| geneid | 26524 |
|---|---|
| ensemblid | ENSG00000150457.9 |
| hgncid | 6515 |
| symbol | LATS2 |
| name | large tumor suppressor kinase 2 |
| refseq_nuc | NM_014572.3 |
| refseq_prot | NP_055387.2 |
| ensembl_nuc | ENST00000382592.5 |
| ensembl_prot | ENSP00000372035.4 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 20973036 |
| end | 21061586 |
| strand | - |
| ver | v1.2 |
| region | chr13:20973036-21061586 |
| region5000 | chr13:20968036-21066586 |
| regionname0 | LATS2_chr13_20973036_21061586 |
| regionname5000 | LATS2_chr13_20968036_21066586 |
| 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 | 0/1 | 1090 | 95 | 4 | 24 | 53 | 4 | 9 | 42 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0002 | 0/0 | 1088 | 83 | 12 | 17 | 48 | 1 | 5 | 38 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0003 | 0/0 | 1088 | 78 | 32 | 14 | 22 | 1 | 9 | 17 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0004 | 1/0 | 1088 | 34 | 15 | 6 | 0 | 4 | 8 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0005 | 0/0 | 1090 | 7 | 5 | 1 | 0 | 0 | 1 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0006 | 0/0 | 1090 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0007 | 0/0 | 1088 | 5 | 0 | 0 | 5 | 0 | 0 | 5 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0008 | 0/0 | 1090 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0009 | 0/0 | 1088 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0010 | 0/0 | 1088 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0011 | 0/0 | 1088 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0012 | 0/0 | 1090 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0013 | 0/0 | 1092 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| 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 | 0/1 | 3273 | 88 | 4 | 22 | 49 | 4 | 8 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| c0002 | 0/0 | 3267 | 60 | 5 | 13 | 37 | 0 | 5 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| c0003 | 0/0 | 3267 | 30 | 6 | 7 | 11 | 0 | 6 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| c0004 | 0/0 | 3267 | 28 | 11 | 5 | 0 | 4 | 8 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| c0005 | 0/0 | 3267 | 26 | 7 | 4 | 11 | 1 | 3 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| c0006 | 0/0 | 3267 | 14 | 1 | 3 | 9 | 1 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| c0007 | 0/0 | 3267 | 7 | 7 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| c0008 | 0/0 | 3267 | 6 | 4 | 2 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| c0009 | 0/0 | 3267 | 6 | 6 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| c0010 | 0/0 | 3273 | 5 | 0 | 1 | 3 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| c0011 | 0/0 | 3273 | 5 | 5 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| c0012 | 0/0 | 3273 | 4 | 3 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| c0013 | 0/0 | 3267 | 4 | 0 | 0 | 4 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| c0014 | 0/0 | 3267 | 3 | 3 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| c0015 | 1/0 | 3267 | 3 | 2 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| c0016 | 0/0 | 3273 | 3 | 2 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| c0017 | 0/0 | 3267 | 2 | 1 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| c0018 | 0/0 | 3267 | 2 | 2 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| c0019 | 0/0 | 3267 | 2 | 1 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| c0020 | 0/0 | 3267 | 2 | 0 | 2 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| c0021 | 0/0 | 3267 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| c0022 | 0/0 | 3273 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| c0023 | 0/0 | 3267 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| c0024 | 0/0 | 3267 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| c0025 | 0/0 | 3267 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| c0026 | 0/0 | 3273 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| c0027 | 0/0 | 3267 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| c0028 | 0/0 | 3267 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| c0029 | 0/0 | 3279 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| c0030 | 0/0 | 3273 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| c0031 | 0/0 | 3273 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| c0032 | 0/0 | 3267 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| c0033 | 0/0 | 3273 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| c0034 | 0/0 | 3267 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| c0035 | 0/0 | 3267 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| c0036 | 0/0 | 3267 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| 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 | 0/1 | 2278 | 69 | 13 | 21 | 24 | 2 | 8 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| t0002 | 0/0 | 2277 | 53 | 10 | 13 | 21 | 2 | 7 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| t0003 | 0/0 | 2287 | 46 | 0 | 11 | 31 | 0 | 4 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| t0004 | 1/0 | 2280 | 22 | 7 | 3 | 10 | 1 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| t0005 | 0/0 | 2281 | 18 | 4 | 5 | 0 | 3 | 6 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| t0006 | 0/0 | 2288 | 9 | 0 | 0 | 8 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| t0007 | 0/0 | 2278 | 9 | 0 | 1 | 7 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| t0008 | 0/0 | 2280 | 8 | 8 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| t0009 | 0/0 | 2279 | 8 | 4 | 4 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| t0010 | 0/0 | 2279 | 8 | 3 | 1 | 3 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| t0011 | 0/0 | 2286 | 6 | 5 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| t0012 | 0/0 | 2286 | 5 | 0 | 1 | 4 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| t0013 | 0/0 | 2276 | 4 | 0 | 0 | 4 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| t0014 | 0/0 | 2283 | 3 | 3 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| t0015 | 0/0 | 2279 | 3 | 0 | 0 | 3 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| t0016 | 0/0 | 2278 | 3 | 3 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| t0017 | 0/0 | 2278 | 3 | 0 | 0 | 3 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| t0018 | 0/0 | 2281 | 3 | 3 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| t0019 | 0/0 | 2284 | 2 | 2 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| t0020 | 0/0 | 2282 | 2 | 1 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| t0021 | 0/0 | 2280 | 2 | 0 | 0 | 0 | 0 | 2 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| t0022 | 0/0 | 2278 | 2 | 0 | 0 | 2 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| t0023 | 0/0 | 2285 | 2 | 1 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| t0024 | 0/0 | 2286 | 2 | 0 | 0 | 2 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| t0025 | 0/0 | 2282 | 2 | 1 | 0 | 0 | 1 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| t0026 | 0/0 | 2280 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| t0027 | 0/0 | 2277 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| t0028 | 0/0 | 2283 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| t0029 | 0/0 | 2288 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| t0030 | 0/0 | 2284 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| t0031 | 0/0 | 2280 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| t0032 | 0/0 | 2278 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| t0033 | 0/0 | 2280 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| t0034 | 0/0 | 2278 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| t0035 | 0/0 | 2287 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| t0036 | 0/0 | 2281 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| t0037 | 0/0 | 2278 | 1 | 0 | 0 | 0 | 1 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| t0038 | 0/0 | 2287 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| t0039 | 0/0 | 2287 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| t0040 | 0/0 | 2289 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| t0041 | 0/0 | 2281 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| t0042 | 0/0 | 2287 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| t0043 | 0/0 | 2277 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| t0044 | 0/0 | 2280 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| t0045 | 0/0 | 2281 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| t0046 | 0/0 | 2280 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| t0047 | 0/0 | 2279 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| 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 | 2 | 0 | 2 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0024 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0086 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| 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 | 0/1 | 3273 | 88 | 4 | 22 | 49 | 4 | 8 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0001c0010 | 0/0 | 3273 | 5 | 0 | 1 | 3 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0001c0030 | 0/0 | 3273 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0001c0031 | 0/0 | 3273 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0002c0002 | 0/0 | 3267 | 60 | 5 | 13 | 37 | 0 | 5 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0002c0006 | 0/0 | 3267 | 14 | 1 | 3 | 9 | 1 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0002c0014 | 0/0 | 3267 | 3 | 3 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0002c0017 | 0/0 | 3267 | 2 | 1 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0002c0024 | 0/0 | 3267 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0002c0027 | 0/0 | 3267 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0002c0028 | 0/0 | 3267 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0002c0034 | 0/0 | 3267 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0003c0003 | 0/0 | 3267 | 30 | 6 | 7 | 11 | 0 | 6 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0003c0005 | 0/0 | 3267 | 26 | 7 | 4 | 11 | 1 | 3 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0003c0007 | 0/0 | 3267 | 7 | 7 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0003c0008 | 0/0 | 3267 | 6 | 4 | 2 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0003c0009 | 0/0 | 3267 | 6 | 6 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0003c0023 | 0/0 | 3267 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0003c0032 | 0/0 | 3267 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0003c0036 | 0/0 | 3267 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0004c0004 | 0/0 | 3267 | 28 | 11 | 5 | 0 | 4 | 8 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0004c0015 | 1/0 | 3267 | 3 | 2 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0004c0019 | 0/0 | 3267 | 2 | 1 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0004c0035 | 0/0 | 3267 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0005c0012 | 0/0 | 3273 | 4 | 3 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0005c0016 | 0/0 | 3273 | 3 | 2 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0006c0011 | 0/0 | 3273 | 5 | 5 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0007c0013 | 0/0 | 3267 | 4 | 0 | 0 | 4 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0007c0021 | 0/0 | 3267 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0008c0026 | 0/0 | 3273 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0008c0033 | 0/0 | 3273 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0009c0020 | 0/0 | 3267 | 2 | 0 | 2 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0010c0018 | 0/0 | 3267 | 2 | 2 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0011c0025 | 0/0 | 3267 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0012c0022 | 0/0 | 3273 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0013c0029 | 0/0 | 3279 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5550 | 52 | 4 | 18 | 21 | 2 | 6 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0001c0001t0002 | 0/0 | 5549 | 9 | 0 | 3 | 5 | 1 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0001c0001t0003 | 0/0 | 5559 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0001c0001t0004 | 0/0 | 5552 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0001c0001t0006 | 0/0 | 5560 | 6 | 0 | 0 | 6 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0001c0001t0010 | 0/0 | 5551 | 4 | 0 | 0 | 3 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0001c0001t0012 | 0/0 | 5558 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0001c0001t0013 | 0/0 | 5548 | 4 | 0 | 0 | 4 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0001c0001t0017 | 0/0 | 5550 | 2 | 0 | 0 | 2 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0001c0001t0022 | 0/0 | 5550 | 2 | 0 | 0 | 2 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0001c0001t0027 | 0/0 | 5549 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0001c0001t0029 | 0/0 | 5560 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0001c0001t0034 | 0/0 | 5550 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0001c0001t0037 | 0/0 | 5550 | 1 | 0 | 0 | 0 | 1 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0001c0001t0043 | 0/0 | 5549 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0001c0001t0047 | 0/0 | 5551 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0001c0010t0001 | 0/0 | 5550 | 4 | 0 | 1 | 2 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0001c0010t0015 | 0/0 | 5551 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0001c0030t0001 | 0/0 | 5550 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0001c0031t0006 | 0/0 | 5560 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0002c0002t0003 | 0/0 | 5553 | 44 | 0 | 11 | 29 | 0 | 4 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0002c0002t0006 | 0/0 | 5554 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0002c0002t0007 | 0/0 | 5544 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0002c0002t0010 | 0/0 | 5545 | 2 | 1 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0002c0002t0011 | 0/0 | 5552 | 4 | 3 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0002c0002t0012 | 0/0 | 5552 | 3 | 0 | 0 | 3 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0002c0002t0023 | 0/0 | 5551 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0002c0002t0024 | 0/0 | 5552 | 2 | 0 | 0 | 2 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0002c0002t0040 | 0/0 | 5555 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0002c0002t0042 | 0/0 | 5553 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0002c0006t0004 | 0/0 | 5546 | 14 | 1 | 3 | 9 | 1 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0002c0014t0018 | 0/0 | 5547 | 2 | 2 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0002c0014t0038 | 0/0 | 5553 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0002c0017t0006 | 0/0 | 5554 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0002c0017t0011 | 0/0 | 5552 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0002c0024t0023 | 0/0 | 5551 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0002c0027t0039 | 0/0 | 5553 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0002c0028t0041 | 0/0 | 5547 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0002c0034t0035 | 0/0 | 5553 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0003c0003t0001 | 0/0 | 5544 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0003c0003t0002 | 0/0 | 5543 | 16 | 2 | 6 | 4 | 0 | 4 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0003c0003t0004 | 0/0 | 5546 | 3 | 3 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0003c0003t0007 | 0/0 | 5544 | 7 | 0 | 1 | 5 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0003c0003t0017 | 0/0 | 5544 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0003c0003t0025 | 0/0 | 5548 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0003c0003t0044 | 0/0 | 5546 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0003c0005t0001 | 0/0 | 5544 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0003c0005t0002 | 0/0 | 5543 | 20 | 5 | 3 | 8 | 1 | 3 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0003c0005t0004 | 0/0 | 5546 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0003c0005t0012 | 0/0 | 5552 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0003c0005t0015 | 0/0 | 5545 | 2 | 0 | 0 | 2 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0003c0005t0033 | 0/0 | 5546 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0003c0007t0008 | 0/0 | 5546 | 5 | 5 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0003c0007t0016 | 0/0 | 5544 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0003c0007t0036 | 0/0 | 5547 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0003c0008t0008 | 0/0 | 5546 | 2 | 2 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0003c0008t0009 | 0/0 | 5545 | 3 | 1 | 2 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0003c0008t0046 | 0/0 | 5546 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0003c0009t0008 | 0/0 | 5546 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0003c0009t0009 | 0/0 | 5545 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0003c0009t0016 | 0/0 | 5544 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0003c0009t0026 | 0/0 | 5546 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0003c0009t0031 | 0/0 | 5546 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0003c0009t0032 | 0/0 | 5544 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0003c0023t0002 | 0/0 | 5543 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0003c0032t0016 | 0/0 | 5544 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0003c0036t0009 | 0/0 | 5545 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0004c0004t0001 | 0/0 | 5544 | 2 | 2 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0004c0004t0004 | 0/0 | 5546 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0004c0004t0005 | 0/0 | 5547 | 16 | 3 | 5 | 0 | 3 | 5 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0004c0004t0014 | 0/0 | 5549 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0004c0004t0019 | 0/0 | 5550 | 2 | 2 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0004c0004t0021 | 0/0 | 5546 | 2 | 0 | 0 | 0 | 0 | 2 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0004c0004t0025 | 0/0 | 5548 | 1 | 0 | 0 | 0 | 1 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0004c0004t0028 | 0/0 | 5549 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0004c0004t0030 | 0/0 | 5550 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0004c0004t0045 | 0/0 | 5547 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0004c0015t0004 | 1/0 | 5546 | 1 | 0 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0004c0015t0005 | 0/0 | 5547 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0004c0015t0018 | 0/0 | 5547 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0004c0019t0020 | 0/0 | 5548 | 2 | 1 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0004c0035t0009 | 0/0 | 5545 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0005c0012t0001 | 0/0 | 5550 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0005c0012t0002 | 0/0 | 5549 | 3 | 3 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0005c0016t0005 | 0/0 | 5553 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0005c0016t0014 | 0/0 | 5555 | 2 | 2 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0006c0011t0001 | 0/0 | 5550 | 5 | 5 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0007c0013t0002 | 0/0 | 5543 | 3 | 0 | 0 | 3 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0007c0013t0007 | 0/0 | 5544 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0007c0021t0002 | 0/0 | 5543 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0008c0026t0011 | 0/0 | 5558 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0008c0033t0001 | 0/0 | 5550 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0009c0020t0009 | 0/0 | 5545 | 2 | 0 | 2 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0010c0018t0010 | 0/0 | 5545 | 2 | 2 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0011c0025t0003 | 0/0 | 5553 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0012c0022t0004 | 0/0 | 5552 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| a0013c0029t0001 | 0/0 | 5556 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | copy fasta | chr13 | 20968036 | 21066586 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0024 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0004g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0006g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0006g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0006g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0006g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0006g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0006g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0010g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0010g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0010g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0010g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0012g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0013g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0013g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0013g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0013g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0017g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0017g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0022g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0022g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0027g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0029g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0034g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0037g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0043g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0001t0047g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0010t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0010t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0010t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0010t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0010t0015g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0030t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0001c0031t0006g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0003g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0003g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0003g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0003g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0003g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0003g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0003g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0003g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0003g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0006g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0007g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0010g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0010g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0011g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0011g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0011g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0011g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0012g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0012g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0012g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0023g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0024g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0024g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0040g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0002t0042g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0006t0004g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0006t0004g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0006t0004g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0006t0004g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0006t0004g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0006t0004g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0006t0004g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0006t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0006t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0006t0004g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0006t0004g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0006t0004g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0006t0004g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0006t0004g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0014t0018g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0014t0018g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0014t0038g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0017t0006g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0017t0011g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0024t0023g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0027t0039g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0028t0041g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0002c0034t0035g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0003t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0003t0002g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0003t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0003t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0003t0002g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0003t0002g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0003t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0003t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0003t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0003t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0003t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0003t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0003t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0003t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0003t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0003t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0003t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0003t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0003t0004g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0003t0004g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0003t0007g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0003t0007g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0003t0007g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0003t0007g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0003t0007g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0003t0007g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0003t0007g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0003t0017g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0003t0025g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0003t0044g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0005t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0005t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0005t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0005t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0005t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0005t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0005t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0005t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0005t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0005t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0005t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0005t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0005t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0005t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0005t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0005t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0005t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0005t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0005t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0005t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0005t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0005t0004g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0005t0012g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0005t0015g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0005t0015g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0005t0033g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0007t0008g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0007t0008g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0007t0008g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0007t0008g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0007t0008g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0007t0016g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0007t0036g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0008t0008g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0008t0008g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0008t0009g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0008t0009g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0008t0009g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0008t0046g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0009t0008g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0009t0009g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0009t0016g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0009t0026g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0009t0031g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0009t0032g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0023t0002g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0032t0016g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0003c0036t0009g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0004c0004t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0004c0004t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0004c0004t0004g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0004c0004t0005g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0004c0004t0005g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0004c0004t0005g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0004c0004t0005g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0004c0004t0005g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0004c0004t0005g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0004c0004t0005g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0004c0004t0005g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0004c0004t0005g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0004c0004t0005g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0004c0004t0005g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0004c0004t0005g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0004c0004t0005g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0004c0004t0005g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0004c0004t0005g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0004c0004t0005g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0004c0004t0014g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0004c0004t0019g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0004c0004t0019g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0004c0004t0021g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0004c0004t0021g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0004c0004t0025g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0004c0004t0028g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0004c0004t0030g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0004c0004t0045g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0004c0015t0004g0086 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0004c0015t0005g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0004c0015t0018g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0004c0019t0020g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0004c0019t0020g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0004c0035t0009g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0005c0012t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0005c0012t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0005c0012t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0005c0012t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0005c0016t0005g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0005c0016t0014g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0005c0016t0014g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0006c0011t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0006c0011t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0006c0011t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0006c0011t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0006c0011t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0007c0013t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0007c0013t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0007c0013t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0007c0013t0007g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0007c0021t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0008c0026t0011g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0008c0033t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0009c0020t0009g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0010c0018t0010g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0010c0018t0010g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0011c0025t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0012c0022t0004g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| a0013c0029t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0249 | EUR | GBR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG00099 | hp2 | a0004 | c0004 | t0005 | g0002 | EUR | GBR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG00280 | hp1 | a0001 | c0001 | t0037 | g0186 | EUR | FIN | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG00280 | hp2 | a0002 | c0006 | t0004 | g0258 | EUR | FIN | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG00423 | hp1 | a0001 | c0001 | t0006 | g0234 | EAS | CHS | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | CHS | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG00438 | hp1 | a0001 | c0001 | t0022 | g0174 | EAS | CHS | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG00438 | hp2 | a0002 | c0002 | t0003 | g0142 | EAS | CHS | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | CHS | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG00597 | hp2 | a0002 | c0006 | t0004 | g0210 | EAS | CHS | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG00621 | hp1 | a0002 | c0002 | t0003 | g0160 | EAS | CHS | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG00621 | hp2 | a0003 | c0005 | t0002 | g0060 | EAS | CHS | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG00639 | hp1 | a0002 | c0024 | t0023 | g0038 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG00639 | hp2 | a0004 | c0004 | t0005 | g0257 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG00642 | hp2 | a0003 | c0003 | t0002 | g0018 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG00735 | hp1 | a0005 | c0012 | t0001 | g0033 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG00735 | hp2 | a0002 | c0002 | t0011 | g0285 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG00738 | hp2 | a0002 | c0002 | t0003 | g0096 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0228 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG00741 | hp2 | a0003 | c0005 | t0002 | g0050 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG01070 | hp1 | a0003 | c0003 | t0002 | g0170 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG01070 | hp2 | a0009 | c0020 | t0009 | g0001 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG01071 | hp2 | a0009 | c0020 | t0009 | g0001 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG01074 | hp2 | a0003 | c0003 | t0002 | g0175 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0218 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG01099 | hp1 | a0001 | c0030 | t0001 | g0091 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG01099 | hp2 | a0003 | c0003 | t0002 | g0173 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG01106 | hp1 | a0004 | c0004 | t0005 | g0266 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG01106 | hp2 | a0001 | c0001 | t0027 | g0226 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG01109 | hp1 | a0003 | c0023 | t0002 | g0006 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG01167 | hp2 | a0003 | c0005 | t0002 | g0068 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG01168 | hp1 | a0002 | c0002 | t0003 | g0102 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG01168 | hp2 | a0003 | c0005 | t0002 | g0067 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG01175 | hp1 | a0004 | c0004 | t0005 | g0247 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG01175 | hp2 | a0003 | c0005 | t0012 | g0077 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG01243 | hp1 | a0004 | c0019 | t0020 | g0305 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG01243 | hp2 | a0003 | c0008 | t0009 | g0088 | AMR | PUR | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | CLM | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG01255 | hp2 | a0002 | c0002 | t0010 | g0118 | AMR | CLM | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG01257 | hp1 | a0002 | c0002 | t0003 | g0134 | AMR | CLM | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG01257 | hp2 | a0003 | c0003 | t0007 | g0313 | AMR | CLM | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG01258 | hp1 | a0002 | c0002 | t0003 | g0116 | AMR | CLM | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG01258 | hp2 | a0003 | c0003 | t0002 | g0255 | AMR | CLM | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG01261 | hp1 | a0002 | c0002 | t0003 | g0115 | AMR | CLM | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG01261 | hp2 | a0001 | c0010 | t0001 | g0074 | AMR | CLM | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG01358 | hp1 | a0002 | c0006 | t0004 | g0021 | AMR | CLM | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG01361 | hp1 | a0004 | c0004 | t0005 | g0261 | AMR | CLM | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | CLM | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG01433 | hp1 | a0004 | c0004 | t0005 | g0270 | AMR | CLM | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG01433 | hp2 | a0003 | c0008 | t0009 | g0296 | AMR | CLM | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | CLM | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG01496 | hp2 | a0002 | c0006 | t0004 | g0022 | AMR | CLM | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0227 | EUR | IBS | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG01515 | hp2 | a0004 | c0004 | t0025 | g0268 | EUR | IBS | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG01516 | hp1 | a0004 | c0004 | t0005 | g0089 | EUR | IBS | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG01516 | hp2 | a0004 | c0004 | t0005 | g0269 | EUR | IBS | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG01884 | hp1 | a0003 | c0036 | t0009 | g0310 | AFR | ACB | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG01928 | hp1 | a0002 | c0002 | t0003 | g0106 | AMR | PEL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PEL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG01934 | hp1 | a0002 | c0002 | t0003 | g0113 | AMR | PEL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PEL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PEL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG01943 | hp2 | a0002 | c0006 | t0004 | g0015 | AMR | PEL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0225 | AMR | PEL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PEL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG01981 | hp2 | a0002 | c0002 | t0003 | g0094 | AMR | PEL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | PEL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02004 | hp2 | a0002 | c0002 | t0003 | g0108 | AMR | PEL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02015 | hp2 | a0002 | c0002 | t0003 | g0149 | EAS | KHV | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02027 | hp1 | a0003 | c0005 | t0002 | g0055 | EAS | KHV | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02027 | hp2 | a0001 | c0001 | t0013 | g0189 | EAS | KHV | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02055 | hp1 | a0003 | c0005 | t0004 | g0078 | AFR | ACB | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02055 | hp2 | a0003 | c0003 | t0025 | g0287 | AFR | ACB | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02056 | hp1 | a0002 | c0002 | t0003 | g0145 | EAS | KHV | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | KHV | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02071 | hp1 | a0001 | c0001 | t0006 | g0188 | EAS | KHV | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02071 | hp2 | a0003 | c0005 | t0002 | g0059 | EAS | KHV | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0161 | EAS | KHV | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02074 | hp2 | a0002 | c0002 | t0003 | g0155 | EAS | KHV | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02083 | hp1 | a0001 | c0001 | t0029 | g0193 | EAS | KHV | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02083 | hp2 | a0002 | c0002 | t0003 | g0154 | EAS | KHV | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02135 | hp1 | a0003 | c0003 | t0007 | g0111 | EAS | KHV | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02135 | hp2 | a0001 | c0010 | t0001 | g0064 | EAS | KHV | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02145 | hp1 | a0003 | c0008 | t0008 | g0291 | AFR | ACB | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02145 | hp2 | a0002 | c0006 | t0004 | g0020 | AFR | ACB | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02148 | hp1 | a0003 | c0003 | t0002 | g0016 | AMR | PEL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02148 | hp2 | a0002 | c0002 | t0003 | g0148 | AMR | PEL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02155 | hp1 | a0003 | c0003 | t0007 | g0135 | EAS | CDX | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02155 | hp2 | a0002 | c0002 | t0012 | g0198 | EAS | CDX | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02257 | hp1 | a0003 | c0005 | t0002 | g0071 | AFR | ACB | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02257 | hp2 | a0003 | c0007 | t0008 | g0070 | AFR | ACB | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02258 | hp1 | a0003 | c0009 | t0032 | g0289 | AFR | ACB | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02258 | hp2 | a0004 | c0004 | t0019 | g0292 | AFR | ACB | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02280 | hp2 | a0003 | c0007 | t0036 | g0051 | AFR | ACB | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02300 | hp1 | a0002 | c0002 | t0003 | g0119 | AMR | PEL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PEL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02451 | hp1 | a0006 | c0011 | t0001 | g0079 | AFR | ACB | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02451 | hp2 | a0002 | c0014 | t0038 | g0040 | AFR | ACB | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02572 | hp1 | a0010 | c0018 | t0010 | g0065 | AFR | GWD | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02572 | hp2 | a0012 | c0022 | t0004 | g0007 | AFR | GWD | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02602 | hp1 | a0002 | c0002 | t0006 | g0159 | SAS | PJL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02602 | hp2 | a0001 | c0010 | t0001 | g0056 | SAS | PJL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02615 | hp1 | a0004 | c0015 | t0005 | g0083 | AFR | GWD | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02615 | hp2 | a0003 | c0003 | t0004 | g0259 | AFR | GWD | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02622 | hp1 | a0003 | c0009 | t0016 | g0307 | AFR | GWD | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02622 | hp2 | a0004 | c0004 | t0005 | g0311 | AFR | GWD | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02630 | hp1 | a0003 | c0008 | t0046 | g0288 | AFR | GWD | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02630 | hp2 | a0003 | c0003 | t0002 | g0172 | AFR | GWD | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02647 | hp1 | a0010 | c0018 | t0010 | g0066 | AFR | GWD | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02647 | hp2 | a0004 | c0004 | t0014 | g0299 | AFR | GWD | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02683 | hp1 | a0001 | c0001 | t0034 | g0216 | SAS | PJL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02683 | hp2 | a0004 | c0004 | t0005 | g0256 | SAS | PJL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02723 | hp1 | a0003 | c0005 | t0002 | g0048 | AFR | GWD | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02723 | hp2 | a0003 | c0009 | t0031 | g0031 | AFR | GWD | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02735 | hp1 | a0002 | c0002 | t0003 | g0157 | SAS | PJL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02735 | hp2 | a0004 | c0004 | t0005 | g0229 | SAS | PJL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02738 | hp1 | a0004 | c0004 | t0021 | g0254 | SAS | PJL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02738 | hp2 | a0004 | c0004 | t0045 | g0314 | SAS | PJL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02809 | hp1 | a0002 | c0002 | t0011 | g0283 | AFR | GWD | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02809 | hp2 | a0002 | c0002 | t0023 | g0087 | AFR | GWD | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02886 | hp1 | a0002 | c0014 | t0018 | g0039 | AFR | GWD | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02886 | hp2 | a0005 | c0012 | t0002 | g0032 | AFR | GWD | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02895 | hp1 | a0003 | c0007 | t0008 | g0044 | AFR | GWD | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02895 | hp2 | a0006 | c0011 | t0001 | g0081 | AFR | GWD | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02897 | hp1 | a0003 | c0009 | t0026 | g0029 | AFR | GWD | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02897 | hp2 | a0003 | c0007 | t0008 | g0045 | AFR | GWD | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02922 | hp1 | a0004 | c0004 | t0001 | g0302 | AFR | ESN | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02922 | hp2 | a0002 | c0014 | t0018 | g0041 | AFR | ESN | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02965 | hp1 | a0002 | c0034 | t0035 | g0027 | AFR | ESN | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02965 | hp2 | a0002 | c0028 | t0041 | g0282 | AFR | ESN | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02970 | hp1 | a0006 | c0011 | t0001 | g0080 | AFR | ESN | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02970 | hp2 | a0003 | c0008 | t0008 | g0293 | AFR | ESN | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02976 | hp1 | a0004 | c0004 | t0005 | g0290 | AFR | ESN | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02976 | hp2 | a0002 | c0017 | t0011 | g0075 | AFR | ESN | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG03017 | hp1 | a0002 | c0002 | t0003 | g0095 | SAS | PJL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG03017 | hp2 | a0001 | c0001 | t0010 | g0099 | SAS | PJL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG03041 | hp1 | a0004 | c0015 | t0018 | g0042 | AFR | GWD | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG03041 | hp2 | a0004 | c0004 | t0005 | g0251 | AFR | GWD | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG03098 | hp1 | a0003 | c0005 | t0002 | g0072 | AFR | MSL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG03098 | hp2 | a0008 | c0026 | t0011 | g0286 | AFR | MSL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG03139 | hp1 | a0005 | c0016 | t0014 | g0036 | AFR | ESN | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | ESN | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG03195 | hp1 | a0006 | c0011 | t0001 | g0085 | AFR | ESN | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG03195 | hp2 | a0005 | c0012 | t0002 | g0030 | AFR | ESN | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG03209 | hp1 | a0003 | c0005 | t0002 | g0049 | AFR | MSL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG03209 | hp2 | a0004 | c0004 | t0030 | g0295 | AFR | MSL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG03225 | hp1 | a0003 | c0009 | t0008 | g0309 | AFR | MSL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG03225 | hp2 | a0003 | c0008 | t0009 | g0294 | AFR | MSL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG03453 | hp1 | a0003 | c0005 | t0001 | g0084 | AFR | MSL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG03453 | hp2 | a0008 | c0033 | t0001 | g0304 | AFR | MSL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG03486 | hp1 | a0003 | c0009 | t0009 | g0308 | AFR | MSL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG03486 | hp2 | a0003 | c0003 | t0004 | g0301 | AFR | MSL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG03490 | hp1 | a0004 | c0004 | t0005 | g0204 | SAS | PJL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG03490 | hp2 | a0003 | c0003 | t0002 | g0008 | SAS | PJL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG03492 | hp1 | a0003 | c0003 | t0002 | g0014 | SAS | PJL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG03540 | hp1 | a0004 | c0035 | t0009 | g0297 | AFR | GWD | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG03540 | hp2 | a0003 | c0032 | t0016 | g0315 | AFR | GWD | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG03654 | hp1 | a0002 | c0002 | t0003 | g0101 | SAS | PJL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG03688 | hp1 | a0004 | c0004 | t0005 | g0230 | SAS | STU | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG03688 | hp2 | a0003 | c0003 | t0001 | g0236 | SAS | STU | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG03704 | hp1 | a0002 | c0002 | t0003 | g0158 | SAS | PJL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG03704 | hp2 | a0003 | c0003 | t0002 | g0017 | SAS | PJL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG03710 | hp2 | a0003 | c0005 | t0002 | g0063 | SAS | PJL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG03831 | hp1 | a0003 | c0003 | t0002 | g0190 | SAS | BEB | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | BEB | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG03834 | hp1 | a0004 | c0004 | t0005 | g0253 | SAS | BEB | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG03834 | hp2 | a0003 | c0005 | t0002 | g0278 | SAS | BEB | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG03927 | hp1 | a0004 | c0004 | t0021 | g0260 | SAS | BEB | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG03927 | hp2 | a0003 | c0003 | t0007 | g0312 | SAS | BEB | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG03942 | hp1 | a0005 | c0016 | t0005 | g0235 | SAS | BEB | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG03942 | hp2 | a0003 | c0005 | t0002 | g0076 | SAS | BEB | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | STU | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | STU | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18612 | hp1 | a0002 | c0027 | t0039 | g0114 | EAS | CHB | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18612 | hp2 | a0002 | c0002 | t0003 | g0151 | EAS | CHB | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18906 | hp1 | a0003 | c0007 | t0016 | g0062 | AFR | YRI | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18906 | hp2 | a0003 | c0005 | t0002 | g0058 | AFR | YRI | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18942 | hp1 | a0001 | c0001 | t0013 | g0167 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18942 | hp2 | a0002 | c0002 | t0003 | g0104 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18943 | hp1 | a0003 | c0003 | t0044 | g0110 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18943 | hp2 | a0003 | c0005 | t0002 | g0057 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18945 | hp2 | a0007 | c0013 | t0007 | g0137 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18946 | hp1 | a0001 | c0001 | t0017 | g0131 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18946 | hp2 | a0003 | c0003 | t0007 | g0120 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18950 | hp1 | a0002 | c0002 | t0003 | g0121 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18951 | hp1 | a0002 | c0002 | t0003 | g0147 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18951 | hp2 | a0002 | c0017 | t0006 | g0004 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18952 | hp1 | a0002 | c0002 | t0003 | g0125 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18952 | hp2 | a0003 | c0003 | t0002 | g0180 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18954 | hp1 | a0003 | c0003 | t0007 | g0105 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18956 | hp1 | a0007 | c0013 | t0002 | g0009 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18956 | hp2 | a0002 | c0002 | t0012 | g0182 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18959 | hp2 | a0002 | c0002 | t0003 | g0126 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18969 | hp1 | a0002 | c0006 | t0004 | g0169 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18969 | hp2 | a0003 | c0005 | t0002 | g0054 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18970 | hp2 | a0001 | c0001 | t0006 | g0194 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18971 | hp1 | a0001 | c0001 | t0010 | g0163 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18971 | hp2 | a0002 | c0002 | t0007 | g0141 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18973 | hp2 | a0002 | c0002 | t0003 | g0117 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18979 | hp1 | a0002 | c0002 | t0003 | g0107 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18979 | hp2 | a0001 | c0001 | t0012 | g0165 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18980 | hp2 | a0002 | c0002 | t0003 | g0124 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18982 | hp1 | a0003 | c0003 | t0017 | g0132 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18982 | hp2 | a0003 | c0003 | t0002 | g0179 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18983 | hp1 | a0001 | c0001 | t0043 | g0139 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18984 | hp1 | a0002 | c0002 | t0003 | g0098 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18984 | hp2 | a0013 | c0029 | t0001 | g0243 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18986 | hp2 | a0003 | c0005 | t0015 | g0005 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18988 | hp1 | a0003 | c0003 | t0002 | g0010 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18988 | hp2 | a0001 | c0001 | t0004 | g0276 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18990 | hp1 | a0003 | c0005 | t0033 | g0073 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18990 | hp2 | a0002 | c0002 | t0003 | g0103 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18991 | hp1 | a0002 | c0002 | t0003 | g0109 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18991 | hp2 | a0002 | c0006 | t0004 | g0219 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18992 | hp1 | a0003 | c0005 | t0015 | g0069 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18992 | hp2 | a0001 | c0001 | t0013 | g0205 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18994 | hp1 | a0002 | c0002 | t0040 | g0143 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18994 | hp2 | a0001 | c0001 | t0006 | g0184 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18998 | hp1 | a0001 | c0001 | t0010 | g0112 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18998 | hp2 | a0002 | c0002 | t0003 | g0123 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18999 | hp1 | a0003 | c0003 | t0007 | g0136 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA18999 | hp2 | a0002 | c0006 | t0004 | g0212 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19000 | hp1 | a0002 | c0002 | t0003 | g0153 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19000 | hp2 | a0001 | c0001 | t0010 | g0162 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19001 | hp1 | a0001 | c0001 | t0017 | g0130 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19001 | hp2 | a0001 | c0010 | t0015 | g0003 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19002 | hp2 | a0002 | c0002 | t0003 | g0122 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19004 | hp1 | a0002 | c0002 | t0042 | g0127 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19005 | hp1 | a0002 | c0002 | t0024 | g0152 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19007 | hp1 | a0002 | c0002 | t0012 | g0244 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19007 | hp2 | a0001 | c0001 | t0022 | g0171 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19011 | hp1 | a0002 | c0006 | t0004 | g0019 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19012 | hp1 | a0003 | c0005 | t0002 | g0053 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19012 | hp2 | a0002 | c0006 | t0004 | g0213 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19030 | hp1 | a0004 | c0019 | t0020 | g0306 | AFR | LWK | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | LWK | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19043 | hp1 | a0003 | c0003 | t0004 | g0300 | AFR | LWK | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19043 | hp2 | a0004 | c0004 | t0019 | g0026 | AFR | LWK | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19057 | hp1 | a0001 | c0001 | t0006 | g0168 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19057 | hp2 | a0007 | c0021 | t0002 | g0013 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19058 | hp1 | a0011 | c0025 | t0003 | g0097 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19058 | hp2 | a0002 | c0006 | t0004 | g0164 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19063 | hp1 | a0003 | c0005 | t0002 | g0043 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19064 | hp1 | a0002 | c0006 | t0004 | g0011 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19064 | hp2 | a0001 | c0010 | t0001 | g0061 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19065 | hp1 | a0002 | c0002 | t0003 | g0129 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19066 | hp1 | a0001 | c0001 | t0006 | g0195 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19066 | hp2 | a0002 | c0002 | t0003 | g0146 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19070 | hp1 | a0002 | c0002 | t0003 | g0150 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19074 | hp1 | a0002 | c0002 | t0003 | g0140 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19076 | hp1 | a0002 | c0002 | t0024 | g0156 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19076 | hp2 | a0007 | c0013 | t0002 | g0093 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19078 | hp1 | a0001 | c0031 | t0006 | g0187 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19078 | hp2 | a0002 | c0002 | t0003 | g0133 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19079 | hp1 | a0001 | c0001 | t0047 | g0100 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19079 | hp2 | a0002 | c0006 | t0004 | g0012 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19081 | hp1 | a0001 | c0001 | t0013 | g0206 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19081 | hp2 | a0002 | c0002 | t0003 | g0144 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19084 | hp2 | a0003 | c0003 | t0002 | g0185 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19085 | hp1 | a0003 | c0005 | t0002 | g0052 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19087 | hp1 | a0002 | c0002 | t0003 | g0138 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19088 | hp2 | a0007 | c0013 | t0002 | g0023 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19091 | hp2 | a0002 | c0002 | t0003 | g0128 | EAS | JPT | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19240 | hp1 | a0004 | c0004 | t0028 | g0025 | AFR | YRI | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA19240 | hp2 | a0005 | c0012 | t0002 | g0028 | AFR | YRI | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA20129 | hp1 | a0006 | c0011 | t0001 | g0082 | AFR | ASW | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA20129 | hp2 | a0004 | c0004 | t0004 | g0298 | AFR | ASW | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA20752 | hp1 | a0003 | c0005 | t0002 | g0037 | EUR | TSI | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0250 | EUR | TSI | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02559 | hp1 | a0003 | c0007 | t0008 | g0047 | AFR | ACB | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG02559 | hp2 | a0002 | c0002 | t0011 | g0034 | AFR | ACB | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG03471 | hp1 | a0002 | c0002 | t0011 | g0284 | AFR | MSL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG03471 | hp2 | a0003 | c0007 | t0008 | g0046 | AFR | MSL | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG06807 | hp1 | a0005 | c0016 | t0014 | g0035 | AFR | USA | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| HG06807 | hp2 | a0003 | c0003 | t0002 | g0231 | AFR | USA | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA20300 | hp1 | a0002 | c0002 | t0010 | g0281 | AFR | USA | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| NA20300 | hp2 | a0004 | c0004 | t0001 | g0303 | AFR | USA | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0024 | REF | REF | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| homoSapiens_grch38 | hp1 | a0004 | c0015 | t0004 | g0086 | REF | REF | LATS2_chr13_20968036_21066586 | LATS2 | chr13 | 20968036 | 21066586 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:20975096
