Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 3987 |
|---|---|
| ensemblid | ENSG00000169756.17 |
| hgncid | 6616 |
| symbol | LIMS1 |
| name | LIM zinc finger domain containing 1 |
| refseq_nuc | NM_001193483.3 |
| refseq_prot | NP_001180412.1 |
| ensembl_nuc | ENST00000544547.6 |
| ensembl_prot | ENSP00000437912.1 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 108534470 |
| end | 108687246 |
| strand | + |
| ver | v1.2 |
| region | chr2:108534470-108687246 |
| region5000 | chr2:108529470-108692246 |
| regionname0 | LIMS1_chr2_108534470_108687246 |
| regionname5000 | LIMS1_chr2_108529470_108692246 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 337 | 242 | 80 | 44 | 63 | 12 | 41 | 59 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| a0002 | 0/0 | 337 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| a0003 | 0/0 | 337 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| a0004 | 0/0 | 337 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 1014 | 137 | 57 | 30 | 21 | 6 | 22 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| c0002 | 0/1 | 1014 | 103 | 21 | 14 | 42 | 6 | 19 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| c0003 | 0/0 | 1014 | 2 | 2 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| c0004 | 0/0 | 1014 | 2 | 2 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| c0005 | 0/0 | 1014 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| c0006 | 0/0 | 1014 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| 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 | 3342 | 63 | 9 | 12 | 25 | 6 | 10 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| t0002 | 0/0 | 3342 | 51 | 20 | 8 | 12 | 2 | 9 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| t0003 | 0/0 | 3341 | 44 | 24 | 10 | 6 | 2 | 2 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| t0004 | 0/0 | 3342 | 21 | 1 | 0 | 11 | 0 | 9 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| t0005 | 0/0 | 3343 | 11 | 1 | 7 | 0 | 0 | 3 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| t0006 | 0/0 | 3342 | 9 | 0 | 3 | 0 | 2 | 4 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| t0007 | 0/0 | 3341 | 5 | 5 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| t0008 | 0/0 | 3341 | 4 | 4 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| t0009 | 0/0 | 3341 | 4 | 0 | 1 | 3 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| t0010 | 1/0 | 3341 | 4 | 3 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| t0011 | 0/0 | 3341 | 4 | 0 | 0 | 1 | 0 | 3 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| t0012 | 0/0 | 3342 | 3 | 2 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| t0013 | 0/0 | 3342 | 2 | 2 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| t0014 | 0/0 | 3341 | 2 | 2 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| t0015 | 0/0 | 3340 | 2 | 1 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| t0016 | 0/0 | 3342 | 2 | 0 | 0 | 2 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| t0017 | 0/0 | 3342 | 2 | 2 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| t0018 | 0/0 | 3342 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| t0019 | 0/0 | 3342 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| t0020 | 0/0 | 3342 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| t0021 | 0/0 | 3342 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| t0022 | 0/0 | 3342 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| t0023 | 0/0 | 3341 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| t0024 | 0/0 | 3342 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| t0025 | 0/0 | 3342 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| t0026 | 0/0 | 3342 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| t0027 | 0/0 | 3341 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| t0028 | 0/0 | 3341 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| t0029 | 0/0 | 3341 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| t0030 | 0/0 | 3342 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| 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 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0012 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0166 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1014 | 137 | 57 | 30 | 21 | 6 | 22 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| a0001c0002 | 0/1 | 1014 | 103 | 21 | 14 | 42 | 6 | 19 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| a0001c0004 | 0/0 | 1014 | 2 | 2 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| a0002c0003 | 0/0 | 1014 | 2 | 2 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| a0003c0005 | 0/0 | 1014 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| a0004c0006 | 0/0 | 1014 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 4355 | 51 | 20 | 8 | 12 | 2 | 9 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| a0001c0001t0003 | 0/0 | 4354 | 44 | 24 | 10 | 6 | 2 | 2 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| a0001c0001t0005 | 0/0 | 4356 | 11 | 1 | 7 | 0 | 0 | 3 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| a0001c0001t0006 | 0/0 | 4355 | 9 | 0 | 3 | 0 | 2 | 4 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| a0001c0001t0010 | 1/0 | 4354 | 4 | 3 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| a0001c0001t0011 | 0/0 | 4354 | 4 | 0 | 0 | 1 | 0 | 3 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| a0001c0001t0014 | 0/0 | 4354 | 2 | 2 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| a0001c0001t0015 | 0/0 | 4353 | 2 | 1 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| a0001c0001t0017 | 0/0 | 4355 | 2 | 2 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| a0001c0001t0019 | 0/0 | 4355 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| a0001c0001t0020 | 0/0 | 4355 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| a0001c0001t0021 | 0/0 | 4355 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| a0001c0001t0022 | 0/0 | 4355 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| a0001c0001t0023 | 0/0 | 4354 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| a0001c0001t0024 | 0/0 | 4355 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| a0001c0001t0028 | 0/0 | 4354 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| a0001c0001t0029 | 0/0 | 4354 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| a0001c0002t0001 | 0/1 | 4355 | 62 | 9 | 12 | 24 | 6 | 10 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| a0001c0002t0004 | 0/0 | 4355 | 20 | 1 | 0 | 11 | 0 | 8 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| a0001c0002t0007 | 0/0 | 4354 | 5 | 5 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| a0001c0002t0008 | 0/0 | 4354 | 4 | 4 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| a0001c0002t0009 | 0/0 | 4354 | 4 | 0 | 1 | 3 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| a0001c0002t0012 | 0/0 | 4355 | 3 | 2 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| a0001c0002t0016 | 0/0 | 4355 | 2 | 0 | 0 | 2 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| a0001c0002t0025 | 0/0 | 4355 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| a0001c0002t0027 | 0/0 | 4354 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| a0001c0002t0030 | 0/0 | 4355 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| a0001c0004t0013 | 0/0 | 4355 | 2 | 2 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| a0002c0003t0018 | 0/0 | 4355 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| a0002c0003t0026 | 0/0 | 4355 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| a0003c0005t0001 | 0/0 | 4355 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| a0004c0006t0004 | 0/0 | 4355 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | copy fasta | chr2 | 108529470 | 108692246 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0003g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0005g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0005g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0005g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0005g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0005g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0005g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0005g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0005g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0005g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0005g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0005g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0006g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0006g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0006g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0006g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0006g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0006g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0006g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0006g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0006g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0010g0166 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0010g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0010g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0010g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0011g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0011g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0011g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0011g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0014g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0014g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0015g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0015g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0017g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0017g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0019g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0020g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0021g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0022g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0023g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0024g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0028g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0001t0029g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0012 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0004g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0004g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0004g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0004g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0004g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0004g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0004g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0004g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0004g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0004g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0004g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0004g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0004g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0007g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0007g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0007g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0007g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0007g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0008g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0008g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0008g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0008g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0009g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0009g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0009g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0009g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0012g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0012g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0012g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0016g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0016g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0025g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0027g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0002t0030g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0004t0013g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0001c0004t0013g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0002c0003t0018g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0002c0003t0026g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0003c0005t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| a0004c0006t0004g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0030 | EUR | GBR | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0106 | EUR | GBR | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG00140 | hp1 | a0001 | c0001 | t0006 | g0171 | EUR | GBR | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0061 | EUR | GBR | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0062 | EUR | FIN | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG00280 | hp2 | a0001 | c0001 | t0006 | g0170 | EUR | FIN | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0137 | EUR | FIN | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0010 | EUR | FIN | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0008 | AMR | PUR | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0188 | AMR | PUR | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG00741 | hp1 | a0001 | c0001 | t0005 | g0172 | AMR | PUR | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG00741 | hp2 | a0001 | c0001 | t0005 | g0077 | AMR | PUR | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0040 | AMR | PUR | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG01070 | hp2 | a0001 | c0001 | t0005 | g0165 | AMR | PUR | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0192 | AMR | PUR | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG01099 | hp1 | a0001 | c0001 | t0005 | g0164 | AMR | PUR | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0066 | AMR | PUR | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG01106 | hp2 | a0001 | c0001 | t0006 | g0177 | AMR | PUR | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0009 | AMR | PUR | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0129 | AMR | PUR | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0097 | AMR | PUR | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0015 | AMR | PUR | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0028 | AMR | PUR | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0107 | AMR | PUR | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG01169 | hp2 | a0001 | c0002 | t0027 | g0016 | AMR | PUR | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG01175 | hp1 | a0001 | c0001 | t0005 | g0180 | AMR | PUR | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0092 | AMR | PUR | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0017 | AMR | PUR | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG01192 | hp2 | a0001 | c0001 | t0006 | g0178 | AMR | PUR | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0143 | AMR | PUR | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG01243 | hp2 | a0001 | c0001 | t0021 | g0120 | AMR | PUR | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0014 | AMR | CLM | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG01256 | hp2 | a0001 | c0001 | t0023 | g0176 | AMR | CLM | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG01257 | hp1 | a0001 | c0001 | t0005 | g0163 | AMR | CLM | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0146 | AMR | CLM | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0145 | AMR | CLM | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG01258 | hp2 | a0001 | c0001 | t0006 | g0175 | AMR | CLM | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG01261 | hp1 | a0001 | c0001 | t0005 | g0169 | AMR | CLM | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG01261 | hp2 | a0001 | c0002 | t0009 | g0080 | AMR | CLM | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0058 | AMR | CLM | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0200 | AMR | CLM | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0190 | AMR | CLM | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0110 | AMR | CLM | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0047 | AMR | CLM | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0198 | AMR | CLM | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0202 | AFR | ACB | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0147 | AFR | ACB | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG01891 | hp1 | a0001 | c0001 | t0029 | g0186 | AFR | ACB | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0206 | AFR | ACB | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0161 | AMR | PEL | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0052 | AMR | PEL | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0076 | AMR | PEL | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0064 | AMR | PEL | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0042 | EAS | KHV | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG02040 | hp2 | a0001 | c0002 | t0012 | g0006 | EAS | KHV | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0212 | AFR | ACB | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0213 | AFR | ACB | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG02056 | hp1 | a0001 | c0001 | t0011 | g0149 | EAS | KHV | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0053 | EAS | KHV | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0155 | AFR | ACB | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0158 | AFR | ACB | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0209 | AFR | ACB | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0184 | AFR | ACB | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG02258 | hp1 | a0001 | c0002 | t0007 | g0215 | AFR | ACB | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0151 | AFR | ACB | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0207 | AFR | ACB | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0090 | AFR | ACB | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0203 | AFR | ACB | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0148 | AFR | ACB | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG02572 | hp1 | a0002 | c0003 | t0026 | g0219 | AFR | GWD | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0141 | AFR | GWD | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0104 | SAS | PJL | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG02602 | hp2 | a0001 | c0002 | t0004 | g0235 | SAS | PJL | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG02622 | hp1 | a0001 | c0002 | t0004 | g0226 | AFR | GWD | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0196 | AFR | GWD | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG02630 | hp1 | a0001 | c0002 | t0008 | g0221 | AFR | GWD | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0050 | AFR | GWD | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG02647 | hp1 | a0001 | c0001 | t0017 | g0157 | AFR | GWD | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG02647 | hp2 | a0001 | c0002 | t0008 | g0223 | AFR | GWD | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG02698 | hp1 | a0001 | c0001 | t0006 | g0173 | SAS | PJL | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG02698 | hp2 | a0001 | c0001 | t0006 | g0101 | SAS | PJL | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0183 | AFR | GWD | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0021 | AFR | GWD | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0082 | AFR | GWD | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0211 | AFR | GWD | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0096 | SAS | PJL | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG02735 | hp2 | a0001 | c0001 | t0005 | g0167 | SAS | PJL | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0152 | SAS | PJL | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG02738 | hp2 | a0001 | c0001 | t0006 | g0179 | SAS | PJL | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0098 | AFR | GWD | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG02818 | hp2 | a0001 | c0001 | t0028 | g0197 | AFR | GWD | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0140 | AFR | GWD | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0029 | AFR | GWD | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG02895 | hp1 | a0001 | c0004 | t0013 | g0074 | AFR | GWD | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG02895 | hp2 | a0001 | c0001 | t0015 | g0210 | AFR | GWD | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0059 | AFR | GWD | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0095 | AFR | GWD | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0094 | AFR | GWD | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG02897 | hp2 | a0001 | c0004 | t0013 | g0073 | AFR | GWD | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0204 | AFR | ESN | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG02922 | hp2 | a0001 | c0002 | t0007 | g0216 | AFR | ESN | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0121 | AFR | ESN | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0089 | AFR | ESN | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0109 | SAS | PJL | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG03017 | hp2 | a0004 | c0006 | t0004 | g0243 | SAS | PJL | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0142 | AFR | GWD | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG03041 | hp2 | a0002 | c0003 | t0018 | g0005 | AFR | GWD | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0208 | AFR | MSL | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0083 | AFR | MSL | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG03195 | hp1 | a0001 | c0002 | t0007 | g0217 | AFR | ESN | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG03195 | hp2 | a0001 | c0002 | t0008 | g0222 | AFR | ESN | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0125 | AFR | MSL | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0138 | AFR | MSL | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG03225 | hp1 | a0001 | c0002 | t0007 | g0214 | AFR | MSL | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0182 | AFR | MSL | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG03239 | hp1 | a0001 | c0001 | t0006 | g0168 | SAS | PJL | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG03239 | hp2 | a0001 | c0002 | t0004 | g0227 | SAS | PJL | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG03453 | hp1 | a0001 | c0002 | t0012 | g0220 | AFR | MSL | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG03453 | hp2 | a0001 | c0002 | t0007 | g0218 | AFR | MSL | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG03486 | hp1 | a0001 | c0001 | t0014 | g0160 | AFR | MSL | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG03486 | hp2 | a0001 | c0001 | t0017 | g0156 | AFR | MSL | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG03491 | hp1 | a0001 | c0001 | t0011 | g0088 | SAS | PJL | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG03491 | hp2 | a0001 | c0002 | t0004 | g0228 | SAS | PJL | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG03492 | hp1 | a0001 | c0001 | t0011 | g0144 | SAS | PJL | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0055 | SAS | PJL | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0102 | AFR | ESN | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0139 | AFR | ESN | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0093 | AFR | GWD | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0187 | AFR | GWD | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG03579 | hp1 | a0001 | c0001 | t0010 | g0195 | AFR | MSL | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0113 | AFR | MSL | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG03654 | hp1 | a0001 | c0002 | t0004 | g0240 | SAS | PJL | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0103 | SAS | PJL | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG03669 | hp1 | a0001 | c0002 | t0004 | g0242 | SAS | PJL | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG03669 | hp2 | a0001 | c0002 | t0030 | g0067 | SAS | PJL | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0037 | SAS | STU | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG03688 | hp2 | a0001 | c0001 | t0005 | g0185 | SAS | STU | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG03704 | hp1 | a0001 | c0001 | t0020 | g0100 | SAS | PJL | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG03704 | hp2 | a0001 | c0002 | t0004 | g0232 | SAS | PJL | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0189 | SAS | PJL | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0011 | SAS | PJL | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG03834 | hp1 | a0001 | c0002 | t0004 | g0245 | SAS | BEB | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0034 | SAS | BEB | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG03927 | hp1 | a0001 | c0001 | t0005 | g0181 | SAS | BEB | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0049 | SAS | BEB | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0069 | SAS | BEB | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0201 | SAS | BEB | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0068 | SAS | STU | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0122 | SAS | STU | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG04184 | hp1 | a0001 | c0002 | t0004 | g0244 | SAS | BEB | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0025 | SAS | BEB | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG04199 | hp1 | a0001 | c0001 | t0011 | g0154 | SAS | STU | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0108 | SAS | STU | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0119 | SAS | STU | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0046 | SAS | STU | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0091 | AFR | YRI | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA18522 | hp2 | a0001 | c0001 | t0010 | g0194 | AFR | YRI | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA18939 | hp2 | a0001 | c0001 | t0015 | g0134 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA18940 | hp2 | a0001 | c0002 | t0004 | g0236 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0130 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA18945 | hp2 | a0001 | c0001 | t0022 | g0112 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA18947 | hp2 | a0001 | c0002 | t0004 | g0237 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA18954 | hp2 | a0001 | c0002 | t0009 | g0081 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA18960 | hp1 | a0001 | c0002 | t0004 | g0230 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA18962 | hp2 | a0001 | c0002 | t0004 | g0225 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0133 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0135 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA18970 | hp2 | a0001 | c0002 | t0009 | g0078 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA18994 | hp2 | a0001 | c0002 | t0004 | g0241 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA18998 | hp1 | a0003 | c0005 | t0001 | g0041 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0132 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0123 | AFR | LWK | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA19030 | hp2 | a0001 | c0001 | t0024 | g0162 | AFR | LWK | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | LWK | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA19043 | hp2 | a0001 | c0002 | t0012 | g0007 | AFR | LWK | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA19056 | hp1 | a0001 | c0002 | t0004 | g0231 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA19056 | hp2 | a0001 | c0002 | t0016 | g0045 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA19062 | hp1 | a0001 | c0002 | t0004 | g0238 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA19062 | hp2 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA19066 | hp1 | a0001 | c0002 | t0004 | g0239 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA19074 | hp1 | a0001 | c0002 | t0025 | g0026 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA19074 | hp2 | a0001 | c0002 | t0004 | g0229 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA19080 | hp1 | a0001 | c0002 | t0004 | g0234 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0054 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA19081 | hp1 | a0001 | c0002 | t0004 | g0233 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA19082 | hp2 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA19083 | hp1 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA19083 | hp2 | a0001 | c0002 | t0016 | g0070 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA19088 | hp2 | a0001 | c0002 | t0009 | g0079 | EAS | JPT | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0150 | AFR | YRI | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0099 | AFR | YRI | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | ASW | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0019 | AFR | ASW | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0013 | EUR | TSI | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0199 | EUR | TSI | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0153 | EUR | TSI | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0071 | EUR | TSI | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0105 | SAS | GIH | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0044 | SAS | GIH | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG02486 | hp1 | a0001 | c0002 | t0008 | g0224 | AFR | ACB | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0060 | AFR | ACB | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0004 | AFR | ACB | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0174 | AFR | ACB | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG03471 | hp1 | a0001 | c0001 | t0010 | g0193 | AFR | MSL | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| HG03471 | hp2 | a0001 | c0001 | t0014 | g0159 | AFR | MSL | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0084 | AFR | USA | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0205 | AFR | USA | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0191 | AFR | LWK | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| NA21309 | hp2 | a0001 | c0001 | t0019 | g0124 | AFR | LWK | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0012 | REF | REF | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0010 | g0166 | REF | REF | LIMS1_chr2_108529470_108692246 | LIMS1 | chr2 | 108529470 | 108692246 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:108659609
|
A | G | 1 | a0004 | 1 | HG03017.hp2 | missense_variant | MODERATE | c.37A>G | p.Met13Val | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/10 | 130/4354 | 37/1014 | 13/337 | chr2 | 108659609 | ||
| chr2:108672387
|
C | T | 1 | a0003 | 1 | NA18998.hp1 | missense_variant | MODERATE | c.322C>T | p.Arg108Cys | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 4/10 | 415/4354 | 322/1014 | 108/337 | chr2 | 108672387 | ||
| chr2:108680724
|
G | A | 1 | a0002 | 2 | HG02572.hp1 HG03041.hp2 |
missense_variant | MODERATE | c.853G>A | p.Val285Met | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 9/10 | 946/4354 | 853/1014 | 285/337 | chr2 | 108680724 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:108672422
|
C | T | 1 | a0001c0004 | 2 | HG02895.hp1 HG02897.hp2 |
synonymous_variant | LOW | c.357C>T | p.Ile119Ile | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 4/10 | 450/4354 | 357/1014 | 119/337 | chr2 | 108672422 | ||
| chr2:108676674
|
A | G | 5 | a0001c0002a0001c0004a0002c0003others(2): Show | 109 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
synonymous_variant | LOW | c.750A>G | p.Ala250Ala | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 7/10 | 843/4354 | 750/1014 | 250/337 | chr2 | 108676674 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:108534528
|
G | A | 4 | a0001c0002t0004a0001c0004t0013a0002c0003t0018others(1): Show | 24 | HG02602.hp2 HG02622.hp1 HG02895.hp1 others(21): Show |
5_prime_UTR_variant | MODIFIER | c.-35G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/10 | 35 | chr2 | 108534528 | |||||
| chr2:108534554
|
A | G | 1 | a0001c0001t0017 | 2 | HG02647.hp1 HG03486.hp2 |
5_prime_UTR_variant | MODIFIER | c.-9A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/10 | 9 | chr2 | 108534554 | |||||
| chr2:108684274
|
T | C | 1 | a0001c0004t0013 | 2 | HG02895.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*275T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 10/10 | 275 | chr2 | 108684274 | |||||
| chr2:108684280
|
C | T | 1 | a0001c0002t0030 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*281C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 10/10 | 281 | chr2 | 108684280 | |||||
| chr2:108684283
|
C | A | 2 | a0001c0002t0004a0004c0006t0004 | 21 | HG02602.hp2 HG02622.hp1 HG03017.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*284C>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 10/10 | 284 | chr2 | 108684283 | |||||
| chr2:108684517
|
A | C | 1 | a0001c0002t0016 | 2 | NA19056.hp2 NA19083.hp2 |
3_prime_UTR_variant | MODIFIER | c.*518A>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 10/10 | 518 | chr2 | 108684517 | |||||
| chr2:108684618
|
C | A | 10 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(7): Show | 79 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*619C>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 10/10 | 619 | chr2 | 108684618 | |||||
| chr2:108684648
|
T | C | 1 | a0001c0001t0014 | 2 | HG03471.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*649T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 10/10 | 649 | chr2 | 108684648 | |||||
| chr2:108684659
|
T | TA | 13 | a0001c0002t0001a0001c0002t0004a0001c0002t0008others(10): Show | 100 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*660_*661insA | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 10/10 | 661 | chr2 | 108684659 | |||||
| chr2:108684773
|
C | T | 1 | a0001c0001t0011 | 4 | HG02056.hp1 HG03491.hp1 HG03492.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*774C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 10/10 | 774 | chr2 | 108684773 | |||||
| chr2:108684826
|
A | G | 1 | a0001c0002t0008 | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*827A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 10/10 | 827 | chr2 | 108684826 | |||||
| chr2:108684833
|
T | C | 1 | a0001c0002t0008 | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*834T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 10/10 | 834 | chr2 | 108684833 | |||||
| chr2:108684867
|
T | G | 1 | a0001c0002t0025 | 1 | NA19074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*868T>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 10/10 | 868 | chr2 | 108684867 | |||||
| chr2:108684942
|
C | A | 31 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(28): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
3_prime_UTR_variant | MODIFIER | c.*943C>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 10/10 | 943 | chr2 | 108684942 | |||||
| chr2:108684947
|
A | T | 1 | a0001c0001t0029 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*948A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 10/10 | 948 | chr2 | 108684947 | |||||
| chr2:108685132
|
G | A | 3 | a0001c0002t0004a0001c0004t0013a0004c0006t0004 | 23 | HG02602.hp2 HG02622.hp1 HG02895.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1133G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 10/10 | 1133 | chr2 | 108685132 | |||||
| chr2:108685231
|
G | C | 8 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(5): Show | 76 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*1232G>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 10/10 | 1232 | chr2 | 108685231 | |||||
| chr2:108685385
|
G | A | 15 | a0001c0002t0001a0001c0002t0004a0001c0002t0007others(12): Show | 109 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*1386G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 10/10 | 1386 | chr2 | 108685385 | |||||
| chr2:108685403
|
C | T | 1 | a0001c0002t0012 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1404C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 10/10 | 1404 | chr2 | 108685403 | |||||
| chr2:108685433
|
G | GT | 3 | a0001c0001t0005a0001c0001t0006a0001c0001t0023 | 21 | HG00140.hp1 HG00280.hp2 HG00741.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1442dupT | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 10/10 | 1443 | INFO_REALIGN_3_PRIME | chr2 | 108685433 | ||||
| chr2:108685441
|
T | C | 2 | a0002c0003t0018a0002c0003t0026 | 2 | HG02572.hp1 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1442T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 10/10 | 1442 | chr2 | 108685441 | |||||
| chr2:108685837
|
G | A | 1 | a0001c0001t0019 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1838G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 10/10 | 1838 | chr2 | 108685837 | |||||
| chr2:108685932
|
G | A | 10 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(7): Show | 79 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*1933G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 10/10 | 1933 | chr2 | 108685932 | |||||
| chr2:108685982
|
T | C | 1 | a0001c0002t0008 | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1983T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 10/10 | 1983 | chr2 | 108685982 | |||||
| chr2:108686050
|
G | A | 1 | a0001c0002t0008 | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2051G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 10/10 | 2051 | chr2 | 108686050 | |||||
| chr2:108686067
|
C | G | 1 | a0001c0001t0022 | 1 | NA18945.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2068C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 10/10 | 2068 | chr2 | 108686067 | |||||
| chr2:108686188
|
G | A | 3 | a0001c0002t0004a0001c0004t0013a0004c0006t0004 | 23 | HG02602.hp2 HG02622.hp1 HG02895.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2189G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 10/10 | 2189 | chr2 | 108686188 | |||||
| chr2:108686212
|
G | A | 1 | a0001c0002t0008 | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2213G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 10/10 | 2213 | chr2 | 108686212 | |||||
| chr2:108686242
|
C | T | 1 | a0001c0002t0012 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2243C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 10/10 | 2243 | chr2 | 108686242 | |||||
| chr2:108686243
|
C | T | 10 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(7): Show | 79 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*2244C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 10/10 | 2244 | chr2 | 108686243 | |||||
| chr2:108686327
|
T | A | 1 | a0001c0001t0020 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2328T>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 10/10 | 2328 | chr2 | 108686327 | |||||
| chr2:108686452
|
G | A | 2 | a0001c0002t0004a0004c0006t0004 | 21 | HG02602.hp2 HG02622.hp1 HG03017.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2453G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 10/10 | 2453 | chr2 | 108686452 | |||||
| chr2:108686458
|
G | A | 2 | a0001c0002t0004a0004c0006t0004 | 21 | HG02602.hp2 HG02622.hp1 HG03017.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2459G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 10/10 | 2459 | chr2 | 108686458 | |||||
| chr2:108686509
|
T | C | 1 | a0001c0001t0021 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2510T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 10/10 | 2510 | chr2 | 108686509 | |||||
| chr2:108686648
|
C | T | 1 | a0001c0001t0021 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2649C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 10/10 | 2649 | chr2 | 108686648 | |||||
| chr2:108686668
|
C | T | 1 | a0001c0001t0028 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2669C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 10/10 | 2669 | chr2 | 108686668 | |||||
| chr2:108686693
|
T | A | 1 | a0001c0001t0021 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2694T>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 10/10 | 2694 | chr2 | 108686693 | |||||
| chr2:108686741
|
A | G | 1 | a0001c0002t0008 | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2742A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 10/10 | 2742 | chr2 | 108686741 | |||||
| chr2:108686775
|
C | CA | 8 | a0001c0001t0002a0001c0001t0005a0001c0001t0017others(5): Show | 69 | HG00099.hp2 HG00741.hp1 HG00741.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*2791dupA | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 10/10 | 2792 | INFO_REALIGN_3_PRIME | chr2 | 108686775 | ||||
| chr2:108686775
|
CA | C | 4 | a0001c0001t0015a0001c0001t0023a0001c0002t0008others(1): Show | 8 | HG01169.hp2 HG01256.hp2 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2791delA | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 10/10 | 2791 | INFO_REALIGN_3_PRIME | chr2 | 108686775 | ||||
| chr2:108687039
|
C | A | 1 | a0001c0002t0009 | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3040C>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 10/10 | 3040 | chr2 | 108687039 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:108534648
|
G | A | 3 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004 | 3 | HG02559.hp1 NA19043.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.32+54G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108534648 | ||||||
| chr2:108534699
|
C | T | 21 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(18): Show | 21 | HG02602.hp2 HG02622.hp1 HG03017.hp2 others(18): Show |
intron_variant | MODIFIER | c.32+105C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108534699 | ||||||
| chr2:108534717
|
T | G | 94 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(91): Show | 94 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.32+123T>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108534717 | ||||||
| chr2:108535077
|
A | G | 2 | a0001c0004t0013g0073a0001c0004t0013g0074 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.32+483A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108535077 | ||||||
| chr2:108535124
|
C | G | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+530C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108535124 | ||||||
| chr2:108535129
|
C | T | 2 | a0001c0002t0012g0220a0002c0003t0026g0219 | 2 | HG02572.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.32+535C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108535129 | ||||||
| chr2:108535151
|
G | T | 2 | a0001c0002t0012g0220a0002c0003t0026g0219 | 2 | HG02572.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.32+557G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108535151 | ||||||
| chr2:108535245
|
A | G | 68 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.32+651A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108535245 | ||||||
| chr2:108535405
|
G | A | 1 | a0002c0003t0018g0005 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.32+811G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108535405 | ||||||
| chr2:108535554
|
A | G | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+960A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108535554 | ||||||
| chr2:108535775
|
A | C | 1 | a0001c0001t0003g0213 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.32+1181A>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108535775 | ||||||
| chr2:108535921
|
T | G | 21 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(18): Show | 21 | HG02602.hp2 HG02622.hp1 HG03017.hp2 others(18): Show |
intron_variant | MODIFIER | c.32+1327T>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108535921 | ||||||
| chr2:108535977
|
TAAC | T | 11 | a0001c0001t0003g0202a0001c0001t0003g0203a0001c0001t0003g0204others(8): Show | 11 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.32+1386_32+1388del others(3): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108535977 | |||||
| chr2:108536094
|
G | A | 1 | a0001c0001t0002g0075 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.32+1500G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108536094 | ||||||
| chr2:108536100
|
A | G | 1 | a0001c0001t0002g0075 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.32+1506A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108536100 | ||||||
| chr2:108536101
|
A | T | 1 | a0001c0001t0002g0075 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.32+1507A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108536101 | ||||||
| chr2:108536103
|
G | A | 1 | a0001c0001t0002g0075 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.32+1509G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108536103 | ||||||
| chr2:108536104
|
A | T | 1 | a0001c0001t0002g0075 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.32+1510A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108536104 | ||||||
| chr2:108536106
|
A | T | 1 | a0001c0001t0002g0075 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.32+1512A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108536106 | ||||||
| chr2:108536132
|
A | G | 2 | a0001c0001t0002g0200a0001c0001t0002g0201 | 2 | HG01346.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.32+1538A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108536132 | ||||||
| chr2:108536134
|
C | T | 1 | a0001c0001t0002g0199 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.32+1540C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108536134 | ||||||
| chr2:108536146
|
A | G | 24 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(21): Show | 24 | HG02602.hp2 HG02622.hp1 HG02895.hp1 others(21): Show |
intron_variant | MODIFIER | c.32+1552A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108536146 | ||||||
| chr2:108536394
|
C | T | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+1800C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108536394 | ||||||
| chr2:108536473
|
T | C | 68 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.32+1879T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108536473 | ||||||
| chr2:108536486
|
T | A | 1 | a0002c0003t0018g0005 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.32+1892T>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108536486 | ||||||
| chr2:108536556
|
T | C | 7 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(4): Show | 7 | HG00323.hp2 HG00639.hp1 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.32+1962T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108536556 | ||||||
| chr2:108536821
|
G | A | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+2227G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108536821 | ||||||
| chr2:108537106
|
A | C | 13 | a0001c0001t0003g0187a0001c0001t0003g0188a0001c0001t0003g0189others(10): Show | 13 | HG00639.hp2 HG01074.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.32+2512A>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108537106 | ||||||
| chr2:108537231
|
G | A | 2 | a0001c0001t0002g0076a0001c0001t0005g0077 | 2 | HG00741.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.32+2637G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108537231 | ||||||
| chr2:108537241
|
G | A | 102 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(99): Show | 102 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.32+2647G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108537241 | ||||||
| chr2:108537434
|
T | C | 2 | a0001c0001t0002g0082a0001c0001t0002g0083 | 2 | HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.32+2840T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108537434 | ||||||
| chr2:108537980
|
A | T | 74 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(71): Show | 74 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.32+3386A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108537980 | ||||||
| chr2:108538001
|
G | A | 2 | a0001c0002t0001g0015a0001c0002t0027g0016 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.32+3407G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108538001 | ||||||
| chr2:108538239
|
C | T | 102 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(99): Show | 102 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.32+3645C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108538239 | ||||||
| chr2:108538324
|
T | A | 1 | a0001c0002t0001g0017 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.32+3730T>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108538324 | ||||||
| chr2:108538706
|
C | T | 1 | a0001c0001t0005g0185 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.32+4112C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108538706 | ||||||
| chr2:108538828
|
T | C | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+4234T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108538828 | ||||||
| chr2:108538915
|
C | T | 1 | a0002c0003t0018g0005 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.32+4321C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108538915 | ||||||
| chr2:108539133
|
G | A | 23 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(20): Show | 23 | HG02602.hp2 HG02622.hp1 HG02895.hp1 others(20): Show |
intron_variant | MODIFIER | c.32+4539G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108539133 | ||||||
| chr2:108539244
|
C | T | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+4650C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108539244 | ||||||
| chr2:108539322
|
C | T | 3 | a0001c0001t0002g0182a0001c0001t0002g0183a0001c0001t0002g0184 | 3 | HG02257.hp2 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.32+4728C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108539322 | ||||||
| chr2:108539498
|
C | T | 74 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(71): Show | 74 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.32+4904C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108539498 | ||||||
| chr2:108539819
|
G | A | 74 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(71): Show | 74 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.32+5225G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108539819 | ||||||
| chr2:108539826
|
T | C | 1 | a0001c0002t0004g0225 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.32+5232T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108539826 | ||||||
| chr2:108539966
|
T | C | 1 | a0001c0001t0029g0186 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.32+5372T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108539966 | ||||||
| chr2:108540139
|
G | A | 225 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(222): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.32+5545G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108540139 | ||||||
| chr2:108540193
|
C | CT | 19 | a0001c0001t0002g0075a0001c0001t0002g0158a0001c0001t0003g0161others(16): Show | 19 | HG01361.hp2 HG01981.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.32+5622dupT | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108540193 | |||||
| chr2:108540193
|
C | CTT | 51 | a0001c0001t0024g0162a0001c0002t0001g0008a0001c0002t0001g0009others(48): Show | 51 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.32+5621_32+5622dup others(2): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108540193 | |||||
| chr2:108540193
|
C | CTTT | 13 | a0001c0002t0001g0017a0001c0002t0001g0061a0001c0002t0001g0062others(10): Show | 13 | HG00140.hp2 HG00280.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.32+5620_32+5622dup others(3): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108540193 | |||||
| chr2:108540193
|
CT | C | 8 | a0001c0001t0002g0084a0001c0001t0002g0085a0001c0001t0002g0086others(5): Show | 8 | HG01168.hp2 HG01257.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.32+5622delT | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108540193 | |||||
| chr2:108540268
|
G | A | 74 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(71): Show | 74 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.32+5674G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108540268 | ||||||
| chr2:108540292
|
G | A | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+5698G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108540292 | ||||||
| chr2:108540722
|
C | A | 1 | a0001c0002t0001g0020 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.32+6128C>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108540722 | ||||||
| chr2:108540770
|
T | C | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+6176T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108540770 | ||||||
| chr2:108541164
|
G | A | 1 | a0002c0003t0018g0005 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.32+6570G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108541164 | ||||||
| chr2:108541407
|
G | C | 21 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(18): Show | 21 | HG02602.hp2 HG02622.hp1 HG03017.hp2 others(18): Show |
intron_variant | MODIFIER | c.32+6813G>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108541407 | ||||||
| chr2:108541522
|
A | G | 24 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(21): Show | 24 | HG02602.hp2 HG02622.hp1 HG02895.hp1 others(21): Show |
intron_variant | MODIFIER | c.32+6928A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108541522 | ||||||
| chr2:108541781
