| geneid | 4008 |
|---|---|
| ensemblid | ENSG00000136153.20 |
| hgncid | 6646 |
| symbol | LMO7 |
| name | LIM domain 7 |
| refseq_nuc | NM_001306080.2 |
| refseq_prot | NP_001293009.1 |
| ensembl_nuc | ENST00000377534.8 |
| ensembl_prot | ENSP00000366757.4 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 75636330 |
| end | 75859866 |
| strand | + |
| ver | v1.2 |
| region | chr13:75636330-75859866 |
| region5000 | chr13:75631330-75864866 |
| regionname0 | LMO7_chr13_75636330_75859866 |
| regionname5000 | LMO7_chr13_75631330_75864866 |
| 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 | 1631 | 76 | 13 | 15 | 39 | 2 | 5 | 29 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0002 | 0/0 | 1631 | 44 | 5 | 15 | 9 | 4 | 11 | 4 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0003 | 0/0 | 1631 | 43 | 0 | 11 | 29 | 1 | 2 | 20 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0004 | 0/0 | 1631 | 25 | 4 | 4 | 10 | 2 | 5 | 10 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0005 | 0/0 | 1631 | 15 | 0 | 0 | 12 | 0 | 3 | 11 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0006 | 0/0 | 1631 | 14 | 10 | 3 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0007 | 0/0 | 1631 | 10 | 6 | 1 | 1 | 0 | 2 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0008 | 0/0 | 1631 | 10 | 4 | 1 | 2 | 0 | 3 | 2 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0009 | 0/0 | 1631 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0010 | 0/0 | 1631 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0011 | 0/0 | 1631 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0012 | 0/0 | 1631 | 4 | 2 | 2 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0013 | 0/0 | 1631 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0014 | 0/0 | 1631 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0015 | 0/0 | 1631 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0016 | 0/0 | 1631 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0017 | 0/0 | 1631 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0018 | 0/0 | 1631 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0019 | 0/0 | 1631 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0020 | 0/0 | 1631 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0021 | 0/0 | 1631 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0022 | 0/0 | 1631 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0023 | 0/0 | 1631 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 4896 | 70 | 12 | 15 | 35 | 2 | 5 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| c0002 | 0/0 | 4896 | 43 | 0 | 11 | 29 | 1 | 2 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| c0003 | 0/0 | 4896 | 25 | 1 | 9 | 7 | 0 | 8 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| c0004 | 0/0 | 4896 | 19 | 3 | 4 | 10 | 1 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| c0005 | 0/0 | 4896 | 15 | 0 | 0 | 12 | 0 | 3 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| c0006 | 0/0 | 4896 | 14 | 10 | 3 | 0 | 1 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| c0007 | 0/0 | 4896 | 12 | 3 | 3 | 2 | 2 | 2 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| c0008 | 0/0 | 4896 | 10 | 4 | 1 | 2 | 0 | 3 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| c0009 | 0/0 | 4896 | 7 | 3 | 1 | 1 | 0 | 2 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| c0010 | 0/0 | 4896 | 6 | 5 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| c0011 | 0/0 | 4896 | 6 | 0 | 3 | 0 | 2 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| c0012 | 0/0 | 4896 | 5 | 4 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| c0013 | 0/0 | 4896 | 5 | 0 | 0 | 0 | 1 | 4 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| c0014 | 0/0 | 4896 | 4 | 2 | 2 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| c0015 | 0/0 | 4896 | 4 | 0 | 0 | 4 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| c0016 | 0/0 | 4896 | 3 | 3 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| c0017 | 0/0 | 4896 | 3 | 0 | 3 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| c0018 | 0/0 | 4896 | 3 | 3 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| c0019 | 0/0 | 4896 | 2 | 0 | 0 | 2 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| c0020 | 0/0 | 4896 | 2 | 0 | 0 | 2 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| c0021 | 0/0 | 4896 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| c0022 | 0/0 | 4896 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| c0023 | 0/0 | 4896 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| c0024 | 0/0 | 4896 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| c0025 | 0/0 | 4896 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| c0026 | 0/0 | 4896 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| c0027 | 0/0 | 4896 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| c0028 | 0/0 | 4896 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| c0029 | 0/0 | 4896 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| c0030 | 0/0 | 4896 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| c0031 | 0/0 | 4896 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| c0032 | 1/0 | 4896 | 1 | 0 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| c0033 | 0/0 | 4896 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| c0034 | 0/0 | 4896 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 2252 | 122 | 22 | 29 | 57 | 3 | 11 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| t0002 | 1/1 | 2252 | 98 | 22 | 18 | 37 | 5 | 14 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| t0003 | 0/0 | 2253 | 26 | 5 | 3 | 11 | 1 | 6 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| t0004 | 0/0 | 2253 | 11 | 5 | 1 | 3 | 1 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| t0005 | 0/0 | 2252 | 3 | 0 | 2 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| t0006 | 0/0 | 2252 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| t0007 | 0/0 | 2253 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| t0008 | 0/0 | 2252 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| t0009 | 0/0 | 2252 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| t0010 | 0/0 | 2252 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| t0011 | 0/0 | 2252 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| t0012 | 0/0 | 2252 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| t0013 | 0/0 | 2252 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| t0014 | 0/0 | 2253 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| t0015 | 0/0 | 2253 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| t0016 | 0/0 | 2252 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| t0017 | 0/0 | 2252 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| 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 | 2 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0052 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0090 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 4896 | 70 | 12 | 15 | 35 | 2 | 5 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0001c0019 | 0/0 | 4896 | 2 | 0 | 0 | 2 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0001c0020 | 0/0 | 4896 | 2 | 0 | 0 | 2 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0001c0021 | 0/0 | 4896 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0001c0032 | 1/0 | 4896 | 1 | 0 