|
G | C | 1 | a0009 | 2 | HG01070.hp2 HG01071.hp2 |
missense_variant | MODERATE | c.3041C>G | p.Ala1014Gly | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 3486/5546 | 3041/3267 | 1014/1088 | chr13 | 20975096 | ||
| chr13:20975100
|
C | T | 1 | a0006 | 5 | HG02451.hp1 HG02895.hp2 HG02970.hp1 others(2): Show |
missense_variant | MODERATE | c.3037G>A | p.Asp1013Asn | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 3482/5546 | 3037/3267 | 1013/1088 | chr13 | 20975100 | ||
| chr13:20981575
|
G | C | 1 | a0006 | 5 | HG02451.hp1 HG02895.hp2 HG02970.hp1 others(2): Show |
missense_variant | MODERATE | c.2556C>G | p.Asp852Glu | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 6/8 | 3001/5546 | 2556/3267 | 852/1088 | chr13 | 20981575 | ||
| chr13:20983392
|
T | C | 1 | a0010 | 2 | HG02572.hp1 HG02647.hp1 |
missense_variant | MODERATE | c.2314A>G | p.Ile772Val | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 5/8 | 2759/5546 | 2314/3267 | 772/1088 | chr13 | 20983392 | ||
| chr13:20988093
|
C | T | 1 | a0012 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.1687G>A | p.Gly563Arg | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/8 | 2132/5546 | 1687/3267 | 563/1088 | chr13 | 20988093 | ||
| chr13:20988343
|
C | CGGGGCG | 5 | a0001a0005a0006others(2): Show | 110 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(107): Show |
disruptive_inframe_insertion | MODERATE | c.1431_1436dupCGCCCC | p.Pro479_Ala480insAl others(4): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/8 | 1881/5546 | 1436/3267 | 479/1088 | chr13 | 20988343 | ||
| chr13:20988343
|
C | CGGGGCGG others(5): Show |
1 | a0013 | 1 | NA18984.hp2 | disruptive_inframe_insertion | MODERATE | c.1425_1436dupCGCCCC others(6): Show |
p.Pro479_Ala480insAl others(10): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/8 | 1881/5546 | 1436/3267 | 479/1088 | chr13 | 20988343 | ||
| chr13:20988693
|
C | T | 11 | a0001a0002a0003others(8): Show | 275 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(272): Show |
missense_variant | MODERATE | c.1087G>A | p.Gly363Ser | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/8 | 1532/5546 | 1087/3267 | 363/1088 | chr13 | 20988693 | ||
| chr13:20988809
|
G | A | 8 | a0001a0003a0006others(5): Show | 189 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(186): Show |
missense_variant | MODERATE | c.971C>T | p.Ala324Val | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/8 | 1416/5546 | 971/3267 | 324/1088 | chr13 | 20988809 | ||
| chr13:20989172
|
G | A | 1 | a0007 | 5 | NA18945.hp2 NA18956.hp1 NA19057.hp2 others(2): Show |
missense_variant | MODERATE | c.608C>T | p.Ala203Val | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/8 | 1053/5546 | 608/3267 | 203/1088 | chr13 | 20989172 | ||
| chr13:20989181
|
C | G | 1 | a0011 | 1 | NA19058.hp1 | missense_variant | MODERATE | c.599G>C | p.Gly200Ala | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/8 | 1044/5546 | 599/3267 | 200/1088 | chr13 | 20989181 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:20975125
|
G | A | 1 | a0002c0027 | 1 | NA18612.hp1 | synonymous_variant | LOW | c.3012C>T | p.Pro1004Pro | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 3457/5546 | 3012/3267 | 1004/1088 | chr13 | 20975125 | ||
| chr13:20975215
|
G | A | 1 | a0002c0034 | 1 | HG02965.hp1 | synonymous_variant | LOW | c.2922C>T | p.Ser974Ser | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 3367/5546 | 2922/3267 | 974/1088 | chr13 | 20975215 | ||
| chr13:20975245
|
G | A | 6 | a0002c0028a0003c0007a0003c0008others(3): Show | 22 | HG01243.hp2 HG01433.hp2 HG01884.hp1 others(19): Show |
synonymous_variant | LOW | c.2892C>T | p.Ala964Ala | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 3337/5546 | 2892/3267 | 964/1088 | chr13 | 20975245 | ||
| chr13:20981470
|
G | A | 1 | a0004c0019 | 2 | HG01243.hp1 NA19030.hp1 |
synonymous_variant | LOW | c.2661C>T | p.Arg887Arg | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 6/8 | 3106/5546 | 2661/3267 | 887/1088 | chr13 | 20981470 | ||
| chr13:20981557
|
C | T | 1 | a0001c0031 | 1 | NA19078.hp1 | synonymous_variant | LOW | c.2574G>A | p.Glu858Glu | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 6/8 | 3019/5546 | 2574/3267 | 858/1088 | chr13 | 20981557 | ||
| chr13:20983240
|
G | C | 1 | a0003c0032 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.2466C>G | p.Ser822Ser | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 5/8 | 2911/5546 | 2466/3267 | 822/1088 | chr13 | 20983240 | ||
| chr13:20983591
|
C | T | 1 | a0001c0030 | 1 | HG01099.hp1 | synonymous_variant | LOW | c.2115G>A | p.Leu705Leu | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 5/8 | 2560/5546 | 2115/3267 | 705/1088 | chr13 | 20983591 | ||
| chr13:20983780
|
C | T | 1 | a0003c0023 | 1 | HG01109.hp1 | synonymous_variant | LOW | c.1926G>A | p.Glu642Glu | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 5/8 | 2371/5546 | 1926/3267 | 642/1088 | chr13 | 20983780 | ||
| chr13:20988178
|
G | A | 2 | a0003c0009a0003c0036 | 7 | HG01884.hp1 HG02258.hp1 HG02622.hp1 others(4): Show |
synonymous_variant | LOW | c.1602C>T | p.Asp534Asp | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/8 | 2047/5546 | 1602/3267 | 534/1088 | chr13 | 20988178 | ||
| chr13:20988223
|
C | T | 1 | a0012c0022 | 1 | HG02572.hp2 | synonymous_variant | LOW | c.1557G>A | p.Pro519Pro | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/8 | 2002/5546 | 1557/3267 | 519/1088 | chr13 | 20988223 | ||
| chr13:20988232
|
C | T | 2 | a0002c0006a0002c0014 | 17 | HG00280.hp2 HG00597.hp2 HG01358.hp1 others(14): Show |
synonymous_variant | LOW | c.1548G>A | p.Pro516Pro | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/8 | 1993/5546 | 1548/3267 | 516/1088 | chr13 | 20988232 | ||
| chr13:20988373
|
A | T | 1 | a0012c0022 | 1 | HG02572.hp2 | synonymous_variant | LOW | c.1407T>A | p.Pro469Pro | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/8 | 1852/5546 | 1407/3267 | 469/1088 | chr13 | 20988373 | ||
| chr13:20988487
|
G | A | 1 | a0005c0012 | 4 | HG00735.hp1 HG02886.hp2 HG03195.hp2 others(1): Show |
synonymous_variant | LOW | c.1293C>T | p.Thr431Thr | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/8 | 1738/5546 | 1293/3267 | 431/1088 | chr13 | 20988487 | ||
| chr13:20988940
|
C | A | 3 | a0002c0024a0002c0034a0008c0033 | 3 | HG00639.hp1 HG02965.hp1 HG03453.hp2 |
synonymous_variant | LOW | c.840G>T | p.Pro280Pro | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/8 | 1285/5546 | 840/3267 | 280/1088 | chr13 | 20988940 | ||
| chr13:20989021
|
G | A | 1 | a0004c0035 | 1 | HG03540.hp1 | synonymous_variant | LOW | c.759C>T | p.Tyr253Tyr | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/8 | 1204/5546 | 759/3267 | 253/1088 | chr13 | 20989021 | ||
| chr13:21045889
|
G | A | 1 | a0003c0036 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.138C>T | p.Ser46Ser | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/8 | 583/5546 | 138/3267 | 46/1088 | chr13 | 21045889 | ||
| chr13:21045946
|
T | C | 25 | a0001c0001a0001c0030a0001c0031others(22): Show | 260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
synonymous_variant | LOW | c.81A>G | p.Lys27Lys | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/8 | 526/5546 | 81/3267 | 27/1088 | chr13 | 21045946 | ||
| chr13:21046000
|
C | T | 1 | a0007c0021 | 1 | NA19057.hp2 | synonymous_variant | LOW | c.27G>A | p.Thr9Thr | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/8 | 472/5546 | 27/3267 | 9/1088 | chr13 | 21046000 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:20973092
|
G | T | 1 | a0001c0001t0034 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1778C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 1778 | chr13 | 20973092 | |||||
| chr13:20973178
|
T | C | 16 | a0001c0001t0002a0001c0001t0027a0001c0010t0015others(13): Show | 69 | HG00621.hp2 HG00642.hp2 HG00741.hp1 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*1692A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 1692 | chr13 | 20973178 | |||||
| chr13:20973242
|
T | C | 1 | a0001c0001t0029 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1628A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 1628 | chr13 | 20973242 | |||||
| chr13:20973514
|
C | CTG | 7 | a0002c0002t0023a0002c0024t0023a0004c0004t0014others(4): Show | 9 | HG00639.hp1 HG02258.hp2 HG02647.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1354_*1355dupCA | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 1355 | chr13 | 20973514 | |||||
| chr13:20973514
|
C | CTGTG | 13 | a0001c0001t0003a0001c0001t0012a0002c0002t0003others(10): Show | 62 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*1352_*1355dupCACA | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 1355 | chr13 | 20973514 | |||||
| chr13:20973514
|
C | CTGTGTG | 7 | a0001c0001t0006a0001c0001t0029a0001c0031t0006others(4): Show | 12 | HG00423.hp1 HG02071.hp1 HG02083.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1350_*1355dupCACA others(2): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 1355 | chr13 | 20973514 | |||||
| chr13:20973514
|
CTG | C | 46 | a0001c0001t0001a0001c0001t0002a0001c0001t0010others(43): Show | 175 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*1354_*1355delCA | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 1354 | chr13 | 20973514 | |||||
| chr13:20973557
|
C | T | 1 | a0002c0027t0039 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1313G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 1313 | chr13 | 20973557 | |||||
| chr13:20973595
|
T | G | 1 | a0003c0009t0032 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1275A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 1275 | chr13 | 20973595 | |||||
| chr13:20973622
|
T | A | 1 | a0001c0001t0022 | 2 | HG00438.hp1 NA19007.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1248A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 1248 | chr13 | 20973622 | |||||
| chr13:20973693
|
A | G | 17 | a0002c0028t0041a0003c0007t0008a0003c0007t0016others(14): Show | 25 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1177T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 1177 | chr13 | 20973693 | |||||
| chr13:20973720
|
A | T | 1 | a0004c0004t0019 | 2 | HG02258.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1150T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 1150 | chr13 | 20973720 | |||||
| chr13:20973845
|
C | T | 28 | a0001c0001t0003a0001c0001t0006a0001c0001t0012others(25): Show | 85 | HG00423.hp1 HG00438.hp2 HG00621.hp1 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*1025G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 1025 | chr13 | 20973845 | |||||
| chr13:20973887
|
A | G | 88 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(85): Show | 291 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(288): Show |
3_prime_UTR_variant | MODIFIER | c.*983T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 983 | chr13 | 20973887 | |||||
| chr13:20973912
|
C | T | 1 | a0004c0004t0028 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*958G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 958 | chr13 | 20973912 | |||||
| chr13:20973971
|
T | TC | 43 | a0001c0001t0003a0001c0001t0006a0001c0001t0012others(40): Show | 123 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*898dupG | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 898 | chr13 | 20973971 | |||||
| chr13:20973971
|
TC | T | 14 | a0001c0001t0002a0001c0001t0027a0001c0010t0015others(11): Show | 67 | HG00621.hp2 HG00642.hp2 HG00741.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*898delG | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 898 | chr13 | 20973971 | |||||
| chr13:20974024
|
TCA | T | 4 | a0001c0001t0013a0001c0001t0017a0001c0001t0043others(1): Show | 8 | HG02027.hp2 NA18942.hp1 NA18946.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*844_*845delTG | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 844 | chr13 | 20974024 | |||||
| chr13:20974056
|
A | G | 1 | a0004c0004t0019 | 2 | HG02258.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*814T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 814 | chr13 | 20974056 | |||||
| chr13:20974418
|
G | A | 1 | a0002c0002t0042 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*452C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 452 | chr13 | 20974418 | |||||
| chr13:20974423
|
C | CT | 30 | a0001c0001t0003a0001c0001t0006a0001c0001t0012others(27): Show | 91 | HG00423.hp1 HG00438.hp2 HG00621.hp1 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*446dupA | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 446 | chr13 | 20974423 | |||||
| chr13:20974632
|
C | T | 4 | a0002c0002t0011a0002c0014t0038a0002c0017t0011others(1): Show | 7 | HG00735.hp2 HG02451.hp2 HG02559.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*238G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 238 | chr13 | 20974632 | |||||
| chr13:20974733
|
A | G | 1 | a0001c0001t0027 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*137T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 137 | chr13 | 20974733 | |||||
| chr13:20974757
|
G | A | 1 | a0001c0001t0037 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*113C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 8/8 | 113 | chr13 | 20974757 | |||||
| chr13:21046056
|
A | G | 1 | a0003c0009t0026 | 1 | HG02897.hp1 | 5_prime_UTR_variant | MODIFIER | c.-30T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/8 | 30 | chr13 | 21046056 | |||||
| chr13:21046083
|
T | TA | 28 | a0001c0001t0003a0001c0001t0010a0001c0001t0017others(25): Show | 85 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(82): Show |
5_prime_UTR_variant | MODIFIER | c.-58dupT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/8 | 58 | chr13 | 21046083 | |||||
| chr13:21046182
|
T | C | 1 | a0001c0001t0047 | 1 | NA19079.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-156A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/8 | chr13 | 21046182 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:20975746
|
C | T | 84 | a0001c0001t0003g0161a0001c0001t0006g0168a0001c0001t0006g0184others(81): Show | 84 | HG00423.hp1 HG00438.hp2 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.2773-382G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20975746 | ||||||
| chr13:20975769
|
C | T | 8 | a0002c0002t0003g0094a0002c0002t0003g0096a0002c0002t0003g0106others(5): Show | 8 | HG00738.hp2 HG01175.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.2773-405G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20975769 | ||||||
| chr13:20975779
|
G | A | 10 | a0002c0024t0023g0038a0004c0004t0014g0299a0004c0004t0019g0026others(7): Show | 10 | HG00639.hp1 HG01243.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.2773-415C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20975779 | ||||||
| chr13:20975926
|
A | C | 182 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(179): Show | 183 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.2773-562T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20975926 | ||||||
| chr13:20975999
|
C | T | 290 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(287): Show | 291 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.2773-635G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20975999 | ||||||
| chr13:20976135
|
CTTG | C | 85 | a0001c0001t0003g0161a0001c0001t0006g0168a0001c0001t0006g0184others(82): Show | 85 | HG00423.hp1 HG00438.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.2773-774_2773-772d others(5): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20976135 | ||||||
| chr13:20976330
|
C | T | 1 | a0003c0008t0046g0288 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2773-966G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20976330 | ||||||
| chr13:20976366
|
G | A | 1 | a0002c0034t0035g0027 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2773-1002C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20976366 | ||||||
| chr13:20976534
|
C | T | 1 | a0003c0003t0004g0300 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2773-1170G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20976534 | ||||||
| chr13:20976704
|
A | T | 107 | a0001c0001t0003g0161a0001c0001t0006g0168a0001c0001t0006g0184others(104): Show | 107 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.2773-1340T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20976704 | ||||||
| chr13:20976830
|
T | C | 290 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(287): Show | 291 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.2773-1466A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20976830 | ||||||
| chr13:20977310
|
C | T | 5 | a0003c0003t0002g0008a0003c0003t0002g0014a0003c0003t0002g0016others(2): Show | 5 | HG00642.hp2 HG02148.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.2773-1946G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20977310 | ||||||
| chr13:20977385
|
CA | C | 86 | a0001c0001t0002g0225a0001c0001t0003g0161a0001c0001t0006g0168others(83): Show | 86 | HG00423.hp1 HG00438.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.2773-2022delT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20977385 | ||||||
| chr13:20977493
|
G | C | 1 | a0004c0004t0005g0270 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2773-2129C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20977493 | ||||||
| chr13:20977622
|
A | ATAAT | 85 | a0001c0001t0003g0161a0001c0001t0006g0168a0001c0001t0006g0184others(82): Show | 85 | HG00423.hp1 HG00438.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.2772+2068_2772+206 others(8): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20977622 | ||||||
| chr13:20977631
|
AATTAAAA others(28): Show |
A | 1 | a0001c0001t0001g0250 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2772+2025_2772+205 others(39): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20977631 | ||||||
| chr13:20977644
|
A | AAGATGGT others(27): Show |
67 | a0001c0001t0002g0166a0001c0001t0002g0176a0001c0001t0002g0177others(64): Show | 67 | HG00621.hp2 HG00642.hp2 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.2772+2013_2772+204 others(38): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20977644 | ||||||
| chr13:20977644
|
A | AAGATGGT others(61): Show |
9 | a0002c0024t0023g0038a0003c0005t0002g0050a0004c0004t0014g0299others(6): Show | 9 | HG00639.hp1 HG00741.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.2772+1979_2772+204 others(72): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20977644 | ||||||
| chr13:20977644
|
A | AAGATGGT others(95): Show |
1 | a0001c0001t0006g0188 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2772+1945_2772+204 others(106): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20977644 | ||||||
| chr13:20977644
|
A | AAGATGGT others(129): Show |
72 | a0001c0001t0003g0161a0001c0001t0006g0168a0001c0001t0006g0184others(69): Show | 72 | HG00423.hp1 HG00438.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.2772+2046_2772+204 others(140): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20977644 | ||||||
| chr13:20977644
|
A | AAGATGGT others(163): Show |
3 | a0002c0002t0012g0182a0004c0019t0020g0305a0004c0019t0020g0306 | 3 | HG01243.hp1 NA18956.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2772+2046_2772+204 others(174): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20977644 | ||||||
| chr13:20977792
|
T | A | 1 | a0001c0001t0001g0274 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2772+1899A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20977792 | ||||||
| chr13:20977793
|
C | A | 1 | a0001c0001t0001g0274 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2772+1898G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20977793 | ||||||
| chr13:20977816
|
A | G | 15 | a0001c0001t0004g0276a0002c0006t0004g0011a0002c0006t0004g0012others(12): Show | 15 | HG00280.hp2 HG00597.hp2 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.2772+1875T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20977816 | ||||||
| chr13:20977838
|
T | C | 22 | a0002c0028t0041g0282a0003c0007t0008g0044a0003c0007t0008g0045others(19): Show | 22 | HG01243.hp2 HG01433.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.2772+1853A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20977838 | ||||||
| chr13:20977845
|
G | A | 74 | a0001c0001t0003g0161a0001c0001t0006g0168a0001c0001t0006g0184others(71): Show | 74 | HG00423.hp1 HG00438.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.2772+1846C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20977845 | ||||||
| chr13:20977848
|
G | C | 5 | a0003c0003t0007g0105a0003c0003t0007g0111a0003c0003t0007g0135others(2): Show | 5 | HG02071.hp2 HG02135.hp1 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.2772+1843C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20977848 | ||||||
| chr13:20978018
|
C | T | 3 | a0004c0004t0019g0026a0004c0004t0019g0292a0004c0004t0030g0295 | 3 | HG02258.hp2 HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2772+1673G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20978018 | ||||||
| chr13:20978065
|
G | A | 3 | a0004c0004t0019g0026a0004c0004t0019g0292a0004c0004t0030g0295 | 3 | HG02258.hp2 HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2772+1626C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20978065 | ||||||
| chr13:20978072
|
T | C | 84 | a0001c0001t0003g0161a0001c0001t0006g0168a0001c0001t0006g0184others(81): Show | 84 | HG00423.hp1 HG00438.hp2 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.2772+1619A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20978072 | ||||||
| chr13:20978129
|
C | T | 68 | a0001c0001t0002g0166a0001c0001t0002g0176a0001c0001t0002g0177others(65): Show | 68 | HG00621.hp2 HG00642.hp2 HG00741.hp1 others(65): Show |
intron_variant | MODIFIER | c.2772+1562G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20978129 | ||||||
| chr13:20978132
|
G | A | 1 | a0003c0008t0009g0088 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2772+1559C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20978132 | ||||||
| chr13:20978303
|
G | C | 1 | a0001c0001t0001g0197 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2772+1388C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20978303 | ||||||
| chr13:20978323
|
C | T | 104 | a0001c0001t0003g0161a0001c0001t0004g0276a0001c0001t0006g0168others(101): Show | 104 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.2772+1368G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20978323 | ||||||
| chr13:20978396
|
T | C | 85 | a0001c0001t0003g0161a0001c0001t0004g0276a0001c0001t0006g0168others(82): Show | 85 | HG00423.hp1 HG00438.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.2772+1295A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20978396 | ||||||
| chr13:20978399
|
T | C | 85 | a0001c0001t0003g0161a0001c0001t0004g0276a0001c0001t0006g0168others(82): Show | 85 | HG00423.hp1 HG00438.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.2772+1292A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20978399 | ||||||
| chr13:20978512
|
A | T | 5 | a0004c0004t0014g0299a0004c0004t0019g0026a0004c0004t0019g0292others(2): Show | 5 | HG02258.hp2 HG02647.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.2772+1179T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20978512 | ||||||
| chr13:20978642
|
C | T | 1 | a0005c0012t0002g0030 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2772+1049G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20978642 | ||||||
| chr13:20978951
|
C | T | 1 | a0003c0005t0002g0067 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2772+740G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20978951 | ||||||
| chr13:20978959
|
G | A | 86 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(83): Show | 86 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.2772+732C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20978959 | ||||||
| chr13:20979095
|
T | C | 71 | a0001c0001t0002g0166a0001c0001t0002g0176a0001c0001t0002g0177others(68): Show | 71 | HG00621.hp2 HG00642.hp2 HG00741.hp1 others(68): Show |
intron_variant | MODIFIER | c.2772+596A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 7/7 | chr13 | 20979095 | ||||||
| chr13:20979832
|
C | T | 74 | a0001c0001t0003g0161a0001c0001t0004g0276a0001c0001t0006g0168others(71): Show | 74 | HG00423.hp1 HG00438.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.2666-35G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 6/7 | chr13 | 20979832 | ||||||
| chr13:20979978
|
G | A | 3 | a0003c0007t0016g0062a0003c0009t0026g0029a0003c0009t0031g0031 | 3 | HG02723.hp2 HG02897.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2666-181C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 6/7 | chr13 | 20979978 | ||||||
| chr13:20980016
|
T | C | 2 | a0003c0032t0016g0315a0012c0022t0004g0007 | 2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2666-219A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 6/7 | chr13 | 20980016 | ||||||
| chr13:20980078
|
A | T | 211 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(208): Show | 212 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.2666-281T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 6/7 | chr13 | 20980078 | ||||||
| chr13:20980254
|
A | C | 236 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(233): Show | 237 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.2666-457T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 6/7 | chr13 | 20980254 | ||||||
| chr13:20980258
|
G | A | 1 | a0002c0006t0004g0015 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2666-461C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 6/7 | chr13 | 20980258 | ||||||
| chr13:20980273
|
G | A | 4 | a0003c0005t0002g0058a0004c0004t0030g0295a0004c0035t0009g0297others(1): Show | 4 | HG03209.hp2 HG03540.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.2666-476C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 6/7 | chr13 | 20980273 | ||||||
| chr13:20980359
|
G | A | 16 | a0001c0001t0001g0092a0001c0001t0034g0216a0002c0006t0004g0011others(13): Show | 16 | HG00280.hp2 HG00597.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.2666-562C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 6/7 | chr13 | 20980359 | ||||||
| chr13:20980498
|
G | A | 1 | a0003c0009t0009g0308 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2666-701C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 6/7 | chr13 | 20980498 | ||||||
| chr13:20980629
|
C | T | 1 | a0004c0004t0005g0229 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2666-832G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 6/7 | chr13 | 20980629 | ||||||
| chr13:20980645
|
G | A | 75 | a0001c0001t0002g0166a0001c0001t0002g0176a0001c0001t0002g0177others(72): Show | 76 | HG00621.hp2 HG00642.hp2 HG00741.hp1 others(73): Show |
intron_variant | MODIFIER | c.2665+821C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 6/7 | chr13 | 20980645 | ||||||
| chr13:20980703
|
A | G | 1 | a0002c0002t0003g0113 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2665+763T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 6/7 | chr13 | 20980703 | ||||||
| chr13:20980921
|
C | T | 205 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(202): Show | 206 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.2665+545G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 6/7 | chr13 | 20980921 | ||||||
| chr13:20981230
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2665+236G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 6/7 | chr13 | 20981230 | ||||||
| chr13:20981405
|
C | G | 121 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(118): Show | 121 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.2665+61G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 6/7 | chr13 | 20981405 | ||||||
| chr13:20981406
|
T | A | 121 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(118): Show | 121 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.2665+60A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 6/7 | chr13 | 20981406 | ||||||
| chr13:20981415
|
G | A | 98 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(95): Show | 98 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.2665+51C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 6/7 | chr13 | 20981415 | ||||||
| chr13:20981419
|
GA | G | 3 | a0002c0024t0023g0038a0002c0034t0035g0027a0008c0033t0001g0304 | 3 | HG00639.hp1 HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2665+46delT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 6/7 | chr13 | 20981419 | ||||||
| chr13:20981461
|
T | C | 3 | a0002c0002t0003g0148a0002c0002t0003g0153a0002c0002t0024g0152 | 3 | HG02148.hp2 NA19000.hp1 NA19005.hp1 |
splice_region_variant&intron_variant | LOW | c.2665+5A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 6/7 | chr13 | 20981461 | ||||||
| chr13:20981702
|
T | C | 1 | a0004c0004t0030g0295 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2483-54A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 5/7 | chr13 | 20981702 | ||||||
| chr13:20981953
|
C | T | 1 | a0003c0003t0002g0170 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2483-305G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 5/7 | chr13 | 20981953 | ||||||
| chr13:20982059
|
G | A | 5 | a0002c0002t0010g0281a0002c0024t0023g0038a0002c0028t0041g0282others(2): Show | 5 | HG00639.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.2483-411C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 5/7 | chr13 | 20982059 | ||||||
| chr13:20982342
|
G | T | 1 | a0001c0001t0001g0273 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2483-694C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 5/7 | chr13 | 20982342 | ||||||
| chr13:20982365
|
G | A | 1 | a0003c0009t0008g0309 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2483-717C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 5/7 | chr13 | 20982365 | ||||||
| chr13:20982374
|
C | T | 21 | a0003c0003t0004g0259a0003c0003t0025g0287a0003c0007t0008g0044others(18): Show | 21 | HG01243.hp2 HG01433.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.2483-726G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 5/7 | chr13 | 20982374 | ||||||
| chr13:20982407
|
G | A | 7 | a0003c0009t0008g0309a0003c0009t0009g0308a0003c0009t0016g0307others(4): Show | 7 | HG01884.hp1 HG02258.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2483-759C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 5/7 | chr13 | 20982407 | ||||||
| chr13:20982468
|
G | A | 63 | a0002c0002t0003g0094a0002c0002t0003g0095a0002c0002t0003g0096others(60): Show | 63 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.2482+756C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 5/7 | chr13 | 20982468 | ||||||
| chr13:20982489
|
T | C | 5 | a0002c0002t0010g0281a0002c0024t0023g0038a0002c0028t0041g0282others(2): Show | 5 | HG00639.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.2482+735A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 5/7 | chr13 | 20982489 | ||||||
| chr13:20982630
|
G | A | 4 | a0001c0001t0001g0192a0001c0001t0001g0221a0001c0001t0001g0279others(1): Show | 4 | HG02056.hp2 NA18954.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.2482+594C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 5/7 | chr13 | 20982630 | ||||||
| chr13:20982861
|
C | T | 14 | a0002c0006t0004g0011a0002c0006t0004g0012a0002c0006t0004g0015others(11): Show | 14 | HG00280.hp2 HG00597.hp2 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.2482+363G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 5/7 | chr13 | 20982861 | ||||||
| chr13:20982948
|
C | T | 205 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(202): Show | 206 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.2482+276G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 5/7 | chr13 | 20982948 | ||||||
| chr13:20982992
|
C | CA | 110 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(107): Show | 110 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.2482+231dupT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 5/7 | chr13 | 20982992 | ||||||
| chr13:20982992
|
C | CAA | 20 | a0001c0001t0002g0227a0002c0006t0004g0011a0002c0006t0004g0012others(17): Show | 20 | HG00280.hp2 HG00597.hp2 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.2482+230_2482+231d others(4): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 5/7 | chr13 | 20982992 | ||||||
| chr13:20982992
|
C | CAAA | 62 | a0001c0001t0002g0218a0001c0001t0002g0225a0001c0001t0002g0228others(59): Show | 63 | HG00621.hp2 HG00642.hp2 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.2482+229_2482+231d others(5): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 5/7 | chr13 | 20982992 | ||||||
| chr13:20982999
|
A | AC | 3 | a0002c0014t0018g0039a0002c0014t0018g0041a0002c0014t0038g0040 | 3 | HG02451.hp2 HG02886.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2482+224_2482+225i others(3): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 5/7 | chr13 | 20982999 | ||||||
| chr13:20983011
|
A | AC | 11 | a0001c0001t0003g0161a0001c0001t0004g0276a0001c0001t0006g0168others(8): Show | 11 | HG00423.hp1 HG02071.hp1 HG02074.hp1 others(8): Show |
intron_variant | MODIFIER | c.2482+212_2482+213i others(3): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 5/7 | chr13 | 20983011 | ||||||
| chr13:20983187
|
C | T | 1 | a0004c0015t0018g0042 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2482+37G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 5/7 | chr13 | 20983187 | ||||||
| chr13:20983961
|
C | T | 17 | a0002c0006t0004g0011a0002c0006t0004g0012a0002c0006t0004g0015others(14): Show | 17 | HG00280.hp2 HG00597.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.1900-155G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20983961 | ||||||
| chr13:20984016
|
C | T | 1 | a0003c0003t0002g0190 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1900-210G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20984016 | ||||||
| chr13:20984056
|
G | A | 2 | a0002c0002t0010g0281a0002c0028t0041g0282 | 2 | HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1900-250C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20984056 | ||||||
| chr13:20984059
|
T | C | 2 | a0002c0002t0010g0281a0002c0028t0041g0282 | 2 | HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1900-253A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20984059 | ||||||
| chr13:20984087
|
T | A | 5 | a0002c0002t0011g0034a0002c0002t0011g0283a0002c0002t0011g0284others(2): Show | 5 | HG00735.hp2 HG02559.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1900-281A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20984087 | ||||||
| chr13:20984125
|
C | T | 274 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(271): Show | 275 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.1900-319G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20984125 | ||||||
| chr13:20984154
|
G | C | 1 | a0003c0032t0016g0315 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1900-348C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20984154 | ||||||
| chr13:20984184
|
T | C | 5 | a0002c0002t0010g0281a0002c0024t0023g0038a0002c0028t0041g0282others(2): Show | 5 | HG00639.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1900-378A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20984184 | ||||||
| chr13:20984266
|
G | A | 1 | a0003c0032t0016g0315 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1900-460C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20984266 | ||||||
| chr13:20984315
|
T | G | 275 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(272): Show | 276 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.1900-509A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20984315 | ||||||
| chr13:20984407
|
A | G | 3 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0252 | 3 | HG00099.hp1 HG01071.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1900-601T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20984407 | ||||||
| chr13:20984489
|
A | G | 1 | a0002c0002t0006g0159 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1900-683T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20984489 | ||||||
| chr13:20984671
|
A | G | 206 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(203): Show | 207 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.1900-865T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20984671 | ||||||
| chr13:20984881
|
A | G | 21 | a0003c0003t0004g0259a0003c0003t0025g0287a0003c0007t0008g0044others(18): Show | 21 | HG01243.hp2 HG01433.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1900-1075T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20984881 | ||||||
| chr13:20984884
|
T | G | 1 | a0003c0007t0036g0051 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1900-1078A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20984884 | ||||||
| chr13:20984912
|
G | C | 1 | a0012c0022t0004g0007 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1900-1106C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20984912 | ||||||
| chr13:20985001
|
G | A | 1 | a0003c0032t0016g0315 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1900-1195C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20985001 | ||||||
| chr13:20985148
|
A | G | 188 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(185): Show | 189 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.1900-1342T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20985148 | ||||||
| chr13:20985266
|
T | C | 2 | a0002c0002t0010g0281a0002c0028t0041g0282 | 2 | HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1900-1460A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20985266 | ||||||
| chr13:20985381
|
T | C | 5 | a0002c0002t0011g0034a0002c0002t0011g0283a0002c0002t0011g0284others(2): Show | 5 | HG00735.hp2 HG02559.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1900-1575A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20985381 | ||||||
| chr13:20985474
|
C | T | 1 | a0012c0022t0004g0007 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1900-1668G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20985474 | ||||||
| chr13:20985518
|
T | C | 1 | a0009c0020t0009g0001 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1900-1712A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20985518 | ||||||
| chr13:20985521
|
T | C | 1 | a0009c0020t0009g0001 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1900-1715A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20985521 | ||||||
| chr13:20985622
|
C | T | 1 | a0001c0001t0001g0217 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1900-1816G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20985622 | ||||||
| chr13:20985719
|
T | C | 275 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(272): Show | 276 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.1900-1913A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20985719 | ||||||
| chr13:20985732
|
C | T | 21 | a0003c0003t0004g0259a0003c0003t0025g0287a0003c0007t0008g0044others(18): Show | 21 | HG01243.hp2 HG01433.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1900-1926G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20985732 | ||||||
| chr13:20985748
|
T | A | 113 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(110): Show | 114 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.1900-1942A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20985748 | ||||||
| chr13:20985839
|
A | C | 4 | a0002c0002t0003g0103a0002c0002t0003g0113a0002c0002t0003g0115others(1): Show | 4 | HG01255.hp2 HG01261.hp1 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.1900-2033T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20985839 | ||||||
| chr13:20985851
|
G | A | 1 | a0001c0001t0001g0271 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1899+2030C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20985851 | ||||||
| chr13:20985875
|
G | A | 1 | a0002c0006t0004g0213 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1899+2006C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20985875 | ||||||
| chr13:20985882
|
C | CT | 275 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(272): Show | 276 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.1899+1998_1899+199 others(5): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20985882 | ||||||
| chr13:20985912
|
T | C | 275 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(272): Show | 276 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.1899+1969A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20985912 | ||||||
| chr13:20985969
|
G | A | 21 | a0003c0003t0004g0259a0003c0003t0025g0287a0003c0007t0008g0044others(18): Show | 21 | HG01243.hp2 HG01433.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1899+1912C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20985969 | ||||||
| chr13:20985996
|
A | G | 24 | a0003c0003t0004g0259a0003c0003t0025g0287a0003c0007t0008g0044others(21): Show | 25 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.1899+1885T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20985996 | ||||||
| chr13:20986005
|
T | C | 64 | a0002c0002t0003g0094a0002c0002t0003g0095a0002c0002t0003g0096others(61): Show | 64 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.1899+1876A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20986005 | ||||||
| chr13:20986257
|
A | T | 311 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(308): Show | 312 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.1899+1624T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20986257 | ||||||
| chr13:20986296
|
T | G | 1 | a0005c0016t0014g0036 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1899+1585A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20986296 | ||||||
| chr13:20986410
|
T | C | 64 | a0002c0002t0003g0094a0002c0002t0003g0095a0002c0002t0003g0096others(61): Show | 64 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.1899+1471A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20986410 | ||||||
| chr13:20986849
|
G | T | 1 | a0002c0002t0023g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1899+1032C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20986849 | ||||||
| chr13:20986952
|
G | A | 2 | a0004c0019t0020g0305a0004c0019t0020g0306 | 2 | HG01243.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1899+929C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20986952 | ||||||
| chr13:20987195
|
A | C | 2 | a0005c0016t0014g0035a0005c0016t0014g0036 | 2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1899+686T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20987195 | ||||||
| chr13:20987212
|
AAAAAATA others(5): Show |
A | 69 | a0001c0001t0002g0218a0001c0001t0002g0225a0001c0001t0002g0227others(66): Show | 70 | HG00621.hp2 HG00642.hp2 HG00741.hp1 others(67): Show |
intron_variant | MODIFIER | c.1899+657_1899+668d others(14): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20987212 | ||||||
| chr13:20987224
|
T | TA | 199 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(196): Show | 199 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.1899+656dupT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20987224 | ||||||
| chr13:20987267
|
G | C | 14 | a0002c0006t0004g0011a0002c0006t0004g0012a0002c0006t0004g0015others(11): Show | 14 | HG00280.hp2 HG00597.hp2 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.1899+614C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20987267 | ||||||
| chr13:20987314
|
A | C | 4 | a0001c0001t0001g0183a0001c0001t0001g0202a0001c0001t0001g0211others(1): Show | 4 | HG00642.hp1 HG02280.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1899+567T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20987314 | ||||||
| chr13:20987338
|
ATC | A | 5 | a0002c0002t0010g0281a0002c0024t0023g0038a0002c0028t0041g0282others(2): Show | 5 | HG00639.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1899+541_1899+542d others(4): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20987338 | ||||||
| chr13:20987402
|
C | G | 2 | a0002c0002t0010g0281a0002c0028t0041g0282 | 2 | HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1899+479G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20987402 | ||||||
| chr13:20987443
|
A | G | 1 | a0003c0032t0016g0315 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1899+438T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20987443 | ||||||
| chr13:20987498
|
C | T | 1 | a0002c0017t0006g0004 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1899+383G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20987498 | ||||||
| chr13:20987624
|
T | C | 3 | a0003c0003t0004g0259a0003c0003t0025g0287a0003c0008t0046g0288 | 3 | HG02055.hp2 HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1899+257A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20987624 | ||||||
| chr13:20987707
|
G | A | 2 | a0002c0002t0010g0281a0002c0028t0041g0282 | 2 | HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1899+174C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20987707 | ||||||
| chr13:20987736
|
T | C | 1 | a0001c0001t0001g0196 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1899+145A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20987736 | ||||||
| chr13:20987826
|
T | C | 2 | a0003c0003t0004g0259a0003c0003t0025g0287 | 2 | HG02055.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1899+55A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 4/7 | chr13 | 20987826 | ||||||
| chr13:20989408
|
G | T | 2 | a0002c0024t0023g0038a0002c0034t0035g0027 | 2 | HG00639.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.476-104C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20989408 | ||||||
| chr13:20989503
|
G | C | 22 | a0002c0002t0010g0281a0002c0006t0004g0011a0002c0006t0004g0012others(19): Show | 22 | HG00280.hp2 HG00597.hp2 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.476-199C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20989503 | ||||||
| chr13:20989576
|
C | T | 274 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(271): Show | 275 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.476-272G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20989576 | ||||||
| chr13:20989862
|
TA | T | 13 | a0003c0003t0002g0008a0003c0003t0002g0010a0003c0003t0002g0014others(10): Show | 13 | HG00642.hp2 HG02148.hp1 HG03490.hp2 others(10): Show |
intron_variant | MODIFIER | c.476-559delT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20989862 | ||||||
| chr13:20990121
|
A | G | 312 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(309): Show | 313 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.476-817T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990121 | ||||||