|
A | G | 147 | a0001c0001t0003g0001a0001c0001t0003g0137a0001c0001t0003g0138others(144): Show | 148 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.32+7187A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108541781 | ||||||
| chr2:108541835
|
C | T | 7 | a0001c0001t0003g0130a0001c0001t0003g0131a0001c0001t0003g0132others(4): Show | 7 | NA18939.hp2 NA18942.hp1 NA18947.hp1 others(4): Show |
intron_variant | MODIFIER | c.32+7241C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108541835 | ||||||
| chr2:108541848
|
G | A | 21 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(18): Show | 21 | HG02602.hp2 HG02622.hp1 HG03017.hp2 others(18): Show |
intron_variant | MODIFIER | c.32+7254G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108541848 | ||||||
| chr2:108541944
|
T | C | 1 | a0001c0002t0001g0008 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.32+7350T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108541944 | ||||||
| chr2:108542344
|
C | G | 1 | a0001c0002t0001g0072 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.32+7750C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108542344 | ||||||
| chr2:108542514
|
C | T | 1 | a0001c0001t0002g0129 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.32+7920C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108542514 | ||||||
| chr2:108542577
|
A | G | 24 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(21): Show | 24 | HG02602.hp2 HG02622.hp1 HG02895.hp1 others(21): Show |
intron_variant | MODIFIER | c.32+7983A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108542577 | ||||||
| chr2:108542858
|
T | C | 1 | a0001c0001t0014g0159 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.32+8264T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108542858 | ||||||
| chr2:108542877
|
C | T | 147 | a0001c0001t0003g0001a0001c0001t0003g0137a0001c0001t0003g0138others(144): Show | 148 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.32+8283C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108542877 | ||||||
| chr2:108542918
|
A | G | 1 | a0001c0002t0001g0071 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.32+8324A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108542918 | ||||||
| chr2:108542975
|
T | G | 2 | a0001c0001t0014g0159a0001c0001t0014g0160 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.32+8381T>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108542975 | ||||||
| chr2:108543307
|
C | G | 2 | a0001c0002t0001g0017a0001c0002t0001g0060 | 2 | HG01192.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.32+8713C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108543307 | ||||||
| chr2:108543307
|
C | T | 2 | a0001c0002t0012g0006a0001c0002t0012g0007 | 2 | HG02040.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.32+8713C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108543307 | ||||||
| chr2:108543355
|
A | G | 74 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(71): Show | 74 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.32+8761A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108543355 | ||||||
| chr2:108543517
|
C | G | 2 | a0001c0002t0004g0244a0004c0006t0004g0243 | 2 | HG03017.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.32+8923C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108543517 | ||||||
| chr2:108543589
|
C | G | 68 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.32+8995C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108543589 | ||||||
| chr2:108543712
|
C | G | 1 | a0001c0002t0001g0059 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.32+9118C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108543712 | ||||||
| chr2:108543745
|
C | G | 1 | a0001c0001t0024g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.32+9151C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108543745 | ||||||
| chr2:108543898
|
C | T | 1 | a0001c0001t0002g0128 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.32+9304C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108543898 | ||||||
| chr2:108544219
|
G | A | 65 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(62): Show | 65 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.32+9625G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108544219 | ||||||
| chr2:108544504
|
A | G | 2 | a0001c0001t0003g0135a0001c0001t0003g0136 | 2 | NA18969.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.32+9910A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108544504 | ||||||
| chr2:108544531
|
C | G | 11 | a0001c0001t0003g0202a0001c0001t0003g0203a0001c0001t0003g0204others(8): Show | 11 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.32+9937C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108544531 | ||||||
| chr2:108544777
|
G | A | 11 | a0001c0001t0003g0202a0001c0001t0003g0203a0001c0001t0003g0204others(8): Show | 11 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.32+10183G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108544777 | ||||||
| chr2:108544802
|
A | G | 40 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0003g0001others(37): Show | 41 | HG00323.hp1 HG00639.hp2 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.32+10208A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108544802 | ||||||
| chr2:108545026
|
G | A | 70 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(67): Show | 70 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.32+10432G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108545026 | ||||||
| chr2:108545240
|
A | G | 2 | a0001c0001t0005g0180a0001c0001t0006g0179 | 2 | HG01175.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.32+10646A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108545240 | ||||||
| chr2:108545488
|
C | T | 20 | a0001c0002t0004g0225a0001c0002t0004g0227a0001c0002t0004g0228others(17): Show | 20 | HG02602.hp2 HG03017.hp2 HG03239.hp2 others(17): Show |
intron_variant | MODIFIER | c.32+10894C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108545488 | ||||||
| chr2:108545533
|
C | T | 1 | a0001c0002t0001g0059 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.32+10939C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108545533 | ||||||
| chr2:108545534
|
G | A | 11 | a0001c0001t0003g0202a0001c0001t0003g0203a0001c0001t0003g0204others(8): Show | 11 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.32+10940G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108545534 | ||||||
| chr2:108545881
|
A | G | 38 | a0001c0001t0003g0001a0001c0001t0003g0137a0001c0001t0003g0138others(35): Show | 39 | HG00323.hp1 HG00639.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.32+11287A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108545881 | ||||||
| chr2:108545941
|
G | A | 3 | a0001c0001t0005g0164a0001c0001t0005g0181a0001c0001t0006g0179 | 3 | HG01099.hp1 HG02738.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.32+11347G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108545941 | ||||||
| chr2:108546031
|
T | C | 74 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(71): Show | 74 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.32+11437T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108546031 | ||||||
| chr2:108546269
|
C | CT | 74 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0085others(71): Show | 74 | HG00099.hp2 HG00741.hp2 HG01168.hp2 others(71): Show |
intron_variant | MODIFIER | c.32+11698dupT | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108546269 | |||||
| chr2:108546269
|
C | CTT | 36 | a0001c0001t0002g0082a0001c0001t0002g0087a0001c0001t0002g0121others(33): Show | 36 | HG01243.hp2 HG02055.hp1 HG02258.hp1 others(33): Show |
intron_variant | MODIFIER | c.32+11697_32+11698d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108546269 | |||||
| chr2:108546269
|
C | CTTT | 9 | a0001c0001t0002g0083a0001c0001t0002g0125a0001c0002t0001g0018others(6): Show | 9 | HG02486.hp1 HG02622.hp1 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.32+11696_32+11698d others(5): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108546269 | |||||
| chr2:108546269
|
C | CTTTT | 43 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0008others(40): Show | 43 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(40): Show |
intron_variant | MODIFIER | c.32+11695_32+11698d others(6): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108546269 | |||||
| chr2:108546269
|
C | CTTTTT | 20 | a0001c0002t0001g0014a0001c0002t0001g0020a0001c0002t0001g0047others(17): Show | 20 | HG01169.hp2 HG01256.hp1 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.32+11694_32+11698d others(7): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108546269 | |||||
| chr2:108546269
|
C | CTTTTTTT others(3): Show |
1 | a0001c0002t0001g0004 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.32+11689_32+11698d others(12): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108546269 | |||||
| chr2:108546310
|
T | C | 1 | a0001c0002t0001g0047 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.32+11716T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108546310 | ||||||
| chr2:108546416
|
G | C | 1 | a0001c0001t0003g0137 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.32+11822G>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108546416 | ||||||
| chr2:108546487
|
G | A | 11 | a0001c0001t0003g0202a0001c0001t0003g0203a0001c0001t0003g0204others(8): Show | 11 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.32+11893G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108546487 | ||||||
| chr2:108546677
|
TC | T | 70 | a0001c0002t0001g0004a0001c0002t0001g0008a0001c0002t0001g0009others(67): Show | 70 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.32+12084delC | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108546677 | ||||||
| chr2:108546678
|
C | CT | 89 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(86): Show | 90 | HG00099.hp2 HG00323.hp1 HG00741.hp2 others(87): Show |
intron_variant | MODIFIER | c.32+12099dupT | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108546678 | |||||
| chr2:108546678
|
C | T | 2 | a0001c0002t0001g0002a0001c0002t0001g0003 | 2 | NA19043.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.32+12084C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108546678 | ||||||
| chr2:108546678
|
CT | C | 29 | a0001c0001t0003g0187a0001c0001t0005g0165a0001c0002t0004g0225others(26): Show | 29 | HG01070.hp2 HG01261.hp2 HG02602.hp2 others(26): Show |
intron_variant | MODIFIER | c.32+12099delT | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108546678 | |||||
| chr2:108546873
|
T | C | 36 | a0001c0001t0003g0001a0001c0001t0003g0137a0001c0001t0003g0138others(33): Show | 37 | HG00323.hp1 HG00639.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.32+12279T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108546873 | ||||||
| chr2:108547022
|
G | A | 11 | a0001c0001t0003g0202a0001c0001t0003g0203a0001c0001t0003g0204others(8): Show | 11 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.32+12428G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108547022 | ||||||
| chr2:108547065
|
G | C | 8 | a0001c0001t0002g0084a0001c0001t0002g0089a0001c0001t0002g0090others(5): Show | 8 | HG01175.hp2 HG02145.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.32+12471G>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108547065 | ||||||
| chr2:108547265
|
T | C | 107 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(104): Show | 107 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.32+12671T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108547265 | ||||||
| chr2:108547397
|
T | C | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+12803T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108547397 | ||||||
| chr2:108547433
|
A | C | 2 | a0001c0002t0012g0006a0001c0002t0012g0007 | 2 | HG02040.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.32+12839A>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108547433 | ||||||
| chr2:108547475
|
A | C | 1 | a0001c0001t0002g0128 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.32+12881A>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108547475 | ||||||
| chr2:108547578
|
T | G | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+12984T>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108547578 | ||||||
| chr2:108547599
|
A | G | 24 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(21): Show | 24 | HG02602.hp2 HG02622.hp1 HG02895.hp1 others(21): Show |
intron_variant | MODIFIER | c.32+13005A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108547599 | ||||||
| chr2:108547603
|
G | T | 3 | a0001c0001t0002g0082a0001c0001t0002g0083a0001c0001t0019g0124 | 3 | HG02723.hp1 HG03098.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.32+13009G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108547603 | ||||||
| chr2:108547789
|
T | C | 2 | a0001c0001t0002g0094a0001c0001t0002g0095 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.32+13195T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108547789 | ||||||
| chr2:108547923
|
G | A | 38 | a0001c0001t0003g0001a0001c0001t0003g0137a0001c0001t0003g0138others(35): Show | 39 | HG00323.hp1 HG00639.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.32+13329G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108547923 | ||||||
| chr2:108548051
|
T | C | 2 | a0001c0002t0012g0006a0001c0002t0012g0007 | 2 | HG02040.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.32+13457T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108548051 | ||||||
| chr2:108548122
|
A | G | 1 | a0001c0001t0003g0211 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.32+13528A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108548122 | ||||||
| chr2:108548289
|
GT | G | 101 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0008others(98): Show | 101 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.32+13707delT | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108548289 | |||||
| chr2:108548294
|
T | G | 1 | a0001c0002t0012g0006 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.32+13700T>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108548294 | ||||||
| chr2:108548358
|
C | T | 14 | a0001c0001t0003g0001a0001c0001t0003g0137a0001c0001t0003g0145others(11): Show | 15 | HG00323.hp1 HG01074.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.32+13764C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108548358 | ||||||
| chr2:108548587
|
A | G | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+13993A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108548587 | ||||||
| chr2:108548676
|
C | T | 1 | a0001c0002t0008g0223 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.32+14082C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108548676 | ||||||
| chr2:108548712
|
C | G | 1 | a0001c0002t0001g0046 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.32+14118C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108548712 | ||||||
| chr2:108548780
|
C | T | 4 | a0001c0001t0002g0094a0001c0001t0002g0095a0001c0001t0002g0098others(1): Show | 4 | HG02818.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+14186C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108548780 | ||||||
| chr2:108548782
|
A | T | 4 | a0001c0001t0002g0094a0001c0001t0002g0095a0001c0001t0002g0098others(1): Show | 4 | HG02818.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+14188A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108548782 | ||||||
| chr2:108548871
|
A | G | 1 | a0001c0001t0002g0093 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.32+14277A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108548871 | ||||||
| chr2:108548916
|
A | G | 68 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.32+14322A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108548916 | ||||||
| chr2:108549075
|
G | A | 1 | a0001c0001t0002g0103 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.32+14481G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108549075 | ||||||
| chr2:108549275
|
G | A | 38 | a0001c0001t0003g0001a0001c0001t0003g0137a0001c0001t0003g0138others(35): Show | 39 | HG00323.hp1 HG00639.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.32+14681G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108549275 | ||||||
| chr2:108549279
|
C | CT | 16 | a0001c0001t0002g0075a0001c0001t0002g0084a0001c0001t0002g0086others(13): Show | 16 | HG02280.hp2 HG02698.hp2 HG02738.hp2 others(13): Show |
intron_variant | MODIFIER | c.32+14718dupT | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108549279 | |||||
| chr2:108549279
|
C | CTT | 10 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0116others(7): Show | 10 | HG00140.hp1 HG00280.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.32+14717_32+14718d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108549279 | |||||
| chr2:108549279
|
C | CTTT | 7 | a0001c0001t0002g0102a0001c0001t0002g0158a0001c0001t0005g0172others(4): Show | 7 | HG00741.hp1 HG01256.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.32+14716_32+14718d others(5): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108549279 | |||||
| chr2:108549279
|
C | CTTTT | 6 | a0001c0001t0002g0097a0001c0001t0002g0119a0001c0001t0006g0177others(3): Show | 6 | HG01106.hp2 HG01167.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.32+14715_32+14718d others(6): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108549279 | |||||
| chr2:108549279
|
CT | C | 41 | a0001c0001t0002g0076a0001c0001t0002g0085a0001c0001t0002g0094others(38): Show | 41 | HG00099.hp2 HG01168.hp2 HG01169.hp1 others(38): Show |
intron_variant | MODIFIER | c.32+14718delT | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108549279 | |||||
| chr2:108549279
|
CTT | C | 18 | a0001c0001t0003g0130a0001c0001t0003g0139a0001c0001t0003g0140others(15): Show | 18 | HG00639.hp2 HG01891.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.32+14717_32+14718d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108549279 | |||||
| chr2:108549279
|
CTTT | C | 9 | a0001c0001t0003g0138a0001c0001t0003g0150a0001c0001t0003g0155others(6): Show | 9 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.32+14716_32+14718d others(5): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108549279 | |||||
| chr2:108549279
|
CTTTT | C | 19 | a0001c0001t0003g0001a0001c0001t0003g0137a0001c0001t0003g0145others(16): Show | 20 | HG00323.hp1 HG01074.hp1 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.32+14715_32+14718d others(6): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108549279 | |||||
| chr2:108549279
|
CTTTTT | C | 7 | a0001c0002t0001g0013a0001c0002t0001g0017a0001c0002t0001g0058others(4): Show | 7 | HG01192.hp1 HG01346.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.32+14714_32+14718d others(7): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108549279 | |||||
| chr2:108549279
|
CTTTTTT | C | 58 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(55): Show | 58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.32+14713_32+14718d others(8): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108549279 | |||||
| chr2:108549279
|
CTTTTTTT | C | 6 | a0001c0002t0001g0023a0001c0002t0001g0027a0001c0002t0012g0006others(3): Show | 6 | HG01169.hp2 HG02040.hp2 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.32+14712_32+14718d others(9): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108549279 | |||||
| chr2:108549279
|
CTTTTTTT others(2): Show |
C | 14 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0232others(11): Show | 14 | HG02602.hp2 HG02622.hp1 HG03017.hp2 others(11): Show |
intron_variant | MODIFIER | c.32+14710_32+14718d others(11): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108549279 | |||||
| chr2:108549279
|
CTTTTTTT others(3): Show |
C | 3 | a0001c0002t0004g0229a0001c0002t0004g0230a0001c0002t0004g0231 | 3 | NA18960.hp1 NA19056.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.32+14709_32+14718d others(12): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108549279 | |||||
| chr2:108549279
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0002g0093 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.32+14707_32+14718d others(14): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108549279 | |||||
| chr2:108549279
|
CTTTTTTT others(14): Show |
C | 3 | a0001c0002t0004g0227a0001c0002t0004g0228a0001c0002t0004g0245 | 3 | HG03239.hp2 HG03491.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.32+14698_32+14718d others(23): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108549279 | |||||
| chr2:108549279
|
CTTTTTTT others(15): Show |
C | 3 | a0001c0001t0002g0182a0001c0001t0002g0183a0001c0001t0002g0184 | 3 | HG02257.hp2 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.32+14697_32+14718d others(24): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108549279 | |||||
| chr2:108549299
|
T | C | 2 | a0001c0002t0001g0002a0001c0002t0001g0003 | 2 | NA19043.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.32+14705T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108549299 | ||||||
| chr2:108549326
|
G | A | 74 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(71): Show | 74 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.32+14732G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108549326 | ||||||
| chr2:108549334
|
G | A | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+14740G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108549334 | ||||||
| chr2:108549741
|
T | C | 38 | a0001c0001t0003g0001a0001c0001t0003g0137a0001c0001t0003g0138others(35): Show | 39 | HG00323.hp1 HG00639.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.32+15147T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108549741 | ||||||
| chr2:108549762
|
G | A | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+15168G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108549762 | ||||||
| chr2:108549808
|
A | G | 1 | a0001c0001t0002g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.32+15214A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108549808 | ||||||
| chr2:108550064
|
T | C | 1 | a0001c0001t0003g0188 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.32+15470T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108550064 | ||||||
| chr2:108550127
|
A | G | 1 | a0001c0002t0001g0025 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.32+15533A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108550127 | ||||||
| chr2:108550211
|
G | A | 24 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(21): Show | 24 | HG02602.hp2 HG02622.hp1 HG02895.hp1 others(21): Show |
intron_variant | MODIFIER | c.32+15617G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108550211 | ||||||
| chr2:108550288
|
G | T | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+15694G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108550288 | ||||||
| chr2:108550359
|
C | A | 1 | a0001c0001t0003g0143 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.32+15765C>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108550359 | ||||||
| chr2:108550360
|
G | A | 2 | a0001c0004t0013g0073a0001c0004t0013g0074 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.32+15766G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108550360 | ||||||
| chr2:108550515
|
A | T | 58 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(55): Show | 58 | HG00099.hp2 HG00741.hp2 HG01070.hp2 others(55): Show |
intron_variant | MODIFIER | c.32+15921A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108550515 | ||||||
| chr2:108550518
|
A | T | 142 | a0001c0001t0002g0075a0001c0001t0002g0086a0001c0001t0002g0087others(139): Show | 143 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.32+15924A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108550518 | ||||||
| chr2:108550563
|
C | T | 1 | a0002c0003t0018g0005 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.32+15969C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108550563 | ||||||
| chr2:108550629
|
C | T | 1 | a0001c0002t0001g0058 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.32+16035C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108550629 | ||||||
| chr2:108550687
|
G | T | 24 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(21): Show | 24 | HG02602.hp2 HG02622.hp1 HG02895.hp1 others(21): Show |
intron_variant | MODIFIER | c.32+16093G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108550687 | ||||||
| chr2:108550746
|
G | T | 1 | a0001c0001t0003g0155 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.32+16152G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108550746 | ||||||
| chr2:108550790
|
T | A | 70 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(67): Show | 70 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.32+16196T>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108550790 | ||||||
| chr2:108550794
|
C | T | 1 | a0001c0002t0001g0046 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.32+16200C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108550794 | ||||||
| chr2:108550825
|
A | G | 65 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(62): Show | 65 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.32+16231A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108550825 | ||||||
| chr2:108550836
|
T | A | 74 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(71): Show | 74 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.32+16242T>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108550836 | ||||||
| chr2:108550887
|
G | A | 1 | a0001c0001t0003g0139 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.32+16293G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108550887 | ||||||
| chr2:108551133
|
C | G | 1 | a0001c0002t0001g0027 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.32+16539C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108551133 | ||||||
| chr2:108551177
|
G | A | 147 | a0001c0001t0003g0001a0001c0001t0003g0137a0001c0001t0003g0138others(144): Show | 148 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.32+16583G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108551177 | ||||||
| chr2:108551290
|
A | G | 24 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(21): Show | 24 | HG02602.hp2 HG02622.hp1 HG02895.hp1 others(21): Show |
intron_variant | MODIFIER | c.32+16696A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108551290 | ||||||
| chr2:108551460
|
G | A | 150 | a0001c0001t0003g0001a0001c0001t0003g0137a0001c0001t0003g0138others(147): Show | 151 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.32+16866G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108551460 | ||||||
| chr2:108551480
|
T | TGC | 4 | a0001c0001t0002g0085a0001c0001t0011g0149a0001c0001t0011g0154others(1): Show | 4 | HG01168.hp2 HG02056.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+16897_32+16898d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108551480 | |||||
| chr2:108551480
|
TGC | T | 28 | a0001c0002t0001g0008a0001c0002t0001g0011a0001c0002t0001g0017others(25): Show | 28 | HG00639.hp1 HG01070.hp1 HG01192.hp1 others(25): Show |
intron_variant | MODIFIER | c.32+16897_32+16898d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108551480 | |||||
| chr2:108551480
|
TGCGC | T | 3 | a0001c0002t0001g0015a0001c0002t0008g0223a0001c0002t0027g0016 | 3 | HG01167.hp2 HG01169.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.32+16895_32+16898d others(6): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108551480 | |||||
| chr2:108551484
|
C | T | 1 | a0002c0003t0018g0005 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.32+16890C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108551484 | ||||||
| chr2:108551487
|
GCGCGCAC others(1): Show |
G | 3 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0224 | 3 | HG02486.hp1 HG02630.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.32+16895_32+16902d others(10): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108551487 | |||||
| chr2:108551489
|
G | GCA | 8 | a0001c0001t0002g0089a0001c0001t0002g0090a0001c0001t0002g0091others(5): Show | 8 | HG00323.hp2 HG01109.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.32+16896_32+16897i others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108551489 | |||||
| chr2:108551489
|
GCGCA | G | 6 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0012others(3): Show | 6 | HG01993.hp2 NA18969.hp1 NA18998.hp1 others(3): Show |
intron_variant | MODIFIER | c.32+16897_32+16900d others(6): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108551489 | |||||
| chr2:108551489
|
GCGCACA | G | 3 | a0001c0001t0002g0082a0001c0002t0001g0023a0002c0003t0018g0005 | 3 | HG02723.hp1 HG03041.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.32+16897_32+16902d others(8): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108551489 | |||||
| chr2:108551489
|
GCGCACAC others(1): Show |
G | 4 | a0001c0002t0001g0004a0001c0002t0001g0018a0001c0002t0012g0006others(1): Show | 4 | HG02040.hp2 HG02559.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+16897_32+16904d others(10): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108551489 | |||||
| chr2:108551489
|
GCGCACAC others(9): Show |
G | 9 | a0001c0002t0001g0020a0001c0002t0001g0024a0001c0002t0001g0025others(6): Show | 9 | HG01106.hp1 HG02040.hp1 HG04184.hp2 others(6): Show |
intron_variant | MODIFIER | c.32+16897_32+16912d others(18): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108551489 | |||||
| chr2:108551491
|
G | A | 29 | a0001c0001t0002g0084a0001c0001t0002g0089a0001c0001t0002g0090others(26): Show | 29 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(26): Show |
intron_variant | MODIFIER | c.32+16897G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108551491 | ||||||
| chr2:108551491
|
G | GCA | 31 | a0001c0001t0002g0076a0001c0001t0002g0086a0001c0001t0002g0096others(28): Show | 31 | HG00099.hp2 HG00741.hp2 HG01169.hp1 others(28): Show |
intron_variant | MODIFIER | c.32+16937_32+16938d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108551491 | |||||
| chr2:108551491
|
G | GCACA | 11 | a0001c0001t0002g0111a0001c0001t0002g0114a0001c0001t0002g0118others(8): Show | 11 | HG01884.hp1 HG03225.hp2 HG03942.hp2 others(8): Show |
intron_variant | MODIFIER | c.32+16935_32+16938d others(6): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108551491 | |||||
| chr2:108551491
|
G | GCACACA | 6 | a0001c0001t0002g0104a0001c0001t0002g0116a0001c0001t0002g0117others(3): Show | 6 | HG01346.hp2 HG02055.hp1 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.32+16933_32+16938d others(8): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108551491 | |||||
| chr2:108551491
|
GCA | G | 24 | a0001c0001t0002g0083a0001c0001t0002g0099a0001c0001t0002g0125others(21): Show | 24 | HG00639.hp2 HG01074.hp2 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.32+16937_32+16938d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108551491 | |||||
| chr2:108551491
|
GCACA | G | 29 | a0001c0001t0002g0094a0001c0001t0002g0095a0001c0001t0002g0121others(26): Show | 29 | HG00140.hp1 HG00280.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.32+16935_32+16938d others(6): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108551491 | |||||
| chr2:108551491
|
GCACACA | G | 29 | a0001c0001t0003g0138a0001c0001t0003g0141a0001c0001t0003g0142others(26): Show | 29 | HG01243.hp1 HG01256.hp2 HG01258.hp2 others(26): Show |
intron_variant | MODIFIER | c.32+16933_32+16938d others(8): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108551491 | |||||
| chr2:108551493
|
A | G | 2 | a0001c0001t0003g0191a0001c0001t0006g0101 | 2 | HG02698.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.32+16899A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108551493 | ||||||
| chr2:108551495
|
A | G | 5 | a0001c0001t0002g0083a0001c0002t0004g0226a0001c0002t0004g0234others(2): Show | 5 | HG02602.hp2 HG02622.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.32+16901A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108551495 | ||||||
| chr2:108551497
|
A | G | 4 | a0001c0002t0004g0244a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 HG04184.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+16903A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108551497 | ||||||
| chr2:108551499
|
A | G | 19 | a0001c0002t0004g0225a0001c0002t0004g0227a0001c0002t0004g0228others(16): Show | 19 | HG02895.hp1 HG02897.hp2 HG03017.hp2 others(16): Show |
intron_variant | MODIFIER | c.32+16905A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108551499 | ||||||
| chr2:108551501
|
A | G | 1 | a0001c0002t0004g0233 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.32+16907A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108551501 | ||||||
| chr2:108551598
|
ATATATAT others(3): Show |
A | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+17022_32+17031d others(12): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108551598 | |||||
| chr2:108551601
|
T | C | 1 | a0001c0002t0004g0236 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.32+17007T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108551601 | ||||||
| chr2:108551604
|
ATATGTAT others(14): Show |
A | 1 | a0001c0002t0004g0236 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.32+17011_32+17031d others(23): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108551604 | ||||||
| chr2:108551606
|
A | ATGTATAT others(13): Show |
1 | a0001c0002t0001g0050 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.32+17051_32+17070d others(22): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108551606 | |||||
| chr2:108551606
|
A | ATGTATAT others(13): Show |
5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+17029_32+17030i others(22): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108551606 | |||||
| chr2:108551606
|
A | ATGTATAT others(3): Show |
2 | a0001c0002t0012g0006a0001c0002t0012g0007 | 2 | HG02040.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.32+17021_32+17022i others(12): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108551606 | |||||
| chr2:108551606
|
ATGTATAT others(13): Show |
A | 2 | a0001c0002t0001g0002a0001c0002t0001g0003 | 2 | NA19043.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.32+17051_32+17070d others(22): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108551606 | |||||
| chr2:108551624
|
A | C | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+17030A>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108551624 | ||||||
| chr2:108551634
|
A | G | 1 | a0001c0002t0004g0236 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.32+17040A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108551634 | ||||||
| chr2:108551636
|
A | T | 1 | a0001c0002t0004g0236 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.32+17042A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108551636 | ||||||
| chr2:108551726
|
AATGTATA others(70): Show |
A | 1 | a0001c0002t0001g0032 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.32+17158_32+17234d others(79): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108551726 | |||||
| chr2:108551752
|
C | G | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+17158C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108551752 | ||||||
| chr2:108551753
|
A | G | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+17159A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108551753 | ||||||
| chr2:108551756
|
C | T | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+17162C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108551756 | ||||||
| chr2:108551757
|
C | G | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+17163C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108551757 | ||||||
| chr2:108551905
|
G | T | 1 | a0001c0002t0001g0004 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.32+17311G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108551905 | ||||||
| chr2:108551919
|
ATG | A | 21 | a0001c0001t0003g0192a0001c0002t0001g0033a0001c0002t0004g0226others(18): Show | 21 | HG01074.hp2 HG02258.hp1 HG02602.hp2 others(18): Show |
intron_variant | MODIFIER | c.32+17329_32+17330d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108551919 | |||||
| chr2:108551923
|
G | A | 126 | a0001c0001t0003g0001a0001c0001t0003g0137a0001c0001t0003g0138others(123): Show | 127 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.32+17329G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108551923 | ||||||
| chr2:108551923
|
GTA | G | 11 | a0001c0001t0003g0202a0001c0001t0003g0203a0001c0001t0003g0204others(8): Show | 11 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.32+17335_32+17336d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108551923 | |||||
| chr2:108551929
|
A | G | 1 | a0001c0001t0014g0159 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.32+17335A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108551929 | ||||||
| chr2:108551929
|
ATG | A | 14 | a0001c0001t0002g0075a0001c0001t0002g0086a0001c0001t0002g0087others(11): Show | 14 | HG01243.hp2 NA18940.hp1 NA18945.hp2 others(11): Show |
intron_variant | MODIFIER | c.32+17359_32+17360d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108551929 | |||||
| chr2:108551931
|
G | A | 15 | a0001c0001t0003g0192a0001c0002t0001g0033a0001c0002t0004g0226others(12): Show | 15 | HG01074.hp2 HG02602.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.32+17337G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108551931 | ||||||
| chr2:108551945
|
G | GTGTATAT others(17): Show |
2 | a0001c0004t0013g0073a0001c0004t0013g0074 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.32+17354_32+17355i others(26): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108551945 | |||||
| chr2:108551947
|
G | A | 8 | a0001c0002t0004g0225a0001c0002t0004g0229a0001c0002t0004g0230others(5): Show | 8 | NA18940.hp2 NA18947.hp2 NA18960.hp1 others(5): Show |
intron_variant | MODIFIER | c.32+17353G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108551947 | ||||||
| chr2:108551949
|
G | A | 21 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(18): Show | 21 | HG02602.hp2 HG02622.hp1 HG02895.hp1 others(18): Show |
intron_variant | MODIFIER | c.32+17355G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108551949 | ||||||
| chr2:108551951
|
G | A | 50 | a0001c0001t0002g0076a0001c0001t0002g0082a0001c0001t0002g0083others(47): Show | 50 | HG00741.hp2 HG01243.hp2 HG01346.hp2 others(47): Show |
intron_variant | MODIFIER | c.32+17357G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108551951 | ||||||
| chr2:108551951
|
G | GTATA | 6 | a0001c0001t0002g0085a0001c0001t0002g0103a0001c0001t0002g0106others(3): Show | 6 | HG00099.hp2 HG01168.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.32+17358_32+17359i others(6): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108551951 | |||||
| chr2:108551951
|
GTGTA | G | 68 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.32+17359_32+17362d others(6): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108551951 | |||||
| chr2:108551953
|
G | A | 87 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(84): Show | 87 | HG00099.hp2 HG00741.hp2 HG01074.hp2 others(84): Show |
intron_variant | MODIFIER | c.32+17359G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108551953 | ||||||
| chr2:108551953
|
G | GTA | 25 | a0001c0001t0003g0001a0001c0001t0003g0137a0001c0001t0003g0138others(22): Show | 26 | HG00323.hp1 HG00639.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.32+17377_32+17378d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108551953 | |||||
| chr2:108551953
|
G | GTATATAT others(5): Show |
1 | a0001c0001t0014g0159 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.32+17367_32+17378d others(14): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108551953 | |||||
| chr2:108551953
|
G | GTGTA | 5 | a0001c0001t0003g0196a0001c0001t0010g0193a0001c0001t0010g0194others(2): Show | 5 | HG02622.hp2 HG02818.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+17360_32+17361i others(6): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108551953 | |||||
| chr2:108551953
|
G | GTGTATAT others(5): Show |
1 | a0001c0001t0014g0160 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.32+17360_32+17361i others(14): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108551953 | |||||
| chr2:108551953
|
GTA | G | 9 | a0001c0002t0001g0046a0001c0002t0001g0049a0001c0002t0007g0214others(6): Show | 9 | HG01169.hp2 HG02258.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.32+17377_32+17378d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108551953 | |||||
| chr2:108551953
|
GTATATA | G | 3 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0081 | 3 | NA18954.hp2 NA18970.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.32+17373_32+17378d others(8): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108551953 | |||||
| chr2:108551955
|
A | G | 13 | a0001c0001t0003g0190a0001c0001t0003g0202a0001c0001t0003g0203others(10): Show | 13 | HG01358.hp1 HG01884.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.32+17361A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108551955 | ||||||
| chr2:108551961
|
A | G | 1 | a0001c0002t0009g0078 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.32+17367A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108551961 | ||||||
| chr2:108551969
|
A | G | 2 | a0001c0002t0012g0006a0001c0002t0012g0007 | 2 | HG02040.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.32+17375A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108551969 | ||||||
| chr2:108552052
|
A | G | 208 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(205): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.32+17458A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108552052 | ||||||
| chr2:108552108
|
A | C | 1 | a0001c0001t0002g0201 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.32+17514A>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108552108 | ||||||
| chr2:108552142
|
A | G | 74 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(71): Show | 74 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.32+17548A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108552142 | ||||||
| chr2:108552190
|
GTATA | G | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+17601_32+17604d others(6): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108552190 | |||||
| chr2:108552231
|
TTATATAT others(2): Show |
T | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+17658_32+17666d others(11): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108552231 | |||||
| chr2:108552240
|
CTATATAT others(58): Show |
C | 1 | a0001c0001t0002g0199 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.32+17655_32+17719d others(67): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108552240 | |||||
| chr2:108552266
|
A | ATAGTATA others(29): Show |
1 | a0001c0001t0002g0117 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.32+17732_32+17767d others(38): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108552266 | |||||
| chr2:108552266
|
ATAGTATA others(29): Show |
A | 16 | a0001c0001t0002g0121a0001c0001t0002g0125a0001c0002t0001g0017others(13): Show | 16 | HG01192.hp1 HG02602.hp2 HG02965.hp1 others(13): Show |
intron_variant | MODIFIER | c.32+17732_32+17767d others(38): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108552266 | |||||
| chr2:108552268
|
A | G | 2 | a0001c0001t0014g0159a0001c0001t0014g0160 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.32+17674A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108552268 | ||||||
| chr2:108552283
|
CTATATAT others(33): Show |
C | 6 | a0001c0002t0004g0229a0001c0002t0004g0230a0001c0002t0004g0234others(3): Show | 6 | NA18947.hp2 NA18960.hp1 NA19062.hp1 others(3): Show |
intron_variant | MODIFIER | c.32+17696_32+17735d others(42): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108552283 | |||||
| chr2:108552302
|
G | A | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+17708G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108552302 | ||||||
| chr2:108552302
|
GTAGTATA others(61): Show |
G | 2 | a0001c0002t0007g0215a0001c0002t0007g0216 | 2 | HG02258.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.32+17734_32+17801d others(70): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108552302 | |||||
| chr2:108552316
|
AAACTATA others(28): Show |
A | 1 | a0001c0002t0004g0236 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.32+17725_32+17759d others(37): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108552316 | |||||
| chr2:108552335
|
C | T | 29 | a0001c0001t0003g0001a0001c0001t0003g0137a0001c0001t0003g0145others(26): Show | 30 | HG00323.hp1 HG00639.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.32+17741C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108552335 | ||||||
| chr2:108552338
|
G | A | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+17744G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108552338 | ||||||
| chr2:108552420
|
A | T | 11 | a0001c0001t0003g0202a0001c0001t0003g0203a0001c0001t0003g0204others(8): Show | 11 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.32+17826A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108552420 | ||||||
| chr2:108552475
|
G | A | 1 | a0001c0002t0004g0237 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.32+17881G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108552475 | ||||||
| chr2:108552488
|
G | C | 1 | a0001c0001t0024g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.32+17894G>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108552488 | ||||||
| chr2:108552581
|
T | A | 4 | a0001c0001t0002g0094a0001c0001t0002g0095a0001c0001t0002g0098others(1): Show | 4 | HG02818.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+17987T>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108552581 | ||||||
| chr2:108552582
|
TTGGGTG | T | 4 | a0001c0001t0002g0094a0001c0001t0002g0095a0001c0001t0002g0098others(1): Show | 4 | HG02818.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+17991_32+17996d others(8): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108552582 | |||||
| chr2:108552585
|
G | GGT | 37 | a0001c0001t0003g0001a0001c0001t0003g0137a0001c0001t0003g0138others(34): Show | 38 | HG00323.hp1 HG00639.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.32+18018_32+18019d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108552585 | |||||
| chr2:108552585
|
G | GGTGTGTG others(1): Show |
3 | a0001c0002t0004g0226a0001c0002t0009g0078a0001c0002t0009g0081 | 3 | HG02622.hp1 NA18954.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.32+18012_32+18019d others(10): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108552585 | |||||
| chr2:108552585
|
G | GGTGTGTG others(3): Show |
19 | a0001c0002t0004g0225a0001c0002t0004g0227a0001c0002t0004g0228others(16): Show | 19 | HG01261.hp2 HG02602.hp2 HG02897.hp2 others(16): Show |
intron_variant | MODIFIER | c.32+18010_32+18019d others(12): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108552585 | |||||
| chr2:108552585
|
G | GGTGTGTG others(5): Show |
4 | a0001c0002t0004g0231a0001c0002t0004g0240a0001c0002t0004g0241others(1): Show | 4 | HG02895.hp1 HG03654.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+18008_32+18019d others(14): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108552585 | |||||
| chr2:108552585
|
G | GGTGTGTG others(11): Show |
1 | a0002c0003t0018g0005 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.32+18002_32+18019d others(20): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108552585 | |||||
| chr2:108552585
|
GGTGTGTG others(1): Show |
G | 57 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(54): Show | 57 | HG00099.hp2 HG00741.hp2 HG01109.hp2 others(54): Show |
intron_variant | MODIFIER | c.32+18012_32+18019d others(10): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108552585 | |||||
| chr2:108552588
|
G | GTGTGTGT others(9): Show |
5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+18009_32+18010i others(18): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108552588 | |||||
| chr2:108552590
|
G | GTGTGTGT others(7): Show |
7 | a0001c0002t0001g0008a0001c0002t0001g0034a0001c0002t0001g0068others(4): Show | 7 | HG00639.hp1 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.32+18009_32+18010i others(16): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108552590 | |||||
| chr2:108552590
|
G | T | 4 | a0001c0001t0002g0094a0001c0001t0002g0095a0001c0001t0002g0098others(1): Show | 4 | HG02818.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+17996G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108552590 | ||||||
| chr2:108552592
|
G | GTGTGTGT others(5): Show |
66 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(63): Show | 66 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.32+18009_32+18010i others(14): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108552592 | |||||
| chr2:108552593
|
T | G | 4 | a0001c0001t0002g0094a0001c0001t0002g0095a0001c0001t0002g0098others(1): Show | 4 | HG02818.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+17999T>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108552593 | ||||||
| chr2:108552610
|
G | GTGTGTGT others(6): Show |
1 | a0001c0002t0004g0236 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.32+18019_32+18020i others(15): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108552610 | |||||
| chr2:108552613
|
T | C | 3 | a0001c0001t0002g0182a0001c0001t0002g0183a0001c0001t0002g0184 | 3 | HG02257.hp2 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.32+18019T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108552613 | ||||||
| chr2:108552814
|
G | C | 1 | a0001c0002t0004g0236 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.32+18220G>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108552814 | ||||||
| chr2:108553419
|
C | T | 1 | a0001c0001t0003g0202 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.32+18825C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108553419 | ||||||
| chr2:108553598
|
T | C | 107 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(104): Show | 107 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.32+19004T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108553598 | ||||||
| chr2:108553610
|
T | C | 74 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(71): Show | 74 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.32+19016T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108553610 | ||||||
| chr2:108553651
|
A | G | 1 | a0001c0002t0025g0026 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.32+19057A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108553651 | ||||||
| chr2:108553723
|
G | A | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+19129G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108553723 | ||||||
| chr2:108553846
|
A | T | 1 | a0001c0002t0004g0236 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.32+19252A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108553846 | ||||||
| chr2:108553850
|
T | G | 145 | a0001c0001t0003g0001a0001c0001t0003g0137a0001c0001t0003g0138others(142): Show | 146 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.32+19256T>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108553850 | ||||||
| chr2:108553943
|
T | C | 1 | a0001c0002t0001g0035 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.32+19349T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108553943 | ||||||
| chr2:108553964
|
A | G | 69 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(66): Show | 69 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.32+19370A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108553964 | ||||||
| chr2:108554018
|
C | T | 1 | a0001c0002t0012g0007 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.32+19424C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108554018 | ||||||
| chr2:108554275
|
A | G | 98 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(95): Show | 98 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.32+19681A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108554275 | ||||||
| chr2:108554383
|
G | C | 161 | a0001c0001t0003g0001a0001c0001t0003g0137a0001c0001t0003g0138others(158): Show | 162 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.32+19789G>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108554383 | ||||||
| chr2:108554457
|
A | G | 2 | a0001c0001t0017g0156a0001c0001t0017g0157 | 2 | HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.32+19863A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108554457 | ||||||
| chr2:108554503
|
G | A | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+19909G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108554503 | ||||||
| chr2:108554657
|
G | C | 1 | a0001c0001t0002g0109 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.32+20063G>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108554657 | ||||||
| chr2:108554743
|
G | A | 2 | a0001c0002t0001g0002a0001c0002t0001g0003 | 2 | NA19043.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.32+20149G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108554743 | ||||||
| chr2:108554851
|
A | C | 1 | a0002c0003t0018g0005 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.32+20257A>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108554851 | ||||||
| chr2:108554917
|
C | A | 38 | a0001c0001t0003g0001a0001c0001t0003g0137a0001c0001t0003g0138others(35): Show | 39 | HG00323.hp1 HG00639.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.32+20323C>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108554917 | ||||||
| chr2:108555005
|
C | A | 74 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(71): Show | 74 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.32+20411C>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108555005 | ||||||