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0002c0003 | 0/0 | 4896 | 25 | 1 | 9 | 7 | 0 | 8 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0002c0007 | 0/0 | 4896 | 12 | 3 | 3 | 2 | 2 | 2 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0002c0011 | 0/0 | 4896 | 6 | 0 | 3 | 0 | 2 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0002c0031 | 0/0 | 4896 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0003c0002 | 0/0 | 4896 | 43 | 0 | 11 | 29 | 1 | 2 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0004c0004 | 0/0 | 4896 | 19 | 3 | 4 | 10 | 1 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0004c0013 | 0/0 | 4896 | 5 | 0 | 0 | 0 | 1 | 4 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0004c0027 | 0/0 | 4896 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0005c0005 | 0/0 | 4896 | 15 | 0 | 0 | 12 | 0 | 3 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0006c0006 | 0/0 | 4896 | 14 | 10 | 3 | 0 | 1 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0007c0009 | 0/0 | 4896 | 7 | 3 | 1 | 1 | 0 | 2 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0007c0016 | 0/0 | 4896 | 3 | 3 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0008c0008 | 0/0 | 4896 | 10 | 4 | 1 | 2 | 0 | 3 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0009c0010 | 0/0 | 4896 | 6 | 5 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0009c0030 | 0/0 | 4896 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0010c0012 | 0/0 | 4896 | 5 | 4 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0011c0015 | 0/0 | 4896 | 4 | 0 | 0 | 4 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0012c0014 | 0/0 | 4896 | 4 | 2 | 2 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0013c0018 | 0/0 | 4896 | 3 | 3 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0014c0017 | 0/0 | 4896 | 3 | 0 | 3 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0015c0029 | 0/0 | 4896 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0016c0024 | 0/0 | 4896 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0017c0023 | 0/0 | 4896 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0018c0028 | 0/0 | 4896 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0019c0034 | 0/0 | 4896 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0020c0033 | 0/0 | 4896 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0021c0026 | 0/0 | 4896 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0022c0025 | 0/0 | 4896 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0023c0022 | 0/0 | 4896 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 7147 | 15 | 1 | 4 | 10 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0001c0001t0002 | 0/1 | 7147 | 53 | 11 | 9 | 25 | 2 | 5 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0001c0001t0003 | 0/0 | 7148 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0001c0001t0008 | 0/0 | 7147 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0001c0019t0002 | 0/0 | 7147 | 2 | 0 | 0 | 2 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0001c0020t0002 | 0/0 | 7147 | 2 | 0 | 0 | 2 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0001c0021t0001 | 0/0 | 7147 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0001c0032t0002 | 1/0 | 7147 | 1 | 0 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0002c0003t0001 | 0/0 | 7147 | 20 | 1 | 5 | 7 | 0 | 7 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0002c0003t0002 | 0/0 | 7147 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0002c0003t0005 | 0/0 | 7147 | 3 | 0 | 2 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0002c0003t0011 | 0/0 | 7147 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0002c0007t0001 | 0/0 | 7147 | 2 | 0 | 1 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0002c0007t0003 | 0/0 | 7148 | 6 | 2 | 2 | 0 | 1 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0002c0007t0004 | 0/0 | 7148 | 3 | 0 | 0 | 1 | 1 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0002c0007t0012 | 0/0 | 7147 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0002c0011t0002 | 0/0 | 7147 | 6 | 0 | 3 | 0 | 2 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0002c0031t0002 | 0/0 | 7147 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0003c0002t0001 | 0/0 | 7147 | 37 | 0 | 11 | 23 | 1 | 2 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0003c0002t0002 | 0/0 | 7147 | 5 | 0 | 0 | 5 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0003c0002t0016 | 0/0 | 7147 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0004c0004t0001 | 0/0 | 7147 | 13 | 0 | 4 | 8 | 1 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0004c0004t0002 | 0/0 | 7147 | 2 | 0 | 0 | 1 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0004c0004t0004 | 0/0 | 7148 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0004c0004t0006 | 0/0 | 7147 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0004c0004t0010 | 0/0 | 7147 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0004c0004t0013 | 0/0 | 7147 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0004c0013t0002 | 0/0 | 7147 | 5 | 0 | 0 | 0 | 1 | 4 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0004c0027t0002 | 0/0 | 7147 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0005c0005t0001 | 0/0 | 7147 | 2 | 0 | 0 | 1 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0005c0005t0003 | 0/0 | 7148 | 10 | 0 | 0 | 9 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0005c0005t0004 | 0/0 | 7148 | 2 | 0 | 0 | 2 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0005c0005t0015 | 0/0 | 7148 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0006c0006t0001 | 0/0 | 7147 | 6 | 4 | 1 | 0 | 1 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0006c0006t0002 | 0/0 | 7147 | 8 | 6 | 2 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0007c0009t0001 | 0/0 | 7147 | 5 | 2 | 1 | 1 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0007c0009t0002 | 0/0 | 7147 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0007c0009t0009 | 0/0 | 7147 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0007c0016t0001 | 0/0 | 7147 | 3 | 3 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0008c0008t0001 | 0/0 | 7147 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0008c0008t0002 | 0/0 | 7147 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0008c0008t0003 | 0/0 | 7148 | 7 | 2 | 0 | 2 | 0 | 3 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0008c0008t0004 | 0/0 | 7148 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0009c0010t0001 | 0/0 | 7147 | 3 | 3 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0009c0010t0002 | 0/0 | 7147 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0009c0010t0003 | 0/0 | 7148 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0009c0010t0017 | 0/0 | 7147 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0009c0030t0001 | 0/0 | 7147 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0010c0012t0001 | 0/0 | 7147 | 4 | 3 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0010c0012t0002 | 0/0 | 7147 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0011c0015t0001 | 0/0 | 7147 | 4 | 0 | 0 | 4 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0012c0014t0001 | 0/0 | 7147 | 2 | 2 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0012c0014t0007 | 0/0 | 7148 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0012c0014t0014 | 0/0 | 7148 