| chr13:20990148
|
T | C | 22 | a0002c0002t0010g0281a0002c0006t0004g0011a0002c0006t0004g0012others(19): Show | 22 | HG00280.hp2 HG00597.hp2 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.476-844A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990148 | ||||||
| chr13:20990152
|
T | C | 1 | a0003c0005t0001g0084 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.476-848A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990152 | ||||||
| chr13:20990340
|
A | AATGTGTG others(312): Show |
1 | a0002c0006t0004g0020 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.475+931_475+932ins others(319): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990340 | ||||||
| chr13:20990340
|
A | AATGTGTG others(315): Show |
3 | a0002c0006t0004g0021a0002c0006t0004g0022a0002c0006t0004g0258 | 3 | HG00280.hp2 HG01358.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.475+931_475+932ins others(322): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990340 | ||||||
| chr13:20990340
|
A | AATGTGTG others(328): Show |
2 | a0002c0014t0018g0041a0002c0014t0038g0040 | 2 | HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.475+931_475+932ins others(335): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990340 | ||||||
| chr13:20990340
|
A | AATGTGTG others(329): Show |
7 | a0002c0006t0004g0011a0002c0006t0004g0015a0002c0006t0004g0019others(4): Show | 7 | HG01943.hp2 HG02886.hp1 NA18969.hp1 others(4): Show |
intron_variant | MODIFIER | c.475+931_475+932ins others(336): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990340 | ||||||
| chr13:20990340
|
A | AATGTGTG others(330): Show |
3 | a0002c0006t0004g0012a0002c0006t0004g0164a0002c0006t0004g0219 | 3 | NA18991.hp2 NA19058.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.475+931_475+932ins others(337): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990340 | ||||||
| chr13:20990340
|
A | AATGTGTG others(332): Show |
1 | a0002c0006t0004g0210 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.475+931_475+932ins others(339): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990340 | ||||||
| chr13:20990411
|
T | G | 1 | a0001c0001t0017g0131 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.475+861A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990411 | ||||||
| chr13:20990413
|
T | A | 1 | a0001c0001t0017g0131 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.475+859A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990413 | ||||||
| chr13:20990461
|
A | AT | 80 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(77): Show | 81 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.475+810dupA | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990461 | ||||||
| chr13:20990461
|
A | ATT | 14 | a0001c0001t0001g0197a0001c0001t0001g0215a0001c0001t0001g0232others(11): Show | 14 | HG01358.hp2 HG02027.hp2 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.475+809_475+810dup others(2): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990461 | ||||||
| chr13:20990461
|
A | ATTTTTTT | 33 | a0001c0001t0002g0225a0001c0001t0002g0228a0001c0001t0027g0226others(30): Show | 33 | HG00621.hp2 HG00642.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.475+804_475+810dup others(7): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990461 | ||||||
| chr13:20990461
|
A | ATTTTTTT others(1): Show |
28 | a0001c0001t0002g0218a0001c0001t0002g0227a0003c0003t0002g0010others(25): Show | 28 | HG01070.hp1 HG01081.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.475+803_475+810dup others(8): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990461 | ||||||
| chr13:20990461
|
A | ATTTTTTT others(2): Show |
12 | a0003c0003t0002g0190a0003c0003t0004g0301a0003c0003t0044g0110others(9): Show | 12 | HG01433.hp2 HG02055.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.475+802_475+810dup others(9): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990461 | ||||||
| chr13:20990461
|
A | ATTTTTTT others(3): Show |
2 | a0003c0005t0002g0059a0003c0008t0046g0288 | 2 | HG02071.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.475+801_475+810dup others(10): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990461 | ||||||
| chr13:20990461
|
A | ATTTTTTT others(5): Show |
1 | a0003c0036t0009g0310 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.475+799_475+810dup others(12): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990461 | ||||||
| chr13:20990461
|
A | ATTTTTTT others(6): Show |
2 | a0010c0018t0010g0065a0010c0018t0010g0066 | 2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.475+798_475+810dup others(13): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990461 | ||||||
| chr13:20990461
|
AT | A | 80 | a0002c0002t0003g0095a0002c0002t0003g0096a0002c0002t0003g0101others(77): Show | 80 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.475+810delA | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990461 | ||||||
| chr13:20990461
|
ATT | A | 10 | a0002c0002t0003g0094a0002c0002t0003g0098a0002c0002t0003g0133others(7): Show | 10 | HG00639.hp1 HG01981.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.475+809_475+810del others(2): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990461 | ||||||
| chr13:20990461
|
ATTTTTTT others(2): Show |
A | 10 | a0002c0006t0004g0011a0002c0006t0004g0012a0002c0006t0004g0015others(7): Show | 10 | HG00597.hp2 HG01943.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.475+802_475+810del others(9): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990461 | ||||||
| chr13:20990461
|
ATTTTTTT others(3): Show |
A | 4 | a0002c0006t0004g0219a0002c0014t0018g0039a0002c0014t0018g0041others(1): Show | 4 | HG02451.hp2 HG02886.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.475+801_475+810del others(10): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990461 | ||||||
| chr13:20990462
|
T | A | 1 | a0001c0001t0017g0131 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.475+810A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990462 | ||||||
| chr13:20990478
|
TTTTTTTT others(3): Show |
T | 3 | a0003c0003t0002g0172a0003c0003t0002g0173a0003c0003t0002g0175 | 3 | HG01074.hp2 HG01099.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.475+784_475+793del others(10): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990478 | ||||||
| chr13:20990488
|
A | T | 186 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(183): Show | 187 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.475+784T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990488 | ||||||
| chr13:20990502
|
T | A | 1 | a0003c0007t0036g0051 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.475+770A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990502 | ||||||
| chr13:20990598
|
A | C | 1 | a0002c0002t0023g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.475+674T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20990598 | ||||||
| chr13:20991158
|
T | G | 1 | a0003c0005t0002g0059 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.475+114A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20991158 | ||||||
| chr13:20991209
|
G | A | 1 | a0001c0001t0004g0276 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.475+63C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 3/7 | chr13 | 20991209 | ||||||
| chr13:20991581
|
G | T | 1 | a0002c0014t0018g0041 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.343-177C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20991581 | ||||||
| chr13:20991714
|
T | C | 1 | a0004c0004t0001g0303 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.343-310A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20991714 | ||||||
| chr13:20991861
|
C | T | 1 | a0003c0003t0002g0172 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.343-457G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20991861 | ||||||
| chr13:20991880
|
C | T | 2 | a0002c0002t0011g0034a0002c0002t0011g0285 | 2 | HG00735.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.343-476G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20991880 | ||||||
| chr13:20991903
|
T | C | 1 | a0003c0003t0025g0287 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.343-499A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20991903 | ||||||
| chr13:20991927
|
G | A | 64 | a0002c0002t0003g0094a0002c0002t0003g0095a0002c0002t0003g0096others(61): Show | 64 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.343-523C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20991927 | ||||||
| chr13:20991947
|
G | A | 1 | a0003c0005t0002g0063 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.343-543C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20991947 | ||||||
| chr13:20991992
|
C | A | 188 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(185): Show | 189 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.343-588G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20991992 | ||||||
| chr13:20992104
|
C | A | 20 | a0003c0003t0004g0259a0003c0007t0008g0044a0003c0007t0008g0045others(17): Show | 20 | HG01243.hp2 HG01433.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.343-700G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20992104 | ||||||
| chr13:20992230
|
A | G | 1 | a0012c0022t0004g0007 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.343-826T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20992230 | ||||||
| chr13:20992236
|
G | A | 1 | a0012c0022t0004g0007 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.343-832C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20992236 | ||||||
| chr13:20992250
|
T | C | 2 | a0002c0002t0010g0281a0002c0028t0041g0282 | 2 | HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.343-846A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20992250 | ||||||
| chr13:20992258
|
G | A | 18 | a0004c0004t0005g0002a0004c0004t0005g0089a0004c0004t0005g0204others(15): Show | 18 | HG00099.hp2 HG00639.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.343-854C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20992258 | ||||||
| chr13:20992325
|
G | A | 26 | a0003c0009t0008g0309a0003c0009t0009g0308a0003c0009t0016g0307others(23): Show | 26 | HG00099.hp2 HG00639.hp2 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.343-921C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20992325 | ||||||
| chr13:20992379
|
T | C | 2 | a0003c0008t0009g0294a0003c0008t0009g0296 | 2 | HG01433.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.343-975A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20992379 | ||||||
| chr13:20992436
|
C | T | 1 | a0003c0007t0036g0051 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.343-1032G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20992436 | ||||||
| chr13:20992437
|
G | A | 7 | a0001c0001t0002g0218a0001c0001t0002g0225a0001c0001t0002g0227others(4): Show | 7 | HG00741.hp1 HG01081.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.343-1033C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20992437 | ||||||
| chr13:20992465
|
G | A | 1 | a0001c0010t0001g0074 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.343-1061C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20992465 | ||||||
| chr13:20992548
|
G | A | 4 | a0005c0012t0001g0033a0005c0012t0002g0028a0005c0012t0002g0030others(1): Show | 4 | HG00735.hp1 HG02886.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.343-1144C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20992548 | ||||||
| chr13:20992763
|
G | A | 17 | a0002c0006t0004g0011a0002c0006t0004g0012a0002c0006t0004g0015others(14): Show | 17 | HG00280.hp2 HG00597.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.343-1359C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20992763 | ||||||
| chr13:20992774
|
C | T | 4 | a0005c0012t0001g0033a0005c0012t0002g0028a0005c0012t0002g0030others(1): Show | 4 | HG00735.hp1 HG02886.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.343-1370G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20992774 | ||||||
| chr13:20992784
|
C | T | 17 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0196others(14): Show | 17 | HG00280.hp1 HG00738.hp1 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.343-1380G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20992784 | ||||||
| chr13:20992906
|
G | T | 1 | a0003c0003t0002g0190 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.343-1502C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20992906 | ||||||
| chr13:20992969
|
G | A | 1 | a0004c0004t0021g0260 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.343-1565C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20992969 | ||||||
| chr13:20993015
|
A | T | 1 | a0002c0017t0011g0075 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.343-1611T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20993015 | ||||||
| chr13:20993035
|
C | CA | 59 | a0001c0001t0002g0225a0001c0001t0002g0228a0002c0002t0003g0103others(56): Show | 59 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.343-1632dupT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20993035 | ||||||
| chr13:20993035
|
C | CAA | 10 | a0002c0002t0003g0155a0002c0002t0012g0244a0002c0002t0024g0156others(7): Show | 11 | HG01070.hp2 HG01071.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.343-1633_343-1632d others(4): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20993035 | ||||||
| chr13:20993035
|
CA | C | 27 | a0002c0002t0003g0128a0002c0006t0004g0011a0002c0006t0004g0012others(24): Show | 27 | HG00280.hp2 HG00597.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.343-1632delT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20993035 | ||||||
| chr13:20993035
|
CAA | C | 16 | a0003c0007t0008g0044a0003c0007t0008g0045a0003c0007t0008g0046others(13): Show | 16 | HG01243.hp2 HG01433.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.343-1633_343-1632d others(4): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20993035 | ||||||
| chr13:20993035
|
CAAAAAA | C | 7 | a0001c0001t0001g0263a0001c0001t0006g0184a0001c0001t0006g0188others(4): Show | 7 | HG00738.hp1 HG02071.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.343-1637_343-1632d others(8): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20993035 | ||||||
| chr13:20993035
|
CAAAAAAA | C | 88 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(85): Show | 88 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.343-1638_343-1632d others(9): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20993035 | ||||||
| chr13:20993035
|
CAAAAAAA others(6): Show |
C | 1 | a0003c0007t0036g0051 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.343-1644_343-1632d others(15): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20993035 | ||||||
| chr13:20993063
|
G | C | 1 | a0002c0002t0011g0283 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.343-1659C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20993063 | ||||||
| chr13:20993063
|
G | T | 1 | a0002c0002t0003g0147 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.343-1659C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20993063 | ||||||
| chr13:20993090
|
G | A | 1 | a0002c0002t0023g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.343-1686C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20993090 | ||||||
| chr13:20993145
|
C | T | 1 | a0005c0012t0002g0032 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.343-1741G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20993145 | ||||||
| chr13:20993397
|
G | A | 1 | a0002c0002t0003g0094 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.343-1993C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20993397 | ||||||
| chr13:20993400
|
A | G | 179 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(176): Show | 180 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(177): Show |
intron_variant | MODIFIER | c.343-1996T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20993400 | ||||||
| chr13:20993432
|
A | G | 188 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(185): Show | 189 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.343-2028T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20993432 | ||||||
| chr13:20993469
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.343-2065G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20993469 | ||||||
| chr13:20993689
|
A | G | 1 | a0009c0020t0009g0001 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.343-2285T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20993689 | ||||||
| chr13:20993799
|
G | A | 1 | a0003c0005t0002g0037 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.343-2395C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20993799 | ||||||
| chr13:20993830
|
A | G | 64 | a0002c0002t0003g0094a0002c0002t0003g0095a0002c0002t0003g0096others(61): Show | 64 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.343-2426T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20993830 | ||||||
| chr13:20994006
|
T | C | 1 | a0001c0001t0001g0092 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.343-2602A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20994006 | ||||||
| chr13:20994167
|
A | G | 1 | a0003c0005t0033g0073 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.343-2763T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20994167 | ||||||
| chr13:20994235
|
C | T | 2 | a0002c0002t0010g0281a0002c0028t0041g0282 | 2 | HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.343-2831G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20994235 | ||||||
| chr13:20994294
|
A | G | 3 | a0002c0014t0018g0039a0002c0014t0018g0041a0002c0014t0038g0040 | 3 | HG02451.hp2 HG02886.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.343-2890T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20994294 | ||||||
| chr13:20994393
|
C | T | 1 | a0002c0002t0003g0133 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.343-2989G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20994393 | ||||||
| chr13:20994512
|
C | T | 1 | a0001c0001t0037g0186 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.343-3108G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20994512 | ||||||
| chr13:20994632
|
T | C | 188 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(185): Show | 189 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.343-3228A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20994632 | ||||||
| chr13:20994675
|
G | T | 4 | a0001c0001t0002g0225a0001c0001t0002g0227a0001c0001t0002g0228others(1): Show | 4 | HG00741.hp1 HG01106.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.343-3271C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20994675 | ||||||
| chr13:20994854
|
C | CA | 67 | a0001c0001t0002g0166a0001c0001t0004g0276a0002c0002t0003g0094others(64): Show | 67 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.343-3451dupT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20994854 | ||||||
| chr13:20994854
|
C | CAA | 187 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(184): Show | 188 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.343-3452_343-3451d others(4): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20994854 | ||||||
| chr13:20994854
|
C | CAAA | 19 | a0001c0001t0006g0184a0002c0002t0010g0281a0002c0006t0004g0011others(16): Show | 19 | HG00280.hp2 HG00597.hp2 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.343-3453_343-3451d others(5): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20994854 | ||||||
| chr13:20994868
|
T | A | 1 | a0003c0007t0036g0051 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.343-3464A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20994868 | ||||||
| chr13:20994955
|
A | T | 4 | a0004c0004t0005g0266a0004c0004t0005g0269a0004c0004t0005g0270others(1): Show | 4 | HG01106.hp1 HG01433.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.343-3551T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20994955 | ||||||
| chr13:20995088
|
T | C | 22 | a0003c0003t0025g0287a0004c0004t0005g0002a0004c0004t0005g0089others(19): Show | 22 | HG00099.hp2 HG00639.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.343-3684A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20995088 | ||||||
| chr13:20995193
|
AT | A | 5 | a0002c0002t0010g0281a0002c0024t0023g0038a0002c0028t0041g0282others(2): Show | 5 | HG00639.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.343-3790delA | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20995193 | ||||||
| chr13:20995205
|
G | A | 3 | a0004c0015t0018g0042a0004c0019t0020g0305a0004c0019t0020g0306 | 3 | HG01243.hp1 HG03041.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.343-3801C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20995205 | ||||||
| chr13:20995206
|
A | G | 64 | a0002c0002t0003g0094a0002c0002t0003g0095a0002c0002t0003g0096others(61): Show | 64 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.343-3802T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20995206 | ||||||
| chr13:20995450
|
T | G | 274 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(271): Show | 275 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.343-4046A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20995450 | ||||||
| chr13:20995505
|
G | C | 3 | a0001c0001t0001g0233a0001c0001t0010g0162a0001c0001t0010g0163 | 3 | HG00423.hp2 NA18971.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.343-4101C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20995505 | ||||||
| chr13:20995576
|
T | C | 1 | a0005c0012t0002g0032 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.343-4172A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20995576 | ||||||
| chr13:20995665
|
A | G | 1 | a0002c0034t0035g0027 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.343-4261T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20995665 | ||||||
| chr13:20995764
|
T | TA | 66 | a0001c0001t0002g0218a0001c0001t0002g0225a0001c0001t0002g0227others(63): Show | 66 | HG00621.hp2 HG00642.hp2 HG00741.hp1 others(63): Show |
intron_variant | MODIFIER | c.343-4361dupT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20995764 | ||||||
| chr13:20995766
|
T | A | 66 | a0001c0001t0002g0218a0001c0001t0002g0225a0001c0001t0002g0227others(63): Show | 66 | HG00621.hp2 HG00642.hp2 HG00741.hp1 others(63): Show |
intron_variant | MODIFIER | c.343-4362A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20995766 | ||||||
| chr13:20995845
|
G | A | 1 | a0003c0032t0016g0315 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.343-4441C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20995845 | ||||||
| chr13:20995876
|
T | C | 1 | a0001c0001t0001g0233 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.343-4472A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20995876 | ||||||
| chr13:20995910
|
G | A | 21 | a0003c0003t0004g0259a0003c0003t0025g0287a0003c0007t0008g0044others(18): Show | 21 | HG01243.hp2 HG01433.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.343-4506C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20995910 | ||||||
| chr13:20996042
|
A | G | 296 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(293): Show | 297 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.343-4638T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20996042 | ||||||
| chr13:20996062
|
A | G | 2 | a0003c0009t0026g0029a0003c0009t0031g0031 | 2 | HG02723.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.343-4658T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20996062 | ||||||
| chr13:20996063
|
G | C | 274 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(271): Show | 275 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.343-4659C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20996063 | ||||||
| chr13:20996107
|
T | G | 188 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(185): Show | 189 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.343-4703A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20996107 | ||||||
| chr13:20996171
|
C | T | 102 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(99): Show | 102 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.343-4767G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20996171 | ||||||
| chr13:20996322
|
A | G | 1 | a0002c0002t0003g0095 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.343-4918T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20996322 | ||||||
| chr13:20996377
|
A | AT | 34 | a0001c0001t0001g0246a0001c0001t0001g0262a0001c0001t0001g0263others(31): Show | 34 | HG00280.hp2 HG00597.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.343-4974dupA | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20996377 | ||||||
| chr13:20996377
|
AT | A | 78 | a0001c0001t0001g0209a0001c0001t0001g0242a0001c0001t0013g0167others(75): Show | 78 | HG00438.hp2 HG00621.hp1 HG00738.hp2 others(75): Show |
intron_variant | MODIFIER | c.343-4974delA | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20996377 | ||||||
| chr13:20996377
|
ATT | A | 33 | a0002c0002t0003g0101a0002c0002t0007g0141a0002c0002t0011g0034others(30): Show | 34 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.343-4975_343-4974d others(4): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20996377 | ||||||
| chr13:20996377
|
ATTT | A | 61 | a0001c0010t0015g0003a0003c0003t0002g0008a0003c0003t0002g0010others(58): Show | 61 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.343-4976_343-4974d others(5): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20996377 | ||||||
| chr13:20996439
|
C | T | 2 | a0001c0001t0003g0161a0001c0001t0012g0165 | 2 | HG02074.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.343-5035G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20996439 | ||||||
| chr13:20996492
|
C | T | 1 | a0001c0030t0001g0091 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.343-5088G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20996492 | ||||||
| chr13:20996497
|
C | G | 1 | a0005c0016t0005g0235 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.343-5093G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20996497 | ||||||
| chr13:20996529
|
C | T | 189 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(186): Show | 190 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.343-5125G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20996529 | ||||||
| chr13:20996679
|
G | A | 1 | a0004c0004t0005g0261 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.343-5275C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20996679 | ||||||
| chr13:20996723
|
T | C | 1 | a0002c0002t0003g0142 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.343-5319A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20996723 | ||||||
| chr13:20996773
|
T | C | 24 | a0004c0004t0005g0002a0004c0004t0005g0089a0004c0004t0005g0204others(21): Show | 24 | HG00099.hp2 HG00639.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.343-5369A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20996773 | ||||||
| chr13:20997002
|
G | A | 64 | a0002c0002t0003g0094a0002c0002t0003g0095a0002c0002t0003g0096others(61): Show | 64 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.343-5598C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20997002 | ||||||
| chr13:20997118
|
G | A | 189 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(186): Show | 190 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.343-5714C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20997118 | ||||||
| chr13:20997234
|
C | T | 311 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(308): Show | 312 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.343-5830G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20997234 | ||||||
| chr13:20997305
|
T | C | 26 | a0002c0002t0010g0281a0002c0006t0004g0011a0002c0006t0004g0012others(23): Show | 26 | HG00280.hp2 HG00597.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.343-5901A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20997305 | ||||||
| chr13:20997639
|
A | G | 94 | a0002c0002t0003g0094a0002c0002t0003g0095a0002c0002t0003g0096others(91): Show | 94 | HG00280.hp2 HG00438.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.343-6235T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20997639 | ||||||
| chr13:20997789
|
A | G | 4 | a0004c0004t0019g0026a0004c0004t0019g0292a0004c0004t0030g0295others(1): Show | 4 | HG02258.hp2 HG03209.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.343-6385T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20997789 | ||||||
| chr13:20997890
|
G | C | 104 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(101): Show | 104 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.343-6486C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20997890 | ||||||
| chr13:20997979
|
T | C | 99 | a0001c0001t0006g0168a0001c0001t0006g0184a0001c0001t0006g0195others(96): Show | 99 | HG00280.hp2 HG00438.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.343-6575A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20997979 | ||||||
| chr13:20997980
|
G | A | 1 | a0002c0002t0003g0148 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.343-6576C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20997980 | ||||||
| chr13:20998140
|
C | T | 1 | a0001c0001t0001g0233 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.343-6736G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20998140 | ||||||
| chr13:20998170
|
G | A | 1 | a0003c0003t0002g0172 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.343-6766C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20998170 | ||||||
| chr13:20998211
|
G | A | 1 | a0012c0022t0004g0007 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.343-6807C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20998211 | ||||||
| chr13:20998365
|
A | T | 2 | a0008c0033t0001g0304a0012c0022t0004g0007 | 2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.343-6961T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20998365 | ||||||
| chr13:20998377
|
TA | T | 109 | a0001c0001t0001g0090a0001c0001t0001g0183a0001c0001t0001g0192others(106): Show | 109 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.343-6974delT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20998377 | ||||||
| chr13:20998513
|
C | T | 2 | a0001c0001t0001g0215a0003c0005t0002g0278 | 2 | HG03654.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.343-7109G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20998513 | ||||||
| chr13:20998518
|
G | GA | 3 | a0003c0003t0004g0259a0003c0003t0025g0287a0003c0008t0046g0288 | 3 | HG02055.hp2 HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.343-7115dupT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20998518 | ||||||
| chr13:20998634
|
C | T | 4 | a0002c0002t0003g0126a0002c0002t0003g0128a0002c0002t0003g0129others(1): Show | 4 | NA18959.hp2 NA19004.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.343-7230G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20998634 | ||||||
| chr13:20998648
|
C | G | 304 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(301): Show | 305 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.343-7244G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20998648 | ||||||
| chr13:20998655
|
T | C | 1 | a0002c0002t0003g0147 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.343-7251A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20998655 | ||||||
| chr13:20998690
|
G | A | 10 | a0002c0002t0012g0244a0002c0006t0004g0011a0002c0006t0004g0015others(7): Show | 10 | HG00597.hp2 HG01358.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.343-7286C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20998690 | ||||||
| chr13:20998705
|
A | C | 13 | a0001c0001t0002g0176a0001c0001t0002g0177a0002c0002t0012g0244others(10): Show | 13 | HG00597.hp2 HG01943.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.343-7301T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20998705 | ||||||
| chr13:20998745
|
G | GCGAGGCG others(9): Show |
50 | a0001c0001t0001g0224a0001c0001t0001g0239a0001c0001t0001g0262others(47): Show | 50 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.343-7357_343-7342d others(18): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20998745 | ||||||
| chr13:20998745
|
G | GCGAGGCG others(10): Show |
4 | a0003c0003t0004g0259a0003c0003t0025g0287a0003c0008t0046g0288others(1): Show | 4 | HG02055.hp2 HG02615.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.343-7358_343-7342d others(19): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20998745 | ||||||
| chr13:20998752
|
G | C | 2 | a0005c0016t0014g0035a0005c0016t0014g0036 | 2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.343-7348C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20998752 | ||||||
| chr13:20998992
|
C | G | 2 | a0004c0004t0001g0302a0004c0004t0001g0303 | 2 | HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.343-7588G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20998992 | ||||||
| chr13:20999024
|
G | A | 1 | a0003c0007t0008g0046 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.343-7620C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20999024 | ||||||
| chr13:20999320
|
C | T | 1 | a0003c0023t0002g0006 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.343-7916G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20999320 | ||||||
| chr13:20999362
|
G | A | 83 | a0002c0002t0003g0094a0002c0002t0003g0095a0002c0002t0003g0096others(80): Show | 84 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(81): Show |
intron_variant | MODIFIER | c.343-7958C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20999362 | ||||||
| chr13:20999501
|
C | A | 2 | a0002c0034t0035g0027a0004c0004t0028g0025 | 2 | HG02965.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.343-8097G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20999501 | ||||||
| chr13:20999544
|
T | C | 10 | a0003c0003t0004g0259a0003c0003t0025g0287a0003c0008t0046g0288others(7): Show | 10 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.343-8140A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20999544 | ||||||
| chr13:20999606
|
C | A | 7 | a0004c0004t0005g0204a0004c0004t0005g0229a0004c0004t0005g0230others(4): Show | 7 | HG02735.hp2 HG02738.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.343-8202G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20999606 | ||||||
| chr13:20999634
|
T | A | 11 | a0002c0002t0012g0244a0003c0003t0004g0259a0003c0003t0025g0287others(8): Show | 11 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.343-8230A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20999634 | ||||||
| chr13:20999710
|
A | C | 1 | a0009c0020t0009g0001 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.343-8306T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20999710 | ||||||
| chr13:20999757
|
C | T | 1 | a0001c0001t0001g0252 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.343-8353G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20999757 | ||||||
| chr13:20999863
|
C | CA | 77 | a0001c0001t0001g0202a0001c0001t0001g0241a0001c0010t0001g0056others(74): Show | 77 | HG00621.hp2 HG00639.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.343-8460dupT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20999863 | ||||||
| chr13:20999863
|
C | CAA | 189 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(186): Show | 190 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.343-8461_343-8460d others(4): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20999863 | ||||||
| chr13:20999863
|
C | CAAA | 27 | a0001c0001t0001g0181a0001c0001t0001g0222a0001c0001t0001g0224others(24): Show | 27 | HG00597.hp1 HG00738.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.343-8462_343-8460d others(5): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20999863 | ||||||
| chr13:20999888
|
C | T | 1 | a0003c0007t0036g0051 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.343-8484G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20999888 | ||||||
| chr13:20999983
|
T | C | 1 | a0009c0020t0009g0001 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.343-8579A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 20999983 | ||||||
| chr13:21000078
|
A | G | 1 | a0003c0032t0016g0315 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.343-8674T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21000078 | ||||||
| chr13:21000123
|
T | C | 2 | a0004c0019t0020g0305a0004c0019t0020g0306 | 2 | HG01243.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.343-8719A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21000123 | ||||||
| chr13:21000253
|
C | T | 76 | a0001c0010t0001g0056a0001c0010t0001g0064a0001c0010t0015g0003others(73): Show | 77 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(74): Show |
intron_variant | MODIFIER | c.343-8849G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21000253 | ||||||
| chr13:21000378
|
C | CATA | 19 | a0001c0001t0022g0171a0002c0002t0003g0148a0002c0002t0003g0153others(16): Show | 19 | HG00597.hp2 HG01243.hp1 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.343-8977_343-8975d others(5): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21000378 | ||||||
| chr13:21000381
|
A | C | 75 | a0001c0010t0001g0056a0001c0010t0001g0064a0001c0010t0015g0003others(72): Show | 76 | HG00621.hp2 HG00741.hp2 HG01070.hp2 others(73): Show |
intron_variant | MODIFIER | c.343-8977T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21000381 | ||||||
| chr13:21000384
|
A | C | 3 | a0002c0002t0010g0281a0002c0028t0041g0282a0012c0022t0004g0007 | 3 | HG02572.hp2 HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.343-8980T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21000384 | ||||||
| chr13:21000489
|
G | A | 77 | a0001c0010t0001g0056a0001c0010t0001g0064a0001c0010t0015g0003others(74): Show | 78 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(75): Show |
intron_variant | MODIFIER | c.343-9085C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21000489 | ||||||
| chr13:21000503
|
G | A | 4 | a0002c0002t0010g0281a0002c0028t0041g0282a0005c0016t0014g0035others(1): Show | 4 | HG02965.hp2 HG03139.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.343-9099C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21000503 | ||||||
| chr13:21000765
|
T | C | 2 | a0005c0016t0014g0035a0005c0016t0014g0036 | 2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.343-9361A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21000765 | ||||||
| chr13:21000770
|
T | C | 54 | a0001c0001t0002g0218a0001c0001t0002g0225a0001c0001t0002g0227others(51): Show | 54 | HG00621.hp2 HG00642.hp2 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.343-9366A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21000770 | ||||||
| chr13:21000795
|
A | G | 1 | a0007c0013t0002g0009 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.343-9391T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21000795 | ||||||
| chr13:21000862
|
G | T | 122 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(119): Show | 122 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.343-9458C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21000862 | ||||||
| chr13:21000866
|
C | T | 7 | a0003c0007t0008g0044a0003c0007t0008g0045a0003c0007t0008g0046others(4): Show | 7 | HG02145.hp1 HG02257.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.343-9462G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21000866 | ||||||
| chr13:21000980
|
A | G | 1 | a0002c0002t0003g0102 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.343-9576T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21000980 | ||||||
| chr13:21000993
|
C | G | 302 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(299): Show | 303 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.343-9589G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21000993 | ||||||
| chr13:21001159
|
C | T | 75 | a0002c0002t0003g0094a0002c0002t0003g0095a0002c0002t0003g0096others(72): Show | 75 | HG00438.hp2 HG00621.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.343-9755G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21001159 | ||||||
| chr13:21001235
|
C | T | 1 | a0001c0001t0001g0209 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.343-9831G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21001235 | ||||||
| chr13:21001244
|
T | G | 1 | a0004c0004t0028g0025 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.343-9840A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21001244 | ||||||
| chr13:21001319
|
C | A | 121 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0178others(118): Show | 121 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.343-9915G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21001319 | ||||||
| chr13:21001379
|
C | T | 2 | a0002c0002t0003g0095a0005c0012t0002g0030 | 2 | HG03017.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.343-9975G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21001379 | ||||||
| chr13:21001380
|
G | A | 76 | a0001c0010t0001g0056a0001c0010t0001g0064a0001c0010t0015g0003others(73): Show | 77 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(74): Show |
intron_variant | MODIFIER | c.343-9976C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21001380 | ||||||
| chr13:21001473
|
G | A | 4 | a0002c0002t0011g0283a0002c0002t0011g0284a0002c0002t0011g0285others(1): Show | 4 | HG00735.hp2 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.343-10069C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21001473 | ||||||
| chr13:21001487
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.343-10083C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21001487 | ||||||
| chr13:21001766
|
T | A | 73 | a0001c0001t0001g0024a0001c0010t0001g0056a0001c0010t0001g0064others(70): Show | 74 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.343-10362A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21001766 | ||||||
| chr13:21001857
|
C | T | 1 | a0001c0001t0001g0277 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.343-10453G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21001857 | ||||||
| chr13:21001873
|
C | T | 2 | a0005c0016t0014g0035a0005c0016t0014g0036 | 2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.343-10469G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21001873 | ||||||
| chr13:21001945
|
G | T | 10 | a0003c0003t0004g0259a0003c0003t0025g0287a0003c0008t0046g0288others(7): Show | 10 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.343-10541C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21001945 | ||||||
| chr13:21001984
|
G | A | 1 | a0001c0001t0013g0205 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.343-10580C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21001984 | ||||||
| chr13:21001990
|
T | C | 175 | a0001c0001t0001g0024a0001c0010t0001g0056a0001c0010t0001g0064others(172): Show | 176 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(173): Show |
intron_variant | MODIFIER | c.343-10586A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21001990 | ||||||
| chr13:21001999
|
C | T | 1 | a0002c0014t0018g0039 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.343-10595G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21001999 | ||||||
| chr13:21002074
|
T | C | 302 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(299): Show | 303 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.343-10670A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21002074 | ||||||
| chr13:21002128
|
T | C | 5 | a0002c0002t0011g0034a0005c0012t0001g0033a0005c0012t0002g0028others(2): Show | 5 | HG00735.hp1 HG02559.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.343-10724A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21002128 | ||||||
| chr13:21002135
|
G | A | 3 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0252 | 3 | HG00099.hp1 HG01071.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.343-10731C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21002135 | ||||||
| chr13:21002150
|
A | T | 176 | a0001c0001t0001g0024a0001c0010t0001g0056a0001c0010t0001g0064others(173): Show | 177 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(174): Show |
intron_variant | MODIFIER | c.343-10746T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21002150 | ||||||
| chr13:21002194
|
T | C | 1 | a0008c0033t0001g0304 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.343-10790A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21002194 | ||||||
| chr13:21002196
|
A | G | 1 | a0008c0026t0011g0286 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.343-10792T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21002196 | ||||||
| chr13:21002197
|
G | A | 10 | a0003c0003t0004g0259a0003c0003t0025g0287a0003c0008t0046g0288others(7): Show | 10 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.343-10793C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21002197 | ||||||
| chr13:21002205
|
G | A | 124 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0178others(121): Show | 124 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.343-10801C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21002205 | ||||||
| chr13:21002374
|
CT | C | 92 | a0001c0001t0001g0024a0001c0001t0001g0197a0001c0001t0001g0267others(89): Show | 93 | HG00597.hp2 HG00621.hp2 HG00639.hp1 others(90): Show |
intron_variant | MODIFIER | c.343-10971delA | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21002374 | ||||||
| chr13:21002606
|
G | A | 1 | a0012c0022t0004g0007 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.343-11202C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21002606 | ||||||
| chr13:21002813
|
C | A | 1 | a0003c0032t0016g0315 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.343-11409G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21002813 | ||||||
| chr13:21002991
|
C | G | 79 | a0002c0002t0003g0094a0002c0002t0003g0095a0002c0002t0003g0096others(76): Show | 79 | HG00438.hp2 HG00621.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.343-11587G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21002991 | ||||||
| chr13:21003212
|
GA | G | 73 | a0001c0001t0001g0024a0001c0010t0001g0056a0001c0010t0001g0064others(70): Show | 74 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.343-11809delT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21003212 | ||||||
| chr13:21003240
|
T | G | 57 | a0001c0001t0001g0024a0001c0010t0001g0056a0001c0010t0001g0064others(54): Show | 57 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(54): Show |
intron_variant | MODIFIER | c.343-11836A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21003240 | ||||||
| chr13:21003397
|
G | A | 1 | a0012c0022t0004g0007 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.343-11993C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21003397 | ||||||
| chr13:21003400
|
C | T | 73 | a0001c0001t0001g0024a0001c0010t0001g0056a0001c0010t0001g0064others(70): Show | 74 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.343-11996G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21003400 | ||||||
| chr13:21003401
|
G | A | 1 | a0003c0008t0009g0088 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.343-11997C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21003401 | ||||||
| chr13:21003444
|
CT | C | 68 | a0001c0001t0001g0024a0001c0001t0001g0221a0001c0010t0001g0056others(65): Show | 69 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(66): Show |
intron_variant | MODIFIER | c.343-12041delA | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21003444 | ||||||
| chr13:21003494
|
G | A | 2 | a0002c0002t0010g0281a0002c0028t0041g0282 | 2 | HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.343-12090C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21003494 | ||||||
| chr13:21003686
|
G | C | 3 | a0001c0001t0002g0227a0001c0001t0002g0228a0001c0001t0027g0226 | 3 | HG00741.hp1 HG01106.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.343-12282C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21003686 | ||||||
| chr13:21003758
|
G | T | 1 | a0004c0004t0028g0025 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.343-12354C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21003758 | ||||||
| chr13:21003846
|
G | A | 1 | a0001c0001t0013g0206 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.343-12442C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21003846 | ||||||
| chr13:21003902
|
C | A | 6 | a0002c0014t0018g0039a0002c0014t0018g0041a0002c0014t0038g0040others(3): Show | 6 | HG01243.hp1 HG02451.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.343-12498G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21003902 | ||||||
| chr13:21003968
|
G | A | 1 | a0003c0005t0001g0084 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.343-12564C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21003968 | ||||||
| chr13:21004011
|
T | C | 10 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0264others(7): Show | 10 | HG00738.hp1 HG01074.hp1 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.343-12607A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21004011 | ||||||
| chr13:21004056
|
C | T | 1 | a0003c0007t0036g0051 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.343-12652G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21004056 | ||||||
| chr13:21004302
|
T | C | 10 | a0003c0005t0002g0058a0003c0007t0008g0044a0003c0007t0008g0045others(7): Show | 10 | HG02145.hp1 HG02257.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.343-12898A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21004302 | ||||||
| chr13:21004382
|
T | C | 3 | a0003c0003t0002g0179a0003c0003t0002g0180a0003c0003t0002g0185 | 3 | NA18952.hp2 NA18982.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.343-12978A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21004382 | ||||||
| chr13:21004394
|
A | T | 3 | a0003c0003t0002g0179a0003c0003t0002g0180a0003c0003t0002g0185 | 3 | NA18952.hp2 NA18982.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.343-12990T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21004394 | ||||||
| chr13:21004434
|
C | CA | 152 | a0001c0001t0001g0024a0001c0010t0001g0056a0001c0010t0001g0064others(149): Show | 152 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(149): Show |
intron_variant | MODIFIER | c.343-13031dupT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21004434 | ||||||
| chr13:21004461
|
T | A | 2 | a0005c0016t0014g0035a0005c0016t0014g0036 | 2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.343-13057A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21004461 | ||||||
| chr13:21004478
|
T | C | 176 | a0001c0001t0001g0024a0001c0010t0001g0056a0001c0010t0001g0064others(173): Show | 177 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(174): Show |
intron_variant | MODIFIER | c.343-13074A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21004478 | ||||||
| chr13:21004488
|
A | T | 13 | a0002c0006t0004g0011a0002c0006t0004g0012a0002c0006t0004g0015others(10): Show | 13 | HG00597.hp2 HG01358.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.343-13084T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21004488 | ||||||
| chr13:21004545
|
CGT | C | 4 | a0002c0006t0004g0169a0002c0006t0004g0212a0002c0006t0004g0213others(1): Show | 4 | NA18969.hp1 NA18991.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.343-13143_343-1314 others(6): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21004545 | ||||||
| chr13:21004803
|
A | T | 1 | a0003c0005t0001g0084 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.343-13399T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21004803 | ||||||
| chr13:21005199
|
C | G | 2 | a0003c0008t0009g0088a0008c0033t0001g0304 | 2 | HG01243.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.343-13795G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21005199 | ||||||
| chr13:21005274
|
T | C | 2 | a0002c0002t0003g0138a0002c0002t0003g0146 | 2 | NA19066.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.343-13870A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21005274 | ||||||
| chr13:21005282
|
A | C | 1 | a0003c0032t0016g0315 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.343-13878T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21005282 | ||||||
| chr13:21005435
|
T | C | 10 | a0003c0003t0004g0259a0003c0003t0025g0287a0003c0008t0046g0288others(7): Show | 10 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.343-14031A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21005435 | ||||||
| chr13:21005533
|
A | G | 1 | a0001c0001t0001g0249 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.343-14129T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21005533 | ||||||
| chr13:21005592
|
G | A | 5 | a0002c0024t0023g0038a0002c0034t0035g0027a0003c0008t0009g0088others(2): Show | 5 | HG00639.hp1 HG01243.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.343-14188C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21005592 | ||||||
| chr13:21005805
|
A | AT | 14 | a0003c0003t0004g0259a0003c0003t0025g0287a0003c0005t0002g0053others(11): Show | 14 | HG01884.hp1 HG02055.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.343-14402dupA | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21005805 | ||||||
| chr13:21005805
|
A | ATT | 207 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0178others(204): Show | 207 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.343-14402_343-1440 others(6): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21005805 | ||||||
| chr13:21005806
|
T | TTTA | 22 | a0001c0001t0006g0184a0001c0001t0012g0165a0002c0002t0024g0156others(19): Show | 22 | HG00597.hp2 HG00639.hp1 HG01358.hp1 others(19): Show |
intron_variant | MODIFIER | c.343-14403_343-1440 others(7): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21005806 | ||||||
| chr13:21005806
|
T | TTTAA | 8 | a0002c0014t0018g0039a0002c0014t0018g0041a0002c0014t0038g0040others(5): Show | 8 | HG01243.hp1 HG01243.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.343-14403_343-1440 others(8): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21005806 | ||||||
| chr13:21005807
|
A | T | 73 | a0001c0001t0001g0024a0001c0010t0001g0056a0001c0010t0001g0064others(70): Show | 74 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.343-14403T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21005807 | ||||||
| chr13:21005808
|
