 32 | HG02145.hp1 HG02145.hp2 HG02257.hp1 others(29): Show |
intron_variant | MODIFIER | c.114-3198A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25125277 | ||||||
| chr16:25125447 | G | T | 1 | a0001c0001t0001g0230 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.114-3028G>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25125447 | ||||||
| chr16:25125458 | C | T | 1 | a0001c0001t0001g0299 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.114-3017C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25125458 | ||||||
| chr16:25125479 | A | G | 1 | a0001c0001t0001g0298 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.114-2996A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25125479 | ||||||
| chr16:25125486 | G | A | 5 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(2): Show | 5 | HG02280.hp1 HG02486.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.114-2989G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25125486 | ||||||
| chr16:25125557 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.114-2918G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25125557 | ||||||
| chr16:25125563 | G | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0291 | 3 | HG01884.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.114-2912G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25125563 | ||||||
| chr16:25125700 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.114-2775C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25125700 | ||||||
| chr16:25125735 | G | A | 2 | a0001c0001t0001g0299a0001c0001t0001g0333 | 2 | HG02145.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.114-2740G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25125735 | ||||||
| chr16:25125763 | C | T | 4 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0004g0015others(1): Show | 4 | HG02717.hp1 HG02965.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.114-2712C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25125763 | ||||||
| chr16:25125766 | G | A | 220 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(217): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.114-2709G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25125766 | ||||||
| chr16:25125838 | G | GTAA | 149 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(146): Show | 155 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.114-2604_114-2602d others(5): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 25125838 | |||||
| chr16:25125838 | G | GTAATAA | 25 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0141others(22): Show | 25 | HG00673.hp1 HG01891.hp1 HG02040.hp1 others(22): Show |
intron_variant | MODIFIER | c.114-2607_114-2602d others(8): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 25125838 | |||||
| chr16:25125838 | G | GTAATAAT others(2): Show |
12 | a0001c0001t0001g0001a0001c0001t0001g0023a0001c0001t0001g0025others(9): Show | 14 | HG00609.hp2 HG02717.hp2 HG02922.hp2 others(11): Show |
intron_variant | MODIFIER | c.114-2610_114-2602d others(11): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 25125838 | |||||
| chr16:25125838 | G | GTAATAAT others(5): Show |
1 | a0001c0001t0001g0334 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.114-2613_114-2602d others(14): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 25125838 | |||||
| chr16:25125838 | GTAA | G | 15 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(12): Show | 16 | HG00099.hp2 HG00280.hp1 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.114-2604_114-2602d others(5): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 25125838 | |||||
| chr16:25125838 | GTAATAA | G | 3 | a0001c0001t0001g0017a0001c0001t0001g0028a0001c0001t0001g0081 | 3 | HG01123.hp1 HG02451.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.114-2607_114-2602d others(8): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 25125838 | |||||
| chr16:25125838 | GTAATAAT others(2): Show |
G | 106 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(103): Show | 111 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.114-2610_114-2602d others(11): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 25125838 | |||||
| chr16:25125838 | GTAATAAT others(5): Show |
G | 3 | a0001c0001t0003g0102a0001c0001t0003g0103a0001c0001t0003g0104 | 3 | HG02109.hp1 HG02257.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.114-2613_114-2602d others(14): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 25125838 | |||||
| chr16:25125931 | A | G | 5 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(2): Show | 5 | HG02280.hp1 HG02486.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.114-2544A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25125931 | ||||||
| chr16:25125968 | G | C | 330 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(327): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.114-2507G>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25125968 | ||||||
| chr16:25125999 | C | T | 2 | a0001c0001t0001g0025a0001c0001t0001g0290 | 2 | HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.114-2476C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25125999 | ||||||
| chr16:25126064 | G | A | 15 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0024others(12): Show | 15 | HG01243.hp2 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.114-2411G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25126064 | ||||||
| chr16:25126069 | T | G | 1 | a0001c0001t0002g0217 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.114-2406T>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25126069 | ||||||
| chr16:25126128 | A | T | 171 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(168): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.114-2347A>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25126128 | ||||||
| chr16:25126158 | C | T | 4 | a0001c0001t0001g0018a0001c0001t0001g0187a0001c0001t0001g0299others(1): Show | 4 | HG02055.hp1 HG02145.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.114-2317C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25126158 | ||||||
| chr16:25126241 | C | T | 1 | a0001c0001t0001g0024 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.114-2234C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25126241 | ||||||
| chr16:25126356 | C | G | 1 | a0001c0001t0001g0149 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.114-2119C>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25126356 | ||||||
| chr16:25126465 | C | T | 1 | a0001c0001t0001g0024 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.114-2010C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25126465 | ||||||
| chr16:25126475 | C | G | 2 | a0001c0001t0001g0025a0001c0001t0001g0290 | 2 | HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.114-2000C>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25126475 | ||||||
| chr16:25126496 | G | A | 2 | a0001c0001t0001g0025a0001c0001t0001g0290 | 2 | HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.114-1979G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25126496 | ||||||
| chr16:25126498 | G | C | 2 | a0001c0001t0001g0025a0001c0001t0001g0290 | 2 | HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.114-1977G>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25126498 | ||||||
| chr16:25126500 | C | T | 2 | a0001c0001t0001g0025a0001c0001t0001g0290 | 2 | HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.114-1975C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25126500 | ||||||
| chr16:25126501 | C | T | 1 | a0001c0001t0001g0268 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.114-1974C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25126501 | ||||||
| chr16:25126502 | G | T | 2 | a0001c0001t0001g0025a0001c0001t0001g0290 | 2 | HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.114-1973G>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25126502 | ||||||
| chr16:25126505 | T | A | 2 | a0001c0001t0001g0025a0001c0001t0001g0290 | 2 | HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.114-1970T>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25126505 | ||||||
| chr16:25126580 | C | T | 7 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.114-1895C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25126580 | ||||||
| chr16:25126629 | G | A | 8 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0024others(5): Show | 8 | HG02055.hp1 HG02145.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.114-1846G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25126629 | ||||||
| chr16:25126634 | A | T | 109 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(106): Show | 114 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.114-1841A>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25126634 | ||||||
| chr16:25126775 | G | A | 27 | a0001c0001t0001g0010a0001c0001t0001g0029a0001c0001t0001g0122others(24): Show | 28 | HG00621.hp2 HG00741.hp1 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.114-1700G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25126775 | ||||||
| chr16:25126838 | A | G | 1 | a0001c0001t0001g0156 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.114-1637A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25126838 | ||||||
| chr16:25126861 | T | A | 6 | a0001c0001t0001g0013a0001c0001t0001g0216a0001c0001t0001g0254others(3): Show | 6 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(3): Show |
intron_variant | MODIFIER | c.114-1614T>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25126861 | ||||||
| chr16:25127060 | A | G | 2 | a0001c0001t0001g0017a0001c0001t0001g0018 | 2 | HG02451.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.114-1415A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25127060 | ||||||
| chr16:25127232 | A | T | 3 | a0001c0001t0001g0187a0001c0001t0001g0299a0001c0001t0001g0333 | 3 | HG02055.hp1 HG02145.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.114-1243A>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25127232 | ||||||
| chr16:25127424 | A | G | 1 | a0001c0001t0001g0334 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.114-1051A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25127424 | ||||||
| chr16:25127649 | A | G | 1 | a0001c0001t0001g0290 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.114-826A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25127649 | ||||||
| chr16:25127729 | G | A | 4 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0004g0015others(1): Show | 4 | HG02717.hp1 HG02965.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.114-746G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25127729 | ||||||
| chr16:25127791 | C | G | 220 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(217): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.114-684C>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25127791 | ||||||
| chr16:25127881 | GTAGTA | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(206): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.114-590_114-586del others(5): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 25127881 | |||||
| chr16:25127955 | T | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(206): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.114-520T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25127955 | ||||||
| chr16:25128078 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.114-397C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25128078 | ||||||
| chr16:25128133 | A | C | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(207): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.114-342A>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25128133 | ||||||
| chr16:25128181 | T | G | 39 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0043others(36): Show | 42 | HG00609.hp2 HG01243.hp2 HG01256.hp1 others(39): Show |
intron_variant | MODIFIER | c.114-294T>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25128181 | ||||||
| chr16:25128283 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.114-192C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25128283 | ||||||
| chr16:25128320 | T | A | 330 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(327): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.114-155T>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25128320 | ||||||
| chr16:25128410 | G | C | 34 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0043others(31): Show | 37 | HG00609.hp2 HG01243.hp2 HG01256.hp1 others(34): Show |
intron_variant | MODIFIER | c.114-65G>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 1/10 | chr16 | 25128410 | ||||||
| chr16:25128648 | G | T | 1 | a0001c0001t0001g0257 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.205+82G>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 2/10 | chr16 | 25128648 | ||||||
| chr16:25128808 | A | G | 4 | a0001c0001t0001g0164a0001c0001t0001g0230a0001c0001t0001g0252others(1): Show | 4 | HG00544.hp1 HG01516.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.205+242A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 2/10 | chr16 | 25128808 | ||||||
| chr16:25128871 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.205+305C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 2/10 | chr16 | 25128871 | ||||||
| chr16:25128933 | C | A | 1 | a0001c0001t0001g0300 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.205+367C>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 2/10 | chr16 | 25128933 | ||||||
| chr16:25129074 | G | A | 2 | a0001c0001t0001g0202a0001c0001t0001g0203 | 2 | HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.205+508G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 2/10 | chr16 | 25129074 | ||||||
| chr16:25129373 | T | G | 1 | a0001c0001t0001g0139 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.205+807T>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 2/10 | chr16 | 25129373 | ||||||
| chr16:25129374 | G | T | 109 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(106): Show | 114 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.205+808G>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 2/10 | chr16 | 25129374 | ||||||
| chr16:25129380 | A | G | 7 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.205+814A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 2/10 | chr16 | 25129380 | ||||||
| chr16:25129471 | T | G | 1 | a0001c0001t0001g0296 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.205+905T>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 2/10 | chr16 | 25129471 | ||||||
| chr16:25129587 | C | T | 3 | a0001c0001t0001g0078a0001c0001t0001g0215a0001c0001t0001g0269 | 3 | HG03669.hp2 HG03688.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.205+1021C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 2/10 | chr16 | 25129587 | ||||||
| chr16:25129918 | A | G | 1 | a0001c0001t0001g0207 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.205+1352A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 2/10 | chr16 | 25129918 | ||||||
| chr16:25129948 | G | A | 2 | a0001c0001t0001g0300a0001c0001t0001g0301 | 2 | HG03098.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.205+1382G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 2/10 | chr16 | 25129948 | ||||||
| chr16:25129963 | G | A | 1 | a0001c0001t0003g0102 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.205+1397G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 2/10 | chr16 | 25129963 | ||||||
| chr16:25130057 | A | G | 3 | a0001c0001t0001g0187a0001c0001t0001g0299a0001c0001t0001g0333 | 3 | HG02055.hp1 HG02145.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.205+1491A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 2/10 | chr16 | 25130057 | ||||||
| chr16:25130060 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.205+1494G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 2/10 | chr16 | 25130060 | ||||||
| chr16:25130196 | C | T | 2 | a0001c0001t0001g0025a0001c0001t0001g0290 | 2 | HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.205+1630C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 2/10 | chr16 | 25130196 | ||||||
| chr16:25130232 | T | C | 7 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.205+1666T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 2/10 | chr16 | 25130232 | ||||||
| chr16:25130316 | G | A | 1 | a0001c0001t0001g0310 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.205+1750G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 2/10 | chr16 | 25130316 | ||||||
| chr16:25130339 | CA | C | 8 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0077others(5): Show | 8 | HG02615.hp1 HG02717.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.205+1792delA | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 25130339 | |||||
| chr16:25130339 | CAA | C | 203 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(200): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.205+1791_205+1792d others(4): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 25130339 | |||||
| chr16:25130355 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.205+1789A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 2/10 | chr16 | 25130355 | ||||||
| chr16:25130379 | C | T | 7 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.205+1813C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 2/10 | chr16 | 25130379 | ||||||
| chr16:25130417 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.205+1851C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 2/10 | chr16 | 25130417 | ||||||
| chr16:25130549 | G | A | 7 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.206-1853G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 2/10 | chr16 | 25130549 | ||||||
