| geneid | 54805 |
|---|---|
| ensemblid | ENSG00000148842.18 |
| hgncid | 103 |
| symbol | CNNM2 |
| name | cyclin and CBS domain divalent metal cation transport mediator 2 |
| refseq_nuc | NM_017649.5 |
| refseq_prot | NP_060119.3 |
| ensembl_nuc | ENST00000369878.9 |
| ensembl_prot | ENSP00000358894.3 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 102918294 |
| end | 103090222 |
| strand | + |
| ver | v1.2 |
| region | chr10:102918294-103090222 |
| region5000 | chr10:102913294-103095222 |
| regionname0 | CNNM2_chr10_102918294_103090222 |
| regionname5000 | CNNM2_chr10_102913294_103095222 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 875 | 253 | 52 | 52 | 109 | 10 | 28 | 72 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0002 | 0/0 | 875 | 13 | 6 | 3 | 0 | 2 | 2 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0003 | 0/0 | 875 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0004 | 0/0 | 875 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0005 | 0/0 | 875 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2628 | 114 | 23 | 28 | 45 | 4 | 12 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| c0002 | 0/0 | 2628 | 69 | 23 | 13 | 25 | 2 | 6 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| c0003 | 0/0 | 2628 | 51 | 4 | 8 | 29 | 1 | 9 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| c0004 | 0/0 | 2628 | 13 | 6 | 3 | 0 | 2 | 2 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| c0005 | 0/0 | 2628 | 8 | 0 | 0 | 7 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| c0006 | 0/0 | 2628 | 7 | 1 | 3 | 0 | 3 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| c0007 | 0/0 | 2628 | 3 | 0 | 0 | 3 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| c0008 | 0/0 | 2628 | 2 | 0 | 0 | 2 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| c0009 | 0/0 | 2628 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| c0010 | 0/0 | 2628 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| c0011 | 0/0 | 2628 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 13229 | 26 | 2 | 2 | 16 | 1 | 5 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0002 | 0/1 | 13218 | 16 | 0 | 4 | 7 | 0 | 4 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0003 | 0/0 | 13231 | 16 | 1 | 5 | 8 | 2 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0004 | 0/0 | 13229 | 14 | 9 | 2 | 2 | 1 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0005 | 0/0 | 13229 | 14 | 8 | 3 | 2 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0006 | 0/0 | 13231 | 8 | 0 | 0 | 7 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0007 | 0/0 | 13230 | 8 | 0 | 1 | 7 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0008 | 0/0 | 13234 | 7 | 0 | 4 | 0 | 1 | 2 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0009 | 0/0 | 13232 | 7 | 0 | 3 | 4 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0010 | 0/0 | 13229 | 5 | 1 | 1 | 0 | 0 | 3 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0011 | 0/0 | 13230 | 5 | 5 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0012 | 0/0 | 13236 | 5 | 1 | 2 | 2 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0013 | 0/0 | 13230 | 4 | 1 | 1 | 0 | 2 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0014 | 0/0 | 13229 | 4 | 0 | 3 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0015 | 0/0 | 13232 | 3 | 0 | 0 | 1 | 0 | 2 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0016 | 0/0 | 13229 | 3 | 0 | 3 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0017 | 0/0 | 13218 | 3 | 1 | 2 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0018 | 0/0 | 13235 | 3 | 0 | 1 | 1 | 1 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0019 | 0/0 | 13241 | 3 | 2 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0020 | 0/0 | 13240 | 3 | 0 | 1 | 2 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0021 | 0/0 | 13241 | 3 | 0 | 1 | 2 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0022 | 0/0 | 13234 | 2 | 0 | 0 | 1 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0023 | 0/0 | 13236 | 2 | 0 | 0 | 2 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0024 | 0/0 | 13229 | 2 | 1 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0025 | 0/0 | 13240 | 2 | 1 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0026 | 0/0 | 13223 | 2 | 2 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0027 | 0/0 | 13233 | 2 | 2 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0028 | 0/0 | 13211 | 2 | 2 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0029 | 0/0 | 13231 | 2 | 0 | 1 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0030 | 0/0 | 13235 | 2 | 0 | 1 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0031 | 0/0 | 13240 | 2 | 0 | 0 | 2 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0032 | 0/0 | 13229 | 2 | 0 | 0 | 2 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0033 | 0/0 | 13230 | 2 | 0 | 0 | 2 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0034 | 0/0 | 13218 | 2 | 0 | 0 | 2 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0035 | 0/0 | 13228 | 2 | 0 | 0 | 0 | 1 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0036 | 0/0 | 13219 | 2 | 0 | 0 | 1 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0037 | 0/0 | 13229 | 2 | 0 | 0 | 2 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0038 | 0/0 | 13237 | 2 | 1 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0039 | 0/0 | 13239 | 2 | 0 | 0 | 2 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0040 | 0/0 | 13242 | 2 | 1 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0041 | 0/0 | 13239 | 2 | 0 | 2 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0042 | 0/0 | 13229 | 2 | 0 | 2 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0043 | 0/0 | 13218 | 2 | 0 | 0 | 2 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0044 | 0/0 | 13231 | 2 | 0 | 2 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0045 | 0/0 | 13218 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0046 | 0/0 | 13235 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0047 | 0/0 | 13235 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0048 | 0/0 | 13228 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0049 | 0/0 | 13229 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0050 | 0/0 | 13233 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0051 | 0/0 | 13229 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0052 | 0/0 | 13229 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0053 | 0/0 | 13230 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0054 | 0/0 | 13231 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0055 | 0/0 | 13223 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0056 | 0/0 | 13239 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0057 | 0/0 | 13248 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0058 | 0/0 | 13249 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0059 | 0/0 | 13272 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0060 | 0/0 | 13254 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0061 | 0/0 | 13257 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0062 | 0/0 | 13238 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0063 | 0/0 | 13234 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0064 | 0/0 | 13216 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0065 | 0/0 | 13228 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0066 | 0/0 | 13230 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0067 | 0/0 | 13230 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0068 | 0/0 | 13232 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0069 | 0/0 | 13232 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0070 | 0/0 | 13233 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0071 | 0/0 | 13229 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0072 | 0/0 | 13236 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0073 | 0/0 | 13218 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0074 | 0/0 | 13237 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0075 | 0/0 | 13247 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0076 | 0/0 | 13248 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0077 | 0/0 | 13230 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0078 | 0/0 | 13231 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0079 | 0/0 | 13231 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0080 | 0/0 | 13229 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0081 | 0/0 | 13229 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0082 | 0/0 | 13229 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0083 | 0/0 | 13235 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0084 | 0/0 | 13218 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0085 | 0/0 | 13241 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0086 | 0/0 | 13230 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0087 | 0/0 | 13227 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0088 | 1/0 | 13230 | 1 | 0 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0089 | 0/0 | 13234 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0090 | 0/0 | 13237 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0091 | 0/0 | 13240 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0092 | 0/0 | 13242 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0093 | 0/0 | 13243 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0094 | 0/0 | 13244 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0095 | 0/0 | 13248 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0096 | 0/0 | 13229 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0097 | 0/0 | 13229 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0098 | 0/0 | 13242 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0099 | 0/0 | 13218 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0100 | 0/0 | 13239 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0101 | 0/0 | 13219 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0102 | 0/0 | 13218 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0103 | 0/0 | 13229 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0104 | 0/0 | 13241 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0105 | 0/0 | 13234 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0106 | 0/0 | 13230 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0107 | 0/0 | 13232 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| t0108 | 0/0 | 13231 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0050 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0103 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2628 | 114 | 23 | 28 | 45 | 4 | 12 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0002 | 0/0 | 2628 | 69 | 23 | 13 | 25 | 2 | 6 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0003 | 0/0 | 2628 | 51 | 4 | 8 | 29 | 1 | 9 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0005 | 0/0 | 2628 | 8 | 0 | 0 | 7 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0006 | 0/0 | 2628 | 7 | 1 | 3 | 0 | 3 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0007 | 0/0 | 2628 | 3 | 0 | 0 | 3 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0010 | 0/0 | 2628 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0002c0004 | 0/0 | 2628 | 13 | 6 | 3 | 0 | 2 | 2 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0003c0008 | 0/0 | 2628 | 2 | 0 | 0 | 2 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0004c0011 | 0/0 | 2628 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0005c0009 | 0/0 | 2628 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/1 | 15845 | 14 | 0 | 4 | 5 | 0 | 4 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0001t0005 | 0/0 | 15856 | 14 | 8 | 3 | 2 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0001t0008 | 0/0 | 15861 | 7 | 0 | 4 | 0 | 1 | 2 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0001t0011 | 0/0 | 15857 | 5 | 5 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0001t0012 | 0/0 | 15863 | 5 | 1 | 2 | 2 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0001t0014 | 0/0 | 15856 | 3 | 0 | 3 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0001t0017 | 0/0 | 15845 | 3 | 1 | 2 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0001t0018 | 0/0 | 15862 | 3 | 0 | 1 | 1 | 1 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0001t0019 | 0/0 | 15868 | 3 | 2 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0001t0020 | 0/0 | 15867 | 3 | 0 | 1 | 2 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0001t0021 | 0/0 | 15868 | 3 | 0 | 1 | 2 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0001t0030 | 0/0 | 15862 | 2 | 0 | 1 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0001t0031 | 0/0 | 15867 | 2 | 0 | 0 | 2 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0001t0034 | 0/0 | 15845 | 2 | 0 | 0 | 2 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0001t0035 | 0/0 | 15855 | 2 | 0 | 0 | 0 | 1 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0001t0036 | 0/0 | 15846 | 2 | 0 | 0 | 1 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0001t0037 | 0/0 | 15856 | 2 | 0 | 0 | 2 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0001t0038 | 0/0 | 15864 | 2 | 1 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0001t0039 | 0/0 | 15866 | 2 | 0 | 0 | 2 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0001t0040 | 0/0 | 15869 | 2 | 1 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0001t0041 | 0/0 | 15866 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0001t0042 | 0/0 | 15856 | 2 | 0 | 2 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0001t0043 | 0/0 | 15845 | 2 | 0 | 0 | 2 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0001t0045 | 0/0 | 15845 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0001t0072 | 0/0 | 15863 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0001t0073 | 0/0 | 15845 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0001t0074 | 0/0 | 15864 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0001t0075 | 0/0 | 15874 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0001t0076 | 0/0 | 15875 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0001t0083 | 0/0 | 15862 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0001t0084 | 0/0 | 15845 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0001t0085 | 0/0 | 15868 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0001t0086 | 0/0 | 15857 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0001t0087 | 0/0 | 15854 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0001t0088 | 1/0 | 15857 | 1 | 0 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0001t0089 | 0/0 | 15861 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0001t0090 | 0/0 | 15864 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0001t0091 | 0/0 | 15867 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0001t0092 | 0/0 | 15869 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0001t0093 | 0/0 | 15870 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0001t0094 | 0/0 | 15871 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0001t0095 | 0/0 | 15875 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0001t0096 | 0/0 | 15856 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0001t0097 | 0/0 | 15856 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0001t0098 | 0/0 | 15869 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0001t0099 | 0/0 | 15845 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0001t0100 | 0/0 | 15866 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0001t0101 | 0/0 | 15846 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0001t0102 | 0/0 | 15845 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0001t0104 | 0/0 | 15868 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0001t0105 | 0/0 | 15861 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0002t0002 | 0/0 | 15845 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0002t0003 | 0/0 | 15858 | 15 | 1 | 4 | 8 | 2 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0002t0004 | 0/0 | 15856 | 10 | 8 | 0 | 2 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0002t0006 | 0/0 | 15858 | 8 | 0 | 0 | 7 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0002t0009 | 0/0 | 15859 | 7 | 0 | 3 | 4 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0002t0013 | 0/0 | 15857 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0002t0015 | 0/0 | 15859 | 3 | 0 | 0 | 1 | 0 | 2 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0002t0024 | 0/0 | 15856 | 2 | 1 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0002t0026 | 0/0 | 15850 | 2 | 2 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0002t0027 | 0/0 | 15860 | 2 | 2 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0002t0029 | 0/0 | 15858 | 2 | 0 | 1 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0002t0044 | 0/0 | 15858 | 2 | 0 | 2 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0002t0052 | 0/0 | 15856 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0002t0053 | 0/0 | 15857 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0002t0054 | 0/0 | 15858 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0002t0062 | 0/0 | 15865 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0002t0063 | 0/0 | 15861 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0002t0064 | 0/0 | 15843 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0002t0065 | 0/0 | 15855 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0002t0068 | 0/0 | 15859 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0002t0069 | 0/0 | 15859 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0002t0070 | 0/0 | 15860 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0002t0071 | 0/0 | 15856 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0002t0106 | 0/0 | 15857 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0002t0107 | 0/0 | 15859 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0002t0108 | 0/0 | 15858 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0003t0001 | 0/0 | 15856 | 26 | 2 | 2 | 16 | 1 | 5 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0003t0007 | 0/0 | 15857 | 7 | 0 | 1 | 6 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0003t0010 | 0/0 | 15856 | 5 | 1 | 1 | 0 | 0 | 3 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0003t0016 | 0/0 | 15856 | 3 | 0 | 3 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0003t0032 | 0/0 | 15856 | 2 | 0 | 0 | 2 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0003t0033 | 0/0 | 15857 | 2 | 0 | 0 | 2 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0003t0051 | 0/0 | 15856 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0003t0079 | 0/0 | 15858 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0003t0080 | 0/0 | 15856 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0003t0081 | 0/0 | 15856 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0003t0082 | 0/0 | 15856 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0003t0103 | 0/0 | 15856 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0005t0022 | 0/0 | 15861 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0005t0023 | 0/0 | 15863 | 2 | 0 | 0 | 2 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0005t0046 | 0/0 | 15862 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0005t0047 | 0/0 | 15862 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0005t0048 | 0/0 | 15855 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0005t0049 | 0/0 | 15856 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0005t0050 | 0/0 | 15860 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0006t0004 | 0/0 | 15856 | 4 | 1 | 2 | 0 | 1 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0006t0013 | 0/0 | 15857 | 3 | 0 | 1 | 0 | 2 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0007t0007 | 0/0 | 15857 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0007t0077 | 0/0 | 15857 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0007t0078 | 0/0 | 15858 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0001c0010t0067 | 0/0 | 15857 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0002c0004t0003 | 0/0 | 15858 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0002c0004t0025 | 0/0 | 15867 | 2 | 1 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0002c0004t0028 | 0/0 | 15838 | 2 | 2 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0002c0004t0055 | 0/0 | 15850 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0002c0004t0056 | 0/0 | 15866 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0002c0004t0057 | 0/0 | 15875 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0002c0004t0058 | 0/0 | 15876 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0002c0004t0059 | 0/0 | 15899 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0002c0004t0060 | 0/0 | 15881 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0002c0004t0061 | 0/0 | 15884 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0002c0004t0066 | 0/0 | 15857 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0003c0008t0002 | 0/0 | 15845 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0003c0008t0014 | 0/0 | 15856 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0004c0011t0041 | 0/0 | 15866 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| a0005c0009t0022 | 0/0 | 15861 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | copy fasta | chr10 | 102913294 | 103095222 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0002g0103 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0005g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0005g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0005g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0005g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0005g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0005g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0005g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0005g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0005g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0005g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0005g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0005g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0005g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0005g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0008g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0008g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0008g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0008g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0008g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0008g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0008g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0011g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0011g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0011g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0011g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0011g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0012g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0012g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0012g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0012g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0012g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0014g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0014g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0014g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0017g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0017g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0017g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0018g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0018g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0018g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0019g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0019g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0019g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0020g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0020g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0020g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0021g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0021g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0021g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0030g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0030g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0031g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0031g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0034g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0034g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0035g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0035g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0036g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0036g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0037g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0037g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0038g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0038g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0039g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0039g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0040g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0040g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0041g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0042g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0042g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0043g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0043g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0045g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0072g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0073g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0074g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0075g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0076g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0083g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0084g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0085g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0086g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0087g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0088g0050 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0089g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0090g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0091g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0092g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0093g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0094g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0095g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0096g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0097g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0098g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0099g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0100g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0101g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0102g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0104g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0001t0105g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0003g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0003g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0003g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0003g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0003g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0003g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0004g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0004g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0004g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0004g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0004g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0004g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0004g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0004g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0004g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0006g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0006g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0006g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0006g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0006g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0006g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0006g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0006g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0009g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0009g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0009g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0009g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0009g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0009g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0009g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0013g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0015g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0015g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0015g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0024g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0024g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0026g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0026g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0027g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0027g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0029g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0029g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0044g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0044g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0052g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0053g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0054g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0062g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0063g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0064g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0065g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0068g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0069g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0070g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0071g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0106g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0107g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0002t0108g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0003t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0003t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0003t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0003t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0003t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0003t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0003t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0003t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0003t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0003t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0003t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0003t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0003t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0003t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0003t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0003t0007g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0003t0007g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0003t0007g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0003t0007g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0003t0007g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0003t0007g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0003t0007g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0003t0010g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0003t0010g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0003t0010g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0003t0010g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0003t0010g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0003t0016g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0003t0016g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0003t0016g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0003t0032g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0003t0032g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0003t0033g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0003t0033g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0003t0051g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0003t0079g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0003t0080g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0003t0081g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0003t0082g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0003t0103g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0005t0022g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0005t0023g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0005t0023g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0005t0046g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0005t0047g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0005t0048g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0005t0049g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0005t0050g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0006t0004g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0006t0004g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0006t0004g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0006t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0006t0013g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0006t0013g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0006t0013g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0007t0007g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0007t0077g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0007t0078g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0001c0010t0067g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0002c0004t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0002c0004t0025g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0002c0004t0025g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0002c0004t0028g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0002c0004t0028g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0002c0004t0055g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0002c0004t0056g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0002c0004t0057g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0002c0004t0058g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0002c0004t0059g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0002c0004t0060g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0002c0004t0061g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0002c0004t0066g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0003c0008t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0003c0008t0014g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0004c0011t0041g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| a0005c0009t0022g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0008 | g0059 | EUR | GBR | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG00099 | hp2 | a0001 | c0003 | t0001 | g0153 | EUR | GBR | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG00408 | hp1 | a0001 | c0002 | t0006 | g0210 | EAS | CHS | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG00408 | hp2 | a0001 | c0001 | t0019 | g0001 | EAS | CHS | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG00544 | hp1 | a0001 | c0001 | t0012 | g0080 | EAS | CHS | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG00544 | hp2 | a0001 | c0003 | t0001 | g0142 | EAS | CHS | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG00558 | hp1 | a0001 | c0001 | t0097 | g0014 | EAS | CHS | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG00558 | hp2 | a0001 | c0001 | t0037 | g0089 | EAS | CHS | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG00597 | hp1 | a0001 | c0001 | t0045 | g0030 | EAS | CHS | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG00597 | hp2 | a0001 | c0002 | t0052 | g0260 | EAS | CHS | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG00609 | hp1 | a0001 | c0002 | t0107 | g0235 | EAS | CHS | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG00609 | hp2 | a0001 | c0002 | t0006 | g0214 | EAS | CHS | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | CHS | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG00621 | hp2 | a0001 | c0002 | t0009 | g0238 | EAS | CHS | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG00639 | hp1 | a0001 | c0006 | t0013 | g0179 | AMR | PUR | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG00639 | hp2 | a0001 | c0002 | t0108 | g0249 | AMR | PUR | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG00642 | hp1 | a0001 | c0001 | t0095 | g0043 | AMR | PUR | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG00642 | hp2 | a0001 | c0002 | t0044 | g0243 | AMR | PUR | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG00673 | hp1 | a0001 | c0002 | t0004 | g0261 | EAS | CHS | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG00673 | hp2 | a0001 | c0002 | t0003 | g0229 | EAS | CHS | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG00733 | hp1 | a0002 | c0004 | t0003 | g0201 | AMR | PUR | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG00733 | hp2 | a0001 | c0001 | t0017 | g0072 | AMR | PUR | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG00735 | hp1 | a0002 | c0004 | t0059 | g0217 | AMR | PUR | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG00735 | hp2 | a0001 | c0002 | t0009 | g0224 | AMR | PUR | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG00738 | hp1 | a0001 | c0006 | t0004 | g0178 | AMR | PUR | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG00738 | hp2 | a0001 | c0001 | t0018 | g0091 | AMR | PUR | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG01070 | hp1 | a0001 | c0001 | t0086 | g0113 | AMR | PUR | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG01070 | hp2 | a0001 | c0002 | t0029 | g0207 | AMR | PUR | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG01071 | hp1 | a0001 | c0002 | t0069 | g0206 | AMR | PUR | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0067 | AMR | PUR | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG01081 | hp1 | a0001 | c0001 | t0101 | g0101 | AMR | PUR | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG01081 | hp2 | a0001 | c0001 | t0005 | g0006 | AMR | PUR | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG01099 | hp2 | a0001 | c0002 | t0003 | g0223 | AMR | PUR | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG01106 | hp1 | a0001 | c0001 | t0030 | g0037 | AMR | PUR | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG01106 | hp2 | a0001 | c0001 | t0017 | g0073 | AMR | PUR | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG01109 | hp1 | a0002 | c0004 | t0025 | g0199 | AMR | PUR | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG01109 | hp2 | a0001 | c0001 | t0005 | g0021 | AMR | PUR | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG01167 | hp1 | a0001 | c0001 | t0005 | g0057 | AMR | PUR | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG01167 | hp2 | a0001 | c0003 | t0010 | g0151 | AMR | PUR | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG01169 | hp1 | a0001 | c0001 | t0008 | g0060 | AMR | PUR | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG01169 | hp2 | a0001 | c0006 | t0004 | g0175 | AMR | PUR | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG01255 | hp1 | a0001 | c0002 | t0044 | g0230 | AMR | CLM | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG01255 | hp2 | a0001 | c0001 | t0012 | g0041 | AMR | CLM | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG01257 | hp1 | a0001 | c0002 | t0009 | g0244 | AMR | CLM | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG01257 | hp2 | a0001 | c0001 | t0042 | g0023 | AMR | CLM | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG01258 | hp1 | a0001 | c0002 | t0009 | g0241 | AMR | CLM | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG01258 | hp2 | a0001 | c0001 | t0008 | g0047 | AMR | CLM | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0062 | AMR | CLM | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG01358 | hp2 | a0001 | c0003 | t0051 | g0136 | AMR | CLM | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG01361 | hp1 | a0001 | c0001 | t0008 | g0252 | AMR | CLM | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG01361 | hp2 | a0001 | c0001 | t0021 | g0055 | AMR | CLM | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | CLM | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG01496 | hp2 | a0001 | c0002 | t0003 | g0253 | AMR | CLM | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG01515 | hp1 | a0001 | c0006 | t0013 | g0173 | EUR | IBS | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG01515 | hp2 | a0001 | c0001 | t0084 | g0016 | EUR | IBS | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG01516 | hp1 | a0001 | c0001 | t0035 | g0111 | EUR | IBS | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG01516 | hp2 | a0002 | c0004 | t0058 | g0203 | EUR | IBS | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG01517 | hp1 | a0002 | c0004 | t0057 | g0202 | EUR | IBS | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG01517 | hp2 | a0001 | c0006 | t0013 | g0174 | EUR | IBS | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0010 | AFR | ACB | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG01884 | hp2 | a0001 | c0002 | t0026 | g0267 | AFR | ACB | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG01934 | hp1 | a0001 | c0003 | t0016 | g0144 | AMR | PEL | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG01934 | hp2 | a0001 | c0001 | t0020 | g0026 | AMR | PEL | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG01943 | hp1 | a0001 | c0003 | t0001 | g0166 | AMR | PEL | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG01943 | hp2 | a0001 | c0001 | t0041 | g0051 | AMR | PEL | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG01952 | hp1 | a0001 | c0002 | t0024 | g0172 | AMR | PEL | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG01952 | hp2 | a0001 | c0001 | t0014 | g0045 | AMR | PEL | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG01978 | hp1 | a0001 | c0003 | t0007 | g0125 | AMR | PEL | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG01978 | hp2 | a0001 | c0001 | t0042 | g0024 | AMR | PEL | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG01981 | hp1 | a0001 | c0001 | t0008 | g0250 | AMR | PEL | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG01981 | hp2 | a0001 | c0001 | t0014 | g0042 | AMR | PEL | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02004 | hp1 | a0001 | c0003 | t0001 | g0168 | AMR | PEL | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02004 | hp2 | a0004 | c0011 | t0041 | g0056 | AMR | PEL | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02027 | hp1 | a0001 | c0001 | t0093 | g0031 | EAS | KHV | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02027 | hp2 | a0001 | c0002 | t0003 | g0233 | EAS | KHV | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02040 | hp1 | a0001 | c0001 | t0039 | g0061 | EAS | KHV | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02040 | hp2 | a0001 | c0002 | t0006 | g0212 | EAS | KHV | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02055 | hp1 | a0001 | c0001 | t0098 | g0033 | AFR | ACB | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02055 | hp2 | a0002 | c0004 | t0025 | g0195 | AFR | ACB | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02056 | hp1 | a0001 | c0002 | t0002 | g0245 | EAS | KHV | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02056 | hp2 | a0003 | c0008 | t0014 | g0074 | EAS | KHV | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02071 | hp1 | a0001 | c0001 | t0083 | g0048 | EAS | KHV | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02071 | hp2 | a0001 | c0007 | t0077 | g0131 | EAS | KHV | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02074 | hp1 | a0001 | c0007 | t0007 | g0129 | EAS | KHV | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02074 | hp2 | a0001 | c0001 | t0092 | g0082 | EAS | KHV | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | KHV | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02083 | hp2 | a0001 | c0003 | t0001 | g0170 | EAS | KHV | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02129 | hp1 | a0001 | c0007 | t0078 | g0132 | EAS | KHV | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02129 | hp2 | a0001 | c0001 | t0039 | g0086 | EAS | KHV | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02135 | hp1 | a0001 | c0002 | t0009 | g0226 | EAS | KHV | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02135 | hp2 | a0001 | c0005 | t0050 | g0191 | EAS | KHV | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02145 | hp1 | a0001 | c0002 | t0063 | g0270 | AFR | ACB | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02145 | hp2 | a0001 | c0001 | t0005 | g0003 | AFR | ACB | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02155 | hp1 | a0001 | c0001 | t0089 | g0092 | EAS | CDX | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02155 | hp2 | a0001 | c0003 | t0001 | g0171 | EAS | CDX | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02257 | hp1 | a0002 | c0004 | t0055 | g0216 | AFR | ACB | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02257 | hp2 | a0001 | c0003 | t0001 | g0157 | AFR | ACB | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02258 | hp1 | a0001 | c0002 | t0004 | g0263 | AFR | ACB | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02258 | hp2 | a0001 | c0010 | t0067 | g0194 | AFR | ACB | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02273 | hp1 | a0001 | c0003 | t0016 | g0145 | AMR | PEL | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02273 | hp2 | a0001 | c0001 | t0014 | g0018 | AMR | PEL | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02280 | hp1 | a0001 | c0002 | t0106 | g0228 | AFR | ACB | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02280 | hp2 | a0001 | c0001 | t0011 | g0013 | AFR | ACB | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02300 | hp1 | a0001 | c0002 | t0003 | g0225 | AMR | PEL | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02300 | hp2 | a0001 | c0003 | t0016 | g0163 | AMR | PEL | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02523 | hp1 | a0001 | c0002 | t0006 | g0208 | EAS | KHV | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02523 | hp2 | a0001 | c0001 | t0100 | g0085 | EAS | KHV | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02572 | hp1 | a0001 | c0001 | t0011 | g0012 | AFR | GWD | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02572 | hp2 | a0001 | c0001 | t0017 | g0063 | AFR | GWD | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02622 | hp1 | a0002 | c0004 | t0028 | g0215 | AFR | GWD | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02622 | hp2 | a0001 | c0002 | t0027 | g0266 | AFR | GWD | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02647 | hp1 | a0001 | c0002 | t0004 | g0262 | AFR | GWD | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02647 | hp2 | a0001 | c0002 | t0062 | g0222 | AFR | GWD | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0069 | SAS | PJL | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02683 | hp2 | a0001 | c0002 | t0029 | g0204 | SAS | PJL | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02717 | hp1 | a0002 | c0004 | t0056 | g0200 | AFR | GWD | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02717 | hp2 | a0001 | c0001 | t0005 | g0008 | AFR | GWD | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02735 | hp1 | a0001 | c0003 | t0010 | g0152 | SAS | PJL | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02735 | hp2 | a0001 | c0002 | t0006 | g0221 | SAS | PJL | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02809 | hp1 | a0001 | c0003 | t0082 | g0154 | AFR | GWD | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02809 | hp2 | a0001 | c0002 | t0004 | g0265 | AFR | GWD | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02896 | hp1 | a0001 | c0001 | t0011 | g0011 | AFR | GWD | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02896 | hp2 | a0002 | c0004 | t0028 | g0196 | AFR | GWD | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02922 | hp1 | a0002 | c0004 | t0066 | g0192 | AFR | ESN | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | ESN | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02970 | hp1 | a0001 | c0001 | t0019 | g0083 | AFR | ESN | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02970 | hp2 | a0001 | c0006 | t0004 | g0182 | AFR | ESN | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0022 | AFR | ESN | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02976 | hp2 | a0001 | c0002 | t0064 | g0248 | AFR | ESN | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG03017 | hp1 | a0001 | c0001 | t0102 | g0110 | SAS | PJL | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG03017 | hp2 | a0001 | c0003 | t0081 | g0165 | SAS | PJL | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG03041 | hp1 | a0001 | c0002 | t0013 | g0257 | AFR | GWD | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG03041 | hp2 | a0001 | c0001 | t0011 | g0114 | AFR | GWD | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG03098 | hp1 | a0001 | c0002 | t0004 | g0255 | AFR | MSL | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG03098 | hp2 | a0001 | c0001 | t0012 | g0020 | AFR | MSL | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG03139 | hp1 | a0001 | c0001 | t0019 | g0084 | AFR | ESN | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG03139 | hp2 | a0001 | c0002 | t0004 | g0264 | AFR | ESN | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG03225 | hp1 | a0001 | c0002 | t0004 | g0256 | AFR | MSL | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG03225 | hp2 | a0001 | c0002 | t0026 | g0269 | AFR | MSL | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG03486 | hp1 | a0001 | c0002 | t0004 | g0258 | AFR | MSL | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG03486 | hp2 | a0001 | c0001 | t0040 | g0035 | AFR | MSL | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0019 | SAS | PJL | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG03490 | hp2 | a0002 | c0004 | t0060 | g0197 | SAS | PJL | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0100 | SAS | PJL | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG03491 | hp2 | a0001 | c0003 | t0010 | g0148 | SAS | PJL | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG03492 | hp1 | a0001 | c0001 | t0036 | g0099 | SAS | PJL | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG03492 | hp2 | a0002 | c0004 | t0061 | g0198 | SAS | PJL | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG03516 | hp1 | a0001 | c0002 | t0053 | g0259 | AFR | ESN | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0002 | AFR | ESN | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG03540 | hp1 | a0001 | c0001 | t0072 | g0115 | AFR | GWD | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG03540 | hp2 | a0001 | c0002 | t0054 | g0193 | AFR | GWD | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG03688 | hp1 | a0001 | c0003 | t0010 | g0137 | SAS | STU | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0028 | SAS | STU | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG03831 | hp1 | a0001 | c0001 | t0073 | g0025 | SAS | BEB | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG03831 | hp2 | a0001 | c0002 | t0068 | g0219 | SAS | BEB | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG03834 | hp1 | a0001 | c0005 | t0022 | g0186 | SAS | BEB | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG03834 | hp2 | a0001 | c0003 | t0001 | g0118 | SAS | BEB | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG03927 | hp1 | a0001 | c0003 | t0001 | g0149 | SAS | BEB | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG03927 | hp2 | a0001 | c0001 | t0035 | g0079 | SAS | BEB | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG03942 | hp1 | a0001 | c0002 | t0070 | g0218 | SAS | BEB | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG03942 | hp2 | a0001 | c0003 | t0001 | g0143 | SAS | BEB | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG04115 | hp1 | a0001 | c0003 | t0001 | g0159 | SAS | STU | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG04115 | hp2 | a0001 | c0002 | t0015 | g0205 | SAS | STU | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG04184 | hp1 | a0001 | c0002 | t0015 | g0220 | SAS | BEB | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG04184 | hp2 | a0001 | c0001 | t0008 | g0017 | SAS | BEB | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG04199 | hp1 | a0001 | c0001 | t0008 | g0090 | SAS | STU | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG04199 | hp2 | a0001 | c0001 | t0005 | g0077 | SAS | STU | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG04228 | hp1 | a0001 | c0003 | t0001 | g0156 | SAS | STU | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG04228 | hp2 | a0001 | c0001 | t0105 | g0093 | SAS | STU | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA18522 | hp1 | a0001 | c0002 | t0027 | g0268 | AFR | YRI | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA18522 | hp2 | a0001 | c0001 | t0011 | g0009 | AFR | YRI | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA18612 | hp1 | a0001 | c0001 | t0094 | g0081 | EAS | CHB | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA18612 | hp2 | a0001 | c0003 | t0001 | g0167 | EAS | CHB | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA18747 | hp1 | a0001 | c0003 | t0007 | g0138 | EAS | CHB | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA18747 | hp2 | a0001 | c0002 | t0006 | g0209 | EAS | CHB | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA18939 | hp1 | a0001 | c0001 | t0040 | g0105 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA18939 | hp2 | a0001 | c0003 | t0033 | g0164 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA18941 | hp1 | a0001 | c0001 | t0021 | g0053 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA18941 | hp2 | a0001 | c0002 | t0003 | g0236 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA18943 | hp1 | a0001 | c0001 | t0020 | g0027 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA18943 | hp2 | a0001 | c0005 | t0049 | g0183 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA18945 | hp2 | a0001 | c0005 | t0023 | g0189 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA18946 | hp1 | a0001 | c0005 | t0023 | g0190 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA18946 | hp2 | a0001 | c0001 | t0005 | g0108 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA18947 | hp1 | a0001 | c0001 | t0018 | g0104 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA18947 | hp2 | a0001 | c0002 | t0004 | g0180 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA18950 | hp1 | a0003 | c0008 | t0002 | g0075 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA18950 | hp2 | a0001 | c0002 | t0009 | g0246 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA18951 | hp1 | a0001 | c0001 | t0038 | g0095 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA18951 | hp2 | a0001 | c0003 | t0033 | g0135 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA18954 | hp1 | a0001 | c0001 | t0031 | g0046 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA18954 | hp2 | a0001 | c0003 | t0001 | g0155 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA18957 | hp1 | a0001 | c0001 | t0091 | g0098 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA18957 | hp2 | a0001 | c0003 | t0007 | g0121 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA18962 | hp1 | a0001 | c0002 | t0009 | g0254 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA18962 | hp2 | a0001 | c0003 | t0001 | g0124 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA18963 | hp1 | a0001 | c0002 | t0003 | g0234 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA18963 | hp2 | a0005 | c0009 | t0022 | g0185 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA18968 | hp1 | a0001 | c0001 | t0090 | g0094 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA18968 | hp2 | a0001 | c0003 | t0001 | g0127 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA18971 | hp1 | a0001 | c0003 | t0001 | g0161 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA18971 | hp2 | a0001 | c0001 | t0021 | g0109 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA18975 | hp1 | a0001 | c0003 | t0001 | g0133 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA18975 | hp2 | a0001 | c0001 | t0030 | g0044 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA18982 | hp1 | a0001 | c0001 | t0034 | g0112 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA18982 | hp2 | a0001 | c0003 | t0001 | g0160 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA18983 | hp1 | a0001 | c0001 | t0005 | g0096 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA18983 | hp2 | a0001 | c0005 | t0048 | g0184 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA18989 | hp1 | a0001 | c0005 | t0047 | g0187 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA18989 | hp2 | a0001 | c0001 | t0074 | g0034 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA18990 | hp1 | a0001 | c0001 | t0099 | g0071 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA18990 | hp2 | a0001 | c0003 | t0103 | g0119 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA18992 | hp1 | a0001 | c0001 | t0096 | g0052 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA18992 | hp2 | a0001 | c0003 | t0001 | g0147 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA18994 | hp1 | a0001 | c0002 | t0003 | g0227 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA18994 | hp2 | a0001 | c0001 | t0085 | g0107 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA18995 | hp1 | a0001 | c0002 | t0003 | g0251 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA18995 | hp2 | a0001 | c0001 | t0036 | g0029 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA19004 | hp1 | a0001 | c0003 | t0001 | g0122 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA19004 | hp2 | a0001 | c0001 | t0034 | g0070 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA19007 | hp1 | a0001 | c0001 | t0012 | g0097 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA19007 | hp2 | a0001 | c0002 | t0006 | g0213 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA19009 | hp1 | a0001 | c0001 | t0037 | g0088 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA19009 | hp2 | a0001 | c0003 | t0001 | g0141 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA19011 | hp1 | a0001 | c0002 | t0003 | g0237 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA19011 | hp2 | a0001 | c0001 | t0043 | g0076 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA19043 | hp1 | a0001 | c0001 | t0005 | g0004 | AFR | LWK | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA19043 | hp2 | a0001 | c0002 | t0071 | g0247 | AFR | LWK | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA19054 | hp1 | a0001 | c0003 | t0032 | g0120 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA19054 | hp2 | a0001 | c0001 | t0075 | g0038 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA19057 | hp1 | a0001 | c0003 | t0007 | g0139 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA19057 | hp2 | a0001 | c0005 | t0046 | g0188 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA19060 | hp1 | a0001 | c0003 | t0007 | g0130 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA19064 | hp1 | a0001 | c0001 | t0076 | g0040 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA19064 | hp2 | a0001 | c0003 | t0080 | g0158 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA19065 | hp1 | a0001 | c0001 | t0020 | g0054 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA19065 | hp2 | a0001 | c0003 | t0001 | g0146 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA19070 | hp1 | a0001 | c0003 | t0001 | g0162 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA19070 | hp2 | a0001 | c0001 | t0031 | g0039 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA19077 | hp1 | a0001 | c0003 | t0079 | g0134 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA19077 | hp2 | a0001 | c0002 | t0015 | g0211 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA19082 | hp1 | a0001 | c0001 | t0043 | g0123 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA19082 | hp2 | a0001 | c0003 | t0001 | g0106 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA19084 | hp1 | a0001 | c0002 | t0006 | g0117 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA19084 | hp2 | a0001 | c0003 | t0007 | g0126 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA19086 | hp1 | a0001 | c0003 | t0007 | g0128 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA19086 | hp2 | a0001 | c0002 | t0003 | g0232 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA19090 | hp2 | a0001 | c0003 | t0032 | g0169 | EAS | JPT | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA20129 | hp1 | a0001 | c0001 | t0005 | g0007 | AFR | ASW | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA20129 | hp2 | a0001 | c0003 | t0001 | g0140 | AFR | ASW | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA20752 | hp1 | a0001 | c0002 | t0003 | g0231 | EUR | TSI | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA20752 | hp2 | a0001 | c0001 | t0018 | g0058 | EUR | TSI | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA20805 | hp1 | a0001 | c0002 | t0003 | g0242 | EUR | TSI | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA20805 | hp2 | a0001 | c0006 | t0004 | g0177 | EUR | TSI | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG01123 | hp1 | a0001 | c0002 | t0003 | g0240 | AMR | CLM | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG01123 | hp2 | a0001 | c0001 | t0012 | g0087 | AMR | CLM | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02109 | hp1 | a0001 | c0002 | t0065 | g0116 | AFR | ACB | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02109 | hp2 | a0001 | c0001 | t0104 | g0032 | AFR | ACB | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02486 | hp1 | a0001 | c0001 | t0087 | g0036 | AFR | ACB | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| HG02486 | hp2 | a0001 | c0002 | t0003 | g0239 | AFR | ACB | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA20300 | hp1 | a0001 | c0001 | t0038 | g0015 | AFR | USA | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA20300 | hp2 | a0001 | c0002 | t0024 | g0181 | AFR | USA | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA21309 | hp1 | a0001 | c0002 | t0004 | g0176 | AFR | LWK | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| NA21309 | hp2 | a0001 | c0003 | t0010 | g0150 | AFR | LWK | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0103 | REF | REF | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0088 | g0050 | REF | REF | CNNM2_chr10_102913294_103095222 | CNNM2 | chr10 | 102913294 | 103095222 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:102918580