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0013c0018t0004 | 0/0 | 7148 | 3 | 3 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0014c0017t0002 | 0/0 | 7147 | 3 | 0 | 3 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0015c0029t0001 | 0/0 | 7147 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0016c0024t0002 | 0/0 | 7147 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0017c0023t0002 | 0/0 | 7147 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0018c0028t0004 | 0/0 | 7148 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0019c0034t0002 | 0/0 | 7147 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0020c0033t0002 | 0/0 | 7147 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0021c0026t0001 | 0/0 | 7147 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0022c0025t0003 | 0/0 | 7148 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| a0023c0022t0001 | 0/0 | 7147 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | copy fasta | chr13 | 75631330 | 75864866 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0002g0052 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0001t0008g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0019t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0019t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0020t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0020t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0021t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0001c0032t0002g0090 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0002c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0002c0003t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0002c0003t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0002c0003t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0002c0003t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0002c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0002c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0002c0003t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0002c0003t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0002c0003t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0002c0003t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0002c0003t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0002c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0002c0003t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0002c0003t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0002c0003t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0002c0003t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0002c0003t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0002c0003t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0002c0003t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0002c0003t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0002c0003t0005g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0002c0003t0005g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0002c0003t0005g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0002c0003t0011g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0002c0007t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0002c0007t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0002c0007t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0002c0007t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0002c0007t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0002c0007t0003g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0002c0007t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0002c0007t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0002c0007t0004g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0002c0007t0004g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0002c0007t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0002c0007t0012g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0002c0011t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0002c0011t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0002c0011t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0002c0011t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0002c0011t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0002c0011t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0002c0031t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0003c0002t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0003c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0003c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0003c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0003c0002t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0003c0002t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0003c0002t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0003c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0003c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0003c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0003c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0003c0002t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0003c0002t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0003c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0003c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0003c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0003c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0003c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0003c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0003c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0003c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0003c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0003c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0003c0002t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0003c0002t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0003c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0003c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0003c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0003c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0003c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0003c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0003c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0003c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0003c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0003c0002t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0003c0002t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0003c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0003c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0003c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0003c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0003c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0003c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0003c0002t0016g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0004c0004t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0004c0004t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0004c0004t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0004c0004t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0004c0004t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0004c0004t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0004c0004t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