| chr16:25130645 | CA | C | 34 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0138others(31): Show | 36 | HG00609.hp2 HG01243.hp2 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.206-1749delA | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 25130645 | |||||
| chr16:25130671 | A | G | 7 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.206-1731A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 2/10 | chr16 | 25130671 | ||||||
| chr16:25130683 | G | A | 2 | a0001c0001t0001g0279a0001c0001t0001g0280 | 2 | NA18963.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.206-1719G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 2/10 | chr16 | 25130683 | ||||||
| chr16:25130736 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.206-1666C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 2/10 | chr16 | 25130736 | ||||||
| chr16:25130775 | A | G | 2 | a0001c0001t0004g0015a0001c0001t0004g0016 | 2 | HG02717.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.206-1627A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 2/10 | chr16 | 25130775 | ||||||
| chr16:25131018 | A | G | 2 | a0001c0001t0004g0015a0001c0001t0004g0016 | 2 | HG02717.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.206-1384A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 2/10 | chr16 | 25131018 | ||||||
| chr16:25131023 | C | G | 7 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.206-1379C>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 2/10 | chr16 | 25131023 | ||||||
| chr16:25131152 | G | T | 3 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0123 | 3 | HG01167.hp1 HG02922.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.206-1250G>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 2/10 | chr16 | 25131152 | ||||||
| chr16:25131154 | T | C | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(218): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.206-1248T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 2/10 | chr16 | 25131154 | ||||||
| chr16:25131225 | C | T | 1 | a0001c0001t0001g0185 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.206-1177C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 2/10 | chr16 | 25131225 | ||||||
| chr16:25131304 | C | T | 7 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.206-1098C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 2/10 | chr16 | 25131304 | ||||||
| chr16:25131332 | T | C | 1 | a0001c0001t0001g0292 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.206-1070T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 2/10 | chr16 | 25131332 | ||||||
| chr16:25131461 | T | C | 1 | a0001c0001t0001g0014 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.206-941T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 2/10 | chr16 | 25131461 | ||||||
| chr16:25131612 | C | T | 7 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.206-790C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 2/10 | chr16 | 25131612 | ||||||
| chr16:25131704 | C | T | 5 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(2): Show | 5 | HG02280.hp1 HG02486.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.206-698C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 2/10 | chr16 | 25131704 | ||||||
| chr16:25131850 | T | A | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(207): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.206-552T>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 2/10 | chr16 | 25131850 | ||||||
| chr16:25131879 | G | A | 1 | a0001c0001t0001g0296 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.206-523G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 2/10 | chr16 | 25131879 | ||||||
| chr16:25131917 | A | G | 2 | a0001c0001t0001g0025a0001c0001t0001g0290 | 2 | HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.206-485A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 2/10 | chr16 | 25131917 | ||||||
| chr16:25132065 | G | A | 7 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.206-337G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 2/10 | chr16 | 25132065 | ||||||
| chr16:25132076 | T | C | 1 | a0001c0001t0001g0254 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.206-326T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 2/10 | chr16 | 25132076 | ||||||
| chr16:25132178 | A | C | 2 | a0001c0001t0001g0145a0001c0001t0001g0146 | 2 | HG01891.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.206-224A>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 2/10 | chr16 | 25132178 | ||||||
| chr16:25132240 | T | A | 4 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0004g0015others(1): Show | 4 | HG02717.hp1 HG02965.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.206-162T>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 2/10 | chr16 | 25132240 | ||||||
| chr16:25132300 | C | G | 1 | a0001c0001t0001g0075 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.206-102C>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 2/10 | chr16 | 25132300 | ||||||
| chr16:25132301 | G | A | 1 | a0001c0001t0001g0024 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.206-101G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 2/10 | chr16 | 25132301 | ||||||
| chr16:25132324 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.206-78T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 2/10 | chr16 | 25132324 | ||||||
| chr16:25132397 | C | G | 1 | a0001c0001t0003g0210 | 1 | HG01175.hp2 | splice_region_variant&intron_variant | LOW | c.206-5C>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 2/10 | chr16 | 25132397 | ||||||
| chr16:25132559 | T | C | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0263 | 3 | NA19002.hp2 NA19060.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.327+36T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25132559 | ||||||
| chr16:25132586 | TAATTCGA others(7): Show |
T | 4 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0004g0015others(1): Show | 4 | HG02717.hp1 HG02965.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+65_327+78delAT others(12): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 25132586 | |||||
| chr16:25132602 | C | T | 4 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0004g0015others(1): Show | 4 | HG02717.hp1 HG02965.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+79C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25132602 | ||||||
| chr16:25132817 | G | A | 4 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0004g0015others(1): Show | 4 | HG02717.hp1 HG02965.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+294G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25132817 | ||||||
| chr16:25132838 | G | A | 5 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG02559.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.327+315G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25132838 | ||||||
| chr16:25132850 | A | G | 4 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0004g0015others(1): Show | 4 | HG02717.hp1 HG02965.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+327A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25132850 | ||||||
| chr16:25132858 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0001g0018 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.327+343_327+352dup others(10): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 25132858 | |||||
| chr16:25132858 | C | CTTTTTTT others(4): Show |
2 | a0001c0001t0004g0015a0001c0001t0004g0016 | 2 | HG02717.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.327+342_327+352dup others(11): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 25132858 | |||||
| chr16:25132858 | C | CTTTTTTT others(5): Show |
3 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0290 | 3 | HG02922.hp2 NA19240.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.327+341_327+352dup others(12): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 25132858 | |||||
| chr16:25132858 | C | CTTTTTTT others(6): Show |
2 | a0001c0001t0001g0014a0001c0001t0001g0019 | 2 | HG02965.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.327+340_327+352dup others(13): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 25132858 | |||||
| chr16:25132858 | C | CTTTTTTT others(7): Show |
1 | a0001c0001t0001g0333 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.327+339_327+352dup others(14): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 25132858 | |||||
| chr16:25132858 | CTT | C | 108 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(105): Show | 113 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.327+351_327+352del others(2): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 25132858 | |||||
| chr16:25132935 | A | G | 5 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG02559.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.327+412A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25132935 | ||||||
| chr16:25133208 | T | C | 5 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG02559.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.327+685T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25133208 | ||||||
| chr16:25133226 | A | G | 2 | a0001c0001t0001g0074a0001c0001t0001g0075 | 2 | HG02040.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.327+703A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25133226 | ||||||
| chr16:25133385 | G | GT | 81 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0029others(78): Show | 82 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.327+892dupT | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 25133385 | |||||
| chr16:25133385 | G | GTT | 34 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0046others(31): Show | 36 | HG00099.hp2 HG00544.hp1 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.327+891_327+892dup others(2): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 25133385 | |||||
| chr16:25133385 | G | GTTT | 8 | a0001c0001t0001g0115a0001c0001t0001g0176a0001c0001t0001g0227others(5): Show | 8 | HG00423.hp2 HG01070.hp1 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.327+890_327+892dup others(3): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 25133385 | |||||
| chr16:25133385 | GT | G | 15 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0022others(12): Show | 16 | HG01074.hp1 HG02109.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.327+892delT | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 25133385 | |||||
| chr16:25133385 | GTT | G | 26 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0140others(23): Show | 28 | HG00609.hp2 HG01884.hp1 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.327+891_327+892del others(2): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 25133385 | |||||
| chr16:25133385 | GTTT | G | 17 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0072others(14): Show | 17 | HG00673.hp2 HG01123.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.327+890_327+892del others(3): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 25133385 | |||||
| chr16:25133385 | GTTTT | G | 90 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(87): Show | 95 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.327+889_327+892del others(4): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 25133385 | |||||
| chr16:25133587 | C | T | 108 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(105): Show | 113 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.327+1064C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25133587 | ||||||
| chr16:25133599 | G | A | 4 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(1): Show | 4 | HG02280.hp1 HG02630.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+1076G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25133599 | ||||||
| chr16:25133755 | C | G | 4 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0004g0015others(1): Show | 4 | HG02717.hp1 HG02965.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+1232C>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25133755 | ||||||
| chr16:25133755 | C | T | 5 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG02559.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.327+1232C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25133755 | ||||||
| chr16:25133810 | G | T | 1 | a0001c0001t0003g0093 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.327+1287G>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25133810 | ||||||
| chr16:25133998 | C | G | 13 | a0001c0001t0001g0010a0001c0001t0001g0029a0001c0001t0001g0122others(10): Show | 14 | HG00741.hp1 HG01175.hp1 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.327+1475C>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25133998 | ||||||
| chr16:25134009 | G | C | 2 | a0001c0001t0004g0015a0001c0001t0004g0016 | 2 | HG02717.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.327+1486G>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25134009 | ||||||
| chr16:25134032 | T | TA | 34 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0012others(31): Show | 38 | HG00609.hp2 HG01256.hp1 HG01258.hp1 others(35): Show |
intron_variant | MODIFIER | c.327+1528dupA | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 25134032 | |||||
| chr16:25134103 | T | C | 1 | a0001c0001t0001g0028 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.327+1580T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25134103 | ||||||
| chr16:25134163 | C | A | 1 | a0001c0001t0001g0017 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.327+1640C>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25134163 | ||||||
| chr16:25134196 | T | C | 5 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG02559.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.327+1673T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25134196 | ||||||
| chr16:25134259 | T | C | 1 | a0001c0001t0001g0082 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.327+1736T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25134259 | ||||||
| chr16:25134445 | G | A | 4 | a0001c0001t0001g0013a0001c0001t0001g0254a0001c0001t0001g0256others(1): Show | 4 | HG00099.hp2 HG00280.hp1 HG00738.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+1922G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25134445 | ||||||
| chr16:25134452 | C | T | 1 | a0001c0001t0001g0012 | 2 | HG01884.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.327+1929C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25134452 | ||||||
| chr16:25134507 | G | A | 1 | a0001c0001t0001g0296 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.327+1984G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25134507 | ||||||
| chr16:25134554 | G | A | 1 | a0002c0002t0001g0153 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.327+2031G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25134554 | ||||||
| chr16:25134560 | C | T | 1 | a0001c0001t0001g0300 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.327+2037C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25134560 | ||||||
| chr16:25134599 | C | T | 7 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(4): Show | 7 | HG02559.hp2 HG02897.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.327+2076C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25134599 | ||||||
| chr16:25134647 | C | G | 1 | a0001c0001t0001g0106 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.327+2124C>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25134647 | ||||||
| chr16:25134683 | C | T | 108 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(105): Show | 113 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.327+2160C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25134683 | ||||||
| chr16:25134701 | A | G | 5 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG02559.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.327+2178A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25134701 | ||||||
| chr16:25134737 | A | T | 1 | a0001c0001t0001g0106 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.327+2214A>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25134737 | ||||||
| chr16:25134834 | C | G | 2 | a0001c0001t0001g0167a0001c0001t0001g0170 | 2 | HG01074.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.327+2311C>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25134834 | ||||||
| chr16:25135124 | T | A | 4 | a0001c0001t0001g0234a0001c0001t0001g0274a0001c0001t0001g0275others(1): Show | 4 | HG02735.hp1 HG03239.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+2601T>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25135124 | ||||||
| chr16:25135139 | G | A | 1 | a0001c0001t0001g0025 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.327+2616G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25135139 | ||||||
| chr16:25135281 | T | A | 1 | a0001c0001t0001g0047 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.327+2758T>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25135281 | ||||||
| chr16:25135284 | A | AAAAAAAA others(39): Show |
1 | a0001c0001t0001g0018 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.327+2762_327+2763i others(48): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 25135284 | |||||
| chr16:25135284 | A | AAAATATA others(15): Show |
1 | a0001c0001t0001g0024 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.327+2762_327+2763i others(24): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 25135284 | |||||
| chr16:25135284 | A | AAAATATA others(7): Show |
3 | a0001c0001t0001g0025a0001c0001t0001g0290a0001c0001t0001g0333 | 3 | HG02559.hp2 HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.327+2762_327+2763i others(16): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 25135284 | |||||
| chr16:25135284 | A | AAT | 28 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0028others(25): Show | 29 | HG00280.hp2 HG00621.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.327+2768_327+2769d others(4): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 25135284 | |||||