| chr2:108555167
|
C | T | 2 | a0001c0001t0002g0076a0001c0001t0005g0077 | 2 | HG00741.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.32+20573C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108555167 | ||||||
| chr2:108555426
|
C | T | 107 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(104): Show | 107 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.32+20832C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108555426 | ||||||
| chr2:108555572
|
C | T | 2 | a0001c0001t0005g0164a0001c0001t0006g0179 | 2 | HG01099.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.32+20978C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108555572 | ||||||
| chr2:108555573
|
G | A | 3 | a0001c0001t0010g0193a0001c0001t0010g0194a0001c0001t0010g0195 | 3 | HG03471.hp1 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.32+20979G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108555573 | ||||||
| chr2:108555802
|
T | C | 1 | a0001c0002t0001g0008 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.32+21208T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108555802 | ||||||
| chr2:108555936
|
A | C | 1 | a0001c0001t0006g0171 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.32+21342A>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108555936 | ||||||
| chr2:108556013
|
A | ACAAATCT others(15): Show |
1 | a0001c0002t0004g0236 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.32+21423_32+21424i others(24): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108556013 | |||||
| chr2:108556131
|
T | C | 29 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(26): Show | 29 | HG02258.hp1 HG02602.hp2 HG02622.hp1 others(26): Show |
intron_variant | MODIFIER | c.32+21537T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108556131 | ||||||
| chr2:108556172
|
C | G | 1 | a0002c0003t0018g0005 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.32+21578C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108556172 | ||||||
| chr2:108556626
|
C | A | 1 | a0001c0001t0029g0186 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.32+22032C>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108556626 | ||||||
| chr2:108556658
|
G | C | 1 | a0001c0001t0003g0151 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.32+22064G>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108556658 | ||||||
| chr2:108556751
|
C | T | 2 | a0001c0001t0003g0139a0001c0001t0003g0142 | 2 | HG03041.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.32+22157C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108556751 | ||||||
| chr2:108556811
|
A | T | 1 | a0001c0002t0001g0032 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.32+22217A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108556811 | ||||||
| chr2:108556838
|
A | G | 68 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.32+22244A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108556838 | ||||||
| chr2:108557026
|
C | T | 1 | a0001c0002t0001g0055 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.32+22432C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108557026 | ||||||
| chr2:108557244
|
A | G | 1 | a0001c0002t0001g0062 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.32+22650A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108557244 | ||||||
| chr2:108557277
|
A | G | 1 | a0001c0002t0001g0040 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.32+22683A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108557277 | ||||||
| chr2:108557474
|
T | C | 109 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(106): Show | 109 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.32+22880T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108557474 | ||||||
| chr2:108557520
|
C | CT | 28 | a0001c0001t0003g0161a0001c0002t0004g0225a0001c0002t0004g0226others(25): Show | 28 | HG01981.hp1 HG02040.hp2 HG02572.hp1 others(25): Show |
intron_variant | MODIFIER | c.32+22938dupT | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108557520 | |||||
| chr2:108557663
|
C | T | 1 | a0001c0002t0001g0018 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.32+23069C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108557663 | ||||||
| chr2:108557780
|
C | T | 154 | a0001c0001t0003g0001a0001c0001t0003g0130a0001c0001t0003g0131others(151): Show | 155 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.32+23186C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108557780 | ||||||
| chr2:108557838
|
A | C | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+23244A>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108557838 | ||||||
| chr2:108557925
|
A | G | 68 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.32+23331A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108557925 | ||||||
| chr2:108557929
|
A | G | 1 | a0001c0002t0001g0054 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.32+23335A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108557929 | ||||||
| chr2:108557979
|
G | A | 25 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(22): Show | 25 | HG02572.hp1 HG02602.hp2 HG02622.hp1 others(22): Show |
intron_variant | MODIFIER | c.32+23385G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108557979 | ||||||
| chr2:108558012
|
A | C | 3 | a0001c0001t0002g0182a0001c0001t0002g0183a0001c0001t0002g0184 | 3 | HG02257.hp2 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.32+23418A>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108558012 | ||||||
| chr2:108558061
|
T | G | 168 | a0001c0001t0003g0001a0001c0001t0003g0130a0001c0001t0003g0131others(165): Show | 169 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.32+23467T>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108558061 | ||||||
| chr2:108558159
|
C | T | 109 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(106): Show | 109 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.32+23565C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108558159 | ||||||
| chr2:108558222
|
CT | C | 103 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(100): Show | 103 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.32+23641delT | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108558222 | |||||
| chr2:108558241
|
G | A | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+23647G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108558241 | ||||||
| chr2:108558291
|
C | T | 1 | a0001c0002t0004g0228 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.32+23697C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108558291 | ||||||
| chr2:108558319
|
G | A | 75 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(72): Show | 75 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.32+23725G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108558319 | ||||||
| chr2:108558430
|
C | T | 75 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(72): Show | 75 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.32+23836C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108558430 | ||||||
| chr2:108558434
|
C | T | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.32+23840C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108558434 | ||||||
| chr2:108558456
|
G | C | 2 | a0001c0001t0002g0126a0001c0001t0002g0127 | 2 | NA18970.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.32+23862G>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108558456 | ||||||
| chr2:108558503
|
C | T | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+23909C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108558503 | ||||||
| chr2:108558555
|
A | G | 1 | a0001c0001t0005g0185 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.32+23961A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108558555 | ||||||
| chr2:108558624
|
T | C | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+24030T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108558624 | ||||||
| chr2:108558675
|
A | AT | 80 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(77): Show | 80 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.32+24094dupT | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108558675 | |||||
| chr2:108558675
|
AT | A | 10 | a0001c0001t0002g0084a0001c0001t0002g0089a0001c0001t0002g0090others(7): Show | 10 | HG01167.hp1 HG01175.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.32+24094delT | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108558675 | |||||
| chr2:108558755
|
C | T | 1 | a0001c0002t0004g0228 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.32+24161C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108558755 | ||||||
| chr2:108558795
|
C | G | 3 | a0001c0001t0003g0131a0001c0001t0003g0132a0001c0001t0003g0133 | 3 | NA18947.hp1 NA18963.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.32+24201C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108558795 | ||||||
| chr2:108558901
|
C | T | 5 | a0001c0001t0003g0189a0001c0001t0003g0190a0001c0001t0003g0191others(2): Show | 5 | HG01074.hp2 HG01358.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.32+24307C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108558901 | ||||||
| chr2:108559267
|
G | C | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+24673G>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108559267 | ||||||
| chr2:108559286
|
G | T | 100 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.32+24692G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108559286 | ||||||
| chr2:108559476
|
C | G | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+24882C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108559476 | ||||||
| chr2:108559476
|
C | T | 1 | a0001c0002t0001g0039 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.32+24882C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108559476 | ||||||
| chr2:108559682
|
G | T | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+25088G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108559682 | ||||||
| chr2:108559944
|
G | T | 45 | a0001c0001t0003g0001a0001c0001t0003g0130a0001c0001t0003g0131others(42): Show | 46 | HG00323.hp1 HG00639.hp2 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.32+25350G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108559944 | ||||||
| chr2:108559989
|
G | A | 1 | a0001c0002t0004g0232 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.32+25395G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108559989 | ||||||
| chr2:108560157
|
T | TG | 25 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(22): Show | 25 | HG02572.hp1 HG02602.hp2 HG02622.hp1 others(22): Show |
intron_variant | MODIFIER | c.32+25564dupG | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108560157 | |||||
| chr2:108560215
|
TC | T | 3 | a0001c0001t0002g0182a0001c0001t0002g0183a0001c0001t0002g0184 | 3 | HG02257.hp2 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.32+25622delC | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108560215 | ||||||
| chr2:108560226
|
A | T | 1 | a0001c0002t0001g0062 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.32+25632A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108560226 | ||||||
| chr2:108560382
|
C | T | 1 | a0001c0001t0014g0160 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.32+25788C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108560382 | ||||||
| chr2:108560396
|
G | T | 1 | a0002c0003t0026g0219 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.32+25802G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108560396 | ||||||
| chr2:108560482
|
C | T | 1 | a0001c0002t0004g0228 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.32+25888C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108560482 | ||||||
| chr2:108560503
|
C | G | 2 | a0001c0002t0007g0215a0001c0002t0007g0216 | 2 | HG02258.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.32+25909C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108560503 | ||||||
| chr2:108560524
|
CTG | C | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+25933_32+25934d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108560524 | |||||
| chr2:108560675
|
A | AAC | 3 | a0001c0001t0002g0094a0001c0001t0002g0095a0001c0001t0002g0099 | 3 | HG02896.hp2 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.32+26093_32+26094d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108560675 | |||||
| chr2:108560777
|
G | C | 4 | a0001c0001t0002g0094a0001c0001t0002g0095a0001c0001t0002g0098others(1): Show | 4 | HG02818.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+26183G>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108560777 | ||||||
| chr2:108561508
|
A | G | 1 | a0001c0001t0014g0159 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.32+26914A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108561508 | ||||||
| chr2:108561550
|
C | T | 1 | a0001c0001t0002g0201 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.32+26956C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108561550 | ||||||
| chr2:108561677
|
C | T | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+27083C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108561677 | ||||||
| chr2:108561689
|
A | G | 1 | a0001c0002t0025g0026 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.32+27095A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108561689 | ||||||
| chr2:108561746
|
G | GT | 72 | a0001c0001t0002g0075a0001c0001t0002g0129a0001c0001t0003g0131others(69): Show | 72 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.32+27166dupT | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108561746 | |||||
| chr2:108561746
|
G | GTT | 22 | a0001c0002t0001g0039a0001c0002t0004g0225a0001c0002t0004g0226others(19): Show | 22 | HG02622.hp1 HG02895.hp1 HG02897.hp2 others(19): Show |
intron_variant | MODIFIER | c.32+27165_32+27166d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108561746 | |||||
| chr2:108561746
|
G | GTTT | 8 | a0001c0002t0004g0235a0001c0002t0004g0236a0001c0002t0008g0221others(5): Show | 8 | HG02486.hp1 HG02572.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.32+27164_32+27166d others(5): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108561746 | |||||
| chr2:108561746
|
G | T | 1 | a0001c0002t0001g0064 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.32+27152G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108561746 | ||||||
| chr2:108561847
|
A | G | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+27253A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108561847 | ||||||
| chr2:108561857
|
C | T | 4 | a0001c0001t0002g0076a0001c0001t0002g0119a0001c0001t0005g0077others(1): Show | 4 | HG00741.hp2 HG01993.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+27263C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108561857 | ||||||
| chr2:108561952
|
C | G | 3 | a0001c0001t0017g0156a0001c0001t0017g0157a0001c0001t0024g0162 | 3 | HG02647.hp1 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.32+27358C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108561952 | ||||||
| chr2:108561997
|
T | C | 100 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.32+27403T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108561997 | ||||||
| chr2:108562044
|
T | C | 1 | a0001c0001t0002g0089 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.32+27450T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108562044 | ||||||
| chr2:108562157
|
C | T | 2 | a0002c0003t0018g0005a0002c0003t0026g0219 | 2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.32+27563C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108562157 | ||||||
| chr2:108562161
|
CTGGCCAT others(10): Show |
C | 4 | a0001c0002t0001g0019a0001c0002t0001g0021a0001c0002t0001g0029others(1): Show | 4 | HG02717.hp2 HG02886.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+27568_32+27584d others(19): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108562161 | ||||||
| chr2:108562263
|
A | C | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.32+27669A>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108562263 | ||||||
| chr2:108562273
|
G | C | 1 | a0001c0002t0007g0215 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.32+27679G>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108562273 | ||||||
| chr2:108562527
|
C | A | 1 | a0001c0001t0002g0118 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.32+27933C>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108562527 | ||||||
| chr2:108562584
|
T | C | 1 | a0001c0002t0001g0044 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.32+27990T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108562584 | ||||||
| chr2:108562821
|
A | T | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+28227A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108562821 | ||||||
| chr2:108562832
|
G | A | 1 | a0001c0002t0001g0014 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.32+28238G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108562832 | ||||||
| chr2:108562915
|
A | G | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+28321A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108562915 | ||||||
| chr2:108562994
|
T | G | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+28400T>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108562994 | ||||||
| chr2:108563060
|
A | G | 1 | a0001c0001t0024g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.32+28466A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108563060 | ||||||
| chr2:108563063
|
A | G | 5 | a0001c0002t0001g0008a0001c0002t0001g0010a0001c0002t0001g0011others(2): Show | 5 | HG00323.hp2 HG00639.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.32+28469A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108563063 | ||||||
| chr2:108563098
|
C | A | 1 | a0001c0002t0009g0081 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.32+28504C>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108563098 | ||||||
| chr2:108563305
|
G | A | 1 | a0001c0002t0008g0221 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.32+28711G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108563305 | ||||||
| chr2:108563316
|
C | G | 21 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(18): Show | 21 | HG02602.hp2 HG02622.hp1 HG03017.hp2 others(18): Show |
intron_variant | MODIFIER | c.32+28722C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108563316 | ||||||
| chr2:108563510
|
TGTG | T | 25 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(22): Show | 25 | HG02572.hp1 HG02602.hp2 HG02622.hp1 others(22): Show |
intron_variant | MODIFIER | c.32+28921_32+28923d others(5): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108563510 | |||||
| chr2:108563749
|
G | T | 1 | a0001c0001t0002g0075 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.32+29155G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108563749 | ||||||
| chr2:108563765
|
C | T | 85 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0111others(82): Show | 85 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.32+29171C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108563765 | ||||||
| chr2:108563786
|
G | A | 1 | a0001c0002t0001g0021 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.32+29192G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108563786 | ||||||
| chr2:108563883
|
A | T | 45 | a0001c0001t0003g0001a0001c0001t0003g0130a0001c0001t0003g0131others(42): Show | 46 | HG00323.hp1 HG00639.hp2 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.32+29289A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108563883 | ||||||
| chr2:108564041
|
C | CA | 95 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(92): Show | 95 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.32+29468dupA | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108564041 | |||||
| chr2:108564041
|
CA | C | 70 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(67): Show | 70 | HG00741.hp2 HG01070.hp2 HG01109.hp2 others(67): Show |
intron_variant | MODIFIER | c.32+29468delA | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108564041 | |||||
| chr2:108564092
|
A | G | 21 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(18): Show | 21 | HG02602.hp2 HG02622.hp1 HG03017.hp2 others(18): Show |
intron_variant | MODIFIER | c.32+29498A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108564092 | ||||||
| chr2:108564160
|
T | C | 154 | a0001c0001t0003g0001a0001c0001t0003g0130a0001c0001t0003g0131others(151): Show | 155 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.32+29566T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108564160 | ||||||
| chr2:108564206
|
G | C | 1 | a0001c0001t0003g0189 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.32+29612G>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108564206 | ||||||
| chr2:108564402
|
C | T | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+29808C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108564402 | ||||||
| chr2:108564414
|
G | A | 75 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(72): Show | 75 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.32+29820G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108564414 | ||||||
| chr2:108564465
|
A | G | 2 | a0001c0004t0013g0073a0001c0004t0013g0074 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.32+29871A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108564465 | ||||||
| chr2:108564479
|
T | G | 25 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(22): Show | 25 | HG02572.hp1 HG02602.hp2 HG02622.hp1 others(22): Show |
intron_variant | MODIFIER | c.32+29885T>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108564479 | ||||||
| chr2:108564706
|
A | G | 7 | a0001c0001t0003g0130a0001c0001t0003g0131a0001c0001t0003g0132others(4): Show | 7 | NA18939.hp2 NA18942.hp1 NA18947.hp1 others(4): Show |
intron_variant | MODIFIER | c.32+30112A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108564706 | ||||||
| chr2:108564797
|
G | C | 1 | a0001c0001t0002g0075 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.32+30203G>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108564797 | ||||||
| chr2:108564951
|
G | A | 1 | a0001c0001t0003g0148 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.32+30357G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108564951 | ||||||
| chr2:108564954
|
C | T | 1 | a0001c0002t0001g0053 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.32+30360C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108564954 | ||||||
| chr2:108564956
|
GCCCTAGC others(14): Show |
G | 109 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(106): Show | 109 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.32+30386_32+30406d others(23): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108564956 | |||||
| chr2:108565035
|
C | CT | 75 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(72): Show | 75 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.32+30442dupT | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108565035 | |||||
| chr2:108565105
|
C | T | 8 | a0001c0001t0003g0187a0001c0001t0003g0188a0001c0001t0003g0189others(5): Show | 8 | HG00639.hp2 HG01074.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.32+30511C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108565105 | ||||||
| chr2:108565449
|
A | G | 2 | a0001c0001t0002g0096a0001c0001t0020g0100 | 2 | HG02735.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.32+30855A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108565449 | ||||||
| chr2:108566138
|
T | C | 25 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(22): Show | 25 | HG02572.hp1 HG02602.hp2 HG02622.hp1 others(22): Show |
intron_variant | MODIFIER | c.32+31544T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108566138 | ||||||
| chr2:108566174
|
C | T | 1 | a0003c0005t0001g0041 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.32+31580C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108566174 | ||||||
| chr2:108566267
|
C | T | 1 | a0001c0002t0009g0080 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.32+31673C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108566267 | ||||||
| chr2:108566420
|
A | G | 1 | a0001c0001t0024g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.32+31826A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108566420 | ||||||
| chr2:108566448
|
T | C | 1 | a0001c0001t0003g0152 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.32+31854T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108566448 | ||||||
| chr2:108566660
|
G | T | 1 | a0001c0002t0001g0021 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.32+32066G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108566660 | ||||||
| chr2:108566836
|
A | G | 1 | a0001c0001t0003g0187 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.32+32242A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108566836 | ||||||
| chr2:108566849
|
A | T | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+32255A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108566849 | ||||||
| chr2:108566884
|
A | G | 1 | a0001c0001t0002g0104 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.32+32290A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108566884 | ||||||
| chr2:108566901
|
G | A | 68 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.32+32307G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108566901 | ||||||
| chr2:108567011
|
A | G | 3 | a0001c0001t0002g0182a0001c0001t0002g0183a0001c0001t0002g0184 | 3 | HG02257.hp2 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.32+32417A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108567011 | ||||||
| chr2:108567950
|
T | C | 1 | a0001c0002t0004g0232 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.32+33356T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108567950 | ||||||
| chr2:108567967
|
C | T | 25 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(22): Show | 25 | HG02572.hp1 HG02602.hp2 HG02622.hp1 others(22): Show |
intron_variant | MODIFIER | c.32+33373C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108567967 | ||||||
| chr2:108568079
|
A | T | 1 | a0002c0003t0026g0219 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.32+33485A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108568079 | ||||||
| chr2:108568207
|
G | T | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+33613G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108568207 | ||||||
| chr2:108568340
|
T | G | 2 | a0001c0001t0002g0123a0001c0001t0021g0120 | 2 | HG01243.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32+33746T>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108568340 | ||||||
| chr2:108568684
|
G | T | 1 | a0001c0001t0014g0160 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.32+34090G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108568684 | ||||||
| chr2:108568804
|
T | C | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+34210T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108568804 | ||||||
| chr2:108568820
|
G | A | 3 | a0001c0002t0001g0022a0001c0002t0001g0033a0001c0002t0001g0051 | 3 | NA18954.hp1 NA18977.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.32+34226G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108568820 | ||||||
| chr2:108568952
|
C | T | 23 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(20): Show | 23 | HG02602.hp2 HG02622.hp1 HG02895.hp1 others(20): Show |
intron_variant | MODIFIER | c.32+34358C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108568952 | ||||||
| chr2:108569112
|
C | T | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.32+34518C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108569112 | ||||||
| chr2:108569190
|
C | T | 4 | a0001c0001t0003g0001a0001c0001t0003g0137a0001c0001t0003g0152others(1): Show | 5 | HG00323.hp1 HG01074.hp1 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.32+34596C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108569190 | ||||||
| chr2:108569325
|
A | C | 68 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.32+34731A>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108569325 | ||||||
| chr2:108569606
|
G | A | 1 | a0001c0002t0008g0223 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.32+35012G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108569606 | ||||||
| chr2:108569622
|
G | A | 90 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(87): Show | 90 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.32+35028G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108569622 | ||||||
| chr2:108569764
|
C | CCTTTTTT others(3): Show |
2 | a0001c0002t0001g0010a0001c0002t0001g0014 | 2 | HG00323.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.32+35170_32+35171i others(12): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108569764 | ||||||
| chr2:108569764
|
C | CCTTTTTT others(4): Show |
23 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0011others(20): Show | 23 | HG00099.hp1 HG00639.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.32+35170_32+35171i others(13): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108569764 | ||||||
| chr2:108569764
|
C | CCTTTTTT others(5): Show |
31 | a0001c0002t0001g0018a0001c0002t0001g0020a0001c0002t0001g0022others(28): Show | 31 | HG01070.hp1 HG01106.hp1 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.32+35170_32+35171i others(14): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108569764 | ||||||
| chr2:108569764
|
C | CCTTTTTT others(6): Show |
7 | a0001c0002t0001g0015a0001c0002t0001g0025a0001c0002t0001g0034others(4): Show | 7 | HG01167.hp2 HG01361.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.32+35170_32+35171i others(15): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108569764 | ||||||
| chr2:108569764
|
C | CCTTTTTT others(21): Show |
1 | a0001c0002t0001g0004 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.32+35170_32+35171i others(30): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108569764 | ||||||
| chr2:108569764
|
C | CT | 7 | a0001c0001t0002g0123a0001c0001t0003g0196a0001c0001t0005g0169others(4): Show | 7 | HG01261.hp1 HG02622.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.32+35189dupT | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108569764 | |||||
| chr2:108569764
|
C | CTTTTTTT others(3): Show |
1 | a0002c0003t0026g0219 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.32+35180_32+35189d others(12): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108569764 | |||||
| chr2:108569764
|
C | CTTTTTTT others(5): Show |
1 | a0001c0002t0009g0078 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.32+35178_32+35189d others(14): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108569764 | |||||
| chr2:108569764
|
C | CTTTTTTT others(12): Show |
2 | a0001c0002t0007g0215a0001c0002t0007g0216 | 2 | HG02258.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.32+35171_32+35189d others(21): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108569764 | |||||
| chr2:108569764
|
C | CTTTTTTT others(13): Show |
1 | a0001c0002t0004g0240 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.32+35189_32+35190i others(22): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108569764 | |||||
| chr2:108569764
|
C | CTTTTTTT others(14): Show |
2 | a0001c0002t0007g0214a0001c0002t0007g0217 | 2 | HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.32+35189_32+35190i others(23): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108569764 | |||||
| chr2:108569764
|
C | CTTTTTTT others(15): Show |
1 | a0001c0002t0007g0218 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.32+35189_32+35190i others(24): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108569764 | |||||
| chr2:108569764
|
C | CTTTTTTT others(19): Show |
1 | a0001c0002t0004g0245 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.32+35189_32+35190i others(28): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108569764 | |||||
| chr2:108569764
|
C | CTTTTTTT others(20): Show |
1 | a0001c0002t0004g0226 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.32+35189_32+35190i others(29): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108569764 | |||||
| chr2:108569764
|
C | CTTTTTTT others(23): Show |
1 | a0001c0002t0004g0225 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.32+35189_32+35190i others(32): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108569764 | |||||
| chr2:108569764
|
C | CTTTTTTT others(24): Show |
3 | a0001c0002t0008g0221a0001c0002t0008g0223a0001c0002t0009g0080 | 3 | HG01261.hp2 HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.32+35189_32+35190i others(33): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108569764 | |||||
| chr2:108569764
|
C | CTTTTTTT others(28): Show |
3 | a0001c0002t0004g0238a0001c0002t0004g0242a0001c0002t0009g0081 | 3 | HG03669.hp1 NA18954.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.32+35189_32+35190i others(37): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108569764 | |||||
| chr2:108569764
|
C | CTTTTTTT others(29): Show |
2 | a0001c0002t0004g0229a0001c0002t0009g0079 | 2 | NA19074.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.32+35189_32+35190i others(38): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108569764 | |||||
| chr2:108569764
|
C | CTTTTTTT others(30): Show |
4 | a0001c0002t0004g0235a0001c0002t0004g0237a0001c0002t0004g0244others(1): Show | 4 | HG02602.hp2 HG03017.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+35189_32+35190i others(39): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108569764 | |||||
| chr2:108569764
|
C | CTTTTTTT others(31): Show |
3 | a0001c0002t0004g0230a0001c0002t0004g0236a0001c0002t0008g0224 | 3 | HG02486.hp1 NA18940.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.32+35189_32+35190i others(40): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108569764 | |||||
| chr2:108569764
|
C | CTTTTTTT others(32): Show |
1 | a0001c0002t0004g0231 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.32+35189_32+35190i others(41): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108569764 | |||||
| chr2:108569764
|
C | CTTTTTTT others(33): Show |
1 | a0001c0002t0004g0241 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.32+35189_32+35190i others(42): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108569764 | |||||
| chr2:108569764
|
C | CTTTTTTT others(35): Show |
3 | a0001c0002t0004g0228a0001c0002t0004g0233a0001c0002t0004g0239 | 3 | HG03491.hp2 NA19066.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.32+35189_32+35190i others(44): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108569764 | |||||
| chr2:108569764
|
C | CTTTTTTT others(36): Show |
2 | a0001c0002t0004g0227a0001c0002t0008g0222 | 2 | HG03195.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.32+35189_32+35190i others(45): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108569764 | |||||
| chr2:108569764
|
C | CTTTTTTT others(41): Show |
1 | a0001c0002t0004g0232 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.32+35189_32+35190i others(50): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108569764 | |||||
| chr2:108569768
|
T | C | 2 | a0001c0002t0001g0061a0001c0002t0001g0062 | 2 | HG00140.hp2 HG00280.hp1 |
intron_variant | MODIFIER | c.32+35174T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108569768 | ||||||
| chr2:108570020
|
A | G | 1 | a0001c0001t0003g0190 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.32+35426A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108570020 | ||||||
| chr2:108570201
|
C | T | 1 | a0001c0002t0001g0027 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.32+35607C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108570201 | ||||||
| chr2:108570315
|
A | C | 2 | a0001c0001t0017g0156a0001c0001t0017g0157 | 2 | HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.32+35721A>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108570315 | ||||||
| chr2:108570322
|
C | T | 1 | a0001c0001t0005g0180 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.32+35728C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108570322 | ||||||
| chr2:108570334
|
G | A | 1 | a0001c0001t0002g0109 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.32+35740G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108570334 | ||||||
| chr2:108570700
|
G | A | 2 | a0001c0002t0001g0061a0001c0002t0001g0062 | 2 | HG00140.hp2 HG00280.hp1 |
intron_variant | MODIFIER | c.32+36106G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108570700 | ||||||
| chr2:108570875
|
G | A | 2 | a0001c0001t0003g0187a0001c0001t0003g0188 | 2 | HG00639.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.32+36281G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108570875 | ||||||
| chr2:108571119
|
G | A | 2 | a0001c0001t0002g0200a0001c0001t0002g0201 | 2 | HG01346.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.32+36525G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108571119 | ||||||
| chr2:108571202
|
T | C | 1 | a0001c0002t0001g0012 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.32+36608T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108571202 | ||||||
| chr2:108571228
|
G | A | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+36634G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108571228 | ||||||
| chr2:108571697
|
G | C | 3 | a0001c0001t0017g0156a0001c0001t0017g0157a0001c0001t0024g0162 | 3 | HG02647.hp1 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.32+37103G>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108571697 | ||||||
| chr2:108571700
|
A | G | 100 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.32+37106A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108571700 | ||||||
| chr2:108571713
|
C | T | 2 | a0001c0002t0007g0215a0001c0002t0007g0216 | 2 | HG02258.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.32+37119C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108571713 | ||||||
| chr2:108572071
|
C | T | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.32+37477C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108572071 | ||||||
| chr2:108572141
|
G | A | 1 | a0001c0002t0012g0220 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.32+37547G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108572141 | ||||||
| chr2:108572380
|
C | CT | 80 | a0001c0001t0002g0094a0001c0001t0002g0095a0001c0001t0002g0123others(77): Show | 80 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.32+37806dupT | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108572380 | |||||
| chr2:108572380
|
C | CTT | 29 | a0001c0001t0003g0139a0001c0001t0003g0142a0001c0002t0001g0004others(26): Show | 29 | HG02486.hp2 HG02559.hp1 HG02572.hp1 others(26): Show |
intron_variant | MODIFIER | c.32+37805_32+37806d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108572380 | |||||
| chr2:108572380
|
CT | C | 13 | a0001c0001t0002g0084a0001c0001t0002g0089a0001c0001t0002g0090others(10): Show | 13 | HG01175.hp2 HG01261.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.32+37806delT | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108572380 | |||||
| chr2:108572437
|
C | T | 1 | a0001c0002t0008g0223 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.32+37843C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108572437 | ||||||
| chr2:108572443
|
C | T | 21 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(18): Show | 21 | HG02602.hp2 HG02622.hp1 HG03017.hp2 others(18): Show |
intron_variant | MODIFIER | c.32+37849C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108572443 | ||||||
| chr2:108572482
|
A | G | 2 | a0002c0003t0018g0005a0002c0003t0026g0219 | 2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.32+37888A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108572482 | ||||||
| chr2:108572538
|
C | A | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.32+37944C>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108572538 | ||||||
| chr2:108572577
|
G | T | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+37983G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108572577 | ||||||
| chr2:108572630
|
C | T | 7 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0114others(4): Show | 7 | NA18968.hp1 NA18977.hp1 NA18993.hp1 others(4): Show |
intron_variant | MODIFIER | c.32+38036C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108572630 | ||||||
| chr2:108572680
|
G | A | 1 | a0001c0002t0001g0052 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.32+38086G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108572680 | ||||||
| chr2:108572782
|
A | C | 2 | a0001c0002t0001g0002a0001c0002t0001g0003 | 2 | NA19043.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.32+38188A>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108572782 | ||||||
| chr2:108572832
|
T | C | 25 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(22): Show | 25 | HG02572.hp1 HG02602.hp2 HG02622.hp1 others(22): Show |
intron_variant | MODIFIER | c.32+38238T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108572832 | ||||||
| chr2:108572954
|
A | G | 1 | a0001c0001t0003g0198 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.32+38360A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108572954 | ||||||
| chr2:108573163
|
A | G | 1 | a0001c0002t0007g0218 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.32+38569A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108573163 | ||||||
| chr2:108573306
|
C | CT | 11 | a0001c0001t0003g0202a0001c0001t0003g0203a0001c0001t0003g0204others(8): Show | 11 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.32+38726dupT | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108573306 | |||||
| chr2:108573320
|
T | C | 93 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(90): Show | 93 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.32+38726T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108573320 | ||||||
| chr2:108573420
|
A | T | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+38826A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108573420 | ||||||
| chr2:108573477
|
TA | T | 25 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(22): Show | 25 | HG02572.hp1 HG02602.hp2 HG02622.hp1 others(22): Show |
intron_variant | MODIFIER | c.32+38884delA | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108573477 | ||||||
| chr2:108573571
|
G | A | 168 | a0001c0001t0003g0001a0001c0001t0003g0130a0001c0001t0003g0131others(165): Show | 169 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.32+38977G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108573571 | ||||||
| chr2:108573749
|
A | G | 1 | a0001c0001t0003g0140 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.32+39155A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108573749 | ||||||
| chr2:108573869
|
A | G | 21 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(18): Show | 21 | HG02602.hp2 HG02622.hp1 HG03017.hp2 others(18): Show |
intron_variant | MODIFIER | c.32+39275A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108573869 | ||||||
| chr2:108574428
|
C | T | 1 | a0001c0002t0001g0008 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.32+39834C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108574428 | ||||||
| chr2:108574484
|
C | T | 1 | a0001c0001t0024g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.32+39890C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108574484 | ||||||
| chr2:108574636
|
A | G | 1 | a0001c0001t0006g0168 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.32+40042A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108574636 | ||||||
| chr2:108575029
|
A | T | 1 | a0001c0001t0003g0188 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.32+40435A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108575029 | ||||||
| chr2:108575199
|
G | A | 1 | a0001c0001t0003g0203 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.32+40605G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108575199 | ||||||
| chr2:108575286
|
T | TA | 75 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(72): Show | 75 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.32+40693dupA | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108575286 | |||||
| chr2:108575415
|
C | G | 2 | a0001c0002t0001g0002a0001c0002t0001g0003 | 2 | NA19043.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.32+40821C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108575415 | ||||||
| chr2:108575457
|
G | A | 1 | a0002c0003t0026g0219 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.32+40863G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108575457 | ||||||
| chr2:108575516
|
T | G | 1 | a0002c0003t0026g0219 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.32+40922T>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108575516 | ||||||
| chr2:108575617
|
A | G | 2 | a0001c0001t0002g0076a0001c0001t0005g0077 | 2 | HG00741.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.32+41023A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108575617 | ||||||
| chr2:108575805
|
TTG | T | 7 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(4): Show | 7 | HG02040.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.32+41222_32+41223d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108575805 | |||||
| chr2:108575821
|
T | A | 168 | a0001c0001t0003g0001a0001c0001t0003g0130a0001c0001t0003g0131others(165): Show | 169 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.32+41227T>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108575821 | ||||||
| chr2:108576142
|
T | C | 2 | a0001c0004t0013g0073a0001c0004t0013g0074 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.32+41548T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108576142 | ||||||
| chr2:108576264
|
A | AGTTTT | 9 | a0001c0001t0003g0150a0001c0001t0003g0151a0001c0001t0003g0196others(6): Show | 9 | HG02258.hp2 HG02622.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.32+41694_32+41698d others(7): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108576264 | |||||
| chr2:108576264
|
AGTTTTGT others(3): Show |
A | 4 | a0001c0001t0017g0156a0001c0001t0017g0157a0001c0001t0024g0162others(1): Show | 4 | HG02559.hp1 HG02647.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+41689_32+41698d others(12): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108576264 | |||||
| chr2:108576280
|
G | C | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+41686G>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108576280 | ||||||
| chr2:108576378
|
C | G | 2 | a0002c0003t0018g0005a0002c0003t0026g0219 | 2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.32+41784C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108576378 | ||||||
| chr2:108576561
|
T | C | 112 | a0001c0001t0017g0156a0001c0001t0017g0157a0001c0001t0024g0162others(109): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.32+41967T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108576561 | ||||||
| chr2:108576774
|
C | T | 7 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140others(4): Show | 7 | HG01243.hp1 HG02055.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.32+42180C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108576774 | ||||||
| chr2:108576784
|
G | A | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+42190G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108576784 | ||||||
| chr2:108576987
|
C | T | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+42393C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108576987 | ||||||
| chr2:108577051
|
A | G | 93 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(90): Show | 93 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.32+42457A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108577051 | ||||||
| chr2:108577504
|
T | G | 1 | a0001c0001t0005g0169 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.32+42910T>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108577504 | ||||||
| chr2:108577610
|
C | T | 93 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(90): Show | 93 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.32+43016C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108577610 | ||||||
| chr2:108577806
|
T | C | 2 | a0002c0003t0018g0005a0002c0003t0026g0219 | 2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.32+43212T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108577806 | ||||||
| chr2:108577810
|
A | T | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+43216A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108577810 | ||||||
| chr2:108577815
|
A | T | 1 | a0001c0002t0001g0034 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.32+43221A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108577815 | ||||||
| chr2:108577949
|
G | A | 1 | a0001c0002t0007g0215 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.32+43355G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108577949 | ||||||
| chr2:108578420
|
A | C | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+43826A>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108578420 | ||||||
| chr2:108578439
|
A | T | 1 | a0001c0002t0001g0022 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.32+43845A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108578439 | ||||||
| chr2:108578517
|
T | C | 1 | a0001c0002t0007g0214 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.32+43923T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108578517 | ||||||
| chr2:108578587
|
A | AT | 98 | a0001c0001t0002g0085a0001c0001t0002g0107a0001c0001t0002g0114others(95): Show | 98 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.32+44016dupT | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108578587 | |||||
| chr2:108578587
|
A | ATT | 17 | a0001c0002t0001g0009a0001c0002t0001g0011a0001c0002t0001g0014others(14): Show | 17 | HG01109.hp1 HG01256.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.32+44015_32+44016d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108578587 | |||||
| chr2:108578623
|
T | G | 1 | a0001c0002t0001g0049 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.32+44029T>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108578623 | ||||||
| chr2:108578625
|
T | C | 100 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.32+44031T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108578625 | ||||||
| chr2:108578695
|
G | A | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.32+44101G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108578695 | ||||||
| chr2:108578777
|
G | A | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+44183G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108578777 | ||||||
| chr2:108578830
|
G | A | 1 | a0001c0002t0001g0027 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.32+44236G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108578830 | ||||||
| chr2:108578956
|
T | A | 93 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(90): Show | 93 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.32+44362T>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108578956 | ||||||
| chr2:108579065
|
C | G | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+44471C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108579065 | ||||||
| chr2:108579066
|
A | G | 1 | a0001c0001t0002g0128 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.32+44472A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108579066 | ||||||
| chr2:108579096
|
A | G | 1 | a0001c0001t0002g0108 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.32+44502A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108579096 | ||||||
| chr2:108579281
|
C | T | 1 | a0001c0002t0001g0048 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.32+44687C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108579281 | ||||||
| chr2:108579403
|
T | C | 68 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.32+44809T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108579403 | ||||||
| chr2:108579562
|
A | G | 1 | a0001c0002t0001g0024 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.32+44968A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108579562 | ||||||
| chr2:108579896
|
G | A | 11 | a0001c0001t0003g0202a0001c0001t0003g0203a0001c0001t0003g0204others(8): Show | 11 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.32+45302G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108579896 | ||||||
| chr2:108579913
|
C | T | 2 | a0001c0004t0013g0073a0001c0004t0013g0074 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.32+45319C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108579913 | ||||||
| chr2:108580179
|
G | A | 7 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(4): Show | 7 | HG02040.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.32+45585G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108580179 | ||||||
| chr2:108580211
|
G | T | 1 | a0001c0001t0002g0122 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.32+45617G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108580211 | ||||||
| chr2:108580254
|
G | T | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+45660G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108580254 | ||||||
| chr2:108580267
|
C | T | 1 | a0001c0002t0001g0034 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.32+45673C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108580267 | ||||||
| chr2:108580307
|
T | G | 68 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.32+45713T>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108580307 | ||||||
| chr2:108580326
|
A | T | 154 | a0001c0001t0003g0001a0001c0001t0003g0130a0001c0001t0003g0131others(151): Show | 155 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.32+45732A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108580326 | ||||||
| chr2:108580330
|