|
A | G | 1 | a0004 | 1 | HG02004.hp2 | missense_variant | MODERATE | c.100A>G | p.Ser34Gly | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/8 | 287/15857 | 100/2628 | 34/875 | chr10 | 102918580 | ||
| chr10:102918593
|
G | A | 1 | a0002 | 13 | HG00733.hp1 HG00735.hp1 HG01109.hp1 others(10): Show |
missense_variant | MODERATE | c.113G>A | p.Arg38Gln | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/8 | 300/15857 | 113/2628 | 38/875 | chr10 | 102918593 | ||
| chr10:102918893
|
C | T | 1 | a0005 | 1 | NA18963.hp2 | missense_variant | MODERATE | c.413C>T | p.Pro138Leu | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/8 | 600/15857 | 413/2628 | 138/875 | chr10 | 102918893 | ||
| chr10:102919084
|
G | A | 1 | a0003 | 2 | HG02056.hp2 NA18950.hp1 |
missense_variant | MODERATE | c.604G>A | p.Ala202Thr | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/8 | 791/15857 | 604/2628 | 202/875 | chr10 | 102919084 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:102918822
|
G | T | 1 | a0001c0007 | 3 | HG02071.hp2 HG02074.hp1 HG02129.hp1 |
synonymous_variant | LOW | c.342G>T | p.Thr114Thr | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/8 | 529/15857 | 342/2628 | 114/875 | chr10 | 102918822 | ||
| chr10:102918840
|
C | T | 1 | a0001c0010 | 1 | HG02258.hp2 | synonymous_variant | LOW | c.360C>T | p.Phe120Phe | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/8 | 547/15857 | 360/2628 | 120/875 | chr10 | 102918840 | ||
| chr10:102919614
|
C | T | 2 | a0001c0005a0005c0009 | 9 | HG02135.hp2 HG03834.hp1 NA18943.hp2 others(6): Show |
synonymous_variant | LOW | c.1134C>T | p.Leu378Leu | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/8 | 1321/15857 | 1134/2628 | 378/875 | chr10 | 102919614 | ||
| chr10:103054405
|
T | C | 8 | a0001c0002a0001c0003a0001c0005others(5): Show | 153 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(150): Show |
synonymous_variant | LOW | c.1842T>C | p.Ser614Ser | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 3/8 | 2029/15857 | 1842/2628 | 614/875 | chr10 | 103054405 | ||
| chr10:103076162
|
C | T | 2 | a0001c0003a0001c0007 | 54 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(51): Show |
synonymous_variant | LOW | c.2310C>T | p.Ala770Ala | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 7/8 | 2497/15857 | 2310/2628 | 770/875 | chr10 | 103076162 | ||
| chr10:103077096
|
C | T | 1 | a0001c0006 | 7 | HG00639.hp1 HG00738.hp1 HG01169.hp2 others(4): Show |
synonymous_variant | LOW | c.2544C>T | p.Asp848Asp | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 2731/15857 | 2544/2628 | 848/875 | chr10 | 103077096 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:103077183
|
C | T | 7 | a0001c0002t0003a0001c0002t0009a0001c0002t0044others(4): Show | 28 | HG00609.hp1 HG00621.hp2 HG00639.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*3C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 3 | chr10 | 103077183 | |||||
| chr10:103077232
|
C | T | 1 | a0001c0002t0108 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*52C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 52 | chr10 | 103077232 | |||||
| chr10:103077298
|
G | A | 1 | a0001c0001t0045 | 1 | HG00597.hp1 | 3_prime_UTR_variant | MODIFIER | c.*118G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 118 | chr10 | 103077298 | |||||
| chr10:103077635
|
C | T | 1 | a0001c0001t0043 | 2 | NA19011.hp2 NA19082.hp1 |
3_prime_UTR_variant | MODIFIER | c.*455C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 455 | chr10 | 103077635 | |||||
| chr10:103077708
|
G | A | 8 | a0001c0005t0022a0001c0005t0023a0001c0005t0046others(5): Show | 9 | HG02135.hp2 HG03834.hp1 NA18943.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*528G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 528 | chr10 | 103077708 | |||||
| chr10:103077974
|
G | A | 1 | a0001c0003t0051 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*794G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 794 | chr10 | 103077974 | |||||
| chr10:103078059
|
G | A | 39 | a0001c0002t0003a0001c0002t0004a0001c0002t0006others(36): Show | 89 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*879G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 879 | chr10 | 103078059 | |||||
| chr10:103078084
|
G | C | 1 | a0001c0002t0024 | 2 | HG01952.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*904G>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 904 | chr10 | 103078084 | |||||
| chr10:103078386
|
G | C | 1 | a0001c0001t0072 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1206G>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 1206 | chr10 | 103078386 | |||||
| chr10:103078517
|
T | A | 1 | a0001c0001t0073 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1337T>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 1337 | chr10 | 103078517 | |||||
| chr10:103078658
|
T | C | 7 | a0001c0001t0014a0001c0001t0030a0001c0001t0031others(4): Show | 11 | HG01106.hp1 HG01952.hp2 HG01981.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1478T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 1478 | chr10 | 103078658 | |||||
| chr10:103078753
|
G | A | 7 | a0001c0002t0004a0001c0002t0013a0001c0002t0024others(4): Show | 22 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1573G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 1573 | chr10 | 103078753 | |||||
| chr10:103078887
|
C | T | 1 | a0001c0001t0105 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1707C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 1707 | chr10 | 103078887 | |||||
| chr10:103078940
|
C | T | 1 | a0001c0001t0104 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1760C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 1760 | chr10 | 103078940 | |||||
| chr10:103078999
|
G | T | 1 | a0001c0003t0103 | 1 | NA18990.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1819G>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 1819 | chr10 | 103078999 | |||||
| chr10:103079273
|
G | A | 1 | a0001c0002t0054 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2093G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 2093 | chr10 | 103079273 | |||||
| chr10:103079307
|
G | A | 1 | a0002c0004t0055 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2127G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 2127 | chr10 | 103079307 | |||||
| chr10:103079395
|
T | C | 54 | a0001c0002t0003a0001c0002t0004a0001c0002t0006others(51): Show | 143 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(140): Show |
3_prime_UTR_variant | MODIFIER | c.*2215T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 2215 | chr10 | 103079395 | |||||
| chr10:103079473
|
T | C | 7 | a0002c0004t0025a0002c0004t0056a0002c0004t0057others(4): Show | 8 | HG00735.hp1 HG01109.hp1 HG01516.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2293T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 2293 | chr10 | 103079473 | |||||
| chr10:103079605
|
G | A | 1 | a0001c0002t0062 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2425G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 2425 | chr10 | 103079605 | |||||
| chr10:103079787
|
C | T | 1 | a0002c0004t0055 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2607C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 2607 | chr10 | 103079787 | |||||
| chr10:103079881
|
C | G | 1 | a0001c0003t0016 | 3 | HG01934.hp1 HG02273.hp1 HG02300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2701C>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 2701 | chr10 | 103079881 | |||||
| chr10:103080476
|
T | C | 1 | a0001c0001t0083 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3296T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 3296 | chr10 | 103080476 | |||||
| chr10:103080618
|
C | T | 1 | a0001c0001t0102 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3438C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 3438 | chr10 | 103080618 | |||||
| chr10:103080676
|
C | T | 39 | a0001c0002t0003a0001c0002t0004a0001c0002t0006others(36): Show | 89 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*3496C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 3496 | chr10 | 103080676 | |||||
| chr10:103080755
|
A | G | 1 | a0001c0001t0101 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3575A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 3575 | chr10 | 103080755 | |||||
| chr10:103080878
|
T | C | 39 | a0001c0002t0003a0001c0002t0004a0001c0002t0006others(36): Show | 89 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*3698T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 3698 | chr10 | 103080878 | |||||
| chr10:103081136
|
G | T | 1 | a0001c0001t0100 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3956G>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 3956 | chr10 | 103081136 | |||||
| chr10:103081210
|
A | G | 15 | a0001c0003t0001a0001c0003t0007a0001c0003t0010others(12): Show | 54 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*4030A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 4030 | chr10 | 103081210 | |||||
| chr10:103081213
|
T | C | 54 | a0001c0002t0003a0001c0002t0004a0001c0002t0006others(51): Show | 143 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(140): Show |
3_prime_UTR_variant | MODIFIER | c.*4033T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 4033 | chr10 | 103081213 | |||||
| chr10:103081559
|
G | C | 4 | a0001c0002t0026a0001c0002t0027a0001c0002t0062others(1): Show | 6 | HG01884.hp2 HG02145.hp1 HG02622.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4379G>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 4379 | chr10 | 103081559 | |||||
| chr10:103081722
|
C | T | 15 | a0001c0003t0001a0001c0003t0007a0001c0003t0010others(12): Show | 54 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*4542C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 4542 | chr10 | 103081722 | |||||
| chr10:103081807
|
C | T | 1 | a0001c0001t0099 | 1 | NA18990.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4627C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 4627 | chr10 | 103081807 | |||||
| chr10:103081814
|
G | A | 2 | a0001c0005t0046a0001c0005t0047 | 2 | NA18989.hp1 NA19057.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4634G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 4634 | chr10 | 103081814 | |||||
| chr10:103081830
|
T | C | 39 | a0001c0002t0003a0001c0002t0004a0001c0002t0006others(36): Show | 89 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*4650T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 4650 | chr10 | 103081830 | |||||
| chr10:103081832
|
C | T | 1 | a0001c0002t0071 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4652C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 4652 | chr10 | 103081832 | |||||
| chr10:103081920
|
T | C | 1 | a0001c0001t0084 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4740T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 4740 | chr10 | 103081920 | |||||
| chr10:103082220
|
C | T | 44 | a0001c0002t0003a0001c0002t0004a0001c0002t0006others(41): Show | 95 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*5040C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 5040 | chr10 | 103082220 | |||||
| chr10:103082380
|
A | G | 1 | a0001c0001t0042 | 2 | HG01257.hp2 HG01978.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5200A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 5200 | chr10 | 103082380 | |||||
| chr10:103082415
|
C | T | 6 | a0001c0002t0006a0001c0002t0015a0001c0002t0029others(3): Show | 16 | HG00408.hp1 HG00609.hp2 HG01070.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*5235C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 5235 | chr10 | 103082415 | |||||
| chr10:103082702
|
C | T | 2 | a0002c0004t0060a0002c0004t0061 | 2 | HG03490.hp2 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5522C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 5522 | chr10 | 103082702 | |||||
| chr10:103082779
|
G | GTC | 7 | a0001c0002t0004a0001c0002t0013a0001c0002t0024others(4): Show | 22 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*5602_*5603dupTC | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 5604 | INFO_REALIGN_3_PRIME | chr10 | 103082779 | ||||
| chr10:103082954
|
ACTTAC | A | 8 | a0001c0005t0022a0001c0005t0023a0001c0005t0046others(5): Show | 9 | HG02135.hp2 HG03834.hp1 NA18943.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5779_*5783delCCTT others(1): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 5779 | INFO_REALIGN_3_PRIME | chr10 | 103082954 | ||||
| chr10:103083140
|
G | A | 1 | a0001c0002t0068 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5960G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 5960 | chr10 | 103083140 | |||||
| chr10:103083391
|
C | T | 39 | a0001c0002t0003a0001c0002t0004a0001c0002t0006others(36): Show | 89 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*6211C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 6211 | chr10 | 103083391 | |||||
| chr10:103083456
|
T | C | 2 | a0001c0001t0034a0001c0001t0099 | 3 | NA18982.hp1 NA18990.hp1 NA19004.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6276T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 6276 | chr10 | 103083456 | |||||
| chr10:103083837
|
G | A | 1 | a0001c0002t0044 | 2 | HG00642.hp2 HG01255.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6657G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 6657 | chr10 | 103083837 | |||||
| chr10:103083886
|
G | A | 1 | a0001c0002t0106 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6706G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 6706 | chr10 | 103083886 | |||||
| chr10:103083958
|
T | A | 1 | a0001c0002t0062 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6778T>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 6778 | chr10 | 103083958 | |||||
| chr10:103084196
|
G | C | 1 | a0001c0001t0085 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7016G>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 7016 | chr10 | 103084196 | |||||
| chr10:103084254
|
A | G | 39 | a0001c0002t0003a0001c0002t0004a0001c0002t0006others(36): Show | 89 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*7074A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 7074 | chr10 | 103084254 | |||||
| chr10:103084392
|
C | T | 1 | a0001c0003t0082 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7212C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 7212 | chr10 | 103084392 | |||||
| chr10:103084408
|
G | A | 1 | a0002c0004t0028 | 2 | HG02622.hp1 HG02896.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7228G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 7228 | chr10 | 103084408 | |||||
| chr10:103084436
|
C | T | 1 | a0001c0002t0062 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7256C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 7256 | chr10 | 103084436 | |||||
| chr10:103084557
|
T | G | 6 | a0001c0002t0006a0001c0002t0015a0001c0002t0029others(3): Show | 16 | HG00408.hp1 HG00609.hp2 HG01070.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*7377T>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 7377 | chr10 | 103084557 | |||||
| chr10:103084790
|
T | C | 1 | a0001c0002t0071 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7610T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 7610 | chr10 | 103084790 | |||||
| chr10:103084939
|
G | T | 1 | a0001c0002t0054 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7759G>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 7759 | chr10 | 103084939 | |||||
| chr10:103084990
|
C | G | 1 | a0001c0003t0081 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7810C>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 7810 | chr10 | 103084990 | |||||
| chr10:103085055
|
C | A | 1 | a0001c0005t0046 | 1 | NA19057.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7875C>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 7875 | chr10 | 103085055 | |||||
| chr10:103085115
|
T | C | 54 | a0001c0001t0017a0001c0002t0003a0001c0002t0004others(51): Show | 145 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*7935T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 7935 | chr10 | 103085115 | |||||
| chr10:103085119
|
C | T | 7 | a0001c0001t0014a0001c0001t0030a0001c0001t0031others(4): Show | 11 | HG01106.hp1 HG01952.hp2 HG01981.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*7939C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 7939 | chr10 | 103085119 | |||||
| chr10:103085171
|
G | T | 39 | a0001c0002t0003a0001c0002t0004a0001c0002t0006others(36): Show | 89 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*7991G>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 7991 | chr10 | 103085171 | |||||
| chr10:103085394
|
A | G | 1 | a0001c0001t0045 | 1 | HG00597.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8214A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 8214 | chr10 | 103085394 | |||||
| chr10:103085469
|
G | A | 2 | a0001c0003t0010a0001c0003t0081 | 6 | HG01167.hp2 HG02735.hp1 HG03017.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*8289G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 8289 | chr10 | 103085469 | |||||
| chr10:103085504
|
G | A | 1 | a0001c0002t0071 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8324G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 8324 | chr10 | 103085504 | |||||
| chr10:103085541
|
C | G | 1 | a0001c0003t0080 | 1 | NA19064.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8361C>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 8361 | chr10 | 103085541 | |||||
| chr10:103085686
|
T | A | 17 | a0001c0002t0004a0001c0002t0013a0001c0002t0024others(14): Show | 34 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*8506T>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 8506 | chr10 | 103085686 | |||||
| chr10:103085708
|
A | T | 1 | a0001c0001t0073 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8528A>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 8528 | chr10 | 103085708 | |||||
| chr10:103085850
|
G | A | 1 | a0001c0002t0107 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8670G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 8670 | chr10 | 103085850 | |||||
| chr10:103085922
|
ACTCATT | A | 2 | a0001c0001t0035a0001c0001t0086 | 3 | HG01070.hp1 HG01516.hp1 HG03927.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8745_*8750delCATT others(2): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 8745 | INFO_REALIGN_3_PRIME | chr10 | 103085922 | ||||
| chr10:103086090
|
T | A | 1 | a0001c0001t0083 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8910T>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 8910 | chr10 | 103086090 | |||||
| chr10:103086421
|
T | C | 15 | a0001c0003t0001a0001c0003t0007a0001c0003t0010others(12): Show | 54 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*9241T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 9241 | chr10 | 103086421 | |||||
| chr10:103086462
|
G | GTTGT | 62 | a0001c0002t0003a0001c0002t0004a0001c0002t0006others(59): Show | 152 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(149): Show |
3_prime_UTR_variant | MODIFIER | c.*9283_*9286dupTTGT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 9287 | INFO_REALIGN_3_PRIME | chr10 | 103086462 | ||||
| chr10:103087040
|
C | T | 38 | a0001c0002t0003a0001c0002t0004a0001c0002t0006others(35): Show | 88 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*9860C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 9860 | chr10 | 103087040 | |||||
| chr10:103087134
|
C | T | 8 | a0001c0001t0020a0001c0001t0021a0001c0001t0041others(5): Show | 13 | HG00558.hp1 HG01257.hp2 HG01361.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*9954C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 9954 | chr10 | 103087134 | |||||
| chr10:103087137
|
A | G | 1 | a0001c0002t0053 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9957A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 9957 | chr10 | 103087137 | |||||
| chr10:103087140
|
A | AT | 3 | a0001c0001t0011a0001c0002t0063a0001c0005t0049 | 7 | HG02145.hp1 HG02280.hp2 HG02572.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*9992dupT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 9993 | INFO_REALIGN_3_PRIME | chr10 | 103087140 | ||||
| chr10:103087140
|
A | ATTTTT | 6 | a0001c0001t0008a0001c0001t0035a0001c0001t0089others(3): Show | 13 | HG00099.hp1 HG01169.hp1 HG01258.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*9988_*9992dupTTTT others(1): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 9993 | INFO_REALIGN_3_PRIME | chr10 | 103087140 | ||||
| chr10:103087140
|
A | ATTTTTT | 6 | a0001c0001t0018a0001c0001t0030a0001c0001t0083others(3): Show | 9 | HG00738.hp2 HG01106.hp1 HG02071.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*9987_*9992dupTTTT others(2): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 9993 | INFO_REALIGN_3_PRIME | chr10 | 103087140 | ||||
| chr10:103087140
|
A | ATTTTTTT | 6 | a0001c0001t0012a0001c0001t0072a0001c0001t0086others(3): Show | 11 | HG00544.hp1 HG01070.hp1 HG01109.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*9986_*9992dupTTTT others(3): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 9993 | INFO_REALIGN_3_PRIME | chr10 | 103087140 | ||||
| chr10:103087140
|
A | ATTTTTTT others(1): Show |
4 | a0001c0001t0038a0001c0001t0074a0001c0001t0090others(1): Show | 6 | NA18945.hp2 NA18946.hp1 NA18951.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*9985_*9992dupTTTT others(4): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 9993 | INFO_REALIGN_3_PRIME | chr10 | 103087140 | ||||
| chr10:103087140
|
A | ATTTTTTT others(3): Show |
4 | a0001c0001t0039a0001c0001t0041a0001c0001t0100others(1): Show | 5 | HG01943.hp2 HG02004.hp2 HG02040.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*9983_*9992dupTTTT others(6): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 9993 | INFO_REALIGN_3_PRIME | chr10 | 103087140 | ||||
| chr10:103087140
|
A | ATTTTTTT others(4): Show |
3 | a0001c0001t0020a0001c0001t0031a0001c0001t0091 | 6 | HG01934.hp2 NA18943.hp1 NA18954.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*9982_*9992dupTTTT others(7): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 9993 | INFO_REALIGN_3_PRIME | chr10 | 103087140 | ||||
| chr10:103087140
|
A | ATTTTTTT others(5): Show |
4 | a0001c0001t0019a0001c0001t0021a0001c0001t0085others(1): Show | 8 | HG00408.hp2 HG01361.hp2 HG02109.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*9981_*9992dupTTTT others(8): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 9993 | INFO_REALIGN_3_PRIME | chr10 | 103087140 | ||||
| chr10:103087140
|
A | ATTTTTTT others(6): Show |
3 | a0001c0001t0040a0001c0001t0092a0001c0001t0098 | 4 | HG02055.hp1 HG02074.hp2 HG03486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*9980_*9992dupTTTT others(9): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 9993 | INFO_REALIGN_3_PRIME | chr10 | 103087140 | ||||
| chr10:103087140
|
A | ATTTTTTT others(7): Show |
1 | a0001c0001t0093 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9979_*9992dupTTTT others(10): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 9993 | INFO_REALIGN_3_PRIME | chr10 | 103087140 | ||||
| chr10:103087140
|
A | ATTTTTTT others(8): Show |
2 | a0001c0001t0094a0002c0004t0057 | 2 | HG01517.hp1 NA18612.hp1 |
3_prime_UTR_variant | MODIFIER | c.*9978_*9992dupTTTT others(11): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 9993 | INFO_REALIGN_3_PRIME | chr10 | 103087140 | ||||
| chr10:103087140
|
A | ATTTTTTT others(9): Show |
1 | a0002c0004t0058 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9977_*9992dupTTTT others(12): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 9993 | INFO_REALIGN_3_PRIME | chr10 | 103087140 | ||||
| chr10:103087140
|
A | ATTTTTTT others(11): Show |
1 | a0001c0001t0075 | 1 | NA19054.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9975_*9992dupTTTT others(14): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 9993 | INFO_REALIGN_3_PRIME | chr10 | 103087140 | ||||
| chr10:103087140
|
A | ATTTTTTT others(12): Show |
2 | a0001c0001t0076a0001c0001t0095 | 2 | HG00642.hp1 NA19064.hp1 |
3_prime_UTR_variant | MODIFIER | c.*9974_*9992dupTTTT others(15): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 9993 | INFO_REALIGN_3_PRIME | chr10 | 103087140 | ||||
| chr10:103087140
|
A | ATTTTTTT others(14): Show |
1 | a0002c0004t0060 | 1 | HG03490.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9972_*9992dupTTTT others(17): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 9993 | INFO_REALIGN_3_PRIME | chr10 | 103087140 | ||||
| chr10:103087140
|
A | ATTTTTTT others(17): Show |
1 | a0002c0004t0061 | 1 | HG03492.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9969_*9992dupTTTT others(20): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 9993 | INFO_REALIGN_3_PRIME | chr10 | 103087140 | ||||
| chr10:103087140
|
A | ATTTTTTT others(32): Show |
1 | a0002c0004t0059 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9992_*9993insTTTT others(35): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 9993 | INFO_REALIGN_3_PRIME | chr10 | 103087140 | ||||
| chr10:103087140
|
AT | A | 5 | a0001c0002t0009a0001c0002t0015a0001c0002t0068others(2): Show | 13 | HG00609.hp1 HG00621.hp2 HG00735.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*9992delT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 9992 | INFO_REALIGN_3_PRIME | chr10 | 103087140 | ||||
| chr10:103087140
|
ATT | A | 9 | a0001c0001t0087a0001c0002t0003a0001c0002t0006others(6): Show | 32 | HG00408.hp1 HG00609.hp2 HG00639.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*9991_*9992delTT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 9991 | INFO_REALIGN_3_PRIME | chr10 | 103087140 | ||||
| chr10:103087140
|
ATTT | A | 5 | a0001c0002t0106a0001c0003t0033a0001c0007t0078others(2): Show | 6 | HG02129.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*9990_*9992delTTT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 9990 | INFO_REALIGN_3_PRIME | chr10 | 103087140 | ||||
| chr10:103087140
|
ATTTT | A | 13 | a0001c0002t0071a0001c0003t0001a0001c0003t0007others(10): Show | 51 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*9989_*9992delTTTT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 9989 | INFO_REALIGN_3_PRIME | chr10 | 103087140 | ||||
| chr10:103087140
|
ATTTTT | A | 4 | a0001c0002t0013a0001c0002t0053a0001c0002t0065others(1): Show | 6 | HG00639.hp1 HG01515.hp1 HG01517.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*9988_*9992delTTTT others(1): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 9988 | INFO_REALIGN_3_PRIME | chr10 | 103087140 | ||||
| chr10:103087140
|
ATTTTTT | A | 4 | a0001c0002t0004a0001c0002t0024a0001c0002t0052others(1): Show | 17 | HG00597.hp2 HG00673.hp1 HG00738.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*9987_*9992delTTTT others(2): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 9987 | INFO_REALIGN_3_PRIME | chr10 | 103087140 | ||||
| chr10:103087140
|
ATTTTTTT others(3): Show |
A | 4 | a0001c0001t0036a0001c0001t0101a0001c0002t0026others(1): Show | 6 | HG01081.hp1 HG01884.hp2 HG02257.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*9983_*9992delTTTT others(6): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 9983 | INFO_REALIGN_3_PRIME | chr10 | 103087140 | ||||
| chr10:103087140
|
ATTTTTTT others(4): Show |
A | 11 | a0001c0001t0002a0001c0001t0017a0001c0001t0034others(8): Show | 28 | HG00597.hp1 HG00621.hp1 HG00733.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*9982_*9992delTTTT others(7): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 9982 | INFO_REALIGN_3_PRIME | chr10 | 103087140 | ||||
| chr10:103087140
|
ATTTTTTT others(10): Show |
A | 1 | a0001c0002t0064 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9976_*9992delTTTT others(13): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 9976 | INFO_REALIGN_3_PRIME | chr10 | 103087140 | ||||
| chr10:103087140
|
ATTTTTTT others(15): Show |
A | 1 | a0002c0004t0028 | 2 | HG02622.hp1 HG02896.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9971_*9992delTTTT others(18): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 9971 | INFO_REALIGN_3_PRIME | chr10 | 103087140 | ||||
| chr10:103087206
|
C | CT | 4 | a0001c0003t0007a0001c0007t0007a0001c0007t0077others(1): Show | 10 | HG01978.hp1 HG02071.hp2 HG02074.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*10028dupT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 10029 | INFO_REALIGN_3_PRIME | chr10 | 103087206 | ||||
| chr10:103087227
|
GA | G | 116 | a0001c0001t0002a0001c0001t0005a0001c0001t0008others(113): Show | 269 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(266): Show |
3_prime_UTR_variant | MODIFIER | c.*10051delA | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 10051 | INFO_REALIGN_3_PRIME | chr10 | 103087227 | ||||
| chr10:103087588
|
G | A | 2 | a0001c0001t0083a0001c0001t0089 | 2 | HG02071.hp1 HG02155.hp1 |
3_prime_UTR_variant | MODIFIER | c.*10408G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 10408 | chr10 | 103087588 | |||||
| chr10:103087985
|
T | C | 1 | a0001c0001t0090 | 1 | NA18968.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10805T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 10805 | chr10 | 103087985 | |||||
| chr10:103088298
|
C | G | 1 | a0001c0001t0097 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11118C>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 11118 | chr10 | 103088298 | |||||
| chr10:103088366
|
G | A | 54 | a0001c0002t0003a0001c0002t0004a0001c0002t0006others(51): Show | 143 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(140): Show |
3_prime_UTR_variant | MODIFIER | c.*11186G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 11186 | chr10 | 103088366 | |||||
| chr10:103088502
|
A | G | 6 | a0001c0001t0037a0001c0001t0085a0001c0001t0091others(3): Show | 7 | HG00558.hp2 HG02074.hp2 HG02523.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*11322A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 11322 | chr10 | 103088502 | |||||
| chr10:103088673
|
C | T | 15 | a0001c0003t0001a0001c0003t0007a0001c0003t0010others(12): Show | 54 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*11493C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 11493 | chr10 | 103088673 | |||||
| chr10:103088693
|
T | G | 1 | a0001c0010t0067 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11513T>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 11513 | chr10 | 103088693 | |||||
| chr10:103088791
|
T | C | 1 | a0001c0007t0077 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11611T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 11611 | chr10 | 103088791 | |||||
| chr10:103089087
|
A | T | 6 | a0001c0002t0006a0001c0002t0015a0001c0002t0029others(3): Show | 16 | HG00408.hp1 HG00609.hp2 HG01070.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*11907A>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 11907 | chr10 | 103089087 | |||||
| chr10:103089098
|
A | T | 6 | a0001c0002t0006a0001c0002t0015a0001c0002t0029others(3): Show | 16 | HG00408.hp1 HG00609.hp2 HG01070.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*11918A>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 11918 | chr10 | 103089098 | |||||
| chr10:103089150
|
A | G | 5 | a0001c0002t0026a0001c0002t0027a0001c0002t0062others(2): Show | 7 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*11970A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 11970 | chr10 | 103089150 | |||||
| chr10:103089359
|
G | C | 16 | a0001c0001t0017a0001c0003t0001a0001c0003t0007others(13): Show | 57 | HG00099.hp2 HG00544.hp2 HG00733.hp2 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*12179G>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 12179 | chr10 | 103089359 | |||||
| chr10:103089387
|
A | C | 6 | a0001c0002t0006a0001c0002t0015a0001c0002t0029others(3): Show | 16 | HG00408.hp1 HG00609.hp2 HG01070.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*12207A>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 12207 | chr10 | 103089387 | |||||
| chr10:103089528
|
A | G | 2 | a0001c0003t0032a0001c0003t0103 | 3 | NA18990.hp2 NA19054.hp1 NA19090.hp2 |
3_prime_UTR_variant | MODIFIER | c.*12348A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 12348 | chr10 | 103089528 | |||||
| chr10:103089711
|
G | A | 53 | a0001c0002t0003a0001c0002t0004a0001c0002t0006others(50): Show | 142 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(139): Show |
3_prime_UTR_variant | MODIFIER | c.*12531G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 12531 | chr10 | 103089711 | |||||
| chr10:103089948
|
G | A | 2 | a0001c0002t0029a0001c0002t0069 | 3 | HG01070.hp2 HG01071.hp1 HG02683.hp2 |
3_prime_UTR_variant | MODIFIER | c.*12768G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 8/8 | 12768 | chr10 | 103089948 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:102920221
|
C | T | 155 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0001t0043g0123others(152): Show | 155 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(152): Show |
intron_variant | MODIFIER | c.1621+120C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102920221 | ||||||
| chr10:102920310
|
G | A | 1 | a0001c0002t0065g0116 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1621+209G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102920310 | ||||||
| chr10:102920376
|
A | AT | 16 | a0001c0002t0004g0255a0001c0002t0004g0256a0001c0002t0004g0258others(13): Show | 16 | HG00597.hp2 HG00673.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1621+288dupT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102920376 | |||||
| chr10:102920380
|
T | A | 69 | a0001c0001t0005g0002a0001c0001t0005g0003a0001c0001t0005g0004others(66): Show | 69 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.1621+279T>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102920380 | ||||||
| chr10:102920383
|
T | A | 1 | a0001c0001t0097g0014 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1621+282T>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102920383 | ||||||
| chr10:102920605
|
A | G | 33 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(30): Show | 33 | HG00609.hp1 HG00621.hp2 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.1621+504A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102920605 | ||||||
| chr10:102920700
|
CA | C | 155 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0001t0043g0123others(152): Show | 155 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(152): Show |
intron_variant | MODIFIER | c.1621+607delA | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102920700 | |||||
| chr10:102920885
|
G | T | 1 | a0001c0003t0001g0171 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1621+784G>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102920885 | ||||||
| chr10:102921218
|
C | T | 6 | a0001c0002t0026g0267a0001c0002t0026g0269a0001c0002t0027g0266others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1621+1117C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102921218 | ||||||
| chr10:102921290
|
C | T | 4 | a0001c0002t0006g0221a0001c0002t0015g0220a0001c0002t0068g0219others(1): Show | 4 | HG02735.hp2 HG03831.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1621+1189C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102921290 | ||||||
| chr10:102921386
|
A | G | 54 | a0001c0001t0043g0123a0001c0003t0001g0118a0001c0003t0001g0122others(51): Show | 54 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(51): Show |
intron_variant | MODIFIER | c.1621+1285A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102921386 | ||||||
| chr10:102921804
|
C | A | 1 | a0001c0001t0038g0015 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1621+1703C>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102921804 | ||||||
| chr10:102921811
|
A | C | 1 | a0001c0001t0072g0115 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1621+1710A>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102921811 | ||||||
| chr10:102921953
|
T | C | 31 | a0001c0002t0004g0176a0001c0002t0004g0180a0001c0002t0004g0255others(28): Show | 31 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.1621+1852T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102921953 | ||||||
| chr10:102922104
|
A | G | 4 | a0001c0002t0004g0262a0001c0002t0004g0263a0001c0002t0004g0264others(1): Show | 4 | HG02258.hp1 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1621+2003A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102922104 | ||||||
| chr10:102922204
|
G | A | 1 | a0001c0001t0084g0016 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1621+2103G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102922204 | ||||||
| chr10:102922328
|
A | AT | 70 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(67): Show | 70 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.1621+2237dupT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102922328 | |||||
| chr10:102922328
|
A | ATT | 31 | a0001c0002t0004g0176a0001c0002t0004g0180a0001c0002t0004g0255others(28): Show | 31 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.1621+2236_1621+223 others(6): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102922328 | |||||
| chr10:102922391
|
T | C | 33 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(30): Show | 33 | HG00609.hp1 HG00621.hp2 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.1621+2290T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102922391 | ||||||
| chr10:102922600
|
T | C | 155 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0001t0043g0123others(152): Show | 155 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(152): Show |
intron_variant | MODIFIER | c.1621+2499T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102922600 | ||||||
| chr10:102922783
|
A | G | 4 | a0001c0002t0006g0221a0001c0002t0015g0220a0001c0002t0068g0219others(1): Show | 4 | HG02735.hp2 HG03831.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1621+2682A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102922783 | ||||||
| chr10:102922845
|
G | A | 54 | a0001c0001t0043g0123a0001c0003t0001g0118a0001c0003t0001g0122others(51): Show | 54 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(51): Show |
intron_variant | MODIFIER | c.1621+2744G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102922845 | ||||||
| chr10:102922937
|
C | CA | 68 | a0001c0001t0008g0017a0001c0001t0008g0250a0001c0001t0008g0252others(65): Show | 68 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.1621+2854dupA | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102922937 | |||||
| chr10:102922985
|
C | A | 3 | a0001c0006t0004g0175a0001c0006t0013g0173a0001c0006t0013g0174 | 3 | HG01169.hp2 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1621+2884C>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102922985 | ||||||
| chr10:102923154
|
G | A | 1 | a0001c0003t0001g0118 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1621+3053G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102923154 | ||||||
| chr10:102923688
|
T | C | 1 | a0001c0001t0014g0018 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1621+3587T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102923688 | ||||||
| chr10:102923929
|
A | G | 13 | a0001c0001t0005g0002a0001c0001t0005g0003a0001c0001t0005g0004others(10): Show | 13 | HG01081.hp2 HG01884.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1621+3828A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102923929 | ||||||
| chr10:102924070
|
G | A | 1 | a0001c0001t0002g0019 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1621+3969G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102924070 | ||||||
| chr10:102924635
|
T | A | 153 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0001t0043g0123others(150): Show | 153 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(150): Show |
intron_variant | MODIFIER | c.1621+4534T>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102924635 | ||||||
| chr10:102924787
|
G | A | 54 | a0001c0001t0043g0123a0001c0003t0001g0118a0001c0003t0001g0122others(51): Show | 54 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(51): Show |
intron_variant | MODIFIER | c.1621+4686G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102924787 | ||||||
| chr10:102925103
|
C | G | 1 | a0001c0002t0065g0116 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1621+5002C>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102925103 | ||||||
| chr10:102925153
|
G | A | 1 | a0001c0002t0003g0223 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1621+5052G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102925153 | ||||||
| chr10:102925188
|
C | T | 9 | a0001c0005t0022g0186a0001c0005t0023g0189a0001c0005t0023g0190others(6): Show | 9 | HG02135.hp2 HG03834.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1621+5087C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102925188 | ||||||
| chr10:102925191
|
G | A | 4 | a0001c0001t0005g0021a0001c0001t0005g0022a0001c0001t0012g0020others(1): Show | 4 | HG01109.hp2 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1621+5090G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102925191 | ||||||
| chr10:102925283
|
C | T | 1 | a0001c0001t0014g0018 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1621+5182C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102925283 | ||||||
| chr10:102925296
|
C | CA | 57 | a0001c0001t0002g0028a0001c0001t0005g0002a0001c0001t0005g0003others(54): Show | 57 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.1621+5225dupA | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102925296 | |||||
| chr10:102925296
|
C | CAA | 26 | a0001c0001t0042g0023a0001c0001t0042g0024a0001c0001t0073g0025others(23): Show | 26 | HG00733.hp1 HG00735.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.1621+5224_1621+522 others(6): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102925296 | |||||
| chr10:102925296
|
C | CAAAAAA | 16 | a0001c0002t0054g0193a0001c0003t0001g0153a0001c0003t0001g0155others(13): Show | 16 | HG00099.hp2 HG01167.hp2 HG02155.hp2 others(13): Show |
intron_variant | MODIFIER | c.1621+5220_1621+522 others(10): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102925296 | |||||
| chr10:102925296
|
C | CAAAAAAA | 11 | a0001c0003t0001g0118a0001c0003t0001g0141a0001c0003t0001g0142others(8): Show | 11 | HG00544.hp2 HG01934.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.1621+5219_1621+522 others(11): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102925296 | |||||
| chr10:102925296
|
C | CAAAAAAA others(1): Show |
11 | a0001c0003t0001g0133a0001c0003t0001g0140a0001c0003t0007g0130others(8): Show | 11 | HG01358.hp2 HG02071.hp2 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.1621+5218_1621+522 others(12): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102925296 | |||||
| chr10:102925296
|
C | CAAAAAAA others(2): Show |
8 | a0001c0003t0001g0124a0001c0003t0001g0127a0001c0003t0001g0170others(5): Show | 8 | HG01978.hp1 HG02074.hp1 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.1621+5217_1621+522 others(13): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102925296 | |||||
| chr10:102925296
|
C | CAAAAAAA others(3): Show |
4 | a0001c0001t0043g0123a0001c0003t0001g0122a0001c0003t0007g0121others(1): Show | 4 | NA18957.hp2 NA19004.hp1 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.1621+5216_1621+522 others(14): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102925296 | |||||
| chr10:102925296
|
C | CAAAAAAA others(4): Show |
2 | a0001c0003t0032g0169a0001c0003t0103g0119 | 2 | NA18990.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1621+5215_1621+522 others(15): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102925296 | |||||
| chr10:102925296
|
CA | C | 7 | a0001c0001t0002g0019a0001c0001t0021g0109a0001c0001t0034g0112others(4): Show | 7 | HG01070.hp1 HG01169.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.1621+5225delA | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102925296 | |||||
| chr10:102925296
|
CAAAAAAA others(3): Show |
C | 5 | a0001c0002t0026g0267a0001c0002t0026g0269a0001c0002t0027g0268others(2): Show | 5 | HG01884.hp2 HG02145.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1621+5216_1621+522 others(14): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102925296 | |||||
| chr10:102925346
|
A | G | 70 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(67): Show | 70 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.1621+5245A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102925346 | ||||||
| chr10:102925351
|
A | C | 13 | a0002c0004t0003g0201a0002c0004t0025g0195a0002c0004t0025g0199others(10): Show | 13 | HG00733.hp1 HG00735.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1621+5250A>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102925351 | ||||||
| chr10:102925542
|
C | A | 53 | a0001c0001t0043g0123a0001c0003t0001g0118a0001c0003t0001g0122others(50): Show | 53 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(50): Show |
intron_variant | MODIFIER | c.1621+5441C>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102925542 | ||||||
| chr10:102925736
|
G | C | 101 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(98): Show | 101 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.1621+5635G>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102925736 | ||||||
| chr10:102925780
|
A | C | 70 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(67): Show | 70 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.1621+5679A>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102925780 | ||||||
| chr10:102926506
|
A | G | 1 | a0001c0003t0010g0150 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1621+6405A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102926506 | ||||||
| chr10:102926644
|
C | T | 9 | a0001c0005t0022g0186a0001c0005t0023g0189a0001c0005t0023g0190others(6): Show | 9 | HG02135.hp2 HG03834.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1621+6543C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102926644 | ||||||
| chr10:102926712
|
A | AT | 13 | a0001c0001t0005g0108a0001c0001t0011g0012a0001c0001t0011g0013others(10): Show | 13 | HG01515.hp1 HG02055.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1621+6632dupT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102926712 | |||||
| chr10:102926712
|
A | ATT | 120 | a0001c0001t0008g0250a0001c0001t0043g0123a0001c0002t0002g0245others(117): Show | 120 | HG00099.hp2 HG00544.hp2 HG00597.hp2 others(117): Show |
intron_variant | MODIFIER | c.1621+6631_1621+663 others(6): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102926712 | |||||
| chr10:102926712
|
A | ATTT | 26 | a0001c0001t0008g0252a0001c0002t0003g0227a0001c0002t0006g0117others(23): Show | 26 | HG00408.hp1 HG00609.hp2 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.1621+6630_1621+663 others(7): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102926712 | |||||
| chr10:102926737
|
A | T | 1 | a0001c0001t0040g0105 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1621+6636A>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102926737 | ||||||
| chr10:102926900
|
G | T | 64 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(61): Show | 64 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.1621+6799G>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102926900 | ||||||
| chr10:102926970
|
C | T | 1 | a0001c0002t0003g0251 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1621+6869C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102926970 | ||||||
| chr10:102927124
|
GTAGT | G | 15 | a0001c0001t0012g0041a0001c0001t0014g0018a0001c0001t0014g0042others(12): Show | 15 | HG00408.hp2 HG00642.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1621+7026_1621+702 others(8): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102927124 | |||||
| chr10:102927313
|
A | G | 1 | a0001c0003t0033g0164 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1621+7212A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102927313 | ||||||
| chr10:102927784
|
C | T | 1 | a0001c0003t0001g0149 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1621+7683C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102927784 | ||||||
| chr10:102928025
|
A | G | 2 | a0001c0005t0023g0189a0001c0005t0023g0190 | 2 | NA18945.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.1621+7924A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102928025 | ||||||
| chr10:102928035
|
C | T | 9 | a0001c0005t0022g0186a0001c0005t0023g0189a0001c0005t0023g0190others(6): Show | 9 | HG02135.hp2 HG03834.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1621+7934C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102928035 | ||||||
| chr10:102928281
|
G | A | 1 | a0001c0001t0008g0047 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1621+8180G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102928281 | ||||||
| chr10:102928358
|
G | A | 13 | a0002c0004t0003g0201a0002c0004t0025g0195a0002c0004t0025g0199others(10): Show | 13 | HG00733.hp1 HG00735.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1621+8257G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102928358 | ||||||
| chr10:102928582
|
CA | C | 113 | a0001c0001t0002g0019a0001c0001t0002g0028a0001c0001t0002g0062others(110): Show | 113 | HG00099.hp1 HG00408.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.1621+8498delA | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102928582 | |||||
| chr10:102928700
|
A | G | 1 | a0001c0001t0073g0025 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1621+8599A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102928700 | ||||||
| chr10:102928872
|
A | G | 6 | a0001c0002t0026g0267a0001c0002t0026g0269a0001c0002t0027g0266others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1621+8771A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102928872 | ||||||
| chr10:102929135
|
C | T | 31 | a0001c0002t0004g0176a0001c0002t0004g0180a0001c0002t0004g0255others(28): Show | 31 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.1621+9034C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102929135 | ||||||
| chr10:102929137
|
G | A | 1 | a0001c0002t0062g0222 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1621+9036G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102929137 | ||||||
| chr10:102929189
|
G | T | 11 | a0001c0002t0004g0255a0001c0002t0004g0256a0001c0002t0004g0258others(8): Show | 11 | HG00597.hp2 HG00673.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1621+9088G>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102929189 | ||||||
| chr10:102929440
|
CT | C | 68 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(65): Show | 68 | HG00408.hp1 HG00609.hp1 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.1621+9345delT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102929440 | |||||
| chr10:102929446
|
T | A | 46 | a0001c0001t0008g0017a0001c0001t0020g0026a0001c0001t0020g0027others(43): Show | 46 | HG00558.hp1 HG00597.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.1621+9345T>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102929446 | ||||||
| chr10:102929446
|
TA | T | 15 | a0001c0001t0002g0019a0001c0001t0005g0003a0001c0001t0005g0022others(12): Show | 15 | HG01070.hp1 HG01081.hp1 HG02004.hp1 others(12): Show |
intron_variant | MODIFIER | c.1621+9362delA | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102929446 | |||||
| chr10:102929447
|
A | T | 3 | a0001c0001t0002g0102a0001c0001t0002g0103a0001c0001t0018g0104 | 3 | NA18945.hp1 NA18947.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1621+9346A>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102929447 | ||||||
| chr10:102929479
|
A | G | 9 | a0002c0004t0003g0201a0002c0004t0025g0195a0002c0004t0025g0199others(6): Show | 9 | HG00733.hp1 HG00735.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1621+9378A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102929479 | ||||||
| chr10:102929556
|
T | G | 1 | a0001c0002t0054g0193 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1621+9455T>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102929556 | ||||||
| chr10:102929701
|
C | T | 70 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(67): Show | 70 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.1621+9600C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102929701 | ||||||
| chr10:102929908
|
A | T | 54 | a0001c0001t0043g0123a0001c0003t0001g0118a0001c0003t0001g0122others(51): Show | 54 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(51): Show |
intron_variant | MODIFIER | c.1621+9807A>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102929908 | ||||||
| chr10:102930233
|
A | G | 70 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(67): Show | 70 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.1621+10132A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102930233 | ||||||
| chr10:102930655
|
A | G | 9 | a0001c0005t0022g0186a0001c0005t0023g0189a0001c0005t0023g0190others(6): Show | 9 | HG02135.hp2 HG03834.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1621+10554A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102930655 | ||||||
| chr10:102930981
|
T | TAATG | 5 | a0001c0001t0005g0057a0001c0001t0008g0017a0001c0001t0008g0059others(2): Show | 5 | HG00099.hp1 HG01167.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1621+10882_1621+10 others(10): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102930981 | |||||
| chr10:102931258
|
A | G | 2 | a0001c0001t0008g0250a0001c0001t0008g0252 | 2 | HG01361.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.1621+11157A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102931258 | ||||||
| chr10:102931356
|
CT | C | 109 | a0001c0001t0002g0019a0001c0001t0002g0028a0001c0001t0002g0062others(106): Show | 109 | HG00099.hp1 HG00408.hp2 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.1621+11273delT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102931356 | |||||
| chr10:102931356
|
CTT | C | 157 | a0001c0001t0005g0004a0001c0001t0008g0250a0001c0001t0008g0252others(154): Show | 157 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(154): Show |
intron_variant | MODIFIER | c.1621+11272_1621+11 others(8): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102931356 | |||||
| chr10:102931735
|
T | G | 11 | a0001c0002t0004g0255a0001c0002t0004g0256a0001c0002t0004g0258others(8): Show | 11 | HG00597.hp2 HG00673.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1621+11634T>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102931735 | ||||||
| chr10:102931810
|
A | G | 22 | a0001c0002t0004g0176a0001c0002t0004g0180a0001c0002t0004g0255others(19): Show | 22 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.1621+11709A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102931810 | ||||||
| chr10:102931846
|
T | TA | 18 | a0001c0001t0039g0061a0001c0002t0004g0255a0001c0002t0004g0256others(15): Show | 18 | HG00735.hp2 HG02040.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1621+11765dupA | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102931846 | |||||
| chr10:102931846
|
TA | T | 9 | a0001c0001t0002g0100a0001c0001t0011g0114a0001c0001t0034g0112others(6): Show | 9 | HG00639.hp2 HG02135.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.1621+11765delA | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102931846 | |||||
| chr10:102931975
|
A | T | 101 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(98): Show | 101 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.1621+11874A>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102931975 | ||||||
| chr10:102932080
|
C | T | 13 | a0002c0004t0003g0201a0002c0004t0025g0195a0002c0004t0025g0199others(10): Show | 13 | HG00733.hp1 HG00735.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1621+11979C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102932080 | ||||||
| chr10:102932384
|
G | A | 1 | a0001c0010t0067g0194 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1621+12283G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102932384 | ||||||
| chr10:102932645
|
C | T | 4 | a0001c0002t0004g0262a0001c0002t0004g0263a0001c0002t0004g0264others(1): Show | 4 | HG02258.hp1 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1621+12544C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102932645 | ||||||
| chr10:102932748
|
T | C | 13 | a0002c0004t0003g0201a0002c0004t0025g0195a0002c0004t0025g0199others(10): Show | 13 | HG00733.hp1 HG00735.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1621+12647T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102932748 | ||||||
| chr10:102932785
|
T | C | 155 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0001t0043g0123others(152): Show | 155 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(152): Show |
intron_variant | MODIFIER | c.1621+12684T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102932785 | ||||||
| chr10:102932876
|
C | A | 54 | a0001c0001t0043g0123a0001c0003t0001g0118a0001c0003t0001g0122others(51): Show | 54 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(51): Show |
intron_variant | MODIFIER | c.1621+12775C>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102932876 | ||||||