| chr16:25135284 | A | AATAT | 8 | a0001c0001t0001g0019a0001c0001t0001g0030a0001c0001t0001g0038others(5): Show | 8 | HG01167.hp1 HG01515.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.327+2766_327+2769d others(6): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 25135284 | |||||
| chr16:25135284 | A | T | 1 | a0001c0001t0001g0047 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.327+2761A>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25135284 | ||||||
| chr16:25135287 | ATATATC | A | 63 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(60): Show | 67 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.327+2770_327+2775d others(8): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 25135287 | |||||
| chr16:25135293 | C | A | 52 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0018others(49): Show | 53 | HG00280.hp2 HG00621.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.327+2770C>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25135293 | ||||||
| chr16:25135293 | C | CTA | 6 | a0001c0001t0001g0222a0001c0001t0001g0230a0001c0001t0001g0288others(3): Show | 6 | HG00099.hp1 HG01069.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.327+2785_327+2786d others(4): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 25135293 | |||||
| chr16:25135297 | A | G | 5 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG02559.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.327+2774A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25135297 | ||||||
| chr16:25135326 | T | G | 5 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG02559.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.327+2803T>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25135326 | ||||||
| chr16:25136017 | G | A | 1 | a0001c0001t0002g0134 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.327+3494G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25136017 | ||||||
| chr16:25136057 | C | T | 108 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(105): Show | 113 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.327+3534C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25136057 | ||||||
| chr16:25136090 | C | CA | 106 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(103): Show | 110 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.327+3588dupA | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 25136090 | |||||
| chr16:25136090 | C | CAA | 13 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0030others(10): Show | 14 | HG00544.hp2 HG01099.hp2 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.327+3587_327+3588d others(4): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 25136090 | |||||
| chr16:25136090 | CA | C | 7 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0145others(4): Show | 7 | HG01891.hp1 HG02451.hp2 HG03516.hp2 others(4): Show |
intron_variant | MODIFIER | c.327+3588delA | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 25136090 | |||||
| chr16:25136108 | A | C | 1 | a0001c0001t0001g0234 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.327+3585A>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25136108 | ||||||
| chr16:25136366 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.328-3805G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25136366 | ||||||
| chr16:25136384 | T | G | 2 | a0001c0001t0001g0014a0001c0001t0001g0019 | 2 | HG02965.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.328-3787T>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25136384 | ||||||
| chr16:25136441 | A | G | 34 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0019others(31): Show | 36 | HG00609.hp2 HG01884.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.328-3730A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25136441 | ||||||
| chr16:25136446 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.328-3725G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25136446 | ||||||
| chr16:25136463 | C | T | 2 | a0001c0001t0001g0238a0001c0001t0001g0264 | 2 | HG04204.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.328-3708C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25136463 | ||||||
| chr16:25136607 | T | G | 108 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(105): Show | 113 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.328-3564T>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25136607 | ||||||
| chr16:25136781 | C | T | 1 | a0001c0001t0001g0160 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.328-3390C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25136781 | ||||||
| chr16:25136797 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.328-3374C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25136797 | ||||||
| chr16:25136837 | C | T | 5 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG02559.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.328-3334C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25136837 | ||||||
| chr16:25136862 | G | A | 5 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG02559.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.328-3309G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25136862 | ||||||
| chr16:25136893 | A | G | 1 | a0001c0001t0001g0168 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.328-3278A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25136893 | ||||||
| chr16:25137160 | G | A | 1 | a0001c0001t0001g0019 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.328-3011G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25137160 | ||||||
| chr16:25137224 | C | T | 1 | a0001c0001t0001g0024 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.328-2947C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25137224 | ||||||
| chr16:25137427 | A | G | 1 | a0001c0001t0001g0227 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.328-2744A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25137427 | ||||||
| chr16:25137535 | C | T | 109 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(106): Show | 114 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.328-2636C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25137535 | ||||||
| chr16:25137741 | G | GC | 151 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(148): Show | 159 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.328-2429dupC | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 25137741 | |||||
| chr16:25137773 | A | C | 1 | a0001c0001t0001g0178 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.328-2398A>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25137773 | ||||||
| chr16:25137885 | A | G | 151 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(148): Show | 159 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.328-2286A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25137885 | ||||||
| chr16:25138047 | G | A | 30 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(27): Show | 32 | HG00609.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.328-2124G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25138047 | ||||||
| chr16:25138062 | C | T | 2 | a0001c0001t0001g0246a0001c0001t0001g0266 | 2 | HG01106.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.328-2109C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25138062 | ||||||
| chr16:25138146 | C | T | 37 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(34): Show | 40 | HG00609.hp2 HG01256.hp1 HG01258.hp1 others(37): Show |
intron_variant | MODIFIER | c.328-2025C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25138146 | ||||||
| chr16:25138240 | G | A | 2 | a0001c0001t0003g0094a0001c0001t0003g0211 | 2 | HG02055.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.328-1931G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25138240 | ||||||
| chr16:25138264 | A | G | 5 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG02559.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.328-1907A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25138264 | ||||||
| chr16:25138357 | A | G | 150 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(147): Show | 158 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.328-1814A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25138357 | ||||||
| chr16:25138359 | G | A | 4 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(1): Show | 4 | HG02280.hp1 HG02630.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-1812G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25138359 | ||||||
| chr16:25138405 | A | G | 168 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0009others(165): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.328-1766A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25138405 | ||||||
| chr16:25138475 | G | C | 5 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG02559.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.328-1696G>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25138475 | ||||||
| chr16:25138776 | C | T | 1 | a0001c0001t0001g0283 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.328-1395C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25138776 | ||||||
| chr16:25138825 | C | T | 2 | a0001c0001t0001g0025a0001c0001t0001g0290 | 2 | HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.328-1346C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25138825 | ||||||
| chr16:25138894 | C | T | 2 | a0001c0001t0001g0025a0001c0001t0001g0290 | 2 | HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.328-1277C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25138894 | ||||||
| chr16:25138965 | G | A | 1 | a0001c0001t0003g0102 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.328-1206G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25138965 | ||||||
| chr16:25139024 | C | G | 1 | a0001c0001t0001g0296 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.328-1147C>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25139024 | ||||||
| chr16:25139152 | C | T | 4 | a0001c0001t0001g0001a0001c0001t0001g0150a0001c0001t0001g0151others(1): Show | 6 | NA18953.hp1 NA18983.hp2 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.328-1019C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25139152 | ||||||
| chr16:25139181 | A | G | 1 | a0001c0001t0003g0093 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.328-990A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25139181 | ||||||
| chr16:25139339 | A | G | 3 | a0001c0001t0001g0002a0001c0001t0001g0180a0001c0001t0001g0184 | 5 | HG01192.hp2 HG01257.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.328-832A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25139339 | ||||||
| chr16:25139414 | G | A | 2 | a0001c0001t0004g0015a0001c0001t0004g0016 | 2 | HG02717.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.328-757G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25139414 | ||||||
| chr16:25139499 | G | A | 2 | a0001c0001t0001g0014a0001c0001t0001g0019 | 2 | HG02965.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.328-672G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25139499 | ||||||
| chr16:25139505 | G | A | 23 | a0001c0001t0001g0028a0001c0001t0001g0068a0001c0001t0001g0081others(20): Show | 23 | HG00280.hp2 HG00621.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.328-666G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25139505 | ||||||
| chr16:25139530 | A | G | 2 | a0001c0001t0004g0015a0001c0001t0004g0016 | 2 | HG02717.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.328-641A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25139530 | ||||||
| chr16:25139691 | G | C | 5 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG02559.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.328-480G>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25139691 | ||||||
| chr16:25139842 | T | C | 1 | a0001c0001t0001g0262 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.328-329T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25139842 | ||||||
| chr16:25139867 | C | T | 5 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG02559.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.328-304C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25139867 | ||||||
| chr16:25139881 | C | G | 1 | a0001c0001t0001g0312 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.328-290C>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25139881 | ||||||
| chr16:25139895 | A | G | 1 | a0001c0001t0001g0333 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.328-276A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25139895 | ||||||
| chr16:25140036 | C | T | 2 | a0001c0001t0001g0025a0001c0001t0001g0290 | 2 | HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.328-135C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25140036 | ||||||
| chr16:25140077 | A | ACT | 151 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(148): Show | 159 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.328-93_328-92dupCT | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 25140077 | |||||
| chr16:25140162 | T | C | 2 | a0001c0001t0001g0014a0001c0001t0001g0019 | 2 | HG02965.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.328-9T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 3/10 | chr16 | 25140162 | ||||||
| chr16:25140291 | A | G | 1 | a0001c0001t0001g0252 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.404+44A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25140291 | ||||||
| chr16:25140335 | C | G | 1 | a0001c0001t0001g0197 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.404+88C>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25140335 | ||||||
| chr16:25140387 | C | T | 1 | a0001c0001t0001g0272 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.404+140C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25140387 | ||||||
| chr16:25140462 | A | G | 2 | a0001c0001t0001g0066a0001c0001t0001g0116 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.404+215A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25140462 | ||||||
| chr16:25140528 | T | G | 1 | a0001c0001t0001g0325 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.404+281T>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25140528 | ||||||
| chr16:25140531 | G | A | 6 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(3): Show | 6 | HG02055.hp1 HG02145.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.404+284G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25140531 | ||||||
| chr16:25140606 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.404+359G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25140606 | ||||||
| chr16:25140694 | C | T | 5 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG02559.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.404+447C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25140694 | ||||||
| chr16:25140948 | CTCTAT | C | 22 | a0001c0001t0001g0028a0001c0001t0001g0068a0001c0001t0001g0081others(19): Show | 22 | HG00280.hp2 HG00621.hp1 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.404+705_404+709del others(5): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 25140948 | |||||
| chr16:25141172 | C | T | 1 | a0001c0001t0001g0187 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.404+925C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25141172 | ||||||
| chr16:25141193 | C | A | 1 | a0001c0001t0001g0008 | 2 | HG01074.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.404+946C>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25141193 | ||||||
| chr16:25141193 | C | T | 2 | a0001c0001t0001g0246a0001c0001t0001g0266 | 2 | HG01106.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.404+946C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25141193 | ||||||
| chr16:25141272 | C | T | 3 | a0001c0001t0001g0144a0001c0001t0001g0155a0001c0001t0001g0156 | 3 | NA18972.hp1 NA18998.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.404+1025C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25141272 | ||||||
| chr16:25141463 | A | G | 1 | a0001c0001t0001g0018 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.404+1216A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25141463 | ||||||
| chr16:25141594 | C | T | 1 | a0001c0001t0001g0143 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.404+1347C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25141594 | ||||||
| chr16:25141597 | T | C | 109 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(106): Show | 114 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.404+1350T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25141597 | ||||||
| chr16:25141612 | C | T | 5 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG02559.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.404+1365C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25141612 | ||||||
| chr16:25141712 | C | G | 1 | a0001c0001t0001g0296 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.404+1465C>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25141712 | ||||||
| chr16:25141752 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.404+1505C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25141752 | ||||||
| chr16:25141817 | G | A | 2 | a0001c0001t0001g0216a0001c0001t0001g0222 | 2 | HG00140.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.404+1570G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25141817 | ||||||
| chr16:25141823 | T | C | 36 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(33): Show | 39 | HG00609.hp2 HG01256.hp1 HG01258.hp1 others(36): Show |
intron_variant | MODIFIER | c.404+1576T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25141823 | ||||||
| chr16:25142000 | C | T | 4 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0004g0015others(1): Show | 4 | HG02717.hp1 HG02965.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.404+1753C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25142000 | ||||||