A | T | 60 | a0001c0001t0001g0024a0001c0010t0001g0056a0001c0010t0001g0064others(57): Show | 61 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.343-14404T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21005808 | ||||||
| chr13:21005809
|
A | T | 1 | a0003c0003t0002g0017 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.343-14405T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21005809 | ||||||
| chr13:21005818
|
A | C | 74 | a0002c0002t0003g0094a0002c0002t0003g0095a0002c0002t0003g0096others(71): Show | 74 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.343-14414T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21005818 | ||||||
| chr13:21005819
|
A | C | 1 | a0003c0007t0036g0051 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.343-14415T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21005819 | ||||||
| chr13:21005841
|
A | G | 241 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0178others(238): Show | 241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.343-14437T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21005841 | ||||||
| chr13:21005853
|
C | G | 15 | a0003c0003t0004g0300a0003c0003t0004g0301a0003c0008t0009g0294others(12): Show | 15 | HG01433.hp2 HG02258.hp2 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.343-14449G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21005853 | ||||||
| chr13:21005880
|
G | A | 1 | a0003c0007t0036g0051 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.343-14476C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21005880 | ||||||
| chr13:21006040
|
G | C | 103 | a0002c0002t0003g0094a0002c0002t0003g0095a0002c0002t0003g0096others(100): Show | 103 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.343-14636C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21006040 | ||||||
| chr13:21006045
|
G | A | 1 | a0003c0003t0002g0017 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.343-14641C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21006045 | ||||||
| chr13:21006069
|
A | G | 73 | a0001c0001t0001g0024a0001c0010t0001g0056a0001c0010t0001g0064others(70): Show | 74 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.343-14665T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21006069 | ||||||
| chr13:21006077
|
C | T | 1 | a0002c0028t0041g0282 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.343-14673G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21006077 | ||||||
| chr13:21006078
|
G | A | 103 | a0002c0002t0003g0094a0002c0002t0003g0095a0002c0002t0003g0096others(100): Show | 103 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.343-14674C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21006078 | ||||||
| chr13:21006175
|
T | C | 3 | a0004c0004t0005g0251a0004c0004t0005g0290a0004c0004t0005g0311 | 3 | HG02622.hp2 HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.343-14771A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21006175 | ||||||
| chr13:21006207
|
G | GA | 99 | a0001c0001t0001g0277a0001c0001t0006g0184a0002c0002t0003g0094others(96): Show | 100 | HG00438.hp2 HG00621.hp1 HG00735.hp1 others(97): Show |
intron_variant | MODIFIER | c.343-14804dupT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21006207 | ||||||
| chr13:21006378
|
A | T | 1 | a0001c0001t0001g0200 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.343-14974T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21006378 | ||||||
| chr13:21006392
|
A | C | 1 | a0003c0005t0002g0037 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.343-14988T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21006392 | ||||||
| chr13:21006540
|
T | C | 13 | a0002c0006t0004g0011a0002c0006t0004g0012a0002c0006t0004g0015others(10): Show | 13 | HG00597.hp2 HG01358.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.343-15136A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21006540 | ||||||
| chr13:21006575
|
T | A | 4 | a0002c0002t0010g0281a0002c0028t0041g0282a0005c0016t0014g0035others(1): Show | 4 | HG02965.hp2 HG03139.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.343-15171A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21006575 | ||||||
| chr13:21006723
|
C | T | 1 | a0003c0007t0036g0051 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.343-15319G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21006723 | ||||||
| chr13:21006823
|
C | T | 56 | a0001c0001t0001g0024a0001c0010t0001g0056a0001c0010t0001g0064others(53): Show | 56 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.343-15419G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21006823 | ||||||
| chr13:21006984
|
G | C | 73 | a0001c0001t0001g0024a0001c0010t0001g0056a0001c0010t0001g0064others(70): Show | 74 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.343-15580C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21006984 | ||||||
| chr13:21007134
|
T | C | 3 | a0003c0003t0004g0259a0003c0003t0025g0287a0003c0008t0046g0288 | 3 | HG02055.hp2 HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.343-15730A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007134 | ||||||
| chr13:21007281
|
C | T | 1 | a0009c0020t0009g0001 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.343-15877G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007281 | ||||||
| chr13:21007287
|
T | C | 7 | a0003c0009t0008g0309a0003c0009t0009g0308a0003c0009t0016g0307others(4): Show | 7 | HG01884.hp1 HG02258.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.343-15883A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007287 | ||||||
| chr13:21007300
|
A | G | 176 | a0001c0001t0001g0024a0001c0010t0001g0056a0001c0010t0001g0064others(173): Show | 177 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(174): Show |
intron_variant | MODIFIER | c.343-15896T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007300 | ||||||
| chr13:21007352
|
G | A | 1 | a0002c0027t0039g0114 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.343-15948C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007352 | ||||||
| chr13:21007373
|
A | T | 1 | a0002c0017t0011g0075 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.343-15969T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007373 | ||||||
| chr13:21007509
|
GAGTAGTT others(218): Show |
G | 1 | a0009c0020t0009g0001 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.343-16330_343-1610 others(4): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007509 | ||||||
| chr13:21007513
|
A | C | 6 | a0002c0014t0018g0039a0002c0014t0018g0041a0002c0014t0038g0040others(3): Show | 6 | HG01243.hp1 HG02451.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.343-16109T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007513 | ||||||
| chr13:21007531
|
G | GAT | 26 | a0001c0010t0001g0056a0001c0010t0001g0064a0001c0010t0015g0003others(23): Show | 26 | HG00621.hp2 HG00741.hp2 HG01257.hp2 others(23): Show |
intron_variant | MODIFIER | c.343-16129_343-1612 others(6): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007531 | ||||||
| chr13:21007531
|
GAT | G | 13 | a0002c0028t0041g0282a0003c0003t0004g0259a0003c0003t0025g0287others(10): Show | 13 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.343-16129_343-1612 others(6): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007531 | ||||||
| chr13:21007531
|
GATATATA others(199): Show |
G | 1 | a0004c0004t0028g0025 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.343-16333_343-1612 others(4): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007531 | ||||||
| chr13:21007532
|
ATATATAT others(197): Show |
A | 1 | a0002c0034t0035g0027 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.343-16332_343-1612 others(4): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007532 | ||||||
| chr13:21007533
|
T | G | 101 | a0002c0002t0003g0094a0002c0002t0003g0095a0002c0002t0003g0096others(98): Show | 101 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(98): Show |
intron_variant | MODIFIER | c.343-16129A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007533 | ||||||
| chr13:21007536
|
ATATATAT others(193): Show |
A | 1 | a0008c0033t0001g0304 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.343-16332_343-1613 others(4): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007536 | ||||||
| chr13:21007538
|
ATATATAG others(191): Show |
A | 1 | a0002c0024t0023g0038 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.343-16332_343-1613 others(4): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007538 | ||||||
| chr13:21007540
|
ATATAGTA others(176): Show |
A | 73 | a0002c0002t0003g0094a0002c0002t0003g0095a0002c0002t0003g0096others(70): Show | 73 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(70): Show |
intron_variant | MODIFIER | c.343-16319_343-1613 others(4): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007540 | ||||||
| chr13:21007542
|
ATAGTATA others(174): Show |
A | 15 | a0002c0002t0011g0034a0002c0006t0004g0011a0002c0006t0004g0012others(12): Show | 15 | HG00735.hp1 HG01358.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.343-16319_343-1613 others(4): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007542 | ||||||
| chr13:21007543
|
T | G | 2 | a0002c0002t0010g0281a0012c0022t0004g0007 | 2 | HG02572.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.343-16139A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007543 | ||||||
| chr13:21007544
|
A | T | 2 | a0002c0002t0010g0281a0012c0022t0004g0007 | 2 | HG02572.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.343-16140T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007544 | ||||||
| chr13:21007544
|
AG | A | 9 | a0002c0006t0004g0164a0002c0006t0004g0210a0002c0014t0018g0039others(6): Show | 9 | HG00597.hp2 HG01243.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.343-16141delC | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007544 | ||||||
| chr13:21007544
|
AGTATATA others(172): Show |
A | 1 | a0005c0012t0002g0030 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.343-16319_343-1614 others(4): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007544 | ||||||
| chr13:21007545
|
G | A | 3 | a0002c0002t0010g0281a0004c0004t0005g0251a0004c0004t0005g0290 | 3 | HG02976.hp1 HG03041.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.343-16141C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007545 | ||||||
| chr13:21007545
|
G | GTA | 15 | a0001c0001t0001g0199a0001c0001t0001g0208a0001c0001t0001g0221others(12): Show | 15 | HG00280.hp1 HG00738.hp1 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.343-16143_343-1614 others(6): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007545 | ||||||
| chr13:21007545
|
G | GTATA | 13 | a0001c0001t0001g0238a0001c0001t0001g0252a0001c0001t0001g0273others(10): Show | 13 | HG00741.hp1 HG01071.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.343-16145_343-1614 others(8): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007545 | ||||||
| chr13:21007545
|
G | GTATATA | 3 | a0001c0010t0001g0061a0001c0030t0001g0091a0003c0003t0002g0179 | 3 | HG01099.hp1 NA18982.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.343-16147_343-1614 others(10): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007545 | ||||||
| chr13:21007545
|
G | GTATATAT others(34): Show |
1 | a0003c0003t0001g0236 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.343-16142_343-1614 others(45): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007545 | ||||||
| chr13:21007545
|
G | T | 32 | a0001c0001t0001g0024a0003c0003t0002g0008a0003c0003t0002g0010others(29): Show | 32 | HG00642.hp2 HG01109.hp1 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.343-16141C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007545 | ||||||
| chr13:21007545
|
GTA | G | 28 | a0001c0001t0001g0192a0001c0001t0001g0196a0001c0001t0001g0200others(25): Show | 28 | HG00280.hp2 HG00639.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.343-16143_343-1614 others(6): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007545 | ||||||
| chr13:21007545
|
GTATA | G | 16 | a0001c0001t0001g0183a0001c0001t0001g0197a0001c0001t0001g0202others(13): Show | 16 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(13): Show |
intron_variant | MODIFIER | c.343-16145_343-1614 others(8): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007545 | ||||||
| chr13:21007545
|
GTATATAT others(3): Show |
G | 1 | a0001c0001t0002g0218 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.343-16151_343-1614 others(14): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007545 | ||||||
| chr13:21007545
|
GTATATAT others(5): Show |
G | 1 | a0001c0001t0022g0174 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.343-16153_343-1614 others(16): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007545 | ||||||
| chr13:21007545
|
GTATATAT others(9): Show |
G | 1 | a0001c0001t0001g0178 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.343-16157_343-1614 others(20): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007545 | ||||||
| chr13:21007546
|
T | A | 32 | a0001c0001t0001g0024a0003c0003t0002g0008a0003c0003t0002g0010others(29): Show | 32 | HG00642.hp2 HG01109.hp1 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.343-16142A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007546 | ||||||
| chr13:21007547
|
A | C | 2 | a0003c0005t0012g0077a0003c0007t0008g0047 | 2 | HG01175.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.343-16143T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007547 | ||||||
| chr13:21007547
|
A | G | 36 | a0001c0001t0001g0024a0001c0001t0006g0168a0001c0001t0006g0195others(33): Show | 36 | HG00642.hp2 HG01109.hp1 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.343-16143T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007547 | ||||||
| chr13:21007549
|
A | ATATATAT others(18): Show |
1 | a0003c0003t0002g0170 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.343-16146_343-1614 others(29): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007549 | ||||||
| chr13:21007549
|
A | ATATATAT others(43): Show |
1 | a0001c0001t0001g0248 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.343-16146_343-1614 others(54): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007549 | ||||||
| chr13:21007549
|
A | G | 4 | a0001c0001t0003g0161a0001c0001t0029g0193a0001c0031t0006g0187others(1): Show | 4 | HG02074.hp1 HG02083.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.343-16145T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007549 | ||||||
| chr13:21007551
|
A | G | 6 | a0001c0001t0004g0276a0001c0001t0006g0184a0001c0001t0006g0188others(3): Show | 6 | HG00423.hp1 HG02071.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.343-16147T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007551 | ||||||
| chr13:21007553
|
A | ATAC | 22 | a0001c0010t0001g0064a0002c0017t0006g0004a0003c0003t0002g0017others(19): Show | 22 | HG00621.hp2 HG01257.hp2 HG02027.hp1 others(19): Show |
intron_variant | MODIFIER | c.343-16150_343-1614 others(7): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007553 | ||||||
| chr13:21007553
|
A | G | 1 | a0003c0032t0016g0315 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.343-16149T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007553 | ||||||
| chr13:21007553
|
ATATATAT others(181): Show |
A | 1 | a0002c0017t0011g0075 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.343-16337_343-1615 others(4): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007553 | ||||||
| chr13:21007555
|
A | AC | 5 | a0001c0010t0001g0056a0001c0010t0015g0003a0002c0028t0041g0282others(2): Show | 5 | HG00741.hp2 HG02602.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.343-16152_343-1615 others(5): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007555 | ||||||
| chr13:21007555
|
A | AG | 5 | a0002c0006t0004g0164a0002c0006t0004g0210a0002c0014t0018g0039others(2): Show | 5 | HG00597.hp2 HG02451.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.343-16152_343-1615 others(5): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007555 | ||||||
| chr13:21007555
|
A | ATATATAT others(12): Show |
1 | a0003c0003t0002g0231 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.343-16152_343-1615 others(23): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007555 | ||||||
| chr13:21007557
|
A | AG | 3 | a0004c0004t0005g0251a0004c0004t0005g0290a0004c0015t0018g0042 | 3 | HG02976.hp1 HG03041.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.343-16154_343-1615 others(5): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007557 | ||||||
| chr13:21007557
|
A | C | 2 | a0005c0016t0014g0035a0005c0016t0014g0036 | 2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.343-16153T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007557 | ||||||
| chr13:21007557
|
ATAT | A | 29 | a0001c0001t0001g0024a0003c0003t0002g0008a0003c0003t0002g0010others(26): Show | 29 | HG00642.hp2 HG01109.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.343-16156_343-1615 others(7): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007557 | ||||||
| chr13:21007559
|
A | AG | 10 | a0003c0003t0004g0259a0003c0003t0025g0287a0003c0008t0046g0288others(7): Show | 10 | HG02055.hp2 HG02258.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.343-16156_343-1615 others(5): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007559 | ||||||
| chr13:21007559
|
ATATATAT others(101): Show |
A | 1 | a0003c0036t0009g0310 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.343-16263_343-1615 others(4): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007559 | ||||||
| chr13:21007561
|
A | ATATATAT others(4): Show |
1 | a0003c0003t0004g0301 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.343-16158_343-1615 others(15): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007561 | ||||||
| chr13:21007561
|
A | ATATATAT others(31): Show |
1 | a0003c0003t0004g0300 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.343-16158_343-1615 others(42): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007561 | ||||||
| chr13:21007561
|
A | C | 28 | a0001c0001t0001g0024a0003c0003t0002g0008a0003c0003t0002g0010others(25): Show | 28 | HG00642.hp2 HG01109.hp1 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.343-16157T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007561 | ||||||
| chr13:21007561
|
A | G | 1 | a0003c0005t0002g0043 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.343-16157T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007561 | ||||||
| chr13:21007563
|
A | AC | 22 | a0001c0010t0001g0064a0002c0017t0006g0004a0003c0003t0002g0017others(19): Show | 22 | HG00621.hp2 HG01257.hp2 HG02027.hp1 others(19): Show |
intron_variant | MODIFIER | c.343-16160_343-1615 others(5): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007563 | ||||||
| chr13:21007563
|
A | G | 2 | a0004c0019t0020g0305a0004c0019t0020g0306 | 2 | HG01243.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.343-16159T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007563 | ||||||
| chr13:21007565
|
A | AC | 4 | a0001c0010t0001g0056a0001c0010t0015g0003a0003c0005t0002g0037others(1): Show | 4 | HG00741.hp2 HG02602.hp2 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.343-16162_343-1616 others(5): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007565 | ||||||
| chr13:21007565
|
ATATATAT others(111): Show |
A | 1 | a0004c0015t0018g0042 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.343-16279_343-1616 others(4): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007565 | ||||||
| chr13:21007566
|
T | C | 1 | a0003c0005t0004g0078 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.343-16162A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007566 | ||||||
| chr13:21007567
|
A | ATATAGTA others(23): Show |
1 | a0004c0004t0019g0026 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.343-16164_343-1616 others(34): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007567 | ||||||
| chr13:21007567
|
A | G | 2 | a0001c0001t0001g0092a0001c0001t0001g0203 | 2 | HG03831.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.343-16163T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007567 | ||||||
| chr13:21007569
|
A | G | 2 | a0001c0001t0001g0092a0001c0001t0001g0203 | 2 | HG03831.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.343-16165T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007569 | ||||||
| chr13:21007571
|
AT | A | 29 | a0001c0001t0001g0024a0003c0003t0002g0008a0003c0003t0002g0010others(26): Show | 29 | HG00642.hp2 HG01109.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.343-16168delA | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007571 | ||||||
| chr13:21007573
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0006g0168 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.343-16170_343-1616 others(15): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007573 | ||||||
| chr13:21007573
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0006g0195 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.343-16170_343-1616 others(17): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007573 | ||||||
| chr13:21007573
|
A | ATATATAT others(10): Show |
1 | a0001c0001t0001g0220 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.343-16170_343-1616 others(21): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007573 | ||||||
| chr13:21007573
|
A | ATATATAT others(49): Show |
1 | a0001c0001t0010g0112 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.343-16170_343-1616 others(60): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007573 | ||||||
| chr13:21007573
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0223 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.343-16170_343-1616 others(25): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007573 | ||||||
| chr13:21007573
|
A | C | 29 | a0001c0001t0001g0024a0003c0003t0002g0008a0003c0003t0002g0010others(26): Show | 29 | HG00642.hp2 HG01109.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.343-16169T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007573 | ||||||
| chr13:21007573
|
A | G | 2 | a0004c0004t0001g0302a0004c0004t0001g0303 | 2 | HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.343-16169T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007573 | ||||||
| chr13:21007573
|
AT | A | 9 | a0003c0003t0004g0259a0003c0003t0025g0287a0003c0008t0046g0288others(6): Show | 9 | HG02055.hp2 HG02258.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.343-16170delA | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007573 | ||||||
| chr13:21007573
|
ATATATAT others(181): Show |
A | 1 | a0003c0008t0009g0088 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.343-16357_343-1617 others(4): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007573 | ||||||
| chr13:21007575
|
A | G | 9 | a0003c0003t0004g0259a0003c0003t0025g0287a0003c0008t0046g0288others(6): Show | 9 | HG02055.hp2 HG02258.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.343-16171T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007575 | ||||||
| chr13:21007575
|
ATATATAT others(6): Show |
A | 1 | a0001c0001t0001g0246 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.343-16184_343-1617 others(17): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007575 | ||||||
| chr13:21007575
|
ATATATAT others(154): Show |
A | 1 | a0002c0014t0018g0041 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.343-16332_343-1617 others(4): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007575 | ||||||
| chr13:21007577
|
A | AC | 22 | a0001c0010t0001g0064a0002c0017t0006g0004a0003c0003t0002g0017others(19): Show | 22 | HG00621.hp2 HG01257.hp2 HG02027.hp1 others(19): Show |
intron_variant | MODIFIER | c.343-16174_343-1617 others(5): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007577 | ||||||
| chr13:21007577
|
A | C | 2 | a0005c0016t0014g0035a0005c0016t0014g0036 | 2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.343-16173T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007577 | ||||||
| chr13:21007577
|
ATATATAT others(152): Show |
A | 2 | a0002c0014t0018g0039a0002c0014t0038g0040 | 2 | HG02451.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.343-16332_343-1617 others(4): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007577 | ||||||
| chr13:21007579
|
ATATATAT others(22): Show |
A | 1 | a0001c0010t0001g0056 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.343-16204_343-1617 others(33): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007579 | ||||||
| chr13:21007579
|
ATATATAT others(85): Show |
A | 1 | a0001c0010t0015g0003 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.343-16267_343-1617 others(96): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007579 | ||||||
| chr13:21007579
|
ATATATAT others(102): Show |
A | 2 | a0003c0005t0002g0037a0003c0005t0002g0050 | 2 | HG00741.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.343-16284_343-1617 others(4): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007579 | ||||||
| chr13:21007583
|
A | G | 1 | a0001c0001t0001g0224 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.343-16179T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007583 | ||||||
| chr13:21007585
|
A | G | 1 | a0001c0001t0001g0224 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.343-16181T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007585 | ||||||
| chr13:21007585
|
ATAGTATA others(170): Show |
A | 2 | a0002c0006t0004g0164a0002c0006t0004g0210 | 2 | HG00597.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.343-16358_343-1618 others(4): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007585 | ||||||
| chr13:21007586
|
T | G | 4 | a0001c0001t0001g0092a0001c0001t0001g0181a0001c0001t0001g0203others(1): Show | 4 | HG00423.hp2 HG02015.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.343-16182A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007586 | ||||||
| chr13:21007587
|
A | AGT | 5 | a0001c0001t0006g0168a0001c0001t0006g0195a0004c0004t0005g0251others(2): Show | 5 | HG02622.hp2 HG02976.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.343-16185_343-1618 others(6): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007587 | ||||||
| chr13:21007587
|
A | ATAGT | 3 | a0001c0001t0047g0100a0004c0004t0030g0295a0004c0035t0009g0297 | 3 | HG03209.hp2 HG03540.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.343-16184_343-1618 others(8): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007587 | ||||||
| chr13:21007587
|
A | ATATATAG others(3): Show |
1 | a0003c0008t0009g0294 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.343-16184_343-1618 others(14): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007587 | ||||||
| chr13:21007587
|
A | T | 4 | a0001c0001t0001g0092a0001c0001t0001g0181a0001c0001t0001g0203others(1): Show | 4 | HG00423.hp2 HG02015.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.343-16183T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007587 | ||||||
| chr13:21007587
|
AG | A | 5 | a0001c0001t0001g0224a0001c0001t0002g0177a0001c0001t0010g0163others(2): Show | 5 | HG00597.hp1 HG02723.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.343-16184delC | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007587 | ||||||
| chr13:21007588
|
G | A | 8 | a0001c0001t0001g0181a0001c0001t0001g0233a0001c0001t0010g0162others(5): Show | 8 | HG00423.hp2 HG01433.hp2 HG02015.hp1 others(5): Show |
intron_variant | MODIFIER | c.343-16184C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007588 | ||||||
| chr13:21007588
|
G | C | 32 | a0001c0001t0001g0024a0003c0003t0002g0008a0003c0003t0002g0010others(29): Show | 32 | HG00642.hp2 HG01109.hp1 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.343-16184C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007588 | ||||||
| chr13:21007590
|
A | G | 3 | a0004c0004t0001g0302a0004c0004t0001g0303a0004c0004t0005g0256 | 3 | HG02683.hp2 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.343-16186T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007590 | ||||||
| chr13:21007596
|
ATATATAG others(4): Show |
A | 1 | a0003c0032t0016g0315 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.343-16203_343-1619 others(15): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007596 | ||||||
| chr13:21007598
|
ATATAGTG others(1): Show |
A | 26 | a0001c0001t0001g0024a0003c0003t0002g0008a0003c0003t0002g0010others(23): Show | 26 | HG00642.hp2 HG01109.hp1 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.343-16202_343-1619 others(12): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007598 | ||||||
| chr13:21007600
|
ATAGTGTG others(3): Show |
A | 19 | a0001c0010t0001g0064a0002c0017t0006g0004a0003c0003t0002g0017others(16): Show | 19 | HG00621.hp2 HG01257.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.343-16206_343-1619 others(14): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007600 | ||||||
| chr13:21007600
|
ATAGTGTG others(62): Show |
A | 1 | a0012c0022t0004g0007 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.343-16265_343-1619 others(73): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007600 | ||||||
| chr13:21007600
|
ATAGTGTG others(81): Show |
A | 2 | a0003c0003t0002g0190a0003c0005t0015g0069 | 2 | HG03831.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.343-16284_343-1619 others(92): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007600 | ||||||
| chr13:21007602
|
AGT | A | 10 | a0001c0001t0001g0200a0001c0001t0001g0248a0001c0001t0001g0252others(7): Show | 10 | HG01071.hp1 HG01361.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.343-16200_343-1619 others(6): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007602 | ||||||
| chr13:21007602
|
AGTGTGTA others(41): Show |
A | 2 | a0003c0009t0008g0309a0003c0009t0032g0289 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.343-16246_343-1619 others(52): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007602 | ||||||
| chr13:21007603
|
G | T | 13 | a0001c0001t0001g0092a0001c0001t0001g0203a0001c0001t0002g0177others(10): Show | 13 | HG02258.hp2 HG02572.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.343-16199C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007603 | ||||||
| chr13:21007603
|
GTGTGTA | G | 6 | a0003c0003t0025g0287a0003c0008t0046g0288a0003c0009t0009g0308others(3): Show | 6 | HG02055.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.343-16205_343-1620 others(10): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007603 | ||||||
| chr13:21007603
|
GTGTGTAT others(79): Show |
G | 1 | a0003c0005t0002g0058 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.343-16285_343-1620 others(90): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007603 | ||||||
| chr13:21007604
|
T | A | 13 | a0001c0001t0001g0092a0001c0001t0001g0203a0001c0001t0002g0177others(10): Show | 13 | HG02258.hp2 HG02572.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.343-16200A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007604 | ||||||
| chr13:21007605
|
G | T | 1 | a0001c0001t0002g0177 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.343-16201C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007605 | ||||||
| chr13:21007606
|
T | A | 1 | a0001c0001t0002g0177 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.343-16202A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007606 | ||||||
| chr13:21007607
|
G | A | 114 | a0001c0001t0001g0090a0001c0001t0001g0178a0001c0001t0001g0181others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.343-16203C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007607 | ||||||
| chr13:21007609
|
A | C | 1 | a0001c0010t0001g0056 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.343-16205T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007609 | ||||||
| chr13:21007609
|
A | G | 5 | a0001c0001t0001g0092a0001c0001t0001g0203a0004c0004t0005g0251others(2): Show | 5 | HG02622.hp2 HG02976.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.343-16205T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007609 | ||||||
| chr13:21007611
|
A | C | 17 | a0001c0010t0001g0064a0002c0017t0006g0004a0003c0003t0007g0312others(14): Show | 17 | HG00621.hp2 HG01257.hp2 HG02027.hp1 others(14): Show |
intron_variant | MODIFIER | c.343-16207T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007611 | ||||||
| chr13:21007611
|
A | G | 2 | a0003c0003t0002g0017a0003c0007t0016g0062 | 2 | HG03704.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.343-16207T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007611 | ||||||
| chr13:21007619
|
ATAGT | A | 27 | a0001c0001t0001g0024a0003c0003t0002g0008a0003c0003t0002g0010others(24): Show | 27 | HG00642.hp2 HG01109.hp1 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.343-16219_343-1621 others(8): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007619 | ||||||
| chr13:21007619
|
ATAGTGTA others(81): Show |
A | 1 | a0003c0003t0004g0259 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.343-16303_343-1621 others(92): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007619 | ||||||
| chr13:21007620
|
T | G | 2 | a0002c0002t0010g0281a0002c0028t0041g0282 | 2 | HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.343-16216A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007620 | ||||||
| chr13:21007621
|
A | T | 2 | a0002c0002t0010g0281a0002c0028t0041g0282 | 2 | HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.343-16217T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007621 | ||||||
| chr13:21007622
|
G | A | 2 | a0002c0002t0010g0281a0002c0028t0041g0282 | 2 | HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.343-16218C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007622 | ||||||
| chr13:21007622
|
G | C | 1 | a0003c0003t0025g0287 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.343-16218C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007622 | ||||||
| chr13:21007622
|
G | T | 1 | a0004c0004t0030g0295 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.343-16218C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007622 | ||||||
| chr13:21007622
|
GTGTATAT others(79): Show |
G | 5 | a0003c0008t0046g0288a0003c0009t0009g0308a0003c0009t0016g0307others(2): Show | 5 | HG02622.hp1 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.343-16304_343-1621 others(90): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007622 | ||||||
| chr13:21007623
|
T | A | 1 | a0004c0004t0030g0295 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.343-16219A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007623 | ||||||
| chr13:21007624
|
G | A | 31 | a0001c0010t0001g0056a0001c0010t0001g0061a0001c0010t0001g0064others(28): Show | 31 | HG00621.hp2 HG01257.hp2 HG02027.hp1 others(28): Show |
intron_variant | MODIFIER | c.343-16220C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007624 | ||||||
| chr13:21007624
|
G | C | 9 | a0003c0003t0002g0255a0003c0005t0002g0043a0003c0005t0002g0067others(6): Show | 9 | HG01167.hp2 HG01168.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.343-16220C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007624 | ||||||
| chr13:21007624
|
GTA | G | 3 | a0003c0003t0004g0300a0003c0003t0004g0301a0003c0008t0009g0294 | 3 | HG03225.hp2 HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.343-16222_343-1622 others(6): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007624 | ||||||
| chr13:21007626
|
A | G | 13 | a0001c0001t0001g0092a0001c0001t0001g0203a0001c0001t0001g0274others(10): Show | 13 | HG02004.hp1 HG02280.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.343-16222T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007626 | ||||||
| chr13:21007628
|
A | G | 1 | a0004c0004t0030g0295 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.343-16224T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007628 | ||||||
| chr13:21007630
|
A | ATATATAG others(21): Show |
1 | a0001c0010t0001g0061 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.343-16227_343-1622 others(32): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007630 | ||||||
| chr13:21007630
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0002g0177 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.343-16227_343-1622 others(15): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007630 | ||||||
| chr13:21007630
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0010g0163 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.343-16227_343-1622 others(17): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007630 | ||||||
| chr13:21007632
|
A | AG | 25 | a0001c0010t0001g0064a0002c0017t0006g0004a0003c0003t0002g0017others(22): Show | 25 | HG00621.hp2 HG01257.hp2 HG02027.hp1 others(22): Show |
intron_variant | MODIFIER | c.343-16229_343-1622 others(5): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007632 | ||||||
| chr13:21007632
|
A | ATATATAG others(4): Show |
5 | a0001c0001t0001g0181a0001c0001t0001g0209a0001c0001t0001g0249others(2): Show | 5 | HG00099.hp1 HG00099.hp2 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.343-16229_343-1622 others(15): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007632 | ||||||
| chr13:21007632
|
A | ATATATAG others(21): Show |
1 | a0001c0001t0001g0252 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.343-16229_343-1622 others(32): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007632 | ||||||
| chr13:21007632
|
A | ATATATAT others(27): Show |
1 | a0004c0004t0019g0292 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.343-16229_343-1622 others(38): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007632 | ||||||
| chr13:21007632
|
A | ATATATAT others(6): Show |
8 | a0001c0001t0001g0197a0001c0001t0001g0245a0001c0001t0001g0280others(5): Show | 8 | HG00639.hp2 HG01358.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.343-16229_343-1622 others(17): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007632 | ||||||
| chr13:21007632
|
A | ATATATAT others(8): Show |
1 | a0004c0004t0019g0026 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.343-16229_343-1622 others(19): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007632 | ||||||
| chr13:21007632
|
A | ATATATAT others(25): Show |
1 | a0003c0008t0009g0296 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.343-16229_343-1622 others(36): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007632 | ||||||
| chr13:21007634
|
A | AG | 25 | a0001c0001t0001g0024a0003c0003t0002g0010a0003c0003t0002g0016others(22): Show | 25 | HG00642.hp2 HG01109.hp1 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.343-16231_343-1623 others(5): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007634 | ||||||
| chr13:21007634
|
A | ATATATAG others(4): Show |
13 | a0001c0001t0001g0215a0001c0001t0001g0274a0001c0001t0003g0161others(10): Show | 13 | HG00423.hp1 HG02004.hp1 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.343-16231_343-1623 others(15): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007634 | ||||||
| chr13:21007636
|
ATATATAT others(7): Show |
A | 1 | a0003c0003t0025g0287 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.343-16246_343-1623 others(18): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007636 | ||||||
| chr13:21007638
|
ATATATAG others(1): Show |
A | 8 | a0001c0001t0001g0279a0001c0001t0002g0207a0001c0001t0047g0100others(5): Show | 8 | HG01099.hp1 HG02056.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.343-16242_343-1623 others(12): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007638 | ||||||
| chr13:21007640
|
ATATAGT | A | 84 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0178others(81): Show | 84 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.343-16242_343-1623 others(10): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007640 | ||||||
| chr13:21007642
|
ATAGT | A | 3 | a0001c0001t0001g0248a0004c0004t0030g0295a0004c0035t0009g0297 | 3 | HG03209.hp2 HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.343-16242_343-1623 others(8): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007642 | ||||||
| chr13:21007644
|
AGTGTGT | A | 44 | a0001c0001t0001g0024a0001c0010t0001g0064a0003c0003t0002g0010others(41): Show | 44 | HG00621.hp2 HG00642.hp2 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.343-16246_343-1624 others(10): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007644 | ||||||
| chr13:21007645
|
G | T | 24 | a0001c0001t0001g0215a0001c0001t0001g0252a0001c0001t0002g0177others(21): Show | 24 | HG00423.hp1 HG01071.hp1 HG01433.hp2 others(21): Show |
intron_variant | MODIFIER | c.343-16241C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007645 | ||||||
| chr13:21007645
|
GTGTGTGT others(56): Show |
G | 2 | a0002c0017t0006g0004a0003c0005t0015g0005 | 2 | NA18951.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.343-16304_343-1624 others(67): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007645 | ||||||
| chr13:21007646
|
T | A | 24 | a0001c0001t0001g0215a0001c0001t0001g0252a0001c0001t0002g0177others(21): Show | 24 | HG00423.hp1 HG01071.hp1 HG01433.hp2 others(21): Show |
intron_variant | MODIFIER | c.343-16242A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007646 | ||||||
| chr13:21007647
|
G | A | 1 | a0004c0019t0020g0305 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.343-16243C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007647 | ||||||
| chr13:21007647
|
G | T | 2 | a0005c0016t0014g0035a0005c0016t0014g0036 | 2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.343-16243C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007647 | ||||||
| chr13:21007648
|
T | A | 2 | a0005c0016t0014g0035a0005c0016t0014g0036 | 2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.343-16244A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007648 | ||||||
| chr13:21007649
|
G | A | 5 | a0002c0002t0010g0281a0002c0028t0041g0282a0003c0032t0016g0315others(2): Show | 5 | HG01243.hp1 HG02965.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.343-16245C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007649 | ||||||
| chr13:21007649
|
G | T | 2 | a0003c0005t0001g0084a0003c0005t0002g0054 | 2 | HG03453.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.343-16245C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007649 | ||||||
| chr13:21007650
|
T | A | 2 | a0003c0005t0001g0084a0003c0005t0002g0054 | 2 | HG03453.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.343-16246A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007650 | ||||||
| chr13:21007651
|
G | A | 22 | a0001c0001t0001g0181a0001c0001t0001g0197a0001c0001t0001g0209others(19): Show | 22 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.343-16247C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007651 | ||||||
| chr13:21007662
|
T | C | 2 | a0002c0002t0010g0281a0002c0028t0041g0282 | 2 | HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.343-16258A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007662 | ||||||
| chr13:21007663
|
AGTGT | A | 20 | a0001c0010t0001g0064a0003c0003t0002g0017a0003c0003t0007g0312others(17): Show | 20 | HG00621.hp2 HG01257.hp2 HG02027.hp1 others(17): Show |
intron_variant | MODIFIER | c.343-16263_343-1626 others(8): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007663 | ||||||
| chr13:21007664
|
G | T | 2 | a0004c0004t0001g0302a0004c0004t0001g0303 | 2 | HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.343-16260C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007664 | ||||||
| chr13:21007664
|
GTGTGTA | G | 28 | a0001c0001t0001g0024a0001c0010t0001g0056a0003c0003t0002g0008others(25): Show | 28 | HG00642.hp2 HG01109.hp1 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.343-16266_343-1626 others(10): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007664 | ||||||
| chr13:21007664
|
GTGTGTAT others(1): Show |
G | 4 | a0002c0002t0010g0281a0002c0028t0041g0282a0010c0018t0010g0065others(1): Show | 4 | HG02572.hp1 HG02647.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.343-16268_343-1626 others(12): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007664 | ||||||
| chr13:21007664
|
GTGTGTAT others(37): Show |
G | 2 | a0003c0005t0002g0048a0003c0005t0002g0049 | 2 | HG02723.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.343-16304_343-1626 others(48): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007664 | ||||||
| chr13:21007665
|
T | A | 2 | a0004c0004t0001g0302a0004c0004t0001g0303 | 2 | HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.343-16261A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007665 | ||||||
| chr13:21007666
|
G | A | 2 | a0005c0016t0014g0035a0005c0016t0014g0036 | 2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.343-16262C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007666 | ||||||
| chr13:21007666
|
G | GTATATAT others(31): Show |
1 | a0004c0035t0009g0297 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.343-16263_343-1626 others(42): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007666 | ||||||
| chr13:21007668
|
G | A | 9 | a0001c0001t0001g0092a0001c0001t0001g0203a0001c0001t0001g0252others(6): Show | 9 | HG01071.hp1 HG01433.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.343-16264C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007668 | ||||||
| chr13:21007668
|
G | C | 1 | a0003c0003t0025g0287 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.343-16264C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007668 | ||||||
| chr13:21007670
|
A | C | 1 | a0012c0022t0004g0007 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.343-16266T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007670 | ||||||
| chr13:21007672
|
A | C | 1 | a0001c0010t0015g0003 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.343-16268T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007672 | ||||||
| chr13:21007681
|
T | G | 28 | a0001c0001t0001g0181a0001c0001t0001g0197a0001c0001t0001g0209others(25): Show | 28 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(25): Show |
intron_variant | MODIFIER | c.343-16277A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007681 | ||||||
| chr13:21007681
|
T | TGTGTATA others(19): Show |
1 | a0001c0001t0001g0237 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.343-16278_343-1627 others(30): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007681 | ||||||
| chr13:21007682
|
A | AGT | 8 | a0001c0001t0001g0267a0004c0004t0001g0302a0004c0004t0001g0303others(5): Show | 8 | HG01255.hp1 HG02258.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.343-16280_343-1627 others(6): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007682 | ||||||
| chr13:21007682
|
A | ATGTGTAT others(19): Show |
1 | a0001c0001t0001g0238 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.343-16279_343-1627 others(30): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007682 | ||||||
| chr13:21007682
|
A | T | 29 | a0001c0001t0001g0181a0001c0001t0001g0197a0001c0001t0001g0209others(26): Show | 29 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(26): Show |
intron_variant | MODIFIER | c.343-16278T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007682 | ||||||
| chr13:21007682
|
AG | A | 8 | a0001c0001t0001g0092a0001c0001t0001g0203a0001c0001t0001g0252others(5): Show | 8 | HG01071.hp1 HG01243.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.343-16279delC | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007682 | ||||||
| chr13:21007683
|
G | A | 2 | a0001c0001t0001g0237a0001c0001t0001g0238 | 2 | NA19011.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.343-16279C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007683 | ||||||
| chr13:21007683
|
G | GTGTGTAT others(14): Show |
1 | a0001c0001t0010g0099 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.343-16280_343-1627 others(25): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007683 | ||||||
| chr13:21007683
|
G | GTGTGTAT others(16): Show |
1 | a0001c0001t0013g0206 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.343-16280_343-1627 others(27): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007683 | ||||||
| chr13:21007683
|
G | GTGTGTAT others(16): Show |
6 | a0001c0001t0001g0178a0001c0001t0001g0183a0001c0001t0001g0211others(3): Show | 6 | HG01515.hp2 HG02280.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.343-16280_343-1627 others(27): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007683 | ||||||
| chr13:21007683
|
G | GTGTGTAT others(18): Show |
7 | a0001c0001t0001g0202a0001c0001t0001g0277a0001c0001t0002g0218others(4): Show | 7 | HG00642.hp1 HG01081.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.343-16280_343-1627 others(29): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007683 | ||||||
| chr13:21007683
|
G | GTGTGTAT others(20): Show |
6 | a0004c0004t0005g0204a0004c0004t0005g0229a0004c0004t0005g0230others(3): Show | 6 | HG02735.hp2 HG02738.hp1 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.343-16280_343-1627 others(31): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007683 | ||||||
| chr13:21007683
|
G | GTGTGTAT others(18): Show |
1 | a0001c0001t0001g0248 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.343-16280_343-1627 others(29): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007683 | ||||||
| chr13:21007683
|
GTA | G | 10 | a0001c0010t0001g0064a0003c0003t0007g0312a0003c0003t0007g0313others(7): Show | 10 | HG00621.hp2 HG01257.hp2 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.343-16281_343-1628 others(6): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007683 | ||||||
| chr13:21007683
|
GTATATAT others(18): Show |
G | 1 | a0003c0005t0001g0084 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.343-16304_343-1628 others(29): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007683 | ||||||
| chr13:21007685
|
A | G | 72 | a0001c0001t0001g0090a0001c0001t0001g0181a0001c0001t0001g0191others(69): Show | 72 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.343-16281T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007685 | ||||||
| chr13:21007687
|
A | G | 65 | a0001c0001t0001g0090a0001c0001t0001g0191a0001c0001t0001g0192others(62): Show | 65 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.343-16283T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007687 | ||||||
| chr13:21007687
|
AT | A | 3 | a0001c0001t0001g0203a0004c0004t0005g0251a0004c0004t0005g0311 | 3 | HG02622.hp2 HG03041.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.343-16284delA | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007687 | ||||||
| chr13:21007689
|
A | C | 4 | a0003c0003t0002g0190a0003c0005t0002g0037a0003c0005t0002g0050others(1): Show | 4 | HG00741.hp2 HG03831.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.343-16285T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007689 | ||||||
| chr13:21007689
|
A | G | 5 | a0001c0001t0001g0203a0001c0001t0001g0252a0004c0004t0005g0251others(2): Show | 5 | HG01071.hp1 HG02622.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.343-16285T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007689 | ||||||
| chr13:21007689
|
ATATATAT others(40): Show |
A | 2 | a0003c0005t0002g0278a0003c0005t0033g0073 | 2 | HG03834.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.343-16332_343-1628 others(51): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007689 | ||||||
| chr13:21007691
|
A | G | 4 | a0001c0001t0001g0092a0001c0001t0001g0203a0004c0004t0005g0251others(1): Show | 4 | HG02622.hp2 HG03041.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.343-16287T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007691 | ||||||
| chr13:21007691
|
ATATATAT others(38): Show |
A | 1 | a0003c0005t0002g0057 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.343-16332_343-1628 others(49): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007691 | ||||||
| chr13:21007693
|
A | AG | 3 | a0002c0002t0010g0281a0002c0028t0041g0282a0010c0018t0010g0065 | 3 | HG02572.hp1 HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.343-16290_343-1628 others(5): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007693 | ||||||
| chr13:21007693
|
A | ATAGTGTA others(25): Show |
1 | a0001c0001t0001g0222 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.343-16290_343-1628 others(36): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007693 | ||||||
| chr13:21007693
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.343-16289T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007693 | ||||||
| chr13:21007693
|
ATATATAG others(9): Show |
A | 1 | a0010c0018t0010g0066 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.343-16305_343-1629 others(20): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007693 | ||||||
| chr13:21007695
|
A | G | 2 | a0002c0002t0010g0281a0002c0028t0041g0282 | 2 | HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.343-16291T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007695 | ||||||
| chr13:21007695
|
ATATAGTA others(3): Show |
A | 1 | a0003c0036t0009g0310 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.343-16301_343-1629 others(14): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007695 | ||||||
| chr13:21007695
|
ATATAGTA others(5): Show |
A | 3 | a0003c0003t0025g0287a0003c0009t0008g0309a0003c0009t0032g0289 | 3 | HG02055.hp2 HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.343-16303_343-1629 others(16): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007695 | ||||||
| chr13:21007697
|
ATAGTATG others(3): Show |
A | 25 | a0001c0001t0001g0024a0001c0010t0001g0056a0003c0003t0002g0010others(22): Show | 25 | HG00642.hp2 HG01167.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.343-16303_343-1629 others(14): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007697 | ||||||
| chr13:21007697
|
ATAGTATG others(5): Show |
A | 1 | a0003c0023t0002g0006 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.343-16305_343-1629 others(16): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007697 | ||||||
| chr13:21007697
|
ATAGTATG others(26): Show |
A | 1 | a0003c0005t0002g0054 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.343-16326_343-1629 others(37): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007697 | ||||||
| chr13:21007698
|
T | C | 2 | a0005c0016t0014g0035a0005c0016t0014g0036 | 2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.343-16294A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007698 | ||||||
| chr13:21007698
|
T | G | 2 | a0003c0032t0016g0315a0004c0019t0020g0305 | 2 | HG01243.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.343-16294A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007698 | ||||||
| chr13:21007699
|