| chr10:102932916
|
C | CA | 6 | a0001c0001t0008g0017a0001c0001t0074g0034a0001c0001t0096g0052others(3): Show | 6 | HG02922.hp1 HG04184.hp2 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.1621+12837dupA | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102932916 | |||||
| chr10:102932916
|
CA | C | 49 | a0001c0001t0005g0108a0001c0001t0008g0250a0001c0001t0008g0252others(46): Show | 49 | HG00408.hp2 HG00609.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.1621+12837delA | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102932916 | |||||
| chr10:102933228
|
C | T | 1 | a0001c0001t0039g0061 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1621+13127C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102933228 | ||||||
| chr10:102933604
|
T | A | 64 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(61): Show | 64 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.1621+13503T>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102933604 | ||||||
| chr10:102933722
|
G | C | 64 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(61): Show | 64 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.1621+13621G>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102933722 | ||||||
| chr10:102933901
|
C | A | 30 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(27): Show | 30 | HG00609.hp1 HG00621.hp2 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.1621+13800C>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102933901 | ||||||
| chr10:102933910
|
C | A | 2 | a0002c0004t0028g0196a0002c0004t0028g0215 | 2 | HG02622.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1621+13809C>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102933910 | ||||||
| chr10:102934003
|
T | G | 1 | a0001c0001t0084g0016 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1621+13902T>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102934003 | ||||||
| chr10:102934007
|
CT | C | 151 | a0001c0001t0005g0108a0001c0001t0008g0250a0001c0001t0008g0252others(148): Show | 151 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(148): Show |
intron_variant | MODIFIER | c.1621+13923delT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102934007 | |||||
| chr10:102934160
|
G | A | 155 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0001t0043g0123others(152): Show | 155 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(152): Show |
intron_variant | MODIFIER | c.1621+14059G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102934160 | ||||||
| chr10:102934275
|
C | CT | 67 | a0001c0001t0005g0004a0001c0001t0008g0047a0001c0001t0008g0250others(64): Show | 67 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.1621+14177dupT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102934275 | |||||
| chr10:102934275
|
C | CTT | 3 | a0001c0002t0002g0245a0001c0002t0009g0246a0001c0002t0015g0220 | 3 | HG02056.hp1 HG04184.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.1621+14176_1621+14 others(8): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102934275 | |||||
| chr10:102934278
|
TC | T | 4 | a0001c0001t0005g0108a0001c0002t0062g0222a0001c0003t0007g0121others(1): Show | 4 | HG02647.hp2 NA18939.hp2 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.1621+14178delC | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102934278 | ||||||
| chr10:102934279
|
C | T | 232 | a0001c0001t0005g0002a0001c0001t0005g0003a0001c0001t0005g0004others(229): Show | 232 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.1621+14178C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102934279 | ||||||
| chr10:102934365
|
C | T | 1 | a0001c0001t0011g0114 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1621+14264C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102934365 | ||||||
| chr10:102934413
|
T | G | 1 | a0001c0002t0029g0204 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1621+14312T>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102934413 | ||||||
| chr10:102934529
|
C | T | 101 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(98): Show | 101 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.1621+14428C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102934529 | ||||||
| chr10:102934704
|
T | A | 1 | a0001c0002t0004g0263 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1621+14603T>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102934704 | ||||||
| chr10:102934897
|
G | A | 54 | a0001c0001t0043g0123a0001c0003t0001g0118a0001c0003t0001g0122others(51): Show | 54 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(51): Show |
intron_variant | MODIFIER | c.1621+14796G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102934897 | ||||||
| chr10:102935158
|
C | CA | 15 | a0001c0001t0002g0028a0001c0001t0002g0062a0001c0001t0002g0064others(12): Show | 15 | HG00621.hp1 HG01358.hp1 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.1621+15081dupA | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102935158 | |||||
| chr10:102935158
|
CA | C | 40 | a0001c0001t0002g0019a0001c0001t0002g0100a0001c0001t0005g0010others(37): Show | 40 | HG00639.hp1 HG00673.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.1621+15081delA | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102935158 | |||||
| chr10:102935158
|
CAA | C | 51 | a0001c0001t0043g0123a0001c0003t0001g0118a0001c0003t0001g0122others(48): Show | 51 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(48): Show |
intron_variant | MODIFIER | c.1621+15080_1621+15 others(8): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102935158 | |||||
| chr10:102935158
|
CAAAAAAA others(3): Show |
C | 69 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(66): Show | 69 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.1621+15072_1621+15 others(16): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102935158 | |||||
| chr10:102935158
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0002t0009g0244 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1621+15071_1621+15 others(17): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102935158 | |||||
| chr10:102935218
|
C | A | 1 | a0001c0002t0002g0245 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1621+15117C>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102935218 | ||||||
| chr10:102935218
|
C | T | 1 | a0001c0001t0011g0011 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1621+15117C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102935218 | ||||||
| chr10:102935316
|
A | T | 1 | a0001c0002t0004g0176 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1621+15215A>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102935316 | ||||||
| chr10:102935438
|
G | A | 33 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(30): Show | 33 | HG00609.hp1 HG00621.hp2 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.1621+15337G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102935438 | ||||||
| chr10:102935587
|
A | G | 1 | a0001c0003t0033g0164 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1621+15486A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102935587 | ||||||
| chr10:102935604
|
A | AT | 20 | a0001c0002t0004g0176a0001c0002t0004g0180a0001c0002t0004g0256others(17): Show | 20 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.1621+15503_1621+15 others(7): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102935604 | ||||||
| chr10:102935604
|
A | T | 1 | a0001c0005t0022g0186 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1621+15503A>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102935604 | ||||||
| chr10:102935605
|
A | AT | 112 | a0001c0001t0002g0065a0001c0001t0008g0250a0001c0001t0008g0252others(109): Show | 112 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.1621+15523dupT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102935605 | |||||
| chr10:102935605
|
A | T | 31 | a0001c0002t0004g0176a0001c0002t0004g0180a0001c0002t0004g0255others(28): Show | 31 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.1621+15504A>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102935605 | ||||||
| chr10:102935774
|
C | CT | 18 | a0001c0001t0002g0065a0001c0001t0002g0078a0001c0001t0005g0077others(15): Show | 18 | HG00738.hp2 HG01952.hp2 HG01978.hp2 others(15): Show |
intron_variant | MODIFIER | c.1621+15697dupT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102935774 | |||||
| chr10:102935774
|
CT | C | 77 | a0001c0001t0008g0250a0001c0002t0002g0245a0001c0002t0003g0223others(74): Show | 77 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.1621+15697delT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102935774 | |||||
| chr10:102935774
|
CTT | C | 20 | a0001c0002t0004g0176a0001c0002t0004g0180a0001c0002t0004g0255others(17): Show | 20 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.1621+15696_1621+15 others(8): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102935774 | |||||
| chr10:102935933
|
T | A | 1 | a0002c0004t0055g0216 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1621+15832T>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102935933 | ||||||
| chr10:102935942
|
T | G | 10 | a0001c0002t0004g0180a0001c0002t0024g0172a0001c0002t0024g0181others(7): Show | 10 | HG00639.hp1 HG00738.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.1621+15841T>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102935942 | ||||||
| chr10:102936067
|
C | T | 4 | a0001c0001t0005g0021a0001c0001t0005g0022a0001c0001t0012g0020others(1): Show | 4 | HG01109.hp2 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1621+15966C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102936067 | ||||||
| chr10:102936469
|
A | G | 1 | a0001c0002t0052g0260 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1621+16368A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102936469 | ||||||
| chr10:102936517
|
C | CT | 8 | a0001c0001t0005g0002a0001c0001t0005g0003a0001c0001t0005g0006others(5): Show | 8 | HG01081.hp2 HG01884.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1621+16432dupT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102936517 | |||||
| chr10:102936517
|
CT | C | 154 | a0001c0001t0002g0066a0001c0001t0008g0250a0001c0001t0008g0252others(151): Show | 154 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(151): Show |
intron_variant | MODIFIER | c.1621+16432delT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102936517 | |||||
| chr10:102936622
|
T | C | 101 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(98): Show | 101 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.1621+16521T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102936622 | ||||||
| chr10:102936967
|
A | G | 1 | a0001c0001t0043g0123 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1621+16866A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102936967 | ||||||
| chr10:102937233
|
ATGATAGC others(2): Show |
A | 54 | a0001c0001t0043g0123a0001c0003t0001g0118a0001c0003t0001g0122others(51): Show | 54 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(51): Show |
intron_variant | MODIFIER | c.1621+17137_1621+17 others(15): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102937233 | |||||
| chr10:102937371
|
CA | C | 99 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(96): Show | 99 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(96): Show |
intron_variant | MODIFIER | c.1621+17283delA | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102937371 | |||||
| chr10:102937612
|
A | G | 9 | a0001c0005t0022g0186a0001c0005t0023g0189a0001c0005t0023g0190others(6): Show | 9 | HG02135.hp2 HG03834.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1621+17511A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102937612 | ||||||
| chr10:102937758
|
C | T | 1 | a0002c0004t0066g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1621+17657C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102937758 | ||||||
| chr10:102937759
|
G | A | 54 | a0001c0001t0043g0123a0001c0003t0001g0118a0001c0003t0001g0122others(51): Show | 54 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(51): Show |
intron_variant | MODIFIER | c.1621+17658G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102937759 | ||||||
| chr10:102937786
|
CT | C | 154 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0001t0043g0123others(151): Show | 154 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(151): Show |
intron_variant | MODIFIER | c.1621+17695delT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102937786 | |||||
| chr10:102937932
|
C | T | 1 | a0001c0002t0106g0228 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1621+17831C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102937932 | ||||||
| chr10:102937950
|
G | A | 50 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(47): Show | 50 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.1621+17849G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102937950 | ||||||
| chr10:102938024
|
C | T | 85 | a0001c0001t0043g0123a0001c0002t0004g0176a0001c0002t0004g0180others(82): Show | 85 | HG00099.hp2 HG00544.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.1621+17923C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102938024 | ||||||
| chr10:102938172
|
G | A | 102 | a0001c0001t0005g0003a0001c0001t0008g0250a0001c0001t0008g0252others(99): Show | 102 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.1621+18071G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102938172 | ||||||
| chr10:102938202
|
G | A | 1 | a0001c0003t0001g0171 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1621+18101G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102938202 | ||||||
| chr10:102938273
|
T | TA | 81 | a0001c0001t0043g0123a0001c0002t0004g0176a0001c0002t0004g0180others(78): Show | 81 | HG00099.hp2 HG00544.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.1621+18185dupA | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102938273 | |||||
| chr10:102938451
|
G | GA | 9 | a0001c0005t0022g0186a0001c0005t0023g0189a0001c0005t0023g0190others(6): Show | 9 | HG02135.hp2 HG03834.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1621+18350_1621+18 others(7): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102938451 | ||||||
| chr10:102938452
|
G | A | 101 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(98): Show | 101 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.1621+18351G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102938452 | ||||||
| chr10:102938619
|
CA | C | 60 | a0001c0001t0008g0017a0001c0001t0012g0080a0001c0001t0074g0034others(57): Show | 60 | HG00099.hp2 HG00544.hp1 HG00673.hp2 others(57): Show |
intron_variant | MODIFIER | c.1621+18543delA | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102938619 | |||||
| chr10:102938619
|
CAA | C | 114 | a0001c0001t0005g0002a0001c0001t0005g0003a0001c0001t0005g0004others(111): Show | 114 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.1621+18542_1621+18 others(8): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102938619 | |||||
| chr10:102938619
|
CAAA | C | 53 | a0001c0002t0003g0253a0001c0002t0004g0176a0001c0002t0004g0180others(50): Show | 53 | HG00408.hp1 HG00597.hp2 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.1621+18541_1621+18 others(9): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102938619 | |||||
| chr10:102938760
|
T | G | 2 | a0001c0001t0040g0035a0001c0001t0087g0036 | 2 | HG02486.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1621+18659T>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102938760 | ||||||
| chr10:102938766
|
G | A | 155 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0001t0043g0123others(152): Show | 155 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(152): Show |
intron_variant | MODIFIER | c.1621+18665G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102938766 | ||||||
| chr10:102938814
|
G | A | 6 | a0001c0003t0010g0137a0001c0003t0010g0148a0001c0003t0010g0150others(3): Show | 6 | HG01167.hp2 HG02735.hp1 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.1621+18713G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102938814 | ||||||
| chr10:102939221
|
T | C | 31 | a0001c0002t0004g0176a0001c0002t0004g0180a0001c0002t0004g0255others(28): Show | 31 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.1621+19120T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102939221 | ||||||
| chr10:102939344
|
C | T | 1 | a0001c0001t0045g0030 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1621+19243C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102939344 | ||||||
| chr10:102939714
|
C | T | 1 | a0001c0001t0097g0014 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1621+19613C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102939714 | ||||||
| chr10:102939794
|
A | T | 1 | a0001c0005t0046g0188 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1621+19693A>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102939794 | ||||||
| chr10:102939949
|
C | G | 2 | a0001c0002t0024g0172a0001c0002t0024g0181 | 2 | HG01952.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1621+19848C>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102939949 | ||||||
| chr10:102940000
|
C | A | 14 | a0001c0001t0043g0123a0001c0003t0001g0127a0001c0003t0001g0133others(11): Show | 14 | HG01978.hp1 HG02071.hp2 HG02074.hp1 others(11): Show |
intron_variant | MODIFIER | c.1621+19899C>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102940000 | ||||||
| chr10:102940000
|
C | CAACAACA others(2): Show |
97 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(94): Show | 97 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.1621+19901_1621+19 others(15): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102940000 | |||||
| chr10:102940000
|
C | CAACAACA others(5): Show |
1 | a0001c0006t0004g0178 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1621+19901_1621+19 others(18): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102940000 | |||||
| chr10:102940003
|
A | C | 170 | a0001c0001t0005g0002a0001c0001t0005g0003a0001c0001t0005g0004others(167): Show | 170 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.1621+19902A>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102940003 | ||||||
| chr10:102940006
|
A | C | 1 | a0001c0001t0040g0105 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1621+19905A>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102940006 | ||||||
| chr10:102940052
|
C | T | 1 | a0002c0004t0055g0216 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1621+19951C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102940052 | ||||||
| chr10:102940338
|
C | T | 1 | a0001c0001t0030g0044 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1621+20237C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102940338 | ||||||
| chr10:102940505
|
G | A | 1 | a0001c0002t0004g0264 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1621+20404G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102940505 | ||||||
| chr10:102940511
|
CG | C | 70 | a0001c0001t0005g0002a0001c0001t0005g0003a0001c0001t0005g0004others(67): Show | 70 | HG00099.hp1 HG00408.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.1621+20413delG | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102940511 | |||||
| chr10:102940575
|
T | C | 2 | a0001c0001t0008g0250a0001c0001t0008g0252 | 2 | HG01361.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.1621+20474T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102940575 | ||||||
| chr10:102940608
|
C | T | 2 | a0001c0001t0008g0250a0001c0001t0008g0252 | 2 | HG01361.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.1621+20507C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102940608 | ||||||
| chr10:102940609
|
A | G | 2 | a0001c0001t0008g0250a0001c0001t0008g0252 | 2 | HG01361.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.1621+20508A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102940609 | ||||||
| chr10:102940617
|
A | G | 2 | a0001c0001t0008g0250a0001c0001t0008g0252 | 2 | HG01361.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.1621+20516A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102940617 | ||||||
| chr10:102940687
|
G | A | 71 | a0001c0001t0011g0011a0001c0002t0004g0176a0001c0002t0004g0180others(68): Show | 71 | HG00408.hp1 HG00597.hp2 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.1621+20586G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102940687 | ||||||
| chr10:102940790
|
T | C | 9 | a0001c0005t0022g0186a0001c0005t0023g0189a0001c0005t0023g0190others(6): Show | 9 | HG02135.hp2 HG03834.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1621+20689T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102940790 | ||||||
| chr10:102941048
|
G | A | 1 | a0001c0001t0096g0052 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1621+20947G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102941048 | ||||||
| chr10:102941061
|
C | T | 2 | a0001c0001t0040g0035a0001c0001t0087g0036 | 2 | HG02486.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1621+20960C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102941061 | ||||||
| chr10:102941095
|
T | C | 6 | a0001c0002t0026g0267a0001c0002t0026g0269a0001c0002t0027g0266others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1621+20994T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102941095 | ||||||
| chr10:102941130
|
A | G | 1 | a0001c0002t0003g0225 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1621+21029A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102941130 | ||||||
| chr10:102941197
|
C | G | 1 | a0002c0004t0066g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1621+21096C>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102941197 | ||||||
| chr10:102941282
|
T | TTATAA | 154 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0001t0043g0123others(151): Show | 154 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(151): Show |
intron_variant | MODIFIER | c.1621+21183_1621+21 others(11): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102941282 | |||||
| chr10:102941354
|
C | T | 2 | a0002c0004t0057g0202a0002c0004t0058g0203 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1621+21253C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102941354 | ||||||
| chr10:102941365
|
A | C | 154 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0001t0043g0123others(151): Show | 154 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(151): Show |
intron_variant | MODIFIER | c.1621+21264A>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102941365 | ||||||
| chr10:102941430
|
A | G | 100 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(97): Show | 100 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.1621+21329A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102941430 | ||||||
| chr10:102941442
|
T | TA | 63 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(60): Show | 63 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.1621+21350dupA | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102941442 | |||||
| chr10:102941494
|
T | C | 3 | a0001c0001t0030g0037a0001c0001t0031g0046a0001c0001t0074g0034 | 3 | HG01106.hp1 NA18954.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.1621+21393T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102941494 | ||||||
| chr10:102941558
|
C | G | 1 | a0001c0005t0022g0186 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1621+21457C>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102941558 | ||||||
| chr10:102941570
|
G | T | 3 | a0001c0003t0001g0157a0001c0003t0001g0166a0001c0003t0001g0168 | 3 | HG01943.hp1 HG02004.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.1621+21469G>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102941570 | ||||||
| chr10:102941840
|
G | T | 1 | a0001c0003t0051g0136 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1621+21739G>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102941840 | ||||||
| chr10:102942067
|
T | G | 2 | a0001c0001t0042g0023a0001c0001t0042g0024 | 2 | HG01257.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.1621+21966T>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102942067 | ||||||
| chr10:102942115
|
A | G | 4 | a0002c0004t0003g0201a0002c0004t0057g0202a0002c0004t0058g0203others(1): Show | 4 | HG00733.hp1 HG00735.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1621+22014A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102942115 | ||||||
| chr10:102942293
|
T | A | 154 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0001t0043g0123others(151): Show | 154 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(151): Show |
intron_variant | MODIFIER | c.1621+22192T>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102942293 | ||||||
| chr10:102942417
|
A | G | 1 | a0001c0002t0004g0180 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1621+22316A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102942417 | ||||||
| chr10:102942656
|
A | C | 22 | a0001c0002t0004g0176a0001c0002t0004g0180a0001c0002t0004g0255others(19): Show | 22 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.1621+22555A>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102942656 | ||||||
| chr10:102942897
|
T | C | 3 | a0001c0001t0002g0062a0001c0001t0002g0067a0001c0001t0101g0101 | 3 | HG01071.hp2 HG01081.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.1621+22796T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102942897 | ||||||
| chr10:102942954
|
C | T | 1 | a0001c0002t0054g0193 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1621+22853C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102942954 | ||||||
| chr10:102943179
|
C | T | 1 | a0001c0001t0011g0009 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1621+23078C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102943179 | ||||||
| chr10:102943238
|
A | G | 1 | a0001c0003t0001g0124 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1621+23137A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102943238 | ||||||
| chr10:102943242
|
C | A | 100 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(97): Show | 100 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.1621+23141C>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102943242 | ||||||
| chr10:102943295
|
G | T | 1 | a0002c0004t0055g0216 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1621+23194G>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102943295 | ||||||
| chr10:102943296
|
C | T | 1 | a0001c0001t0005g0008 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1621+23195C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102943296 | ||||||
| chr10:102943355
|
G | T | 1 | a0001c0001t0002g0028 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1621+23254G>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102943355 | ||||||
| chr10:102943429
|
A | C | 1 | a0002c0004t0066g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1621+23328A>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102943429 | ||||||
| chr10:102943503
|
A | T | 9 | a0001c0005t0022g0186a0001c0005t0023g0189a0001c0005t0023g0190others(6): Show | 9 | HG02135.hp2 HG03834.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1621+23402A>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102943503 | ||||||
| chr10:102943525
|
G | A | 1 | a0001c0002t0062g0222 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1621+23424G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102943525 | ||||||
| chr10:102943558
|
G | A | 3 | a0001c0001t0005g0008a0001c0001t0011g0009a0001c0001t0011g0013 | 3 | HG02280.hp2 HG02717.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1621+23457G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102943558 | ||||||
| chr10:102943620
|
C | T | 6 | a0001c0002t0026g0267a0001c0002t0026g0269a0001c0002t0027g0266others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1621+23519C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102943620 | ||||||
| chr10:102944084
|
C | CT | 25 | a0001c0002t0003g0223a0001c0002t0004g0176a0001c0002t0004g0180others(22): Show | 25 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.1621+24000dupT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102944084 | |||||
| chr10:102944197
|
G | GC | 13 | a0002c0004t0003g0201a0002c0004t0025g0195a0002c0004t0025g0199others(10): Show | 13 | HG00733.hp1 HG00735.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1621+24102dupC | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102944197 | |||||
| chr10:102944260
|
A | G | 154 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0001t0043g0123others(151): Show | 154 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(151): Show |
intron_variant | MODIFIER | c.1621+24159A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102944260 | ||||||
| chr10:102944581
|
C | CGT | 64 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0007others(61): Show | 64 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.1621+24515_1621+24 others(8): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102944581 | |||||
| chr10:102944581
|
C | CGTGT | 78 | a0001c0001t0002g0028a0001c0001t0002g0062a0001c0001t0002g0067others(75): Show | 78 | HG00408.hp2 HG00558.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.1621+24513_1621+24 others(10): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102944581 | |||||
| chr10:102944581
|
C | CGTGTGT | 53 | a0001c0001t0002g0019a0001c0001t0002g0064a0001c0001t0002g0065others(50): Show | 53 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.1621+24511_1621+24 others(12): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102944581 | |||||
| chr10:102944581
|
C | CGTGTGTG others(1): Show |
27 | a0001c0001t0002g0103a0001c0001t0043g0076a0001c0001t0073g0025others(24): Show | 27 | HG00639.hp2 HG01099.hp2 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.1621+24509_1621+24 others(14): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102944581 | |||||
| chr10:102944581
|
C | CGTGTGTG others(3): Show |
3 | a0001c0002t0009g0224a0001c0002t0026g0269a0001c0002t0044g0243 | 3 | HG00642.hp2 HG00735.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1621+24507_1621+24 others(16): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102944581 | |||||
| chr10:102944581
|
CGT | C | 7 | a0001c0001t0002g0068a0001c0001t0005g0003a0001c0001t0085g0107others(4): Show | 7 | HG02074.hp2 HG02083.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1621+24515_1621+24 others(8): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102944581 | |||||
| chr10:102944773
|
C | T | 13 | a0001c0001t0020g0026a0001c0001t0020g0027a0001c0001t0020g0054others(10): Show | 13 | HG00558.hp1 HG01257.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.1621+24672C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102944773 | ||||||
| chr10:102944967
|
G | GTTTTGTT | 84 | a0001c0001t0008g0252a0001c0002t0002g0245a0001c0002t0003g0223others(81): Show | 84 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.1621+24878_1621+24 others(13): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102944967 | |||||
| chr10:102944979
|
G | GT | 7 | a0001c0002t0026g0267a0001c0002t0026g0269a0001c0002t0027g0266others(4): Show | 7 | HG01884.hp2 HG02056.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1621+24889dupT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102944979 | |||||
| chr10:102944979
|
G | GTTTTTTG others(1): Show |
9 | a0001c0005t0022g0186a0001c0005t0023g0189a0001c0005t0023g0190others(6): Show | 9 | HG02135.hp2 HG03834.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1621+24884_1621+24 others(14): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102944979 | |||||
| chr10:102945005
|
A | G | 5 | a0001c0001t0012g0087a0001c0001t0018g0091a0001c0001t0035g0079others(2): Show | 5 | HG00738.hp2 HG01070.hp1 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.1621+24904A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102945005 | ||||||
| chr10:102945093
|
C | T | 1 | a0002c0004t0066g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1621+24992C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102945093 | ||||||
| chr10:102945485
|
G | A | 1 | a0001c0001t0035g0079 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1621+25384G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102945485 | ||||||
| chr10:102945655
|
C | T | 63 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(60): Show | 63 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.1621+25554C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102945655 | ||||||
| chr10:102945682
|
C | A | 6 | a0001c0002t0026g0267a0001c0002t0026g0269a0001c0002t0027g0266others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1621+25581C>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102945682 | ||||||
| chr10:102945784
|
C | A | 1 | a0001c0001t0002g0019 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1621+25683C>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102945784 | ||||||
| chr10:102945949
|
C | G | 38 | a0001c0001t0005g0057a0001c0001t0005g0096a0001c0001t0005g0108others(35): Show | 38 | HG00099.hp1 HG00544.hp1 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.1621+25848C>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102945949 | ||||||
| chr10:102945950
|
T | G | 2 | a0001c0003t0033g0135a0001c0003t0079g0134 | 2 | NA18951.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1621+25849T>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102945950 | ||||||
| chr10:102946316
|
G | A | 2 | a0001c0002t0003g0233a0001c0002t0003g0234 | 2 | HG02027.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.1621+26215G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102946316 | ||||||
| chr10:102946590
|
C | A | 5 | a0001c0002t0026g0267a0001c0002t0026g0269a0001c0002t0027g0266others(2): Show | 5 | HG01884.hp2 HG02145.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1621+26489C>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102946590 | ||||||
| chr10:102946763
|
G | A | 101 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(98): Show | 101 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.1621+26662G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102946763 | ||||||
| chr10:102947117
|
C | T | 1 | a0001c0002t0006g0212 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1621+27016C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102947117 | ||||||
| chr10:102947130
|
T | A | 1 | a0001c0002t0054g0193 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1621+27029T>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102947130 | ||||||
| chr10:102947259
|
A | T | 53 | a0001c0001t0043g0123a0001c0003t0001g0118a0001c0003t0001g0122others(50): Show | 53 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(50): Show |
intron_variant | MODIFIER | c.1621+27158A>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102947259 | ||||||
| chr10:102947454
|
GA | G | 155 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0001t0043g0123others(152): Show | 155 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(152): Show |
intron_variant | MODIFIER | c.1621+27361delA | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102947454 | |||||
| chr10:102947780
|
G | A | 155 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0001t0043g0123others(152): Show | 155 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(152): Show |
intron_variant | MODIFIER | c.1621+27679G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102947780 | ||||||
| chr10:102947970
|
G | A | 12 | a0002c0004t0003g0201a0002c0004t0025g0195a0002c0004t0025g0199others(9): Show | 12 | HG00733.hp1 HG00735.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1621+27869G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102947970 | ||||||
| chr10:102947977
|
C | T | 16 | a0001c0002t0006g0117a0001c0002t0006g0208a0001c0002t0006g0209others(13): Show | 16 | HG00408.hp1 HG00609.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.1621+27876C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102947977 | ||||||
| chr10:102948002
|
G | A | 2 | a0002c0004t0060g0197a0002c0004t0061g0198 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1621+27901G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102948002 | ||||||
| chr10:102948273
|
G | A | 6 | a0001c0001t0002g0064a0001c0001t0002g0065a0001c0001t0036g0029others(3): Show | 6 | HG00597.hp1 HG00621.hp1 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.1621+28172G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102948273 | ||||||
| chr10:102948305
|
T | C | 2 | a0002c0004t0028g0196a0002c0004t0028g0215 | 2 | HG02622.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1621+28204T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102948305 | ||||||
| chr10:102948318
|
C | T | 9 | a0001c0005t0022g0186a0001c0005t0023g0189a0001c0005t0023g0190others(6): Show | 9 | HG02135.hp2 HG03834.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1621+28217C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102948318 | ||||||
| chr10:102948494
|
T | C | 155 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0001t0043g0123others(152): Show | 155 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(152): Show |
intron_variant | MODIFIER | c.1621+28393T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102948494 | ||||||
| chr10:102948555
|
A | G | 79 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(76): Show | 79 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.1621+28454A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102948555 | ||||||
| chr10:102948879
|
T | TACTG | 101 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(98): Show | 101 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.1621+28779_1621+28 others(10): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102948879 | |||||
| chr10:102949147
|
G | A | 1 | a0001c0001t0039g0061 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1621+29046G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102949147 | ||||||
| chr10:102949244
|
C | T | 31 | a0001c0002t0004g0176a0001c0002t0004g0180a0001c0002t0004g0255others(28): Show | 31 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.1621+29143C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102949244 | ||||||
| chr10:102949261
|
C | T | 70 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(67): Show | 70 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.1621+29160C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102949261 | ||||||
| chr10:102949268
|
C | T | 1 | a0001c0001t0102g0110 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1621+29167C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102949268 | ||||||
| chr10:102949306
|
G | A | 4 | a0002c0004t0003g0201a0002c0004t0057g0202a0002c0004t0058g0203others(1): Show | 4 | HG00733.hp1 HG00735.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1621+29205G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102949306 | ||||||
| chr10:102949403
|
G | A | 30 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(27): Show | 30 | HG00609.hp1 HG00621.hp2 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.1621+29302G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102949403 | ||||||
| chr10:102949440
|
G | T | 1 | a0001c0001t0031g0046 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1621+29339G>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102949440 | ||||||
| chr10:102949510
|
A | G | 237 | a0001c0001t0005g0002a0001c0001t0005g0003a0001c0001t0005g0004others(234): Show | 237 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.1621+29409A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102949510 | ||||||
| chr10:102949554
|
C | A | 6 | a0001c0002t0026g0267a0001c0002t0026g0269a0001c0002t0027g0266others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1621+29453C>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102949554 | ||||||
| chr10:102949615
|
C | T | 9 | a0001c0005t0022g0186a0001c0005t0023g0189a0001c0005t0023g0190others(6): Show | 9 | HG02135.hp2 HG03834.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1621+29514C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102949615 | ||||||
| chr10:102949650
|
G | T | 1 | a0001c0002t0062g0222 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1621+29549G>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102949650 | ||||||
| chr10:102949653
|
G | A | 2 | a0001c0003t0001g0146a0001c0003t0001g0147 | 2 | NA18992.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1621+29552G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102949653 | ||||||
| chr10:102949789
|
T | C | 1 | a0001c0005t0022g0186 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1621+29688T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102949789 | ||||||
| chr10:102949817
|
A | G | 1 | a0001c0010t0067g0194 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1621+29716A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102949817 | ||||||
| chr10:102950195
|
G | A | 2 | a0001c0001t0021g0053a0001c0001t0021g0109 | 2 | NA18941.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.1621+30094G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102950195 | ||||||
| chr10:102950294
|
G | A | 2 | a0001c0005t0046g0188a0001c0005t0047g0187 | 2 | NA18989.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1621+30193G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102950294 | ||||||
| chr10:102950688
|
A | G | 1 | a0001c0001t0005g0077 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1621+30587A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102950688 | ||||||
| chr10:102950722
|
C | CAGTACAA others(5): Show |
1 | a0001c0003t0001g0159 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1621+30621_1621+30 others(18): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102950722 | ||||||
| chr10:102950723
|
C | G | 1 | a0001c0003t0001g0159 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1621+30622C>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102950723 | ||||||
| chr10:102950725
|
G | C | 1 | a0001c0003t0001g0159 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1621+30624G>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102950725 | ||||||
| chr10:102950953
|
C | G | 22 | a0001c0002t0004g0176a0001c0002t0004g0180a0001c0002t0004g0255others(19): Show | 22 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.1621+30852C>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102950953 | ||||||
| chr10:102950981
|
C | CT | 6 | a0001c0001t0002g0064a0001c0001t0002g0078a0001c0001t0002g0103others(3): Show | 6 | HG00544.hp1 HG00621.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1621+30904dupT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102950981 | |||||
| chr10:102950981
|
CT | C | 88 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0001t0011g0013others(85): Show | 88 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.1621+30904delT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102950981 | |||||
| chr10:102950981
|
CTT | C | 66 | a0001c0001t0043g0123a0001c0002t0003g0223a0001c0002t0006g0208others(63): Show | 66 | HG00099.hp2 HG00544.hp2 HG00733.hp1 others(63): Show |
intron_variant | MODIFIER | c.1621+30903_1621+30 others(8): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102950981 | |||||
| chr10:102950981
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0100g0085 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1621+30893_1621+30 others(18): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102950981 | |||||
| chr10:102951407
|
G | A | 6 | a0001c0002t0026g0267a0001c0002t0026g0269a0001c0002t0027g0266others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1621+31306G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102951407 | ||||||
| chr10:102952059
|
T | G | 1 | a0001c0001t0094g0081 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1621+31958T>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102952059 | ||||||
| chr10:102952183
|
G | A | 101 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(98): Show | 101 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.1621+32082G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102952183 | ||||||
| chr10:102952264
|
A | T | 1 | a0001c0001t0040g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1621+32163A>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102952264 | ||||||
| chr10:102952415
|
T | C | 1 | a0001c0003t0001g0118 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1621+32314T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102952415 | ||||||
| chr10:102952496
|
G | A | 1 | a0003c0008t0002g0075 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1621+32395G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102952496 | ||||||
| chr10:102952512
|
C | T | 1 | a0001c0002t0027g0268 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1621+32411C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102952512 | ||||||
| chr10:102952528
|
C | T | 1 | a0002c0004t0055g0216 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1621+32427C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102952528 | ||||||
| chr10:102952622
|
C | CA | 100 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0001t0038g0015others(97): Show | 100 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.1621+32538dupA | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102952622 | |||||
| chr10:102952622
|
C | CAA | 50 | a0001c0001t0043g0123a0001c0003t0001g0118a0001c0003t0001g0122others(47): Show | 50 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(47): Show |
intron_variant | MODIFIER | c.1621+32537_1621+32 others(8): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102952622 | |||||
| chr10:102952789
|
G | A | 6 | a0001c0002t0026g0267a0001c0002t0026g0269a0001c0002t0027g0266others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1621+32688G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102952789 | ||||||
| chr10:102953242
|
G | A | 1 | a0001c0003t0082g0154 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1621+33141G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102953242 | ||||||
| chr10:102953319
|
C | T | 54 | a0001c0001t0043g0123a0001c0003t0001g0118a0001c0003t0001g0122others(51): Show | 54 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(51): Show |
intron_variant | MODIFIER | c.1621+33218C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102953319 | ||||||
| chr10:102953356
|
A | C | 54 | a0001c0001t0043g0123a0001c0003t0001g0118a0001c0003t0001g0122others(51): Show | 54 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(51): Show |
intron_variant | MODIFIER | c.1621+33255A>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102953356 | ||||||
| chr10:102953405
|
C | T | 54 | a0001c0001t0043g0123a0001c0003t0001g0118a0001c0003t0001g0122others(51): Show | 54 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(51): Show |
intron_variant | MODIFIER | c.1621+33304C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102953405 | ||||||
| chr10:102953493
|
C | T | 1 | a0001c0005t0046g0188 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1621+33392C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102953493 | ||||||
| chr10:102953544
|
G | T | 1 | a0001c0010t0067g0194 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1621+33443G>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102953544 | ||||||
| chr10:102953752
|
G | C | 1 | a0001c0001t0005g0005 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1621+33651G>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102953752 | ||||||
| chr10:102953907
|
A | G | 1 | a0001c0002t0071g0247 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1621+33806A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102953907 | ||||||
| chr10:102954126
|
C | CT | 7 | a0001c0001t0005g0002a0001c0001t0005g0003a0001c0001t0005g0006others(4): Show | 7 | HG01081.hp2 HG01884.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1621+34042dupT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102954126 | |||||
| chr10:102954126
|
CT | C | 24 | a0001c0002t0003g0234a0001c0002t0006g0117a0001c0002t0006g0208others(21): Show | 24 | HG00408.hp1 HG00609.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.1621+34042delT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102954126 | |||||
| chr10:102954126
|
CTT | C | 129 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(126): Show | 129 | HG00099.hp2 HG00544.hp2 HG00597.hp2 others(126): Show |
intron_variant | MODIFIER | c.1621+34041_1621+34 others(8): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102954126 | |||||
| chr10:102954133
|
T | C | 22 | a0001c0002t0004g0176a0001c0002t0004g0180a0001c0002t0004g0255others(19): Show | 22 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.1621+34032T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102954133 | ||||||
| chr10:102954389
|
G | A | 1 | a0001c0003t0051g0136 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1621+34288G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102954389 | ||||||
| chr10:102954572
|
A | G | 1 | a0001c0002t0003g0225 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1621+34471A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102954572 | ||||||
| chr10:102954582
|
G | C | 1 | a0001c0002t0054g0193 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1621+34481G>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102954582 | ||||||
| chr10:102954650
|
C | T | 1 | a0001c0001t0037g0089 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1621+34549C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102954650 | ||||||
| chr10:102954973
|
G | A | 155 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0001t0043g0123others(152): Show | 155 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(152): Show |
intron_variant | MODIFIER | c.1621+34872G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102954973 | ||||||
| chr10:102954989
|
A | G | 1 | a0001c0001t0102g0110 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1621+34888A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102954989 | ||||||
| chr10:102955005
|
C | G | 1 | a0002c0004t0066g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1621+34904C>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102955005 | ||||||
| chr10:102955381
|
G | A | 9 | a0001c0005t0022g0186a0001c0005t0023g0189a0001c0005t0023g0190others(6): Show | 9 | HG02135.hp2 HG03834.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1621+35280G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102955381 | ||||||
| chr10:102955695
|
C | G | 1 | a0001c0006t0004g0182 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1621+35594C>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102955695 | ||||||
| chr10:102955774
|
A | G | 31 | a0001c0002t0004g0176a0001c0002t0004g0180a0001c0002t0004g0255others(28): Show | 31 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.1621+35673A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102955774 | ||||||
| chr10:102956040
|
C | T | 1 | a0001c0006t0004g0178 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1621+35939C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102956040 | ||||||
| chr10:102956236
|
T | C | 101 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(98): Show | 101 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.1621+36135T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102956236 | ||||||
| chr10:102956288
|
C | CA | 54 | a0001c0001t0005g0010a0001c0001t0074g0034a0001c0001t0075g0038others(51): Show | 54 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(51): Show |
intron_variant | MODIFIER | c.1621+36207dupA | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102956288 | |||||
| chr10:102956288
|
C | CAA | 93 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0001t0043g0123others(90): Show | 93 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(90): Show |
intron_variant | MODIFIER | c.1621+36206_1621+36 others(8): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102956288 | |||||
| chr10:102956288
|
C | CAAA | 7 | a0001c0002t0004g0264a0001c0002t0006g0214a0001c0002t0064g0248others(4): Show | 7 | HG00609.hp1 HG00609.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1621+36205_1621+36 others(9): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102956288 | |||||
| chr10:102956372
|
C | T | 4 | a0001c0002t0004g0262a0001c0002t0004g0263a0001c0002t0004g0264others(1): Show | 4 | HG02258.hp1 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1621+36271C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102956372 | ||||||
| chr10:102956424
|
G | A | 1 | a0001c0003t0010g0150 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1621+36323G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102956424 | ||||||
| chr10:102957001
|
T | G | 1 | a0001c0002t0004g0180 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1621+36900T>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102957001 | ||||||
| chr10:102957002
|
A | T | 16 | a0001c0002t0006g0117a0001c0002t0006g0208a0001c0002t0006g0209others(13): Show | 16 | HG00408.hp1 HG00609.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.1621+36901A>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102957002 | ||||||
| chr10:102957014
|
A | T | 22 | a0001c0002t0004g0176a0001c0002t0004g0180a0001c0002t0004g0255others(19): Show | 22 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.1621+36913A>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102957014 | ||||||
| chr10:102957180
|
C | T | 6 | a0001c0002t0026g0267a0001c0002t0026g0269a0001c0002t0027g0266others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1621+37079C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102957180 | ||||||
| chr10:102957300
|
C | T | 4 | a0001c0002t0004g0262a0001c0002t0004g0263a0001c0002t0004g0264others(1): Show | 4 | HG02258.hp1 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1621+37199C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102957300 | ||||||
| chr10:102957804
|
A | G | 1 | a0001c0002t0027g0268 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1621+37703A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102957804 | ||||||
| chr10:102957817
|
G | T | 1 | a0001c0002t0106g0228 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1621+37716G>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102957817 | ||||||
| chr10:102957887
|
G | T | 1 | a0001c0001t0073g0025 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1621+37786G>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102957887 | ||||||
| chr10:102957912
|
G | A | 13 | a0002c0004t0003g0201a0002c0004t0025g0195a0002c0004t0025g0199others(10): Show | 13 | HG00733.hp1 HG00735.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1621+37811G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102957912 | ||||||
| chr10:102958061
|
T | C | 1 | a0001c0002t0009g0246 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1621+37960T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102958061 | ||||||
| chr10:102958097
|
C | T | 1 | a0001c0001t0014g0042 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1621+37996C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102958097 | ||||||
| chr10:102958179
|
G | A | 1 | a0001c0003t0033g0164 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1621+38078G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102958179 | ||||||
| chr10:102958459
|
GT | G | 104 | a0001c0001t0002g0049a0001c0001t0002g0062a0001c0001t0002g0064others(101): Show | 104 | HG00099.hp1 HG00408.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.1621+38388delT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102958459 | |||||
| chr10:102958459
|
GTT | G | 39 | a0001c0001t0005g0022a0001c0001t0005g0057a0001c0001t0008g0250others(36): Show | 39 | HG00408.hp1 HG00609.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.1621+38387_1621+38 others(8): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102958459 | |||||
| chr10:102958459
|
GTTT | G | 64 | a0001c0001t0043g0123a0001c0002t0003g0227a0001c0002t0006g0209others(61): Show | 64 | HG00099.hp2 HG00544.hp2 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.1621+38386_1621+38 others(9): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102958459 | |||||
| chr10:102958459
|
GTTTT | G | 11 | a0001c0002t0006g0221a0001c0002t0054g0193a0001c0002t0062g0222others(8): Show | 11 | HG02135.hp2 HG02647.hp2 HG02735.hp2 others(8): Show |
intron_variant | MODIFIER | c.1621+38385_1621+38 others(10): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102958459 | |||||
| chr10:102958459
|
GTTTTT | G | 5 | a0001c0005t0022g0186a0001c0005t0023g0190a0001c0005t0048g0184others(2): Show | 5 | HG03834.hp1 NA18943.hp2 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.1621+38384_1621+38 others(11): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102958459 | |||||
| chr10:102958459
|
GTTTTTTT others(6): Show |
G | 2 | a0001c0001t0012g0020a0001c0003t0001g0159 | 2 | HG03098.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1621+38376_1621+38 others(19): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102958459 | |||||
| chr10:102958459
|
GTTTTTTT others(9): Show |
G | 2 | a0001c0001t0005g0007a0001c0001t0005g0010 | 2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1621+38373_1621+38 others(22): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102958459 | |||||
| chr10:102958470
|
T | G | 1 | a0001c0001t0097g0014 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1621+38369T>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102958470 | ||||||
| chr10:102958472
|
T | G | 1 | a0001c0001t0020g0027 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1621+38371T>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102958472 | ||||||
| chr10:102958473
|
T | G | 12 | a0001c0001t0020g0026a0001c0001t0020g0054a0001c0001t0021g0053others(9): Show | 12 | HG00558.hp1 HG01257.hp2 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.1621+38372T>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102958473 | ||||||
| chr10:102958547
|
T | A | 2 | a0001c0002t0003g0233a0001c0002t0003g0234 | 2 | HG02027.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.1621+38446T>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102958547 | ||||||
| chr10:102958606
|
G | A | 6 | a0001c0002t0026g0267a0001c0002t0026g0269a0001c0002t0027g0266others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1621+38505G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102958606 | ||||||
| chr10:102959134
|
C | T | 1 | a0002c0004t0066g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1621+39033C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102959134 | ||||||
| chr10:102959172
|
C | T | 1 | a0001c0003t0082g0154 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1621+39071C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102959172 | ||||||
| chr10:102959339
|
G | A | 54 | a0001c0001t0043g0123a0001c0003t0001g0118a0001c0003t0001g0122others(51): Show | 54 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(51): Show |
intron_variant | MODIFIER | c.1621+39238G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102959339 | ||||||
| chr10:102959461
|
A | G | 3 | a0001c0006t0004g0175a0001c0006t0013g0173a0001c0006t0013g0174 | 3 | HG01169.hp2 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1621+39360A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102959461 | ||||||
| chr10:102959533
|
G | A | 10 | a0001c0002t0004g0180a0001c0002t0024g0172a0001c0002t0024g0181others(7): Show | 10 | HG00639.hp1 HG00738.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.1621+39432G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102959533 | ||||||
| chr10:102959621
|
A | G | 155 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0001t0043g0123others(152): Show | 155 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(152): Show |
intron_variant | MODIFIER | c.1621+39520A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102959621 | ||||||
| chr10:102960062
|
A | AAAAT | 11 | a0002c0004t0003g0201a0002c0004t0025g0195a0002c0004t0025g0199others(8): Show | 11 | HG00733.hp1 HG00735.hp1 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1621+39985_1621+39 others(10): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102960062 | |||||