C | T | 1 | a0001c0001t0014g0159 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.32+45736C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108580330 | ||||||
| chr2:108580455
|
G | A | 1 | a0001c0001t0002g0119 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.32+45861G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108580455 | ||||||
| chr2:108580503
|
C | T | 23 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(20): Show | 23 | HG02602.hp2 HG02622.hp1 HG02895.hp1 others(20): Show |
intron_variant | MODIFIER | c.32+45909C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108580503 | ||||||
| chr2:108580521
|
G | A | 1 | a0001c0001t0003g0189 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.32+45927G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108580521 | ||||||
| chr2:108580693
|
C | A | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+46099C>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108580693 | ||||||
| chr2:108580791
|
C | T | 93 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(90): Show | 93 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.32+46197C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108580791 | ||||||
| chr2:108580969
|
C | T | 2 | a0001c0004t0013g0073a0001c0004t0013g0074 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.32+46375C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108580969 | ||||||
| chr2:108581292
|
C | T | 68 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.32+46698C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108581292 | ||||||
| chr2:108581381
|
A | G | 1 | a0001c0002t0001g0008 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.32+46787A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108581381 | ||||||
| chr2:108581381
|
ATTTC | A | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+46791_32+46794d others(6): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108581381 | |||||
| chr2:108581400
|
A | G | 168 | a0001c0001t0003g0001a0001c0001t0003g0130a0001c0001t0003g0131others(165): Show | 169 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.32+46806A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108581400 | ||||||
| chr2:108581480
|
T | C | 109 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(106): Show | 109 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.32+46886T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108581480 | ||||||
| chr2:108581770
|
G | T | 225 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(222): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.32+47176G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108581770 | ||||||
| chr2:108581913
|
G | A | 3 | a0001c0001t0002g0182a0001c0001t0002g0183a0001c0001t0002g0184 | 3 | HG02257.hp2 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.32+47319G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108581913 | ||||||
| chr2:108581937
|
C | CA | 7 | a0001c0001t0003g0139a0001c0001t0011g0149a0001c0002t0001g0053others(4): Show | 7 | HG02040.hp2 HG02056.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.32+47357dupA | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108581937 | |||||
| chr2:108581952
|
C | A | 1 | a0001c0001t0002g0113 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.32+47358C>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108581952 | ||||||
| chr2:108582074
|
T | C | 68 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.32+47480T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108582074 | ||||||
| chr2:108582247
|
A | C | 1 | a0001c0001t0002g0122 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.32+47653A>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108582247 | ||||||
| chr2:108582340
|
A | G | 25 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(22): Show | 25 | HG02572.hp1 HG02602.hp2 HG02622.hp1 others(22): Show |
intron_variant | MODIFIER | c.32+47746A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108582340 | ||||||
| chr2:108582389
|
A | G | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+47795A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108582389 | ||||||
| chr2:108582634
|
G | T | 1 | a0001c0001t0002g0126 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.32+48040G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108582634 | ||||||
| chr2:108582805
|
G | A | 1 | a0001c0001t0029g0186 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.32+48211G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108582805 | ||||||
| chr2:108582833
|
A | T | 1 | a0001c0001t0003g0161 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.32+48239A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108582833 | ||||||
| chr2:108583177
|
C | T | 23 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(20): Show | 23 | HG02602.hp2 HG02622.hp1 HG02895.hp1 others(20): Show |
intron_variant | MODIFIER | c.32+48583C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108583177 | ||||||
| chr2:108583179
|
C | T | 21 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(18): Show | 21 | HG02602.hp2 HG02622.hp1 HG03017.hp2 others(18): Show |
intron_variant | MODIFIER | c.32+48585C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108583179 | ||||||
| chr2:108583206
|
TA | T | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+48613delA | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108583206 | ||||||
| chr2:108583207
|
AT | A | 125 | a0001c0001t0003g0001a0001c0001t0003g0130a0001c0001t0003g0131others(122): Show | 126 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.32+48629delT | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108583207 | |||||
| chr2:108583207
|
ATT | A | 22 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(19): Show | 22 | HG02602.hp2 HG02622.hp1 HG02895.hp1 others(19): Show |
intron_variant | MODIFIER | c.32+48628_32+48629d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108583207 | |||||
| chr2:108583209
|
T | G | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+48615T>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108583209 | ||||||
| chr2:108583248
|
A | G | 100 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.32+48654A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108583248 | ||||||
| chr2:108583290
|
G | A | 1 | a0001c0001t0003g0212 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.32+48696G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108583290 | ||||||
| chr2:108583327
|
A | G | 168 | a0001c0001t0003g0001a0001c0001t0003g0130a0001c0001t0003g0131others(165): Show | 169 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.32+48733A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108583327 | ||||||
| chr2:108583328
|
T | C | 168 | a0001c0001t0003g0001a0001c0001t0003g0130a0001c0001t0003g0131others(165): Show | 169 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.32+48734T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108583328 | ||||||
| chr2:108583343
|
C | G | 25 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(22): Show | 25 | HG02572.hp1 HG02602.hp2 HG02622.hp1 others(22): Show |
intron_variant | MODIFIER | c.32+48749C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108583343 | ||||||
| chr2:108583364
|
G | T | 1 | a0001c0002t0007g0217 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.32+48770G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108583364 | ||||||
| chr2:108583585
|
G | C | 1 | a0001c0002t0012g0007 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.32+48991G>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108583585 | ||||||
| chr2:108583622
|
A | T | 1 | a0001c0002t0001g0003 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.32+49028A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108583622 | ||||||
| chr2:108583700
|
C | CT | 8 | a0001c0001t0002g0084a0001c0001t0002g0090a0001c0001t0002g0091others(5): Show | 8 | HG01175.hp2 HG01891.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.32+49120dupT | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108583700 | |||||
| chr2:108583700
|
C | CTT | 12 | a0001c0001t0003g0187a0001c0001t0003g0188a0001c0001t0003g0189others(9): Show | 12 | HG00639.hp2 HG01074.hp2 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.32+49119_32+49120d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108583700 | |||||
| chr2:108583700
|
C | CTTTTTT | 9 | a0001c0001t0017g0157a0001c0002t0001g0036a0001c0002t0001g0061others(6): Show | 9 | HG00140.hp2 HG00280.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.32+49115_32+49120d others(8): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108583700 | |||||
| chr2:108583700
|
C | CTTTTTTT | 88 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0008others(85): Show | 88 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(85): Show |
intron_variant | MODIFIER | c.32+49114_32+49120d others(9): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108583700 | |||||
| chr2:108583700
|
C | CTTTTTTT others(1): Show |
5 | a0001c0002t0001g0004a0001c0002t0001g0057a0001c0002t0004g0230others(2): Show | 5 | HG02040.hp2 HG02559.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+49113_32+49120d others(10): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108583700 | |||||
| chr2:108583700
|
C | CTTTTTTT others(2): Show |
5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+49112_32+49120d others(11): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108583700 | |||||
| chr2:108583730
|
T | C | 2 | a0001c0001t0017g0156a0001c0001t0017g0157 | 2 | HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.32+49136T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108583730 | ||||||
| chr2:108583892
|
C | T | 1 | a0001c0001t0021g0120 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.32+49298C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108583892 | ||||||
| chr2:108583973
|
C | T | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+49379C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108583973 | ||||||
| chr2:108584200
|
T | C | 154 | a0001c0001t0003g0001a0001c0001t0003g0130a0001c0001t0003g0131others(151): Show | 155 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.32+49606T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108584200 | ||||||
| chr2:108584209
|
T | G | 45 | a0001c0001t0003g0001a0001c0001t0003g0130a0001c0001t0003g0131others(42): Show | 46 | HG00323.hp1 HG00639.hp2 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.32+49615T>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108584209 | ||||||
| chr2:108584271
|
G | T | 1 | a0001c0002t0001g0009 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.32+49677G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108584271 | ||||||
| chr2:108584412
|
T | C | 1 | a0002c0003t0018g0005 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.32+49818T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108584412 | ||||||
| chr2:108584622
|
C | T | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.32+50028C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108584622 | ||||||
| chr2:108584789
|
A | G | 1 | a0001c0001t0003g0190 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.32+50195A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108584789 | ||||||
| chr2:108584889
|
C | T | 104 | a0001c0001t0003g0202a0001c0001t0003g0203a0001c0001t0003g0204others(101): Show | 104 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.32+50295C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108584889 | ||||||
| chr2:108584942
|
A | G | 7 | a0001c0001t0003g0130a0001c0001t0003g0131a0001c0001t0003g0132others(4): Show | 7 | NA18939.hp2 NA18942.hp1 NA18947.hp1 others(4): Show |
intron_variant | MODIFIER | c.32+50348A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108584942 | ||||||
| chr2:108584980
|
G | C | 68 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.32+50386G>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108584980 | ||||||
| chr2:108585012
|
G | T | 7 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(4): Show | 7 | HG02040.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.32+50418G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108585012 | ||||||
| chr2:108585150
|
C | CA | 95 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(92): Show | 95 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.32+50577dupA | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108585150 | |||||
| chr2:108585150
|
C | CAA | 29 | a0001c0001t0002g0087a0001c0001t0002g0092a0001c0001t0002g0102others(26): Show | 29 | HG00741.hp1 HG01175.hp2 HG01192.hp2 others(26): Show |
intron_variant | MODIFIER | c.32+50576_32+50577d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108585150 | |||||
| chr2:108585189
|
T | C | 43 | a0001c0001t0003g0001a0001c0001t0003g0130a0001c0001t0003g0131others(40): Show | 44 | HG00323.hp1 HG00639.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.32+50595T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108585189 | ||||||
| chr2:108585223
|
T | A | 2 | a0001c0004t0013g0073a0001c0004t0013g0074 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.32+50629T>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108585223 | ||||||
| chr2:108585373
|
G | A | 1 | a0001c0001t0002g0083 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.32+50779G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108585373 | ||||||
| chr2:108585442
|
AT | A | 37 | a0001c0002t0001g0015a0001c0002t0001g0018a0001c0002t0001g0020others(34): Show | 37 | HG01070.hp1 HG01106.hp1 HG01167.hp2 others(34): Show |
intron_variant | MODIFIER | c.32+50852delT | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108585442 | |||||
| chr2:108585459
|
T | G | 2 | a0001c0001t0017g0156a0001c0001t0017g0157 | 2 | HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.32+50865T>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108585459 | ||||||
| chr2:108585550
|
T | C | 3 | a0001c0002t0007g0214a0001c0002t0007g0217a0001c0002t0007g0218 | 3 | HG03195.hp1 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.32+50956T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108585550 | ||||||
| chr2:108585611
|
A | G | 1 | a0001c0001t0017g0157 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.32+51017A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108585611 | ||||||
| chr2:108585799
|
A | C | 7 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(4): Show | 7 | HG02040.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.32+51205A>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108585799 | ||||||
| chr2:108585813
|
T | A | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+51219T>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108585813 | ||||||
| chr2:108585821
|
T | G | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+51227T>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108585821 | ||||||
| chr2:108585951
|
T | TG | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.32+51360dupG | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108585951 | |||||
| chr2:108585965
|
A | G | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.32+51371A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108585965 | ||||||
| chr2:108586068
|
T | C | 1 | a0001c0001t0002g0103 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.32+51474T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108586068 | ||||||
| chr2:108586177
|
G | A | 23 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(20): Show | 23 | HG02602.hp2 HG02622.hp1 HG02895.hp1 others(20): Show |
intron_variant | MODIFIER | c.32+51583G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108586177 | ||||||
| chr2:108586186
|
C | T | 1 | a0001c0002t0009g0079 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.32+51592C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108586186 | ||||||
| chr2:108586198
|
C | CA | 14 | a0001c0001t0002g0123a0001c0001t0003g0136a0001c0001t0003g0138others(11): Show | 14 | HG01168.hp1 HG01981.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.32+51613dupA | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108586198 | |||||
| chr2:108586200
|
A | C | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+51606A>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108586200 | ||||||
| chr2:108586397
|
C | T | 23 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(20): Show | 23 | HG02602.hp2 HG02622.hp1 HG02895.hp1 others(20): Show |
intron_variant | MODIFIER | c.32+51803C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108586397 | ||||||
| chr2:108586559
|
G | T | 21 | a0001c0001t0003g0001a0001c0001t0003g0130a0001c0001t0003g0131others(18): Show | 22 | HG00323.hp1 HG01074.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.32+51965G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108586559 | ||||||
| chr2:108586564
|
G | A | 1 | a0001c0001t0002g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.32+51970G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108586564 | ||||||
| chr2:108586571
|
T | C | 1 | a0001c0001t0002g0084 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.32+51977T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108586571 | ||||||
| chr2:108586649
|
G | T | 93 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(90): Show | 93 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.32+52055G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108586649 | ||||||
| chr2:108587139
|
T | C | 244 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(241): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.32+52545T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108587139 | ||||||
| chr2:108587171
|
G | T | 4 | a0001c0001t0003g0189a0001c0001t0003g0190a0001c0001t0003g0192others(1): Show | 4 | HG01074.hp2 HG01358.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+52577G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108587171 | ||||||
| chr2:108587290
|
T | G | 4 | a0001c0001t0002g0084a0001c0001t0002g0129a0001c0001t0002g0182others(1): Show | 4 | HG01109.hp2 HG02717.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+52696T>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108587290 | ||||||
| chr2:108587290
|
T | TTG | 11 | a0001c0001t0002g0082a0001c0001t0002g0097a0001c0001t0002g0108others(8): Show | 11 | HG01167.hp1 HG01346.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.32+52746_32+52747d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108587290 | |||||
| chr2:108587290
|
T | TTGTG | 7 | a0001c0001t0002g0076a0001c0001t0002g0090a0001c0001t0003g0198others(4): Show | 7 | HG01257.hp1 HG01361.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.32+52744_32+52747d others(6): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108587290 | |||||
| chr2:108587290
|
T | TTGTGTG | 12 | a0001c0001t0002g0092a0001c0001t0002g0093a0001c0001t0002g0098others(9): Show | 12 | HG01074.hp2 HG01175.hp2 HG02602.hp1 others(9): Show |
intron_variant | MODIFIER | c.32+52742_32+52747d others(8): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108587290 | |||||
| chr2:108587290
|
T | TTGTGTGT others(3): Show |
2 | a0001c0001t0002g0091a0001c0001t0005g0180 | 2 | HG01175.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.32+52738_32+52747d others(12): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108587290 | |||||
| chr2:108587290
|
TTG | T | 42 | a0001c0001t0002g0075a0001c0001t0002g0086a0001c0001t0002g0094others(39): Show | 42 | HG00099.hp2 HG01070.hp2 HG01099.hp1 others(39): Show |
intron_variant | MODIFIER | c.32+52746_32+52747d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108587290 | |||||
| chr2:108587290
|
TTGTG | T | 23 | a0001c0001t0002g0105a0001c0001t0003g0001a0001c0001t0003g0130others(20): Show | 24 | HG00280.hp2 HG00323.hp1 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.32+52744_32+52747d others(6): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108587290 | |||||
| chr2:108587290
|
TTGTGTG | T | 24 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0005g0172others(21): Show | 24 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.32+52742_32+52747d others(8): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108587290 | |||||
| chr2:108587290
|
TTGTGTGT others(1): Show |
T | 66 | a0001c0002t0001g0009a0001c0002t0001g0014a0001c0002t0001g0015others(63): Show | 66 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.32+52740_32+52747d others(10): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108587290 | |||||
| chr2:108587290
|
TTGTGTGT others(3): Show |
T | 2 | a0001c0001t0002g0127a0001c0001t0019g0124 | 2 | NA18999.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.32+52738_32+52747d others(12): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108587290 | |||||
| chr2:108587290
|
TTGTGTGT others(5): Show |
T | 6 | a0001c0002t0004g0239a0001c0002t0008g0221a0001c0002t0008g0222others(3): Show | 6 | HG02486.hp1 HG02572.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.32+52736_32+52747d others(14): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108587290 | |||||
| chr2:108587290
|
TTGTGTGT others(9): Show |
T | 2 | a0001c0001t0002g0087a0001c0002t0007g0216 | 2 | HG02922.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.32+52732_32+52747d others(18): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108587290 | |||||
| chr2:108587290
|
TTGTGTGT others(11): Show |
T | 4 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0217others(1): Show | 4 | HG02258.hp1 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+52730_32+52747d others(20): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108587290 | |||||
| chr2:108587290
|
TTGTGTGT others(19): Show |
T | 11 | a0001c0001t0003g0202a0001c0001t0003g0203a0001c0001t0003g0204others(8): Show | 11 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.32+52722_32+52747d others(28): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108587290 | |||||
| chr2:108587292
|
G | T | 2 | a0001c0002t0001g0019a0001c0002t0001g0020 | 2 | NA19087.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.32+52698G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108587292 | ||||||
| chr2:108587294
|
G | T | 2 | a0001c0002t0001g0029a0001c0002t0001g0059 | 2 | HG02886.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.32+52700G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108587294 | ||||||
| chr2:108587296
|
G | T | 1 | a0001c0002t0030g0067 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.32+52702G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108587296 | ||||||
| chr2:108587298
|
G | T | 10 | a0001c0002t0001g0008a0001c0002t0001g0010a0001c0002t0001g0011others(7): Show | 10 | HG00323.hp2 HG00639.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.32+52704G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108587298 | ||||||
| chr2:108587300
|
G | T | 49 | a0001c0002t0001g0009a0001c0002t0001g0014a0001c0002t0001g0015others(46): Show | 49 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(46): Show |
intron_variant | MODIFIER | c.32+52706G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108587300 | ||||||
| chr2:108587388
|
A | G | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+52794A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108587388 | ||||||
| chr2:108587657
|
A | G | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+53063A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108587657 | ||||||
| chr2:108587725
|
A | G | 1 | a0001c0002t0012g0220 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.32+53131A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108587725 | ||||||
| chr2:108587775
|
G | A | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+53181G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108587775 | ||||||
| chr2:108587818
|
C | T | 1 | a0001c0002t0001g0072 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.32+53224C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108587818 | ||||||
| chr2:108587878
|
G | C | 93 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(90): Show | 93 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.32+53284G>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108587878 | ||||||
| chr2:108587891
|
G | A | 2 | a0001c0002t0001g0015a0001c0002t0027g0016 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.32+53297G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108587891 | ||||||
| chr2:108587925
|
ATGTAG | A | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.32+53337_32+53341d others(7): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108587925 | |||||
| chr2:108587987
|
G | A | 1 | a0001c0001t0002g0200 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.32+53393G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108587987 | ||||||
| chr2:108588185
|
T | C | 1 | a0001c0001t0005g0169 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.32+53591T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108588185 | ||||||
| chr2:108588270
|
GA | G | 220 | a0001c0001t0002g0076a0001c0001t0002g0082a0001c0001t0002g0083others(217): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.32+53687delA | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108588270 | |||||
| chr2:108588357
|
A | G | 1 | a0001c0001t0003g0203 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.32+53763A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108588357 | ||||||
| chr2:108588670
|
T | G | 39 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(36): Show | 39 | HG00099.hp2 HG00741.hp2 HG01168.hp2 others(36): Show |
intron_variant | MODIFIER | c.32+54076T>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108588670 | ||||||
| chr2:108588900
|
A | G | 1 | a0001c0002t0001g0049 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.32+54306A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108588900 | ||||||
| chr2:108589168
|
A | G | 100 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.32+54574A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108589168 | ||||||
| chr2:108589249
|
A | G | 2 | a0001c0001t0017g0156a0001c0001t0017g0157 | 2 | HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.32+54655A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108589249 | ||||||
| chr2:108589283
|
A | G | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.32+54689A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108589283 | ||||||
| chr2:108589312
|
A | G | 1 | a0001c0002t0004g0226 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.32+54718A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108589312 | ||||||
| chr2:108589385
|
A | G | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.32+54791A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108589385 | ||||||
| chr2:108589404
|
A | G | 2 | a0001c0001t0014g0159a0001c0001t0014g0160 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.32+54810A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108589404 | ||||||
| chr2:108589649
|
A | T | 4 | a0001c0001t0003g0001a0001c0001t0003g0137a0001c0001t0003g0152others(1): Show | 5 | HG00323.hp1 HG01074.hp1 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.32+55055A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108589649 | ||||||
| chr2:108589683
|
A | G | 45 | a0001c0001t0003g0001a0001c0001t0003g0130a0001c0001t0003g0131others(42): Show | 46 | HG00323.hp1 HG00639.hp2 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.32+55089A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108589683 | ||||||
| chr2:108590008
|
T | G | 68 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.32+55414T>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108590008 | ||||||
| chr2:108590211
|
A | AG | 3 | a0001c0002t0004g0231a0001c0002t0004g0236a0001c0002t0004g0241 | 3 | NA18940.hp2 NA18994.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.32+55619dupG | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108590211 | |||||
| chr2:108590262
|
A | G | 21 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(18): Show | 21 | HG02602.hp2 HG02622.hp1 HG03017.hp2 others(18): Show |
intron_variant | MODIFIER | c.32+55668A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108590262 | ||||||
| chr2:108590487
|
C | T | 4 | a0001c0002t0004g0231a0001c0002t0004g0233a0001c0002t0004g0236others(1): Show | 4 | NA18940.hp2 NA18994.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+55893C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108590487 | ||||||
| chr2:108590572
|
AAG | A | 3 | a0001c0001t0017g0156a0001c0001t0017g0157a0001c0001t0024g0162 | 3 | HG02647.hp1 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.32+55981_32+55982d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108590572 | |||||
| chr2:108590787
|
G | T | 244 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(241): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.32+56193G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108590787 | ||||||
| chr2:108590791
|
G | T | 1 | a0001c0001t0002g0109 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.32+56197G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108590791 | ||||||
| chr2:108590818
|
C | G | 1 | a0001c0002t0001g0021 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.32+56224C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108590818 | ||||||
| chr2:108590892
|
C | T | 1 | a0001c0001t0003g0137 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.32+56298C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108590892 | ||||||
| chr2:108590976
|
A | G | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+56382A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108590976 | ||||||
| chr2:108591276
|
C | T | 1 | a0001c0002t0025g0026 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.32+56682C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108591276 | ||||||
| chr2:108591293
|
T | G | 93 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(90): Show | 93 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.32+56699T>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108591293 | ||||||
| chr2:108591352
|
C | T | 6 | a0001c0002t0004g0229a0001c0002t0004g0230a0001c0002t0004g0234others(3): Show | 6 | NA18947.hp2 NA18960.hp1 NA19062.hp1 others(3): Show |
intron_variant | MODIFIER | c.32+56758C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108591352 | ||||||
| chr2:108591460
|
T | A | 1 | a0001c0002t0008g0223 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.32+56866T>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108591460 | ||||||
| chr2:108591632
|
A | T | 199 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.32+57038A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108591632 | ||||||
| chr2:108591657
|
A | G | 109 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(106): Show | 109 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.32+57063A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108591657 | ||||||
| chr2:108591788
|
A | T | 1 | a0001c0001t0003g0211 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.32+57194A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108591788 | ||||||
| chr2:108591796
|
TTTTTG | T | 67 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0008others(64): Show | 67 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.32+57207_32+57211d others(7): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108591796 | |||||
| chr2:108591797
|
T | A | 2 | a0002c0003t0018g0005a0002c0003t0026g0219 | 2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.32+57203T>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108591797 | ||||||
| chr2:108591797
|
TTTTG | T | 20 | a0001c0002t0001g0004a0001c0002t0001g0049a0001c0002t0001g0058others(17): Show | 20 | HG01346.hp1 HG02559.hp1 HG02602.hp2 others(17): Show |
intron_variant | MODIFIER | c.32+57207_32+57210d others(6): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108591797 | |||||
| chr2:108591798
|
TTTG | T | 8 | a0001c0002t0004g0237a0001c0002t0004g0238a0001c0002t0004g0241others(5): Show | 8 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.32+57207_32+57209d others(5): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108591798 | |||||
| chr2:108591799
|
TTG | T | 11 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(8): Show | 11 | HG01261.hp2 HG02040.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.32+57207_32+57208d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108591799 | |||||
| chr2:108591801
|
G | T | 3 | a0001c0002t0012g0220a0002c0003t0018g0005a0002c0003t0026g0219 | 3 | HG02572.hp1 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.32+57207G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108591801 | ||||||
| chr2:108591801
|
GT | G | 45 | a0001c0001t0003g0001a0001c0001t0003g0130a0001c0001t0003g0131others(42): Show | 46 | HG00323.hp1 HG00639.hp2 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.32+57218delT | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108591801 | |||||
| chr2:108591825
|
C | T | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+57231C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108591825 | ||||||
| chr2:108591939
|
C | T | 68 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.32+57345C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108591939 | ||||||
| chr2:108591971
|
C | T | 168 | a0001c0001t0003g0001a0001c0001t0003g0130a0001c0001t0003g0131others(165): Show | 169 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.32+57377C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108591971 | ||||||
| chr2:108591978
|
A | G | 36 | a0001c0001t0003g0001a0001c0001t0003g0130a0001c0001t0003g0131others(33): Show | 37 | HG00323.hp1 HG00639.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.32+57384A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108591978 | ||||||
| chr2:108591984
|
G | A | 2 | a0002c0003t0018g0005a0002c0003t0026g0219 | 2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.32+57390G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108591984 | ||||||
| chr2:108592094
|
C | A | 1 | a0001c0002t0016g0045 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.32+57500C>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108592094 | ||||||
| chr2:108592261
|
C | T | 154 | a0001c0001t0003g0001a0001c0001t0003g0130a0001c0001t0003g0131others(151): Show | 155 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.32+57667C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108592261 | ||||||
| chr2:108592415
|
T | C | 45 | a0001c0001t0003g0001a0001c0001t0003g0130a0001c0001t0003g0131others(42): Show | 46 | HG00323.hp1 HG00639.hp2 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.32+57821T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108592415 | ||||||
| chr2:108592475
|
G | A | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.32+57881G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108592475 | ||||||
| chr2:108592557
|
A | G | 1 | a0001c0002t0009g0078 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.32+57963A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108592557 | ||||||
| chr2:108592684
|
T | C | 1 | a0001c0001t0015g0134 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.32+58090T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108592684 | ||||||
| chr2:108592795
|
G | T | 2 | a0001c0001t0003g0208a0001c0001t0015g0210 | 2 | HG02895.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.32+58201G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108592795 | ||||||
| chr2:108592901
|
T | A | 1 | a0001c0001t0003g0148 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.32+58307T>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108592901 | ||||||
| chr2:108592910
|
A | G | 1 | a0001c0001t0003g0188 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.32+58316A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108592910 | ||||||
| chr2:108593230
|
TG | T | 7 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(4): Show | 7 | HG02040.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.32+58638delG | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108593230 | |||||
| chr2:108593261
|
C | G | 3 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0081 | 3 | NA18954.hp2 NA18970.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.32+58667C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108593261 | ||||||
| chr2:108593276
|
C | A | 21 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(18): Show | 21 | HG02602.hp2 HG02622.hp1 HG03017.hp2 others(18): Show |
intron_variant | MODIFIER | c.32+58682C>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108593276 | ||||||
| chr2:108593457
|
A | G | 1 | a0001c0002t0004g0235 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.32+58863A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108593457 | ||||||
| chr2:108593816
|
C | T | 1 | a0001c0001t0003g0189 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.32+59222C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108593816 | ||||||
| chr2:108594398
|
C | T | 95 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(92): Show | 95 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.32+59804C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108594398 | ||||||
| chr2:108594504
|
G | C | 154 | a0001c0001t0003g0001a0001c0001t0003g0130a0001c0001t0003g0131others(151): Show | 155 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.32+59910G>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108594504 | ||||||
| chr2:108594890
|
T | C | 1 | a0001c0002t0001g0004 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.32+60296T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108594890 | ||||||
| chr2:108594890
|
TA | T | 21 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(18): Show | 21 | HG02602.hp2 HG02622.hp1 HG03017.hp2 others(18): Show |
intron_variant | MODIFIER | c.32+60304delA | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108594890 | |||||
| chr2:108595047
|
C | G | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.32+60453C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108595047 | ||||||
| chr2:108595263
|
G | A | 2 | a0001c0004t0013g0073a0001c0004t0013g0074 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.32+60669G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108595263 | ||||||
| chr2:108595702
|
C | A | 2 | a0001c0001t0002g0102a0001c0001t0002g0158 | 2 | HG02145.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.32+61108C>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108595702 | ||||||
| chr2:108595804
|
C | A | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+61210C>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108595804 | ||||||
| chr2:108595966
|
T | A | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+61372T>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108595966 | ||||||
| chr2:108595971
|
GGCTTATG others(2): Show |
G | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+61379_32+61387d others(11): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108595971 | |||||
| chr2:108596152
|
C | T | 4 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0142others(1): Show | 4 | HG01243.hp1 HG03041.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+61558C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108596152 | ||||||
| chr2:108596202
|
C | T | 1 | a0001c0002t0012g0006 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.32+61608C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108596202 | ||||||
| chr2:108596203
|
G | A | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+61609G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108596203 | ||||||
| chr2:108596257
|
G | A | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+61663G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108596257 | ||||||
| chr2:108596463
|
T | G | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+61869T>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108596463 | ||||||
| chr2:108596549
|
G | A | 1 | a0001c0001t0005g0165 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.32+61955G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108596549 | ||||||
| chr2:108596560
|
A | G | 7 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(4): Show | 7 | HG02040.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.32+61966A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108596560 | ||||||
| chr2:108596683
|
C | T | 1 | a0001c0002t0001g0035 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.32+62089C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108596683 | ||||||
| chr2:108596869
|
A | T | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+62275A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108596869 | ||||||
| chr2:108596915
|
G | GT | 9 | a0001c0001t0003g0139a0001c0001t0003g0152a0001c0001t0003g0188others(6): Show | 9 | HG00639.hp2 HG01261.hp2 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.32+62344dupT | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108596915 | |||||
| chr2:108596915
|
GT | G | 99 | a0001c0001t0002g0076a0001c0001t0002g0082a0001c0001t0002g0083others(96): Show | 99 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.32+62344delT | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108596915 | |||||
| chr2:108596915
|
GTT | G | 84 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(81): Show | 84 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.32+62343_32+62344d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108596915 | |||||
| chr2:108596916
|
T | G | 1 | a0001c0001t0014g0160 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.32+62322T>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108596916 | ||||||
| chr2:108597044
|
G | A | 2 | a0001c0002t0001g0015a0001c0002t0027g0016 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.32+62450G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108597044 | ||||||
| chr2:108597106
|
C | T | 1 | a0001c0001t0021g0120 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.33-62499C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108597106 | ||||||
| chr2:108597194
|
C | T | 68 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.33-62411C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108597194 | ||||||
| chr2:108597199
|
G | C | 1 | a0001c0002t0030g0067 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.33-62406G>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108597199 | ||||||
| chr2:108597433
|
G | A | 1 | a0001c0002t0012g0220 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.33-62172G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108597433 | ||||||
| chr2:108597640
|
T | C | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-61965T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108597640 | ||||||
| chr2:108597693
|
C | CT | 20 | a0001c0001t0002g0082a0001c0001t0002g0083a0001c0001t0002g0084others(17): Show | 20 | HG00099.hp2 HG01884.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.33-61894dupT | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108597693 | |||||
| chr2:108597693
|
C | CTT | 61 | a0001c0001t0003g0208a0001c0001t0003g0212a0001c0002t0001g0002others(58): Show | 61 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.33-61895_33-61894d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108597693 | |||||
| chr2:108597693
|
C | CTTT | 10 | a0001c0002t0001g0022a0001c0002t0001g0025a0001c0002t0001g0049others(7): Show | 10 | HG01981.hp2 HG02056.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.33-61896_33-61894d others(5): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108597693 | |||||
| chr2:108597693
|
C | CTTTT | 19 | a0001c0002t0001g0037a0001c0002t0004g0225a0001c0002t0004g0226others(16): Show | 19 | HG02602.hp2 HG02622.hp1 HG03017.hp2 others(16): Show |
intron_variant | MODIFIER | c.33-61897_33-61894d others(6): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108597693 | |||||
| chr2:108597693
|
CT | C | 55 | a0001c0001t0003g0001a0001c0001t0003g0130a0001c0001t0003g0131others(52): Show | 56 | HG00323.hp1 HG00639.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.33-61894delT | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108597693 | |||||
| chr2:108597919
|
C | G | 1 | a0001c0001t0003g0212 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.33-61686C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108597919 | ||||||
| chr2:108597944
|
A | G | 154 | a0001c0001t0003g0001a0001c0001t0003g0130a0001c0001t0003g0131others(151): Show | 155 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.33-61661A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108597944 | ||||||
| chr2:108598208
|
G | A | 93 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(90): Show | 93 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.33-61397G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108598208 | ||||||
| chr2:108598492
|
T | C | 154 | a0001c0001t0003g0001a0001c0001t0003g0130a0001c0001t0003g0131others(151): Show | 155 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.33-61113T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108598492 | ||||||
| chr2:108598493
|
G | A | 220 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(217): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.33-61112G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108598493 | ||||||
| chr2:108598493
|
G | C | 5 | a0001c0001t0003g0196a0001c0001t0010g0193a0001c0001t0010g0194others(2): Show | 5 | HG02622.hp2 HG02818.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-61112G>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108598493 | ||||||
| chr2:108598582
|
T | C | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.33-61023T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108598582 | ||||||
| chr2:108598861
|
A | G | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-60744A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108598861 | ||||||
| chr2:108599214
|
T | C | 93 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(90): Show | 93 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.33-60391T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108599214 | ||||||
| chr2:108599295
|
G | A | 109 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(106): Show | 109 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.33-60310G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108599295 | ||||||
| chr2:108599360
|
A | G | 1 | a0001c0001t0002g0096 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.33-60245A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108599360 | ||||||
| chr2:108599506
|
T | C | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-60099T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108599506 | ||||||
| chr2:108599532
|
T | G | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-60073T>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108599532 | ||||||
| chr2:108599615
|
G | A | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.33-59990G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108599615 | ||||||
| chr2:108599643
|
A | G | 7 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(4): Show | 7 | HG02040.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.33-59962A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108599643 | ||||||
| chr2:108599670
|
A | G | 1 | a0001c0001t0005g0180 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.33-59935A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108599670 | ||||||
| chr2:108599705
|
G | T | 93 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(90): Show | 93 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.33-59900G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108599705 | ||||||
| chr2:108599834
|
A | G | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.33-59771A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108599834 | ||||||
| chr2:108599934
|
C | T | 93 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(90): Show | 93 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.33-59671C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108599934 | ||||||
| chr2:108599977
|
G | A | 2 | a0001c0001t0005g0164a0001c0001t0006g0179 | 2 | HG01099.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.33-59628G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108599977 | ||||||
| chr2:108599991
|
T | A | 79 | a0001c0001t0005g0163a0001c0001t0005g0180a0001c0002t0001g0002others(76): Show | 79 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.33-59614T>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108599991 | ||||||
| chr2:108600039
|
T | TTTG | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-59549_33-59547d others(5): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108600039 | |||||
| chr2:108600076
|
C | T | 1 | a0001c0001t0003g0188 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.33-59529C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108600076 | ||||||
| chr2:108600084
|
C | G | 10 | a0001c0001t0005g0163a0001c0001t0005g0180a0001c0002t0001g0004others(7): Show | 10 | HG01175.hp1 HG01257.hp1 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.33-59521C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108600084 | ||||||
| chr2:108600135
|
C | T | 23 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(20): Show | 23 | HG02602.hp2 HG02622.hp1 HG02895.hp1 others(20): Show |
intron_variant | MODIFIER | c.33-59470C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108600135 | ||||||
| chr2:108600302
|
C | T | 93 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(90): Show | 93 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.33-59303C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108600302 | ||||||
| chr2:108600396
|
G | A | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.33-59209G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108600396 | ||||||
| chr2:108600572
|
C | T | 1 | a0001c0001t0002g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.33-59033C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108600572 | ||||||
| chr2:108600770
|
A | G | 2 | a0001c0001t0011g0088a0001c0001t0011g0144 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.33-58835A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108600770 | ||||||
| chr2:108600890
|
G | GTTCTT | 23 | a0001c0001t0003g0131a0001c0001t0003g0139a0001c0001t0003g0142others(20): Show | 23 | HG01261.hp2 HG01891.hp1 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.33-58714_33-58710d others(7): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108600890 | |||||
| chr2:108600891
|
T | TTCTTC | 20 | a0001c0001t0002g0076a0001c0001t0002g0082a0001c0001t0002g0098others(17): Show | 20 | HG00140.hp1 HG00280.hp2 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.33-58674_33-58670d others(7): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108600891 | |||||
| chr2:108600891
|
T | TTCTTCTC others(3): Show |
4 | a0001c0001t0002g0094a0001c0001t0002g0095a0001c0001t0005g0174others(1): Show | 4 | HG02559.hp2 HG02698.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-58679_33-58670d others(12): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108600891 | |||||
| chr2:108600891
|
T | TTCTTCTC others(8): Show |
2 | a0001c0001t0002g0083a0001c0001t0017g0156 | 2 | HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.33-58684_33-58670d others(17): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108600891 | |||||
| chr2:108600891
|
T | TTCTTCTC others(13): Show |
5 | a0001c0001t0002g0182a0001c0001t0003g0207a0001c0001t0003g0212others(2): Show | 5 | HG02055.hp1 HG02280.hp1 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-58689_33-58670d others(22): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108600891 | |||||
| chr2:108600891
|
T | TTCTTCTC others(18): Show |
5 | a0001c0001t0003g0203a0001c0001t0003g0205a0001c0001t0003g0208others(2): Show | 5 | HG02451.hp1 HG02647.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-58694_33-58670d others(27): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108600891 | |||||
| chr2:108600891
|
T | TTCTTCTC others(23): Show |
5 | a0001c0001t0003g0202a0001c0001t0003g0204a0001c0001t0003g0206others(2): Show | 5 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-58699_33-58670d others(32): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108600891 | |||||
| chr2:108600891
|
T | TTCTTTTC others(3): Show |
16 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(13): Show | 16 | HG02602.hp2 HG02622.hp1 HG02895.hp1 others(13): Show |
intron_variant | MODIFIER | c.33-58710_33-58709i others(12): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108600891 | |||||
| chr2:108600891
|
T | TTCTTTTC others(8): Show |
4 | a0001c0002t0004g0244a0001c0002t0009g0079a0001c0002t0009g0081others(1): Show | 4 | HG02572.hp1 HG04184.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-58710_33-58709i others(17): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108600891 | |||||
| chr2:108600891
|
T | TTCTTTTC others(13): Show |
1 | a0001c0002t0009g0078 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.33-58710_33-58709i others(22): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108600891 | |||||
| chr2:108600891
|
T | TTCTTTTC others(18): Show |
1 | a0002c0003t0018g0005 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.33-58710_33-58709i others(27): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108600891 | |||||
| chr2:108600891
|
TTCTTC | T | 17 | a0001c0001t0002g0085a0001c0001t0002g0090a0001c0001t0002g0092others(14): Show | 17 | HG00099.hp2 HG01168.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.33-58674_33-58670d others(7): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108600891 | |||||
| chr2:108600891
|
TTCTTCTC others(3): Show |