A | AGT | 3 | a0001c0001t0001g0183a0001c0001t0001g0248a0001c0001t0002g0218 | 3 | HG01081.hp2 HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.343-16297_343-1629 others(6): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007699 | ||||||
| chr13:21007699
|
A | AGTGTATA others(24): Show |
1 | a0002c0006t0004g0258 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.343-16296_343-1629 others(35): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007699 | ||||||
| chr13:21007699
|
A | ATAGTGTA others(3): Show |
1 | a0001c0001t0001g0245 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.343-16296_343-1629 others(14): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007699 | ||||||
| chr13:21007699
|
A | ATATAGTG others(5): Show |
4 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0010g0112others(1): Show | 4 | HG00099.hp1 NA18998.hp1 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.343-16296_343-1629 others(16): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007699 | ||||||
| chr13:21007699
|
A | ATATAGTG others(5): Show |
2 | a0001c0001t0001g0280a0001c0001t0043g0139 | 2 | NA18983.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.343-16296_343-1629 others(16): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007699 | ||||||
| chr13:21007699
|
A | ATATATAG others(3): Show |
1 | a0003c0003t0001g0236 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.343-16296_343-1629 others(14): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007699 | ||||||
| chr13:21007699
|
A | ATATATAG others(5): Show |
2 | a0001c0001t0004g0276a0001c0001t0029g0193 | 2 | HG02083.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.343-16296_343-1629 others(16): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007699 | ||||||
| chr13:21007699
|
A | ATATATAG others(7): Show |
2 | a0001c0001t0006g0184a0001c0001t0012g0165 | 2 | NA18979.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.343-16296_343-1629 others(18): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007699 | ||||||
| chr13:21007699
|
A | ATATATAG others(7): Show |
2 | a0001c0001t0001g0274a0001c0001t0013g0167 | 2 | HG02004.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.343-16296_343-1629 others(18): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007699 | ||||||
| chr13:21007699
|
A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0197 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.343-16296_343-1629 others(16): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007699 | ||||||
| chr13:21007699
|
A | ATATATAT others(7): Show |
5 | a0001c0001t0001g0215a0001c0001t0006g0188a0001c0001t0006g0194others(2): Show | 5 | HG00423.hp1 HG02071.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.343-16296_343-1629 others(18): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007699 | ||||||
| chr13:21007699
|
A | ATATATAT others(9): Show |
2 | a0001c0001t0003g0161a0001c0001t0006g0168 | 2 | HG02074.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.343-16296_343-1629 others(20): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007699 | ||||||
| chr13:21007699
|
A | ATATATAT others(7): Show |
1 | a0004c0004t0005g0002 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.343-16296_343-1629 others(18): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007699 | ||||||
| chr13:21007699
|
A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0209 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.343-16296_343-1629 others(24): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007699 | ||||||
| chr13:21007699
|
A | ATATATAT others(9): Show |
1 | a0004c0004t0005g0257 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.343-16296_343-1629 others(20): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007699 | ||||||
| chr13:21007699
|
A | T | 2 | a0003c0032t0016g0315a0004c0019t0020g0305 | 2 | HG01243.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.343-16295T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007699 | ||||||
| chr13:21007699
|
AG | A | 6 | a0001c0001t0001g0222a0002c0002t0010g0281a0002c0028t0041g0282others(3): Show | 6 | HG02280.hp2 HG02622.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.343-16296delC | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007699 | ||||||
| chr13:21007699
|
AGTATG | A | 5 | a0001c0001t0001g0092a0001c0001t0001g0203a0001c0001t0001g0252others(2): Show | 5 | HG01071.hp1 HG02572.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.343-16300_343-1629 others(9): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007699 | ||||||
| chr13:21007700
|
G | A | 25 | a0001c0001t0001g0209a0001c0001t0001g0215a0001c0001t0001g0245others(22): Show | 25 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(22): Show |
intron_variant | MODIFIER | c.343-16296C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007700 | ||||||
| chr13:21007700
|
G | C | 1 | a0001c0010t0015g0003 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.343-16296C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007700 | ||||||
| chr13:21007700
|
G | GTGTA | 16 | a0001c0001t0001g0178a0001c0001t0001g0211a0001c0001t0001g0237others(13): Show | 16 | HG01106.hp1 HG01433.hp1 HG01515.hp2 others(13): Show |
intron_variant | MODIFIER | c.343-16297_343-1629 others(8): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007700 | ||||||
| chr13:21007700
|
G | GTGTATAT others(20): Show |
1 | a0001c0001t0001g0223 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.343-16297_343-1629 others(31): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007700 | ||||||
| chr13:21007700
|
G | GTGTATAT others(22): Show |
5 | a0001c0001t0002g0166a0001c0001t0002g0176a0001c0001t0002g0177others(2): Show | 5 | HG02683.hp1 NA18986.hp1 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.343-16297_343-1629 others(33): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007700 | ||||||
| chr13:21007700
|
G | GTGTATAT others(20): Show |
2 | a0003c0003t0002g0172a0003c0003t0002g0173 | 2 | HG01099.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.343-16297_343-1629 others(31): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007700 | ||||||
| chr13:21007700
|
G | GTGTATAT others(22): Show |
5 | a0001c0001t0001g0224a0001c0001t0002g0207a0003c0003t0002g0179others(2): Show | 5 | HG00597.hp1 NA18952.hp2 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.343-16297_343-1629 others(33): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007700 | ||||||
| chr13:21007700
|
G | GTGTATAT others(24): Show |
7 | a0001c0001t0001g0220a0001c0001t0001g0232a0001c0001t0001g0240others(4): Show | 7 | HG01943.hp1 NA18950.hp2 NA18992.hp2 others(4): Show |
intron_variant | MODIFIER | c.343-16297_343-1629 others(35): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007700 | ||||||
| chr13:21007700
|
G | GTGTATAT others(26): Show |
2 | a0001c0001t0001g0214a0001c0001t0001g0221 | 2 | NA18954.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.343-16297_343-1629 others(37): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007700 | ||||||
| chr13:21007700
|
G | GTGTATAT others(28): Show |
1 | a0001c0001t0001g0246 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.343-16297_343-1629 others(39): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007700 | ||||||
| chr13:21007700
|
G | GTGTATAT others(22): Show |
2 | a0001c0001t0001g0263a0003c0003t0002g0175 | 2 | HG00738.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.343-16297_343-1629 others(33): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007700 | ||||||
| chr13:21007700
|
G | GTGTATAT others(24): Show |
1 | a0004c0004t0005g0269 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.343-16297_343-1629 others(35): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007700 | ||||||
| chr13:21007700
|
G | GTGTATAT others(24): Show |
4 | a0001c0001t0001g0262a0001c0001t0017g0131a0001c0001t0047g0100others(1): Show | 4 | HG01928.hp2 NA18946.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.343-16297_343-1629 others(35): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007700 | ||||||
| chr13:21007700
|
G | GTGTATAT others(26): Show |
13 | a0001c0001t0001g0199a0001c0001t0001g0265a0001c0001t0001g0267others(10): Show | 13 | HG01070.hp1 HG01074.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.343-16297_343-1629 others(37): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007700 | ||||||
| chr13:21007700
|
G | GTGTATAT others(28): Show |
1 | a0001c0001t0001g0200 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.343-16297_343-1629 others(39): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007700 | ||||||
| chr13:21007700
|
G | GTGTATAT others(53): Show |
1 | a0001c0001t0001g0217 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.343-16297_343-1629 others(64): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007700 | ||||||
| chr13:21007700
|
G | GTGTATAT others(24): Show |
3 | a0001c0001t0001g0192a0004c0004t0005g0247a0004c0004t0005g0261 | 3 | HG01175.hp1 HG01361.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.343-16297_343-1629 others(35): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007700 | ||||||
| chr13:21007700
|
G | GTGTATAT others(26): Show |
1 | a0004c0004t0005g0089 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.343-16297_343-1629 others(37): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007700 | ||||||
| chr13:21007700
|
G | GTGTATAT others(26): Show |
7 | a0001c0001t0001g0196a0001c0001t0001g0208a0001c0001t0002g0227others(4): Show | 7 | HG00280.hp1 HG00438.hp1 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.343-16297_343-1629 others(37): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007700 | ||||||
| chr13:21007700
|
G | GTGTATAT others(28): Show |
5 | a0001c0001t0001g0191a0001c0001t0001g0233a0001c0001t0001g0279others(2): Show | 5 | HG00423.hp2 HG02056.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.343-16297_343-1629 others(39): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007700 | ||||||
| chr13:21007700
|
G | GTGTATAT others(30): Show |
2 | a0001c0001t0001g0090a0001c0030t0001g0091 | 2 | HG01099.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.343-16297_343-1629 others(41): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007700 | ||||||
| chr13:21007700
|
G | GTGTATAT others(28): Show |
1 | a0004c0015t0005g0083 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.343-16297_343-1629 others(39): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007700 | ||||||
| chr13:21007700
|
G | GTGTATAT others(30): Show |
1 | a0001c0001t0027g0226 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.343-16297_343-1629 others(41): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007700 | ||||||
| chr13:21007700
|
G | GTGTGTAT others(45): Show |
1 | a0001c0001t0001g0181 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.343-16297_343-1629 others(56): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007700 | ||||||
| chr13:21007700
|
G | T | 2 | a0004c0004t0001g0302a0004c0004t0001g0303 | 2 | HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.343-16296C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007700 | ||||||
| chr13:21007701
|
T | A | 2 | a0004c0004t0001g0302a0004c0004t0001g0303 | 2 | HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.343-16297A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007701 | ||||||
| chr13:21007701
|
T | TGTATATA others(8): Show |
2 | a0004c0004t0019g0292a0004c0004t0030g0295 | 2 | HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.343-16298_343-1629 others(19): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007701 | ||||||
| chr13:21007702
|
A | G | 7 | a0001c0010t0001g0061a0003c0007t0036g0051a0004c0004t0001g0302others(4): Show | 7 | HG02258.hp2 HG02280.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.343-16298T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007702 | ||||||
| chr13:21007704
|
G | A | 148 | a0001c0001t0001g0090a0001c0001t0001g0178a0001c0001t0001g0181others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.343-16300C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007704 | ||||||
| chr13:21007705
|
T | C | 2 | a0002c0002t0010g0281a0002c0028t0041g0282 | 2 | HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.343-16301A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007705 | ||||||
| chr13:21007706
|
A | G | 2 | a0003c0007t0036g0051a0003c0036t0009g0310 | 2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.343-16302T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007706 | ||||||
| chr13:21007708
|
A | C | 3 | a0003c0003t0004g0259a0003c0003t0025g0287a0003c0009t0032g0289 | 3 | HG02055.hp2 HG02258.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.343-16304T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007708 | ||||||
| chr13:21007708
|
A | G | 26 | a0001c0001t0001g0024a0001c0010t0001g0056a0003c0003t0002g0010others(23): Show | 26 | HG00642.hp2 HG01167.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.343-16304T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007708 | ||||||
| chr13:21007710
|
A | AG | 8 | a0003c0003t0002g0190a0003c0005t0002g0037a0003c0005t0002g0050others(5): Show | 8 | HG00741.hp2 HG02572.hp1 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.343-16307_343-1630 others(5): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007710 | ||||||
| chr13:21007710
|
A | C | 1 | a0003c0023t0002g0006 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.343-16306T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007710 | ||||||
| chr13:21007710
|
A | G | 1 | a0010c0018t0010g0066 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.343-16306T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007710 | ||||||
| chr13:21007712
|
A | G | 1 | a0001c0010t0015g0003 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.343-16308T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007712 | ||||||
| chr13:21007720
|
A | C | 1 | a0012c0022t0004g0007 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.343-16316T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007720 | ||||||
| chr13:21007720
|
A | G | 1 | a0003c0003t0002g0017 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.343-16316T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007720 | ||||||
| chr13:21007721
|
T | C | 2 | a0001c0001t0001g0221a0003c0008t0046g0288 | 2 | HG02630.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.343-16317A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007721 | ||||||
| chr13:21007721
|
TAGTATAT others(24): Show |
T | 10 | a0001c0010t0001g0064a0003c0003t0007g0312a0003c0003t0007g0313others(7): Show | 10 | HG00621.hp2 HG01257.hp2 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.343-16348_343-1631 others(35): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007721 | ||||||
| chr13:21007723
|
G | A | 1 | a0004c0004t0019g0026 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.343-16319C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007723 | ||||||
| chr13:21007723
|
G | GTA | 3 | a0002c0017t0006g0004a0003c0005t0015g0005a0010c0018t0010g0065 | 3 | HG02572.hp1 NA18951.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.343-16321_343-1632 others(6): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007723 | ||||||
| chr13:21007723
|
G | GTATATAT others(8): Show |
1 | a0010c0018t0010g0066 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.343-16334_343-1632 others(19): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007723 | ||||||
| chr13:21007723
|
G | GTGTATAT others(18): Show |
2 | a0005c0016t0014g0035a0005c0016t0014g0036 | 2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.343-16320_343-1631 others(29): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007723 | ||||||
| chr13:21007725
|
A | G | 1 | a0001c0001t0001g0191 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.343-16321T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007725 | ||||||
| chr13:21007727
|
ATATATAT others(2): Show |
A | 5 | a0003c0003t0002g0016a0003c0005t0002g0071a0003c0005t0002g0072others(2): Show | 5 | HG01109.hp1 HG02055.hp1 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.343-16332_343-1632 others(13): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007727 | ||||||
| chr13:21007729
|
ATATATAG | A | 19 | a0001c0001t0001g0024a0003c0003t0002g0008a0003c0003t0002g0014others(16): Show | 19 | HG00642.hp2 HG01175.hp2 HG01258.hp2 others(16): Show |
intron_variant | MODIFIER | c.343-16332_343-1632 others(11): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007729 | ||||||
| chr13:21007731
|
A | G | 1 | a0003c0005t0002g0054 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.343-16327T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007731 | ||||||
| chr13:21007731
|
ATATAG | A | 6 | a0001c0010t0001g0056a0003c0003t0002g0010a0003c0005t0001g0084others(3): Show | 6 | HG01167.hp2 HG01168.hp2 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.343-16332_343-1632 others(9): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007731 | ||||||
| chr13:21007734
|
T | G | 1 | a0003c0007t0036g0051 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.343-16330A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007734 | ||||||
| chr13:21007735
|
A | T | 1 | a0003c0007t0036g0051 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.343-16331T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007735 | ||||||
| chr13:21007735
|
AG | A | 4 | a0003c0005t0002g0054a0004c0019t0020g0305a0004c0019t0020g0306others(1): Show | 4 | HG01243.hp1 HG02572.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.343-16332delC | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007735 | ||||||
| chr13:21007736
|
G | A | 2 | a0003c0007t0036g0051a0004c0015t0018g0042 | 2 | HG02280.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.343-16332C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007736 | ||||||
| chr13:21007736
|
G | C | 9 | a0003c0003t0004g0259a0003c0003t0025g0287a0003c0008t0046g0288others(6): Show | 9 | HG02055.hp2 HG02258.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.343-16332C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007736 | ||||||
| chr13:21007736
|
G | T | 1 | a0004c0035t0009g0297 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.343-16332C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007736 | ||||||
| chr13:21007736
|
GTATA | G | 5 | a0002c0002t0003g0101a0002c0002t0003g0109a0002c0002t0003g0122others(2): Show | 5 | HG01255.hp2 HG02809.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.343-16336_343-1633 others(8): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007736 | ||||||
| chr13:21007737
|
T | A | 1 | a0004c0035t0009g0297 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.343-16333A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007737 | ||||||
| chr13:21007737
|
T | G | 1 | a0002c0034t0035g0027 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.343-16333A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007737 | ||||||
| chr13:21007738
|
A | ATATATAT others(6): Show |
1 | a0003c0005t0002g0050 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.343-16335_343-1633 others(17): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007738 | ||||||
| chr13:21007738
|
A | G | 124 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0178others(121): Show | 124 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.343-16334T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007738 | ||||||
| chr13:21007739
|
T | G | 1 | a0004c0004t0028g0025 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.343-16335A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007739 | ||||||
| chr13:21007740
|
A | ATATATAT others(4): Show |
3 | a0003c0003t0002g0190a0003c0005t0002g0037a0003c0005t0015g0069 | 3 | HG03831.hp1 NA18992.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.343-16337_343-1633 others(15): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007740 | ||||||
| chr13:21007740
|
A | G | 3 | a0001c0001t0001g0209a0001c0001t0017g0130a0004c0004t0021g0254 | 3 | HG01167.hp1 HG02738.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.343-16336T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007740 | ||||||
| chr13:21007742
|
A | G | 1 | a0002c0017t0011g0075 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.343-16338T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007742 | ||||||
| chr13:21007749
|
T | TA | 3 | a0003c0009t0008g0309a0003c0009t0009g0308a0003c0009t0016g0307 | 3 | HG02622.hp1 HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.343-16346dupT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007749 | ||||||
| chr13:21007750
|
A | T | 1 | a0003c0005t0002g0076 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.343-16346T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007750 | ||||||
| chr13:21007751
|
TA | T | 7 | a0001c0010t0001g0056a0002c0014t0018g0039a0003c0005t0002g0057others(4): Show | 7 | HG01168.hp2 HG01175.hp2 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.343-16348delT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007751 | ||||||
| chr13:21007752
|
A | T | 3 | a0003c0005t0002g0043a0003c0005t0002g0068a0003c0005t0002g0076 | 3 | HG01167.hp2 HG03942.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.343-16348T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007752 | ||||||
| chr13:21007753
|
TA | T | 4 | a0003c0003t0002g0010a0003c0003t0002g0255a0003c0005t0001g0084others(1): Show | 4 | HG01258.hp2 HG03453.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.343-16350delT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007753 | ||||||
| chr13:21007753
|
TATATA | T | 13 | a0002c0002t0003g0138a0002c0002t0003g0146a0002c0002t0003g0147others(10): Show | 13 | HG02148.hp2 HG02155.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.343-16354_343-1635 others(9): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007753 | ||||||
| chr13:21007754
|
A | T | 32 | a0001c0010t0001g0056a0001c0010t0001g0064a0002c0014t0018g0039others(29): Show | 32 | HG00621.hp2 HG01167.hp2 HG01168.hp2 others(29): Show |
intron_variant | MODIFIER | c.343-16350T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007754 | ||||||
| chr13:21007755
|
TA | T | 3 | a0003c0008t0009g0296a0004c0004t0019g0292a0004c0004t0030g0295 | 3 | HG01433.hp2 HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.343-16352delT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007755 | ||||||
| chr13:21007755
|
TATATA | T | 41 | a0002c0002t0003g0094a0002c0002t0003g0095a0002c0002t0003g0096others(38): Show | 41 | HG00438.hp2 HG00621.hp1 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.343-16356_343-1635 others(9): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007755 | ||||||
| chr13:21007756
|
A | ATTTTT | 3 | a0001c0010t0015g0003a0002c0017t0006g0004a0003c0005t0015g0005 | 3 | NA18951.hp2 NA18986.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.343-16353_343-1635 others(9): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007756 | ||||||
| chr13:21007756
|
A | T | 46 | a0001c0001t0001g0024a0001c0010t0001g0056a0001c0010t0001g0064others(43): Show | 46 | HG00621.hp2 HG00642.hp2 HG01167.hp2 others(43): Show |
intron_variant | MODIFIER | c.343-16352T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007756 | ||||||
| chr13:21007756
|
ATATAT | A | 7 | a0002c0002t0003g0098a0002c0002t0003g0124a0002c0002t0003g0150others(4): Show | 7 | HG02602.hp1 NA18612.hp2 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.343-16357_343-1635 others(9): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007756 | ||||||
| chr13:21007757
|
TATA | T | 3 | a0002c0002t0011g0034a0002c0002t0040g0143a0005c0012t0001g0033 | 3 | HG00735.hp1 HG02559.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.343-16356_343-1635 others(7): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007757 | ||||||
| chr13:21007758
|
A | AT | 18 | a0001c0001t0001g0090a0001c0030t0001g0091a0002c0006t0004g0258others(15): Show | 18 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.343-16355dupA | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007758 | ||||||
| chr13:21007758
|
A | T | 64 | a0001c0001t0001g0024a0001c0010t0001g0056a0001c0010t0001g0064others(61): Show | 65 | HG00621.hp2 HG00642.hp2 HG01070.hp2 others(62): Show |
intron_variant | MODIFIER | c.343-16354T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007758 | ||||||
| chr13:21007760
|
A | AT | 19 | a0001c0001t0001g0199a0001c0001t0001g0248a0001c0001t0001g0249others(16): Show | 19 | HG00099.hp1 HG00741.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.343-16357dupA | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007760 | ||||||
| chr13:21007760
|
A | T | 101 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0010t0001g0056others(98): Show | 102 | HG00099.hp2 HG00280.hp2 HG00621.hp2 others(99): Show |
intron_variant | MODIFIER | c.343-16356T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007760 | ||||||
| chr13:21007761
|
T | TA | 83 | a0001c0001t0001g0092a0001c0001t0001g0178a0001c0001t0001g0183others(80): Show | 83 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.343-16358_343-1635 others(5): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007761 | ||||||
| chr13:21007761
|
T | TAATATAT others(7): Show |
1 | a0003c0036t0009g0310 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.343-16358_343-1635 others(18): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007761 | ||||||
| chr13:21007761
|
T | TATA | 7 | a0001c0001t0001g0217a0001c0001t0001g0232a0001c0001t0001g0239others(4): Show | 7 | HG01081.hp1 NA18945.hp1 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.343-16358_343-1635 others(7): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007761 | ||||||
| chr13:21007761
|
T | TATATA | 3 | a0001c0001t0001g0181a0005c0016t0014g0035a0005c0016t0014g0036 | 3 | HG02015.hp1 HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.343-16358_343-1635 others(9): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007761 | ||||||
| chr13:21007762
|
T | A | 13 | a0002c0006t0004g0011a0002c0006t0004g0012a0002c0006t0004g0015others(10): Show | 13 | HG01070.hp1 HG01496.hp2 HG01943.hp2 others(10): Show |
intron_variant | MODIFIER | c.343-16358A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007762 | ||||||
| chr13:21007763
|
T | A | 15 | a0001c0001t0001g0092a0001c0001t0001g0209a0001c0001t0001g0221others(12): Show | 15 | HG01167.hp1 HG01884.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.343-16359A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007763 | ||||||
| chr13:21007764
|
T | A | 3 | a0003c0009t0026g0029a0003c0009t0031g0031a0003c0032t0016g0315 | 3 | HG02723.hp2 HG02897.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.343-16360A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007764 | ||||||
| chr13:21007765
|
T | A | 3 | a0003c0005t0002g0058a0005c0016t0014g0035a0005c0016t0014g0036 | 3 | HG03139.hp1 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.343-16361A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007765 | ||||||
| chr13:21007767
|
T | A | 2 | a0003c0005t0002g0058a0005c0016t0014g0036 | 2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.343-16363A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21007767 | ||||||
| chr13:21008027
|
G | C | 2 | a0002c0034t0035g0027a0004c0004t0028g0025 | 2 | HG02965.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.343-16623C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21008027 | ||||||
| chr13:21008051
|
A | G | 24 | a0002c0006t0004g0011a0002c0006t0004g0012a0002c0006t0004g0015others(21): Show | 24 | HG00597.hp2 HG00639.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.343-16647T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21008051 | ||||||
| chr13:21008190
|
GCTA | G | 24 | a0002c0006t0004g0011a0002c0006t0004g0012a0002c0006t0004g0015others(21): Show | 24 | HG00597.hp2 HG00639.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.343-16789_343-1678 others(7): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21008190 | ||||||
| chr13:21008305
|
T | C | 175 | a0001c0001t0001g0024a0001c0010t0001g0056a0001c0010t0001g0064others(172): Show | 176 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(173): Show |
intron_variant | MODIFIER | c.343-16901A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21008305 | ||||||
| chr13:21008478
|
T | C | 1 | a0009c0020t0009g0001 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.343-17074A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21008478 | ||||||
| chr13:21008580
|
A | T | 1 | a0001c0001t0001g0246 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.343-17176T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21008580 | ||||||
| chr13:21008757
|
C | A | 10 | a0002c0002t0011g0283a0002c0002t0011g0284a0002c0002t0011g0285others(7): Show | 10 | HG00735.hp2 HG02451.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.343-17353G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21008757 | ||||||
| chr13:21008781
|
C | T | 41 | a0001c0001t0001g0181a0001c0001t0001g0192a0001c0001t0001g0199others(38): Show | 41 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.343-17377G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21008781 | ||||||
| chr13:21009015
|
A | C | 2 | a0003c0005t0002g0058a0003c0007t0036g0051 | 2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.343-17611T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21009015 | ||||||
| chr13:21009034
|
G | C | 1 | a0001c0001t0001g0264 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.343-17630C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21009034 | ||||||
| chr13:21009094
|
C | T | 1 | a0002c0002t0010g0118 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.343-17690G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21009094 | ||||||
| chr13:21009146
|
C | T | 2 | a0002c0002t0010g0281a0002c0028t0041g0282 | 2 | HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.343-17742G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21009146 | ||||||
| chr13:21009193
|
A | G | 105 | a0002c0002t0003g0094a0002c0002t0003g0095a0002c0002t0003g0096others(102): Show | 105 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.343-17789T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21009193 | ||||||
| chr13:21009202
|
G | A | 310 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(307): Show | 311 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.343-17798C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21009202 | ||||||
| chr13:21009410
|
C | T | 1 | a0003c0003t0002g0010 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.343-18006G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21009410 | ||||||
| chr13:21009433
|
A | G | 103 | a0002c0002t0003g0094a0002c0002t0003g0095a0002c0002t0003g0096others(100): Show | 103 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.343-18029T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21009433 | ||||||
| chr13:21009641
|
T | C | 1 | a0001c0001t0001g0196 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.343-18237A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21009641 | ||||||
| chr13:21009705
|
G | A | 103 | a0002c0002t0003g0094a0002c0002t0003g0095a0002c0002t0003g0096others(100): Show | 103 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.343-18301C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21009705 | ||||||
| chr13:21009881
|
C | T | 1 | a0002c0028t0041g0282 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.343-18477G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21009881 | ||||||
| chr13:21010027
|
C | T | 6 | a0002c0014t0018g0039a0002c0014t0018g0041a0002c0014t0038g0040others(3): Show | 6 | HG01243.hp1 HG02451.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.343-18623G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21010027 | ||||||
| chr13:21010092
|
C | T | 1 | a0009c0020t0009g0001 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.343-18688G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21010092 | ||||||
| chr13:21010093
|
G | T | 1 | a0001c0001t0001g0203 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.343-18689C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21010093 | ||||||
| chr13:21010177
|
G | T | 1 | a0001c0001t0001g0178 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.343-18773C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21010177 | ||||||
| chr13:21010196
|
T | TCAAA | 3 | a0001c0010t0001g0056a0003c0005t0002g0059a0003c0005t0015g0069 | 3 | HG02071.hp2 HG02602.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.343-18796_343-1879 others(8): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21010196 | ||||||
| chr13:21010196
|
T | TCAAACAA others(1): Show |
50 | a0001c0001t0001g0024a0001c0010t0001g0064a0001c0010t0015g0003others(47): Show | 50 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.343-18793_343-1879 others(12): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21010196 | ||||||
| chr13:21010201
|
A | AAAAC | 14 | a0001c0001t0003g0161a0001c0001t0004g0276a0001c0001t0006g0168others(11): Show | 14 | HG00423.hp1 HG02055.hp2 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.343-18801_343-1879 others(8): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21010201 | ||||||
| chr13:21010201
|
A | AAAACAAA others(1): Show |
95 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0252others(92): Show | 95 | HG00099.hp1 HG00438.hp2 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.343-18805_343-1879 others(12): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21010201 | ||||||
| chr13:21010201
|
A | AAAACAAA others(5): Show |
103 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0178others(100): Show | 103 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.343-18809_343-1879 others(16): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21010201 | ||||||
| chr13:21010201
|
A | AAAACAAA others(9): Show |
13 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0223others(10): Show | 14 | HG00423.hp2 HG00597.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.343-18813_343-1879 others(20): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21010201 | ||||||
| chr13:21010201
|
A | AAACAAAC others(8): Show |
1 | a0001c0001t0002g0227 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.343-18798_343-1879 others(19): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21010201 | ||||||
| chr13:21010201
|
A | ACAAACAA others(2): Show |
17 | a0002c0006t0004g0011a0002c0006t0004g0012a0002c0006t0004g0015others(14): Show | 17 | HG00597.hp2 HG00639.hp1 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.343-18798_343-1879 others(13): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21010201 | ||||||
| chr13:21010201
|
A | ACAAACAA others(10): Show |
1 | a0003c0008t0009g0088 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.343-18798_343-1879 others(21): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21010201 | ||||||
| chr13:21010201
|
A | C | 56 | a0001c0001t0001g0024a0001c0010t0001g0056a0001c0010t0001g0064others(53): Show | 56 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.343-18797T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21010201 | ||||||
| chr13:21010548
|
T | C | 1 | a0001c0001t0002g0218 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.343-19144A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21010548 | ||||||
| chr13:21010727
|
G | T | 1 | a0001c0001t0002g0225 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.343-19323C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21010727 | ||||||
| chr13:21010824
|
T | C | 1 | a0003c0005t0004g0078 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.343-19420A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21010824 | ||||||
| chr13:21011181
|
C | T | 1 | a0003c0007t0016g0062 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.343-19777G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21011181 | ||||||
| chr13:21011182
|
T | G | 10 | a0003c0003t0004g0259a0003c0003t0025g0287a0003c0008t0046g0288others(7): Show | 10 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.343-19778A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21011182 | ||||||
| chr13:21011472
|
C | G | 1 | a0002c0017t0011g0075 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.343-20068G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21011472 | ||||||
| chr13:21011652
|
T | TAAGCAGC others(12): Show |
2 | a0001c0001t0001g0183a0001c0001t0001g0211 | 2 | HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.343-20249_343-2024 others(23): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21011652 | ||||||
| chr13:21011656
|
G | T | 2 | a0001c0001t0001g0183a0001c0001t0001g0211 | 2 | HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.343-20252C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21011656 | ||||||
| chr13:21011845
|
C | A | 300 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(297): Show | 301 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.343-20441G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21011845 | ||||||
| chr13:21011905
|
T | G | 73 | a0001c0001t0001g0024a0001c0010t0001g0056a0001c0010t0001g0064others(70): Show | 74 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.343-20501A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21011905 | ||||||
| chr13:21011927
|
T | A | 79 | a0002c0002t0003g0094a0002c0002t0003g0095a0002c0002t0003g0096others(76): Show | 79 | HG00438.hp2 HG00621.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.343-20523A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21011927 | ||||||
| chr13:21012207
|
A | T | 75 | a0001c0001t0001g0024a0001c0001t0037g0186a0001c0010t0001g0056others(72): Show | 76 | HG00280.hp1 HG00621.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.343-20803T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21012207 | ||||||
| chr13:21012234
|
C | A | 1 | a0009c0020t0009g0001 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.343-20830G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21012234 | ||||||
| chr13:21012275
|
G | A | 5 | a0002c0002t0011g0034a0005c0012t0001g0033a0005c0012t0002g0028others(2): Show | 5 | HG00735.hp1 HG02559.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.343-20871C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21012275 | ||||||
| chr13:21012359
|
G | A | 10 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(7): Show | 10 | HG00597.hp1 HG02056.hp2 NA18954.hp2 others(7): Show |
intron_variant | MODIFIER | c.343-20955C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21012359 | ||||||
| chr13:21012508
|
C | T | 310 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(307): Show | 311 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.343-21104G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21012508 | ||||||
| chr13:21012724
|
T | A | 2 | a0003c0008t0009g0088a0008c0033t0001g0304 | 2 | HG01243.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.343-21320A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21012724 | ||||||
| chr13:21012739
|
C | A | 2 | a0004c0004t0001g0302a0004c0004t0001g0303 | 2 | HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.343-21335G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21012739 | ||||||
| chr13:21012744
|
C | T | 6 | a0002c0014t0018g0039a0002c0014t0018g0041a0002c0014t0038g0040others(3): Show | 6 | HG01243.hp1 HG02451.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.343-21340G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21012744 | ||||||
| chr13:21012785
|
A | ACC | 15 | a0002c0002t0003g0104a0002c0006t0004g0011a0002c0006t0004g0012others(12): Show | 15 | HG00597.hp2 HG01358.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.343-21383_343-2138 others(6): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21012785 | ||||||
| chr13:21012785
|
AC | A | 80 | a0001c0001t0001g0024a0001c0001t0001g0181a0001c0001t0001g0220others(77): Show | 81 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.343-21382delG | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21012785 | ||||||
| chr13:21012788
|
C | A | 73 | a0001c0001t0001g0024a0001c0010t0001g0056a0001c0010t0001g0064others(70): Show | 74 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.343-21384G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21012788 | ||||||
| chr13:21012795
|
C | G | 1 | a0002c0002t0003g0109 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.343-21391G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21012795 | ||||||
| chr13:21012995
|
G | A | 1 | a0002c0002t0003g0102 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.343-21591C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21012995 | ||||||
| chr13:21013223
|
G | T | 5 | a0002c0002t0011g0034a0005c0012t0001g0033a0005c0012t0002g0028others(2): Show | 5 | HG00735.hp1 HG02559.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.343-21819C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21013223 | ||||||
| chr13:21013224
|
C | A | 5 | a0002c0002t0011g0034a0005c0012t0001g0033a0005c0012t0002g0028others(2): Show | 5 | HG00735.hp1 HG02559.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.343-21820G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21013224 | ||||||
| chr13:21013327
|
C | T | 1 | a0003c0003t0002g0190 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.343-21923G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21013327 | ||||||
| chr13:21013328
|
G | A | 74 | a0002c0002t0003g0094a0002c0002t0003g0095a0002c0002t0003g0096others(71): Show | 74 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.343-21924C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21013328 | ||||||
| chr13:21013466
|
G | C | 2 | a0002c0002t0003g0157a0002c0002t0003g0158 | 2 | HG02735.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.343-22062C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21013466 | ||||||
| chr13:21013474
|
C | T | 5 | a0002c0024t0023g0038a0002c0034t0035g0027a0003c0008t0009g0088others(2): Show | 5 | HG00639.hp1 HG01243.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.343-22070G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21013474 | ||||||
| chr13:21013742
|
G | A | 5 | a0002c0024t0023g0038a0002c0034t0035g0027a0003c0008t0009g0088others(2): Show | 5 | HG00639.hp1 HG01243.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.343-22338C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21013742 | ||||||
| chr13:21013788
|
A | G | 10 | a0003c0005t0002g0058a0003c0007t0008g0044a0003c0007t0008g0045others(7): Show | 10 | HG02145.hp1 HG02257.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.343-22384T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21013788 | ||||||
| chr13:21013791
|
C | T | 1 | a0003c0007t0036g0051 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.343-22387G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21013791 | ||||||
| chr13:21013853
|
C | T | 1 | a0003c0007t0016g0062 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.343-22449G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21013853 | ||||||
| chr13:21013941
|
A | G | 1 | a0009c0020t0009g0001 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.343-22537T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21013941 | ||||||
| chr13:21013956
|
G | A | 14 | a0001c0001t0006g0234a0002c0006t0004g0011a0002c0006t0004g0012others(11): Show | 14 | HG00423.hp1 HG00597.hp2 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.343-22552C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21013956 | ||||||
| chr13:21013963
|
C | G | 1 | a0003c0003t0002g0190 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.343-22559G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21013963 | ||||||
| chr13:21013977
|
CAAA | C | 13 | a0002c0006t0004g0011a0002c0006t0004g0012a0002c0006t0004g0015others(10): Show | 13 | HG00597.hp2 HG01358.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.343-22576_343-2257 others(7): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21013977 | ||||||
| chr13:21014110
|
A | G | 13 | a0002c0006t0004g0011a0002c0006t0004g0012a0002c0006t0004g0015others(10): Show | 13 | HG00597.hp2 HG01358.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.343-22706T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21014110 | ||||||
| chr13:21014191
|
G | A | 13 | a0002c0006t0004g0011a0002c0006t0004g0012a0002c0006t0004g0015others(10): Show | 13 | HG00597.hp2 HG01358.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.343-22787C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21014191 | ||||||
| chr13:21014243
|
C | A | 1 | a0003c0007t0036g0051 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.343-22839G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21014243 | ||||||
| chr13:21014243
|
C | G | 4 | a0001c0001t0001g0199a0004c0004t0005g0204a0004c0004t0005g0229others(1): Show | 4 | HG01884.hp2 HG02735.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.343-22839G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21014243 | ||||||
| chr13:21014597
|
C | T | 10 | a0003c0003t0004g0259a0003c0003t0025g0287a0003c0008t0046g0288others(7): Show | 10 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.343-23193G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21014597 | ||||||
| chr13:21014769
|
G | C | 2 | a0003c0007t0008g0046a0003c0007t0008g0070 | 2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.343-23365C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21014769 | ||||||
| chr13:21014981
|
G | A | 74 | a0002c0002t0003g0094a0002c0002t0003g0095a0002c0002t0003g0096others(71): Show | 74 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.343-23577C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21014981 | ||||||
| chr13:21015201
|
G | A | 4 | a0002c0002t0011g0283a0002c0002t0011g0284a0002c0002t0011g0285others(1): Show | 4 | HG00735.hp2 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.343-23797C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21015201 | ||||||
| chr13:21015586
|
G | C | 2 | a0002c0034t0035g0027a0004c0004t0028g0025 | 2 | HG02965.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.343-24182C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21015586 | ||||||
| chr13:21015819
|
C | T | 1 | a0002c0024t0023g0038 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.343-24415G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21015819 | ||||||
| chr13:21015866
|
A | G | 2 | a0003c0003t0004g0300a0003c0003t0004g0301 | 2 | HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.343-24462T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21015866 | ||||||
| chr13:21015950
|
C | T | 103 | a0002c0002t0003g0094a0002c0002t0003g0095a0002c0002t0003g0096others(100): Show | 103 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.343-24546G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21015950 | ||||||
| chr13:21016145
|
A | G | 1 | a0002c0002t0023g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.343-24741T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21016145 | ||||||
| chr13:21016470
|
G | A | 3 | a0002c0024t0023g0038a0002c0034t0035g0027a0004c0004t0028g0025 | 3 | HG00639.hp1 HG02965.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.343-25066C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21016470 | ||||||
| chr13:21016493
|
T | C | 1 | a0012c0022t0004g0007 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.343-25089A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21016493 | ||||||
| chr13:21016525
|
C | T | 5 | a0002c0002t0011g0034a0005c0012t0001g0033a0005c0012t0002g0028others(2): Show | 5 | HG00735.hp1 HG02559.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.343-25121G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21016525 | ||||||
| chr13:21016599
|
G | A | 6 | a0003c0008t0009g0294a0003c0008t0009g0296a0004c0004t0019g0026others(3): Show | 6 | HG01433.hp2 HG02258.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.343-25195C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21016599 | ||||||
| chr13:21016793
|
C | A | 1 | a0003c0003t0007g0105 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.343-25389G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21016793 | ||||||
| chr13:21016838
|
T | G | 2 | a0001c0001t0001g0183a0001c0001t0001g0211 | 2 | HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.343-25434A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21016838 | ||||||
| chr13:21016849
|
A | C | 79 | a0002c0002t0003g0094a0002c0002t0003g0095a0002c0002t0003g0096others(76): Show | 79 | HG00438.hp2 HG00621.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.343-25445T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21016849 | ||||||
| chr13:21017054
|
C | T | 3 | a0001c0001t0001g0239a0001c0001t0001g0242a0001c0001t0001g0246 | 3 | NA18945.hp1 NA18973.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.343-25650G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21017054 | ||||||
| chr13:21017167
|
A | G | 1 | a0001c0001t0001g0265 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.343-25763T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21017167 | ||||||
| chr13:21017314
|
G | C | 1 | a0004c0035t0009g0297 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.343-25910C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21017314 | ||||||
| chr13:21017457
|
G | A | 124 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0178others(121): Show | 124 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.343-26053C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21017457 | ||||||
| chr13:21017625
|
CT | C | 293 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(290): Show | 293 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.343-26222delA | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21017625 | ||||||
| chr13:21017652
|
A | C | 73 | a0001c0001t0001g0024a0001c0010t0001g0056a0001c0010t0001g0064others(70): Show | 74 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.343-26248T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21017652 | ||||||
| chr13:21017868
|
C | T | 1 | a0004c0004t0014g0299 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.343-26464G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21017868 | ||||||
| chr13:21018389
|
G | GC | 176 | a0001c0001t0001g0024a0001c0010t0001g0056a0001c0010t0001g0064others(173): Show | 177 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(174): Show |
intron_variant | MODIFIER | c.343-26986_343-2698 others(5): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21018389 | ||||||
| chr13:21018445
|
G | A | 1 | a0001c0001t0001g0272 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.343-27041C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21018445 | ||||||
| chr13:21018555
|
T | G | 302 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(299): Show | 303 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.342+27130A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21018555 | ||||||
| chr13:21018572
|
C | T | 1 | a0003c0007t0016g0062 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.342+27113G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21018572 | ||||||
| chr13:21018692
|
C | T | 6 | a0003c0008t0009g0294a0003c0008t0009g0296a0004c0004t0019g0026others(3): Show | 6 | HG01433.hp2 HG02258.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.342+26993G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21018692 | ||||||
| chr13:21018723
|
G | A | 1 | a0009c0020t0009g0001 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.342+26962C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21018723 | ||||||
| chr13:21018980
|
C | G | 176 | a0001c0001t0001g0024a0001c0010t0001g0056a0001c0010t0001g0064others(173): Show | 177 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(174): Show |
intron_variant | MODIFIER | c.342+26705G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21018980 | ||||||
| chr13:21019155
|
T | C | 6 | a0001c0001t0001g0233a0001c0001t0010g0162a0001c0001t0010g0163others(3): Show | 6 | HG00423.hp2 NA18952.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.342+26530A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019155 | ||||||
| chr13:21019292
|
G | A | 73 | a0001c0001t0001g0024a0001c0010t0001g0056a0001c0010t0001g0064others(70): Show | 74 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.342+26393C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019292 | ||||||
| chr13:21019298
|
G | GTTA | 3 | a0002c0006t0004g0015a0002c0006t0004g0169a0004c0004t0014g0299 | 3 | HG01943.hp2 HG02647.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.342+26384_342+2638 others(7): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019298 | ||||||
| chr13:21019298
|
GTTA | G | 122 | a0001c0001t0001g0090a0001c0001t0001g0178a0001c0001t0001g0183others(119): Show | 123 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(120): Show |
intron_variant | MODIFIER | c.342+26384_342+2638 others(7): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019298 | ||||||
| chr13:21019298
|
GTTATTA | G | 85 | a0001c0001t0001g0092a0001c0001t0001g0181a0001c0001t0001g0191others(82): Show | 85 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.342+26381_342+2638 others(10): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019298 | ||||||
| chr13:21019298
|
GTTATTAT others(2): Show |
G | 52 | a0001c0001t0001g0209a0001c0001t0001g0233a0001c0001t0001g0245others(49): Show | 52 | HG00423.hp2 HG00642.hp2 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.342+26378_342+2638 others(13): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019298 | ||||||
| chr13:21019298
|
GTTATTAT others(5): Show |
G | 10 | a0001c0001t0001g0024a0001c0001t0006g0195a0002c0006t0004g0022others(7): Show | 10 | HG01496.hp2 HG03490.hp2 HG03492.hp1 others(7): Show |
intron_variant | MODIFIER | c.342+26375_342+2638 others(16): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019298 | ||||||
| chr13:21019298
|
GTTATTAT others(8): Show |
G | 12 | a0001c0001t0001g0214a0003c0003t0004g0259a0003c0003t0025g0287others(9): Show | 12 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.342+26372_342+2638 others(19): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019298 | ||||||
| chr13:21019298
|
GTTATTAT others(14): Show |
G | 2 | a0010c0018t0010g0065a0010c0018t0010g0066 | 2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.342+26366_342+2638 others(25): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019298 | ||||||