| chr16:25142081 | G | A | 109 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(106): Show | 114 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.404+1834G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25142081 | ||||||
| chr16:25142223 | CTG | C | 4 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0004g0015others(1): Show | 4 | HG02717.hp1 HG02965.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.404+1978_404+1979d others(4): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 25142223 | |||||
| chr16:25142458 | C | T | 1 | a0001c0001t0001g0022 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.404+2211C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25142458 | ||||||
| chr16:25142725 | C | G | 7 | a0001c0001t0001g0162a0001c0001t0001g0224a0001c0001t0001g0225others(4): Show | 7 | HG00597.hp2 HG01070.hp1 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.404+2478C>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25142725 | ||||||
| chr16:25142773 | T | C | 1 | a0001c0001t0001g0140 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.404+2526T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25142773 | ||||||
| chr16:25142776 | G | A | 1 | a0001c0001t0001g0024 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.404+2529G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25142776 | ||||||
| chr16:25142966 | G | A | 1 | a0001c0001t0001g0299 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.404+2719G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25142966 | ||||||
| chr16:25143138 | G | C | 1 | a0001c0001t0001g0036 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.404+2891G>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25143138 | ||||||
| chr16:25143154 | G | A | 1 | a0001c0001t0001g0298 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.404+2907G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25143154 | ||||||
| chr16:25143311 | G | A | 109 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(106): Show | 114 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.404+3064G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25143311 | ||||||
| chr16:25143338 | G | C | 5 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG02559.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.404+3091G>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25143338 | ||||||
| chr16:25143349 | A | G | 5 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0149others(2): Show | 5 | HG01884.hp1 HG02258.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.404+3102A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25143349 | ||||||
| chr16:25143587 | AG | A | 3 | a0001c0001t0001g0231a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG01256.hp2 HG03239.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.404+3342delG | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 25143587 | |||||
| chr16:25143728 | A | G | 5 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG02559.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.404+3481A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25143728 | ||||||
| chr16:25143813 | G | C | 146 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(143): Show | 153 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.404+3566G>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25143813 | ||||||
| chr16:25143924 | C | T | 5 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0149others(2): Show | 5 | HG01884.hp1 HG02258.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.404+3677C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25143924 | ||||||
| chr16:25143963 | T | C | 5 | a0001c0001t0001g0029a0001c0001t0001g0122a0001c0001t0001g0284others(2): Show | 5 | HG01175.hp1 HG01261.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.404+3716T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25143963 | ||||||
| chr16:25144018 | A | G | 5 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG02559.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.404+3771A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25144018 | ||||||
| chr16:25144161 | C | T | 1 | a0001c0001t0001g0268 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.404+3914C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25144161 | ||||||
| chr16:25144224 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.404+3977C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25144224 | ||||||
| chr16:25144256 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.404+4009G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25144256 | ||||||
| chr16:25144592 | G | C | 1 | a0002c0002t0001g0153 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.404+4345G>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25144592 | ||||||
| chr16:25144776 | C | G | 2 | a0001c0001t0003g0090a0001c0001t0003g0210 | 2 | HG01175.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.404+4529C>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25144776 | ||||||
| chr16:25144882 | A | G | 109 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(106): Show | 114 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.404+4635A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25144882 | ||||||
| chr16:25144964 | T | A | 109 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(106): Show | 114 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.404+4717T>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25144964 | ||||||
| chr16:25145195 | G | A | 1 | a0001c0001t0001g0174 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.404+4948G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25145195 | ||||||
| chr16:25145203 | T | G | 2 | a0001c0001t0001g0018a0001c0001t0001g0333 | 2 | HG02559.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.404+4956T>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25145203 | ||||||
| chr16:25145205 | T | A | 1 | a0001c0001t0001g0299 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.404+4958T>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25145205 | ||||||
| chr16:25145753 | A | G | 2 | a0001c0001t0004g0015a0001c0001t0004g0016 | 2 | HG02717.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.404+5506A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25145753 | ||||||
| chr16:25145804 | G | A | 2 | a0001c0001t0004g0015a0001c0001t0004g0016 | 2 | HG02717.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.404+5557G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25145804 | ||||||
| chr16:25145922 | C | T | 3 | a0001c0001t0001g0007a0001c0001t0001g0172a0001c0001t0001g0173 | 4 | HG01256.hp1 HG01258.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.405-5632C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25145922 | ||||||
| chr16:25145946 | G | A | 4 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0004g0015others(1): Show | 4 | HG02717.hp1 HG02965.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.405-5608G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25145946 | ||||||
| chr16:25146128 | T | C | 174 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(171): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.405-5426T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25146128 | ||||||
| chr16:25146172 | A | G | 1 | a0001c0001t0001g0012 | 2 | HG01884.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.405-5382A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25146172 | ||||||
| chr16:25146206 | C | T | 7 | a0001c0001t0001g0008a0001c0001t0001g0165a0001c0001t0001g0200others(4): Show | 8 | HG01074.hp1 HG02109.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.405-5348C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25146206 | ||||||
| chr16:25146344 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.405-5210T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25146344 | ||||||
| chr16:25146376 | G | C | 1 | a0001c0001t0003g0093 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.405-5178G>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25146376 | ||||||
| chr16:25146438 | C | A | 170 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(167): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.405-5116C>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25146438 | ||||||
| chr16:25146475 | A | G | 1 | a0001c0001t0001g0219 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.405-5079A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25146475 | ||||||
| chr16:25146507 | A | G | 1 | a0001c0001t0001g0024 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.405-5047A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25146507 | ||||||
| chr16:25146594 | A | G | 5 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG02559.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.405-4960A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25146594 | ||||||
| chr16:25146701 | C | T | 5 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0226others(2): Show | 5 | HG01070.hp1 HG01255.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.405-4853C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25146701 | ||||||
| chr16:25146702 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.405-4852G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25146702 | ||||||
| chr16:25146729 | G | T | 1 | a0001c0001t0001g0067 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.405-4825G>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25146729 | ||||||
| chr16:25147104 | C | T | 1 | a0001c0001t0001g0019 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.405-4450C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25147104 | ||||||
| chr16:25147231 | G | C | 5 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG02559.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.405-4323G>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25147231 | ||||||
| chr16:25147404 | C | T | 36 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(33): Show | 39 | HG00609.hp2 HG01256.hp1 HG01258.hp1 others(36): Show |
intron_variant | MODIFIER | c.405-4150C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25147404 | ||||||
| chr16:25147422 | C | A | 164 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(161): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.405-4132C>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25147422 | ||||||
| chr16:25147478 | A | G | 1 | a0001c0001t0001g0065 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.405-4076A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25147478 | ||||||
| chr16:25147597 | G | A | 110 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(107): Show | 115 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.405-3957G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25147597 | ||||||
| chr16:25147702 | T | C | 1 | a0001c0001t0001g0239 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.405-3852T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25147702 | ||||||
| chr16:25147743 | G | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0287 | 3 | HG02559.hp1 HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.405-3811G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25147743 | ||||||
| chr16:25147768 | T | C | 151 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(148): Show | 159 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.405-3786T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25147768 | ||||||
| chr16:25147778 | A | G | 110 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(107): Show | 115 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.405-3776A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25147778 | ||||||
| chr16:25147824 | A | G | 151 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(148): Show | 159 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.405-3730A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25147824 | ||||||
| chr16:25147960 | A | G | 1 | a0001c0001t0001g0316 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.405-3594A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25147960 | ||||||
| chr16:25148067 | G | T | 1 | a0001c0001t0001g0200 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.405-3487G>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25148067 | ||||||
| chr16:25148094 | C | T | 5 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG02559.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.405-3460C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25148094 | ||||||
| chr16:25148347 | G | C | 34 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(31): Show | 37 | HG00609.hp2 HG01256.hp1 HG01258.hp1 others(34): Show |
intron_variant | MODIFIER | c.405-3207G>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25148347 | ||||||
| chr16:25148455 | G | A | 6 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(3): Show | 6 | HG02055.hp1 HG02145.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.405-3099G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25148455 | ||||||
| chr16:25148537 | C | T | 2 | a0001c0001t0001g0025a0001c0001t0001g0290 | 2 | HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.405-3017C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25148537 | ||||||
| chr16:25148634 | C | A | 1 | a0001c0001t0001g0024 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.405-2920C>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25148634 | ||||||
| chr16:25148819 | T | C | 4 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0290others(1): Show | 4 | HG02559.hp2 HG02922.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.405-2735T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25148819 | ||||||
| chr16:25148819 | T | G | 1 | a0001c0001t0001g0018 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.405-2735T>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25148819 | ||||||
| chr16:25148996 | G | C | 36 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(33): Show | 39 | HG00609.hp2 HG01256.hp1 HG01258.hp1 others(36): Show |
intron_variant | MODIFIER | c.405-2558G>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25148996 | ||||||
| chr16:25149159 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.405-2395G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25149159 | ||||||
| chr16:25149290 | G | A | 3 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0191 | 3 | HG02723.hp1 NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.405-2264G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25149290 | ||||||
| chr16:25149680 | A | G | 1 | a0001c0001t0001g0067 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.405-1874A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25149680 | ||||||
| chr16:25149714 | G | C | 1 | a0001c0001t0001g0067 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.405-1840G>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25149714 | ||||||
| chr16:25149796 | T | C | 1 | a0001c0001t0001g0024 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.405-1758T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25149796 | ||||||
| chr16:25149843 | G | T | 4 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0004g0015others(1): Show | 4 | HG02717.hp1 HG02965.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.405-1711G>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25149843 | ||||||
| chr16:25149910 | C | CA | 110 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(107): Show | 114 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.405-1621dupA | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 25149910 | |||||
| chr16:25149910 | C | CAA | 17 | a0001c0001t0001g0026a0001c0001t0001g0032a0001c0001t0001g0048others(14): Show | 17 | HG01175.hp2 HG02055.hp2 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.405-1622_405-1621d others(4): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 25149910 | |||||
| chr16:25149961 | G | T | 1 | a0001c0001t0001g0024 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.405-1593G>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25149961 | ||||||
| chr16:25150197 | T | C | 110 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(107): Show | 115 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.405-1357T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25150197 | ||||||
| chr16:25150230 | TAAAG | T | 171 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(168): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.405-1321_405-1318d others(6): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 25150230 | |||||
| chr16:25150271 | G | A | 110 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(107): Show | 115 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.405-1283G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25150271 | ||||||
| chr16:25150289 | CTG | C | 3 | a0001c0001t0001g0007a0001c0001t0001g0172a0001c0001t0001g0173 | 4 | HG01256.hp1 HG01258.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.405-1262_405-1261d others(4): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 25150289 | |||||
| chr16:25150333 | G | GT | 95 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(92): Show | 100 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.405-1193dupT | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 25150333 | |||||
| chr16:25150333 | G | GTT | 8 | a0001c0001t0001g0157a0001c0001t0001g0163a0001c0001t0001g0187others(5): Show | 8 | HG00609.hp1 HG01175.hp1 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.405-1194_405-1193d others(4): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 25150333 | |||||