| chr10:102960066
|
T | A | 1 | a0001c0010t0067g0194 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1621+39965T>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102960066 | ||||||
| chr10:102960210
|
C | T | 6 | a0001c0002t0026g0267a0001c0002t0026g0269a0001c0002t0027g0266others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1621+40109C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102960210 | ||||||
| chr10:102960724
|
A | G | 2 | a0001c0002t0003g0232a0001c0002t0009g0246 | 2 | NA18950.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1621+40623A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102960724 | ||||||
| chr10:102960783
|
C | CT | 9 | a0001c0001t0005g0002a0001c0001t0008g0047a0001c0001t0037g0088others(6): Show | 9 | HG01258.hp2 HG02027.hp1 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.1621+40703dupT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102960783 | |||||
| chr10:102960783
|
CT | C | 81 | a0001c0001t0014g0042a0001c0001t0021g0053a0001c0001t0043g0123others(78): Show | 81 | HG00099.hp2 HG00544.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.1621+40703delT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102960783 | |||||
| chr10:102960857
|
C | T | 1 | a0001c0002t0004g0265 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1621+40756C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102960857 | ||||||
| chr10:102960897
|
G | GT | 52 | a0001c0001t0005g0057a0001c0001t0005g0077a0001c0001t0005g0096others(49): Show | 52 | HG00099.hp1 HG00408.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.1621+40809dupT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102960897 | |||||
| chr10:102961077
|
C | T | 1 | a0001c0001t0012g0097 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1621+40976C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102961077 | ||||||
| chr10:102961158
|
G | A | 1 | a0001c0001t0012g0080 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1621+41057G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102961158 | ||||||
| chr10:102961274
|
A | G | 2 | a0001c0001t0002g0100a0001c0001t0036g0099 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1621+41173A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102961274 | ||||||
| chr10:102961287
|
C | T | 6 | a0001c0002t0026g0267a0001c0002t0026g0269a0001c0002t0027g0266others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1621+41186C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102961287 | ||||||
| chr10:102961369
|
A | T | 54 | a0001c0001t0043g0123a0001c0003t0001g0118a0001c0003t0001g0122others(51): Show | 54 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(51): Show |
intron_variant | MODIFIER | c.1621+41268A>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102961369 | ||||||
| chr10:102961850
|
C | T | 2 | a0001c0007t0007g0129a0001c0007t0078g0132 | 2 | HG02074.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.1621+41749C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102961850 | ||||||
| chr10:102961914
|
TATTAA | T | 53 | a0001c0001t0043g0123a0001c0003t0001g0118a0001c0003t0001g0122others(50): Show | 53 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(50): Show |
intron_variant | MODIFIER | c.1621+41815_1621+41 others(11): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102961914 | |||||
| chr10:102961915
|
A | C | 1 | a0001c0002t0063g0270 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1621+41814A>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102961915 | ||||||
| chr10:102961964
|
CTT | C | 31 | a0001c0002t0004g0176a0001c0002t0004g0180a0001c0002t0004g0255others(28): Show | 31 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.1621+41864_1621+41 others(8): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102961964 | ||||||
| chr10:102961968
|
T | C | 10 | a0001c0003t0007g0121a0001c0003t0007g0125a0001c0003t0007g0126others(7): Show | 10 | HG01978.hp1 HG02071.hp2 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.1621+41867T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102961968 | ||||||
| chr10:102962205
|
G | C | 54 | a0001c0001t0043g0123a0001c0003t0001g0118a0001c0003t0001g0122others(51): Show | 54 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(51): Show |
intron_variant | MODIFIER | c.1621+42104G>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102962205 | ||||||
| chr10:102962240
|
G | C | 4 | a0001c0001t0005g0021a0001c0001t0005g0022a0001c0001t0012g0020others(1): Show | 4 | HG01109.hp2 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1621+42139G>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102962240 | ||||||
| chr10:102962690
|
C | CTG | 64 | a0001c0001t0005g0003a0001c0001t0005g0007a0001c0001t0005g0010others(61): Show | 64 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.1621+42629_1621+42 others(8): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102962690 | |||||
| chr10:102962690
|
C | CTGTG | 19 | a0001c0001t0005g0005a0001c0001t0008g0017a0001c0001t0008g0047others(16): Show | 19 | HG00642.hp1 HG01106.hp1 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.1621+42627_1621+42 others(10): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102962690 | |||||
| chr10:102962690
|
C | CTGTGTG | 6 | a0001c0001t0005g0002a0001c0001t0031g0046a0001c0001t0038g0015others(3): Show | 6 | HG00558.hp1 HG02004.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1621+42625_1621+42 others(12): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102962690 | |||||
| chr10:102962690
|
C | CTGTGTGT others(1): Show |
16 | a0001c0001t0005g0004a0001c0001t0020g0026a0001c0001t0020g0027others(13): Show | 16 | HG01257.hp2 HG01361.hp2 HG01934.hp2 others(13): Show |
intron_variant | MODIFIER | c.1621+42623_1621+42 others(14): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102962690 | |||||
| chr10:102962690
|
C | CTGTGTGT others(3): Show |
2 | a0001c0001t0043g0123a0001c0003t0001g0118 | 2 | HG03834.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1621+42621_1621+42 others(16): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102962690 | |||||
| chr10:102962690
|
CTG | C | 56 | a0001c0001t0002g0078a0001c0001t0008g0250a0001c0001t0008g0252others(53): Show | 56 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.1621+42629_1621+42 others(8): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102962690 | |||||
| chr10:102962690
|
CTGTG | C | 12 | a0001c0002t0002g0245a0001c0002t0004g0176a0001c0002t0004g0262others(9): Show | 12 | HG00609.hp2 HG00733.hp1 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.1621+42627_1621+42 others(10): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102962690 | |||||
| chr10:102962690
|
CTGTGTG | C | 13 | a0001c0002t0003g0223a0001c0002t0004g0263a0001c0002t0004g0264others(10): Show | 13 | HG01099.hp2 HG01109.hp1 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.1621+42625_1621+42 others(12): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102962690 | |||||
| chr10:102962690
|
CTGTGTGT others(1): Show |
C | 22 | a0001c0001t0005g0096a0001c0001t0012g0097a0001c0001t0038g0095others(19): Show | 22 | HG00639.hp1 HG00738.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.1621+42623_1621+42 others(14): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102962690 | |||||
| chr10:102962690
|
CTGTGTGT others(3): Show |
C | 6 | a0001c0002t0004g0255a0001c0002t0004g0256a0001c0002t0004g0258others(3): Show | 6 | HG03041.hp1 HG03098.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1621+42621_1621+42 others(16): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102962690 | |||||
| chr10:102962690
|
CTGTGTGT others(5): Show |
C | 1 | a0001c0001t0002g0064 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1621+42619_1621+42 others(18): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102962690 | |||||
| chr10:102962690
|
CTGTGTGT others(7): Show |
C | 13 | a0001c0001t0002g0019a0001c0001t0002g0066a0001c0001t0002g0103others(10): Show | 13 | HG00597.hp1 HG01496.hp1 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.1621+42617_1621+42 others(20): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102962690 | |||||
| chr10:102962690
|
CTGTGTGT others(9): Show |
C | 1 | a0001c0001t0002g0065 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1621+42615_1621+42 others(22): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102962690 | |||||
| chr10:102962877
|
A | C | 2 | a0001c0001t0008g0250a0001c0001t0008g0252 | 2 | HG01361.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.1621+42776A>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102962877 | ||||||
| chr10:102963258
|
C | A | 101 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(98): Show | 101 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.1621+43157C>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102963258 | ||||||
| chr10:102963265
|
C | T | 101 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(98): Show | 101 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.1621+43164C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102963265 | ||||||
| chr10:102963334
|
T | C | 64 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(61): Show | 64 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.1621+43233T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102963334 | ||||||
| chr10:102963644
|
C | CT | 64 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(61): Show | 64 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.1621+43552dupT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102963644 | |||||
| chr10:102963863
|
T | C | 54 | a0001c0001t0043g0123a0001c0003t0001g0118a0001c0003t0001g0122others(51): Show | 54 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(51): Show |
intron_variant | MODIFIER | c.1621+43762T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102963863 | ||||||
| chr10:102964235
|
T | G | 2 | a0001c0002t0004g0261a0001c0002t0052g0260 | 2 | HG00597.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.1621+44134T>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102964235 | ||||||
| chr10:102964443
|
G | A | 101 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(98): Show | 101 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.1621+44342G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102964443 | ||||||
| chr10:102964445
|
T | C | 2 | a0001c0005t0048g0184a0001c0005t0049g0183 | 2 | NA18943.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.1621+44344T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102964445 | ||||||
| chr10:102964507
|
T | A | 35 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(32): Show | 35 | HG00609.hp1 HG00621.hp2 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.1621+44406T>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102964507 | ||||||
| chr10:102964816
|
A | G | 6 | a0001c0003t0010g0137a0001c0003t0010g0148a0001c0003t0010g0150others(3): Show | 6 | HG01167.hp2 HG02735.hp1 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.1621+44715A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102964816 | ||||||
| chr10:102965055
|
A | G | 1 | a0001c0001t0039g0061 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1621+44954A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102965055 | ||||||
| chr10:102965231
|
T | C | 1 | a0001c0002t0004g0261 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1621+45130T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102965231 | ||||||
| chr10:102965413
|
C | T | 64 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(61): Show | 64 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.1621+45312C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102965413 | ||||||
| chr10:102965624
|
A | T | 1 | a0001c0001t0019g0001 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1621+45523A>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102965624 | ||||||
| chr10:102965714
|
T | A | 13 | a0002c0004t0003g0201a0002c0004t0025g0195a0002c0004t0025g0199others(10): Show | 13 | HG00733.hp1 HG00735.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1621+45613T>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102965714 | ||||||
| chr10:102965898
|
A | G | 1 | a0001c0003t0010g0137 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1621+45797A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102965898 | ||||||
| chr10:102966102
|
G | C | 1 | a0001c0002t0071g0247 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1621+46001G>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102966102 | ||||||
| chr10:102966106
|
T | G | 1 | a0001c0003t0007g0126 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1621+46005T>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102966106 | ||||||
| chr10:102966122
|
A | G | 1 | a0001c0003t0001g0124 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1621+46021A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102966122 | ||||||
| chr10:102966182
|
TCTGGAAT others(7): Show |
T | 6 | a0001c0003t0010g0137a0001c0003t0010g0148a0001c0003t0010g0150others(3): Show | 6 | HG01167.hp2 HG02735.hp1 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.1621+46098_1621+46 others(20): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102966182 | |||||
| chr10:102966220
|
T | C | 1 | a0001c0001t0039g0061 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1621+46119T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102966220 | ||||||
| chr10:102966421
|
G | A | 1 | a0001c0006t0013g0179 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1621+46320G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102966421 | ||||||
| chr10:102966730
|
A | T | 4 | a0001c0002t0003g0229a0001c0002t0003g0236a0001c0002t0003g0237others(1): Show | 4 | HG00621.hp2 HG00673.hp2 NA18941.hp2 others(1): Show |
intron_variant | MODIFIER | c.1621+46629A>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102966730 | ||||||
| chr10:102966731
|
A | G | 5 | a0001c0002t0003g0227a0001c0002t0003g0232a0001c0002t0009g0246others(2): Show | 5 | HG00609.hp1 NA18950.hp2 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.1621+46630A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102966731 | ||||||
| chr10:102966916
|
A | G | 101 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(98): Show | 101 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.1621+46815A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102966916 | ||||||
| chr10:102967032
|
G | A | 2 | a0001c0005t0046g0188a0001c0005t0047g0187 | 2 | NA18989.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1621+46931G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102967032 | ||||||
| chr10:102967434
|
T | C | 1 | a0001c0002t0003g0253 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1621+47333T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102967434 | ||||||
| chr10:102967467
|
A | C | 101 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(98): Show | 101 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.1621+47366A>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102967467 | ||||||
| chr10:102967478
|
C | G | 1 | a0001c0001t0005g0108 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1621+47377C>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102967478 | ||||||
| chr10:102967522
|
A | G | 101 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(98): Show | 101 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.1621+47421A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102967522 | ||||||
| chr10:102967547
|
C | T | 35 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(32): Show | 35 | HG00609.hp1 HG00621.hp2 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.1621+47446C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102967547 | ||||||
| chr10:102967576
|
C | T | 101 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(98): Show | 101 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.1621+47475C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102967576 | ||||||
| chr10:102967642
|
G | A | 2 | a0001c0001t0008g0250a0001c0001t0008g0252 | 2 | HG01361.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.1621+47541G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102967642 | ||||||
| chr10:102967698
|
G | A | 4 | a0001c0002t0004g0255a0001c0002t0004g0256a0001c0002t0004g0258others(1): Show | 4 | HG03041.hp1 HG03098.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1621+47597G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102967698 | ||||||
| chr10:102967767
|
G | T | 31 | a0001c0002t0004g0176a0001c0002t0004g0180a0001c0002t0004g0255others(28): Show | 31 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.1621+47666G>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102967767 | ||||||
| chr10:102967774
|
C | T | 2 | a0001c0002t0044g0230a0001c0002t0044g0243 | 2 | HG00642.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.1621+47673C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102967774 | ||||||
| chr10:102967784
|
G | A | 101 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(98): Show | 101 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.1621+47683G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102967784 | ||||||
| chr10:102967788
|
C | T | 1 | a0001c0002t0009g0224 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1621+47687C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102967788 | ||||||
| chr10:102967970
|
TG | T | 4 | a0001c0002t0026g0267a0001c0002t0026g0269a0001c0002t0027g0266others(1): Show | 4 | HG01884.hp2 HG02145.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1621+47870delG | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102967970 | ||||||
| chr10:102968114
|
AAT | A | 155 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0001t0043g0123others(152): Show | 155 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(152): Show |
intron_variant | MODIFIER | c.1621+48024_1621+48 others(8): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102968114 | |||||
| chr10:102968293
|
CTGGAGTG others(960): Show |
C | 1 | a0001c0003t0001g0143 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1621+48206_1621+49 others(6): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102968293 | |||||
| chr10:102968307
|
C | T | 1 | a0001c0002t0009g0254 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1621+48206C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102968307 | ||||||
| chr10:102968315
|
C | T | 1 | a0001c0005t0050g0191 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1621+48214C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102968315 | ||||||
| chr10:102968407
|
C | T | 101 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(98): Show | 101 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.1621+48306C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102968407 | ||||||
| chr10:102968466
|
C | T | 5 | a0001c0002t0004g0255a0001c0002t0004g0256a0001c0002t0004g0258others(2): Show | 5 | HG03041.hp1 HG03098.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1621+48365C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102968466 | ||||||
| chr10:102968608
|
C | CT | 9 | a0001c0005t0022g0186a0001c0005t0023g0189a0001c0005t0023g0190others(6): Show | 9 | HG02135.hp2 HG03834.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1621+48521dupT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102968608 | |||||
| chr10:102968756
|
C | T | 1 | a0001c0001t0002g0078 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1621+48655C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102968756 | ||||||
| chr10:102968859
|
T | C | 154 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0001t0043g0123others(151): Show | 154 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(151): Show |
intron_variant | MODIFIER | c.1621+48758T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102968859 | ||||||
| chr10:102968872
|
G | A | 266 | a0001c0001t0002g0019a0001c0001t0002g0028a0001c0001t0002g0062others(263): Show | 266 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.1621+48771G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102968872 | ||||||
| chr10:102968902
|
A | G | 1 | a0003c0008t0002g0075 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1621+48801A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102968902 | ||||||
| chr10:102968910
|
C | CT | 36 | a0001c0001t0002g0065a0001c0001t0012g0080a0001c0001t0030g0044others(33): Show | 36 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.1621+48830dupT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102968910 | |||||
| chr10:102968910
|
CT | C | 65 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(62): Show | 65 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.1621+48830delT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102968910 | |||||
| chr10:102968963
|
G | C | 1 | a0001c0002t0004g0261 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1621+48862G>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102968963 | ||||||
| chr10:102969328
|
C | T | 1 | a0001c0001t0043g0123 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1621+49227C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102969328 | ||||||
| chr10:102969492
|
G | A | 54 | a0001c0001t0043g0123a0001c0003t0001g0118a0001c0003t0001g0122others(51): Show | 54 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(51): Show |
intron_variant | MODIFIER | c.1621+49391G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102969492 | ||||||
| chr10:102969519
|
C | T | 4 | a0001c0001t0020g0026a0001c0001t0021g0055a0001c0001t0041g0051others(1): Show | 4 | HG01361.hp2 HG01934.hp2 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.1621+49418C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102969519 | ||||||
| chr10:102969589
|
G | A | 1 | a0001c0002t0062g0222 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1621+49488G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102969589 | ||||||
| chr10:102969658
|
C | T | 155 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0001t0043g0123others(152): Show | 155 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(152): Show |
intron_variant | MODIFIER | c.1621+49557C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102969658 | ||||||
| chr10:102969889
|
C | T | 1 | a0001c0003t0007g0125 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1621+49788C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102969889 | ||||||
| chr10:102970043
|
T | C | 8 | a0001c0002t0006g0117a0001c0002t0006g0208a0001c0002t0006g0209others(5): Show | 8 | HG00408.hp1 HG00609.hp2 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.1621+49942T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102970043 | ||||||
| chr10:102970059
|
G | C | 101 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(98): Show | 101 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.1621+49958G>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102970059 | ||||||
| chr10:102970147
|
G | A | 2 | a0001c0001t0020g0026a0001c0001t0021g0055 | 2 | HG01361.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.1621+50046G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102970147 | ||||||
| chr10:102970193
|
A | T | 1 | a0001c0002t0062g0222 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1621+50092A>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102970193 | ||||||
| chr10:102970239
|
T | C | 155 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0001t0043g0123others(152): Show | 155 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(152): Show |
intron_variant | MODIFIER | c.1621+50138T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102970239 | ||||||
| chr10:102970240
|
G | T | 1 | a0001c0003t0007g0125 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1621+50139G>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102970240 | ||||||
| chr10:102970256
|
C | T | 1 | a0001c0001t0073g0025 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1621+50155C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102970256 | ||||||
| chr10:102970407
|
A | G | 1 | a0001c0001t0076g0040 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1621+50306A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102970407 | ||||||
| chr10:102970813
|
A | G | 1 | a0001c0002t0065g0116 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1621+50712A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102970813 | ||||||
| chr10:102970930
|
C | A | 16 | a0001c0002t0006g0117a0001c0002t0006g0208a0001c0002t0006g0209others(13): Show | 16 | HG00408.hp1 HG00609.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.1621+50829C>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102970930 | ||||||
| chr10:102970948
|
T | G | 1 | a0001c0002t0063g0270 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1621+50847T>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102970948 | ||||||
| chr10:102970980
|
C | G | 13 | a0002c0004t0003g0201a0002c0004t0025g0195a0002c0004t0025g0199others(10): Show | 13 | HG00733.hp1 HG00735.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1621+50879C>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102970980 | ||||||
| chr10:102971027
|
C | CA | 6 | a0001c0001t0002g0065a0001c0001t0005g0003a0001c0001t0093g0031others(3): Show | 6 | HG02027.hp1 HG02055.hp2 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.1621+50940dupA | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102971027 | |||||
| chr10:102971027
|
CA | C | 50 | a0001c0001t0043g0123a0001c0003t0001g0122a0001c0003t0001g0124others(47): Show | 50 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(47): Show |
intron_variant | MODIFIER | c.1621+50940delA | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102971027 | |||||
| chr10:102971233
|
A | G | 1 | a0001c0001t0002g0049 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1621+51132A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102971233 | ||||||
| chr10:102971242
|
G | A | 1 | a0002c0004t0066g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1621+51141G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102971242 | ||||||
| chr10:102971262
|
GA | G | 38 | a0001c0002t0004g0176a0001c0002t0004g0180a0001c0002t0004g0255others(35): Show | 38 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.1621+51173delA | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102971262 | |||||
| chr10:102971356
|
CTA | C | 9 | a0001c0005t0022g0186a0001c0005t0023g0189a0001c0005t0023g0190others(6): Show | 9 | HG02135.hp2 HG03834.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1621+51257_1621+51 others(8): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102971356 | |||||
| chr10:102971551
|
A | G | 1 | a0001c0001t0005g0005 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1621+51450A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102971551 | ||||||
| chr10:102971575
|
T | C | 1 | a0002c0004t0066g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1621+51474T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102971575 | ||||||
| chr10:102971984
|
G | A | 1 | a0001c0003t0001g0147 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1621+51883G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102971984 | ||||||
| chr10:102971996
|
A | G | 1 | a0001c0001t0002g0019 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1621+51895A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102971996 | ||||||
| chr10:102972402
|
C | T | 1 | a0001c0001t0074g0034 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1621+52301C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102972402 | ||||||
| chr10:102972502
|
T | G | 1 | a0001c0002t0004g0176 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1621+52401T>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102972502 | ||||||
| chr10:102972588
|
A | G | 1 | a0001c0003t0001g0159 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1621+52487A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102972588 | ||||||
| chr10:102972979
|
T | C | 1 | a0001c0001t0084g0016 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1621+52878T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102972979 | ||||||
| chr10:102973136
|
G | GT | 19 | a0001c0001t0042g0024a0001c0002t0003g0227a0001c0002t0004g0176others(16): Show | 19 | HG00597.hp2 HG00673.hp1 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.1621+53046dupT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102973136 | |||||
| chr10:102973147
|
T | C | 2 | a0001c0001t0038g0015a0001c0002t0062g0222 | 2 | HG02647.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1621+53046T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102973147 | ||||||
| chr10:102973219
|
A | G | 1 | a0001c0002t0009g0226 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1621+53118A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102973219 | ||||||
| chr10:102973239
|
T | C | 10 | a0001c0002t0004g0180a0001c0002t0024g0172a0001c0002t0024g0181others(7): Show | 10 | HG00639.hp1 HG00738.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.1621+53138T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102973239 | ||||||
| chr10:102973283
|
C | CT | 7 | a0001c0001t0019g0083a0001c0001t0019g0084a0001c0002t0026g0267others(4): Show | 7 | HG01884.hp2 HG02145.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1621+53193dupT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102973283 | |||||
| chr10:102973341
|
A | G | 10 | a0001c0002t0004g0180a0001c0002t0024g0172a0001c0002t0024g0181others(7): Show | 10 | HG00639.hp1 HG00738.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.1621+53240A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102973341 | ||||||
| chr10:102973502
|
C | CTG | 3 | a0001c0001t0014g0018a0001c0001t0014g0042a0001c0001t0014g0045 | 3 | HG01952.hp2 HG01981.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.1621+53417_1621+53 others(8): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102973502 | |||||
| chr10:102973518
|
G | GT | 15 | a0001c0001t0005g0002a0001c0001t0005g0003a0001c0001t0005g0006others(12): Show | 15 | HG01081.hp2 HG01884.hp1 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.1621+53431dupT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102973518 | |||||
| chr10:102973518
|
G | T | 2 | a0001c0001t0042g0023a0001c0001t0042g0024 | 2 | HG01257.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.1621+53417G>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102973518 | ||||||
| chr10:102973518
|
GT | G | 67 | a0001c0001t0043g0123a0001c0002t0006g0117a0001c0002t0006g0208others(64): Show | 67 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.1621+53431delT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102973518 | |||||
| chr10:102973520
|
T | G | 2 | a0001c0001t0011g0114a0002c0004t0028g0215 | 2 | HG02622.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1621+53419T>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102973520 | ||||||
| chr10:102973541
|
C | G | 1 | a0001c0001t0031g0046 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1621+53440C>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102973541 | ||||||
| chr10:102973627
|
G | C | 1 | a0001c0002t0004g0176 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1621+53526G>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102973627 | ||||||
| chr10:102973816
|
TC | T | 220 | a0001c0001t0005g0003a0001c0001t0005g0004a0001c0001t0005g0005others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.1621+53726delC | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102973816 | |||||
| chr10:102973820
|
C | A | 1 | a0001c0001t0039g0061 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1621+53719C>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102973820 | ||||||
| chr10:102974136
|
T | A | 155 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0001t0043g0123others(152): Show | 155 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(152): Show |
intron_variant | MODIFIER | c.1621+54035T>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102974136 | ||||||
| chr10:102974578
|
A | AT | 5 | a0001c0001t0042g0023a0001c0001t0042g0024a0001c0001t0073g0025others(2): Show | 5 | HG01257.hp2 HG01978.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1621+54488dupT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102974578 | |||||
| chr10:102974855
|
T | C | 224 | a0001c0001t0005g0002a0001c0001t0005g0003a0001c0001t0005g0004others(221): Show | 224 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.1621+54754T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102974855 | ||||||
| chr10:102974866
|
A | G | 30 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(27): Show | 30 | HG00609.hp1 HG00621.hp2 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.1621+54765A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102974866 | ||||||
| chr10:102974882
|
G | C | 1 | a0001c0001t0002g0065 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1621+54781G>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102974882 | ||||||
| chr10:102975469
|
G | GA | 110 | a0001c0001t0002g0019a0001c0001t0002g0028a0001c0001t0002g0049others(107): Show | 110 | HG00099.hp1 HG00408.hp2 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.1621+55387dupA | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102975469 | |||||
| chr10:102975469
|
G | GAA | 64 | a0001c0001t0002g0102a0001c0001t0008g0250a0001c0001t0008g0252others(61): Show | 64 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.1621+55386_1621+55 others(8): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102975469 | |||||
| chr10:102975469
|
G | GAAA | 32 | a0001c0002t0003g0229a0001c0002t0003g0240a0001c0002t0004g0176others(29): Show | 32 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.1621+55385_1621+55 others(9): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102975469 | |||||
| chr10:102975479
|
A | AC | 54 | a0001c0001t0043g0123a0001c0003t0001g0118a0001c0003t0001g0122others(51): Show | 54 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(51): Show |
intron_variant | MODIFIER | c.1621+55378_1621+55 others(7): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102975479 | ||||||
| chr10:102975609
|
A | G | 101 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(98): Show | 101 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.1621+55508A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102975609 | ||||||
| chr10:102975648
|
T | C | 6 | a0001c0002t0026g0267a0001c0002t0026g0269a0001c0002t0027g0266others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1621+55547T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102975648 | ||||||
| chr10:102976425
|
C | CT | 25 | a0001c0002t0026g0269a0001c0002t0027g0266a0001c0003t0001g0156others(22): Show | 25 | HG01167.hp2 HG01358.hp2 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.1621+56350dupT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102976425 | |||||
| chr10:102976425
|
C | CTTTTT | 21 | a0001c0002t0002g0245a0001c0002t0003g0223a0001c0002t0003g0225others(18): Show | 21 | HG00609.hp1 HG00639.hp2 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.1621+56346_1621+56 others(11): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102976425 | |||||
| chr10:102976425
|
C | CTTTTTT | 7 | a0001c0001t0008g0252a0001c0002t0003g0227a0001c0002t0003g0231others(4): Show | 7 | HG00621.hp2 HG00735.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.1621+56345_1621+56 others(12): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102976425 | |||||
| chr10:102976425
|
CT | C | 86 | a0001c0001t0002g0019a0001c0001t0002g0028a0001c0001t0002g0064others(83): Show | 86 | HG00408.hp2 HG00597.hp1 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.1621+56350delT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102976425 | |||||
| chr10:102976425
|
CTT | C | 43 | a0001c0001t0005g0021a0001c0001t0005g0022a0001c0001t0005g0057others(40): Show | 43 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.1621+56349_1621+56 others(8): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102976425 | |||||
| chr10:102976425
|
CTTTTTTT others(1): Show |
C | 10 | a0001c0002t0044g0230a0002c0004t0003g0201a0002c0004t0025g0195others(7): Show | 10 | HG00733.hp1 HG00735.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1621+56343_1621+56 others(14): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102976425 | |||||
| chr10:102976425
|
CTTTTTTT others(2): Show |
C | 16 | a0001c0002t0006g0117a0001c0002t0006g0208a0001c0002t0006g0209others(13): Show | 16 | HG00408.hp1 HG00609.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.1621+56342_1621+56 others(15): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102976425 | |||||
| chr10:102976493
|
G | T | 1 | a0001c0001t0002g0028 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1621+56392G>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102976493 | ||||||
| chr10:102976588
|
G | T | 101 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(98): Show | 101 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.1621+56487G>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102976588 | ||||||
| chr10:102976594
|
C | T | 64 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(61): Show | 64 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.1621+56493C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102976594 | ||||||
| chr10:102976611
|
A | AT | 20 | a0001c0001t0002g0062a0001c0001t0005g0021a0001c0001t0012g0020others(17): Show | 20 | HG00408.hp1 HG00558.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.1621+56538dupT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102976611 | |||||
| chr10:102976611
|
A | ATT | 41 | a0001c0001t0002g0078a0001c0001t0005g0003a0001c0001t0005g0004others(38): Show | 41 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.1621+56537_1621+56 others(8): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102976611 | |||||
| chr10:102976611
|
A | ATTT | 20 | a0001c0001t0005g0006a0001c0001t0005g0007a0001c0001t0005g0108others(17): Show | 20 | HG01081.hp2 HG01106.hp1 HG01258.hp2 others(17): Show |
intron_variant | MODIFIER | c.1621+56536_1621+56 others(9): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102976611 | |||||
| chr10:102976611
|
A | ATTTT | 7 | a0001c0001t0005g0002a0001c0001t0005g0008a0001c0001t0011g0009others(4): Show | 7 | HG01884.hp2 HG02135.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1621+56535_1621+56 others(10): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102976611 | |||||
| chr10:102976611
|
A | ATTTTTT | 14 | a0001c0001t0008g0252a0001c0002t0003g0223a0001c0002t0003g0225others(11): Show | 14 | HG00639.hp2 HG00735.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.1621+56533_1621+56 others(12): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102976611 | |||||
| chr10:102976611
|
A | ATTTTTTT | 5 | a0001c0001t0008g0250a0001c0002t0003g0239a0001c0002t0044g0243others(2): Show | 5 | HG00642.hp2 HG01981.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1621+56532_1621+56 others(13): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102976611 | |||||
| chr10:102976611
|
A | ATTTTTTT others(4): Show |
2 | a0002c0004t0028g0196a0002c0004t0028g0215 | 2 | HG02622.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1621+56528_1621+56 others(17): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102976611 | |||||
| chr10:102976611
|
A | ATTTTTTT others(5): Show |
1 | a0001c0002t0054g0193 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1621+56527_1621+56 others(18): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102976611 | |||||
| chr10:102976611
|
A | ATTTTTTT others(7): Show |
1 | a0001c0010t0067g0194 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1621+56525_1621+56 others(20): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102976611 | |||||
| chr10:102976611
|
A | ATTTTTTT others(8): Show |
1 | a0001c0002t0071g0247 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1621+56524_1621+56 others(21): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102976611 | |||||
| chr10:102976611
|
A | ATTTTTTT others(11): Show |
1 | a0002c0004t0055g0216 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1621+56521_1621+56 others(24): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102976611 | |||||
| chr10:102976611
|
A | ATTTTTTT others(12): Show |
1 | a0001c0002t0009g0254 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1621+56520_1621+56 others(25): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102976611 | |||||
| chr10:102976611
|
A | ATTTTTTT others(13): Show |
2 | a0001c0002t0003g0236a0001c0002t0107g0235 | 2 | HG00609.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.1621+56519_1621+56 others(26): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102976611 | |||||
| chr10:102976611
|
A | ATTTTTTT others(14): Show |
2 | a0001c0002t0003g0237a0001c0002t0009g0246 | 2 | NA18950.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.1621+56518_1621+56 others(27): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102976611 | |||||
| chr10:102976611
|
A | ATTTTTTT others(15): Show |
4 | a0001c0002t0002g0245a0001c0002t0003g0229a0001c0002t0003g0232others(1): Show | 4 | HG00673.hp2 HG00735.hp1 HG02056.hp1 others(1): Show |
intron_variant | MODIFIER | c.1621+56517_1621+56 others(28): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102976611 | |||||
| chr10:102976611
|
A | ATTTTTTT others(16): Show |
1 | a0002c0004t0003g0201 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1621+56516_1621+56 others(29): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102976611 | |||||
| chr10:102976611
|
A | ATTTTTTT others(17): Show |
3 | a0001c0002t0003g0233a0002c0004t0060g0197a0002c0004t0061g0198 | 3 | HG02027.hp2 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1621+56515_1621+56 others(30): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102976611 | |||||
| chr10:102976611
|
A | ATTTTTTT others(20): Show |
1 | a0001c0002t0009g0238 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1621+56512_1621+56 others(33): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102976611 | |||||
| chr10:102976611
|
A | ATTTTTTT others(21): Show |
1 | a0001c0002t0003g0227 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1621+56511_1621+56 others(34): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102976611 | |||||
| chr10:102976611
|
AT | A | 7 | a0001c0001t0002g0019a0001c0001t0002g0102a0001c0001t0002g0103others(4): Show | 7 | HG02109.hp1 HG02735.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1621+56538delT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102976611 | |||||
| chr10:102976611
|
ATTTTT | A | 20 | a0001c0002t0003g0251a0001c0002t0004g0176a0001c0002t0004g0180others(17): Show | 20 | HG00639.hp1 HG00738.hp1 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.1621+56534_1621+56 others(11): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102976611 | |||||
| chr10:102976611
|
ATTTTTTT others(3): Show |
A | 2 | a0001c0001t0008g0059a0001c0001t0018g0058 | 2 | HG00099.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1621+56529_1621+56 others(16): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102976611 | |||||
| chr10:102976611
|
ATTTTTTT others(4): Show |
A | 15 | a0001c0003t0010g0137a0001c0003t0032g0169a0001c0005t0022g0186others(12): Show | 15 | HG01109.hp1 HG02055.hp2 HG02074.hp1 others(12): Show |
intron_variant | MODIFIER | c.1621+56528_1621+56 others(17): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102976611 | |||||
| chr10:102976611
|
ATTTTTTT others(5): Show |
A | 51 | a0001c0001t0043g0123a0001c0003t0001g0118a0001c0003t0001g0122others(48): Show | 51 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(48): Show |
intron_variant | MODIFIER | c.1621+56527_1621+56 others(18): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102976611 | |||||
| chr10:102976692
|
T | C | 1 | a0001c0002t0062g0222 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1621+56591T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102976692 | ||||||
| chr10:102976806
|
G | A | 101 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(98): Show | 101 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.1621+56705G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102976806 | ||||||
| chr10:102976942
|
T | C | 101 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(98): Show | 101 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.1621+56841T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102976942 | ||||||
| chr10:102976953
|
T | C | 1 | a0001c0010t0067g0194 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1621+56852T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102976953 | ||||||
| chr10:102976964
|
A | G | 155 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0001t0043g0123others(152): Show | 155 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(152): Show |
intron_variant | MODIFIER | c.1621+56863A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102976964 | ||||||
| chr10:102977098
|
A | G | 6 | a0002c0004t0003g0201a0002c0004t0057g0202a0002c0004t0058g0203others(3): Show | 6 | HG00733.hp1 HG00735.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1621+56997A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102977098 | ||||||
| chr10:102977126
|
C | T | 1 | a0001c0001t0018g0104 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1621+57025C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102977126 | ||||||
| chr10:102977343
|
A | C | 1 | a0001c0002t0013g0257 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1621+57242A>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102977343 | ||||||
| chr10:102977411
|
G | A | 1 | a0001c0001t0008g0047 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1621+57310G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102977411 | ||||||
| chr10:102977647
|
T | C | 155 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0001t0043g0123others(152): Show | 155 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(152): Show |
intron_variant | MODIFIER | c.1621+57546T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102977647 | ||||||
| chr10:102977925
|
G | A | 31 | a0001c0002t0004g0176a0001c0002t0004g0180a0001c0002t0004g0255others(28): Show | 31 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.1621+57824G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102977925 | ||||||
| chr10:102977940
|
T | TG | 54 | a0001c0001t0043g0123a0001c0003t0001g0118a0001c0003t0001g0122others(51): Show | 54 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(51): Show |
intron_variant | MODIFIER | c.1621+57840dupG | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102977940 | |||||
| chr10:102977972
|
T | C | 101 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(98): Show | 101 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.1621+57871T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102977972 | ||||||
| chr10:102978058
|
C | T | 1 | a0001c0001t0012g0080 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1621+57957C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102978058 | ||||||
| chr10:102978067
|
G | A | 4 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0011g0011others(1): Show | 4 | HG02572.hp1 HG02896.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1621+57966G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102978067 | ||||||
| chr10:102978072
|
G | A | 12 | a0001c0002t0004g0176a0001c0002t0004g0255a0001c0002t0004g0256others(9): Show | 12 | HG00597.hp2 HG00673.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1621+57971G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102978072 | ||||||
| chr10:102978208
|
CT | C | 5 | a0001c0001t0002g0066a0001c0001t0035g0111a0001c0002t0009g0254others(2): Show | 5 | HG01496.hp1 HG01516.hp1 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.1621+58123delT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102978208 | |||||
| chr10:102978246
|
C | T | 1 | a0001c0001t0005g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1621+58145C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102978246 | ||||||
| chr10:102978531
|
T | C | 1 | a0001c0003t0001g0162 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1621+58430T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102978531 | ||||||
| chr10:102978892
|
G | A | 1 | a0001c0005t0048g0184 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1621+58791G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102978892 | ||||||
| chr10:102979422
|
T | C | 54 | a0001c0001t0043g0123a0001c0003t0001g0118a0001c0003t0001g0122others(51): Show | 54 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(51): Show |
intron_variant | MODIFIER | c.1621+59321T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102979422 | ||||||
| chr10:102979573
|
G | T | 7 | a0001c0001t0037g0088a0001c0001t0037g0089a0001c0001t0085g0107others(4): Show | 7 | HG00558.hp2 HG02074.hp2 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.1621+59472G>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102979573 | ||||||
| chr10:102979768
|
TTAAAAAT others(3): Show |
T | 1 | a0001c0002t0062g0222 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1621+59676_1621+59 others(16): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102979768 | |||||
| chr10:102979796
|
TA | T | 234 | a0001c0001t0005g0002a0001c0001t0005g0003a0001c0001t0005g0004others(231): Show | 234 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.1621+59697delA | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102979796 | |||||
| chr10:102979876
|
A | C | 1 | a0001c0001t0008g0047 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1621+59775A>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102979876 | ||||||
| chr10:102979920
|
A | AT | 53 | a0001c0001t0011g0009a0001c0001t0011g0013a0001c0001t0043g0123others(50): Show | 53 | HG00099.hp2 HG01167.hp2 HG01358.hp2 others(50): Show |
intron_variant | MODIFIER | c.1621+59830dupT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102979920 | |||||
| chr10:102979923
|
T | TA | 4 | a0001c0003t0001g0124a0001c0003t0032g0120a0001c0003t0032g0169others(1): Show | 4 | NA18962.hp2 NA18990.hp2 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.1621+59822_1621+59 others(7): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102979923 | ||||||
| chr10:102980122
|
GCAGGCTG others(20): Show |
G | 1 | a0001c0001t0042g0024 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1621+60037_1621+60 others(33): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102980122 | |||||
| chr10:102980324
|
G | GT | 8 | a0001c0001t0008g0017a0001c0001t0099g0071a0001c0002t0004g0262others(5): Show | 8 | HG01978.hp1 HG02258.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1621+60236dupT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102980324 | |||||
| chr10:102980453
|
A | G | 111 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0001t0012g0041others(108): Show | 111 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.1621+60352A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102980453 | ||||||
| chr10:102980663
|
T | C | 1 | a0001c0001t0019g0001 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1621+60562T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102980663 | ||||||
| chr10:102980811
|
C | A | 101 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(98): Show | 101 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.1621+60710C>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102980811 | ||||||
| chr10:102980826
|
G | A | 8 | a0001c0002t0006g0117a0001c0002t0006g0208a0001c0002t0006g0209others(5): Show | 8 | HG00408.hp1 HG00609.hp2 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.1621+60725G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102980826 | ||||||
| chr10:102981108
|
G | A | 3 | a0001c0001t0012g0097a0001c0001t0038g0095a0001c0001t0090g0094 | 3 | NA18951.hp1 NA18968.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1621+61007G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102981108 | ||||||
| chr10:102981274
|
C | T | 54 | a0001c0001t0043g0123a0001c0003t0001g0118a0001c0003t0001g0122others(51): Show | 54 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(51): Show |
intron_variant | MODIFIER | c.1621+61173C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102981274 | ||||||
| chr10:102981357
|
A | C | 121 | a0001c0001t0043g0123a0001c0002t0004g0176a0001c0002t0004g0180others(118): Show | 121 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.1621+61256A>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102981357 | ||||||
| chr10:102981446
|
CACTT | C | 6 | a0002c0004t0003g0201a0002c0004t0057g0202a0002c0004t0058g0203others(3): Show | 6 | HG00733.hp1 HG00735.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1621+61347_1621+61 others(10): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102981446 | |||||
| chr10:102981565
|
A | AT | 8 | a0001c0001t0040g0035a0001c0002t0026g0267a0001c0002t0026g0269others(5): Show | 8 | HG01884.hp2 HG02145.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1621+61476dupT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102981565 | |||||
| chr10:102981603
|
G | A | 1 | a0001c0001t0002g0028 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1621+61502G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102981603 | ||||||
| chr10:102981826
|
G | T | 10 | a0001c0001t0012g0041a0001c0001t0019g0001a0001c0001t0030g0037others(7): Show | 10 | HG00408.hp2 HG00642.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.1621+61725G>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102981826 | ||||||
| chr10:102982712
|
A | G | 1 | a0001c0002t0004g0176 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1621+62611A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102982712 | ||||||
| chr10:102982786
|
T | C | 1 | a0001c0003t0010g0151 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1621+62685T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102982786 | ||||||
| chr10:102983258
|
ATATT | A | 9 | a0001c0005t0022g0186a0001c0005t0023g0189a0001c0005t0023g0190others(6): Show | 9 | HG02135.hp2 HG03834.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1621+63158_1621+63 others(10): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102983258 | ||||||
| chr10:102983432
|
C | T | 1 | a0001c0003t0010g0148 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1621+63331C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102983432 | ||||||
| chr10:102983772
|
AT | A | 154 | a0001c0001t0005g0005a0001c0001t0008g0250a0001c0001t0008g0252others(151): Show | 154 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(151): Show |
intron_variant | MODIFIER | c.1621+63684delT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102983772 | |||||
| chr10:102983914
|
G | A | 1 | a0001c0001t0038g0015 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1621+63813G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102983914 | ||||||
| chr10:102983937
|
G | A | 4 | a0001c0003t0001g0124a0001c0003t0032g0120a0001c0003t0032g0169others(1): Show | 4 | NA18962.hp2 NA18990.hp2 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.1621+63836G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102983937 | ||||||
| chr10:102984468
|
G | A | 9 | a0001c0001t0020g0026a0001c0001t0020g0027a0001c0001t0020g0054others(6): Show | 9 | HG01361.hp2 HG01934.hp2 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1621+64367G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102984468 | ||||||
| chr10:102984649
|
A | G | 155 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0001t0043g0123others(152): Show | 155 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(152): Show |
intron_variant | MODIFIER | c.1621+64548A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102984649 | ||||||
| chr10:102984728
|
C | T | 1 | a0001c0001t0040g0105 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1621+64627C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102984728 | ||||||
| chr10:102984855
|
C | T | 6 | a0001c0002t0026g0267a0001c0002t0026g0269a0001c0002t0027g0266others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1621+64754C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102984855 | ||||||
| chr10:102985241
|
C | T | 1 | a0001c0005t0050g0191 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1622-64466C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102985241 | ||||||
| chr10:102985379
|
C | T | 8 | a0001c0002t0006g0117a0001c0002t0006g0208a0001c0002t0006g0209others(5): Show | 8 | HG00408.hp1 HG00609.hp2 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.1622-64328C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102985379 | ||||||
| chr10:102985417
|
T | A | 22 | a0001c0002t0004g0176a0001c0002t0004g0180a0001c0002t0004g0255others(19): Show | 22 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.1622-64290T>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102985417 | ||||||
| chr10:102985566
|
G | A | 2 | a0002c0004t0028g0196a0002c0004t0028g0215 | 2 | HG02622.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1622-64141G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102985566 | ||||||
| chr10:102985705
|
G | T | 1 | a0001c0001t0011g0012 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1622-64002G>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102985705 | ||||||
| chr10:102985835
|
G | A | 1 | a0001c0003t0001g0147 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1622-63872G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102985835 | ||||||
| chr10:102985988
|
T | A | 1 | a0001c0001t0043g0123 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1622-63719T>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102985988 | ||||||
| chr10:102986083
|
T | C | 1 | a0001c0001t0097g0014 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1622-63624T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102986083 | ||||||
| chr10:102986322
|
C | T | 1 | a0001c0001t0040g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1622-63385C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102986322 | ||||||
| chr10:102986510
|
C | T | 1 | a0002c0004t0055g0216 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1622-63197C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102986510 | ||||||
| chr10:102986520
|
C | T | 1 | a0002c0004t0055g0216 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1622-63187C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102986520 | ||||||
| chr10:102986617
|
C | CT | 23 | a0001c0002t0003g0225a0001c0002t0004g0176a0001c0002t0004g0180others(20): Show | 23 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.1622-63088dupT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102986617 | |||||
| chr10:102986619
|
T | TA | 68 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(65): Show | 68 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.1622-63078dupA | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102986619 | |||||
| chr10:102986641
|
A | G | 154 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0001t0043g0123others(151): Show | 154 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(151): Show |
intron_variant | MODIFIER | c.1622-63066A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102986641 | ||||||
| chr10:102986711
|
C | T | 23 | a0001c0002t0003g0225a0001c0002t0004g0176a0001c0002t0004g0180others(20): Show | 23 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.1622-62996C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102986711 | ||||||
| chr10:102986779
|
C | CA | 238 | a0001c0001t0002g0019a0001c0001t0002g0062a0001c0001t0002g0064others(235): Show | 238 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.1622-62911dupA | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102986779 | |||||
| chr10:102986779
|
C | CAA | 25 | a0001c0001t0002g0028a0001c0001t0002g0078a0001c0001t0008g0250others(22): Show | 25 | HG00558.hp2 HG00621.hp2 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.1622-62912_1622-62 others(8): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102986779 | |||||
| chr10:102986892
|
A | G | 145 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0001t0043g0123others(142): Show | 145 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(142): Show |