T | 68 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.33-58679_33-58670d others(12): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108600891 | |||||
| chr2:108600891
|
TTCTTCTC others(8): Show |
T | 1 | a0001c0001t0002g0125 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.33-58684_33-58670d others(17): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108600891 | |||||
| chr2:108600896
|
C | T | 37 | a0001c0001t0003g0001a0001c0001t0003g0130a0001c0001t0003g0132others(34): Show | 38 | HG00323.hp1 HG00639.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.33-58709C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108600896 | ||||||
| chr2:108600901
|
C | T | 4 | a0001c0001t0003g0145a0001c0001t0003g0146a0001c0001t0003g0147others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-58704C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108600901 | ||||||
| chr2:108600906
|
C | T | 68 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.33-58699C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108600906 | ||||||
| chr2:108600918
|
C | G | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-58687C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108600918 | ||||||
| chr2:108600921
|
C | CTGTTG | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.33-58683_33-58682i others(7): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108600921 | |||||
| chr2:108600977
|
A | G | 1 | a0001c0002t0001g0046 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.33-58628A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108600977 | ||||||
| chr2:108601074
|
A | C | 1 | a0001c0001t0002g0182 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.33-58531A>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108601074 | ||||||
| chr2:108601117
|
G | C | 21 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(18): Show | 21 | HG02602.hp2 HG02622.hp1 HG03017.hp2 others(18): Show |
intron_variant | MODIFIER | c.33-58488G>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108601117 | ||||||
| chr2:108601445
|
C | T | 37 | a0001c0002t0001g0015a0001c0002t0001g0018a0001c0002t0001g0020others(34): Show | 37 | HG01070.hp1 HG01106.hp1 HG01167.hp2 others(34): Show |
intron_variant | MODIFIER | c.33-58160C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108601445 | ||||||
| chr2:108601560
|
A | C | 225 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(222): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.33-58045A>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108601560 | ||||||
| chr2:108601589
|
A | G | 1 | a0001c0002t0001g0013 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.33-58016A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108601589 | ||||||
| chr2:108601629
|
TC | T | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-57975delC | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108601629 | ||||||
| chr2:108601691
|
A | G | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-57914A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108601691 | ||||||
| chr2:108601961
|
GTTCTA | G | 93 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(90): Show | 93 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.33-57640_33-57636d others(7): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108601961 | |||||
| chr2:108602126
|
T | C | 93 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(90): Show | 93 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.33-57479T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108602126 | ||||||
| chr2:108602565
|
C | T | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-57040C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108602565 | ||||||
| chr2:108602592
|
A | G | 7 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(4): Show | 7 | HG02040.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.33-57013A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108602592 | ||||||
| chr2:108602978
|
C | T | 2 | a0001c0001t0017g0156a0001c0001t0017g0157 | 2 | HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.33-56627C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108602978 | ||||||
| chr2:108602983
|
T | C | 1 | a0001c0002t0004g0232 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.33-56622T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108602983 | ||||||
| chr2:108603037
|
T | C | 45 | a0001c0001t0003g0001a0001c0001t0003g0130a0001c0001t0003g0131others(42): Show | 46 | HG00323.hp1 HG00639.hp2 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.33-56568T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108603037 | ||||||
| chr2:108603081
|
T | C | 1 | a0001c0002t0001g0058 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.33-56524T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108603081 | ||||||
| chr2:108603083
|
A | G | 109 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(106): Show | 109 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.33-56522A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108603083 | ||||||
| chr2:108603390
|
A | G | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-56215A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108603390 | ||||||
| chr2:108603495
|
C | CT | 53 | a0001c0001t0002g0113a0001c0001t0002g0184a0001c0001t0002g0201others(50): Show | 54 | HG00323.hp1 HG00639.hp2 HG01074.hp1 others(51): Show |
intron_variant | MODIFIER | c.33-56089dupT | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108603495 | |||||
| chr2:108603495
|
C | CTT | 10 | a0001c0001t0003g0136a0001c0001t0003g0138a0001c0001t0003g0141others(7): Show | 10 | HG01192.hp1 HG02055.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.33-56090_33-56089d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108603495 | |||||
| chr2:108603495
|
C | CTTT | 52 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(49): Show | 52 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(49): Show |
intron_variant | MODIFIER | c.33-56091_33-56089d others(5): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108603495 | |||||
| chr2:108603495
|
C | CTTTT | 17 | a0001c0002t0001g0009a0001c0002t0001g0012a0001c0002t0001g0018others(14): Show | 17 | HG01106.hp1 HG01109.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.33-56092_33-56089d others(6): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108603495 | |||||
| chr2:108603515
|
T | C | 1 | a0001c0001t0002g0075 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.33-56090T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108603515 | ||||||
| chr2:108603716
|
G | A | 6 | a0001c0002t0004g0229a0001c0002t0004g0230a0001c0002t0004g0234others(3): Show | 6 | NA18947.hp2 NA18960.hp1 NA19062.hp1 others(3): Show |
intron_variant | MODIFIER | c.33-55889G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108603716 | ||||||
| chr2:108603743
|
C | G | 7 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(4): Show | 7 | HG02040.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.33-55862C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108603743 | ||||||
| chr2:108603884
|
G | A | 1 | a0001c0002t0001g0027 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.33-55721G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108603884 | ||||||
| chr2:108604027
|
A | G | 68 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.33-55578A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108604027 | ||||||
| chr2:108604197
|
C | T | 21 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(18): Show | 21 | HG02602.hp2 HG02622.hp1 HG03017.hp2 others(18): Show |
intron_variant | MODIFIER | c.33-55408C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108604197 | ||||||
| chr2:108604278
|
A | G | 7 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(4): Show | 7 | HG02040.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.33-55327A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108604278 | ||||||
| chr2:108604362
|
G | A | 1 | a0001c0002t0001g0010 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.33-55243G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108604362 | ||||||
| chr2:108604454
|
G | A | 68 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.33-55151G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108604454 | ||||||
| chr2:108604589
|
T | C | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-55016T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108604589 | ||||||
| chr2:108604618
|
C | T | 2 | a0001c0001t0002g0076a0001c0001t0005g0077 | 2 | HG00741.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.33-54987C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108604618 | ||||||
| chr2:108604757
|
CAG | C | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-54847_33-54846d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108604757 | ||||||
| chr2:108604862
|
A | G | 2 | a0002c0003t0018g0005a0002c0003t0026g0219 | 2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.33-54743A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108604862 | ||||||
| chr2:108604864
|
T | G | 1 | a0001c0002t0001g0044 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.33-54741T>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108604864 | ||||||
| chr2:108604895
|
T | G | 1 | a0001c0002t0001g0017 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.33-54710T>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108604895 | ||||||
| chr2:108604967
|
G | T | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-54638G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108604967 | ||||||
| chr2:108605076
|
A | G | 1 | a0001c0002t0001g0044 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.33-54529A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108605076 | ||||||
| chr2:108605140
|
G | A | 23 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(20): Show | 23 | HG02602.hp2 HG02622.hp1 HG02895.hp1 others(20): Show |
intron_variant | MODIFIER | c.33-54465G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108605140 | ||||||
| chr2:108605167
|
AAC | A | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-54436_33-54435d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108605167 | |||||
| chr2:108605273
|
G | A | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-54332G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108605273 | ||||||
| chr2:108605378
|
A | G | 1 | a0001c0002t0001g0071 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.33-54227A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108605378 | ||||||
| chr2:108605738
|
A | G | 1 | a0001c0002t0001g0012 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.33-53867A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108605738 | ||||||
| chr2:108605981
|
C | T | 1 | a0002c0003t0026g0219 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.33-53624C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108605981 | ||||||
| chr2:108605985
|
G | A | 7 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(4): Show | 7 | HG02040.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.33-53620G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108605985 | ||||||
| chr2:108605997
|
G | A | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-53608G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108605997 | ||||||
| chr2:108606004
|
T | C | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-53601T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108606004 | ||||||
| chr2:108606043
|
C | T | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-53562C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108606043 | ||||||
| chr2:108606280
|
G | A | 154 | a0001c0001t0003g0001a0001c0001t0003g0130a0001c0001t0003g0131others(151): Show | 155 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.33-53325G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108606280 | ||||||
| chr2:108606531
|
A | G | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.33-53074A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108606531 | ||||||
| chr2:108606534
|
A | G | 1 | a0001c0002t0001g0017 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.33-53071A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108606534 | ||||||
| chr2:108606731
|
T | C | 11 | a0001c0001t0003g0202a0001c0001t0003g0203a0001c0001t0003g0204others(8): Show | 11 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.33-52874T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108606731 | ||||||
| chr2:108606772
|
A | T | 7 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(4): Show | 7 | HG02040.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.33-52833A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108606772 | ||||||
| chr2:108606881
|
A | C | 11 | a0001c0001t0003g0202a0001c0001t0003g0203a0001c0001t0003g0204others(8): Show | 11 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.33-52724A>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108606881 | ||||||
| chr2:108606971
|
G | A | 21 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(18): Show | 21 | HG02602.hp2 HG02622.hp1 HG03017.hp2 others(18): Show |
intron_variant | MODIFIER | c.33-52634G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108606971 | ||||||
| chr2:108607489
|
T | C | 36 | a0001c0001t0003g0001a0001c0001t0003g0130a0001c0001t0003g0131others(33): Show | 37 | HG00323.hp1 HG00639.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.33-52116T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108607489 | ||||||
| chr2:108607721
|
G | T | 1 | a0001c0002t0001g0071 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.33-51884G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108607721 | ||||||
| chr2:108607849
|
A | G | 3 | a0001c0002t0007g0214a0001c0002t0007g0217a0001c0002t0007g0218 | 3 | HG03195.hp1 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.33-51756A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108607849 | ||||||
| chr2:108607867
|
G | T | 1 | a0001c0001t0002g0097 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.33-51738G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108607867 | ||||||
| chr2:108607885
|
A | G | 2 | a0001c0002t0001g0063a0001c0002t0001g0064 | 2 | HG01993.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.33-51720A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108607885 | ||||||
| chr2:108608142
|
C | T | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-51463C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108608142 | ||||||
| chr2:108608263
|
G | A | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.33-51342G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108608263 | ||||||
| chr2:108608265
|
G | A | 154 | a0001c0001t0003g0001a0001c0001t0003g0130a0001c0001t0003g0131others(151): Show | 155 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.33-51340G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108608265 | ||||||
| chr2:108608307
|
C | CT | 5 | a0001c0001t0002g0104a0001c0001t0005g0163a0001c0002t0001g0038others(2): Show | 5 | HG01257.hp1 HG02572.hp1 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-51282dupT | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108608307 | |||||
| chr2:108608392
|
G | A | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.33-51213G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108608392 | ||||||
| chr2:108608529
|
C | G | 1 | a0001c0001t0002g0184 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.33-51076C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108608529 | ||||||
| chr2:108608596
|
G | A | 2 | a0001c0002t0001g0049a0001c0002t0001g0050 | 2 | HG02630.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.33-51009G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108608596 | ||||||
| chr2:108608599
|
C | T | 1 | a0001c0002t0004g0232 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.33-51006C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108608599 | ||||||
| chr2:108609513
|
C | G | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-50092C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108609513 | ||||||
| chr2:108609523
|
C | T | 1 | a0001c0002t0001g0004 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.33-50082C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108609523 | ||||||
| chr2:108609532
|
C | T | 7 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(4): Show | 7 | HG02040.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.33-50073C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108609532 | ||||||
| chr2:108609746
|
C | T | 1 | a0001c0001t0005g0169 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.33-49859C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108609746 | ||||||
| chr2:108609832
|
GT | G | 4 | a0001c0001t0003g0001a0001c0001t0003g0137a0001c0001t0003g0152others(1): Show | 5 | HG00323.hp1 HG01074.hp1 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-49764delT | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108609832 | |||||
| chr2:108609844
|
CTTAAAAA others(4): Show |
C | 4 | a0001c0001t0003g0001a0001c0001t0003g0137a0001c0001t0003g0152others(1): Show | 5 | HG00323.hp1 HG01074.hp1 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-49757_33-49747d others(13): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108609844 | |||||
| chr2:108609865
|
G | A | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.33-49740G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108609865 | ||||||
| chr2:108610012
|
A | G | 21 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(18): Show | 21 | HG02602.hp2 HG02622.hp1 HG03017.hp2 others(18): Show |
intron_variant | MODIFIER | c.33-49593A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108610012 | ||||||
| chr2:108610020
|
G | C | 1 | a0001c0001t0002g0184 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.33-49585G>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108610020 | ||||||
| chr2:108610148
|
A | ATG | 14 | a0001c0001t0002g0085a0001c0001t0002g0098a0001c0001t0002g0106others(11): Show | 14 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.33-49411_33-49410d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108610148 | |||||
| chr2:108610148
|
A | ATGTG | 6 | a0001c0001t0002g0094a0001c0001t0002g0095a0001c0001t0002g0110others(3): Show | 6 | HG00323.hp1 HG01358.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.33-49413_33-49410d others(6): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108610148 | |||||
| chr2:108610148
|
A | ATGTGTG | 3 | a0001c0001t0002g0108a0001c0001t0003g0196a0001c0001t0028g0197 | 3 | HG02622.hp2 HG02818.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.33-49415_33-49410d others(8): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108610148 | |||||
| chr2:108610148
|
ATG | A | 18 | a0001c0001t0002g0084a0001c0001t0002g0113a0001c0001t0003g0001others(15): Show | 19 | HG00140.hp1 HG01074.hp1 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.33-49411_33-49410d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108610148 | |||||
| chr2:108610148
|
ATGTG | A | 33 | a0001c0001t0002g0076a0001c0001t0002g0082a0001c0001t0002g0083others(30): Show | 33 | HG00280.hp2 HG00741.hp1 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.33-49413_33-49410d others(6): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108610148 | |||||
| chr2:108610148
|
ATGTGTG | A | 30 | a0001c0001t0002g0075a0001c0001t0002g0086a0001c0001t0002g0087others(27): Show | 30 | HG01070.hp2 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.33-49415_33-49410d others(8): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108610148 | |||||
| chr2:108610148
|
ATGTGTGT others(1): Show |
A | 21 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140others(18): Show | 21 | HG01243.hp1 HG01257.hp2 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.33-49417_33-49410d others(10): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108610148 | |||||
| chr2:108610148
|
ATGTGTGT others(3): Show |
A | 22 | a0001c0001t0003g0209a0001c0001t0003g0211a0001c0002t0004g0225others(19): Show | 22 | HG02257.hp1 HG02602.hp2 HG02622.hp1 others(19): Show |
intron_variant | MODIFIER | c.33-49419_33-49410d others(12): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108610148 | |||||
| chr2:108610148
|
ATGTGTGT others(5): Show |
A | 6 | a0001c0001t0014g0159a0001c0001t0014g0160a0001c0002t0001g0002others(3): Show | 6 | HG02559.hp1 HG03471.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.33-49421_33-49410d others(14): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108610148 | |||||
| chr2:108610148
|
ATGTGTGT others(7): Show |
A | 7 | a0001c0002t0001g0008a0001c0002t0001g0010a0001c0002t0001g0011others(4): Show | 7 | HG00323.hp2 HG00639.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.33-49423_33-49410d others(16): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108610148 | |||||
| chr2:108610148
|
ATGTGTGT others(9): Show |
A | 57 | a0001c0001t0002g0104a0001c0002t0001g0009a0001c0002t0001g0014others(54): Show | 57 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.33-49425_33-49410d others(18): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108610148 | |||||
| chr2:108610148
|
ATGTGTGT others(11): Show |
A | 1 | a0001c0002t0001g0043 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.33-49427_33-49410d others(20): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108610148 | |||||
| chr2:108610148
|
ATGTGTGT others(17): Show |
A | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-49433_33-49410d others(26): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108610148 | |||||
| chr2:108610417
|
A | G | 1 | a0001c0001t0003g0212 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.33-49188A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108610417 | ||||||
| chr2:108610513
|
G | A | 1 | a0001c0002t0001g0036 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.33-49092G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108610513 | ||||||
| chr2:108610684
|
C | A | 154 | a0001c0001t0003g0001a0001c0001t0003g0130a0001c0001t0003g0131others(151): Show | 155 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.33-48921C>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108610684 | ||||||
| chr2:108610820
|
G | A | 1 | a0001c0001t0003g0213 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.33-48785G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108610820 | ||||||
| chr2:108610851
|
A | G | 1 | a0001c0002t0001g0018 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.33-48754A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108610851 | ||||||
| chr2:108610914
|
T | C | 2 | a0001c0004t0013g0073a0001c0004t0013g0074 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.33-48691T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108610914 | ||||||
| chr2:108610997
|
A | G | 3 | a0001c0002t0007g0214a0001c0002t0007g0217a0001c0002t0007g0218 | 3 | HG03195.hp1 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.33-48608A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108610997 | ||||||
| chr2:108611167
|
C | T | 21 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(18): Show | 21 | HG02602.hp2 HG02622.hp1 HG03017.hp2 others(18): Show |
intron_variant | MODIFIER | c.33-48438C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108611167 | ||||||
| chr2:108611250
|
A | G | 242 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(239): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.33-48355A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108611250 | ||||||
| chr2:108611330
|
A | C | 1 | a0001c0002t0004g0232 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.33-48275A>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108611330 | ||||||
| chr2:108611377
|
G | A | 2 | a0002c0003t0018g0005a0002c0003t0026g0219 | 2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.33-48228G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108611377 | ||||||
| chr2:108611567
|
G | C | 5 | a0001c0001t0003g0189a0001c0001t0003g0190a0001c0001t0003g0191others(2): Show | 5 | HG01074.hp2 HG01358.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-48038G>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108611567 | ||||||
| chr2:108611603
|
G | C | 1 | a0001c0001t0003g0132 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.33-48002G>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108611603 | ||||||
| chr2:108611617
|
C | T | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.33-47988C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108611617 | ||||||
| chr2:108611645
|
C | T | 1 | a0001c0001t0006g0170 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.33-47960C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108611645 | ||||||
| chr2:108611836
|
A | AAT | 34 | a0001c0001t0002g0106a0001c0001t0002g0108a0001c0001t0002g0110others(31): Show | 35 | HG00099.hp2 HG00323.hp1 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.33-47751_33-47750d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108611836 | |||||
| chr2:108611836
|
A | AATAT | 11 | a0001c0001t0003g0130a0001c0001t0003g0135a0001c0001t0003g0136others(8): Show | 11 | HG00639.hp2 HG01074.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.33-47753_33-47750d others(6): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108611836 | |||||
| chr2:108611836
|
A | AATATAT | 5 | a0001c0001t0003g0187a0001c0001t0003g0196a0001c0001t0010g0193others(2): Show | 5 | HG02622.hp2 HG02818.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-47755_33-47750d others(8): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108611836 | |||||
| chr2:108611836
|
A | AATATATA others(3): Show |
17 | a0001c0002t0001g0017a0001c0002t0001g0021a0001c0002t0001g0030others(14): Show | 17 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(14): Show |
intron_variant | MODIFIER | c.33-47759_33-47750d others(12): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108611836 | |||||
| chr2:108611836
|
A | AATATATA others(5): Show |
34 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(31): Show | 34 | HG00639.hp1 HG01167.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.33-47761_33-47750d others(14): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108611836 | |||||
| chr2:108611836
|
A | AATATATA others(7): Show |
13 | a0001c0002t0001g0010a0001c0002t0001g0014a0001c0002t0001g0018others(10): Show | 13 | HG00323.hp2 HG01070.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.33-47763_33-47750d others(16): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108611836 | |||||
| chr2:108611836
|
AAT | A | 11 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(8): Show | 11 | HG02040.hp2 HG02258.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.33-47751_33-47750d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108611836 | |||||
| chr2:108611852
|
T | C | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-47753T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108611852 | ||||||
| chr2:108611854
|
T | C | 9 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(6): Show | 9 | HG01261.hp2 HG02258.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.33-47751T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108611854 | ||||||
| chr2:108611854
|
T | TATAC | 23 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(20): Show | 23 | HG02602.hp2 HG02622.hp1 HG02895.hp1 others(20): Show |
intron_variant | MODIFIER | c.33-47750_33-47749i others(6): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108611854 | |||||
| chr2:108611854
|
T | TATATATA others(3): Show |
1 | a0001c0002t0001g0009 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.33-47750_33-47749i others(12): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108611854 | |||||
| chr2:108611854
|
T | TATATATA others(5): Show |
3 | a0001c0002t0001g0029a0001c0002t0001g0047a0001c0002t0001g0059 | 3 | HG01361.hp1 HG02886.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.33-47750_33-47749i others(14): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108611854 | |||||
| chr2:108611921
|
AAT | A | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-47674_33-47673d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108611921 | |||||
| chr2:108611923
|
TATATATA others(12): Show |
T | 1 | a0001c0001t0003g0213 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.33-47665_33-47647d others(21): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108611923 | |||||
| chr2:108611931
|
T | TACATATA others(29): Show |
72 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(69): Show | 72 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.33-47634_33-47599d others(38): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108611931 | |||||
| chr2:108611931
|
T | TACATATA others(65): Show |
6 | a0001c0002t0001g0064a0001c0002t0009g0078a0001c0002t0009g0080others(3): Show | 6 | HG01261.hp2 HG01993.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.33-47670_33-47599d others(74): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108611931 | |||||
| chr2:108611953
|
ATATAT | A | 3 | a0001c0002t0008g0221a0001c0002t0008g0224a0001c0002t0012g0220 | 3 | HG02486.hp1 HG02630.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.33-47646_33-47642d others(7): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108611953 | |||||
| chr2:108611958
|
T | TATACACA others(19): Show |
2 | a0001c0002t0012g0006a0001c0002t0012g0007 | 2 | HG02040.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.33-47647_33-47646i others(28): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108611958 | ||||||
| chr2:108611958
|
T | TATACATA others(19): Show |
2 | a0001c0002t0008g0222a0001c0002t0008g0223 | 2 | HG02647.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.33-47647_33-47646i others(28): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108611958 | ||||||
| chr2:108611958
|
T | TTATATAT others(24): Show |
1 | a0001c0002t0001g0018 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.33-47641_33-47611d others(33): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108611958 | |||||
| chr2:108611969
|
C | T | 2 | a0001c0002t0008g0221a0001c0002t0008g0224 | 2 | HG02486.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.33-47636C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108611969 | ||||||
| chr2:108611994
|
T | TATACACA others(19): Show |
3 | a0001c0002t0008g0221a0001c0002t0008g0224a0001c0002t0012g0220 | 3 | HG02486.hp1 HG02630.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.33-47611_33-47610i others(28): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108611994 | ||||||
| chr2:108612007
|
C | T | 25 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(22): Show | 25 | HG02572.hp1 HG02602.hp2 HG02622.hp1 others(22): Show |
intron_variant | MODIFIER | c.33-47598C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108612007 | ||||||
| chr2:108612010
|
A | AAAATATA others(11): Show |
2 | a0002c0003t0018g0005a0002c0003t0026g0219 | 2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.33-47595_33-47594i others(20): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108612010 | ||||||
| chr2:108612010
|
A | ATAAAATA others(13): Show |
21 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(18): Show | 21 | HG02602.hp2 HG02622.hp1 HG03017.hp2 others(18): Show |
intron_variant | MODIFIER | c.33-47593_33-47592i others(22): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108612010 | |||||
| chr2:108612017
|
T | C | 4 | a0001c0001t0002g0075a0001c0001t0022g0112a0001c0004t0013g0073others(1): Show | 4 | HG02895.hp1 HG02897.hp2 NA18940.hp1 others(1): Show |
intron_variant | MODIFIER | c.33-47588T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108612017 | ||||||
| chr2:108612023
|
C | T | 24 | a0001c0001t0002g0097a0001c0002t0004g0225a0001c0002t0004g0226others(21): Show | 24 | HG01167.hp1 HG02572.hp1 HG02602.hp2 others(21): Show |
intron_variant | MODIFIER | c.33-47582C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108612023 | ||||||
| chr2:108612025
|
C | T | 25 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(22): Show | 25 | HG02572.hp1 HG02602.hp2 HG02622.hp1 others(22): Show |
intron_variant | MODIFIER | c.33-47580C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108612025 | ||||||
| chr2:108612025
|
CAT | C | 28 | a0001c0002t0001g0018a0001c0002t0001g0020a0001c0002t0001g0023others(25): Show | 28 | HG01070.hp1 HG01106.hp1 HG01993.hp2 others(25): Show |
intron_variant | MODIFIER | c.33-47576_33-47575d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108612025 | |||||
| chr2:108612027
|
T | C | 2 | a0001c0004t0013g0073a0001c0004t0013g0074 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.33-47578T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108612027 | ||||||
| chr2:108612029
|
T | C | 11 | a0001c0002t0001g0015a0001c0002t0001g0022a0001c0002t0001g0028others(8): Show | 11 | HG01167.hp2 HG01168.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.33-47576T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108612029 | ||||||
| chr2:108612029
|
T | TAC | 6 | a0001c0001t0002g0116a0001c0001t0005g0164a0001c0001t0022g0112others(3): Show | 6 | HG01099.hp1 HG02486.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.33-47552_33-47551d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108612029 | |||||
| chr2:108612029
|
T | TACAC | 9 | a0001c0001t0005g0172a0001c0001t0006g0170a0001c0001t0006g0171others(6): Show | 9 | HG00140.hp1 HG00280.hp2 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.33-47554_33-47551d others(6): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108612029 | |||||
| chr2:108612029
|
TAC | T | 9 | a0001c0001t0003g0202a0001c0001t0003g0203a0001c0001t0003g0204others(6): Show | 9 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.33-47552_33-47551d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108612029 | |||||
| chr2:108612031
|
C | T | 21 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(18): Show | 21 | HG02602.hp2 HG02622.hp1 HG03017.hp2 others(18): Show |
intron_variant | MODIFIER | c.33-47574C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108612031 | ||||||
| chr2:108612039
|
C | CATAT | 21 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(18): Show | 21 | HG02572.hp1 HG02602.hp2 HG02622.hp1 others(18): Show |
intron_variant | MODIFIER | c.33-47565_33-47564i others(6): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108612039 | |||||
| chr2:108612043
|
CACACACA others(7): Show |
C | 44 | a0001c0001t0003g0001a0001c0001t0003g0130a0001c0001t0003g0131others(41): Show | 45 | HG00323.hp1 HG00639.hp2 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.33-47560_33-47547d others(16): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108612043 | |||||
| chr2:108612045
|
CACACACA others(7): Show |
C | 1 | a0001c0001t0003g0136 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.33-47558_33-47545d others(16): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108612045 | |||||
| chr2:108612051
|
CACAT | C | 8 | a0001c0001t0024g0162a0001c0002t0007g0214a0001c0002t0007g0215others(5): Show | 8 | HG02040.hp2 HG02258.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.33-47552_33-47549d others(6): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108612051 | |||||
| chr2:108612051
|
CACATATA others(11): Show |
C | 2 | a0001c0001t0005g0167a0001c0001t0005g0185 | 2 | HG02735.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.33-47541_33-47524d others(20): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108612051 | |||||
| chr2:108612053
|
C | CACAT | 3 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0019 | 3 | NA19043.hp1 NA20129.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.33-47551_33-47550i others(6): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108612053 | |||||
| chr2:108612053
|
CAT | C | 8 | a0001c0001t0003g0205a0001c0001t0003g0207a0001c0001t0003g0208others(5): Show | 8 | HG02055.hp1 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.33-47536_33-47535d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108612053 | |||||
| chr2:108612053
|
CATAT | C | 3 | a0001c0002t0009g0079a0001c0002t0009g0080a0001c0002t0009g0081 | 3 | HG01261.hp2 NA18954.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.33-47538_33-47535d others(6): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108612053 | |||||
| chr2:108612055
|
T | C | 89 | a0001c0001t0002g0129a0001c0002t0001g0008a0001c0002t0001g0009others(86): Show | 89 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.33-47550T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108612055 | ||||||
| chr2:108612057
|
T | C | 7 | a0001c0002t0001g0004a0001c0002t0001g0044a0001c0002t0009g0078others(4): Show | 7 | HG02559.hp1 HG02572.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.33-47548T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108612057 | ||||||
| chr2:108612069
|
T | C | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.33-47536T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108612069 | ||||||
| chr2:108612267
|
A | G | 154 | a0001c0001t0003g0001a0001c0001t0003g0130a0001c0001t0003g0131others(151): Show | 155 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.33-47338A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108612267 | ||||||
| chr2:108612352
|
C | T | 1 | a0001c0001t0003g0132 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.33-47253C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108612352 | ||||||
| chr2:108612471
|
CT | C | 5 | a0001c0002t0004g0233a0001c0002t0008g0221a0001c0002t0008g0222others(2): Show | 5 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-47122delT | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108612471 | |||||
| chr2:108612482
|
T | C | 5 | a0001c0001t0003g0196a0001c0001t0010g0193a0001c0001t0010g0194others(2): Show | 5 | HG02622.hp2 HG02818.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-47123T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108612482 | ||||||
| chr2:108613283
|
G | A | 2 | a0001c0001t0014g0159a0001c0001t0014g0160 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.33-46322G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108613283 | ||||||
| chr2:108613646
|
A | G | 1 | a0001c0002t0001g0004 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.33-45959A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108613646 | ||||||
| chr2:108613717
|
A | G | 7 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(4): Show | 7 | HG02040.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.33-45888A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108613717 | ||||||
| chr2:108613904
|
A | G | 154 | a0001c0001t0003g0001a0001c0001t0003g0130a0001c0001t0003g0131others(151): Show | 155 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.33-45701A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108613904 | ||||||
| chr2:108613921
|
C | G | 1 | a0001c0002t0012g0006 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.33-45684C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108613921 | ||||||
| chr2:108613933
|
A | G | 93 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(90): Show | 93 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.33-45672A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108613933 | ||||||
| chr2:108614185
|
G | A | 1 | a0001c0002t0004g0240 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.33-45420G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108614185 | ||||||
| chr2:108614696
|
G | A | 1 | a0001c0001t0024g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.33-44909G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108614696 | ||||||
| chr2:108614977
|
A | G | 68 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.33-44628A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108614977 | ||||||
| chr2:108614979
|
T | G | 11 | a0001c0001t0005g0167a0001c0001t0005g0172a0001c0001t0005g0185others(8): Show | 11 | HG00140.hp1 HG00280.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.33-44626T>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108614979 | ||||||
| chr2:108614997
|
G | A | 45 | a0001c0001t0003g0001a0001c0001t0003g0130a0001c0001t0003g0131others(42): Show | 46 | HG00323.hp1 HG00639.hp2 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.33-44608G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108614997 | ||||||
| chr2:108615065
|
C | T | 2 | a0001c0001t0003g0150a0001c0001t0003g0151 | 2 | HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.33-44540C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108615065 | ||||||
| chr2:108615099
|
TTGG | T | 93 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(90): Show | 93 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.33-44501_33-44499d others(5): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108615099 | |||||
| chr2:108615117
|
G | A | 1 | a0001c0002t0009g0080 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.33-44488G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108615117 | ||||||
| chr2:108615158
|
A | G | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-44447A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108615158 | ||||||
| chr2:108615266
|
A | C | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-44339A>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108615266 | ||||||
| chr2:108615517
|
A | G | 1 | a0001c0002t0009g0078 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.33-44088A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108615517 | ||||||
| chr2:108615519
|
T | C | 39 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(36): Show | 39 | HG00099.hp2 HG00741.hp2 HG01168.hp2 others(36): Show |
intron_variant | MODIFIER | c.33-44086T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108615519 | ||||||
| chr2:108615619
|
C | T | 43 | a0001c0001t0003g0001a0001c0001t0003g0130a0001c0001t0003g0131others(40): Show | 44 | HG00323.hp1 HG00639.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.33-43986C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108615619 | ||||||
| chr2:108615932
|
A | C | 45 | a0001c0001t0003g0001a0001c0001t0003g0130a0001c0001t0003g0131others(42): Show | 46 | HG00323.hp1 HG00639.hp2 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.33-43673A>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108615932 | ||||||
| chr2:108616097
|
AC | A | 21 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(18): Show | 21 | HG02602.hp2 HG02622.hp1 HG03017.hp2 others(18): Show |
intron_variant | MODIFIER | c.33-43507delC | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108616097 | ||||||
| chr2:108616107
|
A | G | 1 | a0001c0002t0001g0054 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.33-43498A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108616107 | ||||||
| chr2:108616197
|
C | CT | 80 | a0001c0001t0002g0075a0001c0001t0002g0122a0001c0001t0003g0206others(77): Show | 80 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.33-43384dupT | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108616197 | |||||
| chr2:108616197
|
C | CTT | 22 | a0001c0001t0017g0156a0001c0001t0017g0157a0001c0002t0001g0004others(19): Show | 22 | HG01106.hp1 HG01361.hp1 HG02056.hp2 others(19): Show |
intron_variant | MODIFIER | c.33-43385_33-43384d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108616197 | |||||
| chr2:108616197
|
CT | C | 49 | a0001c0001t0002g0098a0001c0001t0003g0001a0001c0001t0003g0130others(46): Show | 50 | HG00323.hp1 HG00639.hp2 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.33-43384delT | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108616197 | |||||
| chr2:108616368
|
C | T | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-43237C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108616368 | ||||||
| chr2:108616463
|
G | A | 3 | a0001c0001t0003g0001a0001c0001t0003g0137a0001c0001t0003g0153 | 4 | HG00323.hp1 HG01074.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-43142G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108616463 | ||||||
| chr2:108616623
|
C | T | 93 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(90): Show | 93 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.33-42982C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108616623 | ||||||
| chr2:108616684
|
A | G | 1 | a0001c0001t0002g0129 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.33-42921A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108616684 | ||||||
| chr2:108617090
|
G | A | 1 | a0001c0001t0005g0185 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.33-42515G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108617090 | ||||||
| chr2:108617479
|
A | T | 21 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(18): Show | 21 | HG02602.hp2 HG02622.hp1 HG03017.hp2 others(18): Show |
intron_variant | MODIFIER | c.33-42126A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108617479 | ||||||
| chr2:108617624
|
C | G | 26 | a0001c0002t0001g0004a0001c0002t0004g0225a0001c0002t0004g0226others(23): Show | 26 | HG02559.hp1 HG02572.hp1 HG02602.hp2 others(23): Show |
intron_variant | MODIFIER | c.33-41981C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108617624 | ||||||
| chr2:108617742
|
T | G | 1 | a0001c0002t0001g0004 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.33-41863T>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108617742 | ||||||
| chr2:108617858
|
G | T | 67 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0008others(64): Show | 67 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.33-41747G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108617858 | ||||||
| chr2:108618008
|
G | A | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.33-41597G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108618008 | ||||||
| chr2:108618111
|
G | A | 67 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0008others(64): Show | 67 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.33-41494G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108618111 | ||||||
| chr2:108618501
|
C | CCT | 5 | a0001c0002t0001g0004a0001c0002t0009g0078a0001c0002t0009g0079others(2): Show | 5 | HG01261.hp2 HG02559.hp1 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-41087_33-41086d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108618501 | |||||
| chr2:108618644
|
G | A | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-40961G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108618644 | ||||||
| chr2:108618728
|
G | T | 1 | a0001c0002t0001g0020 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.33-40877G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108618728 | ||||||
| chr2:108618779
|
C | T | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-40826C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108618779 | ||||||
| chr2:108618801
|
G | A | 1 | a0001c0001t0002g0089 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.33-40804G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108618801 | ||||||
| chr2:108618811
|
A | C | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-40794A>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108618811 | ||||||
| chr2:108618823
|
C | CA | 8 | a0001c0001t0003g0131a0001c0001t0003g0138a0001c0001t0003g0141others(5): Show | 8 | HG01361.hp2 HG02572.hp2 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.33-40761dupA | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108618823 | |||||
| chr2:108618823
|
CA | C | 119 | a0001c0001t0002g0082a0001c0001t0002g0083a0001c0001t0002g0084others(116): Show | 119 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.33-40761delA | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108618823 | |||||
| chr2:108618823
|
CAA | C | 5 | a0001c0001t0002g0076a0001c0002t0012g0006a0001c0002t0012g0007others(2): Show | 5 | HG01993.hp1 HG02040.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-40762_33-40761d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108618823 | |||||
| chr2:108618875
|
C | T | 2 | a0002c0003t0018g0005a0002c0003t0026g0219 | 2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.33-40730C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108618875 | ||||||
| chr2:108618985
|
TGTTTCAG others(3): Show |
T | 8 | a0001c0001t0003g0187a0001c0001t0003g0188a0001c0001t0003g0189others(5): Show | 8 | HG00639.hp2 HG01074.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.33-40615_33-40606d others(12): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108618985 | |||||
| chr2:108619189
|
A | G | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.33-40416A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108619189 | ||||||
| chr2:108619223
|
T | A | 1 | a0001c0001t0021g0120 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.33-40382T>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108619223 | ||||||
| chr2:108619224
|
A | G | 2 | a0001c0002t0001g0004a0001c0002t0001g0071 | 2 | HG02559.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.33-40381A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108619224 | ||||||
| chr2:108619304
|
G | T | 1 | a0001c0002t0012g0006 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.33-40301G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108619304 | ||||||
| chr2:108619360
|
CT | C | 9 | a0001c0001t0003g0161a0001c0001t0003g0205a0001c0001t0003g0207others(6): Show | 9 | HG01981.hp1 HG02056.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.33-40230delT | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108619360 | |||||
| chr2:108619391
|
T | C | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-40214T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108619391 | ||||||
| chr2:108619465
|
C | G | 1 | a0001c0002t0009g0078 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.33-40140C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108619465 | ||||||
| chr2:108619700
|
CA | C | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.33-39901delA | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108619700 | |||||
| chr2:108619707
|
A | C | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.33-39898A>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108619707 | ||||||
| chr2:108619795
|
A | T | 1 | a0001c0002t0001g0040 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.33-39810A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108619795 | ||||||
| chr2:108619968
|
G | A | 1 | a0001c0001t0006g0168 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.33-39637G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108619968 | ||||||
| chr2:108620007
|
T | A | 1 | a0001c0002t0001g0050 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.33-39598T>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108620007 | ||||||
| chr2:108620047
|
G | A | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-39558G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108620047 | ||||||
| chr2:108620090
|
C | T | 1 | a0001c0002t0001g0057 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.33-39515C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108620090 | ||||||
| chr2:108620116
|
C | A | 6 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140others(3): Show | 6 | HG01243.hp1 HG02572.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.33-39489C>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108620116 | ||||||
| chr2:108620236
|
C | T | 1 | a0002c0003t0026g0219 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.33-39369C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108620236 | ||||||
| chr2:108620304
|
G | C | 8 | a0001c0001t0002g0084a0001c0001t0002g0089a0001c0001t0002g0090others(5): Show | 8 | HG01175.hp2 HG02145.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.33-39301G>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108620304 | ||||||
| chr2:108620348
|
C | G | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-39257C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108620348 | ||||||
| chr2:108620707
|
A | G | 1 | a0001c0001t0002g0089 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.33-38898A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108620707 | ||||||
| chr2:108620833
|
T | G | 90 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(87): Show | 90 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.33-38772T>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108620833 | ||||||
| chr2:108621599
|
C | G | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.33-38006C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108621599 | ||||||
| chr2:108622022
|
C | G | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-37583C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108622022 | ||||||
| chr2:108622067
|
A | G | 2 | a0001c0001t0003g0203a0001c0001t0003g0211 | 2 | HG02451.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.33-37538A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108622067 | ||||||
| chr2:108622189
|
G | A | 1 | a0001c0002t0009g0078 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.33-37416G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108622189 | ||||||
| chr2:108622300
|
A | G | 1 | a0001c0001t0006g0168 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.33-37305A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108622300 | ||||||
| chr2:108622433
|
A | G | 1 | a0002c0003t0018g0005 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.33-37172A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108622433 | ||||||
| chr2:108622436
|
C | T | 1 | a0001c0001t0006g0168 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.33-37169C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108622436 | ||||||
| chr2:108622525
|
T | C | 68 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.33-37080T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108622525 | ||||||
| chr2:108622554
|