| chr16:25150333 | GT | G | 8 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0053others(5): Show | 8 | HG02559.hp2 HG02738.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.405-1193delT | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 25150333 | |||||
| chr16:25150333 | GTT | G | 46 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0026others(43): Show | 47 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(44): Show |
intron_variant | MODIFIER | c.405-1194_405-1193d others(4): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 25150333 | |||||
| chr16:25150333 | GTTT | G | 66 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(63): Show | 70 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.405-1195_405-1193d others(5): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 25150333 | |||||
| chr16:25150333 | GTTTTTTT others(8): Show |
G | 4 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(1): Show | 4 | HG02280.hp1 HG02630.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.405-1207_405-1193d others(17): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 25150333 | |||||
| chr16:25150399 | C | T | 171 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(168): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.405-1155C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25150399 | ||||||
| chr16:25150418 | C | T | 3 | a0001c0001t0003g0102a0001c0001t0003g0103a0001c0001t0003g0104 | 3 | HG02109.hp1 HG02257.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.405-1136C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25150418 | ||||||
| chr16:25150423 | C | T | 2 | a0001c0001t0001g0018a0001c0001t0001g0333 | 2 | HG02559.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.405-1131C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25150423 | ||||||
| chr16:25150431 | G | A | 2 | a0001c0001t0004g0015a0001c0001t0004g0016 | 2 | HG02717.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.405-1123G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25150431 | ||||||
| chr16:25150683 | C | T | 1 | a0001c0001t0001g0287 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.405-871C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25150683 | ||||||
| chr16:25150855 | ATATATT | A | 5 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG02559.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.405-696_405-691del others(6): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 25150855 | |||||
| chr16:25151023 | A | G | 5 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG02559.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.405-531A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25151023 | ||||||
| chr16:25151056 | T | G | 1 | a0001c0001t0001g0112 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.405-498T>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25151056 | ||||||
| chr16:25151182 | T | C | 1 | a0001c0001t0001g0082 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.405-372T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25151182 | ||||||
| chr16:25151183 | T | C | 172 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(169): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.405-371T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25151183 | ||||||
| chr16:25151493 | C | T | 1 | a0001c0001t0001g0024 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.405-61C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25151493 | ||||||
| chr16:25151520 | A | C | 1 | a0001c0001t0001g0024 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.405-34A>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 4/10 | chr16 | 25151520 | ||||||
| chr16:25151696 | G | GGTGT | 4 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0069others(1): Show | 4 | HG02897.hp1 HG02970.hp1 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.466+105_466+108dup others(4): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr16 | 25151696 | |||||
| chr16:25151696 | G | GGTGTGT | 36 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0020others(33): Show | 39 | HG00609.hp2 HG01256.hp1 HG01258.hp1 others(36): Show |
intron_variant | MODIFIER | c.466+103_466+108dup others(6): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr16 | 25151696 | |||||
| chr16:25151696 | G | GGTGTGTG others(1): Show |
250 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(247): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.466+101_466+108dup others(8): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr16 | 25151696 | |||||
| chr16:25151696 | G | GGTGTGTG others(3): Show |
23 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0028others(20): Show | 25 | HG00544.hp1 HG01516.hp2 HG01517.hp1 others(22): Show |
intron_variant | MODIFIER | c.466+99_466+108dupT others(9): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr16 | 25151696 | |||||
| chr16:25151696 | G | GGTGTGTG others(5): Show |
5 | a0001c0001t0001g0057a0001c0001t0001g0111a0001c0001t0001g0113others(2): Show | 5 | HG00621.hp1 HG02080.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.466+97_466+108dupT others(11): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr16 | 25151696 | |||||
| chr16:25151696 | G | GGTGTGTG others(7): Show |
1 | a0001c0001t0001g0030 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.466+95_466+108dupT others(13): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr16 | 25151696 | |||||
| chr16:25151792 | C | G | 110 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(107): Show | 115 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.466+177C>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25151792 | ||||||
| chr16:25151798 | C | G | 5 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG02559.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.466+183C>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25151798 | ||||||
| chr16:25151798 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.466+183C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25151798 | ||||||
| chr16:25151806 | A | G | 5 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG02559.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.466+191A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25151806 | ||||||
| chr16:25151930 | CA | C | 110 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(107): Show | 115 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.466+316delA | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25151930 | ||||||
| chr16:25152291 | G | A | 3 | a0001c0001t0001g0248a0001c0001t0001g0251a0001c0001t0001g0331 | 3 | HG03139.hp1 HG06807.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.466+676G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25152291 | ||||||
| chr16:25152375 | C | T | 1 | a0001c0001t0001g0250 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.466+760C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25152375 | ||||||
| chr16:25152384 | G | C | 2 | a0001c0001t0001g0025a0001c0001t0001g0290 | 2 | HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.466+769G>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25152384 | ||||||
| chr16:25152433 | A | G | 4 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0004g0015others(1): Show | 4 | HG02717.hp1 HG02965.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.466+818A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25152433 | ||||||
| chr16:25152478 | G | A | 110 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(107): Show | 115 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.466+863G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25152478 | ||||||
| chr16:25152490 | G | A | 5 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG02559.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.466+875G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25152490 | ||||||
| chr16:25152541 | A | T | 5 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG02559.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.466+926A>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25152541 | ||||||
| chr16:25152637 | C | T | 5 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG02559.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.466+1022C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25152637 | ||||||
| chr16:25152765 | T | G | 1 | a0001c0001t0001g0289 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.466+1150T>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25152765 | ||||||
| chr16:25152819 | C | T | 5 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0019others(2): Show | 5 | HG02717.hp1 HG02897.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.466+1204C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25152819 | ||||||
| chr16:25152821 | T | G | 1 | a0001c0001t0001g0246 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.466+1206T>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25152821 | ||||||
| chr16:25153054 | G | T | 3 | a0001c0001t0001g0245a0001c0001t0001g0247a0001c0001t0001g0262 | 3 | NA18940.hp2 NA18953.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.466+1439G>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25153054 | ||||||
| chr16:25153061 | A | T | 3 | a0001c0001t0001g0245a0001c0001t0001g0247a0001c0001t0001g0262 | 3 | NA18940.hp2 NA18953.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.466+1446A>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25153061 | ||||||
| chr16:25153104 | C | CG | 6 | a0001c0001t0001g0053a0001c0001t0001g0101a0001c0001t0001g0109others(3): Show | 6 | NA18965.hp1 NA18985.hp2 NA18989.hp2 others(3): Show |
intron_variant | MODIFIER | c.466+1494dupG | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr16 | 25153104 | |||||
| chr16:25153473 | CTCCCAA | C | 119 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(116): Show | 124 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.466+1877_466+1882d others(8): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr16 | 25153473 | |||||
| chr16:25153502 | G | A | 1 | a0001c0001t0001g0019 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.466+1887G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25153502 | ||||||
| chr16:25153520 | T | C | 110 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(107): Show | 115 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.466+1905T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25153520 | ||||||
| chr16:25153589 | CA | C | 330 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(327): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.466+1976delA | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr16 | 25153589 | |||||
| chr16:25153724 | G | A | 4 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(1): Show | 4 | HG02280.hp1 HG02630.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.466+2109G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25153724 | ||||||
| chr16:25153884 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.466+2269C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25153884 | ||||||
| chr16:25153901 | C | T | 165 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(162): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.466+2286C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25153901 | ||||||
| chr16:25153922 | C | G | 5 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG02559.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.466+2307C>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25153922 | ||||||
| chr16:25153974 | C | T | 1 | a0001c0001t0001g0024 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.466+2359C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25153974 | ||||||
| chr16:25154017 | T | C | 7 | a0001c0001t0001g0008a0001c0001t0001g0165a0001c0001t0001g0200others(4): Show | 8 | HG01074.hp1 HG02109.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.466+2402T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25154017 | ||||||
| chr16:25154064 | T | C | 5 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG02559.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.466+2449T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25154064 | ||||||
| chr16:25154096 | G | A | 1 | a0001c0001t0001g0024 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.466+2481G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25154096 | ||||||
| chr16:25154210 | C | T | 1 | a0001c0001t0001g0290 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.466+2595C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25154210 | ||||||
| chr16:25154299 | C | T | 171 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(168): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.466+2684C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25154299 | ||||||
| chr16:25154310 | T | C | 5 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG02559.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.466+2695T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25154310 | ||||||
| chr16:25154489 | C | CT | 15 | a0001c0001t0001g0031a0001c0001t0001g0099a0001c0001t0001g0111others(12): Show | 15 | HG00673.hp2 HG00735.hp1 HG02080.hp1 others(12): Show |
intron_variant | MODIFIER | c.466+2893dupT | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr16 | 25154489 | |||||
| chr16:25154489 | CT | C | 6 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0105others(3): Show | 6 | HG01167.hp2 HG02559.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.466+2893delT | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr16 | 25154489 | |||||
| chr16:25154517 | T | C | 2 | a0001c0001t0004g0015a0001c0001t0004g0016 | 2 | HG02717.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.466+2902T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25154517 | ||||||
| chr16:25154723 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.466+3108C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25154723 | ||||||
| chr16:25154754 | C | CT | 5 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG02559.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.466+3139_466+3140i others(3): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25154754 | ||||||
| chr16:25154913 | G | GATTTTGC others(1): Show |
5 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG02559.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.466+3301_466+3302i others(10): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr16 | 25154913 | |||||
| chr16:25154962 | A | G | 1 | a0001c0001t0001g0024 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.466+3347A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25154962 | ||||||
| chr16:25155088 | A | G | 5 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG02559.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.466+3473A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25155088 | ||||||
| chr16:25155300 | G | A | 4 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0004g0015others(1): Show | 4 | HG02717.hp1 HG02965.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.466+3685G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25155300 | ||||||
| chr16:25155353 | T | A | 3 | a0001c0001t0001g0007a0001c0001t0001g0172a0001c0001t0001g0173 | 4 | HG01256.hp1 HG01258.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.466+3738T>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25155353 | ||||||
| chr16:25155393 | A | G | 1 | a0001c0001t0003g0094 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.466+3778A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25155393 | ||||||
| chr16:25155676 | C | CT | 111 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(108): Show | 116 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.466+4076dupT | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr16 | 25155676 | |||||
| chr16:25155676 | C | CTT | 35 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0107others(32): Show | 38 | HG00609.hp2 HG01256.hp1 HG01258.hp1 others(35): Show |
intron_variant | MODIFIER | c.466+4075_466+4076d others(4): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr16 | 25155676 | |||||
| chr16:25155676 | C | T | 4 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0290others(1): Show | 4 | HG02559.hp2 HG02922.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.466+4061C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25155676 | ||||||
| chr16:25155747 | C | G | 1 | a0001c0001t0001g0115 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.466+4132C>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25155747 | ||||||
| chr16:25155785 | A | T | 1 | a0001c0001t0001g0296 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.466+4170A>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25155785 | ||||||
| chr16:25155809 | T | G | 1 | a0001c0001t0001g0295 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.466+4194T>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25155809 | ||||||
| chr16:25155845 | T | C | 1 | a0001c0001t0001g0059 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.466+4230T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25155845 | ||||||
| chr16:25155921 | A | G | 1 | a0001c0001t0001g0059 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.466+4306A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25155921 | ||||||
| chr16:25156007 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.466+4392A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25156007 | ||||||
| chr16:25156083 | C | T | 2 | a0001c0001t0001g0025a0001c0001t0001g0290 | 2 | HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.466+4468C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25156083 | ||||||
| chr16:25156158 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.466+4543C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25156158 | ||||||
| chr16:25156364 | G | A | 2 | a0001c0001t0001g0187a0001c0001t0001g0299 | 2 | HG02055.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.467-4738G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25156364 | ||||||