intron_variant | MODIFIER | c.1622-62815A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102986892 | ||||||
| chr10:102987483
|
G | A | 6 | a0001c0002t0026g0267a0001c0002t0026g0269a0001c0002t0027g0266others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1622-62224G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102987483 | ||||||
| chr10:102987616
|
C | T | 28 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(25): Show | 28 | HG00609.hp1 HG00621.hp2 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.1622-62091C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102987616 | ||||||
| chr10:102987777
|
A | G | 49 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(46): Show | 49 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.1622-61930A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102987777 | ||||||
| chr10:102987837
|
C | T | 11 | a0001c0002t0003g0225a0001c0002t0004g0180a0001c0002t0024g0172others(8): Show | 11 | HG00639.hp1 HG00738.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1622-61870C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102987837 | ||||||
| chr10:102988014
|
AAAGGCCG others(11): Show |
A | 1 | a0001c0001t0008g0090 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1622-61692_1622-61 others(24): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102988014 | ||||||
| chr10:102988106
|
C | A | 3 | a0001c0001t0014g0018a0001c0001t0014g0042a0001c0001t0014g0045 | 3 | HG01952.hp2 HG01981.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.1622-61601C>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102988106 | ||||||
| chr10:102988127
|
C | A | 1 | a0001c0001t0002g0019 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1622-61580C>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102988127 | ||||||
| chr10:102988128
|
G | C | 1 | a0001c0001t0002g0019 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1622-61579G>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102988128 | ||||||
| chr10:102988157
|
C | T | 2 | a0001c0002t0029g0207a0001c0002t0069g0206 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1622-61550C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102988157 | ||||||
| chr10:102988237
|
G | A | 91 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(88): Show | 91 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.1622-61470G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102988237 | ||||||
| chr10:102988250
|
C | G | 91 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(88): Show | 91 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.1622-61457C>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102988250 | ||||||
| chr10:102988252
|
G | A | 54 | a0001c0001t0043g0123a0001c0003t0001g0118a0001c0003t0001g0122others(51): Show | 54 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(51): Show |
intron_variant | MODIFIER | c.1622-61455G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102988252 | ||||||
| chr10:102988587
|
G | A | 3 | a0001c0001t0002g0069a0001c0001t0002g0100a0001c0001t0036g0099 | 3 | HG02683.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1622-61120G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102988587 | ||||||
| chr10:102988702
|
A | C | 145 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0001t0043g0123others(142): Show | 145 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(142): Show |
intron_variant | MODIFIER | c.1622-61005A>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102988702 | ||||||
| chr10:102988704
|
C | G | 1 | a0001c0002t0064g0248 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1622-61003C>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102988704 | ||||||
| chr10:102988961
|
A | G | 154 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0001t0043g0123others(151): Show | 154 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(151): Show |
intron_variant | MODIFIER | c.1622-60746A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102988961 | ||||||
| chr10:102989359
|
T | G | 1 | a0002c0004t0055g0216 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1622-60348T>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102989359 | ||||||
| chr10:102989487
|
T | TA | 54 | a0001c0001t0018g0104a0001c0001t0043g0123a0001c0002t0006g0214others(51): Show | 54 | HG00099.hp2 HG00544.hp2 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.1622-60210dupA | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102989487 | |||||
| chr10:102989665
|
T | C | 5 | a0001c0002t0026g0267a0001c0002t0026g0269a0001c0002t0027g0266others(2): Show | 5 | HG01884.hp2 HG02145.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1622-60042T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102989665 | ||||||
| chr10:102989837
|
A | G | 1 | a0001c0003t0001g0167 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1622-59870A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102989837 | ||||||
| chr10:102989948
|
C | CTT | 50 | a0001c0001t0043g0123a0001c0003t0001g0118a0001c0003t0001g0122others(47): Show | 50 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(47): Show |
intron_variant | MODIFIER | c.1622-59746_1622-59 others(8): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102989948 | |||||
| chr10:102989948
|
CT | C | 7 | a0001c0001t0005g0007a0001c0001t0005g0057a0001c0001t0008g0250others(4): Show | 7 | HG01109.hp1 HG01167.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.1622-59745delT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102989948 | |||||
| chr10:102989968
|
A | G | 144 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0001t0043g0123others(141): Show | 144 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(141): Show |
intron_variant | MODIFIER | c.1622-59739A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102989968 | ||||||
| chr10:102990590
|
A | C | 1 | a0001c0003t0001g0167 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1622-59117A>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102990590 | ||||||
| chr10:102990749
|
C | T | 4 | a0001c0001t0036g0029a0001c0001t0045g0030a0003c0008t0002g0075others(1): Show | 4 | HG00597.hp1 HG02056.hp2 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.1622-58958C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102990749 | ||||||
| chr10:102991111
|
C | T | 1 | a0001c0003t0032g0169 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1622-58596C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102991111 | ||||||
| chr10:102991252
|
T | C | 1 | a0002c0004t0028g0196 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1622-58455T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102991252 | ||||||
| chr10:102991813
|
A | G | 8 | a0001c0001t0002g0065a0001c0001t0014g0018a0001c0001t0014g0042others(5): Show | 8 | HG00597.hp1 HG01952.hp2 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.1622-57894A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102991813 | ||||||
| chr10:102992014
|
C | T | 1 | a0001c0002t0108g0249 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1622-57693C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102992014 | ||||||
| chr10:102992024
|
A | T | 62 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(59): Show | 62 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.1622-57683A>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102992024 | ||||||
| chr10:102992225
|
C | T | 2 | a0001c0002t0064g0248a0001c0002t0065g0116 | 2 | HG02109.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1622-57482C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102992225 | ||||||
| chr10:102992273
|
C | CT | 6 | a0001c0001t0005g0006a0001c0001t0093g0031a0001c0001t0100g0085others(3): Show | 6 | HG00642.hp2 HG00735.hp2 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.1622-57416dupT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102992273 | |||||
| chr10:102992273
|
C | CTTTTTTT others(2): Show |
15 | a0001c0002t0004g0176a0001c0002t0004g0180a0001c0002t0004g0255others(12): Show | 15 | HG00597.hp2 HG00673.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.1622-57424_1622-57 others(15): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102992273 | |||||
| chr10:102992273
|
C | CTTTTTTT others(3): Show |
7 | a0001c0002t0004g0264a0001c0002t0004g0265a0001c0002t0024g0172others(4): Show | 7 | HG00639.hp1 HG01952.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1622-57425_1622-57 others(16): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102992273 | |||||
| chr10:102992273
|
C | CTTTTTTT others(4): Show |
12 | a0001c0002t0003g0227a0001c0002t0003g0229a0001c0002t0003g0236others(9): Show | 12 | HG00673.hp2 HG01884.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.1622-57426_1622-57 others(17): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102992273 | |||||
| chr10:102992273
|
C | CTTTTTTT others(5): Show |
53 | a0001c0001t0008g0252a0001c0001t0043g0123a0001c0002t0003g0223others(50): Show | 53 | HG00609.hp1 HG00621.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.1622-57427_1622-57 others(18): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102992273 | |||||
| chr10:102992273
|
C | CTTTTTTT others(6): Show |
20 | a0001c0001t0008g0250a0001c0002t0002g0245a0001c0002t0003g0232others(17): Show | 20 | HG00099.hp2 HG00544.hp2 HG01981.hp1 others(17): Show |
intron_variant | MODIFIER | c.1622-57428_1622-57 others(19): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102992273 | |||||
| chr10:102992273
|
C | CTTTTTTT others(7): Show |
13 | a0001c0002t0003g0233a0001c0002t0003g0240a0001c0002t0006g0221others(10): Show | 13 | HG01123.hp1 HG01167.hp2 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.1622-57429_1622-57 others(20): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102992273 | |||||
| chr10:102992273
|
C | CTTTTTTT others(8): Show |
3 | a0001c0002t0006g0213a0001c0002t0029g0204a0001c0002t0064g0248 | 3 | HG02683.hp2 HG02976.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1622-57430_1622-57 others(21): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102992273 | |||||
| chr10:102992273
|
C | CTTTTTTT others(9): Show |
9 | a0001c0002t0006g0208a0001c0002t0006g0212a0001c0002t0006g0214others(6): Show | 9 | HG00609.hp2 HG01070.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.1622-57431_1622-57 others(22): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102992273 | |||||
| chr10:102992273
|
C | CTTTTTTT others(10): Show |
2 | a0001c0002t0006g0210a0001c0002t0065g0116 | 2 | HG00408.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1622-57432_1622-57 others(23): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102992273 | |||||
| chr10:102992273
|
C | CTTTTTTT others(11): Show |
4 | a0001c0002t0006g0117a0001c0002t0006g0209a0001c0003t0001g0171others(1): Show | 4 | HG02155.hp2 HG02257.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.1622-57433_1622-57 others(24): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102992273 | |||||
| chr10:102992273
|
C | CTTTTTTT others(12): Show |
1 | a0001c0002t0015g0205 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1622-57416_1622-57 others(25): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102992273 | |||||
| chr10:102992273
|
CT | C | 14 | a0001c0001t0008g0060a0001c0001t0018g0058a0001c0001t0072g0115others(11): Show | 14 | HG00558.hp1 HG01169.hp1 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.1622-57416delT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102992273 | |||||
| chr10:102992397
|
T | TGAGCAGC others(44): Show |
1 | a0001c0002t0003g0223 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1622-57309_1622-57 others(57): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102992397 | |||||
| chr10:102992426
|
A | G | 1 | a0001c0001t0017g0063 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1622-57281A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102992426 | ||||||
| chr10:102992884
|
A | G | 2 | a0001c0001t0008g0250a0001c0001t0008g0252 | 2 | HG01361.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.1622-56823A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102992884 | ||||||
| chr10:102992910
|
A | G | 9 | a0001c0005t0022g0186a0001c0005t0023g0189a0001c0005t0023g0190others(6): Show | 9 | HG02135.hp2 HG03834.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1622-56797A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102992910 | ||||||
| chr10:102992997
|
A | T | 1 | a0001c0001t0084g0016 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1622-56710A>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102992997 | ||||||
| chr10:102993047
|
A | G | 6 | a0001c0002t0026g0267a0001c0002t0026g0269a0001c0002t0027g0266others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1622-56660A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102993047 | ||||||
| chr10:102993073
|
T | G | 23 | a0001c0002t0003g0225a0001c0002t0004g0176a0001c0002t0004g0180others(20): Show | 23 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.1622-56634T>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102993073 | ||||||
| chr10:102993074
|
A | T | 23 | a0001c0002t0003g0225a0001c0002t0004g0176a0001c0002t0004g0180others(20): Show | 23 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.1622-56633A>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102993074 | ||||||
| chr10:102993115
|
C | T | 1 | a0001c0001t0019g0001 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1622-56592C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102993115 | ||||||
| chr10:102993203
|
G | A | 145 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0001t0043g0123others(142): Show | 145 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(142): Show |
intron_variant | MODIFIER | c.1622-56504G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102993203 | ||||||
| chr10:102993368
|
GACTTTTG others(22): Show |
G | 1 | a0001c0001t0093g0031 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1622-56338_1622-56 others(35): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102993368 | ||||||
| chr10:102993523
|
A | T | 1 | a0001c0001t0096g0052 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1622-56184A>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102993523 | ||||||
| chr10:102993540
|
C | T | 4 | a0001c0001t0019g0083a0001c0001t0019g0084a0001c0001t0038g0015others(1): Show | 4 | HG02109.hp2 HG02970.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1622-56167C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102993540 | ||||||
| chr10:102993672
|
T | A | 1 | a0001c0001t0096g0052 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1622-56035T>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102993672 | ||||||
| chr10:102993714
|
C | T | 3 | a0001c0001t0019g0083a0001c0001t0019g0084a0001c0001t0104g0032 | 3 | HG02109.hp2 HG02970.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1622-55993C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102993714 | ||||||
| chr10:102993750
|
G | A | 69 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(66): Show | 69 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.1622-55957G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102993750 | ||||||
| chr10:102993761
|
G | A | 3 | a0001c0002t0003g0225a0001c0002t0044g0230a0001c0002t0044g0243 | 3 | HG00642.hp2 HG01255.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1622-55946G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102993761 | ||||||
| chr10:102993911
|
GTTCTGGC others(3): Show |
G | 1 | a0001c0006t0004g0175 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1622-55795_1622-55 others(16): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102993911 | ||||||
| chr10:102993918
|
C | A | 50 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(47): Show | 50 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.1622-55789C>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102993918 | ||||||
| chr10:102993969
|
C | T | 10 | a0001c0002t0004g0180a0001c0002t0024g0172a0001c0002t0024g0181others(7): Show | 10 | HG00639.hp1 HG00738.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.1622-55738C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102993969 | ||||||
| chr10:102993971
|
C | T | 1 | a0001c0001t0039g0061 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1622-55736C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102993971 | ||||||
| chr10:102994015
|
C | T | 1 | a0001c0001t0030g0044 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1622-55692C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102994015 | ||||||
| chr10:102994133
|
C | T | 1 | a0001c0010t0067g0194 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1622-55574C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102994133 | ||||||
| chr10:102994184
|
G | A | 1 | a0001c0010t0067g0194 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1622-55523G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102994184 | ||||||
| chr10:102994371
|
A | T | 1 | a0001c0001t0105g0093 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1622-55336A>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102994371 | ||||||
| chr10:102994422
|
A | G | 1 | a0002c0004t0055g0216 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1622-55285A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102994422 | ||||||
| chr10:102994698
|
C | A | 2 | a0001c0002t0029g0207a0001c0002t0069g0206 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1622-55009C>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102994698 | ||||||
| chr10:102994758
|
A | G | 9 | a0001c0005t0022g0186a0001c0005t0023g0189a0001c0005t0023g0190others(6): Show | 9 | HG02135.hp2 HG03834.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1622-54949A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102994758 | ||||||
| chr10:102994982
|
T | G | 1 | a0001c0001t0008g0060 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1622-54725T>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102994982 | ||||||
| chr10:102994983
|
G | T | 1 | a0001c0001t0008g0060 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1622-54724G>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102994983 | ||||||
| chr10:102994984
|
T | G | 1 | a0001c0001t0008g0060 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1622-54723T>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102994984 | ||||||
| chr10:102995001
|
T | G | 1 | a0001c0002t0106g0228 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1622-54706T>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102995001 | ||||||
| chr10:102995009
|
T | A | 3 | a0001c0001t0002g0069a0001c0001t0002g0100a0001c0001t0036g0099 | 3 | HG02683.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1622-54698T>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102995009 | ||||||
| chr10:102995014
|
C | A | 1 | a0001c0002t0106g0228 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1622-54693C>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102995014 | ||||||
| chr10:102995032
|
G | T | 1 | a0001c0002t0003g0223 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1622-54675G>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102995032 | ||||||
| chr10:102995095
|
T | G | 1 | a0001c0001t0005g0057 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1622-54612T>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102995095 | ||||||
| chr10:102995096
|
T | A | 1 | a0001c0001t0005g0057 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1622-54611T>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102995096 | ||||||
| chr10:102995097
|
A | G | 1 | a0001c0001t0005g0057 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1622-54610A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102995097 | ||||||
| chr10:102995111
|
T | C | 1 | a0001c0001t0005g0057 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1622-54596T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102995111 | ||||||
| chr10:102995113
|
C | G | 1 | a0001c0001t0005g0057 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1622-54594C>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102995113 | ||||||
| chr10:102995114
|
T | G | 1 | a0001c0001t0005g0057 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1622-54593T>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102995114 | ||||||
| chr10:102995123
|
G | A | 1 | a0001c0001t0005g0057 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1622-54584G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102995123 | ||||||
| chr10:102995128
|
T | C | 1 | a0001c0001t0005g0057 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1622-54579T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102995128 | ||||||
| chr10:102995135
|
T | TTCCTCCT others(56): Show |
1 | a0001c0001t0005g0057 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1622-54572_1622-54 others(69): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102995135 | ||||||
| chr10:102995137
|
T | C | 1 | a0001c0001t0005g0057 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1622-54570T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102995137 | ||||||
| chr10:102995139
|
A | C | 1 | a0001c0001t0005g0057 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1622-54568A>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102995139 | ||||||
| chr10:102995143
|
T | C | 1 | a0001c0001t0005g0057 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1622-54564T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102995143 | ||||||
| chr10:102995168
|
T | TC | 7 | a0001c0001t0005g0057a0001c0001t0043g0123a0001c0002t0003g0234others(4): Show | 7 | HG00639.hp1 HG01167.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1622-54534dupC | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995168 | |||||
| chr10:102995179
|
C | T | 1 | a0001c0005t0047g0187 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1622-54528C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102995179 | ||||||
| chr10:102995180
|
T | C | 1 | a0001c0005t0047g0187 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1622-54527T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102995180 | ||||||
| chr10:102995192
|
T | A | 1 | a0001c0002t0106g0228 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1622-54515T>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102995192 | ||||||
| chr10:102995201
|
T | TCCCCCTC others(753): Show |
1 | a0001c0003t0001g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1622-54504_1622-54 others(766): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCCTCCC others(821): Show |
1 | a0001c0002t0003g0240 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1622-54504_1622-54 others(834): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(533): Show |
1 | a0001c0006t0004g0175 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(546): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(421): Show |
1 | a0001c0005t0022g0186 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(434): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(547): Show |
1 | a0001c0001t0005g0010 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(560): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(530): Show |
1 | a0001c0001t0005g0021 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(543): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(566): Show |
1 | a0001c0001t0037g0089 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(579): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(797): Show |
1 | a0001c0003t0007g0125 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(810): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(439): Show |
1 | a0001c0001t0005g0003 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(452): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(418): Show |
2 | a0001c0001t0043g0076a0001c0003t0001g0106 | 2 | NA19011.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1622-54503_1622-54 others(431): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(454): Show |
1 | a0001c0001t0034g0070 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(467): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(475): Show |
1 | a0001c0005t0046g0188 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(488): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(565): Show |
1 | a0001c0005t0050g0191 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(578): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(476): Show |
1 | a0001c0005t0047g0187 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(489): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(439): Show |
1 | a0001c0001t0012g0041 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(452): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(457): Show |
2 | a0001c0005t0023g0189a0001c0005t0023g0190 | 2 | NA18945.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.1622-54503_1622-54 others(470): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(475): Show |
1 | a0005c0009t0022g0185 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(488): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(475): Show |
1 | a0001c0001t0039g0061 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(488): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(535): Show |
1 | a0001c0001t0012g0080 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(548): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(493): Show |
2 | a0001c0001t0005g0002a0001c0001t0005g0007 | 2 | HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1622-54503_1622-54 others(506): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(510): Show |
1 | a0001c0001t0008g0090 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(523): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(493): Show |
1 | a0001c0005t0048g0184 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(506): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(511): Show |
1 | a0001c0005t0049g0183 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(524): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(934): Show |
1 | a0001c0002t0106g0228 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(947): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(493): Show |
1 | a0001c0001t0002g0069 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(506): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(476): Show |
1 | a0001c0001t0012g0020 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(489): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(397): Show |
1 | a0001c0001t0002g0019 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(410): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(541): Show |
1 | a0001c0001t0008g0017 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(554): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(457): Show |
1 | a0001c0001t0072g0115 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(470): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(436): Show |
1 | a0001c0001t0020g0027 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(449): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(517): Show |
1 | a0001c0001t0005g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(530): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(475): Show |
1 | a0001c0001t0104g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(488): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(454): Show |
3 | a0001c0001t0017g0073a0001c0001t0034g0112a0001c0001t0098g0033 | 3 | HG01106.hp2 HG02055.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1622-54503_1622-54 others(467): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(493): Show |
3 | a0001c0001t0019g0083a0001c0001t0019g0084a0001c0001t0040g0035 | 3 | HG02970.hp1 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1622-54503_1622-54 others(506): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(472): Show |
1 | a0001c0001t0002g0065 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(485): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(490): Show |
1 | a0003c0008t0014g0074 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(503): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(761): Show |
1 | a0001c0001t0043g0123 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(774): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(762): Show |
1 | a0001c0007t0007g0129 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(775): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(521): Show |
1 | a0001c0001t0093g0031 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(534): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(494): Show |
1 | a0001c0001t0030g0044 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(507): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(480): Show |
1 | a0001c0001t0011g0011 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(493): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(385): Show |
1 | a0001c0001t0031g0046 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(398): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(382): Show |
1 | a0001c0001t0073g0025 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(395): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(481): Show |
1 | a0001c0001t0075g0038 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(494): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(460): Show |
1 | a0001c0001t0005g0005 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(473): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(439): Show |
1 | a0001c0001t0011g0012 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(452): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(436): Show |
2 | a0001c0001t0020g0054a0001c0001t0101g0101 | 2 | HG01081.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1622-54503_1622-54 others(449): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(475): Show |
1 | a0001c0001t0095g0043 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(488): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(454): Show |
2 | a0001c0001t0002g0064a0001c0001t0021g0053 | 2 | HG00621.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.1622-54503_1622-54 others(467): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(493): Show |
2 | a0001c0001t0030g0037a0001c0001t0087g0036 | 2 | HG01106.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1622-54503_1622-54 others(506): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(472): Show |
1 | a0001c0001t0002g0078 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(485): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(472): Show |
2 | a0001c0001t0002g0103a0001c0001t0021g0109 | 2 | NA18971.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1622-54503_1622-54 others(485): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(542): Show |
1 | a0001c0001t0011g0013 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(555): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(574): Show |
2 | a0001c0001t0008g0059a0001c0001t0083g0048 | 2 | HG00099.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.1622-54503_1622-54 others(587): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(511): Show |
2 | a0001c0001t0014g0045a0001c0001t0074g0034 | 2 | HG01952.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.1622-54503_1622-54 others(524): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(511): Show |
1 | a0001c0001t0002g0068 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(524): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(490): Show |
1 | a0001c0001t0045g0030 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(503): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(592): Show |
1 | a0001c0001t0018g0058 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(605): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(541): Show |
1 | a0001c0001t0011g0009 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(554): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(529): Show |
2 | a0001c0001t0008g0047a0001c0001t0039g0086 | 2 | HG01258.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.1622-54503_1622-54 others(542): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(508): Show |
2 | a0001c0001t0002g0100a0001c0001t0036g0099 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1622-54503_1622-54 others(521): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(508): Show |
1 | a0001c0001t0099g0071 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(521): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(610): Show |
1 | a0001c0001t0089g0092 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(623): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(589): Show |
1 | a0001c0001t0005g0108 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(602): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(526): Show |
1 | a0001c0001t0002g0102 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(539): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(583): Show |
1 | a0001c0001t0037g0088 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(596): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(523): Show |
1 | a0001c0001t0040g0105 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(536): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(436): Show |
1 | a0001c0001t0102g0110 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(449): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(791): Show |
1 | a0001c0003t0001g0166 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(804): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(473): Show |
1 | a0001c0001t0036g0029 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(486): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(439): Show |
1 | a0001c0001t0035g0079 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(452): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(499): Show |
1 | a0001c0001t0076g0040 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(512): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(457): Show |
2 | a0001c0001t0012g0087a0001c0001t0018g0091 | 2 | HG00738.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.1622-54503_1622-54 others(470): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(436): Show |
1 | a0001c0001t0002g0067 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(449): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(517): Show |
1 | a0001c0001t0031g0039 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(530): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(475): Show |
2 | a0001c0001t0035g0111a0001c0001t0086g0113 | 2 | HG01070.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.1622-54503_1622-54 others(488): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(454): Show |
1 | a0001c0001t0002g0062 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(467): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(493): Show |
2 | a0001c0001t0014g0018a0001c0001t0019g0001 | 2 | HG00408.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.1622-54503_1622-54 others(506): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(472): Show |
1 | a0003c0008t0002g0075 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(485): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(541): Show |
1 | a0001c0001t0005g0008 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(554): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(529): Show |
7 | a0001c0001t0005g0096a0001c0001t0012g0097a0001c0001t0014g0042others(4): Show | 7 | HG01981.hp2 HG04228.hp2 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.1622-54503_1622-54 others(542): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(550): Show |
1 | a0001c0001t0005g0004 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(563): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(508): Show |
2 | a0001c0001t0002g0066a0001c0001t0017g0072 | 2 | HG00733.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.1622-54503_1622-54 others(521): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(547): Show |
2 | a0001c0001t0018g0104a0001c0001t0094g0081 | 2 | NA18612.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.1622-54503_1622-54 others(560): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(547): Show |
1 | a0001c0001t0005g0022 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(560): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(526): Show |
2 | a0001c0001t0017g0063a0001c0001t0042g0024 | 2 | HG01978.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1622-54503_1622-54 others(539): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(691): Show |
1 | a0001c0001t0100g0085 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(704): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(547): Show |
2 | a0001c0001t0085g0107a0001c0001t0091g0098 | 2 | NA18957.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1622-54503_1622-54 others(560): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(529): Show |
1 | a0001c0001t0092g0082 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(542): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(460): Show |
1 | a0001c0001t0011g0114 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(473): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(439): Show |
1 | a0001c0002t0009g0224 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(452): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(669): Show |
1 | a0001c0003t0016g0144 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(682): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(472): Show |
1 | a0001c0001t0084g0016 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(485): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(490): Show |
4 | a0001c0001t0021g0055a0001c0001t0041g0051a0001c0001t0096g0052others(1): Show | 4 | HG01361.hp2 HG01943.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.1622-54503_1622-54 others(503): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(508): Show |
2 | a0001c0001t0020g0026a0001c0001t0097g0014 | 2 | HG00558.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.1622-54503_1622-54 others(521): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(544): Show |
1 | a0001c0001t0042g0023 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(557): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(892): Show |
1 | a0001c0002t0003g0227 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(905): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(729): Show |
1 | a0002c0004t0028g0196 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(742): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(472): Show |
1 | a0001c0001t0002g0049 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(485): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(508): Show |
1 | a0001c0001t0002g0028 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(521): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(544): Show |
1 | a0001c0001t0005g0077 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(557): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(497): Show |
1 | a0001c0006t0013g0179 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(510): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(648): Show |
1 | a0001c0003t0001g0155 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(661): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(645): Show |
1 | a0001c0003t0001g0141 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(658): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(667): Show |
1 | a0001c0003t0016g0163 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(680): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(704): Show |
1 | a0001c0003t0016g0145 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(717): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(749): Show |
1 | a0001c0003t0051g0136 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(762): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(669): Show |
2 | a0001c0003t0001g0167a0001c0003t0080g0158 | 2 | NA18612.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1622-54503_1622-54 others(682): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(687): Show |
1 | a0001c0003t0001g0140 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(700): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(766): Show |
1 | a0001c0010t0067g0194 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(779): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(822): Show |
1 | a0002c0004t0055g0216 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(835): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(772): Show |
1 | a0001c0002t0070g0218 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(785): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(590): Show |
2 | a0001c0002t0026g0267a0001c0002t0026g0269 | 2 | HG01884.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1622-54503_1622-54 others(603): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(801): Show |
1 | a0001c0002t0107g0235 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(814): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(609): Show |
1 | a0001c0002t0063g0270 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(622): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(642): Show |
1 | a0001c0002t0027g0266 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(655): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(626): Show |
1 | a0001c0002t0027g0268 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(639): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(760): Show |
1 | a0001c0003t0001g0159 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(773): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(920): Show |
1 | a0001c0003t0001g0170 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(933): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(706): Show |
2 | a0001c0003t0001g0146a0001c0003t0001g0147 | 2 | NA18992.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1622-54503_1622-54 others(719): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(837): Show |
1 | a0001c0002t0009g0254 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(850): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(802): Show |
1 | a0001c0002t0003g0239 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(815): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(821): Show |
1 | a0001c0002t0065g0116 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(834): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(876): Show |
1 | a0001c0002t0064g0248 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(889): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(759): Show |
1 | a0001c0003t0001g0143 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(772): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(777): Show |
1 | a0001c0003t0001g0153 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(790): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(778): Show |
1 | a0001c0003t0001g0149 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(791): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(855): Show |
1 | a0002c0004t0066g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(868): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(820): Show |
1 | a0001c0002t0003g0242 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(833): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(821): Show |
1 | a0001c0002t0003g0253 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(834): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(873): Show |
1 | a0002c0004t0028g0215 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(886): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(856): Show |
1 | a0001c0002t0071g0247 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(869): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(741): Show |
1 | a0001c0003t0033g0164 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(754): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(829): Show |
1 | a0001c0003t0001g0168 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(842): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(778): Show |
1 | a0001c0003t0001g0160 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(791): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(796): Show |
1 | a0001c0003t0082g0154 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(809): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(902): Show |
1 | a0001c0003t0001g0133 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(915): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(873): Show |
1 | a0001c0002t0003g0234 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(886): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(856): Show |
1 | a0001c0002t0003g0229 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(869): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(839): Show |
1 | a0001c0002t0003g0237 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(852): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(964): Show |
1 | a0002c0004t0059g0217 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(977): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(820): Show |
1 | a0001c0002t0003g0251 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(833): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(838): Show |
3 | a0001c0002t0003g0231a0001c0002t0003g0233a0001c0002t0009g0246 | 3 | HG02027.hp2 NA18950.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1622-54503_1622-54 others(851): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(821): Show |
1 | a0001c0002t0009g0226 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(834): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(890): Show |
1 | a0001c0002t0003g0225 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(903): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(873): Show |
1 | a0001c0002t0003g0232 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(886): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(759): Show |
1 | a0001c0003t0001g0171 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(772): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(777): Show |
1 | a0001c0003t0033g0135 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(790): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(742): Show |
1 | a0001c0007t0078g0132 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(755): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(795): Show |
1 | a0001c0003t0001g0162 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(808): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(778): Show |
2 | a0001c0003t0001g0142a0001c0003t0007g0126 | 2 | HG00544.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1622-54503_1622-54 others(791): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(813): Show |
1 | a0001c0003t0001g0122 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(826): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(796): Show |
1 | a0001c0003t0001g0161 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(809): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(841): Show |
1 | a0001c0002t0009g0238 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(854): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(874): Show |
1 | a0001c0002t0002g0245 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(887): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(857): Show |
1 | a0001c0002t0003g0236 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(870): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(839): Show |
1 | a0001c0002t0009g0241 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(852): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(838): Show |
1 | a0001c0002t0009g0244 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(851): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(928): Show |
1 | a0002c0004t0057g0202 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(941): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(945): Show |
1 | a0002c0004t0058g0203 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(958): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(793): Show |
1 | a0001c0003t0032g0120 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(806): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(760): Show |
1 | a0001c0007t0077g0131 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(773): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(813): Show |
1 | a0001c0003t0007g0139 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(826): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(796): Show |
2 | a0001c0003t0007g0128a0001c0003t0007g0138 | 2 | NA18747.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1622-54503_1622-54 others(809): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(812): Show |
1 | a0001c0003t0010g0148 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(825): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(848): Show |
1 | a0001c0003t0001g0127 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(861): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(874): Show |
1 | a0001c0002t0044g0230 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(887): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(840): Show |
1 | a0001c0001t0008g0252 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(853): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(928): Show |
2 | a0002c0004t0060g0197a0002c0004t0061g0198 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1622-54503_1622-54 others(941): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(1306): Show |
1 | a0001c0002t0044g0243 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(1319): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(816): Show |
1 | a0001c0003t0007g0121 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(829): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(811): Show |
2 | a0001c0003t0001g0124a0001c0003t0032g0169 | 2 | NA18962.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1622-54503_1622-54 others(824): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(810): Show |
1 | a0001c0003t0103g0119 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(823): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(830): Show |
1 | a0001c0003t0001g0118 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(843): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(813): Show |
1 | a0001c0003t0079g0134 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(826): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(812): Show |
1 | a0001c0003t0081g0165 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(825): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(796): Show |
1 | a0001c0003t0007g0130 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(809): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(848): Show |
1 | a0001c0003t0010g0137 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(861): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(929): Show |
3 | a0002c0004t0025g0195a0002c0004t0025g0199a0002c0004t0056g0200 | 3 | HG01109.hp1 HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1622-54503_1622-54 others(942): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(628): Show |
1 | a0001c0002t0054g0193 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(641): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(830): Show |
1 | a0001c0003t0010g0152 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(843): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(848): Show |
1 | a0001c0003t0010g0150 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(861): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(884): Show |
1 | a0001c0003t0010g0151 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(897): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(771): Show |
1 | a0001c0002t0069g0206 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(784): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(768): Show |
1 | a0001c0002t0029g0207 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(781): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(933): Show |
1 | a0001c0002t0062g0222 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(946): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(735): Show |
1 | a0001c0002t0015g0205 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(748): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(771): Show |
1 | a0001c0002t0068g0219 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(784): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(771): Show |
1 | a0001c0002t0015g0220 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(784): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(850): Show |
1 | a0001c0003t0001g0156 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(863): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(789): Show |
1 | a0001c0002t0006g0221 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(802): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(807): Show |
1 | a0001c0002t0006g0212 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(820): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(842): Show |
1 | a0001c0002t0006g0117 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(855): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(846): Show |
1 | a0001c0002t0006g0208 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(859): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(825): Show |
2 | a0001c0002t0006g0209a0001c0002t0006g0210 | 2 | HG00408.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.1622-54503_1622-54 others(838): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(790): Show |
1 | a0001c0002t0029g0204 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(803): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(843): Show |
1 | a0001c0002t0006g0214 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(856): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(861): Show |
1 | a0001c0002t0006g0213 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(874): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(877): Show |
1 | a0001c0002t0015g0211 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(890): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(568): Show |
1 | a0001c0002t0004g0180 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(581): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(585): Show |
1 | a0001c0002t0052g0260 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(598): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(853): Show |
1 | a0001c0002t0108g0249 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(866): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(586): Show |
1 | a0001c0002t0053g0259 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(599): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(586): Show |
1 | a0001c0002t0004g0264 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(599): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(550): Show |
1 | a0001c0006t0004g0178 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(563): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(876): Show |
1 | a0001c0001t0008g0250 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(889): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(568): Show |
3 | a0001c0002t0004g0256a0001c0002t0004g0258a0001c0002t0013g0257 | 3 | HG03041.hp1 HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1622-54503_1622-54 others(581): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(550): Show |
1 | a0001c0002t0004g0176 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(563): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(535): Show |
1 | a0001c0002t0004g0255 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(548): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(532): Show |
5 | a0001c0002t0024g0172a0001c0002t0024g0181a0001c0006t0004g0182others(2): Show | 5 | HG01515.hp1 HG01517.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.1622-54503_1622-54 others(545): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(548): Show |
1 | a0001c0006t0004g0177 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(561): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(548): Show |
1 | a0001c0002t0004g0261 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(561): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(550): Show |
3 | a0001c0002t0004g0262a0001c0002t0004g0263a0001c0002t0004g0265 | 3 | HG02258.hp1 HG02647.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1622-54503_1622-54 others(563): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(786): Show |
1 | a0002c0004t0003g0201 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(799): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCCTCCCC others(833): Show |
1 | a0001c0002t0003g0223 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(846): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995201
|
T | TCTCCCCT others(553): Show |
1 | a0001c0001t0005g0057 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1622-54505_1622-54 others(566): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995201 | |||||
| chr10:102995203
|
C | CTCCCCCT others(609): Show |
1 | a0001c0001t0008g0060 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1622-54503_1622-54 others(622): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995203 | |||||
| chr10:102995205
|
T | C | 1 | a0001c0001t0008g0060 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1622-54502T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102995205 | ||||||
| chr10:102995318
|
T | G | 3 | a0001c0001t0039g0086a0001c0001t0040g0105a0001c0001t0093g0031 | 3 | HG02027.hp1 HG02129.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.1622-54389T>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102995318 | ||||||
| chr10:102995576
|
TG | T | 5 | a0001c0001t0002g0100a0001c0002t0003g0223a0001c0003t0010g0148others(2): Show | 5 | HG01099.hp2 HG01358.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.1622-54126delG | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102995576 | |||||
| chr10:102995674
|
G | A | 144 | a0001c0001t0002g0062a0001c0001t0008g0250a0001c0001t0008g0252others(141): Show | 144 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(141): Show |
intron_variant | MODIFIER | c.1622-54033G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102995674 | ||||||
| chr10:102995861
|
C | T | 1 | a0001c0003t0051g0136 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1622-53846C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102995861 | ||||||
| chr10:102996028
|
T | A | 1 | a0001c0002t0003g0242 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1622-53679T>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102996028 | ||||||
| chr10:102996169
|
T | C | 9 | a0001c0005t0022g0186a0001c0005t0023g0189a0001c0005t0023g0190others(6): Show | 9 | HG02135.hp2 HG03834.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1622-53538T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102996169 | ||||||
| chr10:102996232
|
A | AT | 16 | a0001c0002t0003g0223a0001c0002t0006g0117a0001c0002t0006g0208others(13): Show | 16 | HG00408.hp1 HG00609.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.1622-53464dupT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102996232 | |||||
| chr10:102996273
|
A | T | 92 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(89): Show | 92 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.1622-53434A>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102996273 | ||||||
| chr10:102996418
|
C | T | 5 | a0001c0002t0026g0267a0001c0002t0026g0269a0001c0002t0027g0266others(2): Show | 5 | HG01884.hp2 HG02145.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1622-53289C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102996418 | ||||||