| chr13:21019301
|
A | G | 2 | a0004c0004t0001g0302a0004c0004t0001g0303 | 2 | HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.342+26384T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019301 | ||||||
| chr13:21019313
|
A | C | 1 | a0004c0015t0018g0042 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.342+26372T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019313 | ||||||
| chr13:21019322
|
A | C | 82 | a0002c0002t0003g0094a0002c0002t0003g0095a0002c0002t0003g0096others(79): Show | 82 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.342+26363T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019322 | ||||||
| chr13:21019328
|
A | C | 5 | a0002c0024t0023g0038a0002c0034t0035g0027a0003c0008t0009g0088others(2): Show | 5 | HG00639.hp1 HG01243.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.342+26357T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019328 | ||||||
| chr13:21019328
|
A | G | 1 | a0009c0020t0009g0001 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.342+26357T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019328 | ||||||
| chr13:21019388
|
G | A | 6 | a0002c0014t0018g0039a0002c0014t0018g0041a0002c0014t0038g0040others(3): Show | 6 | HG01243.hp1 HG02451.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.342+26297C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019388 | ||||||
| chr13:21019493
|
A | ATTT | 99 | a0002c0002t0003g0094a0002c0002t0003g0095a0002c0002t0003g0096others(96): Show | 99 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.342+26189_342+2619 others(7): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019493 | ||||||
| chr13:21019493
|
A | ATTTT | 18 | a0002c0002t0003g0155a0002c0002t0010g0281a0002c0002t0012g0182others(15): Show | 18 | HG01243.hp2 HG02055.hp2 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.342+26188_342+2619 others(8): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019493 | ||||||
| chr13:21019493
|
A | ATTTTT | 12 | a0003c0005t0002g0058a0003c0007t0008g0044a0003c0007t0008g0045others(9): Show | 12 | HG01109.hp1 HG01884.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.342+26187_342+2619 others(9): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019493 | ||||||
| chr13:21019493
|
A | ATTTTTT | 39 | a0001c0001t0001g0024a0001c0010t0001g0056a0001c0010t0015g0003others(36): Show | 39 | HG00621.hp2 HG00741.hp2 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.342+26186_342+2619 others(10): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019493 | ||||||
| chr13:21019493
|
A | ATTTTTTT | 7 | a0001c0010t0001g0064a0003c0003t0002g0018a0003c0005t0002g0059others(4): Show | 7 | HG00642.hp2 HG01175.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.342+26185_342+2619 others(11): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019493 | ||||||
| chr13:21019531
|
C | G | 1 | a0001c0001t0001g0232 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.342+26154G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019531 | ||||||
| chr13:21019632
|
C | T | 1 | a0002c0002t0003g0103 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.342+26053G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019632 | ||||||
| chr13:21019668
|
CA | C | 191 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0178others(188): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.342+26016delT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019668 | ||||||
| chr13:21019668
|
CAA | C | 74 | a0001c0001t0001g0024a0001c0001t0001g0192a0001c0001t0001g0246others(71): Show | 74 | HG00597.hp2 HG00621.hp2 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.342+26015_342+2601 others(6): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019668 | ||||||
| chr13:21019744
|
C | T | 1 | a0002c0002t0003g0102 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.342+25941G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019744 | ||||||
| chr13:21019840
|
G | C | 68 | a0001c0001t0001g0024a0001c0010t0001g0056a0001c0010t0001g0064others(65): Show | 68 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(65): Show |
intron_variant | MODIFIER | c.342+25845C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019840 | ||||||
| chr13:21019887
|
T | C | 2 | a0003c0008t0009g0088a0008c0033t0001g0304 | 2 | HG01243.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.342+25798A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019887 | ||||||
| chr13:21019912
|
C | T | 176 | a0001c0001t0001g0024a0001c0010t0001g0056a0001c0010t0001g0064others(173): Show | 177 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(174): Show |
intron_variant | MODIFIER | c.342+25773G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019912 | ||||||
| chr13:21019973
|
T | TA | 11 | a0002c0002t0003g0106a0002c0002t0003g0155a0002c0024t0023g0038others(8): Show | 11 | HG00639.hp1 HG01175.hp2 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.342+25711dupT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019973 | ||||||
| chr13:21019973
|
T | TAA | 11 | a0002c0006t0004g0011a0002c0006t0004g0012a0002c0006t0004g0015others(8): Show | 11 | HG00597.hp2 HG01496.hp2 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.342+25710_342+2571 others(6): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21019973 | ||||||
| chr13:21020085
|
G | T | 1 | a0002c0002t0003g0142 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.342+25600C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21020085 | ||||||
| chr13:21020146
|
T | TAAAATAT others(1): Show |
100 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0178others(97): Show | 100 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.342+25531_342+2553 others(12): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21020146 | ||||||
| chr13:21020151
|
T | C | 2 | a0003c0008t0009g0088a0008c0033t0001g0304 | 2 | HG01243.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.342+25534A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21020151 | ||||||
| chr13:21020321
|
T | C | 2 | a0003c0003t0004g0300a0003c0003t0004g0301 | 2 | HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.342+25364A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21020321 | ||||||
| chr13:21020524
|
GA | G | 176 | a0001c0001t0001g0024a0001c0010t0001g0056a0001c0010t0001g0064others(173): Show | 177 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(174): Show |
intron_variant | MODIFIER | c.342+25160delT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21020524 | ||||||
| chr13:21020560
|
C | T | 124 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0178others(121): Show | 124 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.342+25125G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21020560 | ||||||
| chr13:21020796
|
C | T | 124 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0178others(121): Show | 124 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.342+24889G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21020796 | ||||||
| chr13:21020894
|
C | T | 1 | a0001c0001t0002g0166 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.342+24791G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21020894 | ||||||
| chr13:21021070
|
T | C | 1 | a0004c0004t0001g0302 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.342+24615A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21021070 | ||||||
| chr13:21021259
|
G | A | 74 | a0002c0002t0003g0094a0002c0002t0003g0095a0002c0002t0003g0096others(71): Show | 74 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.342+24426C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21021259 | ||||||
| chr13:21021319
|
G | A | 58 | a0001c0001t0001g0024a0001c0010t0001g0056a0001c0010t0001g0064others(55): Show | 58 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(55): Show |
intron_variant | MODIFIER | c.342+24366C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21021319 | ||||||
| chr13:21021332
|
G | A | 3 | a0001c0001t0001g0233a0001c0001t0010g0162a0001c0001t0010g0163 | 3 | HG00423.hp2 NA18971.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.342+24353C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21021332 | ||||||
| chr13:21021450
|
G | A | 4 | a0002c0002t0003g0126a0002c0002t0003g0128a0002c0002t0003g0129others(1): Show | 4 | NA18959.hp2 NA19004.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.342+24235C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21021450 | ||||||
| chr13:21021474
|
C | CA | 89 | a0001c0001t0001g0092a0001c0001t0001g0178a0001c0001t0001g0181others(86): Show | 89 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.342+24210dupT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21021474 | ||||||
| chr13:21021474
|
C | CAA | 58 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0183others(55): Show | 58 | HG00423.hp1 HG00639.hp2 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.342+24209_342+2421 others(6): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21021474 | ||||||
| chr13:21021474
|
C | CAAA | 12 | a0001c0001t0001g0222a0003c0003t0002g0172a0003c0003t0004g0300others(9): Show | 12 | HG02055.hp2 HG02145.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.342+24208_342+2421 others(7): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21021474 | ||||||
| chr13:21021474
|
C | CAAAAAAA others(3): Show |
1 | a0003c0008t0009g0296 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.342+24201_342+2421 others(14): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21021474 | ||||||
| chr13:21021474
|
CAAAAAAA others(3): Show |
C | 2 | a0002c0002t0010g0281a0002c0028t0041g0282 | 2 | HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.342+24201_342+2421 others(14): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21021474 | ||||||
| chr13:21021474
|
CAAAAAAA others(4): Show |
C | 2 | a0002c0002t0003g0122a0002c0002t0003g0133 | 2 | NA19002.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.342+24200_342+2421 others(15): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21021474 | ||||||
| chr13:21021474
|
CAAAAAAA others(5): Show |
C | 101 | a0002c0002t0003g0094a0002c0002t0003g0095a0002c0002t0003g0096others(98): Show | 101 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(98): Show |
intron_variant | MODIFIER | c.342+24199_342+2421 others(16): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21021474 | ||||||
| chr13:21021476
|
A | C | 1 | a0001c0001t0001g0277 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.342+24209T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21021476 | ||||||
| chr13:21021534
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.342+24151C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21021534 | ||||||
| chr13:21021680
|
C | T | 1 | a0002c0002t0003g0095 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.342+24005G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21021680 | ||||||
| chr13:21021739
|
C | A | 74 | a0002c0002t0003g0094a0002c0002t0003g0095a0002c0002t0003g0096others(71): Show | 74 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.342+23946G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21021739 | ||||||
| chr13:21021952
|
T | A | 1 | a0001c0001t0001g0277 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.342+23733A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21021952 | ||||||
| chr13:21021953
|
A | T | 1 | a0001c0001t0001g0277 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.342+23732T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21021953 | ||||||
| chr13:21022044
|
G | A | 147 | a0001c0001t0001g0024a0001c0010t0001g0056a0001c0010t0001g0064others(144): Show | 148 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(145): Show |
intron_variant | MODIFIER | c.342+23641C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21022044 | ||||||
| chr13:21022067
|
C | T | 1 | a0002c0024t0023g0038 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.342+23618G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21022067 | ||||||
| chr13:21022111
|
C | A | 1 | a0002c0002t0003g0122 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.342+23574G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21022111 | ||||||
| chr13:21022236
|
CTA | C | 18 | a0002c0006t0004g0011a0002c0006t0004g0012a0002c0006t0004g0015others(15): Show | 18 | HG00597.hp2 HG00639.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.342+23447_342+2344 others(6): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21022236 | ||||||
| chr13:21022263
|
C | T | 1 | a0012c0022t0004g0007 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.342+23422G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21022263 | ||||||
| chr13:21022345
|
G | C | 1 | a0009c0020t0009g0001 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.342+23340C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21022345 | ||||||
| chr13:21022381
|
C | T | 176 | a0001c0001t0001g0024a0001c0010t0001g0056a0001c0010t0001g0064others(173): Show | 177 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(174): Show |
intron_variant | MODIFIER | c.342+23304G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21022381 | ||||||
| chr13:21022422
|
G | T | 4 | a0004c0004t0005g0266a0004c0004t0005g0269a0004c0004t0005g0270others(1): Show | 4 | HG01106.hp1 HG01433.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.342+23263C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21022422 | ||||||
| chr13:21022424
|
C | T | 1 | a0003c0009t0032g0289 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.342+23261G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21022424 | ||||||
| chr13:21022440
|
CCCTGACA others(41): Show |
C | 1 | a0001c0001t0001g0277 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.342+23197_342+2324 others(52): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21022440 | ||||||
| chr13:21022449
|
C | T | 3 | a0004c0015t0018g0042a0004c0019t0020g0305a0004c0019t0020g0306 | 3 | HG01243.hp1 HG03041.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.342+23236G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21022449 | ||||||
| chr13:21022814
|
TA | T | 18 | a0002c0006t0004g0011a0002c0006t0004g0012a0002c0006t0004g0015others(15): Show | 18 | HG00597.hp2 HG00639.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.342+22870delT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21022814 | ||||||
| chr13:21022913
|
T | C | 10 | a0003c0003t0004g0259a0003c0003t0025g0287a0003c0008t0046g0288others(7): Show | 10 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.342+22772A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21022913 | ||||||
| chr13:21023146
|
AGGGCTCC | A | 73 | a0001c0001t0001g0024a0001c0010t0001g0056a0001c0010t0001g0064others(70): Show | 74 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.342+22532_342+2253 others(11): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023146 | ||||||
| chr13:21023157
|
C | T | 73 | a0001c0001t0001g0024a0001c0010t0001g0056a0001c0010t0001g0064others(70): Show | 74 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.342+22528G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023157 | ||||||
| chr13:21023275
|
C | A | 1 | a0012c0022t0004g0007 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.342+22410G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023275 | ||||||
| chr13:21023323
|
C | G | 1 | a0003c0032t0016g0315 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.342+22362G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023323 | ||||||
| chr13:21023495
|
C | CCTCTGTT others(20): Show |
1 | a0002c0002t0023g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.342+22163_342+2218 others(31): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023495 | ||||||
| chr13:21023501
|
T | C | 1 | a0006c0011t0001g0080 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.342+22184A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023501 | ||||||
| chr13:21023649
|
A | C | 1 | a0003c0007t0036g0051 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.342+22036T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023649 | ||||||
| chr13:21023658
|
A | C | 1 | a0001c0001t0013g0189 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.342+22027T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023658 | ||||||
| chr13:21023665
|
AAAAAAAA others(12): Show |
A | 1 | a0003c0032t0016g0315 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.342+22001_342+2201 others(23): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023665 | ||||||
| chr13:21023666
|
AAAAAAAA others(11): Show |
A | 5 | a0001c0001t0001g0197a0001c0001t0001g0209a0001c0001t0001g0265others(2): Show | 5 | HG01070.hp1 HG01167.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.342+22001_342+2201 others(22): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023666 | ||||||
| chr13:21023667
|
AAAAAAAA others(10): Show |
A | 109 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0178others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.342+22001_342+2201 others(21): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023667 | ||||||
| chr13:21023668
|
AAAAAAAA others(9): Show |
A | 10 | a0001c0001t0001g0224a0001c0001t0001g0241a0001c0001t0002g0176others(7): Show | 10 | HG00597.hp1 HG02074.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.342+22001_342+2201 others(20): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023668 | ||||||
| chr13:21023670
|
AAAAAAAA others(7): Show |
A | 5 | a0002c0014t0018g0039a0002c0014t0018g0041a0002c0014t0038g0040others(2): Show | 5 | HG02451.hp2 HG02886.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.342+22001_342+2201 others(18): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023670 | ||||||
| chr13:21023671
|
AAAAAAAA others(6): Show |
A | 2 | a0004c0019t0020g0305a0005c0012t0002g0028 | 2 | HG01243.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.342+22001_342+2201 others(17): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023671 | ||||||
| chr13:21023672
|
AAAAAAAA others(5): Show |
A | 4 | a0002c0002t0011g0034a0005c0012t0001g0033a0005c0012t0002g0030others(1): Show | 4 | HG00735.hp1 HG02559.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.342+22001_342+2201 others(16): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023672 | ||||||
| chr13:21023673
|
AAAAAAAA others(4): Show |
A | 1 | a0004c0004t0028g0025 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.342+22001_342+2201 others(15): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023673 | ||||||
| chr13:21023674
|
AAAAAAAA others(3): Show |
A | 12 | a0002c0002t0012g0198a0002c0017t0011g0075a0002c0034t0035g0027others(9): Show | 12 | HG01243.hp2 HG02155.hp1 HG02155.hp2 others(9): Show |
intron_variant | MODIFIER | c.342+22001_342+2201 others(14): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023674 | ||||||
| chr13:21023675
|
AAAAAAAA others(2): Show |
A | 42 | a0002c0002t0003g0094a0002c0002t0003g0095a0002c0002t0003g0096others(39): Show | 42 | HG00639.hp1 HG00735.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.342+22001_342+2200 others(13): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023675 | ||||||
| chr13:21023676
|
AAAAAAAA others(1): Show |
A | 44 | a0002c0002t0003g0098a0002c0002t0003g0108a0002c0002t0003g0109others(41): Show | 45 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.342+22001_342+2200 others(12): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023676 | ||||||
| chr13:21023677
|
AAAAAAAC | A | 29 | a0001c0010t0001g0056a0002c0006t0004g0021a0002c0006t0004g0213others(26): Show | 29 | HG01167.hp2 HG01168.hp2 HG01257.hp2 others(26): Show |
intron_variant | MODIFIER | c.342+22001_342+2200 others(11): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023677 | ||||||
| chr13:21023678
|
AAAAAAC | A | 21 | a0001c0001t0001g0024a0001c0010t0001g0064a0001c0010t0015g0003others(18): Show | 21 | HG00642.hp2 HG00741.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.342+22001_342+2200 others(10): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023678 | ||||||
| chr13:21023679
|
AAAAAC | A | 11 | a0002c0017t0006g0004a0003c0003t0025g0287a0003c0005t0002g0057others(8): Show | 11 | HG00621.hp2 HG01884.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.342+22001_342+2200 others(9): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023679 | ||||||
| chr13:21023684
|
C | A | 2 | a0005c0016t0014g0035a0005c0016t0014g0036 | 2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.342+22001G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023684 | ||||||
| chr13:21023723
|
C | T | 1 | a0012c0022t0004g0007 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.342+21962G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023723 | ||||||
| chr13:21023745
|
G | T | 79 | a0002c0002t0003g0094a0002c0002t0003g0095a0002c0002t0003g0096others(76): Show | 79 | HG00438.hp2 HG00621.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.342+21940C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023745 | ||||||
| chr13:21023761
|
G | T | 1 | a0003c0032t0016g0315 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.342+21924C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023761 | ||||||
| chr13:21023763
|
C | T | 4 | a0002c0002t0010g0281a0002c0028t0041g0282a0005c0016t0014g0035others(1): Show | 4 | HG02965.hp2 HG03139.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.342+21922G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023763 | ||||||
| chr13:21023768
|
A | G | 176 | a0001c0001t0001g0024a0001c0010t0001g0056a0001c0010t0001g0064others(173): Show | 177 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(174): Show |
intron_variant | MODIFIER | c.342+21917T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023768 | ||||||
| chr13:21023836
|
G | A | 6 | a0002c0014t0018g0039a0002c0014t0018g0041a0002c0014t0038g0040others(3): Show | 6 | HG01243.hp1 HG02451.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.342+21849C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023836 | ||||||
| chr13:21023842
|
G | T | 1 | a0002c0002t0003g0095 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.342+21843C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023842 | ||||||
| chr13:21023881
|
G | C | 1 | a0002c0002t0003g0102 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.342+21804C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023881 | ||||||
| chr13:21023917
|
GA | G | 3 | a0001c0001t0001g0233a0001c0001t0010g0162a0001c0001t0010g0163 | 3 | HG00423.hp2 NA18971.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.342+21767delT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023917 | ||||||
| chr13:21023934
|
T | C | 58 | a0001c0001t0001g0024a0001c0010t0001g0056a0001c0010t0001g0064others(55): Show | 58 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(55): Show |
intron_variant | MODIFIER | c.342+21751A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023934 | ||||||
| chr13:21023968
|
C | A | 18 | a0002c0006t0004g0011a0002c0006t0004g0012a0002c0006t0004g0015others(15): Show | 18 | HG00597.hp2 HG00639.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.342+21717G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21023968 | ||||||
| chr13:21024089
|
T | C | 2 | a0003c0003t0004g0300a0003c0003t0004g0301 | 2 | HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.342+21596A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21024089 | ||||||
| chr13:21024093
|
C | CA | 9 | a0001c0001t0001g0090a0001c0001t0001g0211a0001c0001t0002g0228others(6): Show | 9 | HG00741.hp1 HG01109.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.342+21591dupT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21024093 | ||||||
| chr13:21024093
|
CA | C | 94 | a0001c0010t0001g0064a0002c0002t0003g0094a0002c0002t0003g0095others(91): Show | 94 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.342+21591delT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21024093 | ||||||
| chr13:21024093
|
CAA | C | 70 | a0001c0001t0001g0024a0001c0010t0001g0056a0001c0010t0015g0003others(67): Show | 71 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(68): Show |
intron_variant | MODIFIER | c.342+21590_342+2159 others(6): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21024093 | ||||||
| chr13:21024093
|
CAAAA | C | 6 | a0002c0014t0018g0039a0002c0014t0018g0041a0002c0014t0038g0040others(3): Show | 6 | HG01243.hp1 HG02451.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.342+21588_342+2159 others(8): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21024093 | ||||||
| chr13:21024110
|
A | G | 76 | a0002c0002t0003g0094a0002c0002t0003g0095a0002c0002t0003g0096others(73): Show | 76 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(73): Show |
intron_variant | MODIFIER | c.342+21575T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21024110 | ||||||
| chr13:21024111
|
A | G | 1 | a0003c0003t0002g0016 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.342+21574T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21024111 | ||||||
| chr13:21024119
|
A | G | 5 | a0002c0002t0011g0034a0005c0012t0001g0033a0005c0012t0002g0028others(2): Show | 5 | HG00735.hp1 HG02559.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.342+21566T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21024119 | ||||||
| chr13:21024330
|
G | C | 1 | a0002c0006t0004g0019 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.342+21355C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21024330 | ||||||
| chr13:21024389
|
T | G | 1 | a0001c0001t0010g0099 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.342+21296A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21024389 | ||||||
| chr13:21024553
|
C | T | 1 | a0003c0003t0002g0255 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.342+21132G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21024553 | ||||||
| chr13:21024579
|
CCTCACGG others(7): Show |
C | 3 | a0002c0014t0018g0039a0002c0014t0018g0041a0002c0014t0038g0040 | 3 | HG02451.hp2 HG02886.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.342+21092_342+2110 others(18): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21024579 | ||||||
| chr13:21024583
|
A | T | 1 | a0002c0006t0004g0258 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.342+21102T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21024583 | ||||||
| chr13:21024585
|
G | A | 1 | a0003c0007t0036g0051 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.342+21100C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21024585 | ||||||
| chr13:21024604
|
C | T | 4 | a0002c0002t0010g0281a0002c0028t0041g0282a0005c0016t0014g0035others(1): Show | 4 | HG02965.hp2 HG03139.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.342+21081G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21024604 | ||||||
| chr13:21024682
|
C | T | 2 | a0004c0004t0001g0302a0004c0004t0001g0303 | 2 | HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.342+21003G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21024682 | ||||||
| chr13:21024689
|
TA | T | 248 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0178others(245): Show | 248 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.342+20995delT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21024689 | ||||||
| chr13:21024689
|
TAA | T | 8 | a0001c0001t0004g0276a0001c0001t0017g0130a0002c0028t0041g0282others(5): Show | 8 | HG01243.hp2 HG01516.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.342+20994_342+2099 others(6): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21024689 | ||||||
| chr13:21024740
|
T | A | 1 | a0003c0007t0036g0051 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.342+20945A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21024740 | ||||||
| chr13:21024807
|
T | C | 2 | a0005c0016t0014g0035a0005c0016t0014g0036 | 2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.342+20878A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21024807 | ||||||
| chr13:21025217
|
TA | T | 235 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0178others(232): Show | 236 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.342+20467delT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21025217 | ||||||
| chr13:21025235
|
T | A | 1 | a0012c0022t0004g0007 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.342+20450A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21025235 | ||||||
| chr13:21025249
|
G | A | 3 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0010g0112 | 3 | NA18998.hp1 NA19005.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.342+20436C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21025249 | ||||||
| chr13:21025338
|
G | A | 1 | a0007c0013t0007g0137 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.342+20347C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21025338 | ||||||
| chr13:21025393
|
C | CA | 22 | a0001c0001t0001g0090a0001c0001t0001g0203a0001c0001t0001g0233others(19): Show | 22 | HG00423.hp2 HG00741.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.342+20291dupT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21025393 | ||||||
| chr13:21025406
|
A | C | 73 | a0002c0002t0003g0094a0002c0002t0003g0095a0002c0002t0003g0096others(70): Show | 73 | HG00438.hp2 HG00621.hp1 HG00735.hp2 others(70): Show |
intron_variant | MODIFIER | c.342+20279T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21025406 | ||||||
| chr13:21025413
|
A | AAC | 24 | a0001c0010t0001g0064a0001c0010t0015g0003a0002c0017t0006g0004others(21): Show | 24 | HG00642.hp2 HG01167.hp2 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.342+20271_342+2027 others(6): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21025413 | ||||||
| chr13:21025413
|
A | AC | 55 | a0001c0001t0001g0024a0002c0002t0010g0281a0002c0006t0004g0020others(52): Show | 56 | HG00621.hp2 HG00741.hp2 HG01070.hp2 others(53): Show |
intron_variant | MODIFIER | c.342+20271_342+2027 others(5): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21025413 | ||||||
| chr13:21025413
|
A | C | 95 | a0001c0010t0001g0056a0002c0002t0003g0094a0002c0002t0003g0095others(92): Show | 95 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.342+20272T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21025413 | ||||||
| chr13:21025685
|
G | A | 68 | a0001c0001t0001g0024a0001c0010t0001g0056a0001c0010t0001g0064others(65): Show | 68 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(65): Show |
intron_variant | MODIFIER | c.342+20000C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21025685 | ||||||
| chr13:21025763
|
C | T | 73 | a0001c0001t0001g0024a0001c0010t0001g0056a0001c0010t0001g0064others(70): Show | 74 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.342+19922G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21025763 | ||||||
| chr13:21026167
|
G | A | 2 | a0002c0002t0011g0034a0005c0012t0001g0033 | 2 | HG00735.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.342+19518C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21026167 | ||||||
| chr13:21026188
|
A | G | 1 | a0003c0008t0009g0088 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.342+19497T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21026188 | ||||||
| chr13:21026326
|
TA | T | 246 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0178others(243): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.342+19358delT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21026326 | ||||||
| chr13:21026338
|
A | C | 1 | a0004c0015t0005g0083 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.342+19347T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21026338 | ||||||
| chr13:21026654
|
T | A | 1 | a0009c0020t0009g0001 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.342+19031A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21026654 | ||||||
| chr13:21026731
|
G | A | 1 | a0002c0027t0039g0114 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.342+18954C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21026731 | ||||||
| chr13:21026734
|
T | C | 1 | a0006c0011t0001g0081 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.342+18951A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21026734 | ||||||
| chr13:21026773
|
T | C | 1 | a0012c0022t0004g0007 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.342+18912A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21026773 | ||||||
| chr13:21026965
|
CTGA | C | 6 | a0002c0014t0018g0039a0002c0014t0018g0041a0002c0014t0038g0040others(3): Show | 6 | HG01243.hp1 HG02451.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.342+18717_342+1871 others(7): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21026965 | ||||||
| chr13:21026967
|
G | A | 5 | a0002c0024t0023g0038a0002c0034t0035g0027a0003c0008t0009g0088others(2): Show | 5 | HG00639.hp1 HG01243.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.342+18718C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21026967 | ||||||
| chr13:21027075
|
T | C | 103 | a0002c0002t0003g0094a0002c0002t0003g0095a0002c0002t0003g0096others(100): Show | 103 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.342+18610A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21027075 | ||||||
| chr13:21027544
|
G | A | 2 | a0003c0003t0002g0170a0003c0003t0002g0231 | 2 | HG01070.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.342+18141C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21027544 | ||||||
| chr13:21027570
|
T | C | 10 | a0003c0003t0004g0259a0003c0003t0025g0287a0003c0008t0046g0288others(7): Show | 10 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.342+18115A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21027570 | ||||||
| chr13:21027642
|
A | G | 1 | a0002c0002t0003g0108 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.342+18043T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21027642 | ||||||
| chr13:21027649
|
G | A | 257 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0178others(254): Show | 258 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.342+18036C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21027649 | ||||||
| chr13:21027748
|
C | T | 1 | a0003c0003t0001g0236 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.342+17937G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21027748 | ||||||
| chr13:21028036
|
C | T | 1 | a0003c0009t0031g0031 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.342+17649G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21028036 | ||||||
| chr13:21028176
|
G | A | 2 | a0002c0002t0003g0124a0002c0024t0023g0038 | 2 | HG00639.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.342+17509C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21028176 | ||||||
| chr13:21028199
|
G | A | 2 | a0001c0001t0006g0234a0001c0031t0006g0187 | 2 | HG00423.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.342+17486C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21028199 | ||||||
| chr13:21028391
|
T | C | 4 | a0003c0003t0004g0300a0003c0003t0004g0301a0004c0004t0004g0298others(1): Show | 4 | HG02647.hp2 HG03486.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.342+17294A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21028391 | ||||||
| chr13:21028493
|
A | C | 5 | a0002c0002t0011g0034a0005c0012t0001g0033a0005c0012t0002g0028others(2): Show | 5 | HG00735.hp1 HG02559.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.342+17192T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21028493 | ||||||
| chr13:21028512
|
ATATTTTG others(17): Show |
A | 1 | a0002c0002t0003g0122 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.342+17149_342+1717 others(28): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21028512 | ||||||
| chr13:21028615
|
G | C | 79 | a0002c0002t0003g0094a0002c0002t0003g0095a0002c0002t0003g0096others(76): Show | 79 | HG00438.hp2 HG00621.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.342+17070C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21028615 | ||||||
| chr13:21028663
|
C | T | 1 | a0003c0032t0016g0315 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.342+17022G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21028663 | ||||||
| chr13:21028682
|
T | C | 6 | a0002c0014t0018g0039a0002c0014t0018g0041a0002c0014t0038g0040others(3): Show | 6 | HG01243.hp1 HG02451.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.342+17003A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21028682 | ||||||
| chr13:21028684
|
C | T | 13 | a0002c0006t0004g0011a0002c0006t0004g0012a0002c0006t0004g0015others(10): Show | 13 | HG00597.hp2 HG01358.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.342+17001G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21028684 | ||||||
| chr13:21028858
|
G | A | 1 | a0002c0002t0003g0145 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.342+16827C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21028858 | ||||||
| chr13:21028897
|
G | A | 6 | a0002c0014t0018g0039a0002c0014t0018g0041a0002c0014t0038g0040others(3): Show | 6 | HG01243.hp1 HG02451.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.342+16788C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21028897 | ||||||
| chr13:21029003
|
T | C | 1 | a0001c0001t0001g0273 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.342+16682A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21029003 | ||||||
| chr13:21029073
|
T | C | 1 | a0004c0004t0005g0270 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.342+16612A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21029073 | ||||||
| chr13:21029094
|
C | T | 1 | a0003c0005t0002g0050 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.342+16591G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21029094 | ||||||
| chr13:21029197
|
T | C | 13 | a0002c0006t0004g0011a0002c0006t0004g0012a0002c0006t0004g0015others(10): Show | 13 | HG00597.hp2 HG01358.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.342+16488A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21029197 | ||||||
| chr13:21029284
|
G | A | 105 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0178others(102): Show | 105 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.342+16401C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21029284 | ||||||
| chr13:21029364
|
A | C | 14 | a0003c0003t0004g0300a0003c0003t0004g0301a0003c0007t0036g0051others(11): Show | 14 | HG01433.hp2 HG02258.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.342+16321T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21029364 | ||||||
| chr13:21029501
|
G | C | 2 | a0002c0002t0011g0034a0005c0012t0001g0033 | 2 | HG00735.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.342+16184C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21029501 | ||||||
| chr13:21029503
|
T | C | 13 | a0003c0003t0004g0300a0003c0003t0004g0301a0003c0007t0036g0051others(10): Show | 13 | HG01433.hp2 HG02258.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.342+16182A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21029503 | ||||||
| chr13:21029541
|
C | T | 4 | a0002c0002t0010g0281a0002c0028t0041g0282a0005c0016t0014g0035others(1): Show | 4 | HG02965.hp2 HG03139.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.342+16144G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21029541 | ||||||
| chr13:21029567
|
C | T | 1 | a0002c0006t0004g0022 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.342+16118G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21029567 | ||||||
| chr13:21029575
|
G | A | 1 | a0002c0002t0011g0284 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.342+16110C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21029575 | ||||||
| chr13:21029715
|
C | T | 1 | a0002c0002t0006g0159 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.342+15970G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21029715 | ||||||
| chr13:21029716
|
G | A | 1 | a0012c0022t0004g0007 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.342+15969C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21029716 | ||||||
| chr13:21029901
|
G | A | 314 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(311): Show | 315 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.342+15784C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21029901 | ||||||
| chr13:21029956
|
T | C | 1 | a0003c0032t0016g0315 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.342+15729A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21029956 | ||||||
| chr13:21030038
|
T | C | 256 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0178others(253): Show | 257 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.342+15647A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21030038 | ||||||
| chr13:21030039
|
G | A | 6 | a0002c0014t0018g0039a0002c0014t0018g0041a0002c0014t0038g0040others(3): Show | 6 | HG01243.hp1 HG02451.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.342+15646C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21030039 | ||||||
| chr13:21030134
|
G | A | 1 | a0007c0013t0002g0093 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.342+15551C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21030134 | ||||||
| chr13:21030136
|
A | G | 1 | a0007c0013t0002g0093 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.342+15549T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21030136 | ||||||
| chr13:21030149
|
A | C | 1 | a0007c0013t0002g0093 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.342+15536T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21030149 | ||||||
| chr13:21030317
|
T | C | 257 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0178others(254): Show | 258 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.342+15368A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21030317 | ||||||
| chr13:21030371
|
C | T | 1 | a0003c0007t0036g0051 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.342+15314G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21030371 | ||||||
| chr13:21030457
|
C | T | 6 | a0002c0014t0018g0039a0002c0014t0018g0041a0002c0014t0038g0040others(3): Show | 6 | HG01243.hp1 HG02451.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.342+15228G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21030457 | ||||||
| chr13:21030506
|
G | A | 2 | a0002c0034t0035g0027a0004c0004t0028g0025 | 2 | HG02965.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.342+15179C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21030506 | ||||||
| chr13:21030583
|
C | CCGGA | 5 | a0001c0001t0001g0222a0003c0003t0002g0179a0003c0003t0002g0180others(2): Show | 5 | NA18952.hp2 NA18982.hp1 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.342+15101_342+1510 others(8): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21030583 | ||||||
| chr13:21030588
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.342+15097A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21030588 | ||||||
| chr13:21030591
|
C | CA | 6 | a0001c0010t0001g0064a0003c0003t0002g0190a0003c0005t0002g0060others(3): Show | 6 | HG00621.hp2 HG02135.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.342+15093dupT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21030591 | ||||||
| chr13:21030593
|
AAAAAAAA others(12): Show |
A | 13 | a0002c0006t0004g0011a0002c0006t0004g0012a0002c0006t0004g0015others(10): Show | 13 | HG00597.hp2 HG01358.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.342+15073_342+1509 others(23): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21030593 | ||||||
| chr13:21030607
|
A | G | 1 | a0001c0001t0013g0205 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.342+15078T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21030607 | ||||||
| chr13:21030608
|
A | AG | 110 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0178others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.342+15076_342+1507 others(5): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21030608 | ||||||
| chr13:21030608
|
A | G | 84 | a0001c0001t0001g0242a0001c0001t0002g0207a0001c0001t0003g0161others(81): Show | 84 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.342+15077T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21030608 | ||||||
| chr13:21030609
|
A | G | 4 | a0001c0001t0001g0222a0003c0003t0002g0179a0003c0003t0002g0180others(1): Show | 4 | NA18952.hp2 NA18982.hp2 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.342+15076T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21030609 | ||||||
| chr13:21030612
|
G | A | 216 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0178others(213): Show | 217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.342+15073C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21030612 | ||||||
| chr13:21030612
|
GA | G | 19 | a0001c0001t0013g0205a0002c0014t0018g0039a0002c0014t0018g0041others(16): Show | 19 | HG01243.hp1 HG01433.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.342+15072delT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21030612 | ||||||
| chr13:21030613
|
A | AG | 12 | a0003c0003t0004g0259a0003c0003t0025g0287a0003c0008t0046g0288others(9): Show | 12 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.342+15071_342+1507 others(5): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21030613 | ||||||
| chr13:21030613
|
A | G | 203 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0178others(200): Show | 203 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.342+15072T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21030613 | ||||||
| chr13:21030614
|
A | G | 4 | a0001c0001t0001g0222a0003c0003t0002g0179a0003c0003t0002g0180others(1): Show | 4 | NA18952.hp2 NA18982.hp2 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.342+15071T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21030614 | ||||||
| chr13:21030617
|
A | G | 2 | a0003c0008t0009g0088a0008c0033t0001g0304 | 2 | HG01243.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.342+15068T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21030617 | ||||||
| chr13:21030866
|
T | C | 1 | a0001c0001t0006g0194 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.342+14819A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21030866 | ||||||
| chr13:21030869
|
A | C | 246 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0178others(243): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.342+14816T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21030869 | ||||||
| chr13:21030914
|
A | C | 3 | a0001c0001t0001g0197a0003c0005t0002g0067a0003c0005t0002g0068 | 3 | HG01167.hp2 HG01168.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.342+14771T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21030914 | ||||||
| chr13:21031046
|
T | G | 1 | a0003c0009t0008g0309 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.342+14639A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21031046 | ||||||
| chr13:21031072
|
T | G | 1 | a0004c0004t0005g0251 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.342+14613A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21031072 | ||||||
| chr13:21031290
|
T | C | 2 | a0002c0034t0035g0027a0004c0004t0028g0025 | 2 | HG02965.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.342+14395A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21031290 | ||||||
| chr13:21031347
|
T | C | 3 | a0001c0001t0006g0168a0001c0001t0006g0184a0001c0001t0006g0195 | 3 | NA18994.hp2 NA19057.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.342+14338A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21031347 | ||||||
| chr13:21031349
|
A | G | 2 | a0002c0002t0010g0281a0002c0028t0041g0282 | 2 | HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.342+14336T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21031349 | ||||||
| chr13:21031421
|
A | G | 90 | a0001c0001t0003g0161a0001c0001t0010g0112a0001c0001t0047g0100others(87): Show | 90 | HG00438.hp2 HG00621.hp1 HG00735.hp1 others(87): Show |
intron_variant | MODIFIER | c.342+14264T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21031421 | ||||||
| chr13:21031616
|
T | C | 1 | a0001c0001t0034g0216 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.342+14069A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21031616 | ||||||
| chr13:21032022
|
G | A | 14 | a0002c0006t0004g0011a0002c0006t0004g0012a0002c0006t0004g0015others(11): Show | 14 | HG00597.hp2 HG01358.hp1 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.342+13663C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21032022 | ||||||
| chr13:21032163
|
T | A | 1 | a0002c0002t0003g0095 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.342+13522A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21032163 | ||||||
| chr13:21032288
|
CAG | C | 152 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0178others(149): Show | 153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.342+13395_342+1339 others(6): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21032288 | ||||||
| chr13:21032328
|
C | T | 1 | a0001c0001t0001g0265 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.342+13357G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21032328 | ||||||
| chr13:21032545
|
G | C | 152 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0178others(149): Show | 153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.342+13140C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21032545 | ||||||
| chr13:21032669
|
T | C | 2 | a0002c0002t0003g0157a0002c0002t0003g0158 | 2 | HG02735.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.342+13016A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21032669 | ||||||
| chr13:21032731
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.342+12954G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21032731 | ||||||
| chr13:21032773
|
C | G | 7 | a0003c0008t0009g0088a0003c0009t0008g0309a0003c0009t0009g0308others(4): Show | 7 | HG01243.hp2 HG01884.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.342+12912G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21032773 | ||||||
| chr13:21032801
|
A | G | 1 | a0002c0002t0010g0118 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.342+12884T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21032801 | ||||||
| chr13:21032919
|
G | T | 123 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0178others(120): Show | 124 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.342+12766C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21032919 | ||||||
| chr13:21032950
|
C | G | 1 | a0003c0005t0001g0084 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.342+12735G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21032950 | ||||||
| chr13:21033055
|
G | A | 1 | a0008c0033t0001g0304 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.342+12630C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21033055 | ||||||
| chr13:21033293
|
G | C | 14 | a0002c0006t0004g0011a0002c0006t0004g0012a0002c0006t0004g0015others(11): Show | 14 | HG00597.hp2 HG01358.hp1 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.342+12392C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21033293 | ||||||
| chr13:21033301
|
G | A | 7 | a0002c0014t0018g0039a0002c0014t0018g0041a0002c0014t0038g0040others(4): Show | 7 | HG00639.hp1 HG01243.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.342+12384C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21033301 | ||||||
| chr13:21033461
|
A | G | 152 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0178others(149): Show | 153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.342+12224T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21033461 | ||||||
| chr13:21033595
|
C | T | 1 | a0003c0032t0016g0315 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.342+12090G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21033595 | ||||||
| chr13:21033621
|
G | A | 135 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0178others(132): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.342+12064C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21033621 | ||||||
| chr13:21033631
|
T | C | 7 | a0003c0008t0009g0088a0003c0009t0008g0309a0003c0009t0009g0308others(4): Show | 7 | HG01243.hp2 HG01884.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.342+12054A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21033631 | ||||||
| chr13:21034004
|
T | C | 1 | a0003c0007t0036g0051 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.342+11681A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21034004 | ||||||
| chr13:21034251
|
C | CACAGCCA others(5): Show |
1 | a0005c0016t0005g0235 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.342+11422_342+1143 others(16): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21034251 | ||||||
| chr13:21034338
|
T | C | 2 | a0002c0002t0010g0281a0002c0028t0041g0282 | 2 | HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.342+11347A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21034338 | ||||||
| chr13:21034533
|
C | T | 1 | a0003c0003t0025g0287 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.342+11152G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21034533 | ||||||
| chr13:21034565
|
G | C | 3 | a0003c0003t0002g0172a0003c0003t0002g0173a0003c0003t0002g0175 | 3 | HG01074.hp2 HG01099.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.342+11120C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21034565 | ||||||
| chr13:21034582
|
T | C | 1 | a0012c0022t0004g0007 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.342+11103A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21034582 | ||||||
| chr13:21034611
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.342+11074G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21034611 | ||||||
| chr13:21034700
|
C | G | 127 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0178others(124): Show | 128 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.342+10985G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21034700 | ||||||
| chr13:21034715
|
CACCTGGG others(87): Show |
C | 1 | a0007c0013t0002g0093 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.342+10876_342+1096 others(98): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21034715 | ||||||
| chr13:21034732
|
G | C | 3 | a0004c0004t0005g0204a0004c0004t0005g0229a0004c0004t0005g0230 | 3 | HG02735.hp2 HG03490.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.342+10953C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21034732 | ||||||
| chr13:21034832
|
A | G | 124 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0178others(121): Show | 125 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.342+10853T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21034832 | ||||||