T | C | 100 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.33-37051T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108622554 | ||||||
| chr2:108622588
|
G | A | 11 | a0001c0001t0003g0202a0001c0001t0003g0203a0001c0001t0003g0204others(8): Show | 11 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.33-37017G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108622588 | ||||||
| chr2:108622889
|
T | C | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-36716T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108622889 | ||||||
| chr2:108622917
|
G | A | 7 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(4): Show | 7 | HG02040.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.33-36688G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108622917 | ||||||
| chr2:108622951
|
C | T | 199 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.33-36654C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108622951 | ||||||
| chr2:108622973
|
AT | A | 136 | a0001c0001t0002g0084a0001c0001t0002g0086a0001c0001t0002g0087others(133): Show | 136 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.33-36613delT | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108622973 | |||||
| chr2:108622973
|
ATT | A | 16 | a0001c0001t0003g0205a0001c0001t0003g0207a0001c0001t0006g0173others(13): Show | 16 | HG02040.hp2 HG02280.hp1 HG02647.hp1 others(13): Show |
intron_variant | MODIFIER | c.33-36614_33-36613d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108622973 | |||||
| chr2:108622973
|
ATTT | A | 14 | a0001c0001t0003g0202a0001c0001t0003g0203a0001c0001t0003g0204others(11): Show | 14 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.33-36615_33-36613d others(5): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108622973 | |||||
| chr2:108623159
|
T | G | 2 | a0001c0001t0014g0159a0001c0001t0014g0160 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.33-36446T>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108623159 | ||||||
| chr2:108623184
|
C | T | 1 | a0001c0001t0028g0197 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.33-36421C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108623184 | ||||||
| chr2:108623217
|
GA | G | 90 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(87): Show | 90 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.33-36387delA | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108623217 | ||||||
| chr2:108623219
|
T | C | 90 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(87): Show | 90 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.33-36386T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108623219 | ||||||
| chr2:108623403
|
A | G | 1 | a0001c0002t0001g0032 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.33-36202A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108623403 | ||||||
| chr2:108623413
|
T | A | 91 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(88): Show | 91 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.33-36192T>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108623413 | ||||||
| chr2:108623458
|
ACT | A | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.33-36141_33-36140d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108623458 | |||||
| chr2:108623584
|
A | T | 7 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(4): Show | 7 | HG02040.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.33-36021A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108623584 | ||||||
| chr2:108623610
|
G | A | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-35995G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108623610 | ||||||
| chr2:108623734
|
C | G | 1 | a0001c0002t0012g0007 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.33-35871C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108623734 | ||||||
| chr2:108623786
|
C | T | 104 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(101): Show | 104 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.33-35819C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108623786 | ||||||
| chr2:108623897
|
C | T | 93 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(90): Show | 93 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.33-35708C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108623897 | ||||||
| chr2:108623903
|
G | A | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-35702G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108623903 | ||||||
| chr2:108623945
|
C | T | 208 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(205): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.33-35660C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108623945 | ||||||
| chr2:108624100
|
T | C | 21 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(18): Show | 21 | HG02602.hp2 HG02622.hp1 HG03017.hp2 others(18): Show |
intron_variant | MODIFIER | c.33-35505T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108624100 | ||||||
| chr2:108624309
|
A | G | 1 | a0001c0002t0001g0063 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.33-35296A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108624309 | ||||||
| chr2:108624338
|
T | G | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-35267T>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108624338 | ||||||
| chr2:108624648
|
T | C | 2 | a0002c0003t0018g0005a0002c0003t0026g0219 | 2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.33-34957T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108624648 | ||||||
| chr2:108624676
|
G | T | 1 | a0001c0002t0001g0054 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.33-34929G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108624676 | ||||||
| chr2:108624713
|
C | T | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-34892C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108624713 | ||||||
| chr2:108624791
|
C | T | 1 | a0001c0002t0001g0009 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.33-34814C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108624791 | ||||||
| chr2:108624807
|
G | A | 2 | a0001c0004t0013g0073a0001c0004t0013g0074 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.33-34798G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108624807 | ||||||
| chr2:108625010
|
C | T | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.33-34595C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108625010 | ||||||
| chr2:108625064
|
G | A | 39 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(36): Show | 39 | HG00099.hp2 HG00741.hp2 HG01168.hp2 others(36): Show |
intron_variant | MODIFIER | c.33-34541G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108625064 | ||||||
| chr2:108625237
|
T | C | 1 | a0001c0002t0001g0034 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.33-34368T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108625237 | ||||||
| chr2:108625360
|
A | G | 7 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(4): Show | 7 | HG02040.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.33-34245A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108625360 | ||||||
| chr2:108625439
|
G | A | 2 | a0001c0004t0013g0073a0001c0004t0013g0074 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.33-34166G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108625439 | ||||||
| chr2:108625585
|
C | A | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-34020C>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108625585 | ||||||
| chr2:108625586
|
C | G | 1 | a0001c0001t0002g0114 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.33-34019C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108625586 | ||||||
| chr2:108625587
|
C | A | 1 | a0001c0002t0001g0004 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.33-34018C>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108625587 | ||||||
| chr2:108625596
|
G | T | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-34009G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108625596 | ||||||
| chr2:108625710
|
G | A | 5 | a0001c0002t0001g0015a0001c0002t0001g0028a0001c0002t0001g0047others(2): Show | 5 | HG01167.hp2 HG01168.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-33895G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108625710 | ||||||
| chr2:108626048
|
G | T | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-33557G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108626048 | ||||||
| chr2:108626273
|
A | T | 67 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0008others(64): Show | 67 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.33-33332A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108626273 | ||||||
| chr2:108626532
|
C | T | 1 | a0002c0003t0018g0005 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.33-33073C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108626532 | ||||||
| chr2:108626570
|
C | T | 21 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(18): Show | 21 | HG02602.hp2 HG02622.hp1 HG03017.hp2 others(18): Show |
intron_variant | MODIFIER | c.33-33035C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108626570 | ||||||
| chr2:108626632
|
A | G | 8 | a0001c0001t0002g0084a0001c0001t0002g0089a0001c0001t0002g0090others(5): Show | 8 | HG01175.hp2 HG02145.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.33-32973A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108626632 | ||||||
| chr2:108626643
|
A | G | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-32962A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108626643 | ||||||
| chr2:108626916
|
G | A | 1 | a0001c0001t0002g0076 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.33-32689G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108626916 | ||||||
| chr2:108626958
|
A | C | 1 | a0001c0002t0001g0044 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.33-32647A>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108626958 | ||||||
| chr2:108627150
|
T | G | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-32455T>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108627150 | ||||||
| chr2:108627400
|
G | GT | 5 | a0001c0001t0002g0086a0001c0001t0003g0136a0001c0001t0003g0155others(2): Show | 5 | HG02145.hp1 HG04199.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-32185dupT | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108627400 | |||||
| chr2:108627400
|
GT | G | 117 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(114): Show | 118 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.33-32185delT | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108627400 | |||||
| chr2:108627400
|
GTT | G | 72 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(69): Show | 72 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.33-32186_33-32185d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108627400 | |||||
| chr2:108627400
|
GTTT | G | 6 | a0001c0002t0007g0215a0001c0002t0007g0216a0001c0002t0009g0078others(3): Show | 6 | HG01261.hp2 HG02258.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.33-32187_33-32185d others(5): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108627400 | |||||
| chr2:108627424
|
C | T | 1 | a0001c0002t0001g0024 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.33-32181C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108627424 | ||||||
| chr2:108627436
|
A | G | 3 | a0001c0001t0002g0182a0001c0001t0002g0183a0001c0001t0002g0184 | 3 | HG02257.hp2 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.33-32169A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108627436 | ||||||
| chr2:108627471
|
A | G | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.33-32134A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108627471 | ||||||
| chr2:108627488
|
T | A | 1 | a0001c0002t0004g0226 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.33-32117T>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108627488 | ||||||
| chr2:108627501
|
T | A | 100 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.33-32104T>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108627501 | ||||||
| chr2:108627862
|
A | G | 11 | a0001c0001t0003g0202a0001c0001t0003g0203a0001c0001t0003g0204others(8): Show | 11 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.33-31743A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108627862 | ||||||
| chr2:108628130
|
G | A | 2 | a0001c0001t0002g0075a0001c0001t0022g0112 | 2 | NA18940.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.33-31475G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108628130 | ||||||
| chr2:108628186
|
C | G | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-31419C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108628186 | ||||||
| chr2:108628362
|
T | C | 11 | a0001c0001t0003g0202a0001c0001t0003g0203a0001c0001t0003g0204others(8): Show | 11 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.33-31243T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108628362 | ||||||
| chr2:108628553
|
C | T | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-31052C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108628553 | ||||||
| chr2:108628608
|
C | T | 3 | a0001c0001t0002g0182a0001c0001t0002g0183a0001c0001t0002g0184 | 3 | HG02257.hp2 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.33-30997C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108628608 | ||||||
| chr2:108628612
|
C | T | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-30993C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108628612 | ||||||
| chr2:108628914
|
G | A | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-30691G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108628914 | ||||||
| chr2:108629114
|
TG | T | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-30488delG | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108629114 | |||||
| chr2:108629276
|
G | A | 1 | a0001c0002t0012g0220 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.33-30329G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108629276 | ||||||
| chr2:108629423
|
CATA | C | 61 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(58): Show | 61 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.33-30178_33-30176d others(5): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108629423 | |||||
| chr2:108629436
|
G | A | 2 | a0002c0003t0018g0005a0002c0003t0026g0219 | 2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.33-30169G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108629436 | ||||||
| chr2:108629830
|
T | C | 2 | a0002c0003t0018g0005a0002c0003t0026g0219 | 2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.33-29775T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108629830 | ||||||
| chr2:108629907
|
T | C | 93 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(90): Show | 93 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.33-29698T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108629907 | ||||||
| chr2:108629964
|
G | A | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.33-29641G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108629964 | ||||||
| chr2:108630192
|
CA | C | 38 | a0001c0001t0002g0113a0001c0001t0002g0129a0001c0001t0003g0001others(35): Show | 39 | HG00323.hp1 HG01074.hp1 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.33-29390delA | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108630192 | |||||
| chr2:108630192
|
CAA | C | 73 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(70): Show | 73 | HG00099.hp2 HG00741.hp2 HG01070.hp2 others(70): Show |
intron_variant | MODIFIER | c.33-29391_33-29390d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108630192 | |||||
| chr2:108630192
|
CAAA | C | 13 | a0001c0001t0002g0085a0001c0001t0002g0089a0001c0001t0002g0095others(10): Show | 13 | HG00140.hp1 HG00280.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.33-29392_33-29390d others(5): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108630192 | |||||
| chr2:108630192
|
CAAAA | C | 11 | a0001c0001t0023g0176a0001c0002t0001g0002a0001c0002t0001g0017others(8): Show | 11 | HG01192.hp1 HG01256.hp2 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.33-29393_33-29390d others(6): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108630192 | |||||
| chr2:108630192
|
CAAAAA | C | 64 | a0001c0002t0001g0003a0001c0002t0001g0004a0001c0002t0001g0008others(61): Show | 64 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.33-29394_33-29390d others(7): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108630192 | |||||
| chr2:108630206
|
AAAAAAAA others(3): Show |
A | 1 | a0001c0002t0004g0245 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.33-29395_33-29386d others(12): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108630206 | |||||
| chr2:108630207
|
AAAAAAAA others(2): Show |
A | 18 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(15): Show | 18 | HG02602.hp2 HG02622.hp1 HG03017.hp2 others(15): Show |
intron_variant | MODIFIER | c.33-29394_33-29386d others(11): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108630207 | |||||
| chr2:108630210
|
A | G | 1 | a0001c0001t0024g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.33-29395A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108630210 | ||||||
| chr2:108630212
|
A | G | 9 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(6): Show | 9 | HG01261.hp2 HG02040.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.33-29393A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108630212 | ||||||
| chr2:108630503
|
C | T | 79 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(76): Show | 79 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.33-29102C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108630503 | ||||||
| chr2:108630530
|
T | TAATCAAA others(74): Show |
8 | a0001c0001t0002g0084a0001c0001t0002g0089a0001c0001t0002g0090others(5): Show | 8 | HG01175.hp2 HG02145.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.33-29073_33-28993d others(83): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108630530 | |||||
| chr2:108630881
|
A | G | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-28724A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108630881 | ||||||
| chr2:108630928
|
A | G | 3 | a0001c0001t0002g0082a0001c0001t0002g0083a0001c0001t0019g0124 | 3 | HG02723.hp1 HG03098.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.33-28677A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108630928 | ||||||
| chr2:108630933
|
G | A | 109 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(106): Show | 109 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.33-28672G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108630933 | ||||||
| chr2:108631033
|
A | G | 1 | a0001c0002t0012g0006 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.33-28572A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108631033 | ||||||
| chr2:108631396
|
A | G | 1 | a0001c0001t0003g0147 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.33-28209A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108631396 | ||||||
| chr2:108631514
|
A | G | 1 | a0001c0002t0001g0040 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.33-28091A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108631514 | ||||||
| chr2:108631550
|
CT | C | 92 | a0001c0001t0002g0087a0001c0002t0001g0002a0001c0002t0001g0003others(89): Show | 92 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.33-28041delT | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108631550 | |||||
| chr2:108631589
|
A | G | 21 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(18): Show | 21 | HG02602.hp2 HG02622.hp1 HG03017.hp2 others(18): Show |
intron_variant | MODIFIER | c.33-28016A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108631589 | ||||||
| chr2:108631630
|
C | T | 1 | a0001c0001t0029g0186 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.33-27975C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108631630 | ||||||
| chr2:108631677
|
A | C | 2 | a0001c0001t0014g0159a0001c0001t0014g0160 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.33-27928A>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108631677 | ||||||
| chr2:108631713
|
C | T | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-27892C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108631713 | ||||||
| chr2:108631785
|
G | T | 1 | a0001c0001t0024g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.33-27820G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108631785 | ||||||
| chr2:108632066
|
G | C | 2 | a0001c0001t0002g0108a0001c0001t0002g0110 | 2 | HG01358.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.33-27539G>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108632066 | ||||||
| chr2:108632190
|
C | T | 1 | a0001c0001t0002g0099 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.33-27415C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108632190 | ||||||
| chr2:108632423
|
G | A | 1 | a0001c0001t0003g0191 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.33-27182G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108632423 | ||||||
| chr2:108632524
|
T | G | 2 | a0001c0001t0003g0140a0001c0001t0003g0141 | 2 | HG02572.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.33-27081T>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108632524 | ||||||
| chr2:108632720
|
A | G | 1 | a0001c0001t0024g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.33-26885A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108632720 | ||||||
| chr2:108633003
|
A | T | 1 | a0001c0002t0001g0025 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.33-26602A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108633003 | ||||||
| chr2:108633043
|
G | A | 90 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(87): Show | 90 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.33-26562G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108633043 | ||||||
| chr2:108633077
|
T | C | 2 | a0001c0001t0003g0150a0001c0001t0003g0151 | 2 | HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.33-26528T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108633077 | ||||||
| chr2:108633184
|
G | T | 1 | a0001c0001t0002g0097 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.33-26421G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108633184 | ||||||
| chr2:108633430
|
T | C | 100 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.33-26175T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108633430 | ||||||
| chr2:108633611
|
A | G | 67 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0008others(64): Show | 67 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.33-25994A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108633611 | ||||||
| chr2:108633672
|
G | A | 1 | a0001c0001t0003g0212 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.33-25933G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108633672 | ||||||
| chr2:108633813
|
T | C | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.33-25792T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108633813 | ||||||
| chr2:108633838
|
A | G | 3 | a0001c0001t0002g0182a0001c0001t0002g0183a0001c0001t0002g0184 | 3 | HG02257.hp2 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.33-25767A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108633838 | ||||||
| chr2:108633865
|
G | A | 11 | a0001c0001t0003g0202a0001c0001t0003g0203a0001c0001t0003g0204others(8): Show | 11 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.33-25740G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108633865 | ||||||
| chr2:108633894
|
G | A | 199 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.33-25711G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108633894 | ||||||
| chr2:108634320
|
A | G | 3 | a0001c0001t0002g0109a0001c0001t0002g0200a0001c0001t0002g0201 | 3 | HG01346.hp2 HG03017.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.33-25285A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108634320 | ||||||
| chr2:108634359
|
A | G | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.33-25246A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108634359 | ||||||
| chr2:108634410
|
C | T | 3 | a0001c0001t0017g0156a0001c0001t0017g0157a0001c0001t0024g0162 | 3 | HG02647.hp1 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.33-25195C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108634410 | ||||||
| chr2:108634505
|
T | G | 1 | a0001c0002t0012g0007 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.33-25100T>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108634505 | ||||||
| chr2:108634561
|
G | A | 1 | a0001c0001t0003g0147 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.33-25044G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108634561 | ||||||
| chr2:108634592
|
G | C | 100 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.33-25013G>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108634592 | ||||||
| chr2:108634609
|
G | A | 67 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0008others(64): Show | 67 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.33-24996G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108634609 | ||||||
| chr2:108634692
|
C | T | 23 | a0001c0001t0003g0001a0001c0001t0003g0130a0001c0001t0003g0131others(20): Show | 24 | HG00323.hp1 HG01074.hp1 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.33-24913C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108634692 | ||||||
| chr2:108634718
|
G | A | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-24887G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108634718 | ||||||
| chr2:108634802
|
C | T | 3 | a0001c0001t0017g0156a0001c0001t0017g0157a0001c0001t0024g0162 | 3 | HG02647.hp1 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.33-24803C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108634802 | ||||||
| chr2:108634811
|
G | A | 7 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(4): Show | 7 | HG02040.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.33-24794G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108634811 | ||||||
| chr2:108635195
|
C | T | 79 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(76): Show | 79 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.33-24410C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108635195 | ||||||
| chr2:108635280
|
T | A | 1 | a0001c0002t0012g0007 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.33-24325T>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108635280 | ||||||
| chr2:108635363
|
A | G | 100 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.33-24242A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108635363 | ||||||
| chr2:108635429
|
T | TA | 166 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.33-24155dupA | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108635429 | |||||
| chr2:108635429
|
T | TAA | 17 | a0001c0001t0002g0182a0001c0001t0002g0183a0001c0001t0002g0184others(14): Show | 17 | HG01891.hp2 HG01981.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.33-24156_33-24155d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108635429 | |||||
| chr2:108635429
|
T | TTA | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-24176_33-24175i others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108635429 | ||||||
| chr2:108635577
|
T | G | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-24028T>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108635577 | ||||||
| chr2:108635644
|
GA | G | 79 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(76): Show | 79 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.33-23959delA | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108635644 | |||||
| chr2:108635734
|
C | T | 3 | a0001c0002t0001g0004a0002c0003t0018g0005a0002c0003t0026g0219 | 3 | HG02559.hp1 HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.33-23871C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108635734 | ||||||
| chr2:108635785
|
TC | T | 100 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.33-23813delC | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108635785 | |||||
| chr2:108636106
|
G | A | 1 | a0001c0001t0003g0136 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.33-23499G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108636106 | ||||||
| chr2:108636123
|
C | T | 3 | a0001c0002t0007g0214a0001c0002t0007g0217a0001c0002t0007g0218 | 3 | HG03195.hp1 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.33-23482C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108636123 | ||||||
| chr2:108636240
|
C | A | 1 | a0001c0002t0012g0006 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.33-23365C>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108636240 | ||||||
| chr2:108636292
|
C | G | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-23313C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108636292 | ||||||
| chr2:108636435
|
G | A | 7 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(4): Show | 7 | HG02040.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.33-23170G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108636435 | ||||||
| chr2:108636561
|
CAA | C | 3 | a0001c0001t0002g0094a0001c0001t0002g0095a0001c0001t0002g0099 | 3 | HG02896.hp2 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.33-23042_33-23041d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108636561 | |||||
| chr2:108636610
|
T | G | 1 | a0001c0002t0001g0069 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.33-22995T>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108636610 | ||||||
| chr2:108636673
|
A | G | 2 | a0001c0001t0003g0145a0001c0001t0003g0146 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.33-22932A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108636673 | ||||||
| chr2:108636722
|
G | A | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.33-22883G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108636722 | ||||||
| chr2:108636865
|
G | C | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-22740G>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108636865 | ||||||
| chr2:108636912
|
A | G | 3 | a0001c0002t0004g0227a0001c0002t0004g0228a0001c0002t0004g0245 | 3 | HG03239.hp2 HG03491.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.33-22693A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108636912 | ||||||
| chr2:108637094
|
C | CAT | 10 | a0001c0001t0003g0202a0001c0001t0003g0204a0001c0001t0003g0205others(7): Show | 10 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.33-22506_33-22505d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108637094 | |||||
| chr2:108637094
|
CAT | C | 12 | a0001c0001t0002g0098a0001c0002t0001g0009a0001c0002t0001g0020others(9): Show | 12 | HG01109.hp1 HG01993.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.33-22506_33-22505d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108637094 | |||||
| chr2:108637097
|
ATATG | A | 19 | a0001c0002t0001g0011a0001c0002t0001g0017a0001c0002t0001g0018others(16): Show | 19 | HG00140.hp2 HG00280.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.33-22506_33-22503d others(6): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108637097 | |||||
| chr2:108637097
|
ATATGTG | A | 31 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0008others(28): Show | 31 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.33-22506_33-22501d others(8): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108637097 | |||||
| chr2:108637097
|
ATATGTGT others(1): Show |
A | 8 | a0001c0002t0001g0015a0001c0002t0001g0023a0001c0002t0001g0028others(5): Show | 8 | HG01167.hp2 HG01168.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.33-22506_33-22499d others(10): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108637097 | |||||
| chr2:108637097
|
ATATGTGT others(3): Show |
A | 1 | a0001c0002t0001g0071 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.33-22506_33-22497d others(12): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108637097 | |||||
| chr2:108637099
|
A | ATG | 16 | a0001c0001t0002g0091a0001c0001t0002g0096a0001c0001t0002g0102others(13): Show | 16 | HG00140.hp1 HG00280.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.33-22460_33-22459d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108637099 | |||||
| chr2:108637099
|
A | ATGTG | 40 | a0001c0001t0002g0075a0001c0001t0002g0086a0001c0001t0002g0087others(37): Show | 41 | HG00639.hp2 HG00741.hp1 HG01070.hp2 others(38): Show |
intron_variant | MODIFIER | c.33-22462_33-22459d others(6): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108637099 | |||||
| chr2:108637099
|
A | ATGTGTG | 7 | a0001c0001t0002g0076a0001c0001t0002g0092a0001c0001t0002g0113others(4): Show | 7 | HG01109.hp2 HG01175.hp2 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.33-22464_33-22459d others(8): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108637099 | |||||
| chr2:108637099
|
A | ATGTGTGT others(1): Show |
6 | a0001c0001t0002g0084a0001c0001t0002g0089a0001c0001t0002g0099others(3): Show | 6 | HG01243.hp1 HG02055.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.33-22466_33-22459d others(10): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108637099 | |||||
| chr2:108637099
|
A | ATGTGTGT others(3): Show |
1 | a0001c0001t0005g0077 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.33-22468_33-22459d others(12): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108637099 | |||||
| chr2:108637099
|
A | ATGTGTGT others(5): Show |
1 | a0001c0001t0002g0094 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.33-22470_33-22459d others(14): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108637099 | |||||
| chr2:108637099
|
A | ATGTGTGT others(7): Show |
1 | a0001c0001t0002g0095 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.33-22472_33-22459d others(16): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108637099 | |||||
| chr2:108637099
|
A | G | 6 | a0001c0002t0001g0024a0001c0002t0001g0025a0001c0002t0001g0038others(3): Show | 6 | HG02258.hp1 HG02647.hp2 HG04184.hp2 others(3): Show |
intron_variant | MODIFIER | c.33-22506A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108637099 | ||||||
| chr2:108637099
|
ATG | A | 8 | a0001c0001t0003g0135a0001c0001t0003g0190a0001c0001t0003g0198others(5): Show | 8 | HG01358.hp1 HG01361.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.33-22460_33-22459d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108637099 | |||||
| chr2:108637099
|
ATGTG | A | 16 | a0001c0001t0002g0082a0001c0001t0002g0083a0001c0001t0005g0164others(13): Show | 16 | HG01099.hp1 HG01891.hp1 HG02602.hp2 others(13): Show |
intron_variant | MODIFIER | c.33-22462_33-22459d others(6): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108637099 | |||||
| chr2:108637099
|
ATGTGTG | A | 6 | a0001c0001t0002g0085a0001c0001t0002g0103a0001c0001t0002g0106others(3): Show | 6 | HG00099.hp2 HG01168.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.33-22464_33-22459d others(8): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108637099 | |||||
| chr2:108637101
|
G | A | 1 | a0001c0001t0003g0203 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.33-22504G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108637101 | ||||||
| chr2:108637324
|
G | A | 1 | a0001c0002t0001g0004 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.33-22281G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108637324 | ||||||
| chr2:108637485
|
A | G | 1 | a0001c0002t0001g0054 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.33-22120A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108637485 | ||||||
| chr2:108637581
|
G | A | 1 | a0001c0002t0001g0049 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.33-22024G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108637581 | ||||||
| chr2:108637797
|
A | AT | 65 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(62): Show | 65 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.33-21804dupT | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108637797 | |||||
| chr2:108637863
|
AT | A | 157 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(154): Show | 158 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.33-21726delT | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108637863 | |||||
| chr2:108637883
|
A | G | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-21722A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108637883 | ||||||
| chr2:108638007
|
C | T | 1 | a0002c0003t0018g0005 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.33-21598C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108638007 | ||||||
| chr2:108638013
|
C | T | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-21592C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108638013 | ||||||
| chr2:108638437
|
A | G | 1 | a0001c0001t0014g0159 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.33-21168A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108638437 | ||||||
| chr2:108638468
|
G | A | 1 | a0001c0001t0005g0174 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.33-21137G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108638468 | ||||||
| chr2:108638605
|
G | C | 65 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(62): Show | 65 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.33-21000G>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108638605 | ||||||
| chr2:108638641
|
G | A | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-20964G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108638641 | ||||||
| chr2:108638748
|
G | A | 2 | a0002c0003t0018g0005a0002c0003t0026g0219 | 2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.33-20857G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108638748 | ||||||
| chr2:108638786
|
G | A | 1 | a0001c0002t0001g0003 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.33-20819G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108638786 | ||||||
| chr2:108638828
|
A | G | 90 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(87): Show | 90 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.33-20777A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108638828 | ||||||
| chr2:108638871
|
G | A | 1 | a0001c0001t0002g0091 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.33-20734G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108638871 | ||||||
| chr2:108638899
|
C | T | 1 | a0001c0002t0012g0006 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.33-20706C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108638899 | ||||||
| chr2:108638904
|
G | A | 11 | a0001c0001t0003g0202a0001c0001t0003g0203a0001c0001t0003g0204others(8): Show | 11 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.33-20701G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108638904 | ||||||
| chr2:108638956
|
T | C | 1 | a0001c0001t0002g0111 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.33-20649T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108638956 | ||||||
| chr2:108639075
|
T | A | 1 | a0002c0003t0026g0219 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.33-20530T>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108639075 | ||||||
| chr2:108639492
|
G | A | 1 | a0001c0002t0012g0220 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.33-20113G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108639492 | ||||||
| chr2:108639516
|
C | T | 2 | a0001c0004t0013g0073a0001c0004t0013g0074 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.33-20089C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108639516 | ||||||
| chr2:108639522
|
A | G | 199 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.33-20083A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108639522 | ||||||
| chr2:108639545
|
C | T | 1 | a0001c0001t0003g0203 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.33-20060C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108639545 | ||||||
| chr2:108639938
|
C | A | 1 | a0001c0002t0007g0215 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.33-19667C>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108639938 | ||||||
| chr2:108639945
|
A | C | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-19660A>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108639945 | ||||||
| chr2:108639961
|
G | C | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-19644G>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108639961 | ||||||
| chr2:108640079
|
A | G | 67 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0008others(64): Show | 67 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.33-19526A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108640079 | ||||||
| chr2:108640087
|
T | C | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-19518T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108640087 | ||||||
| chr2:108640361
|
C | T | 1 | a0001c0001t0005g0077 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.33-19244C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108640361 | ||||||
| chr2:108640696
|
G | A | 37 | a0001c0002t0001g0015a0001c0002t0001g0018a0001c0002t0001g0020others(34): Show | 37 | HG01070.hp1 HG01106.hp1 HG01167.hp2 others(34): Show |
intron_variant | MODIFIER | c.33-18909G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108640696 | ||||||
| chr2:108640875
|
A | G | 1 | a0001c0002t0004g0244 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.33-18730A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108640875 | ||||||
| chr2:108640886
|
C | T | 2 | a0002c0003t0018g0005a0002c0003t0026g0219 | 2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.33-18719C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108640886 | ||||||
| chr2:108640930
|
T | C | 2 | a0002c0003t0018g0005a0002c0003t0026g0219 | 2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.33-18675T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108640930 | ||||||
| chr2:108641459
|
G | A | 1 | a0001c0001t0005g0169 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.33-18146G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108641459 | ||||||
| chr2:108641577
|
C | T | 1 | a0001c0001t0005g0165 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.33-18028C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108641577 | ||||||
| chr2:108641645
|
C | G | 2 | a0001c0004t0013g0073a0001c0004t0013g0074 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.33-17960C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108641645 | ||||||
| chr2:108641679
|
G | A | 8 | a0001c0001t0002g0119a0001c0001t0003g0138a0001c0001t0003g0139others(5): Show | 8 | HG01243.hp1 HG02055.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.33-17926G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108641679 | ||||||
| chr2:108641915
|
C | A | 7 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(4): Show | 7 | HG02040.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.33-17690C>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108641915 | ||||||
| chr2:108642124
|
A | G | 1 | a0001c0002t0001g0027 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.33-17481A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108642124 | ||||||
| chr2:108642333
|
GTGTTTTT others(16): Show |
G | 3 | a0001c0002t0001g0014a0001c0002t0001g0023a0002c0003t0026g0219 | 3 | HG01256.hp1 HG02572.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.33-17250_33-17228d others(25): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108642333 | |||||
| chr2:108642335
|
GTTTTTTG others(3): Show |
G | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-17263_33-17254d others(12): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108642335 | |||||
| chr2:108642336
|
TTTTTTGT others(15): Show |
T | 76 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(73): Show | 76 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.33-17263_33-17242d others(24): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108642336 | |||||
| chr2:108642337
|
TTTTTGTT others(14): Show |
T | 13 | a0001c0002t0001g0009a0001c0002t0001g0017a0001c0002t0001g0021others(10): Show | 13 | HG00099.hp1 HG01109.hp1 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.33-17263_33-17243d others(23): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108642337 | |||||
| chr2:108642338
|
TTTTGTTT others(13): Show |
T | 65 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(62): Show | 65 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.33-17263_33-17244d others(22): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108642338 | |||||
| chr2:108642339
|
TTTGTTTT others(12): Show |
T | 10 | a0001c0001t0002g0090a0001c0001t0002g0092a0001c0001t0002g0103others(7): Show | 10 | HG01175.hp1 HG01175.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.33-17263_33-17245d others(21): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108642339 | |||||
| chr2:108642339
|
TTTGTTTT others(19): Show |
T | 10 | a0001c0001t0003g0202a0001c0001t0003g0203a0001c0001t0003g0204others(7): Show | 10 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.33-17263_33-17238d others(28): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108642339 | |||||
| chr2:108642340
|
TTGTTTTT others(11): Show |
T | 1 | a0001c0001t0002g0129 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.33-17263_33-17246d others(20): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108642340 | |||||
| chr2:108642340
|
TTGTTTTT others(18): Show |
T | 1 | a0001c0001t0003g0208 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.33-17263_33-17239d others(27): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108642340 | |||||
| chr2:108642341
|
TGTTTTTT others(17): Show |
T | 1 | a0002c0003t0018g0005 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.33-17263_33-17240d others(26): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108642341 | ||||||
| chr2:108642342
|
G | GT | 5 | a0001c0001t0003g0138a0001c0001t0003g0140a0001c0001t0003g0142others(2): Show | 5 | HG00639.hp2 HG02886.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-17248dupT | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108642342 | |||||
| chr2:108642342
|
G | T | 5 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(2): Show | 5 | HG01261.hp2 HG03453.hp1 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-17263G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108642342 | ||||||
| chr2:108642352
|
TTTTTTGT others(6): Show |
T | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-17247_33-17235d others(15): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108642352 | |||||
| chr2:108642354
|
T | G | 1 | a0001c0001t0003g0189 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.33-17251T>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108642354 | ||||||
| chr2:108642357
|
TG | T | 15 | a0001c0001t0003g0001a0001c0001t0003g0130a0001c0001t0003g0131others(12): Show | 16 | HG00323.hp1 HG01074.hp1 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.33-17247delG | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108642357 | ||||||
| chr2:108642358
|
G | T | 28 | a0001c0001t0003g0132a0001c0001t0003g0138a0001c0001t0003g0139others(25): Show | 28 | HG01243.hp1 HG01257.hp2 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.33-17247G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108642358 | ||||||
| chr2:108642362
|
T | G | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-17243T>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108642362 | ||||||
| chr2:108642365
|
G | T | 183 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.33-17240G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108642365 | ||||||
| chr2:108642384
|
G | A | 54 | a0001c0002t0001g0015a0001c0002t0001g0017a0001c0002t0001g0018others(51): Show | 54 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.33-17221G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108642384 | ||||||
| chr2:108642481
|
T | C | 239 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(236): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.33-17124T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108642481 | ||||||
| chr2:108642549
|
C | T | 2 | a0001c0001t0011g0149a0001c0001t0011g0154 | 2 | HG02056.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.33-17056C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108642549 | ||||||
| chr2:108642601
|
C | T | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.33-17004C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108642601 | ||||||
| chr2:108642605
|
C | T | 23 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(20): Show | 23 | HG02602.hp2 HG02622.hp1 HG02895.hp1 others(20): Show |
intron_variant | MODIFIER | c.33-17000C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108642605 | ||||||
| chr2:108642606
|
G | A | 79 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(76): Show | 79 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.33-16999G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108642606 | ||||||
| chr2:108642700
|
G | A | 25 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(22): Show | 25 | HG02572.hp1 HG02602.hp2 HG02622.hp1 others(22): Show |
intron_variant | MODIFIER | c.33-16905G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108642700 | ||||||
| chr2:108642727
|
G | T | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-16878G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108642727 | ||||||
| chr2:108642948
|
C | T | 1 | a0001c0002t0016g0070 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.33-16657C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108642948 | ||||||
| chr2:108642949
|
A | ATTGGACT others(4): Show |
1 | a0001c0002t0016g0070 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.33-16656_33-16655i others(13): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108642949 | ||||||
| chr2:108642953
|
T | C | 1 | a0001c0002t0016g0070 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.33-16652T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108642953 | ||||||
| chr2:108643127
|
A | G | 2 | a0001c0001t0017g0156a0001c0001t0017g0157 | 2 | HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.33-16478A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108643127 | ||||||
| chr2:108643160
|
G | T | 1 | a0001c0001t0005g0169 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.33-16445G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108643160 | ||||||
| chr2:108643232
|
G | A | 93 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(90): Show | 93 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.33-16373G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108643232 | ||||||
| chr2:108643554
|
TG | T | 76 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(73): Show | 76 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.33-16048delG | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108643554 | |||||
| chr2:108643577
|
C | T | 1 | a0001c0001t0003g0132 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.33-16028C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108643577 | ||||||
| chr2:108643578
|
G | A | 1 | a0001c0001t0002g0091 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.33-16027G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108643578 | ||||||
| chr2:108643588
|
G | GT | 76 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(73): Show | 76 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.33-16007dupT | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108643588 | |||||
| chr2:108643616
|
G | A | 2 | a0001c0001t0002g0075a0001c0001t0022g0112 | 2 | NA18940.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.33-15989G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108643616 | ||||||
| chr2:108643688
|
GA | G | 100 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.33-15916delA | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108643688 | ||||||
| chr2:108643691
|
G | A | 93 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(90): Show | 93 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.33-15914G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108643691 | ||||||
| chr2:108643803
|
C | T | 93 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(90): Show | 93 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.33-15802C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108643803 | ||||||
| chr2:108643825
|
G | C | 1 | a0001c0002t0008g0223 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.33-15780G>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108643825 | ||||||
| chr2:108643838
|
C | G | 1 | a0001c0002t0001g0057 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.33-15767C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108643838 | ||||||
| chr2:108644072
|
G | A | 11 | a0001c0001t0003g0202a0001c0001t0003g0203a0001c0001t0003g0204others(8): Show | 11 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.33-15533G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108644072 | ||||||
| chr2:108644074
|
G | C | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-15531G>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108644074 | ||||||
| chr2:108644146
|
G | A | 2 | a0001c0001t0003g0139a0001c0001t0003g0142 | 2 | HG03041.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.33-15459G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108644146 | ||||||
| chr2:108644150
|
A | C | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-15455A>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108644150 | ||||||
| chr2:108644190
|
C | G | 1 | a0001c0001t0014g0160 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.33-15415C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108644190 | ||||||
| chr2:108644365
|
G | A | 1 | a0001c0001t0002g0091 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.33-15240G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108644365 | ||||||