| chr10:102996425
|
C | T | 92 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(89): Show | 92 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.1622-53282C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102996425 | ||||||
| chr10:102996617
|
T | C | 146 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0001t0043g0123others(143): Show | 146 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(143): Show |
intron_variant | MODIFIER | c.1622-53090T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102996617 | ||||||
| chr10:102996654
|
A | C | 1 | a0001c0003t0001g0147 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1622-53053A>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102996654 | ||||||
| chr10:102996661
|
G | T | 1 | a0001c0001t0012g0080 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1622-53046G>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102996661 | ||||||
| chr10:102996879
|
G | A | 92 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(89): Show | 92 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.1622-52828G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102996879 | ||||||
| chr10:102996973
|
C | T | 1 | a0001c0001t0018g0091 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1622-52734C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102996973 | ||||||
| chr10:102997036
|
A | T | 1 | a0001c0003t0016g0163 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1622-52671A>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102997036 | ||||||
| chr10:102997288
|
G | T | 1 | a0001c0001t0002g0019 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1622-52419G>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102997288 | ||||||
| chr10:102997945
|
A | G | 1 | a0001c0003t0016g0163 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1622-51762A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102997945 | ||||||
| chr10:102997952
|
A | C | 70 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(67): Show | 70 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.1622-51755A>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102997952 | ||||||
| chr10:102997996
|
T | C | 31 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(28): Show | 31 | HG00609.hp1 HG00621.hp2 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.1622-51711T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102997996 | ||||||
| chr10:102998158
|
C | G | 3 | a0001c0002t0064g0248a0001c0002t0065g0116a0001c0002t0071g0247 | 3 | HG02109.hp1 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1622-51549C>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102998158 | ||||||
| chr10:102998468
|
A | G | 1 | a0001c0001t0096g0052 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1622-51239A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102998468 | ||||||
| chr10:102998581
|
C | T | 1 | a0001c0001t0031g0046 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1622-51126C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102998581 | ||||||
| chr10:102998587
|
G | A | 1 | a0001c0002t0106g0228 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1622-51120G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102998587 | ||||||
| chr10:102998588
|
A | T | 1 | a0001c0002t0106g0228 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1622-51119A>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102998588 | ||||||
| chr10:102998675
|
G | A | 1 | a0001c0002t0004g0263 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1622-51032G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102998675 | ||||||
| chr10:102998897
|
C | T | 5 | a0001c0002t0026g0267a0001c0002t0026g0269a0001c0002t0027g0266others(2): Show | 5 | HG01884.hp2 HG02145.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1622-50810C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102998897 | ||||||
| chr10:102998937
|
T | C | 4 | a0001c0002t0004g0262a0001c0002t0004g0263a0001c0002t0004g0264others(1): Show | 4 | HG02258.hp1 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1622-50770T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102998937 | ||||||
| chr10:102998969
|
A | G | 1 | a0001c0010t0067g0194 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1622-50738A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102998969 | ||||||
| chr10:102999049
|
C | CA | 4 | a0001c0001t0005g0003a0001c0002t0003g0251a0001c0002t0026g0267others(1): Show | 4 | HG01884.hp2 HG02145.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.1622-50651dupA | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102999049 | |||||
| chr10:102999076
|
C | CT | 10 | a0001c0002t0004g0180a0001c0002t0024g0172a0001c0002t0024g0181others(7): Show | 10 | HG00639.hp1 HG00738.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.1622-50619dupT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102999076 | |||||
| chr10:102999121
|
A | G | 6 | a0001c0002t0026g0267a0001c0002t0026g0269a0001c0002t0027g0266others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1622-50586A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102999121 | ||||||
| chr10:102999131
|
C | T | 1 | a0002c0004t0066g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1622-50576C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102999131 | ||||||
| chr10:102999202
|
C | G | 1 | a0001c0002t0004g0262 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1622-50505C>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102999202 | ||||||
| chr10:102999220
|
G | A | 1 | a0001c0002t0004g0258 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1622-50487G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102999220 | ||||||
| chr10:102999237
|
A | AT | 30 | a0001c0001t0002g0064a0001c0001t0002g0065a0001c0001t0005g0003others(27): Show | 30 | HG00597.hp1 HG00597.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.1622-50452dupT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102999237 | |||||
| chr10:102999237
|
A | ATT | 50 | a0001c0001t0043g0123a0001c0002t0004g0255a0001c0002t0004g0256others(47): Show | 50 | HG00099.hp2 HG00544.hp2 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.1622-50453_1622-50 others(8): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102999237 | |||||
| chr10:102999237
|
A | ATTT | 6 | a0001c0003t0001g0156a0001c0003t0001g0157a0001c0003t0001g0162others(3): Show | 6 | HG01358.hp2 HG01943.hp1 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.1622-50454_1622-50 others(9): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102999237 | |||||
| chr10:102999237
|
AT | A | 7 | a0001c0001t0005g0022a0001c0001t0011g0114a0001c0001t0030g0044others(4): Show | 7 | HG01515.hp2 HG01517.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1622-50452delT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 102999237 | |||||
| chr10:102999328
|
C | T | 1 | a0001c0010t0067g0194 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1622-50379C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102999328 | ||||||
| chr10:102999434
|
G | C | 234 | a0001c0001t0005g0002a0001c0001t0005g0003a0001c0001t0005g0004others(231): Show | 234 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.1622-50273G>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102999434 | ||||||
| chr10:102999655
|
C | T | 2 | a0001c0001t0083g0048a0001c0001t0089g0092 | 2 | HG02071.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.1622-50052C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102999655 | ||||||
| chr10:102999829
|
A | G | 92 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(89): Show | 92 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.1622-49878A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 102999829 | ||||||
| chr10:103000131
|
G | A | 1 | a0001c0001t0030g0044 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1622-49576G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103000131 | ||||||
| chr10:103000132
|
A | G | 1 | a0001c0001t0030g0044 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1622-49575A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103000132 | ||||||
| chr10:103000177
|
A | T | 9 | a0001c0005t0022g0186a0001c0005t0023g0189a0001c0005t0023g0190others(6): Show | 9 | HG02135.hp2 HG03834.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1622-49530A>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103000177 | ||||||
| chr10:103000231
|
C | T | 3 | a0001c0001t0005g0008a0001c0001t0011g0009a0001c0001t0011g0013 | 3 | HG02280.hp2 HG02717.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1622-49476C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103000231 | ||||||
| chr10:103000242
|
C | CAAAT | 27 | a0001c0001t0002g0019a0001c0001t0002g0065a0001c0001t0002g0066others(24): Show | 27 | HG00597.hp1 HG01071.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.1622-49425_1622-49 others(10): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103000242 | |||||
| chr10:103000242
|
CAAAT | C | 18 | a0001c0001t0005g0008a0001c0001t0005g0057a0001c0001t0008g0060others(15): Show | 18 | HG00408.hp2 HG00544.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.1622-49425_1622-49 others(10): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103000242 | |||||
| chr10:103000242
|
CAAATAAA others(1): Show |
C | 63 | a0001c0001t0005g0004a0001c0001t0005g0021a0001c0001t0005g0022others(60): Show | 63 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.1622-49429_1622-49 others(14): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103000242 | |||||
| chr10:103000242
|
CAAATAAA others(5): Show |
C | 20 | a0001c0002t0004g0180a0001c0002t0024g0172a0001c0002t0024g0181others(17): Show | 20 | HG00639.hp1 HG00733.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.1622-49433_1622-49 others(18): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103000242 | |||||
| chr10:103000242
|
CAAATAAA others(9): Show |
C | 2 | a0002c0004t0055g0216a0002c0004t0066g0192 | 2 | HG02257.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1622-49437_1622-49 others(22): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103000242 | |||||
| chr10:103000246
|
T | C | 13 | a0001c0001t0020g0026a0001c0001t0020g0027a0001c0001t0020g0054others(10): Show | 13 | HG00558.hp1 HG01257.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.1622-49461T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103000246 | ||||||
| chr10:103000250
|
T | C | 1 | a0001c0001t0020g0054 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1622-49457T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103000250 | ||||||
| chr10:103000254
|
T | C | 12 | a0001c0002t0004g0176a0001c0002t0004g0255a0001c0002t0004g0256others(9): Show | 12 | HG00597.hp2 HG00673.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1622-49453T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103000254 | ||||||
| chr10:103000258
|
T | C | 21 | a0001c0002t0004g0180a0001c0002t0004g0255a0001c0002t0004g0256others(18): Show | 21 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.1622-49449T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103000258 | ||||||
| chr10:103000333
|
A | G | 1 | a0002c0004t0066g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1622-49374A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103000333 | ||||||
| chr10:103000523
|
G | A | 1 | a0001c0001t0002g0019 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1622-49184G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103000523 | ||||||
| chr10:103000722
|
G | A | 1 | a0001c0002t0065g0116 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1622-48985G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103000722 | ||||||
| chr10:103000728
|
T | C | 92 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(89): Show | 92 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.1622-48979T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103000728 | ||||||
| chr10:103000966
|
A | G | 1 | a0001c0001t0073g0025 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1622-48741A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103000966 | ||||||
| chr10:103000995
|
G | A | 155 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0001t0043g0123others(152): Show | 155 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(152): Show |
intron_variant | MODIFIER | c.1622-48712G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103000995 | ||||||
| chr10:103001078
|
G | A | 1 | a0001c0001t0012g0087 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1622-48629G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103001078 | ||||||
| chr10:103001088
|
A | G | 1 | a0001c0002t0004g0261 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1622-48619A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103001088 | ||||||
| chr10:103001193
|
T | C | 1 | a0001c0003t0001g0122 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1622-48514T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103001193 | ||||||
| chr10:103001223
|
C | G | 5 | a0001c0001t0005g0057a0001c0001t0008g0017a0001c0001t0008g0059others(2): Show | 5 | HG00099.hp1 HG01167.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1622-48484C>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103001223 | ||||||
| chr10:103001369
|
A | G | 1 | a0003c0008t0014g0074 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1622-48338A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103001369 | ||||||
| chr10:103001402
|
ACT | A | 3 | a0001c0002t0029g0204a0001c0002t0029g0207a0001c0002t0069g0206 | 3 | HG01070.hp2 HG01071.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.1622-48302_1622-48 others(8): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103001402 | |||||
| chr10:103001521
|
A | C | 1 | a0001c0001t0011g0011 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1622-48186A>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103001521 | ||||||
| chr10:103001576
|
C | T | 1 | a0001c0003t0051g0136 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1622-48131C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103001576 | ||||||
| chr10:103001802
|
G | A | 1 | a0001c0001t0020g0054 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1622-47905G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103001802 | ||||||
| chr10:103001849
|
CA | C | 70 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(67): Show | 70 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.1622-47853delA | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103001849 | |||||
| chr10:103002086
|
G | A | 1 | a0002c0004t0066g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1622-47621G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103002086 | ||||||
| chr10:103002173
|
A | G | 52 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(49): Show | 52 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.1622-47534A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103002173 | ||||||
| chr10:103002479
|
C | CT | 57 | a0001c0001t0043g0123a0001c0003t0001g0118a0001c0003t0001g0122others(54): Show | 57 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(54): Show |
intron_variant | MODIFIER | c.1622-47211dupT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103002479 | |||||
| chr10:103002479
|
C | CTT | 12 | a0001c0002t0003g0234a0001c0002t0003g0236a0001c0002t0006g0209others(9): Show | 12 | HG00609.hp2 HG00639.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1622-47212_1622-47 others(8): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103002479 | |||||
| chr10:103002479
|
C | CTTT | 81 | a0001c0001t0008g0250a0001c0002t0002g0245a0001c0002t0003g0225others(78): Show | 81 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.1622-47213_1622-47 others(9): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103002479 | |||||
| chr10:103002516
|
G | A | 1 | a0001c0003t0001g0140 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1622-47191G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103002516 | ||||||
| chr10:103002518
|
C | T | 3 | a0001c0001t0012g0080a0002c0004t0028g0196a0002c0004t0028g0215 | 3 | HG00544.hp1 HG02622.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1622-47189C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103002518 | ||||||
| chr10:103002712
|
C | T | 1 | a0001c0002t0003g0237 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1622-46995C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103002712 | ||||||
| chr10:103002778
|
T | C | 92 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(89): Show | 92 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.1622-46929T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103002778 | ||||||
| chr10:103002841
|
T | G | 6 | a0001c0002t0026g0267a0001c0002t0026g0269a0001c0002t0027g0266others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1622-46866T>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103002841 | ||||||
| chr10:103002852
|
C | T | 6 | a0001c0002t0026g0267a0001c0002t0026g0269a0001c0002t0027g0266others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1622-46855C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103002852 | ||||||
| chr10:103002865
|
A | G | 2 | a0001c0001t0012g0087a0001c0001t0018g0091 | 2 | HG00738.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.1622-46842A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103002865 | ||||||
| chr10:103002965
|
C | T | 10 | a0001c0001t0086g0113a0001c0005t0022g0186a0001c0005t0023g0189others(7): Show | 10 | HG01070.hp1 HG02135.hp2 HG03834.hp1 others(7): Show |
intron_variant | MODIFIER | c.1622-46742C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103002965 | ||||||
| chr10:103002966
|
G | A | 3 | a0001c0001t0005g0004a0001c0001t0005g0021a0001c0001t0005g0022 | 3 | HG01109.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1622-46741G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103002966 | ||||||
| chr10:103003102
|
T | C | 1 | a0001c0007t0007g0129 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1622-46605T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103003102 | ||||||
| chr10:103003116
|
C | CT | 259 | a0001c0001t0002g0019a0001c0001t0002g0028a0001c0001t0002g0062others(256): Show | 259 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(256): Show |
intron_variant | MODIFIER | c.1622-46576dupT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103003116 | |||||
| chr10:103003167
|
C | T | 3 | a0002c0004t0057g0202a0002c0004t0058g0203a0002c0004t0059g0217 | 3 | HG00735.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1622-46540C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103003167 | ||||||
| chr10:103003186
|
C | G | 1 | a0001c0001t0075g0038 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1622-46521C>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103003186 | ||||||
| chr10:103003215
|
C | T | 9 | a0001c0005t0022g0186a0001c0005t0023g0189a0001c0005t0023g0190others(6): Show | 9 | HG02135.hp2 HG03834.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1622-46492C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103003215 | ||||||
| chr10:103003216
|
G | A | 2 | a0001c0001t0040g0035a0001c0001t0087g0036 | 2 | HG02486.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1622-46491G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103003216 | ||||||
| chr10:103003256
|
C | T | 1 | a0001c0001t0037g0088 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1622-46451C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103003256 | ||||||
| chr10:103003547
|
G | T | 1 | a0001c0002t0062g0222 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1622-46160G>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103003547 | ||||||
| chr10:103003551
|
C | T | 70 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(67): Show | 70 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.1622-46156C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103003551 | ||||||
| chr10:103003560
|
A | G | 2 | a0001c0001t0042g0023a0001c0001t0042g0024 | 2 | HG01257.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.1622-46147A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103003560 | ||||||
| chr10:103003665
|
A | G | 3 | a0001c0001t0031g0039a0001c0001t0075g0038a0001c0001t0076g0040 | 3 | NA19054.hp2 NA19064.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1622-46042A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103003665 | ||||||
| chr10:103003681
|
G | A | 1 | a0001c0005t0050g0191 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1622-46026G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103003681 | ||||||
| chr10:103003985
|
A | AT | 48 | a0001c0001t0005g0004a0001c0001t0005g0021a0001c0001t0005g0022others(45): Show | 48 | HG00408.hp1 HG00558.hp2 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.1622-45696dupT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103003985 | |||||
| chr10:103003985
|
A | ATT | 74 | a0001c0001t0002g0066a0001c0001t0008g0250a0001c0001t0043g0123others(71): Show | 74 | HG00544.hp2 HG00609.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.1622-45697_1622-45 others(8): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103003985 | |||||
| chr10:103003985
|
A | ATTT | 23 | a0001c0002t0003g0227a0001c0002t0003g0229a0001c0002t0003g0231others(20): Show | 23 | HG00099.hp2 HG00639.hp2 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.1622-45698_1622-45 others(9): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103003985 | |||||
| chr10:103003985
|
A | ATTTT | 6 | a0001c0002t0003g0242a0001c0002t0071g0247a0001c0003t0001g0141others(3): Show | 6 | HG00733.hp1 HG02055.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.1622-45699_1622-45 others(10): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103003985 | |||||
| chr10:103003985
|
AT | A | 18 | a0001c0001t0005g0057a0001c0001t0012g0020a0001c0001t0020g0026others(15): Show | 18 | HG00738.hp1 HG01070.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.1622-45696delT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103003985 | |||||
| chr10:103003985
|
ATTTTTTT others(3): Show |
A | 3 | a0001c0001t0012g0097a0001c0001t0090g0094a0001c0003t0001g0170 | 3 | HG02083.hp2 NA18968.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1622-45705_1622-45 others(16): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103003985 | |||||
| chr10:103003985
|
ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0038g0095 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1622-45706_1622-45 others(17): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103003985 | |||||
| chr10:103004112
|
C | T | 2 | a0001c0005t0046g0188a0001c0005t0047g0187 | 2 | NA18989.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1622-45595C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103004112 | ||||||
| chr10:103004308
|
C | T | 70 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(67): Show | 70 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.1622-45399C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103004308 | ||||||
| chr10:103004391
|
A | G | 16 | a0001c0002t0006g0117a0001c0002t0006g0208a0001c0002t0006g0209others(13): Show | 16 | HG00408.hp1 HG00609.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.1622-45316A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103004391 | ||||||
| chr10:103004433
|
A | G | 4 | a0001c0002t0004g0262a0001c0002t0004g0263a0001c0002t0004g0264others(1): Show | 4 | HG02258.hp1 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1622-45274A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103004433 | ||||||
| chr10:103004514
|
T | C | 54 | a0001c0001t0043g0123a0001c0003t0001g0118a0001c0003t0001g0122others(51): Show | 54 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(51): Show |
intron_variant | MODIFIER | c.1622-45193T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103004514 | ||||||
| chr10:103004520
|
G | A | 3 | a0001c0001t0002g0069a0001c0001t0002g0100a0001c0001t0036g0099 | 3 | HG02683.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1622-45187G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103004520 | ||||||
| chr10:103004904
|
C | A | 92 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(89): Show | 92 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.1622-44803C>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103004904 | ||||||
| chr10:103005180
|
A | C | 52 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(49): Show | 52 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.1622-44527A>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103005180 | ||||||
| chr10:103005181
|
T | A | 52 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(49): Show | 52 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.1622-44526T>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103005181 | ||||||
| chr10:103005182
|
A | G | 52 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(49): Show | 52 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.1622-44525A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103005182 | ||||||
| chr10:103005192
|
A | G | 52 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(49): Show | 52 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.1622-44515A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103005192 | ||||||
| chr10:103005194
|
C | G | 52 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(49): Show | 52 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.1622-44513C>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103005194 | ||||||
| chr10:103005232
|
T | C | 146 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0001t0043g0123others(143): Show | 146 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(143): Show |
intron_variant | MODIFIER | c.1622-44475T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103005232 | ||||||
| chr10:103005477
|
C | T | 1 | a0001c0001t0039g0061 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1622-44230C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103005477 | ||||||
| chr10:103005645
|
G | A | 1 | a0001c0003t0010g0151 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1622-44062G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103005645 | ||||||
| chr10:103005663
|
T | G | 1 | a0001c0001t0014g0018 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1622-44044T>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103005663 | ||||||
| chr10:103005737
|
T | G | 54 | a0001c0001t0043g0123a0001c0003t0001g0118a0001c0003t0001g0122others(51): Show | 54 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(51): Show |
intron_variant | MODIFIER | c.1622-43970T>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103005737 | ||||||
| chr10:103005848
|
C | T | 22 | a0001c0002t0004g0176a0001c0002t0004g0180a0001c0002t0004g0255others(19): Show | 22 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.1622-43859C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103005848 | ||||||
| chr10:103006014
|
G | A | 1 | a0001c0003t0001g0140 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1622-43693G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103006014 | ||||||
| chr10:103006061
|
T | C | 1 | a0002c0004t0028g0215 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1622-43646T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103006061 | ||||||
| chr10:103006363
|
C | T | 54 | a0001c0001t0043g0123a0001c0003t0001g0118a0001c0003t0001g0122others(51): Show | 54 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(51): Show |
intron_variant | MODIFIER | c.1622-43344C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103006363 | ||||||
| chr10:103006364
|
G | A | 1 | a0001c0002t0026g0269 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1622-43343G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103006364 | ||||||
| chr10:103006452
|
C | T | 2 | a0001c0001t0008g0047a0001c0002t0004g0265 | 2 | HG01258.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1622-43255C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103006452 | ||||||
| chr10:103006512
|
A | G | 1 | a0001c0010t0067g0194 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1622-43195A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103006512 | ||||||
| chr10:103006829
|
C | T | 1 | a0001c0002t0062g0222 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1622-42878C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103006829 | ||||||
| chr10:103006853
|
A | C | 1 | a0001c0001t0002g0049 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1622-42854A>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103006853 | ||||||
| chr10:103006932
|
C | T | 1 | a0001c0002t0006g0208 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1622-42775C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103006932 | ||||||
| chr10:103007016
|
C | T | 1 | a0001c0001t0030g0044 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1622-42691C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103007016 | ||||||
| chr10:103007027
|
TC | T | 7 | a0001c0001t0030g0037a0001c0001t0030g0044a0001c0001t0031g0039others(4): Show | 7 | HG01106.hp1 NA18954.hp1 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.1622-42679delC | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103007027 | ||||||
| chr10:103007117
|
G | A | 70 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(67): Show | 70 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.1622-42590G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103007117 | ||||||
| chr10:103007134
|
C | T | 54 | a0001c0001t0043g0123a0001c0003t0001g0118a0001c0003t0001g0122others(51): Show | 54 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(51): Show |
intron_variant | MODIFIER | c.1622-42573C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103007134 | ||||||
| chr10:103007333
|
C | G | 1 | a0001c0002t0054g0193 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1622-42374C>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103007333 | ||||||
| chr10:103007428
|
T | G | 155 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0001t0043g0123others(152): Show | 155 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(152): Show |
intron_variant | MODIFIER | c.1622-42279T>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103007428 | ||||||
| chr10:103007502
|
C | T | 1 | a0001c0007t0077g0131 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1622-42205C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103007502 | ||||||
| chr10:103007607
|
A | G | 2 | a0002c0004t0057g0202a0002c0004t0058g0203 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1622-42100A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103007607 | ||||||
| chr10:103007950
|
G | T | 1 | a0002c0004t0055g0216 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1622-41757G>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103007950 | ||||||
| chr10:103007982
|
G | A | 1 | a0001c0002t0063g0270 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1622-41725G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103007982 | ||||||
| chr10:103008078
|
A | G | 1 | a0001c0002t0003g0242 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1622-41629A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103008078 | ||||||
| chr10:103008135
|
C | G | 22 | a0001c0002t0004g0176a0001c0002t0004g0180a0001c0002t0004g0255others(19): Show | 22 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.1622-41572C>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103008135 | ||||||
| chr10:103008186
|
A | T | 2 | a0001c0002t0064g0248a0001c0002t0065g0116 | 2 | HG02109.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1622-41521A>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103008186 | ||||||
| chr10:103008239
|
A | T | 2 | a0001c0002t0024g0172a0001c0002t0024g0181 | 2 | HG01952.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1622-41468A>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103008239 | ||||||
| chr10:103008501
|
C | CG | 9 | a0001c0005t0022g0186a0001c0005t0023g0189a0001c0005t0023g0190others(6): Show | 9 | HG02135.hp2 HG03834.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1622-41202dupG | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103008501 | |||||
| chr10:103008502
|
G | A | 1 | a0001c0002t0071g0247 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1622-41205G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103008502 | ||||||
| chr10:103008702
|
C | T | 1 | a0001c0002t0004g0180 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1622-41005C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103008702 | ||||||
| chr10:103008728
|
G | A | 1 | a0001c0002t0003g0239 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1622-40979G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103008728 | ||||||
| chr10:103008778
|
C | CA | 176 | a0001c0001t0002g0019a0001c0001t0002g0062a0001c0001t0002g0064others(173): Show | 176 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.1622-40909dupA | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103008778 | |||||
| chr10:103008778
|
C | CAA | 66 | a0001c0001t0002g0028a0001c0001t0002g0065a0001c0001t0002g0069others(63): Show | 66 | HG00544.hp2 HG00609.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.1622-40910_1622-40 others(8): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103008778 | |||||
| chr10:103008852
|
C | T | 1 | a0001c0002t0071g0247 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1622-40855C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103008852 | ||||||
| chr10:103008877
|
C | T | 70 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(67): Show | 70 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.1622-40830C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103008877 | ||||||
| chr10:103009142
|
G | A | 2 | a0001c0001t0019g0083a0001c0001t0019g0084 | 2 | HG02970.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1622-40565G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103009142 | ||||||
| chr10:103009144
|
C | T | 1 | a0002c0004t0028g0196 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1622-40563C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103009144 | ||||||
| chr10:103009165
|
A | G | 92 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(89): Show | 92 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.1622-40542A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103009165 | ||||||
| chr10:103009275
|
C | CA | 5 | a0001c0002t0026g0267a0001c0002t0026g0269a0001c0002t0027g0266others(2): Show | 5 | HG01884.hp2 HG02145.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1622-40424dupA | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103009275 | |||||
| chr10:103009341
|
T | G | 22 | a0001c0002t0004g0176a0001c0002t0004g0180a0001c0002t0004g0255others(19): Show | 22 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.1622-40366T>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103009341 | ||||||
| chr10:103009511
|
G | A | 22 | a0001c0002t0004g0176a0001c0002t0004g0180a0001c0002t0004g0255others(19): Show | 22 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.1622-40196G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103009511 | ||||||
| chr10:103009518
|
A | C | 54 | a0001c0001t0043g0123a0001c0003t0001g0118a0001c0003t0001g0122others(51): Show | 54 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(51): Show |
intron_variant | MODIFIER | c.1622-40189A>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103009518 | ||||||
| chr10:103009578
|
G | C | 155 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0001t0043g0123others(152): Show | 155 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(152): Show |
intron_variant | MODIFIER | c.1622-40129G>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103009578 | ||||||
| chr10:103009593
|
A | T | 2 | a0001c0005t0046g0188a0001c0005t0047g0187 | 2 | NA18989.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1622-40114A>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103009593 | ||||||
| chr10:103009606
|
G | A | 1 | a0001c0001t0002g0103 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1622-40101G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103009606 | ||||||
| chr10:103009635
|
T | A | 54 | a0001c0001t0043g0123a0001c0003t0001g0118a0001c0003t0001g0122others(51): Show | 54 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(51): Show |
intron_variant | MODIFIER | c.1622-40072T>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103009635 | ||||||
| chr10:103009674
|
C | CA | 18 | a0001c0001t0002g0028a0001c0001t0002g0065a0001c0001t0005g0003others(15): Show | 18 | HG00642.hp1 HG00733.hp1 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.1622-40009dupA | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103009674 | |||||
| chr10:103009674
|
C | CAAA | 48 | a0001c0001t0043g0123a0001c0003t0001g0118a0001c0003t0001g0122others(45): Show | 48 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(45): Show |
intron_variant | MODIFIER | c.1622-40011_1622-40 others(9): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103009674 | |||||
| chr10:103009674
|
CA | C | 58 | a0001c0001t0002g0068a0001c0001t0005g0108a0001c0001t0008g0250others(55): Show | 58 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.1622-40009delA | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103009674 | |||||
| chr10:103009698
|
A | G | 1 | a0001c0010t0067g0194 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1622-40009A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103009698 | ||||||
| chr10:103009706
|
G | GGGAGAAT | 63 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(60): Show | 63 | HG00408.hp1 HG00609.hp2 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.1622-39994_1622-39 others(13): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103009706 | |||||
| chr10:103009706
|
G | T | 5 | a0001c0002t0003g0227a0001c0002t0003g0232a0001c0002t0009g0246others(2): Show | 5 | HG00609.hp1 NA18950.hp2 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.1622-40001G>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103009706 | ||||||
| chr10:103009828
|
T | G | 2 | a0001c0001t0096g0052a0001c0001t0097g0014 | 2 | HG00558.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.1622-39879T>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103009828 | ||||||
| chr10:103009911
|
G | A | 1 | a0001c0001t0005g0108 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1622-39796G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103009911 | ||||||
| chr10:103009939
|
CT | C | 10 | a0001c0001t0005g0022a0001c0005t0022g0186a0001c0005t0023g0189others(7): Show | 10 | HG02135.hp2 HG02976.hp1 HG03834.hp1 others(7): Show |
intron_variant | MODIFIER | c.1622-39755delT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103009939 | |||||
| chr10:103009939
|
CTT | C | 93 | a0001c0001t0008g0090a0001c0001t0008g0250a0001c0001t0008g0252others(90): Show | 93 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.1622-39756_1622-39 others(8): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103009939 | |||||
| chr10:103009952
|
T | C | 54 | a0001c0001t0043g0123a0001c0003t0001g0118a0001c0003t0001g0122others(51): Show | 54 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(51): Show |
intron_variant | MODIFIER | c.1622-39755T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103009952 | ||||||
| chr10:103010229
|
C | CT | 16 | a0001c0002t0006g0117a0001c0002t0006g0208a0001c0002t0006g0209others(13): Show | 16 | HG00408.hp1 HG00609.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.1622-39466dupT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103010229 | |||||
| chr10:103010309
|
C | T | 1 | a0001c0003t0033g0164 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1622-39398C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103010309 | ||||||
| chr10:103010599
|
A | G | 1 | a0001c0003t0001g0142 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1622-39108A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103010599 | ||||||
| chr10:103010667
|
C | T | 12 | a0001c0001t0012g0041a0001c0001t0019g0001a0001c0001t0030g0037others(9): Show | 12 | HG00408.hp2 HG00642.hp1 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.1622-39040C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103010667 | ||||||
| chr10:103010743
|
G | A | 2 | a0001c0001t0075g0038a0001c0001t0076g0040 | 2 | NA19054.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1622-38964G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103010743 | ||||||
| chr10:103010758
|
G | A | 1 | a0001c0003t0001g0127 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1622-38949G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103010758 | ||||||
| chr10:103010801
|
C | T | 2 | a0001c0001t0019g0083a0001c0001t0019g0084 | 2 | HG02970.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1622-38906C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103010801 | ||||||
| chr10:103010945
|
T | C | 268 | a0001c0001t0002g0019a0001c0001t0002g0028a0001c0001t0002g0062others(265): Show | 268 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.1622-38762T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103010945 | ||||||
| chr10:103011008
|
T | C | 1 | a0002c0004t0066g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1622-38699T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103011008 | ||||||
| chr10:103011086
|
C | A | 2 | a0001c0001t0043g0076a0001c0003t0001g0106 | 2 | NA19011.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1622-38621C>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103011086 | ||||||
| chr10:103011272
|
A | G | 155 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0001t0043g0123others(152): Show | 155 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(152): Show |
intron_variant | MODIFIER | c.1622-38435A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103011272 | ||||||
| chr10:103011273
|
T | G | 3 | a0001c0003t0001g0160a0001c0003t0001g0161a0001c0003t0001g0162 | 3 | NA18971.hp1 NA18982.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1622-38434T>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103011273 | ||||||
| chr10:103011434
|
C | T | 1 | a0001c0002t0027g0266 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1622-38273C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103011434 | ||||||
| chr10:103011454
|
A | AAAAAT | 155 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0001t0043g0123others(152): Show | 155 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(152): Show |
intron_variant | MODIFIER | c.1622-38248_1622-38 others(11): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103011454 | |||||
| chr10:103011646
|
C | CTG | 62 | a0001c0001t0005g0003a0001c0001t0005g0007a0001c0001t0005g0008others(59): Show | 62 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.1622-38023_1622-38 others(8): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103011646 | |||||
| chr10:103011646
|
C | CTGTG | 36 | a0001c0001t0005g0021a0001c0001t0011g0013a0001c0001t0020g0054others(33): Show | 36 | HG00558.hp1 HG00609.hp2 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.1622-38025_1622-38 others(10): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103011646 | |||||
| chr10:103011646
|
C | CTGTGTG | 32 | a0001c0001t0002g0019a0001c0001t0002g0064a0001c0001t0002g0065others(29): Show | 32 | HG00597.hp1 HG00621.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.1622-38027_1622-38 others(12): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103011646 | |||||
| chr10:103011646
|
C | CTGTGTGT others(1): Show |
3 | a0001c0001t0005g0006a0001c0002t0003g0233a0001c0002t0009g0238 | 3 | HG00621.hp2 HG01081.hp2 HG02027.hp2 |
intron_variant | MODIFIER | c.1622-38029_1622-38 others(14): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103011646 | |||||
| chr10:103011646
|
C | CTGTGTGT others(3): Show |
5 | a0001c0002t0054g0193a0001c0002t0062g0222a0002c0004t0025g0195others(2): Show | 5 | HG01109.hp1 HG02055.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1622-38031_1622-38 others(16): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103011646 | |||||
| chr10:103011646
|
C | CTGTGTGT others(5): Show |
1 | a0001c0002t0004g0262 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1622-38033_1622-38 others(18): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103011646 | |||||
| chr10:103011646
|
CTG | C | 7 | a0001c0001t0039g0061a0001c0001t0040g0035a0001c0002t0009g0224others(4): Show | 7 | HG00735.hp2 HG02040.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1622-38023_1622-38 others(8): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103011646 | |||||
| chr10:103011646
|
CTGTGTG | C | 3 | a0001c0002t0071g0247a0001c0003t0001g0168a0001c0003t0010g0148 | 3 | HG02004.hp1 HG03491.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1622-38027_1622-38 others(12): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103011646 | |||||
| chr10:103011682
|
G | GTGTGTAT others(3): Show |
1 | a0002c0004t0055g0216 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1622-38022_1622-38 others(16): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103011682 | |||||
| chr10:103011682
|
G | GTGTGTGT others(1): Show |
7 | a0002c0004t0028g0196a0002c0004t0028g0215a0002c0004t0057g0202others(4): Show | 7 | HG00735.hp1 HG01516.hp2 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.1622-38022_1622-38 others(14): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103011682 | |||||
| chr10:103011682
|
G | GTGTGTGT others(5): Show |
1 | a0002c0004t0066g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1622-38022_1622-38 others(18): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103011682 | |||||
| chr10:103011693
|
A | AT | 12 | a0002c0004t0003g0201a0002c0004t0025g0199a0002c0004t0028g0196others(9): Show | 12 | HG00733.hp1 HG00735.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1622-38002dupT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103011693 | |||||
| chr10:103011750
|
G | A | 3 | a0002c0004t0025g0195a0002c0004t0025g0199a0002c0004t0056g0200 | 3 | HG01109.hp1 HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1622-37957G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103011750 | ||||||
| chr10:103011773
|
C | T | 1 | a0001c0007t0077g0131 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1622-37934C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103011773 | ||||||
| chr10:103011790
|
T | A | 1 | a0001c0005t0022g0186 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1622-37917T>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103011790 | ||||||
| chr10:103011811
|
A | G | 9 | a0001c0005t0022g0186a0001c0005t0023g0189a0001c0005t0023g0190others(6): Show | 9 | HG02135.hp2 HG03834.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1622-37896A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103011811 | ||||||
| chr10:103011863
|
T | G | 4 | a0001c0002t0004g0262a0001c0002t0004g0263a0001c0002t0004g0264others(1): Show | 4 | HG02258.hp1 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1622-37844T>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103011863 | ||||||
| chr10:103012069
|
A | G | 9 | a0001c0005t0022g0186a0001c0005t0023g0189a0001c0005t0023g0190others(6): Show | 9 | HG02135.hp2 HG03834.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1622-37638A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103012069 | ||||||
| chr10:103012165
|
A | G | 155 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0001t0043g0123others(152): Show | 155 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(152): Show |
intron_variant | MODIFIER | c.1622-37542A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103012165 | ||||||
| chr10:103012411
|
C | T | 1 | a0001c0002t0054g0193 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1622-37296C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103012411 | ||||||
| chr10:103012507
|
G | T | 1 | a0001c0003t0007g0138 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1622-37200G>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103012507 | ||||||
| chr10:103012596
|
C | T | 2 | a0001c0001t0040g0035a0001c0001t0087g0036 | 2 | HG02486.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1622-37111C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103012596 | ||||||
| chr10:103012639
|
C | CT | 76 | a0001c0001t0002g0065a0001c0001t0008g0250a0001c0001t0008g0252others(73): Show | 76 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.1622-37046dupT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103012639 | |||||
| chr10:103012639
|
C | CTT | 10 | a0001c0002t0009g0224a0001c0002t0026g0267a0001c0002t0026g0269others(7): Show | 10 | HG00735.hp1 HG00735.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1622-37047_1622-37 others(8): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103012639 | |||||
| chr10:103012639
|
CT | C | 17 | a0001c0001t0002g0028a0001c0001t0005g0022a0001c0001t0021g0109others(14): Show | 17 | HG01070.hp1 HG01106.hp1 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.1622-37046delT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103012639 | |||||
| chr10:103012828
|
C | T | 1 | a0001c0001t0005g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1622-36879C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103012828 | ||||||
| chr10:103012830
|
A | G | 14 | a0001c0002t0002g0245a0001c0002t0003g0227a0001c0002t0003g0229others(11): Show | 14 | HG00609.hp1 HG00621.hp2 HG00673.hp2 others(11): Show |
intron_variant | MODIFIER | c.1622-36877A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103012830 | ||||||
| chr10:103012942
|
A | G | 70 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(67): Show | 70 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.1622-36765A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103012942 | ||||||
| chr10:103013032
|
A | G | 1 | a0001c0002t0004g0176 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1622-36675A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103013032 | ||||||
| chr10:103013227
|
T | G | 92 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(89): Show | 92 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.1622-36480T>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103013227 | ||||||
| chr10:103013607
|
C | T | 54 | a0001c0001t0043g0123a0001c0003t0001g0118a0001c0003t0001g0122others(51): Show | 54 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(51): Show |
intron_variant | MODIFIER | c.1622-36100C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103013607 | ||||||
| chr10:103014196
|
A | G | 1 | a0002c0004t0055g0216 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1622-35511A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103014196 | ||||||
| chr10:103014293
|
A | G | 22 | a0001c0002t0004g0176a0001c0002t0004g0180a0001c0002t0004g0255others(19): Show | 22 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.1622-35414A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103014293 | ||||||
| chr10:103014386
|
C | A | 2 | a0001c0002t0064g0248a0001c0002t0065g0116 | 2 | HG02109.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1622-35321C>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103014386 | ||||||
| chr10:103014825
|
A | G | 1 | a0001c0001t0076g0040 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1622-34882A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103014825 | ||||||
| chr10:103014845
|
T | C | 1 | a0001c0010t0067g0194 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1622-34862T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103014845 | ||||||
| chr10:103014892
|
TA | T | 24 | a0001c0001t0002g0100a0001c0002t0004g0176a0001c0002t0004g0180others(21): Show | 24 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.1622-34801delA | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103014892 | |||||
| chr10:103015103
|
G | T | 5 | a0001c0003t0001g0122a0001c0003t0001g0124a0001c0003t0032g0120others(2): Show | 5 | NA18962.hp2 NA18990.hp2 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1622-34604G>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103015103 | ||||||
| chr10:103015118
|
A | G | 1 | a0001c0001t0100g0085 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1622-34589A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103015118 | ||||||
| chr10:103015388
|
T | C | 1 | a0002c0004t0055g0216 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1622-34319T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103015388 | ||||||
| chr10:103015447
|
T | C | 1 | a0001c0002t0054g0193 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1622-34260T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103015447 | ||||||
| chr10:103015474
|
C | CTTT | 155 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0001t0043g0123others(152): Show | 155 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(152): Show |
intron_variant | MODIFIER | c.1622-34231_1622-34 others(9): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103015474 | |||||
| chr10:103015505
|
TA | T | 9 | a0001c0005t0022g0186a0001c0005t0023g0189a0001c0005t0023g0190others(6): Show | 9 | HG02135.hp2 HG03834.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1622-34200delA | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103015505 | |||||
| chr10:103015578
|
C | G | 155 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0001t0043g0123others(152): Show | 155 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(152): Show |
intron_variant | MODIFIER | c.1622-34129C>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103015578 | ||||||
| chr10:103015611
|
T | C | 1 | a0001c0001t0011g0114 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1622-34096T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103015611 | ||||||
| chr10:103015657
|
C | T | 5 | a0001c0001t0002g0028a0001c0001t0002g0069a0001c0001t0002g0100others(2): Show | 5 | HG02683.hp1 HG03491.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.1622-34050C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103015657 | ||||||
| chr10:103015726
|
G | A | 82 | a0001c0001t0005g0002a0001c0001t0005g0003a0001c0001t0005g0004others(79): Show | 82 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.1622-33981G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103015726 | ||||||
| chr10:103015899
|
C | G | 1 | a0002c0004t0028g0215 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1622-33808C>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103015899 | ||||||
| chr10:103015942
|
C | T | 2 | a0001c0003t0001g0146a0001c0003t0001g0147 | 2 | NA18992.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1622-33765C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103015942 | ||||||
| chr10:103016151
|
G | A | 155 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0001t0043g0123others(152): Show | 155 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(152): Show |
intron_variant | MODIFIER | c.1622-33556G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103016151 | ||||||
| chr10:103016325
|
A | C | 2 | a0001c0001t0042g0023a0001c0001t0042g0024 | 2 | HG01257.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.1622-33382A>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103016325 | ||||||
| chr10:103016358
|
T | C | 1 | a0001c0002t0004g0255 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1622-33349T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103016358 | ||||||
| chr10:103016448
|
C | T | 54 | a0001c0001t0043g0123a0001c0003t0001g0118a0001c0003t0001g0122others(51): Show | 54 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(51): Show |
intron_variant | MODIFIER | c.1622-33259C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103016448 | ||||||
| chr10:103016508
|
C | T | 1 | a0001c0002t0062g0222 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1622-33199C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103016508 | ||||||
| chr10:103016634
|
G | A | 22 | a0001c0002t0004g0176a0001c0002t0004g0180a0001c0002t0004g0255others(19): Show | 22 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.1622-33073G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103016634 | ||||||
| chr10:103016718
|
G | A | 92 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(89): Show | 92 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.1622-32989G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103016718 | ||||||
| chr10:103016770
|
G | A | 53 | a0001c0001t0043g0123a0001c0003t0001g0118a0001c0003t0001g0122others(50): Show | 53 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(50): Show |
intron_variant | MODIFIER | c.1622-32937G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103016770 | ||||||
| chr10:103016978
|
CTTTTTT | C | 6 | a0001c0001t0005g0002a0001c0001t0005g0007a0001c0001t0005g0008others(3): Show | 6 | HG01884.hp1 HG02280.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1622-32721_1622-32 others(12): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103016978 | |||||
| chr10:103016986
|
T | C | 1 | a0001c0001t0039g0061 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1622-32721T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103016986 | ||||||
| chr10:103017384
|
G | A | 1 | a0002c0004t0055g0216 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1622-32323G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103017384 | ||||||
| chr10:103017538
|
A | G | 9 | a0001c0005t0022g0186a0001c0005t0023g0189a0001c0005t0023g0190others(6): Show | 9 | HG02135.hp2 HG03834.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1622-32169A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103017538 | ||||||
| chr10:103017675
|
G | C | 2 | a0002c0004t0028g0196a0002c0004t0028g0215 | 2 | HG02622.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1622-32032G>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103017675 | ||||||
| chr10:103017703
|
C | A | 1 | a0001c0003t0001g0162 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1622-32004C>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103017703 | ||||||
| chr10:103017963
|
C | CA | 20 | a0001c0001t0005g0003a0001c0001t0008g0017a0001c0001t0012g0041others(17): Show | 20 | HG00408.hp2 HG00544.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.1622-31726dupA | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103017963 | |||||
| chr10:103017963
|
C | CAAA | 15 | a0001c0002t0006g0117a0001c0002t0006g0208a0001c0002t0006g0209others(12): Show | 15 | HG00408.hp1 HG00609.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.1622-31728_1622-31 others(9): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103017963 | |||||
| chr10:103017963
|
C | CAAAAAAA others(3): Show |
2 | a0001c0002t0004g0265a0001c0002t0054g0193 | 2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1622-31735_1622-31 others(16): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103017963 | |||||
| chr10:103017963
|
C | CAAAAAAA others(4): Show |
15 | a0001c0002t0004g0176a0001c0002t0004g0180a0001c0002t0004g0255others(12): Show | 15 | HG00673.hp1 HG00738.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1622-31736_1622-31 others(17): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103017963 | |||||
| chr10:103017963
|
C | CAAAAAAA others(5): Show |
11 | a0001c0002t0004g0263a0001c0002t0024g0172a0001c0002t0024g0181others(8): Show | 11 | HG00597.hp2 HG00639.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.1622-31737_1622-31 others(18): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103017963 | |||||
| chr10:103017963
|
C | CAAAAAAA others(6): Show |
1 | a0001c0010t0067g0194 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1622-31738_1622-31 others(19): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103017963 | |||||
| chr10:103017963
|
C | CAAAAAAA others(7): Show |
1 | a0001c0002t0063g0270 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1622-31739_1622-31 others(20): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103017963 | |||||
| chr10:103017963
|
C | CAAAAAAA others(8): Show |
5 | a0001c0001t0008g0250a0001c0002t0003g0227a0001c0002t0003g0232others(2): Show | 5 | HG01981.hp1 HG02027.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1622-31740_1622-31 others(21): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103017963 | |||||