| chr16:25156389 | G | T | 1 | a0001c0001t0001g0152 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.467-4713G>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25156389 | ||||||
| chr16:25156567 | C | T | 1 | a0001c0001t0001g0255 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.467-4535C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25156567 | ||||||
| chr16:25156634 | C | T | 5 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG02559.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.467-4468C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25156634 | ||||||
| chr16:25156664 | C | A | 110 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(107): Show | 115 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.467-4438C>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25156664 | ||||||
| chr16:25156665 | C | T | 1 | a0001c0001t0001g0008 | 2 | HG01074.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.467-4437C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25156665 | ||||||
| chr16:25156811 | G | A | 1 | a0001c0001t0001g0024 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.467-4291G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25156811 | ||||||
| chr16:25156843 | G | A | 1 | a0001c0001t0001g0332 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.467-4259G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25156843 | ||||||
| chr16:25156879 | G | A | 5 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG02559.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.467-4223G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25156879 | ||||||
| chr16:25156940 | C | CT | 137 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(134): Show | 145 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.467-4142dupT | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr16 | 25156940 | |||||
| chr16:25156940 | CT | C | 6 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0115others(3): Show | 6 | HG02451.hp2 HG02559.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.467-4142delT | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr16 | 25156940 | |||||
| chr16:25157150 | T | TTG | 105 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(102): Show | 109 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.467-3932_467-3931d others(4): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr16 | 25157150 | |||||
| chr16:25157150 | T | TTGTG | 8 | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0054others(5): Show | 9 | HG01257.hp1 HG01952.hp2 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.467-3934_467-3931d others(6): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr16 | 25157150 | |||||
| chr16:25157222 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.467-3880C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25157222 | ||||||
| chr16:25157283 | C | T | 1 | a0001c0001t0001g0201 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.467-3819C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25157283 | ||||||
| chr16:25157300 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.467-3802C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25157300 | ||||||
| chr16:25157428 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.467-3674G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25157428 | ||||||
| chr16:25157562 | TA | T | 6 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(3): Show | 6 | HG02559.hp2 HG02897.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.467-3530delA | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr16 | 25157562 | |||||
| chr16:25157563 | A | T | 3 | a0001c0001t0001g0049a0001c0001t0001g0058a0001c0001t0001g0095 | 3 | HG00597.hp1 NA18969.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.467-3539A>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25157563 | ||||||
| chr16:25157602 | A | G | 3 | a0001c0001t0001g0007a0001c0001t0001g0172a0001c0001t0001g0173 | 4 | HG01256.hp1 HG01258.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.467-3500A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25157602 | ||||||
| chr16:25157625 | G | T | 2 | a0001c0001t0001g0025a0001c0001t0001g0290 | 2 | HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.467-3477G>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25157625 | ||||||
| chr16:25157666 | A | G | 24 | a0001c0001t0001g0004a0001c0001t0001g0037a0001c0001t0001g0045others(21): Show | 25 | HG00408.hp2 HG00544.hp2 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.467-3436A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25157666 | ||||||
| chr16:25157798 | A | G | 2 | a0001c0001t0001g0018a0001c0001t0001g0333 | 2 | HG02559.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.467-3304A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25157798 | ||||||
| chr16:25157875 | A | G | 1 | a0001c0001t0001g0265 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.467-3227A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25157875 | ||||||
| chr16:25157913 | G | A | 32 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0138others(29): Show | 35 | HG00609.hp2 HG01256.hp1 HG01258.hp1 others(32): Show |
intron_variant | MODIFIER | c.467-3189G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25157913 | ||||||
| chr16:25157928 | T | C | 2 | a0001c0001t0001g0011a0001c0001t0001g0287 | 3 | HG02559.hp1 HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.467-3174T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25157928 | ||||||
| chr16:25158018 | A | G | 6 | a0001c0001t0002g0039a0001c0001t0002g0044a0001c0001t0002g0080others(3): Show | 6 | HG01243.hp2 HG02258.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.467-3084A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25158018 | ||||||
| chr16:25158111 | C | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0019 | 2 | HG02965.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.467-2991C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25158111 | ||||||
| chr16:25158237 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.467-2865C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25158237 | ||||||
| chr16:25158262 | A | T | 5 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG02559.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.467-2840A>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25158262 | ||||||
| chr16:25158309 | G | A | 1 | a0001c0001t0001g0008 | 2 | HG01074.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.467-2793G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25158309 | ||||||
| chr16:25158430 | C | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0019 | 2 | HG02965.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.467-2672C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25158430 | ||||||
| chr16:25158518 | A | G | 110 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(107): Show | 115 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.467-2584A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25158518 | ||||||
| chr16:25158635 | A | C | 1 | a0001c0001t0001g0085 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.467-2467A>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25158635 | ||||||
| chr16:25158828 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.467-2274G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25158828 | ||||||
| chr16:25158887 | G | A | 2 | a0001c0001t0001g0018a0001c0001t0001g0333 | 2 | HG02559.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.467-2215G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25158887 | ||||||
| chr16:25159009 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.467-2093A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25159009 | ||||||
| chr16:25159169 | A | C | 1 | a0001c0001t0001g0193 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.467-1933A>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25159169 | ||||||
| chr16:25159269 | G | A | 119 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(116): Show | 124 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.467-1833G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25159269 | ||||||
| chr16:25159334 | A | G | 1 | a0001c0001t0001g0302 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.467-1768A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25159334 | ||||||
| chr16:25159412 | A | C | 4 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0004g0015others(1): Show | 4 | HG02717.hp1 HG02965.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.467-1690A>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25159412 | ||||||
| chr16:25159564 | A | C | 330 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(327): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.467-1538A>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25159564 | ||||||
| chr16:25159966 | C | CT | 328 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(325): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.467-1123dupT | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr16 | 25159966 | |||||
| chr16:25160004 | C | T | 1 | a0001c0001t0001g0293 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.467-1098C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25160004 | ||||||
| chr16:25160168 | C | T | 5 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG02559.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.467-934C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25160168 | ||||||
| chr16:25160236 | C | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0019 | 2 | HG02965.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.467-866C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25160236 | ||||||
| chr16:25160237 | G | A | 1 | a0001c0001t0001g0313 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.467-865G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25160237 | ||||||
| chr16:25160315 | C | CTG | 330 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(327): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.467-786_467-785dup others(2): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr16 | 25160315 | |||||
| chr16:25160351 | A | G | 119 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(116): Show | 124 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.467-751A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25160351 | ||||||
| chr16:25160363 | GAAT | G | 330 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(327): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.467-735_467-733del others(3): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr16 | 25160363 | |||||
| chr16:25160489 | G | A | 90 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0013others(87): Show | 93 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.467-613G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25160489 | ||||||
| chr16:25160639 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.467-463G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25160639 | ||||||
| chr16:25160840 | G | A | 1 | a0001c0001t0001g0109 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.467-262G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25160840 | ||||||
| chr16:25160880 | A | C | 1 | a0001c0001t0001g0123 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.467-222A>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25160880 | ||||||
| chr16:25160953 | G | T | 118 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(115): Show | 123 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.467-149G>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | chr16 | 25160953 | ||||||
| chr16:25160986 | A | AT | 297 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(294): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.467-104dupT | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr16 | 25160986 | |||||
| chr16:25160986 | A | ATT | 23 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0138others(20): Show | 25 | HG00609.hp2 HG02155.hp2 HG02451.hp1 others(22): Show |
intron_variant | MODIFIER | c.467-105_467-104dup others(2): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr16 | 25160986 | |||||
| chr16:25161315 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.569+111A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 6/10 | chr16 | 25161315 | ||||||
| chr16:25161359 | C | CT | 9 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(6): Show | 9 | HG02056.hp1 HG02559.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.569+169dupT | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 25161359 | |||||
| chr16:25161402 | G | T | 1 | a0001c0001t0001g0058 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.569+198G>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 6/10 | chr16 | 25161402 | ||||||
| chr16:25161419 | A | T | 1 | a0001c0001t0001g0024 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.569+215A>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 6/10 | chr16 | 25161419 | ||||||
| chr16:25161516 | C | G | 1 | a0001c0001t0001g0296 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.569+312C>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 6/10 | chr16 | 25161516 | ||||||
| chr16:25161582 | C | T | 1 | a0001c0001t0001g0241 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.569+378C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 6/10 | chr16 | 25161582 | ||||||
| chr16:25161583 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.569+379G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 6/10 | chr16 | 25161583 | ||||||
| chr16:25161620 | G | A | 1 | a0001c0001t0001g0334 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.569+416G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 6/10 | chr16 | 25161620 | ||||||
| chr16:25161723 | T | C | 2 | a0001c0001t0001g0018a0001c0001t0001g0333 | 2 | HG02559.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.569+519T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 6/10 | chr16 | 25161723 | ||||||
| chr16:25161818 | TA | T | 108 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(105): Show | 113 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.569+625delA | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 25161818 | |||||
| chr16:25161908 | C | G | 1 | a0001c0001t0001g0038 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.569+704C>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 6/10 | chr16 | 25161908 | ||||||
| chr16:25162403 | G | A | 4 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0004g0015others(1): Show | 4 | HG02717.hp1 HG02965.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.569+1199G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 6/10 | chr16 | 25162403 | ||||||
| chr16:25162442 | C | T | 5 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG02559.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.569+1238C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 6/10 | chr16 | 25162442 | ||||||
| chr16:25162462 | C | T | 1 | a0001c0001t0001g0334 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.569+1258C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 6/10 | chr16 | 25162462 | ||||||
| chr16:25162487 | G | A | 1 | a0001c0001t0001g0300 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.569+1283G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 6/10 | chr16 | 25162487 | ||||||
| chr16:25162588 | C | CA | 9 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0036others(6): Show | 9 | HG01175.hp2 HG01261.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.569+1399dupA | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 25162588 | |||||
| chr16:25162599 | AAAAAG | A | 6 | a0001c0001t0001g0188a0001c0001t0001g0206a0001c0001t0001g0207others(3): Show | 6 | HG02257.hp1 HG02572.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.569+1410_569+1414d others(7): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 25162599 | |||||
| chr16:25162678 | A | G | 174 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(171): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.569+1474A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 6/10 | chr16 | 25162678 | ||||||
| chr16:25162749 | C | T | 111 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(108): Show | 116 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.569+1545C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 6/10 | chr16 | 25162749 | ||||||
| chr16:25162860 | A | G | 1 | a0001c0001t0001g0314 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.569+1656A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 6/10 | chr16 | 25162860 | ||||||
| chr16:25162880 | T | TTTTG | 330 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(327): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.569+1681_569+1684d others(6): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 25162880 | |||||
| chr16:25163111 | C | G | 1 | a0001c0001t0001g0188 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.570-1487C>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 6/10 | chr16 | 25163111 | ||||||
| chr16:25163143 | G | A | 2 | a0001c0001t0001g0014a0001c0001t0001g0019 | 2 | HG02965.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.570-1455G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 6/10 | chr16 | 25163143 | ||||||
| chr16:25163197 | G | A | 2 | a0001c0001t0001g0163a0001c0001t0001g0164 | 2 | HG00544.hp1 HG00609.hp1 |
intron_variant | MODIFIER | c.570-1401G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 6/10 | chr16 | 25163197 | ||||||
| chr16:25163244 | G | A | 1 | a0001c0001t0001g0296 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.570-1354G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 6/10 | chr16 | 25163244 | ||||||