| chr2:108644746
|
C | T | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.33-14859C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108644746 | ||||||
| chr2:108644771
|
C | A | 23 | a0001c0001t0003g0001a0001c0001t0003g0130a0001c0001t0003g0131others(20): Show | 24 | HG00323.hp1 HG01074.hp1 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.33-14834C>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108644771 | ||||||
| chr2:108644851
|
A | G | 7 | a0001c0001t0003g0130a0001c0001t0003g0131a0001c0001t0003g0132others(4): Show | 7 | NA18939.hp2 NA18942.hp1 NA18947.hp1 others(4): Show |
intron_variant | MODIFIER | c.33-14754A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108644851 | ||||||
| chr2:108644919
|
A | G | 1 | a0001c0002t0007g0218 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.33-14686A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108644919 | ||||||
| chr2:108645080
|
G | A | 3 | a0001c0001t0002g0082a0001c0001t0002g0083a0001c0001t0019g0124 | 3 | HG02723.hp1 HG03098.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.33-14525G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108645080 | ||||||
| chr2:108645176
|
C | T | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-14429C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108645176 | ||||||
| chr2:108645333
|
A | G | 1 | a0001c0002t0001g0023 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.33-14272A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108645333 | ||||||
| chr2:108645406
|
G | A | 11 | a0001c0001t0003g0202a0001c0001t0003g0203a0001c0001t0003g0204others(8): Show | 11 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.33-14199G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108645406 | ||||||
| chr2:108645433
|
A | G | 1 | a0001c0001t0005g0180 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.33-14172A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108645433 | ||||||
| chr2:108645473
|
T | C | 90 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(87): Show | 90 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.33-14132T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108645473 | ||||||
| chr2:108645522
|
C | G | 2 | a0002c0003t0018g0005a0002c0003t0026g0219 | 2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.33-14083C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108645522 | ||||||
| chr2:108645528
|
A | G | 93 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(90): Show | 93 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.33-14077A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108645528 | ||||||
| chr2:108645666
|
G | A | 3 | a0001c0001t0002g0182a0001c0001t0002g0183a0001c0001t0002g0184 | 3 | HG02257.hp2 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.33-13939G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108645666 | ||||||
| chr2:108645756
|
G | A | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-13849G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108645756 | ||||||
| chr2:108645820
|
C | CA | 17 | a0001c0001t0002g0116a0001c0001t0002g0129a0001c0001t0002g0158others(14): Show | 17 | HG01106.hp2 HG01109.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.33-13771dupA | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108645820 | |||||
| chr2:108645820
|
CA | C | 19 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(16): Show | 19 | HG02602.hp2 HG02622.hp1 HG03017.hp2 others(16): Show |
intron_variant | MODIFIER | c.33-13771delA | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108645820 | |||||
| chr2:108645853
|
A | G | 2 | a0001c0004t0013g0073a0001c0004t0013g0074 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.33-13752A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108645853 | ||||||
| chr2:108645904
|
G | A | 1 | a0001c0001t0002g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.33-13701G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108645904 | ||||||
| chr2:108646142
|
G | A | 100 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.33-13463G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108646142 | ||||||
| chr2:108646549
|
C | G | 1 | a0001c0002t0001g0071 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.33-13056C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108646549 | ||||||
| chr2:108646746
|
G | T | 1 | a0001c0002t0004g0228 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.33-12859G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108646746 | ||||||
| chr2:108646779
|
C | A | 1 | a0001c0001t0003g0143 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.33-12826C>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108646779 | ||||||
| chr2:108646791
|
C | T | 1 | a0001c0002t0001g0055 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.33-12814C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108646791 | ||||||
| chr2:108646866
|
C | T | 93 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(90): Show | 93 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.33-12739C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108646866 | ||||||
| chr2:108646871
|
G | A | 2 | a0001c0004t0013g0073a0001c0004t0013g0074 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.33-12734G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108646871 | ||||||
| chr2:108646942
|
C | T | 4 | a0001c0001t0003g0131a0001c0001t0003g0132a0001c0001t0003g0133others(1): Show | 4 | NA18939.hp2 NA18947.hp1 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.33-12663C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108646942 | ||||||
| chr2:108646963
|
C | T | 1 | a0001c0001t0002g0089 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.33-12642C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108646963 | ||||||
| chr2:108647001
|
A | G | 201 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(198): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.33-12604A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108647001 | ||||||
| chr2:108647159
|
A | G | 19 | a0001c0001t0005g0163a0001c0001t0005g0164a0001c0001t0005g0165others(16): Show | 19 | HG00140.hp1 HG00280.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.33-12446A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108647159 | ||||||
| chr2:108647185
|
A | C | 1 | a0001c0001t0005g0185 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.33-12420A>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108647185 | ||||||
| chr2:108647409
|
C | T | 1 | a0001c0002t0007g0218 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.33-12196C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108647409 | ||||||
| chr2:108647459
|
T | C | 1 | a0001c0002t0001g0004 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.33-12146T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108647459 | ||||||
| chr2:108647554
|
G | A | 6 | a0001c0002t0001g0008a0001c0002t0001g0010a0001c0002t0001g0011others(3): Show | 6 | HG00323.hp2 HG00639.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.33-12051G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108647554 | ||||||
| chr2:108647677
|
C | T | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.33-11928C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108647677 | ||||||
| chr2:108647874
|
A | G | 1 | a0001c0001t0002g0119 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.33-11731A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108647874 | ||||||
| chr2:108647993
|
G | C | 1 | a0001c0002t0007g0218 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.33-11612G>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108647993 | ||||||
| chr2:108648179
|
A | G | 1 | a0001c0001t0002g0091 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.33-11426A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108648179 | ||||||
| chr2:108648180
|
C | T | 7 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0114others(4): Show | 7 | NA18968.hp1 NA18977.hp1 NA18993.hp1 others(4): Show |
intron_variant | MODIFIER | c.33-11425C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108648180 | ||||||
| chr2:108648239
|
C | T | 1 | a0001c0002t0030g0067 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.33-11366C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108648239 | ||||||
| chr2:108648376
|
A | G | 1 | a0001c0002t0012g0220 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.33-11229A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108648376 | ||||||
| chr2:108648441
|
A | C | 67 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0008others(64): Show | 67 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.33-11164A>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108648441 | ||||||
| chr2:108648602
|
C | G | 23 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(20): Show | 23 | HG02602.hp2 HG02622.hp1 HG02895.hp1 others(20): Show |
intron_variant | MODIFIER | c.33-11003C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108648602 | ||||||
| chr2:108648686
|
A | G | 1 | a0001c0001t0003g0191 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.33-10919A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108648686 | ||||||
| chr2:108648781
|
T | C | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-10824T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108648781 | ||||||
| chr2:108648961
|
G | A | 93 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(90): Show | 93 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.33-10644G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108648961 | ||||||
| chr2:108648978
|
C | T | 23 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(20): Show | 23 | HG02602.hp2 HG02622.hp1 HG02895.hp1 others(20): Show |
intron_variant | MODIFIER | c.33-10627C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108648978 | ||||||
| chr2:108649266
|
C | G | 1 | a0001c0001t0002g0119 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.33-10339C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108649266 | ||||||
| chr2:108649418
|
G | A | 1 | a0001c0001t0006g0171 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.33-10187G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108649418 | ||||||
| chr2:108649425
|
C | T | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-10180C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108649425 | ||||||
| chr2:108649432
|
C | T | 2 | a0001c0001t0014g0159a0001c0001t0014g0160 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.33-10173C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108649432 | ||||||
| chr2:108649741
|
A | T | 1 | a0001c0002t0016g0070 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.33-9864A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108649741 | ||||||
| chr2:108649765
|
C | T | 1 | a0001c0001t0002g0099 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.33-9840C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108649765 | ||||||
| chr2:108649891
|
A | G | 39 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(36): Show | 39 | HG00099.hp2 HG00741.hp2 HG01168.hp2 others(36): Show |
intron_variant | MODIFIER | c.33-9714A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108649891 | ||||||
| chr2:108649910
|
T | C | 1 | a0001c0001t0002g0117 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.33-9695T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108649910 | ||||||
| chr2:108649941
|
A | G | 2 | a0001c0002t0001g0002a0001c0002t0001g0003 | 2 | NA19043.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.33-9664A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108649941 | ||||||
| chr2:108650065
|
GACCTGCT | G | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-9538_33-9532del others(7): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108650065 | |||||
| chr2:108650262
|
A | G | 2 | a0001c0002t0001g0022a0001c0002t0001g0051 | 2 | NA18954.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.33-9343A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108650262 | ||||||
| chr2:108650413
|
CT | C | 28 | a0001c0001t0003g0135a0001c0002t0001g0004a0001c0002t0001g0030others(25): Show | 28 | HG00099.hp1 HG02559.hp1 HG02572.hp1 others(25): Show |
intron_variant | MODIFIER | c.33-9176delT | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108650413 | |||||
| chr2:108650418
|
T | C | 79 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(76): Show | 79 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.33-9187T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108650418 | ||||||
| chr2:108650429
|
TC | T | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-9175delC | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108650429 | ||||||
| chr2:108650530
|
G | A | 1 | a0001c0002t0001g0052 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.33-9075G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108650530 | ||||||
| chr2:108650561
|
G | C | 1 | a0001c0002t0001g0039 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.33-9044G>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108650561 | ||||||
| chr2:108650730
|
C | T | 2 | a0001c0001t0003g0150a0001c0001t0003g0151 | 2 | HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.33-8875C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108650730 | ||||||
| chr2:108650742
|
A | G | 1 | a0001c0002t0012g0006 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.33-8863A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108650742 | ||||||
| chr2:108650824
|
A | T | 1 | a0001c0001t0006g0168 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.33-8781A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108650824 | ||||||
| chr2:108650850
|
TTTTA | T | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-8744_33-8741del others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108650850 | |||||
| chr2:108650861
|
T | TATTC | 5 | a0001c0001t0017g0156a0001c0001t0017g0157a0001c0002t0012g0006others(2): Show | 5 | HG02040.hp2 HG02647.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-8726_33-8723dup others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108650861 | |||||
| chr2:108650861
|
TATTC | T | 93 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(90): Show | 93 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.33-8726_33-8723del others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108650861 | |||||
| chr2:108651173
|
T | G | 93 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(90): Show | 93 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.33-8432T>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108651173 | ||||||
| chr2:108651465
|
T | C | 2 | a0002c0003t0018g0005a0002c0003t0026g0219 | 2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.33-8140T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108651465 | ||||||
| chr2:108651665
|
G | A | 7 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140others(4): Show | 7 | HG01243.hp1 HG02055.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.33-7940G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108651665 | ||||||
| chr2:108651693
|
A | G | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-7912A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108651693 | ||||||
| chr2:108651735
|
A | G | 2 | a0001c0004t0013g0073a0001c0004t0013g0074 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.33-7870A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108651735 | ||||||
| chr2:108651933
|
A | G | 109 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(106): Show | 109 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.33-7672A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108651933 | ||||||
| chr2:108651937
|
C | A | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-7668C>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108651937 | ||||||
| chr2:108651965
|
G | C | 2 | a0002c0003t0018g0005a0002c0003t0026g0219 | 2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.33-7640G>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108651965 | ||||||
| chr2:108652074
|
T | G | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-7531T>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108652074 | ||||||
| chr2:108652192
|
A | T | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.33-7413A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108652192 | ||||||
| chr2:108652368
|
G | A | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-7237G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108652368 | ||||||
| chr2:108652375
|
C | CTG | 3 | a0001c0001t0002g0182a0001c0001t0002g0183a0001c0001t0002g0184 | 3 | HG02257.hp2 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.33-7229_33-7228dup others(2): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108652375 | |||||
| chr2:108652465
|
A | G | 23 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(20): Show | 23 | HG02602.hp2 HG02622.hp1 HG02895.hp1 others(20): Show |
intron_variant | MODIFIER | c.33-7140A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108652465 | ||||||
| chr2:108652557
|
A | G | 1 | a0001c0002t0001g0004 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.33-7048A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108652557 | ||||||
| chr2:108652856
|
C | A | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-6749C>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108652856 | ||||||
| chr2:108652924
|
A | G | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.33-6681A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108652924 | ||||||
| chr2:108652963
|
G | C | 1 | a0001c0002t0001g0058 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.33-6642G>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108652963 | ||||||
| chr2:108653010
|
G | T | 93 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(90): Show | 93 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.33-6595G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108653010 | ||||||
| chr2:108653114
|
A | G | 1 | a0001c0002t0025g0026 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.33-6491A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108653114 | ||||||
| chr2:108653124
|
G | A | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.33-6481G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108653124 | ||||||
| chr2:108653564
|
A | C | 2 | a0001c0001t0017g0156a0001c0001t0017g0157 | 2 | HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.33-6041A>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108653564 | ||||||
| chr2:108653590
|
C | T | 93 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(90): Show | 93 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.33-6015C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108653590 | ||||||
| chr2:108653651
|
T | C | 1 | a0001c0001t0002g0097 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.33-5954T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108653651 | ||||||
| chr2:108653729
|
C | T | 1 | a0001c0002t0009g0080 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.33-5876C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108653729 | ||||||
| chr2:108653891
|
G | T | 199 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.33-5714G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108653891 | ||||||
| chr2:108654034
|
GT | G | 100 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.33-5568delT | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108654034 | |||||
| chr2:108654040
|
G | A | 67 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0008others(64): Show | 67 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.33-5565G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108654040 | ||||||
| chr2:108654071
|
C | T | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.33-5534C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108654071 | ||||||
| chr2:108654155
|
C | T | 1 | a0001c0002t0001g0012 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.33-5450C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108654155 | ||||||
| chr2:108654239
|
T | G | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-5366T>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108654239 | ||||||
| chr2:108654363
|
A | G | 1 | a0001c0001t0006g0101 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.33-5242A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108654363 | ||||||
| chr2:108654377
|
C | G | 93 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(90): Show | 93 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.33-5228C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108654377 | ||||||
| chr2:108654468
|
A | G | 1 | a0001c0001t0003g0161 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.33-5137A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108654468 | ||||||
| chr2:108654548
|
G | A | 93 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(90): Show | 93 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.33-5057G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108654548 | ||||||
| chr2:108654572
|
C | A | 1 | a0001c0001t0005g0167 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.33-5033C>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108654572 | ||||||
| chr2:108654622
|
CAG | C | 6 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0114others(3): Show | 6 | NA18968.hp1 NA18977.hp1 NA18993.hp1 others(3): Show |
intron_variant | MODIFIER | c.33-4982_33-4981del others(2): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108654622 | ||||||
| chr2:108654677
|
C | T | 1 | a0001c0002t0001g0071 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.33-4928C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108654677 | ||||||
| chr2:108654680
|
G | A | 20 | a0001c0002t0004g0225a0001c0002t0004g0227a0001c0002t0004g0228others(17): Show | 20 | HG02602.hp2 HG03017.hp2 HG03239.hp2 others(17): Show |
intron_variant | MODIFIER | c.33-4925G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108654680 | ||||||
| chr2:108654761
|
C | T | 1 | a0001c0002t0001g0018 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.33-4844C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108654761 | ||||||
| chr2:108654785
|
G | C | 3 | a0001c0002t0007g0214a0001c0002t0007g0217a0001c0002t0007g0218 | 3 | HG03195.hp1 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.33-4820G>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108654785 | ||||||
| chr2:108654931
|
T | C | 6 | a0001c0001t0003g0131a0001c0001t0003g0132a0001c0001t0003g0133others(3): Show | 6 | NA18939.hp2 NA18947.hp1 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.33-4674T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108654931 | ||||||
| chr2:108655037
|
A | G | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-4568A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108655037 | ||||||
| chr2:108655202
|
G | T | 1 | a0001c0002t0001g0057 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.33-4403G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108655202 | ||||||
| chr2:108655262
|
T | C | 1 | a0001c0002t0001g0003 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.33-4343T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108655262 | ||||||
| chr2:108655392
|
C | T | 23 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(20): Show | 23 | HG02602.hp2 HG02622.hp1 HG02895.hp1 others(20): Show |
intron_variant | MODIFIER | c.33-4213C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108655392 | ||||||
| chr2:108655394
|
G | A | 7 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140others(4): Show | 7 | HG01243.hp1 HG02055.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.33-4211G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108655394 | ||||||
| chr2:108655422
|
G | T | 3 | a0001c0002t0001g0004a0002c0003t0018g0005a0002c0003t0026g0219 | 3 | HG02559.hp1 HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.33-4183G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108655422 | ||||||
| chr2:108655516
|
T | C | 202 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.33-4089T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108655516 | ||||||
| chr2:108655603
|
C | T | 3 | a0001c0002t0009g0079a0001c0002t0009g0080a0001c0002t0009g0081 | 3 | HG01261.hp2 NA18954.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.33-4002C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108655603 | ||||||
| chr2:108655800
|
C | T | 1 | a0001c0002t0009g0081 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.33-3805C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108655800 | ||||||
| chr2:108655817
|
G | C | 1 | a0001c0001t0002g0083 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.33-3788G>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108655817 | ||||||
| chr2:108655935
|
T | C | 1 | a0001c0002t0001g0068 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.33-3670T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108655935 | ||||||
| chr2:108656109
|
A | T | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-3496A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108656109 | ||||||
| chr2:108656186
|
A | G | 93 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(90): Show | 93 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.33-3419A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108656186 | ||||||
| chr2:108656257
|
A | G | 4 | a0001c0001t0002g0096a0001c0001t0002g0122a0001c0001t0003g0143others(1): Show | 4 | HG01243.hp1 HG02735.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.33-3348A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108656257 | ||||||
| chr2:108656282
|
T | G | 109 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(106): Show | 109 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.33-3323T>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108656282 | ||||||
| chr2:108656313
|
CTATCTAT others(5): Show |
C | 20 | a0001c0002t0004g0226a0001c0002t0004g0227a0001c0002t0004g0228others(17): Show | 20 | HG02602.hp2 HG02622.hp1 HG03017.hp2 others(17): Show |
intron_variant | MODIFIER | c.33-3291_33-3280del others(12): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108656313 | ||||||
| chr2:108656313
|
CTATCTAT others(9): Show |
C | 1 | a0001c0002t0004g0225 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.33-3291_33-3276del others(16): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108656313 | ||||||
| chr2:108656317
|
C | A | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.33-3288C>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108656317 | ||||||
| chr2:108656317
|
C | CGATA | 3 | a0001c0002t0001g0021a0001c0002t0001g0029a0001c0002t0001g0059 | 3 | HG02717.hp2 HG02886.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.33-3288_33-3287ins others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108656317 | ||||||
| chr2:108656317
|
C | CGATAGAT others(5): Show |
1 | a0001c0002t0001g0019 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.33-3288_33-3287ins others(12): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108656317 | ||||||
| chr2:108656317
|
CTATA | C | 110 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(107): Show | 110 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.33-3287_33-3284del others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108656317 | ||||||
| chr2:108656317
|
CTATAGAT others(1): Show |
C | 25 | a0001c0001t0002g0182a0001c0001t0002g0183a0001c0001t0002g0184others(22): Show | 25 | HG00140.hp1 HG00280.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.33-3287_33-3280del others(8): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108656317 | ||||||
| chr2:108656318
|
T | G | 28 | a0001c0001t0002g0103a0001c0001t0006g0101a0001c0001t0017g0156others(25): Show | 28 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.33-3287T>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108656318 | ||||||
| chr2:108656318
|
T | TATAG | 17 | a0001c0001t0003g0001a0001c0001t0003g0131a0001c0001t0003g0132others(14): Show | 18 | HG00323.hp1 HG01074.hp1 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.33-3255_33-3252dup others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108656318 | |||||
| chr2:108656318
|
T | TATAGATA others(1): Show |
3 | a0001c0001t0003g0130a0001c0001t0003g0147a0001c0001t0003g0161 | 3 | HG01884.hp2 HG01981.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.33-3259_33-3252dup others(8): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108656318 | |||||
| chr2:108656318
|
TATAG | T | 9 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140others(6): Show | 9 | HG01074.hp2 HG01243.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.33-3255_33-3252del others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108656318 | |||||
| chr2:108656655
|
T | C | 2 | a0001c0002t0001g0002a0001c0002t0001g0003 | 2 | NA19043.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.33-2950T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108656655 | ||||||
| chr2:108656870
|
A | C | 1 | a0001c0001t0011g0154 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.33-2735A>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108656870 | ||||||
| chr2:108656975
|
C | T | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-2630C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108656975 | ||||||
| chr2:108657006
|
T | C | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-2599T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108657006 | ||||||
| chr2:108657016
|
G | A | 3 | a0001c0002t0001g0044a0001c0002t0001g0049a0001c0002t0001g0050 | 3 | HG02630.hp2 HG03927.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.33-2589G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108657016 | ||||||
| chr2:108657016
|
G | T | 12 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(9): Show | 12 | HG01261.hp2 HG02040.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.33-2589G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108657016 | ||||||
| chr2:108657074
|
C | T | 105 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(102): Show | 105 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.33-2531C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108657074 | ||||||
| chr2:108657102
|
A | G | 7 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140others(4): Show | 7 | HG01243.hp1 HG02055.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.33-2503A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108657102 | ||||||
| chr2:108657126
|
A | G | 1 | a0001c0002t0001g0068 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.33-2479A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108657126 | ||||||
| chr2:108657147
|
T | A | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.33-2458T>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108657147 | ||||||
| chr2:108657155
|
A | G | 2 | a0002c0003t0018g0005a0002c0003t0026g0219 | 2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.33-2450A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108657155 | ||||||
| chr2:108657189
|
A | C | 2 | a0002c0003t0018g0005a0002c0003t0026g0219 | 2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.33-2416A>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108657189 | ||||||
| chr2:108657203
|
A | AAG | 105 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(102): Show | 105 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.33-2399_33-2398dup others(2): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108657203 | |||||
| chr2:108657367
|
A | G | 2 | a0002c0003t0018g0005a0002c0003t0026g0219 | 2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.33-2238A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108657367 | ||||||
| chr2:108657383
|
A | G | 7 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(4): Show | 7 | HG00323.hp2 HG00639.hp1 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.33-2222A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108657383 | ||||||
| chr2:108657398
|
A | G | 3 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0224 | 3 | HG02486.hp1 HG02630.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.33-2207A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108657398 | ||||||
| chr2:108657465
|
T | C | 4 | a0001c0002t0004g0231a0001c0002t0004g0233a0001c0002t0004g0236others(1): Show | 4 | NA18940.hp2 NA18994.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.33-2140T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108657465 | ||||||
| chr2:108657486
|
T | C | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-2119T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108657486 | ||||||
| chr2:108657490
|
G | A | 90 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(87): Show | 90 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.33-2115G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108657490 | ||||||
| chr2:108657714
|
C | G | 25 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(22): Show | 25 | HG02572.hp1 HG02602.hp2 HG02622.hp1 others(22): Show |
intron_variant | MODIFIER | c.33-1891C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108657714 | ||||||
| chr2:108657738
|
C | CT | 24 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(21): Show | 24 | HG02572.hp1 HG02622.hp1 HG02895.hp1 others(21): Show |
intron_variant | MODIFIER | c.33-1859dupT | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 108657738 | |||||
| chr2:108657750
|
A | G | 68 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.33-1855A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108657750 | ||||||
| chr2:108657791
|
C | T | 1 | a0001c0002t0001g0011 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.33-1814C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108657791 | ||||||
| chr2:108657798
|
G | T | 25 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(22): Show | 25 | HG02572.hp1 HG02602.hp2 HG02622.hp1 others(22): Show |
intron_variant | MODIFIER | c.33-1807G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108657798 | ||||||
| chr2:108657853
|
C | G | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-1752C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108657853 | ||||||
| chr2:108657946
|
T | C | 23 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(20): Show | 23 | HG02602.hp2 HG02622.hp1 HG02895.hp1 others(20): Show |
intron_variant | MODIFIER | c.33-1659T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108657946 | ||||||
| chr2:108658049
|
A | G | 2 | a0001c0001t0014g0159a0001c0001t0014g0160 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.33-1556A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108658049 | ||||||
| chr2:108658205
|
T | C | 1 | a0001c0002t0001g0071 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.33-1400T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108658205 | ||||||
| chr2:108658384
|
A | G | 127 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(124): Show | 127 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.33-1221A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108658384 | ||||||
| chr2:108658625
|
A | G | 1 | a0001c0002t0001g0020 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.33-980A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108658625 | ||||||
| chr2:108658677
|
A | G | 2 | a0001c0002t0001g0063a0001c0002t0001g0064 | 2 | HG01993.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.33-928A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108658677 | ||||||
| chr2:108658706
|
G | A | 1 | a0001c0002t0001g0028 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.33-899G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108658706 | ||||||
| chr2:108658711
|
G | T | 2 | a0001c0001t0002g0075a0001c0001t0022g0112 | 2 | NA18940.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.33-894G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108658711 | ||||||
| chr2:108658735
|
G | A | 1 | a0001c0001t0003g0190 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.33-870G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108658735 | ||||||
| chr2:108658794
|
C | G | 1 | a0001c0002t0012g0006 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.33-811C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108658794 | ||||||
| chr2:108659045
|
G | A | 11 | a0001c0001t0003g0202a0001c0001t0003g0203a0001c0001t0003g0204others(8): Show | 11 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.33-560G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108659045 | ||||||
| chr2:108659102
|
G | A | 5 | a0001c0001t0003g0189a0001c0001t0003g0190a0001c0001t0003g0191others(2): Show | 5 | HG01074.hp2 HG01358.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-503G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108659102 | ||||||
| chr2:108659117
|
A | G | 27 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(24): Show | 27 | HG01261.hp2 HG02602.hp2 HG02622.hp1 others(24): Show |
intron_variant | MODIFIER | c.33-488A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108659117 | ||||||
| chr2:108659217
|
T | C | 1 | a0001c0001t0003g0155 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.33-388T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108659217 | ||||||
| chr2:108659276
|
C | A | 25 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(22): Show | 25 | HG02572.hp1 HG02602.hp2 HG02622.hp1 others(22): Show |
intron_variant | MODIFIER | c.33-329C>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108659276 | ||||||
| chr2:108659278
|
T | C | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-327T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 1/9 | chr2 | 108659278 | ||||||
| chr2:108659925
|
T | G | 1 | a0001c0001t0002g0115 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.192+161T>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108659925 | ||||||
| chr2:108659930
|
A | G | 7 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140others(4): Show | 7 | HG01243.hp1 HG02055.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.192+166A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108659930 | ||||||
| chr2:108659951
|
A | G | 199 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.192+187A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108659951 | ||||||
| chr2:108660000
|
G | T | 21 | a0001c0001t0003g0001a0001c0001t0003g0130a0001c0001t0003g0131others(18): Show | 22 | HG00323.hp1 HG01074.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.192+236G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108660000 | ||||||
| chr2:108660129
|
C | T | 1 | a0001c0001t0002g0104 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.192+365C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108660129 | ||||||
| chr2:108660136
|
T | C | 1 | a0001c0001t0002g0098 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.192+372T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108660136 | ||||||
| chr2:108660185
|
G | C | 3 | a0001c0001t0017g0156a0001c0001t0017g0157a0001c0001t0024g0162 | 3 | HG02647.hp1 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.192+421G>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108660185 | ||||||
| chr2:108660306
|
C | T | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.192+542C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108660306 | ||||||
| chr2:108660316
|
A | G | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.192+552A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108660316 | ||||||
| chr2:108660405
|
A | G | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.192+641A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108660405 | ||||||
| chr2:108660410
|
C | T | 97 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(94): Show | 97 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.192+646C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108660410 | ||||||
| chr2:108660626
|
T | C | 2 | a0001c0001t0003g0190a0001c0001t0003g0192 | 2 | HG01074.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.192+862T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108660626 | ||||||
| chr2:108660783
|
C | T | 68 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.192+1019C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108660783 | ||||||
| chr2:108660991
|
T | C | 1 | a0001c0002t0004g0239 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.192+1227T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108660991 | ||||||
| chr2:108661173
|
A | G | 1 | a0001c0002t0001g0046 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.192+1409A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108661173 | ||||||
| chr2:108661314
|
C | T | 3 | a0001c0001t0003g0204a0001c0001t0003g0206a0001c0001t0003g0209 | 3 | HG01891.hp2 HG02257.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.192+1550C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108661314 | ||||||
| chr2:108661336
|
C | CT | 105 | a0001c0001t0003g0202a0001c0001t0003g0203a0001c0001t0003g0204others(102): Show | 105 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.192+1585dupT | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 108661336 | |||||
| chr2:108661336
|
C | CTT | 11 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(8): Show | 11 | HG01261.hp2 HG02040.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.192+1584_192+1585d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 108661336 | |||||
| chr2:108661352
|
C | G | 1 | a0001c0001t0005g0185 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.192+1588C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108661352 | ||||||
| chr2:108661365
|
G | A | 1 | a0002c0003t0018g0005 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.192+1601G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108661365 | ||||||
| chr2:108661394
|
T | C | 1 | a0001c0002t0001g0020 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.192+1630T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108661394 | ||||||
| chr2:108661472
|
G | A | 4 | a0001c0002t0004g0231a0001c0002t0004g0233a0001c0002t0004g0236others(1): Show | 4 | NA18940.hp2 NA18994.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.192+1708G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108661472 | ||||||
| chr2:108661500
|
G | A | 1 | a0001c0002t0001g0054 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.192+1736G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108661500 | ||||||
| chr2:108661516
|
T | A | 1 | a0001c0001t0002g0127 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.192+1752T>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108661516 | ||||||
| chr2:108661674
|
G | A | 1 | a0001c0001t0005g0181 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.192+1910G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108661674 | ||||||
| chr2:108661714
|
G | T | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.192+1950G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108661714 | ||||||
| chr2:108661735
|
A | G | 2 | a0001c0002t0007g0215a0001c0002t0007g0216 | 2 | HG02258.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.192+1971A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108661735 | ||||||
| chr2:108661764
|
G | C | 239 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(236): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.192+2000G>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108661764 | ||||||
| chr2:108661824
|
G | C | 1 | a0001c0002t0004g0225 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.192+2060G>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108661824 | ||||||
| chr2:108661863
|
C | T | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.192+2099C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108661863 | ||||||
| chr2:108661943
|
G | A | 90 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(87): Show | 90 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.192+2179G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108661943 | ||||||
| chr2:108661982
|
C | G | 1 | a0001c0002t0001g0029 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.192+2218C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108661982 | ||||||
| chr2:108662028
|
A | G | 1 | a0001c0001t0024g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.192+2264A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108662028 | ||||||
| chr2:108662044
|
G | A | 68 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.192+2280G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108662044 | ||||||
| chr2:108662091
|
G | A | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.192+2327G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108662091 | ||||||
| chr2:108662130
|
G | A | 2 | a0001c0001t0017g0156a0001c0001t0017g0157 | 2 | HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.192+2366G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108662130 | ||||||
| chr2:108662158
|
C | G | 11 | a0001c0001t0003g0202a0001c0001t0003g0203a0001c0001t0003g0204others(8): Show | 11 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.192+2394C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108662158 | ||||||
| chr2:108662179
|
T | G | 4 | a0001c0001t0017g0156a0001c0001t0017g0157a0001c0001t0024g0162others(1): Show | 4 | HG02647.hp1 HG03486.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.192+2415T>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108662179 | ||||||
| chr2:108662367
|
T | C | 3 | a0001c0001t0003g0208a0001c0001t0014g0159a0001c0001t0014g0160 | 3 | HG03098.hp1 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.192+2603T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108662367 | ||||||
| chr2:108662485
|
A | G | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.192+2721A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108662485 | ||||||
| chr2:108662548
|
A | C | 1 | a0001c0001t0006g0168 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.192+2784A>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108662548 | ||||||
| chr2:108662605
|
A | G | 1 | a0001c0002t0009g0080 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.192+2841A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108662605 | ||||||
| chr2:108662678
|
G | A | 26 | a0001c0002t0001g0042a0001c0002t0004g0225a0001c0002t0004g0226others(23): Show | 26 | HG02040.hp1 HG02572.hp1 HG02602.hp2 others(23): Show |
intron_variant | MODIFIER | c.192+2914G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108662678 | ||||||
| chr2:108662816
|
G | A | 1 | a0001c0002t0012g0006 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.192+3052G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108662816 | ||||||
| chr2:108662866
|
T | G | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.192+3102T>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108662866 | ||||||
| chr2:108663061
|
A | G | 68 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.192+3297A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108663061 | ||||||
| chr2:108663097
|
A | G | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.192+3333A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108663097 | ||||||
| chr2:108663118
|
T | C | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.192+3354T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108663118 | ||||||
| chr2:108663304
|
C | T | 1 | a0001c0002t0001g0042 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.192+3540C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108663304 | ||||||
| chr2:108663375
|
A | C | 5 | a0001c0002t0001g0039a0001c0002t0009g0078a0001c0002t0009g0079others(2): Show | 5 | HG01261.hp2 NA18954.hp2 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.192+3611A>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108663375 | ||||||
| chr2:108663390
|
CT | C | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.192+3629delT | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 108663390 | |||||
| chr2:108663514
|
G | A | 1 | a0001c0002t0001g0021 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.192+3750G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108663514 | ||||||
| chr2:108663527
|
A | T | 90 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(87): Show | 90 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.192+3763A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108663527 | ||||||
| chr2:108663716
|
G | A | 1 | a0002c0003t0026g0219 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.192+3952G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108663716 | ||||||
| chr2:108663723
|
C | T | 11 | a0001c0001t0003g0202a0001c0001t0003g0203a0001c0001t0003g0204others(8): Show | 11 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.192+3959C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108663723 | ||||||
| chr2:108663726
|
T | G | 3 | a0001c0001t0017g0156a0001c0001t0017g0157a0001c0001t0024g0162 | 3 | HG02647.hp1 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.192+3962T>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108663726 | ||||||
| chr2:108663750
|
T | A | 5 | a0001c0001t0003g0189a0001c0001t0003g0190a0001c0001t0003g0191others(2): Show | 5 | HG01074.hp2 HG01358.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.192+3986T>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108663750 | ||||||
| chr2:108663757
|
A | T | 1 | a0001c0002t0001g0064 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.192+3993A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108663757 | ||||||
| chr2:108663763
|
A | T | 65 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0010others(62): Show | 65 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.192+3999A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108663763 | ||||||
| chr2:108663818
|
G | C | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.192+4054G>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108663818 | ||||||
| chr2:108663853
|
C | G | 1 | a0001c0002t0001g0061 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.192+4089C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108663853 | ||||||
| chr2:108663871
|
G | C | 100 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(97): Show | 100 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.192+4107G>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108663871 | ||||||
| chr2:108663978
|
T | C | 39 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(36): Show | 39 | HG00099.hp2 HG00741.hp2 HG01168.hp2 others(36): Show |
intron_variant | MODIFIER | c.192+4214T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108663978 | ||||||
| chr2:108664012
|
C | T | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.192+4248C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108664012 | ||||||
| chr2:108664045
|
T | C | 68 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.192+4281T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108664045 | ||||||
| chr2:108664160
|
G | A | 1 | a0001c0001t0014g0160 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.192+4396G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108664160 | ||||||
| chr2:108664295
|
C | T | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.192+4531C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108664295 | ||||||
| chr2:108664296
|
G | A | 1 | a0001c0002t0001g0071 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.192+4532G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108664296 | ||||||
| chr2:108664296
|
G | C | 1 | a0001c0001t0003g0213 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.192+4532G>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108664296 | ||||||
| chr2:108664360
|
G | A | 90 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(87): Show | 90 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.192+4596G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108664360 | ||||||
| chr2:108664364
|
T | G | 1 | a0001c0001t0014g0159 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.192+4600T>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108664364 | ||||||
| chr2:108664811
|
A | G | 1 | a0001c0001t0002g0113 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.192+5047A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108664811 | ||||||
| chr2:108664840
|
G | T | 68 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.192+5076G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108664840 | ||||||
| chr2:108665320
|
T | C | 1 | a0001c0002t0001g0004 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.193-5461T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108665320 | ||||||
| chr2:108665450
|
G | A | 1 | a0001c0001t0006g0178 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.193-5331G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108665450 | ||||||
| chr2:108665613
|
A | G | 2 | a0001c0002t0012g0006a0001c0002t0012g0007 | 2 | HG02040.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.193-5168A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108665613 | ||||||
| chr2:108665671
|
C | T | 1 | a0001c0001t0002g0098 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.193-5110C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108665671 | ||||||
| chr2:108665776
|
G | A | 1 | a0001c0002t0001g0063 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.193-5005G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108665776 | ||||||
| chr2:108665824
|
A | G | 5 | a0001c0001t0003g0145a0001c0001t0003g0146a0001c0001t0003g0147others(2): Show | 5 | HG01257.hp2 HG01258.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.193-4957A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108665824 | ||||||
| chr2:108666033
|