| chr10:103017963
|
C | CAAAAAAA others(9): Show |
22 | a0001c0001t0008g0252a0001c0002t0002g0245a0001c0002t0003g0223others(19): Show | 22 | HG00609.hp1 HG00621.hp2 HG00673.hp2 others(19): Show |
intron_variant | MODIFIER | c.1622-31741_1622-31 others(22): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103017963 | |||||
| chr10:103017963
|
C | CAAAAAAA others(10): Show |
4 | a0001c0002t0009g0241a0001c0002t0044g0243a0001c0002t0108g0249others(1): Show | 4 | HG00639.hp2 HG00642.hp2 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.1622-31742_1622-31 others(23): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103017963 | |||||
| chr10:103017963
|
C | CAAAAAAA others(11): Show |
6 | a0001c0002t0003g0237a0001c0002t0003g0239a0001c0002t0003g0251others(3): Show | 6 | HG02055.hp2 HG02486.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1622-31743_1622-31 others(24): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103017963 | |||||
| chr10:103017963
|
C | CAAAAAAA others(12): Show |
2 | a0002c0004t0055g0216a0002c0004t0056g0200 | 2 | HG02257.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1622-31726_1622-31 others(25): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103017963 | |||||
| chr10:103017963
|
CA | C | 76 | a0001c0001t0002g0064a0001c0001t0005g0096a0001c0001t0012g0097others(73): Show | 76 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.1622-31726delA | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103017963 | |||||
| chr10:103018115
|
C | A | 70 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(67): Show | 70 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.1622-31592C>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103018115 | ||||||
| chr10:103018209
|
C | T | 1 | a0001c0001t0073g0025 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1622-31498C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103018209 | ||||||
| chr10:103018215
|
G | A | 1 | a0001c0001t0035g0111 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1622-31492G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103018215 | ||||||
| chr10:103018510
|
C | G | 92 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(89): Show | 92 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.1622-31197C>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103018510 | ||||||
| chr10:103018686
|
C | CT | 6 | a0001c0001t0002g0069a0001c0001t0005g0006a0001c0001t0012g0097others(3): Show | 6 | HG01081.hp2 HG01952.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1622-31000dupT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103018686 | |||||
| chr10:103018686
|
C | CTTTTT | 11 | a0001c0002t0004g0261a0001c0002t0024g0172a0001c0002t0024g0181others(8): Show | 11 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(8): Show |
intron_variant | MODIFIER | c.1622-31004_1622-31 others(11): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103018686 | |||||
| chr10:103018686
|
C | CTTTTTT | 27 | a0001c0002t0004g0176a0001c0002t0004g0180a0001c0002t0004g0262others(24): Show | 27 | HG00733.hp1 HG00735.hp1 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.1622-31005_1622-31 others(12): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103018686 | |||||
| chr10:103018686
|
C | CTTTTTTT | 21 | a0001c0002t0004g0256a0001c0002t0004g0258a0001c0002t0006g0117others(18): Show | 21 | HG00408.hp1 HG00609.hp2 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.1622-31006_1622-31 others(13): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103018686 | |||||
| chr10:103018686
|
C | CTTTTTTT others(1): Show |
6 | a0001c0002t0004g0255a0001c0005t0022g0186a0001c0005t0023g0189others(3): Show | 6 | HG03098.hp1 HG03834.hp1 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.1622-31007_1622-31 others(14): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103018686 | |||||
| chr10:103018686
|
CTTTT | C | 7 | a0001c0003t0001g0157a0001c0003t0080g0158a0001c0005t0046g0188others(4): Show | 7 | HG02071.hp2 HG02074.hp1 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.1622-31003_1622-31 others(10): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103018686 | |||||
| chr10:103018686
|
CTTTTT | C | 49 | a0001c0001t0043g0123a0001c0003t0001g0118a0001c0003t0001g0122others(46): Show | 49 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(46): Show |
intron_variant | MODIFIER | c.1622-31004_1622-31 others(11): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103018686 | |||||
| chr10:103018686
|
CTTTTTT | C | 30 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(27): Show | 30 | HG00609.hp1 HG00621.hp2 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.1622-31005_1622-31 others(12): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103018686 | |||||
| chr10:103018849
|
G | A | 1 | a0001c0002t0054g0193 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1622-30858G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103018849 | ||||||
| chr10:103018999
|
G | A | 22 | a0001c0002t0004g0176a0001c0002t0004g0180a0001c0002t0004g0255others(19): Show | 22 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.1622-30708G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103018999 | ||||||
| chr10:103019006
|
G | A | 1 | a0001c0001t0042g0023 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1622-30701G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103019006 | ||||||
| chr10:103019055
|
C | T | 54 | a0001c0001t0043g0123a0001c0003t0001g0118a0001c0003t0001g0122others(51): Show | 54 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(51): Show |
intron_variant | MODIFIER | c.1622-30652C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103019055 | ||||||
| chr10:103019062
|
G | C | 2 | a0001c0001t0005g0057a0001c0001t0008g0060 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1622-30645G>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103019062 | ||||||
| chr10:103019085
|
C | T | 2 | a0001c0002t0044g0230a0001c0002t0044g0243 | 2 | HG00642.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.1622-30622C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103019085 | ||||||
| chr10:103019086
|
G | A | 3 | a0001c0001t0005g0008a0001c0001t0011g0009a0001c0001t0011g0013 | 3 | HG02280.hp2 HG02717.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1622-30621G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103019086 | ||||||
| chr10:103019221
|
A | G | 14 | a0001c0001t0005g0096a0001c0001t0012g0097a0001c0001t0037g0088others(11): Show | 14 | HG00558.hp2 HG02027.hp1 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.1622-30486A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103019221 | ||||||
| chr10:103019245
|
G | C | 1 | a0001c0001t0002g0028 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1622-30462G>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103019245 | ||||||
| chr10:103019268
|
C | CA | 8 | a0001c0001t0008g0047a0001c0002t0006g0221a0001c0002t0015g0220others(5): Show | 8 | HG01258.hp2 HG02280.hp1 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.1622-30422dupA | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103019268 | |||||
| chr10:103019268
|
C | CAA | 6 | a0001c0002t0026g0267a0001c0002t0026g0269a0001c0002t0027g0266others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1622-30423_1622-30 others(8): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103019268 | |||||
| chr10:103019443
|
C | G | 2 | a0002c0004t0003g0201a0002c0004t0059g0217 | 2 | HG00733.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.1622-30264C>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103019443 | ||||||
| chr10:103019880
|
T | G | 1 | a0001c0002t0003g0223 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1622-29827T>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103019880 | ||||||
| chr10:103019893
|
A | T | 1 | a0001c0002t0054g0193 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1622-29814A>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103019893 | ||||||
| chr10:103020028
|
C | T | 1 | a0001c0002t0062g0222 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1622-29679C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103020028 | ||||||
| chr10:103020040
|
T | C | 1 | a0001c0002t0003g0242 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1622-29667T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103020040 | ||||||
| chr10:103020281
|
G | A | 54 | a0001c0001t0043g0123a0001c0003t0001g0118a0001c0003t0001g0122others(51): Show | 54 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(51): Show |
intron_variant | MODIFIER | c.1622-29426G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103020281 | ||||||
| chr10:103020655
|
T | C | 3 | a0001c0003t0001g0160a0001c0003t0001g0161a0001c0003t0001g0162 | 3 | NA18971.hp1 NA18982.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1622-29052T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103020655 | ||||||
| chr10:103020790
|
AAGGGCGC others(3): Show |
A | 92 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(89): Show | 92 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.1622-28912_1622-28 others(16): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103020790 | |||||
| chr10:103020807
|
T | C | 92 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(89): Show | 92 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.1622-28900T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103020807 | ||||||
| chr10:103020943
|
T | A | 9 | a0001c0005t0022g0186a0001c0005t0023g0189a0001c0005t0023g0190others(6): Show | 9 | HG02135.hp2 HG03834.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1622-28764T>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103020943 | ||||||
| chr10:103021031
|
A | G | 1 | a0001c0006t0013g0179 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1622-28676A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103021031 | ||||||
| chr10:103021122
|
C | T | 2 | a0001c0001t0012g0087a0001c0001t0018g0091 | 2 | HG00738.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.1622-28585C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103021122 | ||||||
| chr10:103021134
|
C | T | 1 | a0001c0001t0011g0114 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1622-28573C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103021134 | ||||||
| chr10:103021268
|
G | A | 1 | a0001c0005t0022g0186 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1622-28439G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103021268 | ||||||
| chr10:103021538
|
T | C | 1 | a0001c0001t0008g0047 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1622-28169T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103021538 | ||||||
| chr10:103021544
|
G | A | 6 | a0002c0004t0003g0201a0002c0004t0057g0202a0002c0004t0058g0203others(3): Show | 6 | HG00733.hp1 HG00735.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1622-28163G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103021544 | ||||||
| chr10:103021634
|
T | C | 1 | a0001c0006t0004g0175 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1622-28073T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103021634 | ||||||
| chr10:103021761
|
C | CAGA | 92 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(89): Show | 92 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.1622-27944_1622-27 others(9): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103021761 | |||||
| chr10:103021835
|
T | C | 2 | a0001c0001t0012g0020a0001c0001t0072g0115 | 2 | HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1622-27872T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103021835 | ||||||
| chr10:103021865
|
G | A | 2 | a0001c0001t0083g0048a0001c0001t0089g0092 | 2 | HG02071.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.1622-27842G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103021865 | ||||||
| chr10:103021980
|
T | G | 1 | a0001c0002t0003g0223 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1622-27727T>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103021980 | ||||||
| chr10:103022432
|
A | G | 6 | a0001c0002t0026g0267a0001c0002t0026g0269a0001c0002t0027g0266others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1622-27275A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103022432 | ||||||
| chr10:103022543
|
C | T | 5 | a0001c0002t0026g0267a0001c0002t0026g0269a0001c0002t0027g0266others(2): Show | 5 | HG01884.hp2 HG02145.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1622-27164C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103022543 | ||||||
| chr10:103022619
|
C | G | 1 | a0001c0002t0054g0193 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1622-27088C>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103022619 | ||||||
| chr10:103022686
|
A | G | 5 | a0001c0002t0026g0267a0001c0002t0026g0269a0001c0002t0027g0266others(2): Show | 5 | HG01884.hp2 HG02145.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1622-27021A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103022686 | ||||||
| chr10:103022800
|
T | C | 92 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(89): Show | 92 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.1622-26907T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103022800 | ||||||
| chr10:103022802
|
G | A | 1 | a0001c0002t0015g0205 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1622-26905G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103022802 | ||||||
| chr10:103022844
|
G | A | 7 | a0001c0001t0037g0088a0001c0001t0037g0089a0001c0001t0085g0107others(4): Show | 7 | HG00558.hp2 HG02074.hp2 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.1622-26863G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103022844 | ||||||
| chr10:103022910
|
A | AT | 37 | a0001c0001t0005g0057a0001c0001t0005g0096a0001c0001t0005g0108others(34): Show | 37 | HG00099.hp1 HG00544.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.1622-26788dupT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103022910 | |||||
| chr10:103023029
|
A | G | 1 | a0001c0001t0012g0080 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1622-26678A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103023029 | ||||||
| chr10:103023087
|
T | A | 1 | a0001c0002t0062g0222 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1622-26620T>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103023087 | ||||||
| chr10:103023096
|
C | G | 155 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0001t0043g0123others(152): Show | 155 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(152): Show |
intron_variant | MODIFIER | c.1622-26611C>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103023096 | ||||||
| chr10:103023304
|
C | T | 1 | a0001c0001t0002g0028 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1622-26403C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103023304 | ||||||
| chr10:103023509
|
T | C | 1 | a0002c0004t0055g0216 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1622-26198T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103023509 | ||||||
| chr10:103023580
|
C | G | 1 | a0001c0001t0008g0090 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1622-26127C>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103023580 | ||||||
| chr10:103023646
|
A | T | 1 | a0002c0004t0066g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1622-26061A>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103023646 | ||||||
| chr10:103023702
|
C | T | 1 | a0001c0003t0001g0106 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1622-26005C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103023702 | ||||||
| chr10:103023848
|
C | A | 2 | a0001c0003t0010g0152a0001c0003t0081g0165 | 2 | HG02735.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1622-25859C>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103023848 | ||||||
| chr10:103023898
|
G | A | 1 | a0001c0002t0009g0254 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1622-25809G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103023898 | ||||||
| chr10:103023935
|
A | G | 1 | a0001c0001t0030g0037 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1622-25772A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103023935 | ||||||
| chr10:103024072
|
T | C | 13 | a0002c0004t0003g0201a0002c0004t0025g0195a0002c0004t0025g0199others(10): Show | 13 | HG00733.hp1 HG00735.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1622-25635T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103024072 | ||||||
| chr10:103024076
|
T | C | 92 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(89): Show | 92 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.1622-25631T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103024076 | ||||||
| chr10:103024285
|
A | G | 9 | a0001c0005t0022g0186a0001c0005t0023g0189a0001c0005t0023g0190others(6): Show | 9 | HG02135.hp2 HG03834.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1622-25422A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103024285 | ||||||
| chr10:103024626
|
G | C | 1 | a0001c0007t0077g0131 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1622-25081G>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103024626 | ||||||
| chr10:103024767
|
C | T | 1 | a0001c0002t0107g0235 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1622-24940C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103024767 | ||||||
| chr10:103025037
|
A | G | 2 | a0001c0001t0012g0087a0001c0001t0018g0091 | 2 | HG00738.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.1622-24670A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103025037 | ||||||
| chr10:103025122
|
C | T | 1 | a0001c0003t0001g0167 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1622-24585C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103025122 | ||||||
| chr10:103025161
|
C | T | 54 | a0001c0001t0043g0123a0001c0003t0001g0118a0001c0003t0001g0122others(51): Show | 54 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(51): Show |
intron_variant | MODIFIER | c.1622-24546C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103025161 | ||||||
| chr10:103025287
|
C | T | 1 | a0001c0003t0001g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1622-24420C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103025287 | ||||||
| chr10:103025381
|
G | A | 1 | a0001c0001t0072g0115 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1622-24326G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103025381 | ||||||
| chr10:103025909
|
T | G | 6 | a0001c0002t0026g0267a0001c0002t0026g0269a0001c0002t0027g0266others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1622-23798T>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103025909 | ||||||
| chr10:103025980
|
T | C | 16 | a0001c0002t0006g0117a0001c0002t0006g0208a0001c0002t0006g0209others(13): Show | 16 | HG00408.hp1 HG00609.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.1622-23727T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103025980 | ||||||
| chr10:103026396
|
T | A | 1 | a0001c0003t0001g0140 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1622-23311T>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103026396 | ||||||
| chr10:103026556
|
G | A | 92 | a0001c0001t0008g0250a0001c0001t0008g0252a0001c0002t0002g0245others(89): Show | 92 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.1622-23151G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103026556 | ||||||
| chr10:103026601
|
C | CA | 14 | a0001c0001t0002g0066a0001c0001t0005g0003a0001c0001t0008g0252others(11): Show | 14 | HG00408.hp1 HG00642.hp2 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.1622-23082dupA | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103026601 | |||||
| chr10:103026601
|
C | CAA | 11 | a0001c0001t0020g0026a0001c0001t0020g0027a0001c0001t0020g0054others(8): Show | 11 | HG00558.hp1 HG01257.hp2 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.1622-23083_1622-23 others(8): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103026601 | |||||
| chr10:103026601
|
CA | C | 31 | a0001c0001t0002g0019a0001c0001t0012g0020a0001c0001t0018g0104others(28): Show | 31 | HG00673.hp2 HG01070.hp2 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.1622-23082delA | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103026601 | |||||
| chr10:103026601
|
CAA | C | 70 | a0001c0001t0043g0123a0001c0002t0004g0180a0001c0002t0004g0261others(67): Show | 70 | HG00099.hp2 HG00544.hp2 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.1622-23083_1622-23 others(8): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103026601 | |||||
| chr10:103026601
|
CAAA | C | 8 | a0001c0003t0007g0125a0001c0003t0007g0126a0001c0003t0007g0130others(5): Show | 8 | HG01978.hp1 HG02071.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1622-23084_1622-23 others(9): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103026601 | |||||
| chr10:103026736
|
T | C | 1 | a0001c0003t0016g0145 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1622-22971T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103026736 | ||||||
| chr10:103026774
|
G | A | 1 | a0001c0003t0001g0156 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1622-22933G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103026774 | ||||||
| chr10:103027094
|
A | G | 1 | a0001c0001t0014g0042 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1622-22613A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103027094 | ||||||
| chr10:103027107
|
C | T | 3 | a0001c0001t0014g0018a0001c0001t0014g0042a0001c0001t0014g0045 | 3 | HG01952.hp2 HG01981.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.1622-22600C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103027107 | ||||||
| chr10:103027262
|
C | A | 87 | a0001c0001t0005g0096a0001c0001t0008g0250a0001c0001t0008g0252others(84): Show | 87 | HG00408.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1622-22445C>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103027262 | ||||||
| chr10:103027296
|
G | A | 1 | a0001c0002t0071g0247 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1622-22411G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103027296 | ||||||
| chr10:103027734
|
A | T | 1 | a0001c0010t0067g0194 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1622-21973A>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103027734 | ||||||
| chr10:103027837
|
G | A | 1 | a0001c0001t0034g0112 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1622-21870G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103027837 | ||||||
| chr10:103028321
|
T | C | 2 | a0001c0005t0046g0188a0001c0005t0047g0187 | 2 | NA18989.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1622-21386T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103028321 | ||||||
| chr10:103028418
|
T | C | 1 | a0003c0008t0002g0075 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1622-21289T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103028418 | ||||||
| chr10:103028459
|
T | A | 1 | a0001c0002t0004g0261 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1622-21248T>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103028459 | ||||||
| chr10:103028814
|
CT | C | 60 | a0001c0002t0002g0245a0001c0002t0003g0223a0001c0002t0003g0225others(57): Show | 60 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.1622-20880delT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103028814 | |||||
| chr10:103028814
|
CTTTTTTT others(8): Show |
C | 3 | a0001c0001t0002g0069a0001c0001t0002g0100a0001c0001t0036g0099 | 3 | HG02683.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1622-20879_1622-20 others(21): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103028814 | |||||
| chr10:103028826
|
TTC | T | 5 | a0001c0001t0012g0020a0001c0001t0021g0055a0001c0001t0072g0115others(2): Show | 5 | HG01361.hp2 HG02074.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.1622-20879_1622-20 others(8): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103028826 | |||||
| chr10:103028827
|
T | C | 2 | a0001c0002t0003g0239a0001c0002t0044g0243 | 2 | HG00642.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1622-20880T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103028827 | ||||||
| chr10:103028828
|
C | CT | 6 | a0001c0002t0006g0221a0001c0002t0015g0220a0001c0002t0068g0219others(3): Show | 6 | HG01516.hp2 HG02055.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.1622-20865dupT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103028828 | |||||
| chr10:103028828
|
C | T | 4 | a0001c0001t0005g0007a0001c0001t0005g0010a0001c0002t0003g0239others(1): Show | 4 | HG00642.hp2 HG01884.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1622-20879C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103028828 | ||||||
| chr10:103028828
|
CT | C | 166 | a0001c0001t0002g0019a0001c0001t0002g0028a0001c0001t0002g0062others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.1622-20865delT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103028828 | |||||
| chr10:103028829
|
T | C | 7 | a0001c0001t0005g0007a0001c0001t0005g0010a0001c0001t0012g0020others(4): Show | 7 | HG01361.hp2 HG01884.hp1 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.1622-20878T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103028829 | ||||||
| chr10:103028891
|
C | T | 2 | a0001c0001t0019g0083a0001c0001t0019g0084 | 2 | HG02970.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1622-20816C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103028891 | ||||||
| chr10:103028984
|
A | AG | 90 | a0001c0002t0002g0245a0001c0002t0003g0223a0001c0002t0003g0225others(87): Show | 90 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.1622-20723_1622-20 others(7): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103028984 | ||||||
| chr10:103029068
|
C | T | 2 | a0001c0002t0064g0248a0001c0002t0065g0116 | 2 | HG02109.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1622-20639C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103029068 | ||||||
| chr10:103029069
|
G | A | 22 | a0001c0002t0004g0176a0001c0002t0004g0180a0001c0002t0004g0255others(19): Show | 22 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.1622-20638G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103029069 | ||||||
| chr10:103029300
|
TA | T | 12 | a0001c0001t0002g0049a0001c0001t0005g0022a0001c0001t0021g0053others(9): Show | 12 | HG01099.hp1 HG02135.hp2 HG02976.hp1 others(9): Show |
intron_variant | MODIFIER | c.1622-20388delA | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103029300 | |||||
| chr10:103029328
|
C | T | 1 | a0001c0003t0001g0142 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1622-20379C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103029328 | ||||||
| chr10:103029364
|
A | G | 9 | a0001c0005t0022g0186a0001c0005t0023g0189a0001c0005t0023g0190others(6): Show | 9 | HG02135.hp2 HG03834.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1622-20343A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103029364 | ||||||
| chr10:103029412
|
T | C | 9 | a0001c0005t0022g0186a0001c0005t0023g0189a0001c0005t0023g0190others(6): Show | 9 | HG02135.hp2 HG03834.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1622-20295T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103029412 | ||||||
| chr10:103029679
|
C | T | 2 | a0002c0004t0055g0216a0002c0004t0066g0192 | 2 | HG02257.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1622-20028C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103029679 | ||||||
| chr10:103029718
|
T | G | 54 | a0001c0001t0043g0123a0001c0003t0001g0118a0001c0003t0001g0122others(51): Show | 54 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(51): Show |
intron_variant | MODIFIER | c.1622-19989T>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103029718 | ||||||
| chr10:103029726
|
C | T | 7 | a0001c0001t0030g0037a0001c0001t0030g0044a0001c0001t0031g0039others(4): Show | 7 | HG01106.hp1 NA18954.hp1 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.1622-19981C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103029726 | ||||||
| chr10:103029737
|
G | A | 10 | a0002c0004t0025g0195a0002c0004t0025g0199a0002c0004t0028g0196others(7): Show | 10 | HG00735.hp1 HG01109.hp1 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.1622-19970G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103029737 | ||||||
| chr10:103029771
|
C | T | 10 | a0001c0002t0026g0267a0001c0002t0026g0269a0001c0002t0027g0266others(7): Show | 10 | HG01167.hp2 HG01884.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1622-19936C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103029771 | ||||||
| chr10:103029823
|
G | A | 54 | a0001c0001t0043g0123a0001c0003t0001g0118a0001c0003t0001g0122others(51): Show | 54 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(51): Show |
intron_variant | MODIFIER | c.1622-19884G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103029823 | ||||||
| chr10:103029879
|
AT | A | 149 | a0001c0001t0043g0123a0001c0002t0002g0245a0001c0002t0003g0223others(146): Show | 149 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.1622-19827delT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103029879 | ||||||
| chr10:103029880
|
T | A | 4 | a0001c0001t0040g0105a0001c0002t0063g0270a0001c0003t0001g0133others(1): Show | 4 | HG02145.hp1 HG03942.hp2 NA18939.hp1 others(1): Show |
intron_variant | MODIFIER | c.1622-19827T>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103029880 | ||||||
| chr10:103029916
|
G | C | 1 | a0001c0003t0079g0134 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1622-19791G>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103029916 | ||||||
| chr10:103030041
|
A | T | 9 | a0001c0005t0022g0186a0001c0005t0023g0189a0001c0005t0023g0190others(6): Show | 9 | HG02135.hp2 HG03834.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1622-19666A>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103030041 | ||||||
| chr10:103030068
|
G | A | 2 | a0001c0001t0043g0076a0001c0003t0001g0106 | 2 | NA19011.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1622-19639G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103030068 | ||||||
| chr10:103030219
|
A | G | 1 | a0001c0002t0004g0262 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1622-19488A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103030219 | ||||||
| chr10:103031087
|
A | G | 1 | a0001c0010t0067g0194 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1622-18620A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103031087 | ||||||
| chr10:103031242
|
T | C | 90 | a0001c0002t0002g0245a0001c0002t0003g0223a0001c0002t0003g0225others(87): Show | 90 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.1622-18465T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103031242 | ||||||
| chr10:103031577
|
T | G | 1 | a0001c0003t0001g0159 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1622-18130T>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103031577 | ||||||
| chr10:103031836
|
T | TG | 3 | a0001c0002t0024g0172a0001c0002t0024g0181a0001c0006t0004g0178 | 3 | HG00738.hp1 HG01952.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1622-17870dupG | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103031836 | |||||
| chr10:103031837
|
GC | G | 75 | a0001c0002t0002g0245a0001c0002t0003g0223a0001c0002t0003g0225others(72): Show | 75 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.1622-17869delC | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103031837 | ||||||
| chr10:103031838
|
C | G | 15 | a0001c0002t0003g0227a0001c0002t0004g0180a0001c0002t0009g0224others(12): Show | 15 | HG00597.hp2 HG00639.hp1 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.1622-17869C>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103031838 | ||||||
| chr10:103031838
|
CG | C | 176 | a0001c0001t0002g0019a0001c0001t0002g0028a0001c0001t0002g0062others(173): Show | 176 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.1622-17861delG | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103031838 | |||||
| chr10:103032003
|
C | T | 49 | a0001c0002t0002g0245a0001c0002t0003g0223a0001c0002t0003g0225others(46): Show | 49 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.1622-17704C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103032003 | ||||||
| chr10:103032080
|
G | A | 13 | a0002c0004t0003g0201a0002c0004t0025g0195a0002c0004t0025g0199others(10): Show | 13 | HG00733.hp1 HG00735.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1622-17627G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103032080 | ||||||
| chr10:103032177
|
C | T | 1 | a0001c0003t0007g0130 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1622-17530C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103032177 | ||||||
| chr10:103032204
|
C | A | 3 | a0002c0004t0025g0195a0002c0004t0025g0199a0002c0004t0056g0200 | 3 | HG01109.hp1 HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1622-17503C>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103032204 | ||||||
| chr10:103032215
|
C | T | 1 | a0001c0001t0008g0090 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1622-17492C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103032215 | ||||||
| chr10:103032491
|
A | G | 68 | a0001c0002t0002g0245a0001c0002t0003g0223a0001c0002t0003g0225others(65): Show | 68 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.1622-17216A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103032491 | ||||||
| chr10:103032493
|
CAG | C | 55 | a0001c0001t0043g0123a0001c0003t0001g0106a0001c0003t0001g0118others(52): Show | 55 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(52): Show |
intron_variant | MODIFIER | c.1622-17213_1622-17 others(8): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103032493 | ||||||
| chr10:103032609
|
T | G | 1 | a0001c0003t0001g0156 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1622-17098T>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103032609 | ||||||
| chr10:103032643
|
A | G | 22 | a0001c0002t0004g0176a0001c0002t0004g0180a0001c0002t0004g0255others(19): Show | 22 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.1622-17064A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103032643 | ||||||
| chr10:103032661
|
CT | C | 85 | a0001c0001t0002g0066a0001c0001t0002g0068a0001c0001t0005g0002others(82): Show | 85 | HG00099.hp1 HG00408.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.1622-17025delT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103032661 | |||||
| chr10:103032661
|
CTT | C | 65 | a0001c0001t0005g0022a0001c0001t0011g0114a0001c0001t0042g0023others(62): Show | 65 | HG00408.hp1 HG00609.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.1622-17026_1622-17 others(8): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103032661 | |||||
| chr10:103032661
|
CTTT | C | 37 | a0001c0002t0003g0231a0001c0002t0004g0176a0001c0002t0004g0180others(34): Show | 37 | HG00597.hp2 HG00609.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.1622-17027_1622-17 others(9): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103032661 | |||||
| chr10:103032697
|
C | T | 1 | a0001c0002t0054g0193 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1622-17010C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103032697 | ||||||
| chr10:103032704
|
T | C | 3 | a0001c0001t0017g0063a0001c0001t0017g0072a0001c0001t0017g0073 | 3 | HG00733.hp2 HG01106.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1622-17003T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103032704 | ||||||
| chr10:103032777
|
C | T | 1 | a0002c0004t0066g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1622-16930C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103032777 | ||||||
| chr10:103032819
|
T | C | 1 | a0001c0001t0002g0028 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1622-16888T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103032819 | ||||||
| chr10:103032859
|
T | C | 1 | a0001c0003t0010g0150 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1622-16848T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103032859 | ||||||
| chr10:103032937
|
G | A | 1 | a0001c0001t0002g0078 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1622-16770G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103032937 | ||||||
| chr10:103033153
|
T | C | 5 | a0001c0001t0005g0057a0001c0001t0008g0017a0001c0001t0008g0059others(2): Show | 5 | HG00099.hp1 HG01167.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1622-16554T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103033153 | ||||||
| chr10:103033283
|
G | A | 22 | a0001c0002t0004g0176a0001c0002t0004g0180a0001c0002t0004g0255others(19): Show | 22 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.1622-16424G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103033283 | ||||||
| chr10:103033478
|
G | A | 90 | a0001c0002t0002g0245a0001c0002t0003g0223a0001c0002t0003g0225others(87): Show | 90 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.1622-16229G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103033478 | ||||||
| chr10:103033549
|
T | A | 1 | a0001c0001t0008g0059 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1622-16158T>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103033549 | ||||||
| chr10:103033678
|
G | C | 22 | a0001c0002t0004g0176a0001c0002t0004g0180a0001c0002t0004g0255others(19): Show | 22 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.1622-16029G>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103033678 | ||||||
| chr10:103033726
|
C | T | 1 | a0001c0001t0031g0046 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1622-15981C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103033726 | ||||||
| chr10:103033727
|
C | T | 9 | a0001c0005t0022g0186a0001c0005t0023g0189a0001c0005t0023g0190others(6): Show | 9 | HG02135.hp2 HG03834.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1622-15980C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103033727 | ||||||
| chr10:103033807
|
A | G | 4 | a0001c0001t0085g0107a0001c0001t0091g0098a0001c0001t0092g0082others(1): Show | 4 | HG02074.hp2 NA18612.hp1 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.1622-15900A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103033807 | ||||||
| chr10:103033864
|
A | G | 1 | a0001c0002t0006g0209 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1622-15843A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103033864 | ||||||
| chr10:103033891
|
T | C | 54 | a0001c0001t0043g0123a0001c0003t0001g0106a0001c0003t0001g0118others(51): Show | 54 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(51): Show |
intron_variant | MODIFIER | c.1622-15816T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103033891 | ||||||
| chr10:103033893
|
C | T | 1 | a0002c0004t0055g0216 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1622-15814C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103033893 | ||||||
| chr10:103033966
|
A | G | 68 | a0001c0002t0002g0245a0001c0002t0003g0223a0001c0002t0003g0225others(65): Show | 68 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.1622-15741A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103033966 | ||||||
| chr10:103034147
|
C | T | 54 | a0001c0001t0043g0123a0001c0003t0001g0106a0001c0003t0001g0118others(51): Show | 54 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(51): Show |
intron_variant | MODIFIER | c.1622-15560C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103034147 | ||||||
| chr10:103034235
|
G | T | 4 | a0002c0004t0003g0201a0002c0004t0057g0202a0002c0004t0058g0203others(1): Show | 4 | HG00733.hp1 HG00735.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1622-15472G>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103034235 | ||||||
| chr10:103034316
|
GT | G | 90 | a0001c0001t0042g0023a0001c0002t0002g0245a0001c0002t0003g0223others(87): Show | 90 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.1622-15379delT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103034316 | |||||
| chr10:103034329
|
G | T | 55 | a0001c0001t0043g0123a0001c0003t0001g0106a0001c0003t0001g0118others(52): Show | 55 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(52): Show |
intron_variant | MODIFIER | c.1622-15378G>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103034329 | ||||||
| chr10:103034335
|
A | AAAAAC | 90 | a0001c0002t0002g0245a0001c0002t0003g0223a0001c0002t0003g0225others(87): Show | 90 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.1622-15357_1622-15 others(11): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103034335 | |||||
| chr10:103034435
|
G | A | 5 | a0001c0002t0026g0267a0001c0002t0026g0269a0001c0002t0027g0266others(2): Show | 5 | HG01884.hp2 HG02145.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1622-15272G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103034435 | ||||||
| chr10:103034945
|
C | T | 3 | a0001c0001t0005g0021a0001c0001t0005g0022a0001c0002t0004g0176 | 3 | HG01109.hp2 HG02976.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1622-14762C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103034945 | ||||||
| chr10:103034972
|
C | CA | 22 | a0001c0001t0002g0062a0001c0001t0008g0017a0001c0001t0011g0114others(19): Show | 22 | HG00408.hp2 HG00642.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.1622-14717dupA | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103034972 | |||||
| chr10:103034972
|
C | CAAAAAAA others(1): Show |
9 | a0002c0004t0003g0201a0002c0004t0025g0199a0002c0004t0055g0216others(6): Show | 9 | HG00733.hp1 HG01109.hp1 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.1622-14724_1622-14 others(14): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103034972 | |||||
| chr10:103034972
|
C | CAAAAAAA others(4): Show |
5 | a0001c0005t0022g0186a0001c0005t0023g0190a0001c0005t0046g0188others(2): Show | 5 | HG02135.hp2 HG03834.hp1 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.1622-14727_1622-14 others(17): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103034972 | |||||
| chr10:103034972
|
C | CAAAAAAA others(5): Show |
4 | a0001c0005t0023g0189a0001c0005t0047g0187a0001c0005t0049g0183others(1): Show | 4 | NA18943.hp2 NA18945.hp2 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.1622-14728_1622-14 others(18): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103034972 | |||||
| chr10:103034972
|
C | CAAAAAAA others(6): Show |
1 | a0001c0002t0062g0222 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1622-14729_1622-14 others(19): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103034972 | |||||
| chr10:103034972
|
C | CAAAAAAA others(7): Show |
3 | a0001c0002t0026g0267a0001c0002t0026g0269a0001c0002t0027g0268 | 3 | HG01884.hp2 HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1622-14730_1622-14 others(20): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103034972 | |||||
| chr10:103034972
|
C | CAAAAAAA others(8): Show |
4 | a0001c0002t0006g0208a0001c0002t0027g0266a0001c0002t0054g0193others(1): Show | 4 | HG02145.hp1 HG02523.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1622-14731_1622-14 others(21): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103034972 | |||||
| chr10:103034972
|
C | CAAAAAAA others(9): Show |
11 | a0001c0002t0006g0117a0001c0002t0006g0212a0001c0002t0006g0214others(8): Show | 11 | HG00609.hp2 HG00639.hp1 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.1622-14732_1622-14 others(22): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103034972 | |||||
| chr10:103034972
|
C | CAAAAAAA others(10): Show |
24 | a0001c0002t0003g0223a0001c0002t0003g0229a0001c0002t0003g0231others(21): Show | 24 | HG00408.hp1 HG00621.hp2 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.1622-14733_1622-14 others(23): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103034972 | |||||
| chr10:103034972
|
C | CAAAAAAA others(11): Show |
18 | a0001c0002t0002g0245a0001c0002t0003g0225a0001c0002t0003g0227others(15): Show | 18 | HG00597.hp2 HG00609.hp1 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.1622-14734_1622-14 others(24): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103034972 | |||||
| chr10:103034972
|
C | CAAAAAAA others(12): Show |
10 | a0001c0002t0003g0234a0001c0002t0003g0239a0001c0002t0003g0240others(7): Show | 10 | HG01123.hp1 HG01258.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.1622-14717_1622-14 others(25): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103034972 | |||||
| chr10:103034972
|
C | CAAAAAAA others(13): Show |
3 | a0001c0002t0003g0233a0001c0002t0004g0255a0001c0002t0009g0246 | 3 | HG02027.hp2 HG03098.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.1622-14717_1622-14 others(26): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103034972 | |||||
| chr10:103034972
|
C | CAAAAAAA others(14): Show |
2 | a0001c0002t0003g0251a0001c0002t0009g0226 | 2 | HG02135.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.1622-14717_1622-14 others(27): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103034972 | |||||
| chr10:103034987
|
A | AAAAT | 50 | a0001c0001t0043g0123a0001c0003t0001g0106a0001c0003t0001g0118others(47): Show | 50 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(47): Show |
intron_variant | MODIFIER | c.1622-14719_1622-14 others(10): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103034987 | |||||
| chr10:103034987
|
A | T | 3 | a0001c0003t0001g0141a0001c0003t0001g0155a0001c0003t0051g0136 | 3 | HG01358.hp2 NA18954.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.1622-14720A>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103034987 | ||||||
| chr10:103035011
|
A | G | 11 | a0001c0002t0004g0255a0001c0002t0004g0256a0001c0002t0004g0258others(8): Show | 11 | HG00597.hp2 HG00673.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1622-14696A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103035011 | ||||||
| chr10:103035070
|
A | G | 1 | a0002c0004t0055g0216 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1622-14637A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103035070 | ||||||
| chr10:103035190
|
G | A | 145 | a0001c0001t0043g0123a0001c0002t0002g0245a0001c0002t0003g0223others(142): Show | 145 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(142): Show |
intron_variant | MODIFIER | c.1622-14517G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103035190 | ||||||
| chr10:103035227
|
G | C | 22 | a0001c0002t0004g0176a0001c0002t0004g0180a0001c0002t0004g0255others(19): Show | 22 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.1622-14480G>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103035227 | ||||||
| chr10:103035294
|
A | G | 1 | a0001c0005t0047g0187 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1622-14413A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103035294 | ||||||
| chr10:103035377
|
C | T | 49 | a0001c0002t0002g0245a0001c0002t0003g0223a0001c0002t0003g0225others(46): Show | 49 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.1622-14330C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103035377 | ||||||
| chr10:103035469
|
A | G | 1 | a0001c0001t0002g0103 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1622-14238A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103035469 | ||||||
| chr10:103035508
|
G | A | 1 | a0002c0004t0066g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1622-14199G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103035508 | ||||||
| chr10:103035652
|
C | T | 90 | a0001c0002t0002g0245a0001c0002t0003g0223a0001c0002t0003g0225others(87): Show | 90 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.1622-14055C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103035652 | ||||||
| chr10:103035772
|
C | T | 1 | a0001c0001t0100g0085 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1622-13935C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103035772 | ||||||
| chr10:103035966
|
T | G | 28 | a0001c0002t0002g0245a0001c0002t0003g0223a0001c0002t0003g0225others(25): Show | 28 | HG00609.hp1 HG00621.hp2 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.1622-13741T>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103035966 | ||||||
| chr10:103035979
|
C | T | 6 | a0001c0002t0026g0267a0001c0002t0026g0269a0001c0002t0027g0266others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1622-13728C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103035979 | ||||||
| chr10:103036077
|
T | C | 13 | a0002c0004t0003g0201a0002c0004t0025g0195a0002c0004t0025g0199others(10): Show | 13 | HG00733.hp1 HG00735.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1622-13630T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103036077 | ||||||
| chr10:103036078
|
A | G | 240 | a0001c0001t0002g0065a0001c0001t0005g0002a0001c0001t0005g0003others(237): Show | 240 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1622-13629A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103036078 | ||||||
| chr10:103036128
|
G | GAC | 60 | a0001c0001t0005g0004a0001c0001t0043g0123a0001c0001t0105g0093others(57): Show | 60 | HG00099.hp2 HG00544.hp2 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.1622-13560_1622-13 others(8): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103036128 | |||||
| chr10:103036149
|
T | A | 9 | a0001c0005t0022g0186a0001c0005t0023g0189a0001c0005t0023g0190others(6): Show | 9 | HG02135.hp2 HG03834.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1622-13558T>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103036149 | ||||||
| chr10:103036160
|
G | A | 1 | a0001c0010t0067g0194 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1622-13547G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103036160 | ||||||
| chr10:103036336
|
C | A | 6 | a0001c0002t0026g0267a0001c0002t0026g0269a0001c0002t0027g0266others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1622-13371C>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103036336 | ||||||
| chr10:103036381
|
T | C | 22 | a0001c0002t0004g0176a0001c0002t0004g0180a0001c0002t0004g0255others(19): Show | 22 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.1622-13326T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103036381 | ||||||
| chr10:103036487
|
G | A | 16 | a0001c0002t0006g0117a0001c0002t0006g0208a0001c0002t0006g0209others(13): Show | 16 | HG00408.hp1 HG00609.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.1622-13220G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103036487 | ||||||
| chr10:103036588
|
T | C | 90 | a0001c0002t0002g0245a0001c0002t0003g0223a0001c0002t0003g0225others(87): Show | 90 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.1622-13119T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103036588 | ||||||
| chr10:103036704
|
C | T | 6 | a0001c0002t0026g0267a0001c0002t0026g0269a0001c0002t0027g0266others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1622-13003C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103036704 | ||||||
| chr10:103036823
|
A | G | 1 | a0001c0001t0074g0034 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1622-12884A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103036823 | ||||||
| chr10:103036895
|
T | G | 68 | a0001c0002t0002g0245a0001c0002t0003g0223a0001c0002t0003g0225others(65): Show | 68 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.1622-12812T>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103036895 | ||||||
| chr10:103037030
|
A | C | 90 | a0001c0002t0002g0245a0001c0002t0003g0223a0001c0002t0003g0225others(87): Show | 90 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.1622-12677A>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103037030 | ||||||
| chr10:103037177
|
T | A | 9 | a0001c0005t0022g0186a0001c0005t0023g0189a0001c0005t0023g0190others(6): Show | 9 | HG02135.hp2 HG03834.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1622-12530T>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103037177 | ||||||
| chr10:103037526
|
G | A | 13 | a0001c0001t0020g0026a0001c0001t0020g0027a0001c0001t0020g0054others(10): Show | 13 | HG00558.hp1 HG01257.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.1622-12181G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103037526 | ||||||
| chr10:103037666
|
A | C | 90 | a0001c0002t0002g0245a0001c0002t0003g0223a0001c0002t0003g0225others(87): Show | 90 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.1622-12041A>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103037666 | ||||||
| chr10:103037812
|
G | C | 5 | a0001c0002t0026g0267a0001c0002t0026g0269a0001c0002t0027g0266others(2): Show | 5 | HG01884.hp2 HG02145.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1622-11895G>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103037812 | ||||||
| chr10:103038029
|
G | A | 6 | a0001c0002t0026g0267a0001c0002t0026g0269a0001c0002t0027g0266others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1622-11678G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103038029 | ||||||
| chr10:103039175
|
C | T | 1 | a0001c0003t0007g0130 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1622-10532C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103039175 | ||||||
| chr10:103039204
|
C | T | 1 | a0001c0002t0054g0193 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1622-10503C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103039204 | ||||||
| chr10:103039217
|
C | T | 1 | a0001c0001t0037g0088 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1622-10490C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103039217 | ||||||
| chr10:103039454
|
C | T | 1 | a0001c0001t0005g0006 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1622-10253C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103039454 | ||||||
| chr10:103039510
|
T | A | 22 | a0001c0002t0004g0176a0001c0002t0004g0180a0001c0002t0004g0255others(19): Show | 22 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.1622-10197T>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103039510 | ||||||
| chr10:103039626
|
T | C | 1 | a0001c0002t0054g0193 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1622-10081T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103039626 | ||||||
| chr10:103039911
|
G | A | 90 | a0001c0002t0002g0245a0001c0002t0003g0223a0001c0002t0003g0225others(87): Show | 90 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.1622-9796G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103039911 | ||||||
| chr10:103040209
|
CATT | C | 5 | a0001c0002t0004g0255a0001c0002t0004g0256a0001c0002t0004g0258others(2): Show | 5 | HG03041.hp1 HG03098.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1622-9495_1622-949 others(7): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103040209 | |||||
| chr10:103040287
|
T | C | 33 | a0001c0002t0002g0245a0001c0002t0003g0223a0001c0002t0003g0225others(30): Show | 33 | HG00609.hp1 HG00621.hp2 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.1622-9420T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103040287 | ||||||
| chr10:103040342
|
G | T | 1 | a0001c0001t0002g0066 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1622-9365G>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103040342 | ||||||
| chr10:103040391
|
G | A | 9 | a0001c0005t0022g0186a0001c0005t0023g0189a0001c0005t0023g0190others(6): Show | 9 | HG02135.hp2 HG03834.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1622-9316G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103040391 | ||||||
| chr10:103040448
|
T | C | 22 | a0001c0002t0004g0176a0001c0002t0004g0180a0001c0002t0004g0255others(19): Show | 22 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.1622-9259T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103040448 | ||||||
| chr10:103040601
|
C | T | 1 | a0001c0002t0009g0238 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1622-9106C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103040601 | ||||||
| chr10:103040686
|
G | GC | 3 | a0001c0001t0002g0062a0001c0001t0002g0067a0001c0001t0101g0101 | 3 | HG01071.hp2 HG01081.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.1622-9020dupC | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103040686 | |||||
| chr10:103041197
|
C | T | 3 | a0001c0001t0030g0037a0001c0001t0031g0046a0001c0001t0074g0034 | 3 | HG01106.hp1 NA18954.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.1622-8510C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103041197 | ||||||
| chr10:103041297
|
C | G | 2 | a0001c0005t0046g0188a0001c0005t0047g0187 | 2 | NA18989.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1622-8410C>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103041297 | ||||||
| chr10:103041330
|
A | G | 13 | a0002c0004t0003g0201a0002c0004t0025g0195a0002c0004t0025g0199others(10): Show | 13 | HG00733.hp1 HG00735.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1622-8377A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103041330 | ||||||
| chr10:103041895
|
C | T | 1 | a0001c0002t0009g0246 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1622-7812C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103041895 | ||||||
| chr10:103042109
|
C | T | 41 | a0001c0002t0004g0176a0001c0002t0004g0180a0001c0002t0004g0255others(38): Show | 41 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.1622-7598C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103042109 | ||||||
| chr10:103042112
|
C | T | 1 | a0001c0010t0067g0194 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1622-7595C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103042112 | ||||||
| chr10:103042135
|
A | G | 1 | a0001c0010t0067g0194 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1622-7572A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103042135 | ||||||
| chr10:103042314
|
T | C | 90 | a0001c0002t0002g0245a0001c0002t0003g0223a0001c0002t0003g0225others(87): Show | 90 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.1622-7393T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103042314 | ||||||
| chr10:103042727
|
G | A | 1 | a0001c0001t0014g0042 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1622-6980G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103042727 | ||||||
| chr10:103042915
|
A | C | 1 | a0001c0001t0005g0008 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1622-6792A>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103042915 | ||||||
| chr10:103043013
|
A | T | 9 | a0001c0005t0022g0186a0001c0005t0023g0189a0001c0005t0023g0190others(6): Show | 9 | HG02135.hp2 HG03834.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1622-6694A>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103043013 | ||||||
| chr10:103043130
|
G | A | 1 | a0001c0001t0098g0033 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1622-6577G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103043130 | ||||||
| chr10:103043305
|
C | A | 22 | a0001c0002t0004g0176a0001c0002t0004g0180a0001c0002t0004g0255others(19): Show | 22 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.1622-6402C>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103043305 | ||||||
| chr10:103043557
|
T | C | 16 | a0001c0002t0006g0117a0001c0002t0006g0208a0001c0002t0006g0209others(13): Show | 16 | HG00408.hp1 HG00609.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.1622-6150T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103043557 | ||||||
| chr10:103043678
|
T | C | 1 | a0001c0003t0001g0156 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1622-6029T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103043678 | ||||||
| chr10:103043927
|
A | C | 1 | a0001c0002t0062g0222 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1622-5780A>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103043927 | ||||||
| chr10:103044198
|
C | T | 7 | a0001c0006t0004g0175a0001c0006t0004g0177a0001c0006t0004g0178others(4): Show | 7 | HG00639.hp1 HG00738.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.1622-5509C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103044198 | ||||||
| chr10:103044263
|
A | C | 1 | a0001c0003t0010g0137 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1622-5444A>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103044263 | ||||||
| chr10:103044551
|
GA | G | 150 | a0001c0002t0002g0245a0001c0002t0003g0223a0001c0002t0003g0225others(147): Show | 150 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(147): Show |
intron_variant | MODIFIER | c.1622-5142delA | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103044551 | |||||
| chr10:103044906
|
C | T | 1 | a0001c0002t0065g0116 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1622-4801C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103044906 | ||||||