| chr13:21034912
|
C | T | 3 | a0003c0003t0004g0259a0003c0003t0025g0287a0003c0008t0046g0288 | 3 | HG02055.hp2 HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.342+10773G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21034912 | ||||||
| chr13:21035001
|
C | T | 3 | a0003c0003t0004g0259a0003c0003t0025g0287a0003c0008t0046g0288 | 3 | HG02055.hp2 HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.342+10684G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21035001 | ||||||
| chr13:21035010
|
C | A | 128 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0178others(125): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.342+10675G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21035010 | ||||||
| chr13:21035046
|
CAT | C | 3 | a0001c0001t0001g0191a0001c0001t0001g0208a0001c0001t0037g0186 | 3 | HG00280.hp1 HG01361.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.342+10637_342+1063 others(6): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21035046 | ||||||
| chr13:21035143
|
T | A | 4 | a0002c0002t0011g0283a0002c0002t0011g0284a0002c0002t0011g0285others(1): Show | 4 | HG00735.hp2 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.342+10542A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21035143 | ||||||
| chr13:21035213
|
G | A | 9 | a0002c0002t0011g0034a0003c0009t0026g0029a0003c0009t0031g0031others(6): Show | 9 | HG00735.hp1 HG02559.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.342+10472C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21035213 | ||||||
| chr13:21035447
|
C | T | 1 | a0003c0007t0036g0051 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.342+10238G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21035447 | ||||||
| chr13:21035577
|
G | A | 124 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0178others(121): Show | 125 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.342+10108C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21035577 | ||||||
| chr13:21035625
|
G | A | 2 | a0001c0001t0002g0218a0003c0008t0008g0291 | 2 | HG01081.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.342+10060C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21035625 | ||||||
| chr13:21035698
|
T | C | 3 | a0001c0001t0001g0191a0001c0001t0001g0208a0001c0001t0037g0186 | 3 | HG00280.hp1 HG01361.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.342+9987A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21035698 | ||||||
| chr13:21035727
|
T | G | 2 | a0003c0003t0002g0016a0003c0003t0002g0018 | 2 | HG00642.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.342+9958A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21035727 | ||||||
| chr13:21035777
|
G | A | 1 | a0002c0002t0023g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.342+9908C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21035777 | ||||||
| chr13:21035929
|
T | G | 2 | a0004c0004t0001g0302a0004c0004t0001g0303 | 2 | HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.342+9756A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21035929 | ||||||
| chr13:21036043
|
C | T | 25 | a0001c0001t0001g0024a0002c0006t0004g0011a0002c0006t0004g0012others(22): Show | 25 | HG00597.hp2 HG00642.hp2 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.342+9642G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21036043 | ||||||
| chr13:21036050
|
C | T | 4 | a0002c0002t0011g0283a0002c0002t0011g0284a0002c0002t0011g0285others(1): Show | 4 | HG00735.hp2 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.342+9635G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21036050 | ||||||
| chr13:21036085
|
C | T | 2 | a0002c0002t0003g0116a0002c0002t0003g0134 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.342+9600G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21036085 | ||||||
| chr13:21036116
|
G | A | 1 | a0004c0015t0005g0083 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.342+9569C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21036116 | ||||||
| chr13:21036156
|
G | A | 6 | a0003c0008t0009g0088a0003c0009t0008g0309a0003c0009t0009g0308others(3): Show | 6 | HG01243.hp2 HG01884.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.342+9529C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21036156 | ||||||
| chr13:21036176
|
G | A | 1 | a0002c0002t0003g0095 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.342+9509C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21036176 | ||||||
| chr13:21036209
|
T | G | 1 | a0007c0013t0002g0093 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.342+9476A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21036209 | ||||||
| chr13:21036330
|
C | A | 3 | a0003c0003t0004g0259a0003c0003t0025g0287a0003c0008t0046g0288 | 3 | HG02055.hp2 HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.342+9355G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21036330 | ||||||
| chr13:21036419
|
T | A | 1 | a0003c0007t0036g0051 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.342+9266A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21036419 | ||||||
| chr13:21036512
|
C | T | 25 | a0001c0001t0001g0024a0002c0006t0004g0011a0002c0006t0004g0012others(22): Show | 25 | HG00597.hp2 HG00642.hp2 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.342+9173G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21036512 | ||||||
| chr13:21036644
|
G | A | 2 | a0002c0034t0035g0027a0004c0004t0028g0025 | 2 | HG02965.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.342+9041C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21036644 | ||||||
| chr13:21036667
|
A | G | 163 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(160): Show | 164 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.342+9018T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21036667 | ||||||
| chr13:21036705
|
G | A | 4 | a0002c0002t0011g0283a0002c0002t0011g0284a0002c0002t0011g0285others(1): Show | 4 | HG00735.hp2 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.342+8980C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21036705 | ||||||
| chr13:21036713
|
C | T | 1 | a0003c0005t0033g0073 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.342+8972G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21036713 | ||||||
| chr13:21036767
|
C | T | 1 | a0004c0015t0018g0042 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.342+8918G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21036767 | ||||||
| chr13:21036774
|
AAAC | A | 138 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0178others(135): Show | 139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.342+8908_342+8910d others(5): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21036774 | ||||||
| chr13:21037049
|
G | C | 1 | a0007c0013t0002g0093 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.342+8636C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21037049 | ||||||
| chr13:21037050
|
C | G | 1 | a0007c0013t0002g0093 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.342+8635G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21037050 | ||||||
| chr13:21037163
|
G | A | 3 | a0003c0003t0004g0259a0003c0003t0025g0287a0003c0008t0046g0288 | 3 | HG02055.hp2 HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.342+8522C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21037163 | ||||||
| chr13:21037222
|
T | C | 68 | a0001c0001t0003g0161a0001c0001t0010g0112a0001c0001t0047g0100others(65): Show | 68 | HG00438.hp2 HG00621.hp1 HG00738.hp2 others(65): Show |
intron_variant | MODIFIER | c.342+8463A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21037222 | ||||||
| chr13:21037268
|
A | G | 1 | a0012c0022t0004g0007 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.342+8417T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21037268 | ||||||
| chr13:21037334
|
G | C | 1 | a0001c0001t0001g0222 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.342+8351C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21037334 | ||||||
| chr13:21037345
|
A | G | 1 | a0001c0001t0001g0262 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.342+8340T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21037345 | ||||||
| chr13:21037469
|
CG | C | 96 | a0001c0001t0003g0161a0001c0001t0010g0112a0001c0001t0047g0100others(93): Show | 96 | HG00438.hp2 HG00621.hp1 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.342+8215delC | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21037469 | ||||||
| chr13:21037470
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.342+8215C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21037470 | ||||||
| chr13:21037520
|
A | G | 3 | a0003c0003t0004g0259a0003c0003t0025g0287a0003c0008t0046g0288 | 3 | HG02055.hp2 HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.342+8165T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21037520 | ||||||
| chr13:21037652
|
C | T | 272 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(269): Show | 273 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.342+8033G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21037652 | ||||||
| chr13:21037743
|
G | A | 1 | a0002c0002t0003g0113 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.342+7942C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21037743 | ||||||
| chr13:21037803
|
GCCAGGGT others(8): Show |
G | 7 | a0003c0008t0009g0088a0003c0009t0008g0309a0003c0009t0009g0308others(4): Show | 7 | HG01243.hp2 HG01884.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.342+7867_342+7881d others(17): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21037803 | ||||||
| chr13:21037810
|
T | A | 1 | a0003c0007t0008g0070 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.342+7875A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21037810 | ||||||
| chr13:21037826
|
G | A | 1 | a0001c0001t0001g0242 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.342+7859C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21037826 | ||||||
| chr13:21037840
|
T | C | 12 | a0003c0003t0004g0300a0003c0003t0004g0301a0003c0008t0009g0294others(9): Show | 12 | HG01433.hp2 HG02258.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.342+7845A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21037840 | ||||||
| chr13:21037879
|
G | A | 1 | a0008c0033t0001g0304 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.342+7806C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21037879 | ||||||
| chr13:21037880
|
T | C | 1 | a0007c0013t0002g0093 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.342+7805A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21037880 | ||||||
| chr13:21037911
|
AG | A | 4 | a0003c0005t0002g0048a0003c0005t0002g0049a0003c0005t0002g0071others(1): Show | 4 | HG02257.hp1 HG02723.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.342+7773delC | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21037911 | ||||||
| chr13:21037979
|
C | T | 1 | a0003c0008t0008g0291 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.342+7706G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21037979 | ||||||
| chr13:21037989
|
C | T | 4 | a0003c0005t0002g0048a0003c0005t0002g0049a0003c0005t0002g0071others(1): Show | 4 | HG02257.hp1 HG02723.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.342+7696G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21037989 | ||||||
| chr13:21037992
|
G | A | 3 | a0003c0032t0016g0315a0004c0004t0004g0298a0004c0004t0014g0299 | 3 | HG02647.hp2 HG03540.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.342+7693C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21037992 | ||||||
| chr13:21038010
|
C | T | 25 | a0001c0001t0001g0024a0002c0006t0004g0011a0002c0006t0004g0012others(22): Show | 25 | HG00597.hp2 HG00642.hp2 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.342+7675G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21038010 | ||||||
| chr13:21038020
|
C | T | 29 | a0001c0001t0001g0024a0002c0002t0011g0283a0002c0002t0011g0284others(26): Show | 29 | HG00597.hp2 HG00642.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.342+7665G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21038020 | ||||||
| chr13:21038066
|
A | G | 124 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0178others(121): Show | 125 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.342+7619T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21038066 | ||||||
| chr13:21038086
|
A | C | 1 | a0007c0013t0002g0093 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.342+7599T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21038086 | ||||||
| chr13:21038113
|
G | A | 165 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(162): Show | 166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.342+7572C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21038113 | ||||||
| chr13:21038169
|
G | A | 1 | a0003c0008t0009g0088 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.342+7516C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21038169 | ||||||
| chr13:21038322
|
G | A | 1 | a0003c0005t0015g0069 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.342+7363C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21038322 | ||||||
| chr13:21038336
|
T | C | 3 | a0003c0003t0004g0259a0003c0003t0025g0287a0003c0008t0046g0288 | 3 | HG02055.hp2 HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.342+7349A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21038336 | ||||||
| chr13:21038425
|
A | T | 3 | a0002c0002t0003g0107a0002c0002t0003g0117a0002c0002t0003g0123 | 3 | NA18973.hp2 NA18979.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.342+7260T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21038425 | ||||||
| chr13:21038515
|
C | T | 1 | a0002c0006t0004g0022 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.342+7170G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21038515 | ||||||
| chr13:21038544
|
T | C | 6 | a0003c0008t0009g0294a0003c0008t0009g0296a0004c0004t0019g0026others(3): Show | 6 | HG01433.hp2 HG02258.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.342+7141A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21038544 | ||||||
| chr13:21038652
|
G | A | 135 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0178others(132): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.342+7033C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21038652 | ||||||
| chr13:21038742
|
C | T | 2 | a0003c0003t0002g0016a0003c0003t0002g0018 | 2 | HG00642.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.342+6943G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21038742 | ||||||
| chr13:21038904
|
C | T | 7 | a0003c0008t0009g0088a0003c0009t0008g0309a0003c0009t0009g0308others(4): Show | 7 | HG01243.hp2 HG01884.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.342+6781G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21038904 | ||||||
| chr13:21038920
|
T | C | 273 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(270): Show | 274 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.342+6765A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21038920 | ||||||
| chr13:21038924
|
G | C | 3 | a0003c0003t0004g0259a0003c0003t0025g0287a0003c0008t0046g0288 | 3 | HG02055.hp2 HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.342+6761C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21038924 | ||||||
| chr13:21038965
|
T | C | 24 | a0001c0001t0001g0024a0002c0006t0004g0011a0002c0006t0004g0012others(21): Show | 24 | HG00597.hp2 HG00642.hp2 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.342+6720A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21038965 | ||||||
| chr13:21038965
|
T | G | 1 | a0007c0013t0002g0093 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.342+6720A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21038965 | ||||||
| chr13:21038986
|
C | G | 25 | a0001c0001t0001g0024a0002c0006t0004g0011a0002c0006t0004g0012others(22): Show | 25 | HG00597.hp2 HG00642.hp2 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.342+6699G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21038986 | ||||||
| chr13:21039049
|
T | A | 1 | a0007c0013t0002g0093 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.342+6636A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21039049 | ||||||
| chr13:21039130
|
T | C | 142 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0178others(139): Show | 143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.342+6555A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21039130 | ||||||
| chr13:21039137
|
C | G | 1 | a0001c0001t0001g0024 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.342+6548G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21039137 | ||||||
| chr13:21039423
|
A | G | 1 | a0007c0013t0002g0093 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.342+6262T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21039423 | ||||||
| chr13:21039424
|
G | A | 1 | a0007c0013t0002g0093 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.342+6261C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21039424 | ||||||
| chr13:21039425
|
A | G | 1 | a0007c0013t0002g0093 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.342+6260T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21039425 | ||||||
| chr13:21039530
|
G | C | 1 | a0002c0002t0006g0159 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.342+6155C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21039530 | ||||||
| chr13:21039659
|
A | G | 1 | a0007c0013t0002g0093 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.342+6026T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21039659 | ||||||
| chr13:21039768
|
T | G | 1 | a0007c0013t0002g0093 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.342+5917A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21039768 | ||||||
| chr13:21039864
|
A | C | 10 | a0002c0002t0011g0283a0002c0002t0011g0284a0002c0002t0011g0285others(7): Show | 10 | HG00735.hp2 HG02809.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.342+5821T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21039864 | ||||||
| chr13:21039941
|
C | T | 5 | a0006c0011t0001g0079a0006c0011t0001g0080a0006c0011t0001g0081others(2): Show | 5 | HG02451.hp1 HG02895.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.342+5744G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21039941 | ||||||
| chr13:21039998
|
G | A | 1 | a0003c0008t0009g0296 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.342+5687C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21039998 | ||||||
| chr13:21040059
|
G | C | 1 | a0001c0001t0027g0226 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.342+5626C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21040059 | ||||||
| chr13:21040073
|
CA | C | 6 | a0001c0001t0001g0275a0002c0002t0003g0095a0002c0002t0003g0102others(3): Show | 6 | HG01168.hp1 HG01496.hp1 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.342+5611delT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21040073 | ||||||
| chr13:21040361
|
C | T | 164 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(161): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.342+5324G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21040361 | ||||||
| chr13:21040373
|
T | C | 7 | a0002c0002t0011g0034a0003c0009t0026g0029a0003c0009t0031g0031others(4): Show | 7 | HG00735.hp1 HG02559.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.342+5312A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21040373 | ||||||
| chr13:21040376
|
C | CA | 29 | a0001c0001t0001g0024a0001c0001t0022g0171a0002c0006t0004g0011others(26): Show | 29 | HG00642.hp2 HG01243.hp1 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.342+5308dupT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21040376 | ||||||
| chr13:21040376
|
C | CAAAAAAA others(5): Show |
1 | a0005c0016t0014g0036 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.342+5297_342+5308d others(14): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21040376 | ||||||
| chr13:21040376
|
C | CAAAAAAA others(6): Show |
1 | a0005c0016t0014g0035 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.342+5296_342+5308d others(15): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21040376 | ||||||
| chr13:21040388
|
A | G | 1 | a0012c0022t0004g0007 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.342+5297T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21040388 | ||||||
| chr13:21040392
|
G | A | 11 | a0002c0002t0011g0283a0002c0002t0011g0284a0002c0002t0011g0285others(8): Show | 11 | HG00735.hp2 HG02055.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.342+5293C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21040392 | ||||||
| chr13:21040396
|
G | A | 4 | a0003c0003t0025g0287a0003c0008t0046g0288a0005c0016t0014g0035others(1): Show | 4 | HG02055.hp2 HG02630.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.342+5289C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21040396 | ||||||
| chr13:21040402
|
G | A | 2 | a0003c0003t0025g0287a0003c0008t0046g0288 | 2 | HG02055.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.342+5283C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21040402 | ||||||
| chr13:21040416
|
T | G | 2 | a0003c0003t0025g0287a0003c0008t0046g0288 | 2 | HG02055.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.342+5269A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21040416 | ||||||
| chr13:21040426
|
G | T | 8 | a0001c0001t0004g0276a0001c0001t0006g0168a0001c0001t0006g0188others(5): Show | 8 | HG00423.hp1 HG02071.hp1 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.342+5259C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21040426 | ||||||
| chr13:21040561
|
T | G | 7 | a0002c0002t0011g0034a0003c0009t0026g0029a0003c0009t0031g0031others(4): Show | 7 | HG00735.hp1 HG02559.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.342+5124A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21040561 | ||||||
| chr13:21040587
|
C | T | 3 | a0002c0002t0003g0148a0002c0002t0003g0153a0002c0002t0024g0152 | 3 | HG02148.hp2 NA19000.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.342+5098G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21040587 | ||||||
| chr13:21040598
|
G | A | 76 | a0001c0001t0003g0161a0001c0001t0010g0099a0001c0001t0010g0112others(73): Show | 76 | HG00438.hp2 HG00621.hp1 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.342+5087C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21040598 | ||||||
| chr13:21040977
|
C | CT | 11 | a0002c0002t0011g0283a0002c0002t0011g0284a0002c0002t0011g0285others(8): Show | 11 | HG00735.hp2 HG02809.hp1 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.342+4707dupA | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21040977 | ||||||
| chr13:21041117
|
C | T | 1 | a0004c0004t0005g0089 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.342+4568G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21041117 | ||||||
| chr13:21041165
|
G | C | 1 | a0001c0001t0001g0024 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.342+4520C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21041165 | ||||||
| chr13:21041201
|
T | A | 1 | a0002c0002t0003g0133 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.342+4484A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21041201 | ||||||
| chr13:21041275
|
TCC | T | 4 | a0002c0002t0011g0283a0002c0002t0011g0284a0002c0002t0011g0285others(1): Show | 4 | HG00735.hp2 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.342+4408_342+4409d others(4): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21041275 | ||||||
| chr13:21041316
|
A | G | 12 | a0002c0002t0011g0283a0002c0002t0011g0284a0002c0002t0011g0285others(9): Show | 12 | HG00735.hp2 HG02055.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.342+4369T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21041316 | ||||||
| chr13:21041346
|
T | C | 129 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0178others(126): Show | 130 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.342+4339A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21041346 | ||||||
| chr13:21041932
|
C | T | 164 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(161): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.342+3753G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21041932 | ||||||
| chr13:21042004
|
A | T | 4 | a0002c0002t0011g0283a0002c0002t0011g0284a0002c0002t0011g0285others(1): Show | 4 | HG00735.hp2 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.342+3681T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21042004 | ||||||
| chr13:21042058
|
T | A | 8 | a0002c0002t0011g0283a0002c0002t0011g0284a0002c0002t0011g0285others(5): Show | 8 | HG00735.hp2 HG02809.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.342+3627A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21042058 | ||||||
| chr13:21042340
|
T | C | 74 | a0001c0001t0003g0161a0001c0001t0010g0099a0001c0001t0010g0112others(71): Show | 74 | HG00438.hp2 HG00621.hp1 HG00738.hp2 others(71): Show |
intron_variant | MODIFIER | c.342+3345A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21042340 | ||||||
| chr13:21042793
|
C | G | 11 | a0002c0002t0011g0034a0003c0003t0025g0287a0003c0008t0046g0288others(8): Show | 11 | HG00735.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.342+2892G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21042793 | ||||||
| chr13:21042843
|
G | A | 240 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(237): Show | 241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.342+2842C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21042843 | ||||||
| chr13:21042857
|
G | A | 9 | a0002c0002t0011g0034a0003c0009t0026g0029a0003c0009t0031g0031others(6): Show | 9 | HG00735.hp1 HG02559.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.342+2828C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21042857 | ||||||
| chr13:21042909
|
G | C | 15 | a0003c0003t0004g0300a0003c0003t0004g0301a0003c0008t0008g0291others(12): Show | 15 | HG01433.hp2 HG02145.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.342+2776C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21042909 | ||||||
| chr13:21042923
|
G | C | 1 | a0003c0023t0002g0006 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.342+2762C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21042923 | ||||||
| chr13:21042938
|
T | C | 282 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(279): Show | 283 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.342+2747A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21042938 | ||||||
| chr13:21042973
|
G | A | 6 | a0002c0006t0004g0258a0004c0004t0005g0002a0004c0004t0005g0247others(3): Show | 6 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(3): Show |
intron_variant | MODIFIER | c.342+2712C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21042973 | ||||||
| chr13:21042988
|
A | C | 76 | a0001c0001t0003g0161a0001c0001t0010g0099a0001c0001t0010g0112others(73): Show | 76 | HG00438.hp2 HG00621.hp1 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.342+2697T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21042988 | ||||||
| chr13:21042993
|
AC | A | 90 | a0001c0001t0001g0090a0001c0001t0001g0178a0001c0001t0001g0181others(87): Show | 91 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.342+2691delG | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21042993 | ||||||
| chr13:21042994
|
C | A | 193 | a0001c0001t0001g0024a0001c0001t0001g0092a0001c0001t0001g0248others(190): Show | 193 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.342+2691G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21042994 | ||||||
| chr13:21043198
|
C | T | 1 | a0003c0005t0004g0078 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.342+2487G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21043198 | ||||||
| chr13:21043220
|
C | T | 6 | a0002c0017t0011g0075a0006c0011t0001g0079a0006c0011t0001g0080others(3): Show | 6 | HG02451.hp1 HG02895.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.342+2465G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21043220 | ||||||
| chr13:21043248
|
G | A | 2 | a0002c0006t0004g0011a0002c0006t0004g0012 | 2 | NA19064.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.342+2437C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21043248 | ||||||
| chr13:21043351
|
C | G | 4 | a0001c0001t0002g0225a0001c0001t0002g0227a0001c0001t0002g0228others(1): Show | 4 | HG00741.hp1 HG01106.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.342+2334G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21043351 | ||||||
| chr13:21043413
|
G | T | 259 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(256): Show | 260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.342+2272C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21043413 | ||||||
| chr13:21043509
|
G | A | 8 | a0002c0002t0011g0283a0002c0002t0011g0284a0002c0002t0011g0285others(5): Show | 8 | HG00735.hp2 HG02809.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.342+2176C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21043509 | ||||||
| chr13:21043595
|
C | T | 1 | a0001c0001t0001g0274 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.342+2090G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21043595 | ||||||
| chr13:21043688
|
G | T | 11 | a0002c0002t0011g0034a0003c0003t0025g0287a0003c0008t0046g0288others(8): Show | 11 | HG00735.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.342+1997C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21043688 | ||||||
| chr13:21043707
|
T | C | 2 | a0003c0003t0025g0287a0003c0008t0046g0288 | 2 | HG02055.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.342+1978A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21043707 | ||||||
| chr13:21043839
|
G | A | 1 | a0003c0023t0002g0006 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.342+1846C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21043839 | ||||||
| chr13:21043867
|
C | A | 11 | a0002c0002t0011g0034a0003c0003t0025g0287a0003c0008t0046g0288others(8): Show | 11 | HG00735.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.342+1818G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21043867 | ||||||
| chr13:21043965
|
C | T | 11 | a0002c0002t0011g0034a0003c0003t0025g0287a0003c0008t0046g0288others(8): Show | 11 | HG00735.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.342+1720G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21043965 | ||||||
| chr13:21043998
|
G | C | 4 | a0003c0008t0009g0088a0004c0019t0020g0305a0004c0019t0020g0306others(1): Show | 4 | HG01243.hp1 HG01243.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.342+1687C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21043998 | ||||||
| chr13:21044024
|
T | C | 1 | a0004c0035t0009g0297 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.342+1661A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21044024 | ||||||
| chr13:21044046
|
A | G | 265 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(262): Show | 266 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.342+1639T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21044046 | ||||||
| chr13:21044262
|
G | A | 15 | a0003c0003t0004g0300a0003c0003t0004g0301a0003c0008t0008g0291others(12): Show | 15 | HG01433.hp2 HG02145.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.342+1423C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21044262 | ||||||
| chr13:21044466
|
G | A | 4 | a0002c0002t0011g0283a0002c0002t0011g0284a0002c0002t0011g0285others(1): Show | 4 | HG00735.hp2 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.342+1219C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21044466 | ||||||
| chr13:21044689
|
G | GGT | 8 | a0002c0024t0023g0038a0003c0005t0002g0052a0003c0005t0002g0053others(5): Show | 8 | HG00639.hp1 HG01243.hp2 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.342+994_342+995dup others(2): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21044689 | ||||||
| chr13:21044689
|
G | GGTGTGTG others(3): Show |
1 | a0004c0015t0018g0042 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.342+986_342+995dup others(10): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21044689 | ||||||
| chr13:21044689
|
GGT | G | 21 | a0002c0017t0006g0004a0002c0017t0011g0075a0003c0005t0002g0057others(18): Show | 21 | HG01243.hp1 HG02451.hp1 HG02572.hp1 others(18): Show |
intron_variant | MODIFIER | c.342+994_342+995del others(2): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21044689 | ||||||
| chr13:21044689
|
GGTGT | G | 16 | a0001c0001t0001g0191a0001c0001t0001g0208a0001c0001t0001g0264others(13): Show | 16 | HG00280.hp1 HG00438.hp1 HG00621.hp2 others(13): Show |
intron_variant | MODIFIER | c.342+992_342+995del others(4): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21044689 | ||||||
| chr13:21044689
|
GGTGTGT | G | 38 | a0001c0001t0001g0192a0001c0001t0001g0220a0001c0001t0001g0237others(35): Show | 38 | HG00099.hp1 HG00735.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.342+990_342+995del others(6): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21044689 | ||||||
| chr13:21044689
|
GGTGTGTG others(1): Show |
G | 97 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0178others(94): Show | 98 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.342+988_342+995del others(8): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21044689 | ||||||
| chr13:21044689
|
GGTGTGTG others(3): Show |
G | 26 | a0001c0001t0001g0248a0001c0001t0002g0227a0001c0001t0002g0228others(23): Show | 26 | HG00280.hp2 HG00438.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.342+986_342+995del others(10): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21044689 | ||||||
| chr13:21044689
|
GGTGTGTG others(5): Show |
G | 74 | a0001c0001t0010g0112a0001c0001t0010g0162a0001c0001t0010g0163others(71): Show | 74 | HG00621.hp1 HG00735.hp2 HG00738.hp2 others(71): Show |
intron_variant | MODIFIER | c.342+984_342+995del others(12): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21044689 | ||||||
| chr13:21044689
|
GGTGTGTG others(7): Show |
G | 2 | a0001c0001t0022g0171a0002c0002t0003g0147 | 2 | NA18951.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.342+982_342+995del others(14): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21044689 | ||||||
| chr13:21044689
|
GGTGTGTG others(9): Show |
G | 1 | a0002c0002t0003g0098 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.342+980_342+995del others(16): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21044689 | ||||||
| chr13:21044689
|
GGTGTGTG others(13): Show |
G | 1 | a0001c0001t0001g0252 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.342+976_342+995del others(20): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21044689 | ||||||
| chr13:21044689
|
GGTGTGTG others(19): Show |
G | 18 | a0001c0001t0001g0024a0002c0006t0004g0011a0002c0006t0004g0012others(15): Show | 18 | HG00642.hp2 HG01358.hp1 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.342+970_342+995del others(26): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21044689 | ||||||
| chr13:21044693
|
T | G | 3 | a0003c0009t0026g0029a0003c0009t0031g0031a0005c0012t0002g0032 | 3 | HG02723.hp2 HG02886.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.342+992A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21044693 | ||||||
| chr13:21044697
|
T | G | 2 | a0002c0002t0011g0034a0005c0012t0001g0033 | 2 | HG00735.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.342+988A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21044697 | ||||||
| chr13:21044728
|
GTGTGTGT others(4): Show |
G | 1 | a0004c0004t0005g0230 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.342+946_342+956del others(11): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21044728 | ||||||
| chr13:21044752
|
T | C | 1 | a0002c0002t0003g0125 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.342+933A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21044752 | ||||||
| chr13:21044856
|
T | C | 1 | a0001c0001t0001g0090 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.342+829A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21044856 | ||||||
| chr13:21044870
|
CA | C | 259 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(256): Show | 260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.342+814delT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21044870 | ||||||
| chr13:21044908
|
T | C | 2 | a0005c0016t0014g0035a0005c0016t0014g0036 | 2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.342+777A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21044908 | ||||||
| chr13:21044975
|
G | A | 4 | a0002c0014t0018g0039a0002c0014t0018g0041a0002c0014t0038g0040others(1): Show | 4 | HG00639.hp1 HG02451.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.342+710C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21044975 | ||||||
| chr13:21045106
|
CTG | C | 164 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(161): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.342+577_342+578del others(2): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21045106 | ||||||
| chr13:21045331
|
C | T | 18 | a0001c0001t0001g0024a0002c0006t0004g0011a0002c0006t0004g0012others(15): Show | 18 | HG00642.hp2 HG01358.hp1 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.342+354G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21045331 | ||||||
| chr13:21045341
|
G | A | 15 | a0003c0003t0004g0300a0003c0003t0004g0301a0003c0008t0008g0291others(12): Show | 15 | HG01433.hp2 HG02145.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.342+344C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21045341 | ||||||
| chr13:21045360
|
CA | C | 4 | a0002c0034t0035g0027a0003c0032t0016g0315a0004c0004t0019g0026others(1): Show | 4 | HG02965.hp1 HG03540.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.342+324delT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 2/7 | chr13 | 21045360 | ||||||
| chr13:21046325
|
A | G | 1 | a0012c0022t0004g0007 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-204-95T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21046325 | ||||||
| chr13:21046330
|
G | A | 2 | a0003c0003t0025g0287a0003c0008t0046g0288 | 2 | HG02055.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.-204-100C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21046330 | ||||||
| chr13:21046450
|
C | T | 4 | a0001c0001t0001g0233a0003c0003t0002g0179a0003c0003t0002g0180others(1): Show | 4 | HG00423.hp2 NA18952.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.-204-220G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21046450 | ||||||
| chr13:21046671
|
C | A | 1 | a0001c0001t0001g0223 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-204-441G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21046671 | ||||||
| chr13:21046981
|
T | C | 4 | a0001c0001t0002g0207a0001c0001t0013g0189a0001c0001t0013g0205others(1): Show | 4 | HG02027.hp2 NA18980.hp1 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.-204-751A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21046981 | ||||||
| chr13:21047024
|
G | A | 1 | a0002c0027t0039g0114 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-204-794C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21047024 | ||||||
| chr13:21047027
|
A | G | 1 | a0012c0022t0004g0007 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-204-797T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21047027 | ||||||
| chr13:21047149
|
G | A | 8 | a0002c0002t0011g0283a0002c0002t0011g0284a0002c0002t0011g0285others(5): Show | 8 | HG00735.hp2 HG02809.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-204-919C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21047149 | ||||||
| chr13:21047152
|
C | A | 1 | a0004c0035t0009g0297 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-204-922G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21047152 | ||||||
| chr13:21047191
|
G | A | 2 | a0002c0002t0003g0153a0002c0002t0024g0152 | 2 | NA19000.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.-204-961C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21047191 | ||||||
| chr13:21047222
|
C | T | 4 | a0002c0002t0011g0283a0002c0002t0011g0284a0002c0002t0011g0285others(1): Show | 4 | HG00735.hp2 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-204-992G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21047222 | ||||||
| chr13:21047403
|
T | C | 3 | a0003c0009t0008g0309a0003c0009t0009g0308a0003c0009t0032g0289 | 3 | HG02258.hp1 HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-204-1173A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21047403 | ||||||
| chr13:21047419
|
C | T | 164 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(161): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.-204-1189G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21047419 | ||||||
| chr13:21047482
|
T | C | 1 | a0002c0002t0003g0123 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-204-1252A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21047482 | ||||||
| chr13:21047499
|
C | T | 8 | a0002c0002t0011g0283a0002c0002t0011g0284a0002c0002t0011g0285others(5): Show | 8 | HG00735.hp2 HG02809.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-204-1269G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21047499 | ||||||
| chr13:21047645
|
G | A | 7 | a0002c0002t0011g0034a0003c0009t0026g0029a0003c0009t0031g0031others(4): Show | 7 | HG00735.hp1 HG02559.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-204-1415C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21047645 | ||||||
| chr13:21047669
|
C | T | 8 | a0002c0002t0011g0283a0002c0002t0011g0284a0002c0002t0011g0285others(5): Show | 8 | HG00735.hp2 HG02809.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-204-1439G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21047669 | ||||||
| chr13:21047806
|
T | C | 4 | a0001c0001t0001g0275a0002c0034t0035g0027a0004c0004t0019g0026others(1): Show | 4 | HG01496.hp1 HG02965.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-204-1576A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21047806 | ||||||
| chr13:21047840
|
G | C | 3 | a0002c0034t0035g0027a0004c0004t0019g0026a0004c0004t0028g0025 | 3 | HG02965.hp1 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-204-1610C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21047840 | ||||||
| chr13:21047851
|
G | T | 2 | a0004c0019t0020g0305a0004c0019t0020g0306 | 2 | HG01243.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-204-1621C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21047851 | ||||||
| chr13:21047895
|
T | C | 3 | a0002c0034t0035g0027a0004c0004t0019g0026a0004c0004t0028g0025 | 3 | HG02965.hp1 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-204-1665A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21047895 | ||||||
| chr13:21047928
|
G | A | 19 | a0002c0002t0011g0034a0002c0002t0011g0283a0002c0002t0011g0284others(16): Show | 19 | HG00735.hp1 HG00735.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.-204-1698C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21047928 | ||||||
| chr13:21048082
|
T | C | 267 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(264): Show | 268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.-204-1852A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21048082 | ||||||
| chr13:21048273
|
C | T | 2 | a0003c0005t0002g0037a0003c0005t0002g0050 | 2 | HG00741.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-204-2043G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21048273 | ||||||
| chr13:21048444
|
C | T | 19 | a0002c0002t0011g0034a0002c0002t0011g0283a0002c0002t0011g0284others(16): Show | 19 | HG00735.hp1 HG00735.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.-204-2214G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21048444 | ||||||
| chr13:21048602
|
C | T | 1 | a0003c0003t0002g0190 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-204-2372G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21048602 | ||||||
| chr13:21048613
|
T | C | 259 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(256): Show | 260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.-204-2383A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21048613 | ||||||
| chr13:21048706
|
G | A | 122 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0178others(119): Show | 123 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.-204-2476C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21048706 | ||||||
| chr13:21048719
|
C | T | 11 | a0002c0002t0011g0034a0003c0003t0025g0287a0003c0008t0046g0288others(8): Show | 11 | HG00735.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-204-2489G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21048719 | ||||||
| chr13:21048768
|
C | T | 2 | a0002c0002t0010g0281a0002c0028t0041g0282 | 2 | HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-204-2538G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21048768 | ||||||
| chr13:21048773
|
G | A | 1 | a0009c0020t0009g0001 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-204-2543C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21048773 | ||||||
| chr13:21048845
|
AAAAAATA others(5): Show |
A | 4 | a0002c0002t0011g0283a0002c0002t0011g0284a0002c0002t0011g0285others(1): Show | 4 | HG00735.hp2 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-204-2627_-204-261 others(16): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21048845 | ||||||
| chr13:21048853
|
A | G | 1 | a0001c0001t0001g0252 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-204-2623T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21048853 | ||||||
| chr13:21049139
|
T | C | 11 | a0002c0002t0011g0034a0003c0003t0025g0287a0003c0008t0046g0288others(8): Show | 11 | HG00735.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-204-2909A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21049139 | ||||||
| chr13:21049172
|
G | A | 2 | a0004c0004t0005g0229a0004c0004t0005g0230 | 2 | HG02735.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.-204-2942C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21049172 | ||||||
| chr13:21049191
|
G | A | 1 | a0001c0001t0002g0227 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-204-2961C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21049191 | ||||||
| chr13:21049278
|
T | C | 8 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0241others(5): Show | 8 | NA18945.hp1 NA18950.hp2 NA18970.hp1 others(5): Show |
intron_variant | MODIFIER | c.-204-3048A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21049278 | ||||||
| chr13:21049329
|
G | A | 1 | a0003c0032t0016g0315 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-204-3099C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21049329 | ||||||
| chr13:21049330
|
G | A | 76 | a0001c0001t0003g0161a0001c0001t0010g0099a0001c0001t0010g0112others(73): Show | 76 | HG00438.hp2 HG00621.hp1 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.-204-3100C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21049330 | ||||||
| chr13:21049367
|
C | T | 1 | a0001c0001t0022g0171 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-204-3137G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21049367 | ||||||
| chr13:21049622
|
C | T | 240 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(237): Show | 241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.-204-3392G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21049622 | ||||||
| chr13:21049636
|
A | G | 2 | a0001c0001t0006g0184a0001c0001t0012g0165 | 2 | NA18979.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.-204-3406T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21049636 | ||||||
| chr13:21049644
|
A | G | 260 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(257): Show | 261 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.-204-3414T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21049644 | ||||||
| chr13:21049662
|
A | G | 1 | a0004c0015t0018g0042 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-204-3432T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21049662 | ||||||
| chr13:21049694
|
G | A | 1 | a0003c0007t0008g0070 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-204-3464C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21049694 | ||||||
| chr13:21049709
|
C | T | 2 | a0003c0003t0025g0287a0003c0008t0046g0288 | 2 | HG02055.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.-204-3479G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21049709 | ||||||
| chr13:21049710
|
A | G | 7 | a0002c0002t0011g0034a0003c0009t0026g0029a0003c0009t0031g0031others(4): Show | 7 | HG00735.hp1 HG02559.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-204-3480T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21049710 | ||||||
| chr13:21049732
|
C | A | 15 | a0003c0003t0004g0300a0003c0003t0004g0301a0003c0008t0008g0291others(12): Show | 15 | HG01433.hp2 HG02145.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.-204-3502G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21049732 | ||||||
| chr13:21049849
|
T | C | 122 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0178others(119): Show | 123 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.-204-3619A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21049849 | ||||||
| chr13:21049872
|
G | A | 2 | a0003c0003t0025g0287a0003c0008t0046g0288 | 2 | HG02055.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.-204-3642C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21049872 | ||||||
| chr13:21049877
|
T | C | 1 | a0004c0004t0005g0269 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-204-3647A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21049877 | ||||||
| chr13:21049938
|
C | G | 2 | a0002c0002t0003g0116a0002c0002t0003g0134 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-204-3708G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21049938 | ||||||
| chr13:21049973
|
T | C | 11 | a0002c0002t0011g0034a0003c0003t0025g0287a0003c0008t0046g0288others(8): Show | 11 | HG00735.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-204-3743A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21049973 | ||||||
| chr13:21049974
|
A | G | 1 | a0003c0009t0009g0308 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-204-3744T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21049974 | ||||||
| chr13:21050027
|
G | A | 2 | a0003c0005t0002g0067a0003c0005t0002g0068 | 2 | HG01167.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.-204-3797C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050027 | ||||||
| chr13:21050110
|
ACT | A | 9 | a0002c0002t0011g0034a0003c0009t0026g0029a0003c0009t0031g0031others(6): Show | 9 | HG00735.hp1 HG02559.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-204-3882_-204-388 others(6): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050110 | ||||||
| chr13:21050119
|
C | CATAG | 4 | a0003c0009t0026g0029a0003c0009t0031g0031a0005c0012t0002g0028others(1): Show | 4 | HG02723.hp2 HG02897.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-204-3893_-204-389 others(8): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050119 | ||||||
| chr13:21050125
|
C | CAGACAGA others(49): Show |
1 | a0003c0003t0002g0173 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-204-3896_-204-389 others(60): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050125 | ||||||
| chr13:21050125
|
C | CAGACAGA others(29): Show |
1 | a0004c0004t0014g0299 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-204-3896_-204-389 others(40): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050125 | ||||||
| chr13:21050125
|
C | CAGACAGA others(33): Show |
1 | a0004c0004t0004g0298 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-204-3896_-204-389 others(44): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050125 | ||||||
| chr13:21050125
|
C | CAGACAGA others(37): Show |
1 | a0003c0003t0002g0172 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-204-3896_-204-389 others(48): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050125 | ||||||
| chr13:21050125
|
C | CAGACAGA others(21): Show |
5 | a0003c0008t0008g0293a0003c0008t0009g0294a0003c0008t0009g0296others(2): Show | 5 | HG01433.hp2 HG02970.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-204-3896_-204-389 others(32): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050125 | ||||||
| chr13:21050125
|
C | CAGACAGA others(25): Show |
2 | a0003c0008t0008g0291a0004c0004t0019g0292 | 2 | HG02145.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.-204-3896_-204-389 others(36): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050125 | ||||||
| chr13:21050125
|
C | CAGAT | 7 | a0003c0005t0002g0037a0003c0005t0002g0048a0003c0005t0002g0049others(4): Show | 7 | HG00741.hp2 HG01109.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-204-3899_-204-389 others(8): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050125 | ||||||
| chr13:21050125
|
C | T | 9 | a0002c0002t0011g0034a0003c0009t0026g0029a0003c0009t0031g0031others(6): Show | 9 | HG00735.hp1 HG02559.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-204-3895G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050125 | ||||||
| chr13:21050125
|
CAGAT | C | 3 | a0002c0014t0018g0039a0002c0014t0018g0041a0002c0014t0038g0040 | 3 | HG02451.hp2 HG02886.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-204-3899_-204-389 others(8): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050125 | ||||||
| chr13:21050129
|
T | C | 228 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(225): Show | 229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.-204-3899A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050129 | ||||||
| chr13:21050133
|
T | C | 31 | a0001c0001t0001g0024a0002c0002t0003g0124a0002c0006t0004g0011others(28): Show | 31 | HG00642.hp2 HG01074.hp2 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.-204-3903A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050133 | ||||||
| chr13:21050137
|
T | C | 1 | a0002c0006t0004g0021 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-204-3907A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050137 | ||||||
| chr13:21050139
|
G | C | 1 | a0003c0003t0002g0173 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-204-3909C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050139 | ||||||
| chr13:21050143
|
G | C | 6 | a0003c0003t0002g0172a0003c0003t0002g0173a0003c0003t0025g0287others(3): Show | 6 | HG01099.hp2 HG02055.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-204-3913C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050143 | ||||||