| chr16:25163329 | C | T | 11 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(8): Show | 11 | HG00099.hp1 HG00735.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.570-1269C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 6/10 | chr16 | 25163329 | ||||||
| chr16:25163346 | A | G | 120 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(117): Show | 125 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.570-1252A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 6/10 | chr16 | 25163346 | ||||||
| chr16:25163362 | G | A | 2 | a0001c0001t0003g0103a0001c0001t0003g0104 | 2 | HG02109.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.570-1236G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 6/10 | chr16 | 25163362 | ||||||
| chr16:25163467 | C | CAAAAAAA others(44): Show |
1 | a0001c0001t0001g0247 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.570-1112_570-1111i others(53): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 25163467 | |||||
| chr16:25163467 | CA | C | 113 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(110): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.570-1112delA | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 25163467 | |||||
| chr16:25163541 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.570-1057C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 6/10 | chr16 | 25163541 | ||||||
| chr16:25163801 | G | A | 171 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(168): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.570-797G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 6/10 | chr16 | 25163801 | ||||||
| chr16:25164346 | A | G | 1 | a0001c0001t0001g0222 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.570-252A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 6/10 | chr16 | 25164346 | ||||||
| chr16:25164435 | G | A | 2 | a0001c0001t0001g0240a0001c0001t0001g0268 | 2 | HG03669.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.570-163G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 6/10 | chr16 | 25164435 | ||||||
| chr16:25164895 | A | G | 1 | a0001c0001t0001g0137 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.690+177A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 7/10 | chr16 | 25164895 | ||||||
| chr16:25164896 | C | A | 1 | a0001c0001t0001g0137 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.690+178C>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 7/10 | chr16 | 25164896 | ||||||
| chr16:25164897 | T | C | 1 | a0001c0001t0001g0137 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.690+179T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 7/10 | chr16 | 25164897 | ||||||
| chr16:25164947 | A | G | 7 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(4): Show | 7 | HG02559.hp2 HG02717.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.690+229A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 7/10 | chr16 | 25164947 | ||||||
| chr16:25165021 | T | TG | 6 | a0001c0001t0001g0067a0001c0001t0001g0152a0001c0001t0001g0162others(3): Show | 6 | HG01175.hp2 HG02055.hp1 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.690+307dupG | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 25165021 | |||||
| chr16:25165108 | C | CTG | 329 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(326): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.690+391_690+392dup others(2): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 25165108 | |||||
| chr16:25165156 | C | G | 1 | a0001c0001t0001g0115 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.690+438C>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 7/10 | chr16 | 25165156 | ||||||
| chr16:25165449 | G | A | 172 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(169): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.690+731G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 7/10 | chr16 | 25165449 | ||||||
| chr16:25165517 | CT | C | 73 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(70): Show | 78 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.690+810delT | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 25165517 | |||||
| chr16:25165591 | C | G | 34 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(31): Show | 37 | HG00609.hp2 HG01256.hp1 HG01258.hp1 others(34): Show |
intron_variant | MODIFIER | c.690+873C>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 7/10 | chr16 | 25165591 | ||||||
| chr16:25165621 | G | A | 110 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(107): Show | 115 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.690+903G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 7/10 | chr16 | 25165621 | ||||||
| chr16:25165659 | A | G | 1 | a0001c0001t0001g0334 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.690+941A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 7/10 | chr16 | 25165659 | ||||||
| chr16:25165664 | T | G | 1 | a0001c0001t0001g0069 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.690+946T>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 7/10 | chr16 | 25165664 | ||||||
| chr16:25166035 | A | G | 152 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(149): Show | 160 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.690+1317A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 7/10 | chr16 | 25166035 | ||||||
| chr16:25166086 | A | G | 1 | a0001c0001t0001g0290 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.690+1368A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 7/10 | chr16 | 25166086 | ||||||
| chr16:25166142 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.690+1424C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 7/10 | chr16 | 25166142 | ||||||
| chr16:25166143 | G | A | 2 | a0001c0001t0001g0018a0001c0001t0001g0333 | 2 | HG02559.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.690+1425G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 7/10 | chr16 | 25166143 | ||||||
| chr16:25166219 | G | A | 172 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(169): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.690+1501G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 7/10 | chr16 | 25166219 | ||||||
| chr16:25166269 | C | CA | 110 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(107): Show | 114 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.690+1567dupA | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 25166269 | |||||
| chr16:25166269 | CA | C | 7 | a0001c0001t0001g0188a0001c0001t0001g0225a0001c0001t0001g0231others(4): Show | 7 | HG01256.hp2 HG02004.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.690+1567delA | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 25166269 | |||||
| chr16:25166319 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.690+1601T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 7/10 | chr16 | 25166319 | ||||||
| chr16:25166377 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.690+1659C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 7/10 | chr16 | 25166377 | ||||||
| chr16:25166491 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.690+1773C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 7/10 | chr16 | 25166491 | ||||||
| chr16:25166493 | C | T | 1 | a0001c0001t0001g0046 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.690+1775C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 7/10 | chr16 | 25166493 | ||||||
| chr16:25166555 | C | T | 9 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0055others(6): Show | 10 | HG00423.hp1 HG00673.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.690+1837C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 7/10 | chr16 | 25166555 | ||||||
| chr16:25166556 | A | G | 2 | a0001c0001t0001g0014a0001c0001t0001g0019 | 2 | HG02965.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.690+1838A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 7/10 | chr16 | 25166556 | ||||||
| chr16:25166599 | C | T | 1 | a0001c0001t0001g0024 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.690+1881C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 7/10 | chr16 | 25166599 | ||||||
| chr16:25166697 | C | T | 2 | a0001c0001t0001g0271a0001c0001t0001g0272 | 2 | HG02738.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.690+1979C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 7/10 | chr16 | 25166697 | ||||||
| chr16:25166904 | G | A | 7 | a0001c0001t0001g0008a0001c0001t0001g0165a0001c0001t0001g0200others(4): Show | 8 | HG01074.hp1 HG02109.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.690+2186G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 7/10 | chr16 | 25166904 | ||||||
| chr16:25167080 | G | A | 2 | a0001c0001t0002g0080a0001c0001t0002g0195 | 2 | HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.691-2032G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 7/10 | chr16 | 25167080 | ||||||
| chr16:25167284 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.691-1828C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 7/10 | chr16 | 25167284 | ||||||
| chr16:25167356 | C | T | 1 | a0001c0001t0001g0037 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.691-1756C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 7/10 | chr16 | 25167356 | ||||||
| chr16:25167502 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.691-1610G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 7/10 | chr16 | 25167502 | ||||||
| chr16:25167549 | C | T | 1 | a0001c0001t0001g0300 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.691-1563C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 7/10 | chr16 | 25167549 | ||||||
| chr16:25167602 | A | G | 1 | a0001c0001t0001g0333 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.691-1510A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 7/10 | chr16 | 25167602 | ||||||
| chr16:25167974 | C | G | 7 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(4): Show | 7 | HG02559.hp2 HG02717.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.691-1138C>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 7/10 | chr16 | 25167974 | ||||||
| chr16:25168036 | C | T | 1 | a0001c0001t0001g0051 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.691-1076C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 7/10 | chr16 | 25168036 | ||||||
| chr16:25168048 | C | T | 5 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(2): Show | 5 | HG02055.hp1 HG02145.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.691-1064C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 7/10 | chr16 | 25168048 | ||||||
| chr16:25168056 | C | CT | 37 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(34): Show | 40 | HG00609.hp2 HG01256.hp1 HG01258.hp1 others(37): Show |
intron_variant | MODIFIER | c.691-1046dupT | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 25168056 | |||||
| chr16:25168062 | T | A | 2 | a0001c0001t0004g0015a0001c0001t0004g0016 | 2 | HG02717.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.691-1050T>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 7/10 | chr16 | 25168062 | ||||||
| chr16:25168211 | G | C | 5 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(2): Show | 5 | HG02055.hp1 HG02145.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.691-901G>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 7/10 | chr16 | 25168211 | ||||||
| chr16:25168246 | A | G | 110 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(107): Show | 115 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.691-866A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 7/10 | chr16 | 25168246 | ||||||
| chr16:25168293 | C | A | 1 | a0001c0001t0001g0316 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.691-819C>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 7/10 | chr16 | 25168293 | ||||||
| chr16:25168337 | C | T | 1 | a0001c0001t0002g0134 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.691-775C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 7/10 | chr16 | 25168337 | ||||||
| chr16:25168376 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.691-736G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 7/10 | chr16 | 25168376 | ||||||
| chr16:25168451 | T | G | 1 | a0001c0001t0001g0284 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.691-661T>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 7/10 | chr16 | 25168451 | ||||||
| chr16:25168722 | G | T | 1 | a0001c0001t0003g0093 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.691-390G>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 7/10 | chr16 | 25168722 | ||||||
| chr16:25169069 | G | A | 1 | a0001c0001t0001g0290 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.691-43G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 7/10 | chr16 | 25169069 | ||||||
| chr16:25169289 | G | A | 331 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(328): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.792+76G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 8/10 | chr16 | 25169289 | ||||||
| chr16:25169360 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.792+147T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 8/10 | chr16 | 25169360 | ||||||
| chr16:25169393 | C | G | 1 | a0001c0001t0001g0333 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.792+180C>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 8/10 | chr16 | 25169393 | ||||||
| chr16:25169435 | G | A | 172 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(169): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.792+222G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 8/10 | chr16 | 25169435 | ||||||
| chr16:25169578 | A | G | 110 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(107): Show | 115 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.792+365A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 8/10 | chr16 | 25169578 | ||||||
| chr16:25169621 | T | C | 110 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(107): Show | 115 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.792+408T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 8/10 | chr16 | 25169621 | ||||||
| chr16:25169729 | G | A | 2 | a0001c0001t0004g0015a0001c0001t0004g0016 | 2 | HG02717.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.792+516G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 8/10 | chr16 | 25169729 | ||||||
| chr16:25169757 | C | CT | 111 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(108): Show | 116 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.792+552dupT | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 25169757 | |||||
| chr16:25169782 | A | AATC | 7 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0025others(4): Show | 7 | HG02559.hp2 HG02717.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.792+571_792+573dup others(3): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 25169782 | |||||
| chr16:25169910 | G | T | 1 | a0001c0001t0001g0332 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.792+697G>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 8/10 | chr16 | 25169910 | ||||||
| chr16:25170017 | C | T | 2 | a0001c0001t0001g0018a0001c0001t0001g0333 | 2 | HG02559.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.793-697C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 8/10 | chr16 | 25170017 | ||||||
| chr16:25170078 | G | T | 1 | a0001c0001t0001g0261 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.793-636G>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 8/10 | chr16 | 25170078 | ||||||
| chr16:25170353 | T | TC | 27 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0138others(24): Show | 30 | HG00609.hp2 HG01256.hp1 HG01258.hp1 others(27): Show |
intron_variant | MODIFIER | c.793-355dupC | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 25170353 | |||||
| chr16:25170390 | T | A | 172 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(169): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.793-324T>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 8/10 | chr16 | 25170390 | ||||||
| chr16:25170700 | G | A | 2 | a0001c0001t0001g0248a0001c0001t0001g0251 | 2 | HG03139.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.793-14G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 8/10 | chr16 | 25170700 | ||||||
| chr16:25170711 | T | C | 57 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0017others(54): Show | 59 | HG00621.hp2 HG00741.hp1 HG01175.hp1 others(56): Show |
splice_region_variant&intron_variant | LOW | c.793-3T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 8/10 | chr16 | 25170711 | ||||||
| chr16:25170835 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.884+30G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 9/10 | chr16 | 25170835 | ||||||
| chr16:25171040 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.884+235G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 9/10 | chr16 | 25171040 | ||||||
| chr16:25171080 | G | A | 112 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(109): Show | 117 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.884+275G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 9/10 | chr16 | 25171080 | ||||||
| chr16:25171160 | T | TG | 110 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(107): Show | 115 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.884+359dupG | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr16 | 25171160 | |||||
| chr16:25171386 | T | C | 1 | a0001c0001t0001g0023 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.884+581T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 9/10 | chr16 | 25171386 | ||||||
| chr16:25171445 | C | A | 2 | a0001c0001t0001g0035a0001c0001t0001g0042 | 2 | NA18963.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.884+640C>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 9/10 | chr16 | 25171445 | ||||||