| chr10:103044937
|
C | G | 2 | a0002c0004t0028g0196a0002c0004t0028g0215 | 2 | HG02622.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1622-4770C>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103044937 | ||||||
| chr10:103044981
|
G | A | 1 | a0001c0005t0023g0189 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1622-4726G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103044981 | ||||||
| chr10:103045285
|
A | G | 1 | a0001c0001t0011g0011 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1622-4422A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103045285 | ||||||
| chr10:103045593
|
C | A | 2 | a0001c0001t0012g0020a0001c0001t0072g0115 | 2 | HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1622-4114C>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103045593 | ||||||
| chr10:103045853
|
C | A | 21 | a0001c0002t0004g0176a0001c0002t0004g0180a0001c0002t0004g0255others(18): Show | 21 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.1622-3854C>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103045853 | ||||||
| chr10:103046089
|
C | T | 15 | a0001c0001t0005g0002a0001c0001t0005g0003a0001c0001t0005g0004others(12): Show | 15 | HG01081.hp2 HG01109.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.1622-3618C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103046089 | ||||||
| chr10:103046090
|
G | A | 3 | a0001c0002t0064g0248a0001c0002t0065g0116a0001c0002t0071g0247 | 3 | HG02109.hp1 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1622-3617G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103046090 | ||||||
| chr10:103046273
|
C | T | 1 | a0001c0001t0005g0003 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1622-3434C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103046273 | ||||||
| chr10:103046442
|
T | G | 1 | a0001c0001t0017g0073 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1622-3265T>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103046442 | ||||||
| chr10:103046854
|
A | G | 1 | a0001c0005t0022g0186 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1622-2853A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103046854 | ||||||
| chr10:103046872
|
A | T | 3 | a0001c0002t0064g0248a0001c0002t0065g0116a0001c0002t0071g0247 | 3 | HG02109.hp1 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1622-2835A>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103046872 | ||||||
| chr10:103046897
|
A | C | 151 | a0001c0002t0002g0245a0001c0002t0003g0223a0001c0002t0003g0225others(148): Show | 151 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(148): Show |
intron_variant | MODIFIER | c.1622-2810A>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103046897 | ||||||
| chr10:103046897
|
A | T | 2 | a0001c0002t0044g0230a0001c0002t0044g0243 | 2 | HG00642.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.1622-2810A>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103046897 | ||||||
| chr10:103046956
|
C | T | 1 | a0001c0001t0005g0002 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1622-2751C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103046956 | ||||||
| chr10:103047013
|
A | G | 5 | a0001c0001t0005g0057a0001c0001t0008g0017a0001c0001t0008g0059others(2): Show | 5 | HG00099.hp1 HG01167.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1622-2694A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103047013 | ||||||
| chr10:103047127
|
G | A | 22 | a0001c0002t0004g0176a0001c0002t0004g0180a0001c0002t0004g0255others(19): Show | 22 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.1622-2580G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103047127 | ||||||
| chr10:103047141
|
G | C | 54 | a0001c0003t0001g0106a0001c0003t0001g0118a0001c0003t0001g0122others(51): Show | 54 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(51): Show |
intron_variant | MODIFIER | c.1622-2566G>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103047141 | ||||||
| chr10:103047311
|
C | G | 1 | a0001c0001t0042g0024 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1622-2396C>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103047311 | ||||||
| chr10:103047885
|
C | T | 10 | a0001c0001t0039g0061a0001c0005t0022g0186a0001c0005t0023g0189others(7): Show | 10 | HG02040.hp1 HG02135.hp2 HG03834.hp1 others(7): Show |
intron_variant | MODIFIER | c.1622-1822C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103047885 | ||||||
| chr10:103047923
|
T | A | 6 | a0001c0002t0026g0267a0001c0002t0026g0269a0001c0002t0027g0266others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1622-1784T>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103047923 | ||||||
| chr10:103048032
|
C | T | 2 | a0001c0003t0001g0146a0001c0003t0001g0147 | 2 | NA18992.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1622-1675C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103048032 | ||||||
| chr10:103048169
|
C | T | 22 | a0001c0002t0004g0176a0001c0002t0004g0180a0001c0002t0004g0255others(19): Show | 22 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.1622-1538C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103048169 | ||||||
| chr10:103048214
|
A | AT | 74 | a0001c0001t0002g0078a0001c0001t0005g0003a0001c0001t0005g0004others(71): Show | 74 | HG00099.hp2 HG00544.hp2 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.1622-1475dupT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103048214 | |||||
| chr10:103048214
|
A | ATT | 7 | a0001c0001t0005g0002a0001c0001t0005g0021a0001c0001t0008g0250others(4): Show | 7 | HG01109.hp2 HG01943.hp1 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.1622-1476_1622-147 others(6): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103048214 | |||||
| chr10:103048217
|
T | G | 32 | a0001c0002t0002g0245a0001c0002t0003g0223a0001c0002t0003g0225others(29): Show | 32 | HG00609.hp1 HG00621.hp2 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.1622-1490T>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103048217 | ||||||
| chr10:103048302
|
G | T | 49 | a0001c0002t0002g0245a0001c0002t0003g0223a0001c0002t0003g0225others(46): Show | 49 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.1622-1405G>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103048302 | ||||||
| chr10:103048325
|
C | G | 9 | a0001c0005t0022g0186a0001c0005t0023g0189a0001c0005t0023g0190others(6): Show | 9 | HG02135.hp2 HG03834.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1622-1382C>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103048325 | ||||||
| chr10:103048588
|
G | GTGACAGG others(298): Show |
4 | a0002c0004t0057g0202a0002c0004t0058g0203a0002c0004t0060g0197others(1): Show | 4 | HG01516.hp2 HG01517.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.1622-1103_1622-110 others(309): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103048588 | |||||
| chr10:103048588
|
G | GTGACAGG others(298): Show |
2 | a0002c0004t0003g0201a0002c0004t0059g0217 | 2 | HG00733.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.1622-1103_1622-110 others(309): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103048588 | |||||
| chr10:103048588
|
G | GTGACAGG others(316): Show |
2 | a0002c0004t0055g0216a0002c0004t0066g0192 | 2 | HG02257.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1622-1103_1622-110 others(327): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103048588 | |||||
| chr10:103048588
|
G | GTGACAGG others(319): Show |
1 | a0002c0004t0028g0196 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1622-1103_1622-110 others(330): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103048588 | |||||
| chr10:103048588
|
G | GTGACAGG others(320): Show |
1 | a0002c0004t0028g0215 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1622-1103_1622-110 others(331): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103048588 | |||||
| chr10:103048588
|
G | GTGACAGG others(322): Show |
1 | a0002c0004t0056g0200 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1622-1103_1622-110 others(333): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103048588 | |||||
| chr10:103048588
|
G | GTGACAGG others(323): Show |
2 | a0002c0004t0025g0195a0002c0004t0025g0199 | 2 | HG01109.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1622-1103_1622-110 others(334): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 103048588 | |||||
| chr10:103048627
|
C | T | 1 | a0001c0001t0030g0044 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1622-1080C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103048627 | ||||||
| chr10:103048795
|
T | A | 1 | a0001c0001t0084g0016 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1622-912T>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103048795 | ||||||
| chr10:103048866
|
T | A | 1 | a0001c0002t0065g0116 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1622-841T>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103048866 | ||||||
| chr10:103048919
|
G | A | 1 | a0001c0003t0010g0150 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1622-788G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103048919 | ||||||
| chr10:103048997
|
T | C | 1 | a0001c0001t0011g0114 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1622-710T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103048997 | ||||||
| chr10:103049034
|
C | T | 2 | a0001c0001t0012g0020a0001c0001t0072g0115 | 2 | HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1622-673C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103049034 | ||||||
| chr10:103049071
|
C | G | 9 | a0001c0005t0022g0186a0001c0005t0023g0189a0001c0005t0023g0190others(6): Show | 9 | HG02135.hp2 HG03834.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1622-636C>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103049071 | ||||||
| chr10:103049240
|
G | A | 22 | a0001c0002t0004g0176a0001c0002t0004g0180a0001c0002t0004g0255others(19): Show | 22 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.1622-467G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103049240 | ||||||
| chr10:103049430
|
G | A | 1 | a0001c0003t0001g0155 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1622-277G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103049430 | ||||||
| chr10:103049513
|
G | A | 1 | a0001c0001t0084g0016 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1622-194G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103049513 | ||||||
| chr10:103049701
|
C | T | 3 | a0001c0001t0005g0008a0001c0001t0011g0009a0001c0001t0011g0013 | 3 | HG02280.hp2 HG02717.hp2 NA18522.hp2 |
splice_region_variant&intron_variant | LOW | c.1622-6C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 1/7 | chr10 | 103049701 | ||||||
| chr10:103050039
|
G | A | 1 | a0001c0002t0004g0180 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1765+189G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 2/7 | chr10 | 103050039 | ||||||
| chr10:103050343
|
C | G | 11 | a0001c0001t0014g0018a0001c0001t0014g0042a0001c0001t0014g0045others(8): Show | 11 | HG01106.hp1 HG01952.hp2 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.1765+493C>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 2/7 | chr10 | 103050343 | ||||||
| chr10:103050536
|
C | CA | 6 | a0001c0001t0073g0025a0001c0001t0083g0048a0001c0002t0064g0248others(3): Show | 6 | HG02071.hp1 HG02109.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1765+702dupA | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 103050536 | |||||
| chr10:103050536
|
CA | C | 63 | a0001c0002t0027g0268a0001c0003t0001g0106a0001c0003t0001g0118others(60): Show | 63 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(60): Show |
intron_variant | MODIFIER | c.1765+702delA | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 103050536 | |||||
| chr10:103050659
|
G | A | 1 | a0001c0001t0043g0123 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1765+809G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 2/7 | chr10 | 103050659 | ||||||
| chr10:103051218
|
G | A | 1 | a0001c0002t0064g0248 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1765+1368G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 2/7 | chr10 | 103051218 | ||||||
| chr10:103051328
|
G | C | 16 | a0001c0002t0006g0117a0001c0002t0006g0208a0001c0002t0006g0209others(13): Show | 16 | HG00408.hp1 HG00609.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.1765+1478G>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 2/7 | chr10 | 103051328 | ||||||
| chr10:103051446
|
T | A | 1 | a0001c0003t0007g0128 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1765+1596T>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 2/7 | chr10 | 103051446 | ||||||
| chr10:103051446
|
T | C | 53 | a0001c0003t0001g0106a0001c0003t0001g0118a0001c0003t0001g0122others(50): Show | 53 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(50): Show |
intron_variant | MODIFIER | c.1765+1596T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 2/7 | chr10 | 103051446 | ||||||
| chr10:103051595
|
C | T | 1 | a0001c0003t0007g0128 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1765+1745C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 2/7 | chr10 | 103051595 | ||||||
| chr10:103051596
|
T | G | 1 | a0001c0003t0007g0128 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1765+1746T>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 2/7 | chr10 | 103051596 | ||||||
| chr10:103051913
|
G | A | 1 | a0001c0003t0001g0159 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1765+2063G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 2/7 | chr10 | 103051913 | ||||||
| chr10:103051942
|
C | T | 152 | a0001c0002t0003g0223a0001c0002t0003g0225a0001c0002t0003g0227others(149): Show | 152 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(149): Show |
intron_variant | MODIFIER | c.1765+2092C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 2/7 | chr10 | 103051942 | ||||||
| chr10:103052003
|
G | A | 15 | a0001c0001t0005g0002a0001c0001t0005g0003a0001c0001t0005g0004others(12): Show | 15 | HG01081.hp2 HG01109.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.1765+2153G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 2/7 | chr10 | 103052003 | ||||||
| chr10:103052043
|
G | A | 6 | a0001c0003t0010g0137a0001c0003t0010g0148a0001c0003t0010g0150others(3): Show | 6 | HG01167.hp2 HG02735.hp1 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.1765+2193G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 2/7 | chr10 | 103052043 | ||||||
| chr10:103052149
|
C | T | 6 | a0001c0002t0026g0267a0001c0002t0026g0269a0001c0002t0027g0266others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1766-2180C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 2/7 | chr10 | 103052149 | ||||||
| chr10:103052291
|
C | A | 1 | a0001c0001t0097g0014 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1766-2038C>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 2/7 | chr10 | 103052291 | ||||||
| chr10:103052291
|
C | CA | 10 | a0001c0001t0005g0002a0001c0001t0005g0003a0001c0001t0005g0007others(7): Show | 10 | HG01884.hp1 HG02074.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1766-2025dupA | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 103052291 | |||||
| chr10:103052295
|
A | C | 68 | a0001c0002t0003g0223a0001c0002t0003g0225a0001c0002t0003g0227others(65): Show | 68 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.1766-2034A>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 2/7 | chr10 | 103052295 | ||||||
| chr10:103052384
|
T | A | 5 | a0001c0002t0026g0267a0001c0002t0026g0269a0001c0002t0027g0266others(2): Show | 5 | HG01884.hp2 HG02145.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1766-1945T>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 2/7 | chr10 | 103052384 | ||||||
| chr10:103052518
|
CT | C | 120 | a0001c0002t0003g0223a0001c0002t0003g0225a0001c0002t0003g0227others(117): Show | 120 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.1766-1797delT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 103052518 | |||||
| chr10:103052518
|
CTT | C | 22 | a0001c0002t0004g0176a0001c0002t0004g0180a0001c0002t0004g0255others(19): Show | 22 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.1766-1798_1766-179 others(6): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 103052518 | |||||
| chr10:103052547
|
T | TC | 5 | a0001c0002t0004g0255a0001c0002t0004g0256a0001c0002t0004g0258others(2): Show | 5 | HG03041.hp1 HG03098.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1766-1781dupC | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 103052547 | |||||
| chr10:103052574
|
T | C | 143 | a0001c0002t0003g0223a0001c0002t0003g0225a0001c0002t0003g0227others(140): Show | 143 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(140): Show |
intron_variant | MODIFIER | c.1766-1755T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 2/7 | chr10 | 103052574 | ||||||
| chr10:103052970
|
A | G | 1 | a0001c0010t0067g0194 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1766-1359A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 2/7 | chr10 | 103052970 | ||||||
| chr10:103053042
|
T | C | 3 | a0001c0001t0017g0063a0001c0001t0017g0072a0001c0001t0017g0073 | 3 | HG00733.hp2 HG01106.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1766-1287T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 2/7 | chr10 | 103053042 | ||||||
| chr10:103053104
|
A | G | 13 | a0002c0004t0003g0201a0002c0004t0025g0195a0002c0004t0025g0199others(10): Show | 13 | HG00733.hp1 HG00735.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1766-1225A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 2/7 | chr10 | 103053104 | ||||||
| chr10:103053140
|
A | G | 143 | a0001c0002t0003g0223a0001c0002t0003g0225a0001c0002t0003g0227others(140): Show | 143 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(140): Show |
intron_variant | MODIFIER | c.1766-1189A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 2/7 | chr10 | 103053140 | ||||||
| chr10:103053148
|
A | C | 1 | a0001c0001t0020g0054 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1766-1181A>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 2/7 | chr10 | 103053148 | ||||||
| chr10:103053320
|
G | A | 2 | a0001c0005t0023g0189a0001c0005t0023g0190 | 2 | NA18945.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.1766-1009G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 2/7 | chr10 | 103053320 | ||||||
| chr10:103053360
|
T | A | 1 | a0001c0001t0011g0011 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1766-969T>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 2/7 | chr10 | 103053360 | ||||||
| chr10:103053511
|
G | A | 268 | a0001c0001t0002g0019a0001c0001t0002g0028a0001c0001t0002g0062others(265): Show | 268 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.1766-818G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 2/7 | chr10 | 103053511 | ||||||
| chr10:103053684
|
A | G | 3 | a0001c0002t0029g0204a0001c0002t0029g0207a0001c0002t0069g0206 | 3 | HG01070.hp2 HG01071.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.1766-645A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 2/7 | chr10 | 103053684 | ||||||
| chr10:103054144
|
G | A | 1 | a0001c0001t0008g0090 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1766-185G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 2/7 | chr10 | 103054144 | ||||||
| chr10:103054147
|
G | A | 1 | a0001c0002t0004g0265 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1766-182G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 2/7 | chr10 | 103054147 | ||||||
| chr10:103054590
|
GTGTTTTG others(15): Show |
G | 53 | a0001c0003t0001g0106a0001c0003t0001g0118a0001c0003t0001g0122others(50): Show | 53 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(50): Show |
intron_variant | MODIFIER | c.1903+136_1903+157d others(24): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 103054590 | |||||
| chr10:103054610
|
T | C | 28 | a0001c0002t0002g0245a0001c0002t0003g0223a0001c0002t0003g0225others(25): Show | 28 | HG00609.hp1 HG00621.hp2 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.1903+144T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 3/7 | chr10 | 103054610 | ||||||
| chr10:103055511
|
T | A | 62 | a0001c0002t0002g0245a0001c0002t0003g0223a0001c0002t0003g0225others(59): Show | 62 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.1903+1045T>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 3/7 | chr10 | 103055511 | ||||||
| chr10:103055588
|
G | A | 9 | a0001c0002t0003g0231a0001c0002t0003g0239a0001c0002t0003g0240others(6): Show | 9 | HG00639.hp2 HG00733.hp1 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.1903+1122G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 3/7 | chr10 | 103055588 | ||||||
| chr10:103055948
|
C | A | 1 | a0001c0010t0067g0194 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1904-847C>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 3/7 | chr10 | 103055948 | ||||||
| chr10:103056016
|
A | T | 1 | a0001c0001t0002g0066 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1904-779A>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 3/7 | chr10 | 103056016 | ||||||
| chr10:103056023
|
G | T | 2 | a0001c0002t0026g0267a0001c0002t0026g0269 | 2 | HG01884.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1904-772G>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 3/7 | chr10 | 103056023 | ||||||
| chr10:103056070
|
A | G | 55 | a0001c0002t0107g0235a0001c0003t0001g0106a0001c0003t0001g0118others(52): Show | 55 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.1904-725A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 3/7 | chr10 | 103056070 | ||||||
| chr10:103056087
|
C | CA | 36 | a0001c0001t0096g0052a0001c0002t0002g0245a0001c0002t0003g0223others(33): Show | 36 | HG00609.hp1 HG00621.hp2 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.1904-694dupA | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 103056087 | |||||
| chr10:103056087
|
CA | C | 9 | a0001c0001t0011g0011a0001c0001t0031g0046a0001c0002t0015g0205others(6): Show | 9 | HG01884.hp2 HG02145.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1904-694delA | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 103056087 | |||||
| chr10:103056114
|
AAAAAG | A | 54 | a0001c0003t0001g0106a0001c0003t0001g0118a0001c0003t0001g0122others(51): Show | 54 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(51): Show |
intron_variant | MODIFIER | c.1904-676_1904-672d others(7): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 103056114 | |||||
| chr10:103056253
|
A | G | 1 | a0002c0004t0066g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1904-542A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 3/7 | chr10 | 103056253 | ||||||
| chr10:103056268
|
T | A | 1 | a0001c0002t0054g0193 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1904-527T>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 3/7 | chr10 | 103056268 | ||||||
| chr10:103056282
|
G | A | 1 | a0001c0001t0005g0108 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1904-513G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 3/7 | chr10 | 103056282 | ||||||
| chr10:103056488
|
G | A | 5 | a0001c0002t0026g0267a0001c0002t0026g0269a0001c0002t0027g0266others(2): Show | 5 | HG01884.hp2 HG02145.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1904-307G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 3/7 | chr10 | 103056488 | ||||||
| chr10:103056510
|
G | A | 1 | a0001c0002t0062g0222 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1904-285G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 3/7 | chr10 | 103056510 | ||||||
| chr10:103056712
|
T | C | 5 | a0001c0001t0012g0087a0001c0001t0018g0091a0001c0001t0035g0079others(2): Show | 5 | HG00738.hp2 HG01070.hp1 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.1904-83T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 3/7 | chr10 | 103056712 | ||||||
| chr10:103056978
|
T | C | 1 | a0002c0004t0055g0216 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2073+14T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103056978 | ||||||
| chr10:103057190
|
C | G | 153 | a0001c0002t0002g0245a0001c0002t0003g0223a0001c0002t0003g0225others(150): Show | 153 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(150): Show |
intron_variant | MODIFIER | c.2073+226C>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103057190 | ||||||
| chr10:103057274
|
C | T | 22 | a0001c0002t0004g0176a0001c0002t0004g0180a0001c0002t0004g0255others(19): Show | 22 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.2073+310C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103057274 | ||||||
| chr10:103057381
|
C | T | 1 | a0001c0001t0039g0086 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2073+417C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103057381 | ||||||
| chr10:103057465
|
TA | T | 6 | a0001c0001t0011g0011a0001c0001t0034g0112a0001c0001t0073g0025others(3): Show | 6 | HG00735.hp1 HG02896.hp1 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.2073+516delA | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 103057465 | |||||
| chr10:103057626
|
T | C | 16 | a0001c0002t0006g0117a0001c0002t0006g0208a0001c0002t0006g0209others(13): Show | 16 | HG00408.hp1 HG00609.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.2073+662T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103057626 | ||||||
| chr10:103057915
|
G | T | 2 | a0002c0004t0028g0196a0002c0004t0028g0215 | 2 | HG02622.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.2073+951G>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103057915 | ||||||
| chr10:103057952
|
A | G | 40 | a0001c0001t0005g0057a0001c0001t0005g0096a0001c0001t0005g0108others(37): Show | 40 | HG00099.hp1 HG00544.hp1 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.2073+988A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103057952 | ||||||
| chr10:103058002
|
G | T | 2 | a0001c0001t0012g0020a0001c0001t0072g0115 | 2 | HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2073+1038G>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103058002 | ||||||
| chr10:103058018
|
T | C | 1 | a0001c0001t0002g0103 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2073+1054T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103058018 | ||||||
| chr10:103058099
|
T | C | 2 | a0001c0002t0064g0248a0001c0002t0065g0116 | 2 | HG02109.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2073+1135T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103058099 | ||||||
| chr10:103058125
|
T | G | 1 | a0001c0002t0004g0264 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2073+1161T>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103058125 | ||||||
| chr10:103058222
|
TG | T | 5 | a0001c0002t0004g0255a0001c0002t0004g0256a0001c0002t0004g0258others(2): Show | 5 | HG03041.hp1 HG03098.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2073+1259delG | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103058222 | ||||||
| chr10:103058555
|
G | A | 1 | a0001c0002t0071g0247 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2073+1591G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103058555 | ||||||
| chr10:103058782
|
G | T | 2 | a0001c0003t0001g0146a0001c0003t0001g0147 | 2 | NA18992.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.2073+1818G>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103058782 | ||||||
| chr10:103058950
|
AGTTT | A | 17 | a0001c0002t0006g0117a0001c0002t0006g0208a0001c0002t0006g0209others(14): Show | 17 | HG00408.hp1 HG00609.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.2073+1995_2073+199 others(8): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 103058950 | |||||
| chr10:103059527
|
A | G | 3 | a0001c0001t0014g0018a0001c0001t0014g0042a0001c0001t0014g0045 | 3 | HG01952.hp2 HG01981.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.2073+2563A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103059527 | ||||||
| chr10:103059701
|
A | G | 1 | a0001c0003t0010g0137 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2073+2737A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103059701 | ||||||
| chr10:103059750
|
TA | T | 89 | a0001c0002t0003g0223a0001c0002t0003g0225a0001c0002t0003g0227others(86): Show | 89 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.2073+2796delA | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 103059750 | |||||
| chr10:103059799
|
A | G | 31 | a0001c0002t0003g0223a0001c0002t0003g0225a0001c0002t0003g0227others(28): Show | 31 | HG00609.hp1 HG00621.hp2 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.2073+2835A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103059799 | ||||||
| chr10:103059855
|
A | G | 1 | a0001c0002t0003g0223 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2073+2891A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103059855 | ||||||
| chr10:103059887
|
A | T | 1 | a0001c0002t0002g0245 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2073+2923A>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103059887 | ||||||
| chr10:103060001
|
T | C | 2 | a0002c0004t0057g0202a0002c0004t0058g0203 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2073+3037T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103060001 | ||||||
| chr10:103060013
|
A | G | 152 | a0001c0002t0003g0223a0001c0002t0003g0225a0001c0002t0003g0227others(149): Show | 152 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(149): Show |
intron_variant | MODIFIER | c.2073+3049A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103060013 | ||||||
| chr10:103060190
|
A | T | 6 | a0001c0001t0014g0018a0001c0001t0014g0042a0001c0001t0014g0045others(3): Show | 6 | HG01952.hp2 HG01981.hp2 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.2073+3226A>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103060190 | ||||||
| chr10:103060273
|
A | G | 1 | a0002c0004t0066g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2073+3309A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103060273 | ||||||
| chr10:103060309
|
C | G | 1 | a0001c0001t0008g0090 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2073+3345C>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103060309 | ||||||
| chr10:103060507
|
T | C | 1 | a0001c0002t0004g0256 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2073+3543T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103060507 | ||||||
| chr10:103060528
|
G | A | 1 | a0001c0003t0001g0118 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2073+3564G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103060528 | ||||||
| chr10:103060582
|
C | A | 9 | a0001c0005t0022g0186a0001c0005t0023g0189a0001c0005t0023g0190others(6): Show | 9 | HG02135.hp2 HG03834.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.2073+3618C>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103060582 | ||||||
| chr10:103060839
|
G | T | 1 | a0001c0002t0062g0222 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2073+3875G>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103060839 | ||||||
| chr10:103061231
|
A | C | 1 | a0001c0003t0051g0136 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2073+4267A>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103061231 | ||||||
| chr10:103061434
|
T | C | 28 | a0001c0002t0002g0245a0001c0002t0003g0223a0001c0002t0003g0225others(25): Show | 28 | HG00609.hp1 HG00621.hp2 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.2073+4470T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103061434 | ||||||
| chr10:103061486
|
G | T | 1 | a0001c0001t0008g0252 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2073+4522G>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103061486 | ||||||
| chr10:103061499
|
A | T | 10 | a0001c0002t0004g0180a0001c0002t0024g0172a0001c0002t0024g0181others(7): Show | 10 | HG00639.hp1 HG00738.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.2073+4535A>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103061499 | ||||||
| chr10:103061706
|
T | C | 1 | a0001c0001t0002g0102 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.2073+4742T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103061706 | ||||||
| chr10:103061866
|
T | TA | 83 | a0001c0002t0002g0245a0001c0002t0003g0223a0001c0002t0003g0225others(80): Show | 83 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.2073+4911dupA | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 103061866 | |||||
| chr10:103061866
|
T | TAA | 7 | a0001c0002t0026g0267a0001c0002t0026g0269a0001c0002t0027g0266others(4): Show | 7 | HG01884.hp2 HG02145.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.2073+4910_2073+491 others(6): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 103061866 | |||||
| chr10:103061924
|
A | G | 2 | a0002c0004t0028g0196a0002c0004t0028g0215 | 2 | HG02622.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.2073+4960A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103061924 | ||||||
| chr10:103062189
|
G | A | 30 | a0001c0002t0003g0223a0001c0002t0003g0225a0001c0002t0003g0227others(27): Show | 30 | HG00609.hp1 HG00621.hp2 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.2073+5225G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103062189 | ||||||
| chr10:103062252
|
C | T | 22 | a0001c0002t0004g0176a0001c0002t0004g0180a0001c0002t0004g0255others(19): Show | 22 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.2073+5288C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103062252 | ||||||
| chr10:103062505
|
T | C | 1 | a0001c0001t0002g0066 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2073+5541T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103062505 | ||||||
| chr10:103062674
|
C | G | 89 | a0001c0002t0003g0223a0001c0002t0003g0225a0001c0002t0003g0227others(86): Show | 89 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.2073+5710C>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103062674 | ||||||
| chr10:103062931
|
A | G | 22 | a0001c0002t0004g0176a0001c0002t0004g0180a0001c0002t0004g0255others(19): Show | 22 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.2074-5698A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103062931 | ||||||
| chr10:103062978
|
G | A | 5 | a0001c0001t0005g0005a0001c0001t0005g0021a0001c0001t0005g0022others(2): Show | 5 | HG01109.hp2 HG02572.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.2074-5651G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103062978 | ||||||
| chr10:103063052
|
G | C | 89 | a0001c0002t0003g0223a0001c0002t0003g0225a0001c0002t0003g0227others(86): Show | 89 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.2074-5577G>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103063052 | ||||||
| chr10:103063197
|
T | C | 1 | a0001c0003t0001g0156 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2074-5432T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103063197 | ||||||
| chr10:103063295
|
C | T | 6 | a0001c0002t0026g0267a0001c0002t0026g0269a0001c0002t0027g0266others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.2074-5334C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103063295 | ||||||
| chr10:103063561
|
C | T | 6 | a0001c0001t0005g0004a0001c0001t0005g0005a0001c0001t0005g0021others(3): Show | 6 | HG01109.hp2 HG02572.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.2074-5068C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103063561 | ||||||
| chr10:103063917
|
C | T | 12 | a0002c0004t0025g0195a0002c0004t0025g0199a0002c0004t0028g0196others(9): Show | 12 | HG00735.hp1 HG01109.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.2074-4712C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103063917 | ||||||
| chr10:103064055
|
G | T | 1 | a0001c0002t0071g0247 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2074-4574G>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103064055 | ||||||
| chr10:103064152
|
A | T | 90 | a0001c0002t0002g0245a0001c0002t0003g0223a0001c0002t0003g0225others(87): Show | 90 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.2074-4477A>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103064152 | ||||||
| chr10:103064176
|
C | A | 1 | a0001c0010t0067g0194 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2074-4453C>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103064176 | ||||||
| chr10:103064322
|
A | T | 2 | a0001c0002t0009g0254a0001c0002t0107g0235 | 2 | HG00609.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.2074-4307A>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103064322 | ||||||
| chr10:103064382
|
A | G | 1 | a0001c0003t0001g0140 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2074-4247A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103064382 | ||||||
| chr10:103064388
|
G | GT | 50 | a0001c0002t0002g0245a0001c0002t0003g0223a0001c0002t0003g0225others(47): Show | 50 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.2074-4233dupT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 103064388 | |||||
| chr10:103064442
|
A | G | 153 | a0001c0002t0002g0245a0001c0002t0003g0223a0001c0002t0003g0225others(150): Show | 153 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(150): Show |
intron_variant | MODIFIER | c.2074-4187A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103064442 | ||||||
| chr10:103064567
|
T | A | 144 | a0001c0002t0002g0245a0001c0002t0003g0223a0001c0002t0003g0225others(141): Show | 144 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(141): Show |
intron_variant | MODIFIER | c.2074-4062T>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103064567 | ||||||
| chr10:103064630
|
G | A | 54 | a0001c0003t0001g0106a0001c0003t0001g0118a0001c0003t0001g0122others(51): Show | 54 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(51): Show |
intron_variant | MODIFIER | c.2074-3999G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103064630 | ||||||
| chr10:103065010
|
G | A | 269 | a0001c0001t0002g0019a0001c0001t0002g0028a0001c0001t0002g0049others(266): Show | 269 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.2074-3619G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103065010 | ||||||
| chr10:103065068
|
T | C | 1 | a0001c0002t0003g0223 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2074-3561T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103065068 | ||||||
| chr10:103065375
|
C | T | 89 | a0001c0002t0003g0223a0001c0002t0003g0225a0001c0002t0003g0227others(86): Show | 89 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.2074-3254C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103065375 | ||||||
| chr10:103065395
|
T | G | 13 | a0001c0001t0020g0026a0001c0001t0020g0027a0001c0001t0020g0054others(10): Show | 13 | HG00558.hp1 HG01257.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.2074-3234T>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103065395 | ||||||
| chr10:103065504
|
T | G | 1 | a0001c0001t0005g0022 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2074-3125T>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103065504 | ||||||
| chr10:103065625
|
A | G | 3 | a0001c0006t0004g0175a0001c0006t0013g0173a0001c0006t0013g0174 | 3 | HG01169.hp2 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.2074-3004A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103065625 | ||||||
| chr10:103065821
|
T | C | 14 | a0001c0002t0003g0223a0001c0002t0003g0225a0001c0002t0003g0231others(11): Show | 14 | HG00639.hp2 HG00642.hp2 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.2074-2808T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103065821 | ||||||
| chr10:103065897
|
G | A | 1 | a0001c0002t0003g0225 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2074-2732G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103065897 | ||||||
| chr10:103065908
|
C | G | 53 | a0001c0003t0001g0106a0001c0003t0001g0118a0001c0003t0001g0122others(50): Show | 53 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(50): Show |
intron_variant | MODIFIER | c.2074-2721C>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103065908 | ||||||
| chr10:103066001
|
C | T | 1 | a0001c0003t0001g0106 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2074-2628C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103066001 | ||||||
| chr10:103066089
|
C | T | 8 | a0001c0001t0005g0057a0001c0001t0005g0108a0001c0001t0008g0017others(5): Show | 8 | HG00099.hp1 HG01167.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.2074-2540C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103066089 | ||||||
| chr10:103066239
|
A | G | 3 | a0002c0004t0025g0195a0002c0004t0025g0199a0002c0004t0056g0200 | 3 | HG01109.hp1 HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.2074-2390A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103066239 | ||||||
| chr10:103066256
|
C | G | 2 | a0001c0002t0003g0233a0001c0002t0003g0234 | 2 | HG02027.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.2074-2373C>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103066256 | ||||||
| chr10:103066491
|
C | T | 1 | a0001c0002t0065g0116 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2074-2138C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103066491 | ||||||
| chr10:103066504
|
T | C | 153 | a0001c0002t0002g0245a0001c0002t0003g0223a0001c0002t0003g0225others(150): Show | 153 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(150): Show |
intron_variant | MODIFIER | c.2074-2125T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103066504 | ||||||
| chr10:103066575
|
A | C | 269 | a0001c0001t0002g0019a0001c0001t0002g0028a0001c0001t0002g0049others(266): Show | 269 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.2074-2054A>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103066575 | ||||||
| chr10:103067096
|
CT | C | 14 | a0001c0001t0005g0108a0001c0001t0031g0046a0001c0003t0001g0160others(11): Show | 14 | HG02135.hp2 HG03834.hp1 NA18943.hp2 others(11): Show |
intron_variant | MODIFIER | c.2074-1517delT | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 103067096 | |||||
| chr10:103067441
|
C | G | 89 | a0001c0002t0003g0223a0001c0002t0003g0225a0001c0002t0003g0227others(86): Show | 89 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.2074-1188C>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103067441 | ||||||
| chr10:103067519
|
C | T | 1 | a0001c0002t0054g0193 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2074-1110C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | chr10 | 103067519 | ||||||
| chr10:103068269
|
GGAGGCCA others(7): Show |
G | 54 | a0001c0003t0001g0106a0001c0003t0001g0118a0001c0003t0001g0122others(51): Show | 54 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(51): Show |
intron_variant | MODIFIER | c.2074-356_2074-343d others(16): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr10 | 103068269 | |||||
| chr10:103068794
|
C | A | 3 | a0001c0001t0005g0008a0001c0001t0011g0009a0001c0001t0011g0013 | 3 | HG02280.hp2 HG02717.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2167+72C>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 5/7 | chr10 | 103068794 | ||||||
| chr10:103068910
|
C | G | 1 | a0002c0004t0055g0216 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2167+188C>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 5/7 | chr10 | 103068910 | ||||||
| chr10:103068982
|
C | T | 5 | a0001c0002t0003g0227a0001c0002t0003g0232a0001c0002t0009g0246others(2): Show | 5 | HG00609.hp1 NA18950.hp2 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.2167+260C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 5/7 | chr10 | 103068982 | ||||||
| chr10:103069208
|
C | T | 1 | a0001c0002t0003g0231 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2167+486C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 5/7 | chr10 | 103069208 | ||||||
| chr10:103069345
|
G | A | 152 | a0001c0002t0003g0223a0001c0002t0003g0225a0001c0002t0003g0227others(149): Show | 152 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(149): Show |
intron_variant | MODIFIER | c.2167+623G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 5/7 | chr10 | 103069345 | ||||||
| chr10:103069576
|
C | T | 4 | a0001c0001t0020g0026a0001c0001t0021g0055a0001c0001t0041g0051others(1): Show | 4 | HG01361.hp2 HG01934.hp2 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.2167+854C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 5/7 | chr10 | 103069576 | ||||||
| chr10:103069712
|
C | T | 52 | a0001c0003t0001g0106a0001c0003t0001g0118a0001c0003t0001g0122others(49): Show | 52 | HG00099.hp2 HG00544.hp2 HG01167.hp2 others(49): Show |
intron_variant | MODIFIER | c.2167+990C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 5/7 | chr10 | 103069712 | ||||||
| chr10:103069713
|
G | A | 1 | a0001c0001t0104g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2167+991G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 5/7 | chr10 | 103069713 | ||||||
| chr10:103069719
|
T | G | 1 | a0001c0002t0062g0222 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2167+997T>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 5/7 | chr10 | 103069719 | ||||||
| chr10:103069762
|
A | G | 2 | a0001c0002t0064g0248a0001c0002t0065g0116 | 2 | HG02109.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2167+1040A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 5/7 | chr10 | 103069762 | ||||||
| chr10:103069770
|
G | A | 1 | a0001c0003t0010g0137 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2167+1048G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 5/7 | chr10 | 103069770 | ||||||
| chr10:103069933
|
A | G | 3 | a0001c0001t0005g0008a0001c0001t0011g0009a0001c0001t0011g0013 | 3 | HG02280.hp2 HG02717.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2167+1211A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 5/7 | chr10 | 103069933 | ||||||
| chr10:103070036
|
G | A | 20 | a0001c0002t0004g0176a0001c0002t0004g0180a0001c0002t0004g0255others(17): Show | 20 | HG00639.hp1 HG00738.hp1 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.2167+1314G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 5/7 | chr10 | 103070036 | ||||||
| chr10:103070141
|
C | T | 87 | a0001c0002t0003g0223a0001c0002t0003g0225a0001c0002t0003g0227others(84): Show | 87 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.2167+1419C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 5/7 | chr10 | 103070141 | ||||||
| chr10:103070184
|
G | C | 1 | a0001c0003t0001g0166 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2167+1462G>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 5/7 | chr10 | 103070184 | ||||||
| chr10:103070265
|
A | G | 1 | a0001c0002t0006g0117 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2168-1509A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 5/7 | chr10 | 103070265 | ||||||
| chr10:103070453
|
A | G | 67 | a0001c0002t0003g0223a0001c0002t0003g0225a0001c0002t0003g0227others(64): Show | 67 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.2168-1321A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 5/7 | chr10 | 103070453 | ||||||
| chr10:103070788
|
G | C | 3 | a0001c0003t0001g0127a0001c0003t0001g0133a0001c0003t0001g0170 | 3 | HG02083.hp2 NA18968.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.2168-986G>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 5/7 | chr10 | 103070788 | ||||||
| chr10:103070831
|
G | A | 47 | a0001c0002t0003g0223a0001c0002t0003g0225a0001c0002t0003g0227others(44): Show | 47 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.2168-943G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 5/7 | chr10 | 103070831 | ||||||
| chr10:103070877
|
C | T | 22 | a0001c0002t0004g0176a0001c0002t0004g0180a0001c0002t0004g0255others(19): Show | 22 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.2168-897C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 5/7 | chr10 | 103070877 | ||||||
| chr10:103070943
|
G | C | 9 | a0001c0005t0022g0186a0001c0005t0023g0189a0001c0005t0023g0190others(6): Show | 9 | HG02135.hp2 HG03834.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.2168-831G>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 5/7 | chr10 | 103070943 | ||||||
| chr10:103071062
|
A | G | 143 | a0001c0002t0003g0223a0001c0002t0003g0225a0001c0002t0003g0227others(140): Show | 143 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(140): Show |
intron_variant | MODIFIER | c.2168-712A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 5/7 | chr10 | 103071062 | ||||||
| chr10:103072415
|
ACTTCTCC others(23): Show |
A | 3 | a0001c0001t0043g0076a0001c0001t0043g0123a0001c0003t0001g0140 | 3 | NA19011.hp2 NA19082.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2233+616_2233+645d others(32): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 103072415 | |||||
| chr10:103072425
|
A | ACCACCAG others(53): Show |
1 | a0001c0006t0004g0175 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.2233+616_2233+675d others(62): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 103072425 | |||||
| chr10:103072435
|
A | G | 6 | a0001c0002t0026g0267a0001c0002t0026g0269a0001c0002t0027g0266others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.2233+596A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 6/7 | chr10 | 103072435 | ||||||
| chr10:103072455
|
A | ACCACCAG others(23): Show |
1 | a0001c0001t0002g0069 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2233+675_2233+704d others(32): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 103072455 | |||||
| chr10:103072455
|
ACCACCAG others(23): Show |
A | 2 | a0001c0001t0019g0083a0001c0001t0019g0084 | 2 | HG02970.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2233+675_2233+704d others(32): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 103072455 | |||||
| chr10:103072476
|
C | T | 1 | a0001c0002t0070g0218 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2233+637C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 6/7 | chr10 | 103072476 | ||||||
| chr10:103072499
|
G | A | 1 | a0001c0010t0067g0194 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2233+660G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 6/7 | chr10 | 103072499 | ||||||
| chr10:103072591
|
C | G | 1 | a0001c0001t0005g0077 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2233+752C>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 6/7 | chr10 | 103072591 | ||||||
| chr10:103072824
|
C | T | 1 | a0001c0001t0041g0051 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2233+985C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 6/7 | chr10 | 103072824 | ||||||
| chr10:103072883
|
C | T | 1 | a0001c0002t0062g0222 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2233+1044C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 6/7 | chr10 | 103072883 | ||||||
| chr10:103072884
|
G | A | 1 | a0002c0004t0028g0215 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2233+1045G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 6/7 | chr10 | 103072884 | ||||||
| chr10:103073021
|
T | A | 7 | a0001c0003t0001g0122a0001c0003t0001g0124a0001c0003t0032g0120others(4): Show | 7 | NA18951.hp2 NA18962.hp2 NA18990.hp2 others(4): Show |
intron_variant | MODIFIER | c.2233+1182T>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 6/7 | chr10 | 103073021 | ||||||
| chr10:103073100
|
C | T | 10 | a0002c0004t0025g0195a0002c0004t0025g0199a0002c0004t0055g0216others(7): Show | 10 | HG00735.hp1 HG01109.hp1 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.2233+1261C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 6/7 | chr10 | 103073100 | ||||||
| chr10:103073291
|
G | A | 18 | a0001c0002t0006g0117a0001c0002t0006g0208a0001c0002t0006g0209others(15): Show | 18 | HG00408.hp1 HG00609.hp2 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.2233+1452G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 6/7 | chr10 | 103073291 | ||||||
| chr10:103073317
|
A | G | 28 | a0001c0002t0003g0223a0001c0002t0003g0225a0001c0002t0003g0227others(25): Show | 28 | HG00609.hp1 HG00621.hp2 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.2233+1478A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 6/7 | chr10 | 103073317 | ||||||
| chr10:103073404
|
C | T | 22 | a0001c0002t0004g0176a0001c0002t0004g0180a0001c0002t0004g0255others(19): Show | 22 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.2233+1565C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 6/7 | chr10 | 103073404 | ||||||
| chr10:103073457
|
G | T | 1 | a0001c0001t0008g0047 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.2233+1618G>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 6/7 | chr10 | 103073457 | ||||||
| chr10:103073507
|
C | T | 1 | a0001c0001t0075g0038 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2233+1668C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 6/7 | chr10 | 103073507 | ||||||
| chr10:103073589
|
C | T | 2 | a0001c0001t0012g0020a0001c0001t0072g0115 | 2 | HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2233+1750C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 6/7 | chr10 | 103073589 | ||||||
| chr10:103073620
|
C | G | 89 | a0001c0002t0003g0223a0001c0002t0003g0225a0001c0002t0003g0227others(86): Show | 89 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.2233+1781C>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 6/7 | chr10 | 103073620 | ||||||
| chr10:103073628
|
G | A | 1 | a0001c0002t0062g0222 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2233+1789G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 6/7 | chr10 | 103073628 | ||||||
| chr10:103073778
|
C | T | 9 | a0001c0005t0022g0186a0001c0005t0023g0189a0001c0005t0023g0190others(6): Show | 9 | HG02135.hp2 HG03834.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.2233+1939C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 6/7 | chr10 | 103073778 | ||||||
| chr10:103073779
|
G | A | 29 | a0001c0002t0003g0223a0001c0002t0003g0225a0001c0002t0003g0227others(26): Show | 29 | HG00609.hp1 HG00621.hp2 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.2233+1940G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 6/7 | chr10 | 103073779 | ||||||
| chr10:103073797
|
A | G | 269 | a0001c0001t0002g0019a0001c0001t0002g0028a0001c0001t0002g0049others(266): Show | 269 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.2233+1958A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 6/7 | chr10 | 103073797 | ||||||
| chr10:103073863
|
C | T | 1 | a0001c0001t0096g0052 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.2233+2024C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 6/7 | chr10 | 103073863 | ||||||
| chr10:103073868
|
C | CA | 23 | a0001c0002t0004g0176a0001c0002t0004g0180a0001c0002t0004g0256others(20): Show | 23 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.2233+2055dupA | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 103073868 | |||||
| chr10:103073868
|
CA | C | 100 | a0001c0001t0002g0019a0001c0001t0002g0028a0001c0001t0002g0049others(97): Show | 100 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.2233+2055delA | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 103073868 | |||||
| chr10:103073868
|
CAA | C | 39 | a0001c0001t0002g0100a0001c0001t0034g0112a0001c0001t0040g0105others(36): Show | 39 | HG00609.hp1 HG00621.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.2233+2054_2233+205 others(6): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 103073868 | |||||
| chr10:103073868
|
CAAA | C | 14 | a0001c0002t0006g0117a0001c0002t0006g0208a0001c0002t0006g0209others(11): Show | 14 | HG00408.hp1 HG00609.hp2 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.2233+2053_2233+205 others(7): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 103073868 | |||||
| chr10:103073868
|
CAAAA | C | 9 | a0001c0002t0003g0231a0001c0002t0003g0239a0001c0002t0003g0240others(6): Show | 9 | HG00639.hp2 HG00733.hp1 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.2233+2052_2233+205 others(8): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 103073868 | |||||
| chr10:103073868
|
CAAAAAAA others(5): Show |
C | 2 | a0001c0005t0048g0184a0001c0005t0049g0183 | 2 | NA18943.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.2233+2044_2233+205 others(16): Show |
CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 103073868 | |||||
| chr10:103073907
|
C | T | 3 | a0001c0001t0035g0079a0001c0001t0035g0111a0001c0001t0086g0113 | 3 | HG01070.hp1 HG01516.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.2233+2068C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 6/7 | chr10 | 103073907 | ||||||
| chr10:103073929
|
T | C | 3 | a0001c0001t0017g0063a0001c0001t0017g0072a0001c0001t0017g0073 | 3 | HG00733.hp2 HG01106.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.2233+2090T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 6/7 | chr10 | 103073929 | ||||||
| chr10:103074117
|
G | A | 1 | a0001c0001t0002g0102 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.2234-1969G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 6/7 | chr10 | 103074117 | ||||||
| chr10:103074165
|
A | G | 22 | a0001c0002t0004g0176a0001c0002t0004g0180a0001c0002t0004g0255others(19): Show | 22 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.2234-1921A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 6/7 | chr10 | 103074165 | ||||||
| chr10:103074179
|
T | C | 1 | a0001c0001t0005g0003 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2234-1907T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 6/7 | chr10 | 103074179 | ||||||
| chr10:103074398
|
A | G | 1 | a0002c0004t0066g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2234-1688A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 6/7 | chr10 | 103074398 | ||||||
| chr10:103074651
|
G | C | 1 | a0002c0004t0028g0196 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2234-1435G>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 6/7 | chr10 | 103074651 | ||||||
| chr10:103074991
|
C | T | 1 | a0001c0002t0004g0258 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2234-1095C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 6/7 | chr10 | 103074991 | ||||||
| chr10:103075119
|
C | T | 35 | a0001c0001t0005g0057a0001c0001t0005g0096a0001c0001t0005g0108others(32): Show | 35 | HG00099.hp1 HG00544.hp1 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.2234-967C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 6/7 | chr10 | 103075119 | ||||||
| chr10:103075924
|
C | T | 1 | a0001c0001t0031g0039 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2234-162C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 6/7 | chr10 | 103075924 | ||||||
| chr10:103076290
|
T | C | 143 | a0001c0002t0003g0223a0001c0002t0003g0225a0001c0002t0003g0227others(140): Show | 143 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(140): Show |
intron_variant | MODIFIER | c.2418+20T>C | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 7/7 | chr10 | 103076290 | ||||||
| chr10:103076297
|
G | A | 1 | a0001c0003t0103g0119 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.2418+27G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 7/7 | chr10 | 103076297 | ||||||
| chr10:103076344
|
C | A | 22 | a0001c0002t0004g0176a0001c0002t0004g0180a0001c0002t0004g0255others(19): Show | 22 | HG00597.hp2 HG00639.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.2418+74C>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 7/7 | chr10 | 103076344 | ||||||
| chr10:103076371
|
T | G | 1 | a0001c0002t0006g0214 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2418+101T>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 7/7 | chr10 | 103076371 | ||||||
| chr10:103076555
|
T | G | 1 | a0002c0004t0028g0196 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2418+285T>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 7/7 | chr10 | 103076555 | ||||||
| chr10:103076754
|
A | G | 2 | a0001c0001t0012g0041a0001c0001t0095g0043 | 2 | HG00642.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.2419-217A>G | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 7/7 | chr10 | 103076754 | ||||||
| chr10:103076891
|
G | A | 1 | a0001c0003t0016g0145 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2419-80G>A | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 7/7 | chr10 | 103076891 | ||||||
| chr10:103076918
|
C | T | 5 | a0001c0002t0026g0267a0001c0002t0026g0269a0001c0002t0027g0266others(2): Show | 5 | HG01884.hp2 HG02145.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.2419-53C>T | CNNM2 | ENSG00000148842.18 | transcript | ENST00000369878.9 | protein_coding | 7/7 | chr10 | 103076918 |