| chr13:21050147
|
G | C | 13 | a0003c0003t0002g0172a0003c0003t0002g0173a0003c0003t0025g0287others(10): Show | 13 | HG01099.hp2 HG01433.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.-204-3917C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | ||||||
| chr13:21050147
|
G | GATAGATA others(13): Show |
2 | a0002c0002t0011g0034a0005c0012t0001g0033 | 2 | HG00735.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(24): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | ||||||
| chr13:21050147
|
G | GATAGATA others(25): Show |
1 | a0003c0032t0016g0315 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-204-3918_-204-391 others(36): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | ||||||
| chr13:21050147
|
G | GATAGATA others(29): Show |
4 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0237others(1): Show | 4 | NA19011.hp2 NA19084.hp1 NA19085.hp2 others(1): Show |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(40): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | ||||||
| chr13:21050147
|
G | GATAGATA others(33): Show |
1 | a0001c0001t0001g0224 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-204-3918_-204-391 others(44): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | ||||||
| chr13:21050147
|
G | GATAGATA others(17): Show |
2 | a0001c0001t0001g0249a0001c0001t0001g0250 | 2 | HG00099.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(28): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | ||||||
| chr13:21050147
|
G | GATAGATA others(25): Show |
1 | a0001c0001t0001g0274 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-204-3918_-204-391 others(36): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | ||||||
| chr13:21050147
|
G | GATAGATA others(29): Show |
3 | a0001c0001t0001g0220a0001c0001t0001g0279a0002c0002t0003g0142 | 3 | HG00438.hp2 HG02056.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(40): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | ||||||
| chr13:21050147
|
G | GATAGATA others(33): Show |
1 | a0004c0004t0045g0314 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-204-3918_-204-391 others(44): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | ||||||
| chr13:21050147
|
G | GATAGATA others(41): Show |
2 | a0002c0002t0003g0095a0002c0002t0003g0125 | 2 | HG03017.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(52): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | ||||||
| chr13:21050147
|
G | GATAGATA others(25): Show |
1 | a0001c0001t0001g0209 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-204-3918_-204-391 others(36): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | ||||||
| chr13:21050147
|
G | GATAGATA others(29): Show |
10 | a0001c0001t0001g0248a0001c0001t0001g0252a0002c0006t0004g0258others(7): Show | 10 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(7): Show |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(40): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | ||||||
| chr13:21050147
|
G | GATAGATA others(33): Show |
5 | a0001c0001t0001g0272a0002c0002t0003g0098a0003c0003t0007g0312others(2): Show | 5 | HG01074.hp1 HG01257.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(44): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | ||||||
| chr13:21050147
|
G | GATAGATA others(37): Show |
9 | a0001c0001t0001g0221a0002c0002t0003g0148a0002c0002t0003g0149others(6): Show | 9 | HG02015.hp2 HG02148.hp2 HG03927.hp1 others(6): Show |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(48): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | ||||||
| chr13:21050147
|
G | GATAGATA others(41): Show |
7 | a0001c0001t0001g0280a0001c0001t0017g0130a0001c0001t0017g0131others(4): Show | 7 | HG01361.hp1 HG02074.hp2 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(52): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | ||||||
| chr13:21050147
|
G | GATAGATA others(25): Show |
1 | a0002c0002t0003g0096 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-204-3918_-204-391 others(36): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | ||||||
| chr13:21050147
|
G | GATAGATA others(29): Show |
2 | a0001c0001t0001g0208a0001c0001t0001g0263 | 2 | HG00738.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(40): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | ||||||
| chr13:21050147
|
G | GATAGATA others(33): Show |
10 | a0001c0001t0001g0092a0001c0001t0001g0264a0001c0001t0001g0265others(7): Show | 10 | HG01106.hp1 HG01255.hp1 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(44): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | ||||||
| chr13:21050147
|
G | GATAGATA others(37): Show |
8 | a0001c0001t0001g0271a0002c0002t0003g0138a0002c0002t0003g0140others(5): Show | 8 | HG01433.hp1 HG02300.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(48): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | ||||||
| chr13:21050147
|
G | GATAGATA others(41): Show |
15 | a0001c0001t0001g0273a0001c0001t0010g0112a0002c0002t0003g0094others(12): Show | 15 | HG00621.hp1 HG01928.hp1 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(52): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | ||||||
| chr13:21050147
|
G | GATAGATA others(45): Show |
11 | a0002c0002t0003g0116a0002c0002t0003g0117a0002c0002t0003g0119others(8): Show | 11 | HG01255.hp2 HG01257.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(56): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | ||||||
| chr13:21050147
|
G | GATAGATA others(49): Show |
1 | a0002c0002t0003g0124 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-204-3918_-204-391 others(60): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | ||||||
| chr13:21050147
|
G | GATAGATA others(33): Show |
29 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0196others(26): Show | 29 | HG00423.hp1 HG00642.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(44): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | ||||||
| chr13:21050147
|
G | GATAGATA others(37): Show |
9 | a0001c0001t0001g0024a0001c0001t0001g0214a0001c0001t0001g0215others(6): Show | 9 | HG00642.hp2 HG02683.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(48): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | ||||||
| chr13:21050147
|
G | GATAGATA others(41): Show |
7 | a0001c0001t0043g0139a0002c0002t0011g0283a0002c0006t0004g0219others(4): Show | 7 | HG02809.hp1 HG02965.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(52): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | ||||||
| chr13:21050147
|
G | GATAGATA others(45): Show |
14 | a0001c0001t0003g0161a0002c0002t0003g0101a0002c0002t0003g0102others(11): Show | 14 | HG01168.hp1 HG01358.hp1 HG02074.hp1 others(11): Show |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(56): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | ||||||
| chr13:21050147
|
G | GATAGATA others(49): Show |
8 | a0001c0001t0010g0162a0001c0001t0010g0163a0002c0002t0003g0115others(5): Show | 8 | HG01261.hp1 HG01496.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(60): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | ||||||
| chr13:21050147
|
G | GATAGATA others(57): Show |
1 | a0003c0003t0007g0136 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-204-3918_-204-391 others(68): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | ||||||
| chr13:21050147
|
G | GATAGATA others(33): Show |
4 | a0001c0001t0002g0166a0001c0001t0002g0176a0001c0001t0002g0177others(1): Show | 4 | NA19004.hp2 NA19065.hp2 NA19087.hp2 others(1): Show |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(44): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | ||||||
| chr13:21050147
|
G | GATAGATA others(37): Show |
18 | a0001c0001t0001g0233a0001c0001t0001g0239a0001c0001t0001g0240others(15): Show | 19 | HG00280.hp1 HG00423.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(48): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | ||||||
| chr13:21050147
|
G | GATAGATA others(41): Show |
12 | a0001c0001t0001g0211a0001c0001t0001g0246a0002c0006t0004g0011others(9): Show | 12 | HG00597.hp2 HG02148.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(52): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | ||||||
| chr13:21050147
|
G | GATAGATA others(45): Show |
9 | a0001c0001t0001g0217a0001c0001t0002g0218a0002c0006t0004g0169others(6): Show | 9 | HG01081.hp1 HG01081.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(56): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | ||||||
| chr13:21050147
|
G | GATAGATA others(49): Show |
4 | a0001c0001t0047g0100a0002c0002t0011g0285a0002c0002t0040g0143others(1): Show | 4 | HG00735.hp2 NA18994.hp1 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(60): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | ||||||
| chr13:21050147
|
G | GATAGATA others(53): Show |
2 | a0002c0002t0003g0154a0003c0009t0008g0309 | 2 | HG02083.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(64): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | ||||||
| chr13:21050147
|
G | GATAGATA others(57): Show |
1 | a0007c0013t0007g0137 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-204-3918_-204-391 others(68): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | ||||||
| chr13:21050147
|
G | GATAGATA others(37): Show |
1 | a0001c0001t0022g0174 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-204-3918_-204-391 others(48): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | ||||||
| chr13:21050147
|
G | GATAGATA others(41): Show |
14 | a0001c0001t0001g0090a0001c0001t0001g0178a0001c0001t0001g0181others(11): Show | 14 | HG01106.hp2 HG01109.hp2 HG01515.hp1 others(11): Show |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(52): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | ||||||
| chr13:21050147
|
G | GATAGATA others(45): Show |
1 | a0002c0006t0004g0015 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-204-3918_-204-391 others(56): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | ||||||
| chr13:21050147
|
G | GATAGATA others(49): Show |
1 | a0002c0006t0004g0019 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-204-3918_-204-391 others(60): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | ||||||
| chr13:21050147
|
G | GATAGATA others(53): Show |
2 | a0001c0001t0010g0099a0003c0009t0032g0289 | 2 | HG02258.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(64): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | ||||||
| chr13:21050147
|
G | GATAGATA others(41): Show |
4 | a0002c0006t0004g0164a0003c0003t0002g0008a0003c0003t0002g0014others(1): Show | 4 | HG01074.hp2 HG03490.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(52): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | ||||||
| chr13:21050147
|
G | GATAGATA others(45): Show |
2 | a0004c0004t0001g0302a0004c0004t0005g0089 | 2 | HG01516.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-204-3918_-204-391 others(56): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | ||||||
| chr13:21050147
|
G | GATAGATA others(57): Show |
1 | a0003c0009t0009g0308 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-204-3918_-204-391 others(68): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | ||||||
| chr13:21050147
|
GATAC | G | 5 | a0002c0024t0023g0038a0003c0005t0002g0037a0003c0005t0002g0050others(2): Show | 5 | HG00639.hp1 HG00741.hp2 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.-204-3921_-204-391 others(8): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | ||||||
| chr13:21050147
|
GATACATA others(5): Show |
G | 1 | a0004c0015t0018g0042 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-204-3929_-204-391 others(16): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050147 | ||||||
| chr13:21050175
|
G | C | 1 | a0003c0032t0016g0315 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-204-3945C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050175 | ||||||
| chr13:21050199
|
AG | A | 4 | a0001c0010t0015g0003a0002c0017t0006g0004a0003c0005t0015g0005others(1): Show | 4 | NA18951.hp2 NA18986.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.-204-3970delC | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050199 | ||||||
| chr13:21050227
|
G | T | 8 | a0002c0002t0011g0283a0002c0002t0011g0284a0002c0002t0011g0285others(5): Show | 8 | HG00735.hp2 HG02809.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-204-3997C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050227 | ||||||
| chr13:21050242
|
C | T | 124 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0178others(121): Show | 124 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-204-4012G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050242 | ||||||
| chr13:21050254
|
A | G | 9 | a0002c0014t0018g0039a0002c0014t0018g0041a0002c0014t0038g0040others(6): Show | 9 | HG00639.hp1 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-204-4024T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050254 | ||||||
| chr13:21050255
|
T | C | 2 | a0005c0016t0014g0035a0005c0016t0014g0036 | 2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-204-4025A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050255 | ||||||
| chr13:21050361
|
G | GA | 76 | a0001c0001t0003g0161a0001c0001t0010g0099a0001c0001t0010g0112others(73): Show | 76 | HG00438.hp2 HG00621.hp1 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.-204-4132dupT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050361 | ||||||
| chr13:21050531
|
T | C | 1 | a0004c0015t0018g0042 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-204-4301A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050531 | ||||||
| chr13:21050604
|
C | T | 8 | a0002c0002t0011g0283a0002c0002t0011g0284a0002c0002t0011g0285others(5): Show | 8 | HG00735.hp2 HG02809.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-204-4374G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050604 | ||||||
| chr13:21050631
|
A | G | 259 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(256): Show | 260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.-204-4401T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050631 | ||||||
| chr13:21050748
|
G | A | 1 | a0004c0015t0005g0083 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-204-4518C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050748 | ||||||
| chr13:21050869
|
G | T | 4 | a0003c0003t0004g0300a0003c0003t0004g0301a0004c0004t0004g0298others(1): Show | 4 | HG02647.hp2 HG03486.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.-204-4639C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050869 | ||||||
| chr13:21050929
|
C | T | 1 | a0003c0032t0016g0315 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-204-4699G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050929 | ||||||
| chr13:21050944
|
G | A | 7 | a0001c0001t0017g0130a0001c0001t0017g0131a0002c0002t0003g0126others(4): Show | 7 | NA18946.hp1 NA18959.hp2 NA18982.hp1 others(4): Show |
intron_variant | MODIFIER | c.-204-4714C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21050944 | ||||||
| chr13:21051042
|
T | C | 2 | a0004c0004t0005g0229a0004c0004t0005g0230 | 2 | HG02735.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.-204-4812A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21051042 | ||||||
| chr13:21051052
|
T | C | 11 | a0002c0002t0011g0034a0003c0003t0025g0287a0003c0008t0046g0288others(8): Show | 11 | HG00735.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-204-4822A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21051052 | ||||||
| chr13:21051087
|
C | A | 27 | a0001c0001t0001g0024a0002c0006t0004g0011a0002c0006t0004g0012others(24): Show | 27 | HG00642.hp2 HG01243.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.-204-4857G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21051087 | ||||||
| chr13:21051092
|
G | A | 11 | a0002c0002t0011g0034a0003c0003t0025g0287a0003c0008t0046g0288others(8): Show | 11 | HG00735.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-204-4862C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21051092 | ||||||
| chr13:21051146
|
G | C | 5 | a0006c0011t0001g0079a0006c0011t0001g0080a0006c0011t0001g0081others(2): Show | 5 | HG02451.hp1 HG02895.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-204-4916C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21051146 | ||||||
| chr13:21051148
|
A | G | 8 | a0002c0002t0011g0283a0002c0002t0011g0284a0002c0002t0011g0285others(5): Show | 8 | HG00735.hp2 HG02809.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-204-4918T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21051148 | ||||||
| chr13:21051267
|
G | A | 4 | a0002c0002t0011g0283a0002c0002t0011g0284a0002c0002t0011g0285others(1): Show | 4 | HG00735.hp2 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-204-5037C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21051267 | ||||||
| chr13:21051288
|
T | G | 1 | a0007c0013t0002g0023 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-204-5058A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21051288 | ||||||
| chr13:21051315
|
A | G | 8 | a0002c0002t0011g0283a0002c0002t0011g0284a0002c0002t0011g0285others(5): Show | 8 | HG00735.hp2 HG02809.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-204-5085T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21051315 | ||||||
| chr13:21051334
|
C | T | 122 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0178others(119): Show | 123 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.-204-5104G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21051334 | ||||||
| chr13:21051382
|
A | G | 5 | a0003c0009t0008g0309a0003c0009t0009g0308a0003c0009t0016g0307others(2): Show | 5 | HG01884.hp1 HG02258.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-204-5152T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21051382 | ||||||
| chr13:21051535
|
T | C | 2 | a0003c0003t0002g0170a0003c0003t0002g0231 | 2 | HG01070.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-204-5305A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21051535 | ||||||
| chr13:21051566
|
C | T | 5 | a0003c0007t0008g0044a0003c0007t0008g0045a0003c0007t0008g0046others(2): Show | 5 | HG02257.hp2 HG02559.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-204-5336G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21051566 | ||||||
| chr13:21051739
|
G | C | 8 | a0002c0002t0011g0283a0002c0002t0011g0284a0002c0002t0011g0285others(5): Show | 8 | HG00735.hp2 HG02809.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-204-5509C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21051739 | ||||||
| chr13:21051778
|
G | A | 8 | a0002c0002t0011g0283a0002c0002t0011g0284a0002c0002t0011g0285others(5): Show | 8 | HG00735.hp2 HG02809.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-204-5548C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21051778 | ||||||
| chr13:21051792
|
CTAAAAGT others(7): Show |
C | 1 | a0001c0001t0022g0171 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-204-5576_-204-556 others(18): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21051792 | ||||||
| chr13:21051865
|
GA | G | 76 | a0001c0001t0003g0161a0001c0001t0010g0099a0001c0001t0010g0112others(73): Show | 76 | HG00438.hp2 HG00621.hp1 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.-204-5636delT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21051865 | ||||||
| chr13:21051920
|
G | A | 1 | a0001c0001t0001g0232 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-204-5690C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21051920 | ||||||
| chr13:21051955
|
T | A | 1 | a0002c0002t0024g0156 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-204-5725A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21051955 | ||||||
| chr13:21052013
|
G | A | 14 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0264others(11): Show | 14 | HG00738.hp1 HG01074.hp1 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.-204-5783C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21052013 | ||||||
| chr13:21052348
|
C | G | 5 | a0003c0009t0008g0309a0003c0009t0009g0308a0003c0009t0016g0307others(2): Show | 5 | HG01884.hp1 HG02258.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-204-6118G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21052348 | ||||||
| chr13:21052734
|
A | G | 37 | a0001c0001t0001g0024a0002c0002t0011g0034a0002c0002t0011g0283others(34): Show | 37 | HG00642.hp2 HG00735.hp1 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.-204-6504T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21052734 | ||||||
| chr13:21052773
|
GTGCCTGC others(3): Show |
G | 22 | a0001c0001t0001g0024a0002c0006t0004g0011a0002c0006t0004g0012others(19): Show | 22 | HG00642.hp2 HG01358.hp1 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.-204-6553_-204-654 others(14): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21052773 | ||||||
| chr13:21052795
|
T | C | 2 | a0004c0004t0004g0298a0004c0004t0014g0299 | 2 | HG02647.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-204-6565A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21052795 | ||||||
| chr13:21052894
|
G | A | 1 | a0003c0005t0002g0043 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-204-6664C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21052894 | ||||||
| chr13:21052947
|
G | C | 259 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(256): Show | 260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.-204-6717C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21052947 | ||||||
| chr13:21052988
|
G | A | 222 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0178others(219): Show | 223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.-204-6758C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21052988 | ||||||
| chr13:21053041
|
C | G | 21 | a0001c0001t0001g0024a0002c0006t0004g0011a0002c0006t0004g0012others(18): Show | 21 | HG00642.hp2 HG01358.hp1 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.-204-6811G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21053041 | ||||||
| chr13:21053213
|
A | G | 37 | a0001c0001t0001g0024a0002c0002t0011g0034a0002c0002t0011g0283others(34): Show | 37 | HG00642.hp2 HG00735.hp1 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.-204-6983T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21053213 | ||||||
| chr13:21053220
|
T | A | 1 | a0003c0032t0016g0315 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-204-6990A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21053220 | ||||||
| chr13:21053233
|
C | CA | 61 | a0001c0001t0001g0024a0001c0001t0001g0092a0001c0001t0001g0233others(58): Show | 61 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.-204-7004dupT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21053233 | ||||||
| chr13:21053233
|
CA | C | 88 | a0001c0001t0002g0166a0001c0001t0003g0161a0001c0001t0006g0168others(85): Show | 88 | HG00438.hp2 HG00738.hp2 HG01070.hp1 others(85): Show |
intron_variant | MODIFIER | c.-204-7004delT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21053233 | ||||||
| chr13:21053414
|
C | T | 1 | a0004c0004t0028g0025 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-204-7184G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21053414 | ||||||
| chr13:21053425
|
T | C | 222 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0178others(219): Show | 223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.-204-7195A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21053425 | ||||||
| chr13:21053439
|
G | A | 1 | a0007c0013t0007g0137 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-204-7209C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21053439 | ||||||
| chr13:21053446
|
G | A | 2 | a0003c0003t0025g0287a0003c0008t0046g0288 | 2 | HG02055.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.-204-7216C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21053446 | ||||||
| chr13:21053492
|
C | T | 2 | a0004c0004t0005g0290a0004c0004t0005g0311 | 2 | HG02622.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-204-7262G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21053492 | ||||||
| chr13:21053503
|
G | A | 1 | a0004c0015t0005g0083 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-204-7273C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21053503 | ||||||
| chr13:21053518
|
A | C | 1 | a0002c0002t0003g0138 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-204-7288T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21053518 | ||||||
| chr13:21053716
|
A | G | 259 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(256): Show | 260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.-204-7486T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21053716 | ||||||
| chr13:21053748
|
A | C | 4 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0241others(1): Show | 4 | NA18945.hp1 NA18950.hp2 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.-204-7518T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21053748 | ||||||
| chr13:21053868
|
G | A | 26 | a0001c0001t0001g0024a0002c0002t0011g0283a0002c0002t0011g0284others(23): Show | 26 | HG00642.hp2 HG00735.hp2 HG01358.hp1 others(23): Show |
intron_variant | MODIFIER | c.-205+7478C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21053868 | ||||||
| chr13:21053930
|
C | T | 265 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(262): Show | 266 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.-205+7416G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21053930 | ||||||
| chr13:21053935
|
G | C | 4 | a0002c0002t0011g0283a0002c0002t0011g0284a0002c0002t0011g0285others(1): Show | 4 | HG00735.hp2 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-205+7411C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21053935 | ||||||
| chr13:21053948
|
T | G | 1 | a0001c0001t0004g0276 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-205+7398A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21053948 | ||||||
| chr13:21053949
|
G | T | 1 | a0001c0001t0004g0276 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-205+7397C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21053949 | ||||||
| chr13:21053952
|
T | G | 1 | a0001c0001t0004g0276 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-205+7394A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21053952 | ||||||
| chr13:21053955
|
G | C | 22 | a0001c0001t0003g0161a0001c0001t0010g0162a0001c0001t0010g0163others(19): Show | 22 | HG00438.hp2 HG02015.hp2 HG02056.hp1 others(19): Show |
intron_variant | MODIFIER | c.-205+7391C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21053955 | ||||||
| chr13:21053992
|
T | C | 2 | a0002c0002t0003g0157a0002c0002t0003g0158 | 2 | HG02735.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-205+7354A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21053992 | ||||||
| chr13:21054026
|
G | A | 4 | a0002c0002t0011g0283a0002c0002t0011g0284a0002c0002t0011g0285others(1): Show | 4 | HG00735.hp2 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-205+7320C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054026 | ||||||
| chr13:21054142
|
T | C | 264 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(261): Show | 265 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.-205+7204A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054142 | ||||||
| chr13:21054505
|
C | A | 11 | a0002c0002t0011g0034a0003c0003t0025g0287a0003c0008t0046g0288others(8): Show | 11 | HG00735.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-205+6841G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054505 | ||||||
| chr13:21054588
|
C | T | 11 | a0002c0002t0011g0034a0003c0003t0025g0287a0003c0008t0046g0288others(8): Show | 11 | HG00735.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-205+6758G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054588 | ||||||
| chr13:21054661
|
C | T | 233 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0178others(230): Show | 234 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.-205+6685G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054661 | ||||||
| chr13:21054671
|
T | C | 2 | a0003c0003t0025g0287a0003c0008t0046g0288 | 2 | HG02055.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.-205+6675A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054671 | ||||||
| chr13:21054734
|
T | TAAACAGA | 38 | a0001c0001t0001g0024a0002c0002t0011g0034a0002c0002t0011g0283others(35): Show | 38 | HG00642.hp2 HG00735.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.-205+6611_-205+661 others(11): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054734 | ||||||
| chr13:21054734
|
T | TGAACAGA | 222 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0178others(219): Show | 223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.-205+6611_-205+661 others(11): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054734 | ||||||
| chr13:21054803
|
G | T | 259 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(256): Show | 260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.-205+6543C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054803 | ||||||
| chr13:21054804
|
T | G | 222 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0178others(219): Show | 223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.-205+6542A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054804 | ||||||
| chr13:21054860
|
T | C | 2 | a0001c0001t0001g0274a0001c0001t0001g0275 | 2 | HG01496.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.-205+6486A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054860 | ||||||
| chr13:21054884
|
G | C | 8 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0241others(5): Show | 8 | NA18945.hp1 NA18950.hp2 NA18970.hp1 others(5): Show |
intron_variant | MODIFIER | c.-205+6462C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054884 | ||||||
| chr13:21054896
|
A | T | 1 | a0001c0001t0012g0165 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-205+6450T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054896 | ||||||
| chr13:21054897
|
C | G | 1 | a0001c0001t0012g0165 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-205+6449G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054897 | ||||||
| chr13:21054899
|
A | G | 1 | a0001c0001t0012g0165 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-205+6447T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054899 | ||||||
| chr13:21054901
|
C | G | 1 | a0001c0001t0012g0165 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-205+6445G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054901 | ||||||
| chr13:21054903
|
G | C | 1 | a0001c0030t0001g0091 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-205+6443C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054903 | ||||||
| chr13:21054910
|
T | G | 1 | a0001c0001t0012g0165 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-205+6436A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054910 | ||||||
| chr13:21054912
|
T | G | 1 | a0001c0001t0012g0165 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-205+6434A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054912 | ||||||
| chr13:21054915
|
T | C | 1 | a0001c0001t0012g0165 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-205+6431A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054915 | ||||||
| chr13:21054917
|
T | C | 1 | a0001c0001t0012g0165 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-205+6429A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054917 | ||||||
| chr13:21054918
|
C | G | 1 | a0001c0001t0012g0165 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-205+6428G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054918 | ||||||
| chr13:21054924
|
C | A | 1 | a0001c0001t0012g0165 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-205+6422G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054924 | ||||||
| chr13:21054925
|
C | G | 1 | a0001c0001t0012g0165 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-205+6421G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054925 | ||||||
| chr13:21054926
|
C | G | 1 | a0001c0001t0012g0165 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-205+6420G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054926 | ||||||
| chr13:21054927
|
A | T | 1 | a0001c0001t0012g0165 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-205+6419T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054927 | ||||||
| chr13:21054928
|
C | G | 1 | a0001c0001t0012g0165 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-205+6418G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054928 | ||||||
| chr13:21054929
|
C | A | 1 | a0001c0001t0012g0165 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-205+6417G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054929 | ||||||
| chr13:21054930
|
A | G | 1 | a0001c0001t0012g0165 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-205+6416T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054930 | ||||||
| chr13:21054931
|
T | G | 1 | a0001c0001t0012g0165 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-205+6415A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054931 | ||||||
| chr13:21054937
|
G | C | 1 | a0001c0001t0012g0165 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-205+6409C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054937 | ||||||
| chr13:21054939
|
C | T | 1 | a0001c0001t0012g0165 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-205+6407G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054939 | ||||||
| chr13:21054966
|
G | T | 1 | a0001c0001t0012g0165 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-205+6380C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054966 | ||||||
| chr13:21054967
|
T | G | 1 | a0001c0001t0012g0165 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-205+6379A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054967 | ||||||
| chr13:21054968
|
C | T | 1 | a0001c0001t0012g0165 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-205+6378G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054968 | ||||||
| chr13:21054986
|
T | C | 26 | a0001c0001t0001g0024a0002c0002t0011g0283a0002c0002t0011g0284others(23): Show | 26 | HG00642.hp2 HG00735.hp2 HG01358.hp1 others(23): Show |
intron_variant | MODIFIER | c.-205+6360A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054986 | ||||||
| chr13:21054987
|
G | GT | 26 | a0001c0001t0001g0024a0002c0002t0011g0283a0002c0002t0011g0284others(23): Show | 26 | HG00642.hp2 HG00735.hp2 HG01358.hp1 others(23): Show |
intron_variant | MODIFIER | c.-205+6358_-205+635 others(5): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21054987 | ||||||
| chr13:21055063
|
T | C | 1 | a0004c0015t0018g0042 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-205+6283A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21055063 | ||||||
| chr13:21055064
|
A | G | 1 | a0003c0036t0009g0310 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-205+6282T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21055064 | ||||||
| chr13:21055065
|
G | A | 220 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0178others(217): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.-205+6281C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21055065 | ||||||
| chr13:21055238
|
A | G | 11 | a0002c0002t0011g0034a0003c0003t0025g0287a0003c0008t0046g0288others(8): Show | 11 | HG00735.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-205+6108T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21055238 | ||||||
| chr13:21055250
|
C | T | 259 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(256): Show | 260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.-205+6096G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21055250 | ||||||
| chr13:21055271
|
A | G | 2 | a0004c0004t0019g0026a0004c0004t0028g0025 | 2 | NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-205+6075T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21055271 | ||||||
| chr13:21055308
|
TA | T | 221 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0178others(218): Show | 222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.-205+6037delT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21055308 | ||||||
| chr13:21055381
|
C | T | 1 | a0002c0002t0003g0095 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-205+5965G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21055381 | ||||||
| chr13:21055724
|
C | T | 18 | a0001c0001t0001g0024a0002c0006t0004g0011a0002c0006t0004g0012others(15): Show | 18 | HG00642.hp2 HG01358.hp1 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.-205+5622G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21055724 | ||||||
| chr13:21055810
|
A | C | 1 | a0001c0001t0004g0276 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-205+5536T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21055810 | ||||||
| chr13:21055844
|
C | T | 26 | a0001c0001t0001g0024a0002c0002t0011g0283a0002c0002t0011g0284others(23): Show | 26 | HG00642.hp2 HG00735.hp2 HG01358.hp1 others(23): Show |
intron_variant | MODIFIER | c.-205+5502G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21055844 | ||||||
| chr13:21055901
|
T | C | 1 | a0002c0002t0006g0159 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-205+5445A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21055901 | ||||||
| chr13:21055997
|
G | A | 31 | a0001c0001t0001g0092a0001c0001t0001g0248a0001c0001t0001g0249others(28): Show | 31 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(28): Show |
intron_variant | MODIFIER | c.-205+5349C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21055997 | ||||||
| chr13:21056071
|
G | T | 76 | a0001c0001t0003g0161a0001c0001t0010g0099a0001c0001t0010g0112others(73): Show | 76 | HG00438.hp2 HG00621.hp1 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.-205+5275C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21056071 | ||||||
| chr13:21056096
|
T | C | 1 | a0003c0036t0009g0310 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-205+5250A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21056096 | ||||||
| chr13:21056131
|
T | C | 76 | a0001c0001t0003g0161a0001c0001t0010g0099a0001c0001t0010g0112others(73): Show | 76 | HG00438.hp2 HG00621.hp1 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.-205+5215A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21056131 | ||||||
| chr13:21056150
|
G | C | 3 | a0002c0034t0035g0027a0004c0004t0019g0026a0004c0004t0028g0025 | 3 | HG02965.hp1 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-205+5196C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21056150 | ||||||
| chr13:21056153
|
G | A | 76 | a0001c0001t0003g0161a0001c0001t0010g0099a0001c0001t0010g0112others(73): Show | 76 | HG00438.hp2 HG00621.hp1 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.-205+5193C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21056153 | ||||||
| chr13:21056276
|
T | C | 1 | a0012c0022t0004g0007 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-205+5070A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21056276 | ||||||
| chr13:21056286
|
G | A | 76 | a0001c0001t0003g0161a0001c0001t0010g0099a0001c0001t0010g0112others(73): Show | 76 | HG00438.hp2 HG00621.hp1 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.-205+5060C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21056286 | ||||||
| chr13:21056409
|
T | C | 1 | a0003c0023t0002g0006 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-205+4937A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21056409 | ||||||
| chr13:21056765
|
G | C | 1 | a0003c0008t0009g0088 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-205+4581C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21056765 | ||||||
| chr13:21056850
|
A | G | 259 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(256): Show | 260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.-205+4496T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21056850 | ||||||
| chr13:21056927
|
C | T | 1 | a0012c0022t0004g0007 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-205+4419G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21056927 | ||||||
| chr13:21057011
|
A | G | 4 | a0002c0002t0011g0283a0002c0002t0011g0284a0002c0002t0011g0285others(1): Show | 4 | HG00735.hp2 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-205+4335T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21057011 | ||||||
| chr13:21057041
|
C | T | 1 | a0002c0002t0003g0094 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-205+4305G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21057041 | ||||||
| chr13:21057060
|
G | A | 76 | a0001c0001t0003g0161a0001c0001t0010g0099a0001c0001t0010g0112others(73): Show | 76 | HG00438.hp2 HG00621.hp1 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.-205+4286C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21057060 | ||||||
| chr13:21057105
|
C | A | 4 | a0002c0002t0011g0283a0002c0002t0011g0284a0002c0002t0011g0285others(1): Show | 4 | HG00735.hp2 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-205+4241G>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21057105 | ||||||
| chr13:21057359
|
C | G | 4 | a0002c0002t0011g0283a0002c0002t0011g0284a0002c0002t0011g0285others(1): Show | 4 | HG00735.hp2 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-205+3987G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21057359 | ||||||
| chr13:21057564
|
C | T | 2 | a0003c0003t0025g0287a0003c0008t0046g0288 | 2 | HG02055.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.-205+3782G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21057564 | ||||||
| chr13:21057635
|
T | TA | 101 | a0001c0001t0001g0024a0001c0001t0003g0161a0001c0001t0010g0099others(98): Show | 101 | HG00438.hp2 HG00621.hp1 HG00642.hp2 others(98): Show |
intron_variant | MODIFIER | c.-205+3710dupT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21057635 | ||||||
| chr13:21057636
|
A | T | 121 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0178others(118): Show | 122 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.-205+3710T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21057636 | ||||||
| chr13:21057644
|
A | T | 1 | a0012c0022t0004g0007 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-205+3702T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21057644 | ||||||
| chr13:21057669
|
G | A | 5 | a0002c0014t0018g0039a0002c0014t0018g0041a0002c0014t0038g0040others(2): Show | 5 | HG00639.hp1 HG02451.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-205+3677C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21057669 | ||||||
| chr13:21057757
|
G | C | 7 | a0002c0002t0011g0034a0003c0009t0026g0029a0003c0009t0031g0031others(4): Show | 7 | HG00735.hp1 HG02559.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-205+3589C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21057757 | ||||||
| chr13:21057805
|
TA | T | 313 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(310): Show | 314 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.-205+3540delT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21057805 | ||||||
| chr13:21057833
|
G | A | 3 | a0002c0002t0010g0281a0002c0028t0041g0282a0003c0008t0009g0088 | 3 | HG01243.hp2 HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-205+3513C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21057833 | ||||||
| chr13:21057991
|
C | T | 5 | a0002c0014t0018g0039a0002c0014t0018g0041a0002c0014t0038g0040others(2): Show | 5 | HG00639.hp1 HG02451.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-205+3355G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21057991 | ||||||
| chr13:21058089
|
G | A | 146 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0178others(143): Show | 147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.-205+3257C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21058089 | ||||||
| chr13:21058188
|
T | C | 2 | a0005c0016t0014g0035a0005c0016t0014g0036 | 2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-205+3158A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21058188 | ||||||
| chr13:21058333
|
C | T | 11 | a0002c0002t0011g0034a0003c0003t0025g0287a0003c0008t0046g0288others(8): Show | 11 | HG00735.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-205+3013G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21058333 | ||||||
| chr13:21058596
|
T | C | 1 | a0012c0022t0004g0007 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-205+2750A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21058596 | ||||||
| chr13:21058605
|
C | T | 2 | a0004c0019t0020g0305a0004c0019t0020g0306 | 2 | HG01243.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-205+2741G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21058605 | ||||||
| chr13:21058772
|
G | T | 76 | a0001c0001t0003g0161a0001c0001t0010g0099a0001c0001t0010g0112others(73): Show | 76 | HG00438.hp2 HG00621.hp1 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.-205+2574C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21058772 | ||||||
| chr13:21058941
|
G | GA | 12 | a0002c0002t0011g0034a0003c0003t0025g0287a0003c0008t0046g0288others(9): Show | 12 | HG00735.hp1 HG02055.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-205+2404dupT | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21058941 | ||||||
| chr13:21058979
|
T | C | 1 | a0001c0001t0001g0277 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-205+2367A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21058979 | ||||||
| chr13:21059013
|
A | G | 1 | a0003c0005t0002g0037 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-205+2333T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21059013 | ||||||
| chr13:21059166
|
T | G | 1 | a0002c0002t0003g0160 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-205+2180A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21059166 | ||||||
| chr13:21059170
|
T | C | 2 | a0005c0016t0014g0035a0005c0016t0014g0036 | 2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-205+2176A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21059170 | ||||||
| chr13:21059233
|
T | A | 76 | a0001c0001t0003g0161a0001c0001t0010g0099a0001c0001t0010g0112others(73): Show | 76 | HG00438.hp2 HG00621.hp1 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.-205+2113A>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21059233 | ||||||
| chr13:21059308
|
A | G | 180 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(177): Show | 181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.-205+2038T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21059308 | ||||||
| chr13:21059345
|
C | T | 7 | a0002c0002t0011g0034a0003c0009t0026g0029a0003c0009t0031g0031others(4): Show | 7 | HG00735.hp1 HG02559.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-205+2001G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21059345 | ||||||
| chr13:21059411
|
T | C | 86 | a0001c0001t0003g0161a0001c0001t0010g0099a0001c0001t0010g0112others(83): Show | 86 | HG00438.hp2 HG00621.hp1 HG00735.hp1 others(83): Show |
intron_variant | MODIFIER | c.-205+1935A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21059411 | ||||||
| chr13:21059458
|
G | A | 1 | a0001c0001t0003g0161 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-205+1888C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21059458 | ||||||
| chr13:21059506
|
A | G | 1 | a0002c0006t0004g0164 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-205+1840T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21059506 | ||||||
| chr13:21059508
|
A | C | 1 | a0002c0006t0004g0164 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-205+1838T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21059508 | ||||||
| chr13:21059516
|
A | ACAGGAGA others(15): Show |
1 | a0002c0006t0004g0164 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-205+1829_-205+183 others(26): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21059516 | ||||||
| chr13:21059518
|
C | G | 1 | a0002c0006t0004g0164 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-205+1828G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21059518 | ||||||
| chr13:21059542
|
C | T | 1 | a0002c0006t0004g0164 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-205+1804G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21059542 | ||||||
| chr13:21059545
|
A | T | 1 | a0002c0006t0004g0164 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-205+1801T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21059545 | ||||||
| chr13:21059553
|
C | G | 1 | a0002c0006t0004g0164 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-205+1793G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21059553 | ||||||
| chr13:21059555
|
A | T | 1 | a0002c0006t0004g0164 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-205+1791T>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21059555 | ||||||
| chr13:21059679
|
T | G | 2 | a0001c0001t0010g0162a0001c0001t0010g0163 | 2 | NA18971.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.-205+1667A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21059679 | ||||||
| chr13:21059686
|
T | C | 2 | a0004c0019t0020g0305a0004c0019t0020g0306 | 2 | HG01243.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-205+1660A>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21059686 | ||||||
| chr13:21059720
|
C | G | 9 | a0002c0002t0011g0034a0003c0009t0026g0029a0003c0009t0031g0031others(6): Show | 9 | HG00735.hp1 HG02559.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-205+1626G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21059720 | ||||||
| chr13:21060047
|
AG | A | 5 | a0003c0009t0008g0309a0003c0009t0009g0308a0003c0009t0016g0307others(2): Show | 5 | HG01884.hp1 HG02258.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-205+1298delC | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21060047 | ||||||
| chr13:21060193
|
C | G | 169 | a0001c0001t0001g0024a0001c0001t0001g0178a0001c0001t0001g0181others(166): Show | 170 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.-205+1153G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21060193 | ||||||
| chr13:21060243
|
C | T | 1 | a0003c0009t0032g0289 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-205+1103G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21060243 | ||||||
| chr13:21060324
|
G | T | 2 | a0003c0003t0025g0287a0003c0008t0046g0288 | 2 | HG02055.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.-205+1022C>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21060324 | ||||||
| chr13:21060353
|
A | C | 1 | a0012c0022t0004g0007 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-205+993T>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21060353 | ||||||
| chr13:21060504
|
C | T | 1 | a0003c0023t0002g0006 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-205+842G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21060504 | ||||||
| chr13:21060585
|
C | T | 3 | a0001c0010t0015g0003a0002c0017t0006g0004a0003c0005t0015g0005 | 3 | NA18951.hp2 NA18986.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.-205+761G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21060585 | ||||||
| chr13:21060613
|
G | C | 82 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0003g0161others(79): Show | 82 | HG00438.hp2 HG00621.hp1 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.-205+733C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21060613 | ||||||
| chr13:21060631
|
A | G | 82 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0003g0161others(79): Show | 82 | HG00438.hp2 HG00621.hp1 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.-205+715T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21060631 | ||||||
| chr13:21060657
|
G | C | 1 | a0002c0002t0023g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-205+689C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21060657 | ||||||
| chr13:21060676
|
C | G | 1 | a0002c0002t0023g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-205+670G>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21060676 | ||||||
| chr13:21060844
|
G | A | 2 | a0001c0001t0001g0279a0001c0001t0001g0280 | 2 | HG02056.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.-205+502C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21060844 | ||||||
| chr13:21060861
|
G | A | 2 | a0002c0002t0010g0281a0002c0028t0041g0282 | 2 | HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-205+485C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21060861 | ||||||
| chr13:21060901
|
A | G | 314 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0092others(311): Show | 315 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.-205+445T>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21060901 | ||||||
| chr13:21060910
|
T | G | 226 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0178others(223): Show | 227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.-205+436A>C | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21060910 | ||||||
| chr13:21060926
|
G | A | 4 | a0002c0002t0011g0283a0002c0002t0011g0284a0002c0002t0011g0285others(1): Show | 4 | HG00735.hp2 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-205+420C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21060926 | ||||||
| chr13:21060973
|
G | A | 1 | a0004c0004t0005g0311 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-205+373C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21060973 | ||||||
| chr13:21061004
|
G | A | 29 | a0002c0002t0011g0283a0002c0002t0011g0284a0002c0002t0011g0285others(26): Show | 29 | HG00735.hp2 HG01243.hp1 HG01433.hp2 others(26): Show |
intron_variant | MODIFIER | c.-205+342C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21061004 | ||||||
| chr13:21061015
|
G | GC | 25 | a0003c0003t0004g0300a0003c0003t0004g0301a0003c0003t0025g0287others(22): Show | 25 | HG01243.hp1 HG01433.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.-205+330dupG | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21061015 | ||||||
| chr13:21061124
|
G | A | 3 | a0003c0003t0007g0312a0003c0003t0007g0313a0004c0004t0045g0314 | 3 | HG01257.hp2 HG02738.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-205+222C>T | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21061124 | ||||||
| chr13:21061244
|
G | C | 1 | a0003c0032t0016g0315 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-205+102C>G | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21061244 | ||||||
| chr13:21061321
|
C | T | 1 | a0004c0004t0005g0002 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-205+25G>A | LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | 21061321 |