C | CTT | 199 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.193-4747_193-4746d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 108666033 | |||||
| chr2:108666084
|
C | T | 2 | a0001c0001t0020g0100a0001c0002t0007g0218 | 2 | HG03453.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.193-4697C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108666084 | ||||||
| chr2:108666208
|
C | T | 2 | a0002c0003t0018g0005a0002c0003t0026g0219 | 2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.193-4573C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108666208 | ||||||
| chr2:108666347
|
A | G | 1 | a0001c0001t0011g0154 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.193-4434A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108666347 | ||||||
| chr2:108666443
|
C | T | 1 | a0001c0002t0001g0044 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.193-4338C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108666443 | ||||||
| chr2:108666562
|
G | A | 3 | a0001c0001t0017g0156a0001c0001t0017g0157a0001c0001t0024g0162 | 3 | HG02647.hp1 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.193-4219G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108666562 | ||||||
| chr2:108666612
|
G | C | 21 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(18): Show | 21 | HG02602.hp2 HG02622.hp1 HG03017.hp2 others(18): Show |
intron_variant | MODIFIER | c.193-4169G>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108666612 | ||||||
| chr2:108666713
|
T | C | 7 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(4): Show | 7 | HG02040.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.193-4068T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108666713 | ||||||
| chr2:108666736
|
C | G | 2 | a0001c0001t0003g0139a0001c0001t0003g0142 | 2 | HG03041.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.193-4045C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108666736 | ||||||
| chr2:108666797
|
A | T | 59 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(56): Show | 59 | HG00099.hp2 HG00741.hp2 HG01109.hp2 others(56): Show |
intron_variant | MODIFIER | c.193-3984A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108666797 | ||||||
| chr2:108666915
|
C | T | 1 | a0001c0001t0002g0105 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.193-3866C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108666915 | ||||||
| chr2:108667023
|
A | G | 76 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(73): Show | 76 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.193-3758A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108667023 | ||||||
| chr2:108667114
|
C | G | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.193-3667C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108667114 | ||||||
| chr2:108667197
|
A | G | 3 | a0001c0002t0004g0229a0001c0002t0004g0238a0001c0002t0004g0239 | 3 | NA19062.hp1 NA19066.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.193-3584A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108667197 | ||||||
| chr2:108667330
|
C | T | 3 | a0001c0002t0004g0229a0001c0002t0004g0238a0001c0002t0004g0239 | 3 | NA19062.hp1 NA19066.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.193-3451C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108667330 | ||||||
| chr2:108667354
|
TA | T | 3 | a0001c0002t0004g0229a0001c0002t0004g0238a0001c0002t0004g0239 | 3 | NA19062.hp1 NA19066.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.193-3425delA | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 108667354 | |||||
| chr2:108667379
|
G | A | 3 | a0001c0002t0004g0229a0001c0002t0004g0238a0001c0002t0004g0239 | 3 | NA19062.hp1 NA19066.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.193-3402G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108667379 | ||||||
| chr2:108667413
|
G | A | 3 | a0001c0002t0004g0229a0001c0002t0004g0238a0001c0002t0004g0239 | 3 | NA19062.hp1 NA19066.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.193-3368G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108667413 | ||||||
| chr2:108667454
|
C | T | 4 | a0001c0002t0004g0229a0001c0002t0004g0238a0001c0002t0004g0239others(1): Show | 4 | NA19043.hp2 NA19062.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-3327C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108667454 | ||||||
| chr2:108667458
|
C | G | 1 | a0001c0001t0003g0155 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.193-3323C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108667458 | ||||||
| chr2:108667506
|
TC | T | 3 | a0001c0002t0004g0229a0001c0002t0004g0238a0001c0002t0004g0239 | 3 | NA19062.hp1 NA19066.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.193-3274delC | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108667506 | ||||||
| chr2:108667508
|
A | G | 3 | a0001c0002t0004g0229a0001c0002t0004g0238a0001c0002t0004g0239 | 3 | NA19062.hp1 NA19066.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.193-3273A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108667508 | ||||||
| chr2:108667520
|
T | TATA | 90 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(87): Show | 90 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.193-3260_193-3258d others(5): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 108667520 | |||||
| chr2:108667532
|
CT | C | 3 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0224 | 3 | HG02486.hp1 HG02630.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.193-3243delT | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 108667532 | |||||
| chr2:108667535
|
T | C | 3 | a0001c0002t0004g0229a0001c0002t0004g0238a0001c0002t0004g0239 | 3 | NA19062.hp1 NA19066.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.193-3246T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108667535 | ||||||
| chr2:108667536
|
TTTAAAAA others(1): Show |
T | 3 | a0001c0002t0004g0229a0001c0002t0004g0238a0001c0002t0004g0239 | 3 | NA19062.hp1 NA19066.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.193-3244_193-3237d others(10): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108667536 | ||||||
| chr2:108667537
|
T | A | 1 | a0001c0001t0006g0177 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.193-3244T>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108667537 | ||||||
| chr2:108667537
|
TTA | T | 5 | a0001c0002t0001g0029a0001c0002t0008g0223a0001c0002t0016g0045others(2): Show | 5 | HG02572.hp1 HG02647.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.193-3243_193-3242d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108667537 | ||||||
| chr2:108667538
|
T | A | 10 | a0001c0001t0002g0087a0001c0001t0003g0189a0001c0001t0005g0165others(7): Show | 10 | HG00741.hp1 HG01070.hp2 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.193-3243T>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108667538 | ||||||
| chr2:108667538
|
T | TA | 11 | a0001c0001t0003g0138a0001c0001t0003g0139a0001c0001t0003g0140others(8): Show | 11 | HG01243.hp1 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.193-3229dupA | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 108667538 | |||||
| chr2:108667538
|
TA | T | 60 | a0001c0002t0001g0002a0001c0002t0001g0004a0001c0002t0001g0015others(57): Show | 60 | HG01070.hp1 HG01106.hp1 HG01167.hp2 others(57): Show |
intron_variant | MODIFIER | c.193-3229delA | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 108667538 | |||||
| chr2:108667539
|
A | T | 4 | a0001c0001t0003g0202a0001c0001t0006g0168a0001c0001t0017g0156others(1): Show | 4 | HG01884.hp1 HG02647.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-3242A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108667539 | ||||||
| chr2:108667547
|
A | T | 1 | a0001c0002t0012g0007 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.193-3234A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108667547 | ||||||
| chr2:108667549
|
A | AATATATA others(3): Show |
1 | a0001c0001t0002g0097 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.193-3231_193-3230i others(12): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 108667549 | |||||
| chr2:108667549
|
A | T | 9 | a0001c0001t0014g0159a0001c0002t0007g0214a0001c0002t0007g0215others(6): Show | 9 | HG02258.hp1 HG02572.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.193-3232A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108667549 | ||||||
| chr2:108667551
|
A | AAAAAAAT | 6 | a0001c0001t0005g0163a0001c0001t0005g0169a0001c0001t0005g0180others(3): Show | 6 | HG01175.hp1 HG01257.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.193-3229_193-3228i others(9): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 108667551 | |||||
| chr2:108667551
|
A | AAAAATAT | 22 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0086others(19): Show | 22 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.193-3229_193-3228i others(9): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 108667551 | |||||
| chr2:108667551
|
A | AAAATAT | 15 | a0001c0001t0002g0085a0001c0001t0002g0096a0001c0001t0002g0107others(12): Show | 15 | HG01168.hp2 HG01169.hp1 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.193-3229_193-3228i others(8): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 108667551 | |||||
| chr2:108667551
|
A | AAAATATA others(1): Show |
6 | a0001c0001t0002g0106a0001c0001t0002g0128a0001c0001t0003g0211others(3): Show | 6 | HG00099.hp2 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.193-3229_193-3228i others(10): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 108667551 | |||||
| chr2:108667551
|
A | AAATATAT | 9 | a0001c0001t0002g0082a0001c0001t0002g0083a0001c0001t0002g0098others(6): Show | 9 | HG00741.hp2 HG01346.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.193-3229_193-3228i others(9): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 108667551 | |||||
| chr2:108667551
|
A | AAATATAT others(4): Show |
3 | a0001c0001t0002g0129a0001c0001t0002g0182a0001c0001t0002g0184 | 3 | HG01109.hp2 HG02257.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.193-3229_193-3228i others(13): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 108667551 | |||||
| chr2:108667551
|
A | AAATATAT others(8): Show |
1 | a0001c0001t0002g0183 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.193-3229_193-3228i others(17): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 108667551 | |||||
| chr2:108667551
|
A | AT | 23 | a0001c0001t0003g0001a0001c0001t0003g0130a0001c0001t0003g0131others(20): Show | 24 | HG00323.hp1 HG00639.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.193-3230_193-3229i others(3): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108667551 | ||||||
| chr2:108667551
|
A | ATATATAT | 3 | a0001c0001t0002g0094a0001c0001t0002g0095a0001c0001t0002g0099 | 3 | HG02896.hp2 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.193-3230_193-3229i others(9): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108667551 | ||||||
| chr2:108667551
|
A | ATATATAT others(2): Show |
4 | a0001c0001t0002g0084a0001c0001t0002g0089a0001c0001t0002g0092others(1): Show | 4 | HG01175.hp2 HG02145.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.193-3230_193-3229i others(11): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108667551 | ||||||
| chr2:108667551
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0002g0113 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.193-3230_193-3229i others(13): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108667551 | ||||||
| chr2:108667551
|
A | T | 27 | a0001c0001t0002g0091a0001c0001t0002g0097a0001c0001t0003g0148others(24): Show | 27 | HG01167.hp1 HG01243.hp2 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.193-3230A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108667551 | ||||||
| chr2:108667552
|
AT | A | 22 | a0001c0002t0001g0003a0001c0002t0001g0008a0001c0002t0001g0009others(19): Show | 22 | HG00099.hp1 HG00639.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.193-3228delT | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108667552 | ||||||
| chr2:108667553
|
T | A | 3 | a0001c0001t0003g0140a0001c0002t0001g0029a0001c0002t0008g0224 | 3 | HG02486.hp1 HG02886.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.193-3228T>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108667553 | ||||||
| chr2:108667553
|
TA | T | 3 | a0001c0002t0004g0229a0001c0002t0004g0238a0001c0002t0004g0239 | 3 | NA19062.hp1 NA19066.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.193-3227delA | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108667553 | ||||||
| chr2:108667555
|
T | A | 2 | a0001c0002t0001g0037a0001c0002t0001g0050 | 2 | HG02630.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.193-3226T>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108667555 | ||||||
| chr2:108667573
|
G | A | 10 | a0001c0002t0004g0229a0001c0002t0004g0238a0001c0002t0004g0239others(7): Show | 10 | HG02040.hp2 HG02486.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.193-3208G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108667573 | ||||||
| chr2:108667651
|
T | TATCTA | 4 | a0001c0002t0001g0004a0001c0002t0004g0229a0001c0002t0004g0238others(1): Show | 4 | HG02559.hp1 NA19062.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-3129_193-3128i others(7): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 108667651 | |||||
| chr2:108667654
|
C | T | 4 | a0001c0002t0001g0004a0001c0002t0004g0229a0001c0002t0004g0238others(1): Show | 4 | HG02559.hp1 NA19062.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-3127C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108667654 | ||||||
| chr2:108667698
|
T | C | 2 | a0001c0004t0013g0073a0001c0004t0013g0074 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.193-3083T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108667698 | ||||||
| chr2:108667799
|
G | T | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.193-2982G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108667799 | ||||||
| chr2:108667899
|
A | G | 1 | a0001c0001t0003g0213 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.193-2882A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108667899 | ||||||
| chr2:108668154
|
T | C | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.193-2627T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108668154 | ||||||
| chr2:108668293
|
C | T | 1 | a0001c0002t0025g0026 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.193-2488C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108668293 | ||||||
| chr2:108668324
|
CTAACTG | C | 11 | a0001c0001t0003g0202a0001c0001t0003g0203a0001c0001t0003g0204others(8): Show | 11 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.193-2451_193-2446d others(8): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 108668324 | |||||
| chr2:108668397
|
C | A | 2 | a0002c0003t0018g0005a0002c0003t0026g0219 | 2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.193-2384C>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108668397 | ||||||
| chr2:108668399
|
T | G | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.193-2382T>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108668399 | ||||||
| chr2:108668412
|
C | G | 1 | a0001c0001t0002g0086 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.193-2369C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108668412 | ||||||
| chr2:108668517
|
C | T | 1 | a0001c0001t0005g0174 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.193-2264C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108668517 | ||||||
| chr2:108668597
|
T | A | 1 | a0001c0001t0002g0129 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.193-2184T>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108668597 | ||||||
| chr2:108668647
|
G | A | 109 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(106): Show | 109 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.193-2134G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108668647 | ||||||
| chr2:108669280
|
C | T | 68 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.193-1501C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108669280 | ||||||
| chr2:108669406
|
A | G | 12 | a0001c0001t0002g0084a0001c0001t0002g0089a0001c0001t0002g0090others(9): Show | 12 | HG01167.hp1 HG01175.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.193-1375A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108669406 | ||||||
| chr2:108669463
|
G | A | 199 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.193-1318G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108669463 | ||||||
| chr2:108669466
|
A | T | 1 | a0001c0002t0001g0027 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.193-1315A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108669466 | ||||||
| chr2:108669553
|
C | A | 4 | a0001c0001t0002g0094a0001c0001t0002g0095a0001c0001t0002g0098others(1): Show | 4 | HG02818.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-1228C>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108669553 | ||||||
| chr2:108669659
|
G | C | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.193-1122G>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108669659 | ||||||
| chr2:108669722
|
TA | T | 110 | a0001c0001t0002g0183a0001c0002t0001g0002a0001c0002t0001g0003others(107): Show | 110 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.193-1047delA | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 108669722 | |||||
| chr2:108669794
|
A | G | 3 | a0001c0002t0001g0019a0001c0002t0001g0029a0001c0002t0001g0059 | 3 | HG02886.hp2 HG02896.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.193-987A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108669794 | ||||||
| chr2:108669841
|
G | A | 1 | a0001c0002t0016g0070 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.193-940G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108669841 | ||||||
| chr2:108669842
|
G | C | 5 | a0001c0002t0004g0231a0001c0002t0004g0233a0001c0002t0004g0236others(2): Show | 5 | NA18940.hp2 NA18994.hp2 NA19056.hp1 others(2): Show |
intron_variant | MODIFIER | c.193-939G>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108669842 | ||||||
| chr2:108669870
|
A | C | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.193-911A>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108669870 | ||||||
| chr2:108669892
|
T | C | 1 | a0001c0002t0001g0038 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.193-889T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108669892 | ||||||
| chr2:108670166
|
GT | G | 79 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(76): Show | 79 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.193-609delT | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 108670166 | |||||
| chr2:108670203
|
G | A | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.193-578G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108670203 | ||||||
| chr2:108670211
|
C | CG | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.193-570_193-569ins others(1): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108670211 | ||||||
| chr2:108670334
|
A | C | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.193-447A>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108670334 | ||||||
| chr2:108670347
|
A | G | 199 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.193-434A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108670347 | ||||||
| chr2:108670391
|
C | T | 1 | a0001c0001t0002g0098 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.193-390C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108670391 | ||||||
| chr2:108670398
|
C | T | 11 | a0001c0001t0003g0202a0001c0001t0003g0203a0001c0001t0003g0204others(8): Show | 11 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.193-383C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108670398 | ||||||
| chr2:108670421
|
A | G | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.193-360A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108670421 | ||||||
| chr2:108670574
|
A | G | 1 | a0001c0001t0002g0075 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.193-207A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108670574 | ||||||
| chr2:108670733
|
T | C | 1 | a0001c0002t0012g0220 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.193-48T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108670733 | ||||||
| chr2:108670735
|
C | T | 1 | a0001c0002t0012g0220 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.193-46C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 2/9 | chr2 | 108670735 | ||||||
| chr2:108670949
|
T | C | 11 | a0001c0001t0003g0202a0001c0001t0003g0203a0001c0001t0003g0204others(8): Show | 11 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.259+102T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 3/9 | chr2 | 108670949 | ||||||
| chr2:108670991
|
G | A | 1 | a0001c0001t0003g0131 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.259+144G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 3/9 | chr2 | 108670991 | ||||||
| chr2:108671047
|
A | G | 1 | a0001c0002t0001g0004 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.259+200A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 3/9 | chr2 | 108671047 | ||||||
| chr2:108671089
|
C | T | 93 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(90): Show | 93 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.259+242C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 3/9 | chr2 | 108671089 | ||||||
| chr2:108671090
|
G | A | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.259+243G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 3/9 | chr2 | 108671090 | ||||||
| chr2:108671156
|
A | C | 1 | a0001c0001t0002g0122 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.259+309A>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 3/9 | chr2 | 108671156 | ||||||
| chr2:108671227
|
G | A | 1 | a0001c0001t0006g0179 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.259+380G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 3/9 | chr2 | 108671227 | ||||||
| chr2:108671447
|
A | G | 1 | a0001c0002t0009g0078 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.259+600A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 3/9 | chr2 | 108671447 | ||||||
| chr2:108671467
|
A | G | 11 | a0001c0001t0003g0202a0001c0001t0003g0203a0001c0001t0003g0204others(8): Show | 11 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.259+620A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 3/9 | chr2 | 108671467 | ||||||
| chr2:108671597
|
G | A | 1 | a0001c0001t0022g0112 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.260-728G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 3/9 | chr2 | 108671597 | ||||||
| chr2:108671646
|
G | A | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.260-679G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 3/9 | chr2 | 108671646 | ||||||
| chr2:108671687
|
A | G | 1 | a0001c0002t0009g0080 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.260-638A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 3/9 | chr2 | 108671687 | ||||||
| chr2:108671763
|
C | A | 4 | a0001c0001t0002g0094a0001c0001t0002g0095a0001c0001t0002g0098others(1): Show | 4 | HG02818.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.260-562C>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 3/9 | chr2 | 108671763 | ||||||
| chr2:108671813
|
T | C | 4 | a0001c0001t0002g0094a0001c0001t0002g0095a0001c0001t0002g0098others(1): Show | 4 | HG02818.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.260-512T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 3/9 | chr2 | 108671813 | ||||||
| chr2:108671977
|
C | T | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.260-348C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 3/9 | chr2 | 108671977 | ||||||
| chr2:108672024
|
G | A | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.260-301G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 3/9 | chr2 | 108672024 | ||||||
| chr2:108672028
|
G | A | 2 | a0001c0001t0005g0163a0001c0001t0005g0180 | 2 | HG01175.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.260-297G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 3/9 | chr2 | 108672028 | ||||||
| chr2:108672165
|
CA | C | 203 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(200): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.260-137delA | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 108672165 | |||||
| chr2:108672165
|
CAA | C | 20 | a0001c0001t0002g0107a0001c0001t0002g0182a0001c0001t0002g0183others(17): Show | 20 | HG00140.hp1 HG00323.hp2 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.260-138_260-137del others(2): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 108672165 | |||||
| chr2:108672229
|
T | C | 109 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(106): Show | 109 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.260-96T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 3/9 | chr2 | 108672229 | ||||||
| chr2:108672245
|
A | G | 67 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0008others(64): Show | 67 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.260-80A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 3/9 | chr2 | 108672245 | ||||||
| chr2:108672504
|
T | C | 1 | a0001c0001t0002g0127 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.380+59T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 4/9 | chr2 | 108672504 | ||||||
| chr2:108672533
|
G | T | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.380+88G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 4/9 | chr2 | 108672533 | ||||||
| chr2:108672605
|
G | A | 3 | a0001c0002t0007g0214a0001c0002t0007g0217a0001c0002t0007g0218 | 3 | HG03195.hp1 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.380+160G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 4/9 | chr2 | 108672605 | ||||||
| chr2:108673116
|
A | G | 1 | a0001c0002t0001g0021 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.530+87A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 5/9 | chr2 | 108673116 | ||||||
| chr2:108673129
|
A | C | 46 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(43): Show | 46 | HG00099.hp2 HG00741.hp2 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.530+100A>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 5/9 | chr2 | 108673129 | ||||||
| chr2:108673180
|
T | C | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.530+151T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 5/9 | chr2 | 108673180 | ||||||
| chr2:108673207
|
G | A | 1 | a0001c0001t0002g0116 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.530+178G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 5/9 | chr2 | 108673207 | ||||||
| chr2:108673207
|
G | GTT | 11 | a0001c0001t0003g0202a0001c0001t0003g0203a0001c0001t0003g0204others(8): Show | 11 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.530+180_530+181dup others(2): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 108673207 | |||||
| chr2:108673263
|
C | CACCCTCC others(33): Show |
1 | a0001c0002t0001g0051 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.530+238_530+277dup others(40): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 108673263 | |||||
| chr2:108673563
|
A | T | 19 | a0001c0001t0005g0163a0001c0001t0005g0164a0001c0001t0005g0165others(16): Show | 19 | HG00140.hp1 HG00280.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.530+534A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 5/9 | chr2 | 108673563 | ||||||
| chr2:108673666
|
G | A | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.530+637G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 5/9 | chr2 | 108673666 | ||||||
| chr2:108673820
|
T | C | 2 | a0002c0003t0018g0005a0002c0003t0026g0219 | 2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.530+791T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 5/9 | chr2 | 108673820 | ||||||
| chr2:108674186
|
C | T | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.530+1157C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 5/9 | chr2 | 108674186 | ||||||
| chr2:108674207
|
A | G | 1 | a0002c0003t0026g0219 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.530+1178A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 5/9 | chr2 | 108674207 | ||||||
| chr2:108674251
|
A | G | 79 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(76): Show | 79 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.530+1222A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 5/9 | chr2 | 108674251 | ||||||
| chr2:108674253
|
C | T | 1 | a0001c0002t0001g0048 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.530+1224C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 5/9 | chr2 | 108674253 | ||||||
| chr2:108674380
|
T | G | 1 | a0001c0002t0004g0226 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.530+1351T>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 5/9 | chr2 | 108674380 | ||||||
| chr2:108674450
|
C | CAGTG | 4 | a0001c0001t0003g0145a0001c0001t0003g0146a0001c0001t0003g0147others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.530+1422_531-1424d others(6): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 108674450 | |||||
| chr2:108674471
|
C | G | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.531-1407C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 5/9 | chr2 | 108674471 | ||||||
| chr2:108674578
|
A | G | 1 | a0001c0001t0002g0104 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.531-1300A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 5/9 | chr2 | 108674578 | ||||||
| chr2:108674628
|
G | A | 1 | a0001c0001t0003g0198 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.531-1250G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 5/9 | chr2 | 108674628 | ||||||
| chr2:108674638
|
A | G | 199 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.531-1240A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 5/9 | chr2 | 108674638 | ||||||
| chr2:108674686
|
A | G | 68 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.531-1192A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 5/9 | chr2 | 108674686 | ||||||
| chr2:108674719
|
C | CA | 23 | a0001c0001t0002g0122a0001c0001t0003g0130a0001c0001t0003g0131others(20): Show | 23 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.531-1140dupA | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 108674719 | |||||
| chr2:108674719
|
CA | C | 8 | a0001c0001t0002g0095a0001c0001t0002g0102a0001c0001t0002g0158others(5): Show | 8 | HG01261.hp2 HG02145.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.531-1140delA | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 108674719 | |||||
| chr2:108674719
|
CAA | C | 96 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(93): Show | 96 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.531-1141_531-1140d others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 108674719 | |||||
| chr2:108674820
|
C | T | 2 | a0001c0001t0002g0123a0001c0001t0021g0120 | 2 | HG01243.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.531-1058C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 5/9 | chr2 | 108674820 | ||||||
| chr2:108675061
|
A | G | 1 | a0001c0001t0011g0154 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.531-817A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 5/9 | chr2 | 108675061 | ||||||
| chr2:108675071
|
G | T | 23 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(20): Show | 23 | HG02602.hp2 HG02622.hp1 HG02895.hp1 others(20): Show |
intron_variant | MODIFIER | c.531-807G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 5/9 | chr2 | 108675071 | ||||||
| chr2:108675277
|
C | T | 1 | a0001c0002t0001g0009 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.531-601C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 5/9 | chr2 | 108675277 | ||||||
| chr2:108675292
|
T | A | 68 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.531-586T>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 5/9 | chr2 | 108675292 | ||||||
| chr2:108675330
|
G | A | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.531-548G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 5/9 | chr2 | 108675330 | ||||||
| chr2:108675330
|
G | C | 2 | a0001c0002t0001g0022a0001c0002t0001g0051 | 2 | NA18954.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.531-548G>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 5/9 | chr2 | 108675330 | ||||||
| chr2:108675443
|
CT | C | 68 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.531-433delT | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 108675443 | |||||
| chr2:108675450
|
G | T | 1 | a0001c0001t0006g0171 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.531-428G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 5/9 | chr2 | 108675450 | ||||||
| chr2:108675470
|
A | T | 1 | a0001c0001t0010g0195 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.531-408A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 5/9 | chr2 | 108675470 | ||||||
| chr2:108675472
|
A | C | 1 | a0001c0001t0010g0195 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.531-406A>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 5/9 | chr2 | 108675472 | ||||||
| chr2:108675599
|
A | G | 1 | a0001c0002t0001g0063 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.531-279A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 5/9 | chr2 | 108675599 | ||||||
| chr2:108675713
|
A | G | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.531-165A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 5/9 | chr2 | 108675713 | ||||||
| chr2:108675763
|
A | G | 11 | a0001c0001t0002g0084a0001c0001t0002g0089a0001c0001t0002g0090others(8): Show | 11 | HG01109.hp2 HG01167.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.531-115A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 5/9 | chr2 | 108675763 | ||||||
| chr2:108675824
|
T | C | 199 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.531-54T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 5/9 | chr2 | 108675824 | ||||||
| chr2:108675860
|
T | C | 11 | a0001c0001t0003g0202a0001c0001t0003g0203a0001c0001t0003g0204others(8): Show | 11 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.531-18T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 5/9 | chr2 | 108675860 | ||||||
| chr2:108676269
|
A | T | 1 | a0001c0002t0004g0225 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.681+241A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 6/9 | chr2 | 108676269 | ||||||
| chr2:108676314
|
A | G | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.681+286A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 6/9 | chr2 | 108676314 | ||||||
| chr2:108676381
|
C | A | 1 | a0001c0002t0001g0050 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.682-225C>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 6/9 | chr2 | 108676381 | ||||||
| chr2:108676434
|
A | C | 90 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(87): Show | 90 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.682-172A>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 6/9 | chr2 | 108676434 | ||||||
| chr2:108676493
|
T | C | 6 | a0001c0002t0001g0008a0001c0002t0001g0010a0001c0002t0001g0011others(3): Show | 6 | HG00323.hp2 HG00639.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.682-113T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 6/9 | chr2 | 108676493 | ||||||
| chr2:108676523
|
T | C | 68 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.682-83T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 6/9 | chr2 | 108676523 | ||||||
| chr2:108676902
|
A | G | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.774+204A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 7/9 | chr2 | 108676902 | ||||||
| chr2:108676951
|
G | C | 67 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0008others(64): Show | 67 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.774+253G>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 7/9 | chr2 | 108676951 | ||||||
| chr2:108676979
|
T | C | 1 | a0001c0001t0002g0116 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.774+281T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 7/9 | chr2 | 108676979 | ||||||
| chr2:108677212
|
C | T | 23 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(20): Show | 23 | HG02602.hp2 HG02622.hp1 HG02895.hp1 others(20): Show |
intron_variant | MODIFIER | c.774+514C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 7/9 | chr2 | 108677212 | ||||||
| chr2:108677261
|
A | T | 1 | a0001c0001t0003g0148 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.774+563A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 7/9 | chr2 | 108677261 | ||||||
| chr2:108677425
|
C | A | 1 | a0001c0001t0002g0103 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.775-554C>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 7/9 | chr2 | 108677425 | ||||||
| chr2:108677653
|
C | A | 1 | a0001c0002t0001g0010 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.775-326C>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 7/9 | chr2 | 108677653 | ||||||
| chr2:108677660
|
G | A | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.775-319G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 7/9 | chr2 | 108677660 | ||||||
| chr2:108678132
|
A | T | 93 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(90): Show | 93 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.823+105A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 8/9 | chr2 | 108678132 | ||||||
| chr2:108678364
|
C | T | 1 | a0001c0002t0007g0216 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.823+337C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 8/9 | chr2 | 108678364 | ||||||
| chr2:108678436
|
T | TA | 68 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.823+410dupA | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 108678436 | |||||
| chr2:108678638
|
A | C | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.823+611A>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 8/9 | chr2 | 108678638 | ||||||
| chr2:108678737
|
A | G | 67 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0008others(64): Show | 67 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.823+710A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 8/9 | chr2 | 108678737 | ||||||
| chr2:108678977
|
C | G | 1 | a0002c0003t0018g0005 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.823+950C>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 8/9 | chr2 | 108678977 | ||||||
| chr2:108679019
|
C | T | 2 | a0002c0003t0018g0005a0002c0003t0026g0219 | 2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.823+992C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 8/9 | chr2 | 108679019 | ||||||
| chr2:108679083
|
G | C | 1 | a0004c0006t0004g0243 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.823+1056G>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 8/9 | chr2 | 108679083 | ||||||
| chr2:108679096
|
A | G | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.823+1069A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 8/9 | chr2 | 108679096 | ||||||
| chr2:108679154
|
G | A | 1 | a0001c0002t0001g0019 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.823+1127G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 8/9 | chr2 | 108679154 | ||||||
| chr2:108679190
|
G | A | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.823+1163G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 8/9 | chr2 | 108679190 | ||||||
| chr2:108679249
|
C | T | 1 | a0001c0002t0001g0004 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.823+1222C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 8/9 | chr2 | 108679249 | ||||||
| chr2:108679300
|
G | A | 1 | a0001c0001t0019g0124 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.823+1273G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 8/9 | chr2 | 108679300 | ||||||
| chr2:108679360
|
A | T | 7 | a0001c0001t0002g0086a0001c0001t0002g0087a0001c0001t0002g0114others(4): Show | 7 | NA18968.hp1 NA18977.hp1 NA18993.hp1 others(4): Show |
intron_variant | MODIFIER | c.823+1333A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 8/9 | chr2 | 108679360 | ||||||
| chr2:108679384
|
A | G | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.824-1311A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 8/9 | chr2 | 108679384 | ||||||
| chr2:108679507
|
G | A | 79 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(76): Show | 79 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.824-1188G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 8/9 | chr2 | 108679507 | ||||||
| chr2:108679754
|
C | CAAAATA | 97 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(94): Show | 97 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.824-936_824-931dup others(6): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 108679754 | |||||
| chr2:108679803
|
T | C | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.824-892T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 8/9 | chr2 | 108679803 | ||||||
| chr2:108680029
|
G | A | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.824-666G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 8/9 | chr2 | 108680029 | ||||||
| chr2:108680108
|
C | T | 93 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(90): Show | 93 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.824-587C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 8/9 | chr2 | 108680108 | ||||||
| chr2:108680183
|
A | G | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.824-512A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 8/9 | chr2 | 108680183 | ||||||
| chr2:108680200
|
C | T | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.824-495C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 8/9 | chr2 | 108680200 | ||||||
| chr2:108680204
|
A | G | 21 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(18): Show | 21 | HG02602.hp2 HG02622.hp1 HG03017.hp2 others(18): Show |
intron_variant | MODIFIER | c.824-491A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 8/9 | chr2 | 108680204 | ||||||
| chr2:108680316
|
G | A | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.824-379G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 8/9 | chr2 | 108680316 | ||||||
| chr2:108680352
|
C | T | 5 | a0001c0002t0007g0214a0001c0002t0007g0215a0001c0002t0007g0216others(2): Show | 5 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.824-343C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 8/9 | chr2 | 108680352 | ||||||
| chr2:108680365
|
C | CA | 94 | a0001c0001t0002g0076a0001c0001t0002g0082a0001c0001t0002g0083others(91): Show | 94 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.824-308dupA | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 108680365 | |||||
| chr2:108680365
|
C | CAA | 7 | a0001c0001t0002g0075a0001c0001t0002g0090a0001c0001t0002g0092others(4): Show | 7 | HG01175.hp1 HG01175.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.824-309_824-308dup others(2): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 108680365 | |||||
| chr2:108680365
|
CA | C | 22 | a0001c0002t0001g0036a0001c0002t0001g0052a0001c0002t0004g0225others(19): Show | 22 | HG01981.hp2 HG02572.hp1 HG02622.hp1 others(19): Show |
intron_variant | MODIFIER | c.824-308delA | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 108680365 | |||||
| chr2:108680410
|
AC | A | 76 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(73): Show | 76 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.824-283delC | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 108680410 | |||||
| chr2:108680474
|
T | C | 109 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(106): Show | 109 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.824-221T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 8/9 | chr2 | 108680474 | ||||||
| chr2:108680528
|
C | A | 93 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(90): Show | 93 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.824-167C>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 8/9 | chr2 | 108680528 | ||||||
| chr2:108680540
|
T | TA | 14 | a0001c0001t0002g0083a0001c0001t0002g0087a0001c0001t0002g0106others(11): Show | 14 | HG00099.hp2 HG01257.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.824-131dupA | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 108680540 | |||||
| chr2:108680540
|
TA | T | 13 | a0001c0001t0002g0076a0001c0001t0002g0089a0001c0001t0002g0094others(10): Show | 13 | HG00741.hp2 HG01261.hp2 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.824-131delA | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 108680540 | |||||
| chr2:108680541
|
A | T | 3 | a0001c0002t0001g0019a0001c0002t0001g0029a0001c0002t0001g0059 | 3 | HG02886.hp2 HG02896.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.824-154A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 8/9 | chr2 | 108680541 | ||||||
| chr2:108680542
|
A | T | 1 | a0001c0002t0012g0006 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.824-153A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 8/9 | chr2 | 108680542 | ||||||
| chr2:108680560
|
AAAAAG | A | 8 | a0001c0002t0001g0028a0001c0002t0001g0038a0001c0002t0001g0056others(5): Show | 8 | HG01168.hp1 HG02895.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.824-134_824-130del others(5): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 8/9 | chr2 | 108680560 | ||||||
| chr2:108680561
|
AAAAG | A | 83 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0004others(80): Show | 83 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.824-133_824-130del others(4): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 8/9 | chr2 | 108680561 | ||||||
| chr2:108680940
|
C | A | 1 | a0001c0002t0004g0226 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.899+170C>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 9/9 | chr2 | 108680940 | ||||||
| chr2:108681287
|
G | A | 4 | a0001c0002t0009g0078a0001c0002t0009g0079a0001c0002t0009g0080others(1): Show | 4 | HG01261.hp2 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.899+517G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 9/9 | chr2 | 108681287 | ||||||
| chr2:108681347
|
A | G | 1 | a0001c0002t0001g0071 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.899+577A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 9/9 | chr2 | 108681347 | ||||||
| chr2:108681413
|
G | A | 1 | a0001c0001t0002g0184 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.899+643G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 9/9 | chr2 | 108681413 | ||||||
| chr2:108681428
|
T | A | 195 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(192): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.899+658T>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 9/9 | chr2 | 108681428 | ||||||
| chr2:108681429
|
T | A | 4 | a0001c0002t0004g0231a0001c0002t0004g0233a0001c0002t0004g0236others(1): Show | 4 | NA18940.hp2 NA18994.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.899+659T>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 9/9 | chr2 | 108681429 | ||||||
| chr2:108681646
|
C | T | 3 | a0001c0001t0002g0182a0001c0001t0002g0183a0001c0001t0002g0184 | 3 | HG02257.hp2 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.899+876C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 9/9 | chr2 | 108681646 | ||||||
| chr2:108681723
|
C | A | 1 | a0001c0002t0009g0078 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.899+953C>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 9/9 | chr2 | 108681723 | ||||||
| chr2:108681754
|
G | A | 1 | a0001c0001t0003g0213 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.899+984G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 9/9 | chr2 | 108681754 | ||||||
| chr2:108681868
|
G | A | 1 | a0001c0001t0002g0129 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.899+1098G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 9/9 | chr2 | 108681868 | ||||||
| chr2:108681922
|
G | A | 198 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(195): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.899+1152G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 9/9 | chr2 | 108681922 | ||||||
| chr2:108682005
|
T | C | 2 | a0001c0001t0003g0139a0001c0001t0003g0142 | 2 | HG03041.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.899+1235T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 9/9 | chr2 | 108682005 | ||||||
| chr2:108682017
|
ATTCAT | A | 21 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(18): Show | 21 | HG02602.hp2 HG02622.hp1 HG03017.hp2 others(18): Show |
intron_variant | MODIFIER | c.899+1251_899+1255d others(7): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 108682017 | |||||
| chr2:108682107
|
A | G | 3 | a0001c0001t0002g0082a0001c0001t0002g0083a0001c0001t0019g0124 | 3 | HG02723.hp1 HG03098.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.899+1337A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 9/9 | chr2 | 108682107 | ||||||
| chr2:108682162
|
T | C | 79 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(76): Show | 79 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.899+1392T>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 9/9 | chr2 | 108682162 | ||||||
| chr2:108682351
|
T | A | 23 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0227others(20): Show | 23 | HG02602.hp2 HG02622.hp1 HG02895.hp1 others(20): Show |
intron_variant | MODIFIER | c.900-1534T>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 9/9 | chr2 | 108682351 | ||||||
| chr2:108682478
|
C | A | 2 | a0001c0004t0013g0073a0001c0004t0013g0074 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.900-1407C>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 9/9 | chr2 | 108682478 | ||||||
| chr2:108682756
|
A | G | 1 | a0001c0002t0001g0050 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.900-1129A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 9/9 | chr2 | 108682756 | ||||||
| chr2:108683046
|
G | T | 1 | a0001c0001t0003g0192 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.900-839G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 9/9 | chr2 | 108683046 | ||||||
| chr2:108683212
|
C | T | 1 | a0001c0002t0001g0037 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.900-673C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 9/9 | chr2 | 108683212 | ||||||
| chr2:108683251
|
G | C | 1 | a0001c0001t0002g0075 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.900-634G>C | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 9/9 | chr2 | 108683251 | ||||||
| chr2:108683253
|
T | A | 1 | a0001c0001t0002g0075 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.900-632T>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 9/9 | chr2 | 108683253 | ||||||
| chr2:108683254
|
G | T | 1 | a0001c0001t0002g0075 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.900-631G>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 9/9 | chr2 | 108683254 | ||||||
| chr2:108683255
|
C | A | 1 | a0001c0001t0002g0075 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.900-630C>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 9/9 | chr2 | 108683255 | ||||||
| chr2:108683264
|
A | G | 1 | a0001c0001t0002g0075 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.900-621A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 9/9 | chr2 | 108683264 | ||||||
| chr2:108683265
|
A | T | 1 | a0001c0001t0002g0075 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.900-620A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 9/9 | chr2 | 108683265 | ||||||
| chr2:108683268
|
A | T | 1 | a0001c0001t0002g0075 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.900-617A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 9/9 | chr2 | 108683268 | ||||||
| chr2:108683269
|
A | G | 1 | a0001c0001t0002g0075 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.900-616A>G | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 9/9 | chr2 | 108683269 | ||||||
| chr2:108683272
|
A | T | 1 | a0001c0001t0002g0075 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.900-613A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 9/9 | chr2 | 108683272 | ||||||
| chr2:108683506
|
C | T | 3 | a0001c0001t0017g0156a0001c0001t0017g0157a0001c0001t0024g0162 | 3 | HG02647.hp1 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.900-379C>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 9/9 | chr2 | 108683506 | ||||||
| chr2:108683539
|
C | CA | 173 | a0001c0001t0002g0076a0001c0001t0002g0082a0001c0001t0002g0083others(170): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.900-326dupA | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 108683539 | |||||
| chr2:108683539
|
C | CAA | 10 | a0001c0001t0002g0075a0001c0001t0002g0114a0001c0001t0002g0119others(7): Show | 10 | HG01192.hp2 HG02559.hp1 HG02738.hp2 others(7): Show |
intron_variant | MODIFIER | c.900-327_900-326dup others(2): Show |
LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 108683539 | |||||
| chr2:108683580
|
T | A | 244 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0082others(241): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.900-305T>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 9/9 | chr2 | 108683580 | ||||||
| chr2:108683690
|
A | T | 4 | a0001c0002t0008g0221a0001c0002t0008g0222a0001c0002t0008g0223others(1): Show | 4 | HG02486.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.900-195A>T | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 9/9 | chr2 | 108683690 | ||||||
| chr2:108683792
|
G | A | 1 | a0001c0001t0002g0075 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.900-93G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 9/9 | chr2 | 108683792 | ||||||
| chr2:108683802
|
G | A | 3 | a0001c0002t0012g0006a0001c0002t0012g0007a0001c0002t0012g0220 | 3 | HG02040.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.900-83G>A | LIMS1 | ENSG00000169756.17 | transcript | ENST00000544547.6 | protein_coding | 9/9 | chr2 | 108683802 |