| chr16:25171449 | A | C | 2 | a0001c0001t0001g0187a0001c0001t0001g0299 | 2 | HG02055.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.884+644A>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 9/10 | chr16 | 25171449 | ||||||
| chr16:25171729 | A | G | 1 | a0001c0001t0001g0244 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.884+924A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 9/10 | chr16 | 25171729 | ||||||
| chr16:25171891 | A | C | 1 | a0001c0001t0001g0274 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.884+1086A>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 9/10 | chr16 | 25171891 | ||||||
| chr16:25172001 | A | G | 119 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(116): Show | 124 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.884+1196A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 9/10 | chr16 | 25172001 | ||||||
| chr16:25172124 | G | A | 2 | a0001c0001t0001g0025a0001c0001t0001g0290 | 2 | HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.884+1319G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 9/10 | chr16 | 25172124 | ||||||
| chr16:25172189 | C | T | 1 | a0001c0001t0001g0316 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.884+1384C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 9/10 | chr16 | 25172189 | ||||||
| chr16:25172256 | G | A | 1 | a0001c0001t0001g0319 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.884+1451G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 9/10 | chr16 | 25172256 | ||||||
| chr16:25172308 | C | CAA | 109 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(106): Show | 114 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.884+1516_884+1517d others(4): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr16 | 25172308 | |||||
| chr16:25172418 | C | T | 1 | a0001c0001t0001g0333 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.884+1613C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 9/10 | chr16 | 25172418 | ||||||
| chr16:25172419 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.884+1614G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 9/10 | chr16 | 25172419 | ||||||
| chr16:25172485 | A | G | 1 | a0001c0001t0001g0290 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.884+1680A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 9/10 | chr16 | 25172485 | ||||||
| chr16:25172572 | C | G | 2 | a0001c0001t0001g0025a0001c0001t0001g0290 | 2 | HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.884+1767C>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 9/10 | chr16 | 25172572 | ||||||
| chr16:25172681 | C | T | 110 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(107): Show | 115 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.884+1876C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 9/10 | chr16 | 25172681 | ||||||
| chr16:25172982 | A | T | 1 | a0001c0001t0002g0218 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.885-1955A>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 9/10 | chr16 | 25172982 | ||||||
| chr16:25173326 | GC | G | 30 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0138others(27): Show | 33 | HG00609.hp2 HG01256.hp1 HG01258.hp1 others(30): Show |
intron_variant | MODIFIER | c.885-1609delC | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr16 | 25173326 | |||||
| chr16:25173338 | G | A | 2 | a0001c0001t0001g0167a0001c0001t0001g0170 | 2 | HG01074.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.885-1599G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 9/10 | chr16 | 25173338 | ||||||
| chr16:25173715 | G | GT | 110 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(107): Show | 115 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.885-1213dupT | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr16 | 25173715 | |||||
| chr16:25173805 | A | G | 3 | a0001c0001t0001g0011a0001c0001t0001g0287a0001c0001t0001g0301 | 4 | HG02559.hp1 HG02818.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.885-1132A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 9/10 | chr16 | 25173805 | ||||||
| chr16:25173864 | C | A | 119 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(116): Show | 124 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.885-1073C>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 9/10 | chr16 | 25173864 | ||||||
| chr16:25174132 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.885-805G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 9/10 | chr16 | 25174132 | ||||||
| chr16:25174246 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.885-691G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 9/10 | chr16 | 25174246 | ||||||
| chr16:25174247 | C | A | 1 | a0001c0001t0001g0124 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.885-690C>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 9/10 | chr16 | 25174247 | ||||||
| chr16:25174346 | C | CTCTCTTA others(14): Show |
2 | a0001c0001t0001g0202a0001c0001t0001g0203 | 2 | HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.885-589_885-569dup others(21): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr16 | 25174346 | |||||
| chr16:25174490 | C | G | 1 | a0001c0001t0001g0268 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.885-447C>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 9/10 | chr16 | 25174490 | ||||||
| chr16:25174505 | G | C | 1 | a0001c0001t0001g0264 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.885-432G>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 9/10 | chr16 | 25174505 | ||||||
| chr16:25174510 | A | G | 2 | a0001c0001t0001g0014a0001c0001t0001g0019 | 2 | HG02965.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.885-427A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 9/10 | chr16 | 25174510 | ||||||
| chr16:25174676 | A | G | 33 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0020others(30): Show | 36 | HG00609.hp2 HG01256.hp1 HG01258.hp1 others(33): Show |
intron_variant | MODIFIER | c.885-261A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 9/10 | chr16 | 25174676 | ||||||
| chr16:25175204 | C | A | 22 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(19): Show | 24 | HG00609.hp2 HG02155.hp2 NA18941.hp1 others(21): Show |
intron_variant | MODIFIER | c.982+170C>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 10/10 | chr16 | 25175204 | ||||||
| chr16:25175206 | G | A | 1 | a0001c0001t0001g0024 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.982+172G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 10/10 | chr16 | 25175206 | ||||||
| chr16:25175211 | A | T | 22 | a0001c0001t0001g0001a0001c0001t0001g0138a0001c0001t0001g0139others(19): Show | 24 | HG00609.hp2 HG02155.hp2 NA18941.hp1 others(21): Show |
intron_variant | MODIFIER | c.982+177A>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 10/10 | chr16 | 25175211 | ||||||
| chr16:25175349 | C | T | 1 | a0001c0001t0001g0279 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.982+315C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 10/10 | chr16 | 25175349 | ||||||
| chr16:25175452 | C | T | 1 | a0001c0001t0001g0292 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.982+418C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 10/10 | chr16 | 25175452 | ||||||
| chr16:25175469 | C | CA | 114 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(111): Show | 119 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.982+449dupA | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 25175469 | |||||
| chr16:25175469 | C | CAA | 41 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0018others(38): Show | 44 | HG00609.hp2 HG01256.hp1 HG01258.hp1 others(41): Show |
intron_variant | MODIFIER | c.982+448_982+449dup others(2): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 25175469 | |||||
| chr16:25175491 | G | A | 1 | a0001c0001t0001g0238 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.982+457G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 10/10 | chr16 | 25175491 | ||||||
| chr16:25175857 | A | G | 35 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(32): Show | 38 | HG00609.hp2 HG01256.hp1 HG01258.hp1 others(35): Show |
intron_variant | MODIFIER | c.982+823A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 10/10 | chr16 | 25175857 | ||||||
| chr16:25176000 | C | T | 2 | a0001c0001t0001g0025a0001c0001t0001g0290 | 2 | HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.982+966C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 10/10 | chr16 | 25176000 | ||||||
| chr16:25176186 | G | C | 1 | a0001c0001t0001g0334 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.982+1152G>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 10/10 | chr16 | 25176186 | ||||||
| chr16:25176228 | C | A | 1 | a0001c0001t0001g0105 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.982+1194C>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 10/10 | chr16 | 25176228 | ||||||
| chr16:25176229 | C | G | 4 | a0001c0001t0001g0188a0001c0001t0001g0206a0001c0001t0001g0209others(1): Show | 4 | HG02572.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.982+1195C>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 10/10 | chr16 | 25176229 | ||||||
| chr16:25176261 | G | A | 1 | a0001c0001t0002g0080 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.982+1227G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 10/10 | chr16 | 25176261 | ||||||
| chr16:25176266 | A | G | 2 | a0001c0001t0004g0015a0001c0001t0004g0016 | 2 | HG02717.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.982+1232A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 10/10 | chr16 | 25176266 | ||||||
| chr16:25176289 | G | A | 30 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0138others(27): Show | 33 | HG00609.hp2 HG01256.hp1 HG01258.hp1 others(30): Show |
intron_variant | MODIFIER | c.982+1255G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 10/10 | chr16 | 25176289 | ||||||
| chr16:25176297 | G | T | 1 | a0001c0001t0001g0064 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.982+1263G>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 10/10 | chr16 | 25176297 | ||||||
| chr16:25176336 | C | T | 1 | a0001c0001t0001g0244 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.982+1302C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 10/10 | chr16 | 25176336 | ||||||
| chr16:25176346 | G | A | 2 | a0001c0001t0001g0025a0001c0001t0001g0290 | 2 | HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.982+1312G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 10/10 | chr16 | 25176346 | ||||||
| chr16:25176347 | T | C | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(220): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.982+1313T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 10/10 | chr16 | 25176347 | ||||||
| chr16:25176427 | A | G | 3 | a0001c0001t0001g0043a0001c0001t0001g0194a0001c0001t0001g0213 | 3 | HG02622.hp1 HG02809.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.982+1393A>G | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 10/10 | chr16 | 25176427 | ||||||
| chr16:25176550 | C | CT | 37 | a0001c0001t0001g0042a0001c0001t0001g0050a0001c0001t0001g0051others(34): Show | 37 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.983-1421dupT | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 25176550 | |||||
| chr16:25176550 | C | CTT | 19 | a0001c0001t0001g0012a0001c0001t0001g0028a0001c0001t0001g0045others(16): Show | 20 | HG00280.hp2 HG00738.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.983-1422_983-1421d others(4): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 25176550 | |||||
| chr16:25176550 | CTT | C | 11 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0049others(8): Show | 11 | HG02155.hp2 HG02559.hp2 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.983-1422_983-1421d others(4): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 25176550 | |||||
| chr16:25176550 | CTTT | C | 32 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0018others(29): Show | 35 | HG00609.hp2 HG01167.hp1 HG01256.hp1 others(32): Show |
intron_variant | MODIFIER | c.983-1423_983-1421d others(5): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 25176550 | |||||
| chr16:25176550 | CTTTT | C | 26 | a0001c0001t0001g0017a0001c0001t0001g0021a0001c0001t0001g0101others(23): Show | 26 | HG00438.hp1 HG01106.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.983-1424_983-1421d others(6): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 25176550 | |||||
| chr16:25176550 | CTTTTT | C | 147 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(144): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.983-1425_983-1421d others(7): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 25176550 | |||||
| chr16:25176550 | CTTTTTT | C | 6 | a0001c0001t0001g0160a0001c0001t0001g0170a0001c0001t0001g0244others(3): Show | 6 | HG01099.hp1 HG02293.hp1 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.983-1426_983-1421d others(8): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 25176550 | |||||
| chr16:25176550 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0024 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.983-1433_983-1421d others(15): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 25176550 | |||||
| chr16:25176550 | CTTTTTTT others(7): Show |
C | 2 | a0001c0001t0004g0015a0001c0001t0004g0016 | 2 | HG02717.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.983-1434_983-1421d others(16): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 25176550 | |||||
| chr16:25176550 | CTTTTTTT others(10): Show |
C | 2 | a0001c0001t0001g0242a0001c0001t0001g0307 | 2 | NA18947.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.983-1437_983-1421d others(19): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 25176550 | |||||
| chr16:25176591 | C | T | 181 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(178): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.983-1410C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 10/10 | chr16 | 25176591 | ||||||
| chr16:25176615 | G | A | 2 | a0001c0001t0001g0018a0001c0001t0001g0333 | 2 | HG02559.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.983-1386G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 10/10 | chr16 | 25176615 | ||||||
| chr16:25176648 | G | A | 7 | a0001c0001t0001g0008a0001c0001t0001g0165a0001c0001t0001g0200others(4): Show | 8 | HG01074.hp1 HG02109.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.983-1353G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 10/10 | chr16 | 25176648 | ||||||
| chr16:25176763 | T | C | 1 | a0001c0001t0001g0012 | 2 | HG01884.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.983-1238T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 10/10 | chr16 | 25176763 | ||||||
| chr16:25176803 | C | T | 34 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(31): Show | 37 | HG00609.hp2 HG01256.hp1 HG01258.hp1 others(34): Show |
intron_variant | MODIFIER | c.983-1198C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 10/10 | chr16 | 25176803 | ||||||
| chr16:25176820 | C | A | 1 | a0001c0001t0001g0244 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.983-1181C>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 10/10 | chr16 | 25176820 | ||||||
| chr16:25176906 | G | A | 2 | a0001c0001t0001g0222a0001c0001t0001g0291 | 2 | HG01433.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.983-1095G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 10/10 | chr16 | 25176906 | ||||||
| chr16:25177014 | T | A | 1 | a0001c0001t0001g0288 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.983-987T>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 10/10 | chr16 | 25177014 | ||||||
| chr16:25177041 | G | A | 2 | a0001c0001t0001g0052a0001c0001t0001g0333 | 2 | HG01257.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.983-960G>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 10/10 | chr16 | 25177041 | ||||||
| chr16:25177134 | G | C | 2 | a0001c0001t0004g0015a0001c0001t0004g0016 | 2 | HG02717.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.983-867G>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 10/10 | chr16 | 25177134 | ||||||
| chr16:25177143 | G | GTACTCCA | 184 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(181): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.983-857_983-851dup others(7): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 25177143 | |||||
| chr16:25177168 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.983-833C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 10/10 | chr16 | 25177168 | ||||||
| chr16:25177250 | T | A | 4 | a0001c0001t0001g0018a0001c0001t0001g0025a0001c0001t0001g0290others(1): Show | 4 | HG02559.hp2 HG02897.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.983-751T>A | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 10/10 | chr16 | 25177250 | ||||||
| chr16:25177538 | T | C | 23 | a0001c0001t0001g0004a0001c0001t0001g0037a0001c0001t0001g0045others(20): Show | 24 | HG00408.hp2 HG00544.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.983-463T>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 10/10 | chr16 | 25177538 | ||||||
| chr16:25177859 | TCATTTTA others(27): Show |
T | 1 | a0001c0001t0001g0290 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.983-141_983-108del others(34): Show |
LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 10/10 | chr16 | 25177859 | ||||||
| chr16:25177888 | C | T | 1 | a0001c0001t0002g0131 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.983-113C>T | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 10/10 | chr16 | 25177888 | ||||||
| chr16:25177930 | G | C | 1 | a0001c0001t0001g0056 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.983-71G>C | LCMT1 | ENSG00000205629.12 | transcript | ENST00000399069.8 | protein_coding | 10/10 | chr16 | 25177930 |