0004c0004t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0004c0004t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0004c0004t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0004c0004t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0004c0004t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0004c0004t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0004c0004t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0004c0004t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0004c0004t0004g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0004c0004t0006g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0004c0004t0010g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0004c0004t0013g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0004c0013t0002g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0004c0013t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0004c0013t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0004c0013t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0004c0013t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0004c0027t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0005c0005t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0005c0005t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0005c0005t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0005c0005t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0005c0005t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0005c0005t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0005c0005t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0005c0005t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0005c0005t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0005c0005t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0005c0005t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0005c0005t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0005c0005t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0005c0005t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0005c0005t0015g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0006c0006t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0006c0006t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0006c0006t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0006c0006t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0006c0006t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0006c0006t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0006c0006t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0006c0006t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0006c0006t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0006c0006t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0006c0006t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0006c0006t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0006c0006t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0006c0006t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0007c0009t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0007c0009t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0007c0009t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0007c0009t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0007c0009t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0007c0009t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0007c0009t0009g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0007c0016t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0007c0016t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0008c0008t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0008c0008t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0008c0008t0003g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0008c0008t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0008c0008t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0008c0008t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0008c0008t0003g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0008c0008t0003g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0008c0008t0003g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0008c0008t0004g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0009c0010t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0009c0010t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0009c0010t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0009c0010t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0009c0010t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0009c0010t0017g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0009c0030t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0010c0012t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0010c0012t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0010c0012t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0010c0012t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0010c0012t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0011c0015t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0011c0015t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0011c0015t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0011c0015t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0012c0014t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0012c0014t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0012c0014t0007g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0012c0014t0014g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0013c0018t0004g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0013c0018t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0013c0018t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0014c0017t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0014c0017t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0014c0017t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0015c0029t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0016c0024t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0017c0023t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0018c0028t0004g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0019c0034t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0020c0033t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0021c0026t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0022c0025t0003g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| a0023c0022t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0085 | EUR | GBR | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG00099 | hp2 | a0002 | c0011 | t0002 | g0084 | EUR | GBR | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG00140 | hp1 | a0002 | c0011 | t0002 | g0075 | EUR | GBR | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG00140 | hp2 | a0006 | c0006 | t0001 | g0183 | EUR | GBR | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG00280 | hp1 | a0003 | c0002 | t0001 | g0141 | EUR | FIN | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0053 | EUR | FIN | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG00438 | hp1 | a0002 | c0003 | t0001 | g0146 | EAS | CHS | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG00438 | hp2 | a0003 | c0002 | t0001 | g0224 | EAS | CHS | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | CHS | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG00621 | hp1 | a0001 | c0020 | t0002 | g0269 | EAS | CHS | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG00621 | hp2 | a0003 | c0002 | t0002 | g0270 | EAS | CHS | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG00639 | hp1 | a0002 | c0007 | t0003 | g0178 | AMR | PUR | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG00639 | hp2 | a0018 | c0028 | t0004 | g0133 | AMR | PUR | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG00673 | hp1 | a0002 | c0003 | t0001 | g0256 | EAS | CHS | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG00673 | hp2 | a0001 | c0019 | t0002 | g0267 | EAS | CHS | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG00735 | hp1 | a0009 | c0010 | t0017 | g0004 | AMR | PUR | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0082 | AMR | PUR | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG00738 | hp2 | a0002 | c0011 | t0002 | g0076 | AMR | PUR | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG01070 | hp1 | a0003 | c0002 | t0001 | g0158 | AMR | PUR | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG01070 | hp2 | a0004 | c0004 | t0001 | g0232 | AMR | PUR | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG01081 | hp1 | a0012 | c0014 | t0014 | g0185 | AMR | PUR | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG01081 | hp2 | a0007 | c0009 | t0001 | g0152 | AMR | PUR | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG01099 | hp1 | a0002 | c0003 | t0005 | g0070 | AMR | PUR | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0099 | AMR | PUR | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG01106 | hp1 | a0002 | c0003 | t0001 | g0192 | AMR | PUR | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG01106 | hp2 | a0006 | c0006 | t0002 | g0095 | AMR | PUR | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG01109 | hp1 | a0006 | c0006 | t0001 | g0132 | AMR | PUR | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG01109 | hp2 | a0003 | c0002 | t0001 | g0179 | AMR | PUR | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG01167 | hp1 | a0014 | c0017 | t0002 | g0027 | AMR | PUR | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG01167 | hp2 | a0003 | c0002 | t0001 | g0216 | AMR | PUR | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG01168 | hp1 | a0002 | c0003 | t0001 | g0139 | AMR | PUR | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG01168 | hp2 | a0002 | c0011 | t0002 | g0031 | AMR | PUR | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG01169 | hp1 | a0014 | c0017 | t0002 | g0028 | AMR | PUR | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG01169 | hp2 | a0002 | c0003 | t0001 | g0138 | AMR | PUR | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG01175 | hp1 | a0003 | c0002 | t0001 | g0215 | AMR | PUR | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG01175 | hp2 | a0002 | c0003 | t0001 | g0126 | AMR | PUR | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG01192 | hp1 | a0001 | c0001 | t0008 | g0044 | AMR | PUR | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG01192 | hp2 | a0004 | c0004 | t0001 | g0235 | AMR | PUR | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG01243 | hp1 | a0008 | c0008 | t0001 | g0089 | AMR | PUR | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG01255 | hp1 | a0012 | c0014 | t0007 | g0049 | AMR | CLM | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG01255 | hp2 | a0003 | c0002 | t0001 | g0237 | AMR | CLM | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG01256 | hp1 | a0006 | c0006 | t0002 | g0097 | AMR | CLM | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0045 | AMR | CLM | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG01257 | hp1 | a0002 | c0003 | t0005 | g0030 | AMR | CLM | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG01261 | hp1 | a0002 | c0007 | t0003 | g0181 | AMR | CLM | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG01346 | hp1 | a0002 | c0003 | t0011 | g0161 | AMR | CLM | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG01361 | hp1 | a0002 | c0003 | t0001 | g0137 | AMR | CLM | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG01361 | hp2 | a0004 | c0004 | t0001 | g0236 | AMR | CLM | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG01433 | hp1 | a0014 | c0017 | t0002 | g0037 | AMR | CLM | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG01433 | hp2 | a0003 | c0002 | t0001 | g0157 | AMR | CLM | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG01496 | hp1 | a0002 | c0011 | t0002 | g0038 | AMR | CLM | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0078 | AMR | CLM | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG01515 | hp1 | a0004 | c0004 | t0001 | g0120 | EUR | IBS | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG01515 | hp2 | a0002 | c0007 | t0004 | g0260 | EUR | IBS | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG01884 | hp1 | a0004 | c0027 | t0002 | g0092 | AFR | ACB | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0107 | AFR | ACB | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG01891 | hp1 | a0007 | c0009 | t0001 | g0165 | AFR | ACB | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG01891 | hp2 | a0010 | c0012 | t0001 | g0247 | AFR | ACB | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG01928 | hp1 | a0003 | c0002 | t0001 | g0195 | AMR | PEL | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0065 | AMR | PEL | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG01952 | hp1 | a0003 | c0002 | t0001 | g0191 | AMR | PEL | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG01952 | hp2 | a0002 | c0007 | t0001 | g0129 | AMR | PEL | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG01981 | hp1 | a0010 | c0012 | t0001 | g0140 | AMR | PEL | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG01981 | hp2 | a0002 | c0003 | t0002 | g0134 | AMR | PEL | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG01993 | hp1 | a0003 | c0002 | t0001 | g0217 | AMR | PEL | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PEL | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG02040 | hp1 | a0002 | c0003 | t0001 | g0257 | EAS | KHV | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG02040 | hp2 | a0003 | c0002 | t0001 | g0204 | EAS | KHV | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | KHV | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG02056 | hp2 | a0003 | c0002 | t0001 | g0222 | EAS | KHV | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | KHV | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG02074 | hp2 | a0002 | c0007 | t0001 | g0234 | EAS | KHV | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | KHV | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG02129 | hp2 | a0003 | c0002 | t0001 | g0205 | EAS | KHV | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG02132 | hp1 | a0003 | c0002 | t0002 | g0266 | EAS | KHV | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | KHV | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG02135 | hp1 | a0003 | c0002 | t0001 | g0194 | EAS | KHV | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG02135 | hp2 | a0007 | c0009 | t0001 | g0163 | EAS | KHV | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CDX | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG02165 | hp2 | a0003 | c0002 | t0016 | g0223 | EAS | CDX | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG02258 | hp1 | a0002 | c0007 | t0012 | g0156 | AFR | ACB | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0088 | AFR | ACB | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG02273 | hp1 | a0004 | c0004 | t0001 | g0231 | AMR | PEL | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0063 | AMR | PEL | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0083 | AFR | ACB | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG02280 | hp2 | a0002 | c0003 | t0001 | g0203 | AFR | ACB | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0265 | AMR | PEL | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG02293 | hp2 | a0003 | c0002 | t0001 | g0196 | AMR | PEL | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG02451 | hp1 | a0004 | c0004 | t0004 | g0081 | AFR | ACB | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | KHV | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG02523 | hp2 | a0005 | c0005 | t0003 | g0254 | EAS | KHV | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0048 | AFR | GWD | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG02647 | hp2 | a0006 | c0006 | t0002 | g0094 | AFR | GWD | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG02698 | hp1 | a0019 | c0034 | t0002 | g0073 | SAS | PJL | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG02698 | hp2 | a0005 | c0005 | t0003 | g0115 | SAS | PJL | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG02723 | hp1 | a0006 | c0006 | t0002 | g0102 | AFR | GWD | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG02723 | hp2 | a0013 | c0018 | t0004 | g0011 | AFR | GWD | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG02735 | hp1 | a0004 | c0013 | t0002 | g0019 | SAS | PJL | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG02735 | hp2 | a0002 | c0003 | t0001 | g0211 | SAS | PJL | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG02809 | hp1 | a0015 | c0029 | t0001 | g0118 | AFR | GWD | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG02809 | hp2 | a0009 | c0030 | t0001 | g0170 | AFR | GWD | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG02818 | hp1 | a0004 | c0004 | t0006 | g0103 | AFR | GWD | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG02818 | hp2 | a0012 | c0014 | t0001 | g0002 | AFR | GWD | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG02895 | hp1 | a0007 | c0016 | t0001 | g0001 | AFR | GWD | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG02895 | hp2 | a0012 | c0014 | t0001 | g0003 | AFR | GWD | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG02896 | hp1 | a0006 | c0006 | t0001 | g0175 | AFR | GWD | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG02896 | hp2 | a0013 | c0018 | t0004 | g0010 | AFR | GWD | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG02897 | hp1 | a0006 | c0006 | t0001 | g0174 | AFR | GWD | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG02897 | hp2 | a0007 | c0016 | t0001 | g0001 | AFR | GWD | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0106 | AFR | ESN | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG02922 | hp2 | a0008 | c0008 | t0003 | g0111 | AFR | ESN | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG02970 | hp1 | a0004 | c0004 | t0010 | g0119 | AFR | ESN | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG02970 | hp2 | a0008 | c0008 | t0004 | g0087 | AFR | ESN | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG03017 | hp1 | a0005 | c0005 | t0015 | g0171 | SAS | PJL | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG03017 | hp2 | a0007 | c0009 | t0002 | g0067 | SAS | PJL | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | GWD | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG03041 | hp2 | a0007 | c0009 | t0009 | g0251 | AFR | GWD | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG03098 | hp1 | a0006 | c0006 | t0001 | g0172 | AFR | MSL | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG03098 | hp2 | a0009 | c0010 | t0001 | g0250 | AFR | MSL | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG03139 | hp1 | a0010 | c0012 | t0002 | g0105 | AFR | ESN | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG03139 | hp2 | a0007 | c0009 | t0001 | g0166 | AFR | ESN | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG03195 | hp1 | a0008 | c0008 | t0002 | g0077 | AFR | ESN | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG03195 | hp2 | a0007 | c0016 | t0001 | g0252 | AFR | ESN | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG03225 | hp1 | a0006 | c0006 | t0002 | g0108 | AFR | MSL | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG03225 | hp2 | a0013 | c0018 | t0004 | g0056 | AFR | MSL | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG03486 | hp1 | a0006 | c0006 | t0002 | g0096 | AFR | MSL | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG03486 | hp2 | a0009 | c0010 | t0001 | g0249 | AFR | MSL | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG03490 | hp1 | a0004 | c0013 | t0002 | g0059 | SAS | PJL | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG03490 | hp2 | a0002 | c0007 | t0004 | g0098 | SAS | PJL | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG03491 | hp1 | a0002 | c0003 | t0001 | g0238 | SAS | PJL | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0020 | SAS | PJL | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG03492 | hp1 | a0004 | c0013 | t0002 | g0061 | SAS | PJL | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0062 | SAS | PJL | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG03579 | hp1 | a0009 | c0010 | t0003 | g0244 | AFR | MSL | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG03579 | hp2 | a0002 | c0007 | t0003 | g0246 | AFR | MSL | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0036 | SAS | PJL | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG03654 | hp2 | a0002 | c0003 | t0001 | g0154 | SAS | PJL | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG03669 | hp1 | a0008 | c0008 | t0003 | g0169 | SAS | PJL | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG03669 | hp2 | a0002 | c0007 | t0003 | g0176 | SAS | PJL | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG03704 | hp1 | a0008 | c0008 | t0003 | g0168 | SAS | PJL | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG03704 | hp2 | a0002 | c0003 | t0005 | g0033 | SAS | PJL | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG03710 | hp1 | a0007 | c0009 | t0001 | g0162 | SAS | PJL | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG03710 | hp2 | a0002 | c0003 | t0001 | g0239 | SAS | PJL | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG03831 | hp1 | a0002 | c0003 | t0001 | g0121 | SAS | BEB | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG03831 | hp2 | a0005 | c0005 | t0001 | g0125 | SAS | BEB | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG03834 | hp1 | a0003 | c0002 | t0001 | g0213 | SAS | BEB | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG03834 | hp2 | a0004 | c0004 | t0002 | g0060 | SAS | BEB | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | BEB | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG03927 | hp2 | a0002 | c0003 | t0001 | g0220 | SAS | BEB | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG03942 | hp1 | a0003 | c0002 | t0001 | g0212 | SAS | BEB | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG03942 | hp2 | a0020 | c0033 | t0002 | g0074 | SAS | BEB | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG04184 | hp1 | a0004 | c0013 | t0002 | g0057 | SAS | BEB | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG04184 | hp2 | a0002 | c0003 | t0001 | g0240 | SAS | BEB | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0016 | SAS | STU | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG04199 | hp2 | a0008 | c0008 | t0003 | g0241 | SAS | STU | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0079 | AFR | YRI | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA18522 | hp2 | a0008 | c0008 | t0003 | g0160 | AFR | YRI | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA18747 | hp1 | a0003 | c0002 | t0001 | g0219 | EAS | CHB | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA18747 | hp2 | a0002 | c0003 | t0001 | g0259 | EAS | CHB | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA18906 | hp1 | a0006 | c0006 | t0002 | g0093 | AFR | YRI | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA18906 | hp2 | a0006 | c0006 | t0001 | g0245 | AFR | YRI | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA18940 | hp2 | a0005 | c0005 | t0004 | g0264 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA18941 | hp2 | a0011 | c0015 | t0001 | g0197 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA18942 | hp2 | a0005 | c0005 | t0003 | g0127 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA18944 | hp2 | a0005 | c0005 | t0003 | g0164 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA18946 | hp1 | a0003 | c0002 | t0001 | g0229 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA18949 | hp1 | a0002 | c0003 | t0001 | g0253 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA18949 | hp2 | a0004 | c0004 | t0001 | g0188 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA18951 | hp2 | a0005 | c0005 | t0003 | g0144 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA18953 | hp1 | a0003 | c0002 | t0001 | g0243 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA18954 | hp2 | a0004 | c0004 | t0001 | g0187 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA18960 | hp1 | a0001 | c0020 | t0002 | g0271 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA18960 | hp2 | a0003 | c0002 | t0002 | g0046 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA18965 | hp1 | a0016 | c0024 | t0002 | g0086 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA18969 | hp1 | a0005 | c0005 | t0003 | g0112 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA18969 | hp2 | a0004 | c0004 | t0001 | g0199 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA18970 | hp1 | a0003 | c0002 | t0001 | g0142 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA18979 | hp1 | a0003 | c0002 | t0001 | g0214 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA18980 | hp2 | a0003 | c0002 | t0001 | g0226 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA18983 | hp1 | a0002 | c0003 | t0001 | g0258 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA18983 | hp2 | a0001 | c0019 | t0002 | g0268 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA18986 | hp1 | a0023 | c0022 | t0001 | g0136 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA18986 | hp2 | a0011 | c0015 | t0001 | g0242 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA18987 | hp1 | a0003 | c0002 | t0002 | g0064 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA18987 | hp2 | a0002 | c0007 | t0004 | g0261 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA18990 | hp1 | a0003 | c0002 | t0001 | g0209 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA18990 | hp2 | a0021 | c0026 | t0001 | g0122 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA18993 | hp1 | a0005 | c0005 | t0003 | g0128 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA18998 | hp2 | a0003 | c0002 | t0001 | g0206 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA18999 | hp1 | a0004 | c0004 | t0001 | g0190 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA19001 | hp2 | a0005 | c0005 | t0003 | g0124 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA19003 | hp2 | a0003 | c0002 | t0001 | g0225 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA19005 | hp1 | a0017 | c0023 | t0002 | g0050 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA19007 | hp1 | a0005 | c0005 | t0004 | g0263 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA19007 | hp2 | a0004 | c0004 | t0001 | g0148 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA19011 | hp2 | a0003 | c0002 | t0002 | g0262 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA19012 | hp2 | a0003 | c0002 | t0001 | g0227 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA19043 | hp1 | a0002 | c0007 | t0003 | g0173 | AFR | LWK | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0047 | AFR | LWK | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA19054 | hp1 | a0004 | c0004 | t0013 | g0189 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA19054 | hp2 | a0008 | c0008 | t0003 | g0110 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA19055 | hp1 | a0005 | c0005 | t0001 | g0114 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA19055 | hp2 | a0003 | c0002 | t0001 | g0200 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA19056 | hp1 | a0003 | c0002 | t0001 | g0198 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA19057 | hp1 | a0003 | c0002 | t0001 | g0228 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA19057 | hp2 | a0004 | c0004 | t0001 | g0149 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA19058 | hp1 | a0003 | c0002 | t0001 | g0186 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA19060 | hp1 | a0003 | c0002 | t0001 | g0193 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA19060 | hp2 | a0002 | c0003 | t0001 | g0255 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA19063 | hp1 | a0003 | c0002 | t0001 | g0230 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA19065 | hp1 | a0005 | c0005 | t0003 | g0145 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA19065 | hp2 | a0004 | c0004 | t0002 | g0032 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA19070 | hp2 | a0005 | c0005 | t0003 | g0147 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA19076 | hp1 | a0003 | c0002 | t0001 | g0123 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA19077 | hp1 | a0003 | c0002 | t0001 | g0006 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA19077 | hp2 | a0011 | c0015 | t0001 | g0221 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA19082 | hp1 | a0008 | c0008 | t0003 | g0005 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA19082 | hp2 | a0004 | c0004 | t0001 | g0202 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA19085 | hp2 | a0004 | c0004 | t0001 | g0210 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA19091 | hp2 | a0011 | c0015 | t0001 | g0155 | EAS | JPT | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA20129 | hp1 | a0010 | c0012 | t0001 | g0130 | AFR | ASW | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0080 | AFR | ASW | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA20752 | hp1 | a0002 | c0007 | t0003 | g0180 | EUR | TSI | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA20752 | hp2 | a0004 | c0013 | t0002 | g0104 | EUR | TSI | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA20905 | hp1 | a0002 | c0011 | t0002 | g0071 | SAS | GIH | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA20905 | hp2 | a0022 | c0025 | t0003 | g0177 | SAS | GIH | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG01123 | hp1 | a0003 | c0002 | t0001 | g0233 | AMR | CLM | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0153 | AMR | CLM | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG02559 | hp1 | a0002 | c0031 | t0002 | g0091 | AFR | ACB | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | ACB | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG06807 | hp1 | a0010 | c0012 | t0001 | g0131 | AFR | USA | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| HG06807 | hp2 | a0009 | c0010 | t0002 | g0015 | AFR | USA | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0101 | AFR | USA | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA20300 | hp2 | a0009 | c0010 | t0001 | g0248 | AFR | USA | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA21309 | hp1 | a0006 | c0006 | t0002 | g0100 | AFR | LWK | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| NA21309 | hp2 | a0001 | c0021 | t0001 | g0182 | AFR | LWK | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0052 | REF | REF | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| homoSapiens_grch38 | hp1 | a0001 | c0032 | t0002 | g0090 | REF | REF | LMO7_chr13_75631330_75864866 | LMO7 | chr13 | 75631330 | 75864866 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:75800870
|
G | C | 1 | a0008 | 10 | HG01243.hp1 HG02922.hp2 HG02970.hp2 others(7): Show |
missense_variant | MODERATE | c.649G>C | p.Gly217Arg | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 7/31 | 977/7147 | 649/4896 | 217/1631 | chr13 | 75800870 | ||
| chr13:75804355
|
C | T | 1 | a0015 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.728C>T | p.Ser243Leu | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 8/31 | 1056/7147 | 728/4896 | 243/1631 | chr13 | 75804355 | ||
| chr13:75805660
|
G | A | 1 | a0023 | 1 | NA18986.hp1 | missense_variant | MODERATE | c.1096G>A | p.Asp366Asn | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 9/31 | 1424/7147 | 1096/4896 | 366/1631 | chr13 | 75805660 | ||
| chr13:75807893
|
G | A | 2 | a0016a0017 | 2 | NA18965.hp1 NA19005.hp1 |
missense_variant | MODERATE | c.1610G>A | p.Arg537Lys | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 10/31 | 1938/7147 | 1610/4896 | 537/1631 | chr13 | 75807893 | ||
| chr13:75807964
|
C | T | 2 | a0003a0018 | 44 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(41): Show |
missense_variant | MODERATE | c.1681C>T | p.Leu561Phe | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 10/31 | 2009/7147 | 1681/4896 | 561/1631 | chr13 | 75807964 | ||
| chr13:75821206
|
C | T | 1 | a0005 | 15 | HG02523.hp2 HG02698.hp2 HG03017.hp1 others(12): Show |
missense_variant | MODERATE | c.2237C>T | p.Pro746Leu | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 14/31 | 2565/7147 | 2237/4896 | 746/1631 | chr13 | 75821206 | ||
| chr13:75821328
|
C | T | 3 | a0007a0016a0017 | 12 | HG01081.hp2 HG01891.hp1 HG02135.hp2 others(9): Show |
missense_variant | MODERATE | c.2359C>T | p.Pro787Ser | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 14/31 | 2687/7147 | 2359/4896 | 787/1631 | chr13 | 75821328 | ||
| chr13:75821484
|
C | T | 5 | a0004a0011a0013others(2): Show | 34 | HG01070.hp2 HG01192.hp2 HG01361.hp2 others(31): Show |
missense_variant | MODERATE | c.2515C>T | p.Arg839Cys | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 14/31 | 2843/7147 | 2515/4896 | 839/1631 | chr13 | 75821484 | ||
| chr13:75823574
|
G | A | 1 | a0014 | 3 | HG01167.hp1 HG01169.hp1 HG01433.hp1 |
missense_variant | MODERATE | c.2650G>A | p.Ala884Thr | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/31 | 2978/7147 | 2650/4896 | 884/1631 | chr13 | 75823574 | ||
| chr13:75823595
|
G | A | 12 | a0004a0005a0006others(9): Show | 90 | HG00140.hp2 HG00735.hp1 HG01070.hp2 others(87): Show |
missense_variant | MODERATE | c.2671G>A | p.Val891Ile | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/31 | 2999/7147 | 2671/4896 | 891/1631 | chr13 | 75823595 | ||
| chr13:75823650
|
C | T | 1 | a0018 | 1 | HG00639.hp2 | missense_variant | MODERATE | c.2726C>T | p.Pro909Leu | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/31 | 3054/7147 | 2726/4896 | 909/1631 | chr13 | 75823650 | ||
| chr13:75834235
|
C | A | 1 | a0022 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.3074C>A | p.Ala1025Glu | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 17/31 | 3402/7147 | 3074/4896 | 1025/1631 | chr13 | 75834235 | ||
| chr13:75840433
|
G | C | 2 | a0019a0020 | 2 | HG02698.hp1 HG03942.hp2 |
missense_variant | MODERATE | c.3520G>C | p.Asp1174His | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 22/31 | 3848/7147 | 3520/4896 | 1174/1631 | chr13 | 75840433 | ||
| chr13:75841898
|
G | A | 1 | a0017 | 1 | NA19005.hp1 | missense_variant | MODERATE | c.3946G>A | p.Glu1316Lys | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 24/31 | 4274/7147 | 3946/4896 | 1316/1631 | chr13 | 75841898 | ||
| chr13:75841932
|
G | A | 1 | a0013 | 3 | HG02723.hp2 HG02896.hp2 HG03225.hp2 |
missense_variant | MODERATE | c.3980G>A | p.Arg1327His | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 24/31 | 4308/7147 | 3980/4896 | 1327/1631 | chr13 | 75841932 | ||
| chr13:75849112
|
T | C | 19 | a0002a0003a0004others(16): Show | 191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
missense_variant | MODERATE | c.4184T>C | p.Met1395Thr | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 27/31 | 4512/7147 | 4184/4896 | 1395/1631 | chr13 | 75849112 | ||
| chr13:75849215
|
C | A | 1 | a0021 | 1 | NA18990.hp2 | missense_variant | MODERATE | c.4287C>A | p.His1429Gln | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 27/31 | 4615/7147 | 4287/4896 | 1429/1631 | chr13 | 75849215 | ||
| chr13:75853211
|
C | A | 3 | a0006a0009a0010 | 26 | HG00140.hp2 HG00735.hp1 HG01106.hp2 others(23): Show |
missense_variant | MODERATE | c.4484C>A | p.Pro1495Gln | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 28/31 | 4812/7147 | 4484/4896 | 1495/1631 | chr13 | 75853211 | ||
| chr13:75853267
|
G | A | 1 | a0006 | 14 | HG00140.hp2 HG01106.hp2 HG01109.hp1 others(11): Show |
missense_variant | MODERATE | c.4540G>A | p.Val1514Met | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 28/31 | 4868/7147 | 4540/4896 | 1514/1631 | chr13 | 75853267 | ||
| chr13:75853274
|
C | G | 2 | a0006a0010 | 19 | HG00140.hp2 HG01106.hp2 HG01109.hp1 others(16): Show |
missense_variant | MODERATE | c.4547C>G | p.Pro1516Arg | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 28/31 | 4875/7147 | 4547/4896 | 1516/1631 | chr13 | 75853274 | ||
| chr13:75855277
|
G | A | 1 | a0011 | 4 | NA18941.hp2 NA18986.hp2 NA19077.hp2 others(1): Show |
missense_variant | MODERATE | c.4679G>A | p.Arg1560His | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 29/31 | 5007/7147 | 4679/4896 | 1560/1631 | chr13 | 75855277 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:75760973
|
A | G | 4 | a0002c0011a0004c0013a0019c0034others(1): Show | 13 | HG00099.hp2 HG00140.hp1 HG00738.hp2 others(10): Show |
synonymous_variant | LOW | c.252A>G | p.Gly84Gly | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/31 | 580/7147 | 252/4896 | 84/1631 | chr13 | 75760973 | ||
| chr13:75796701
|
T | C | 1 | a0007c0016 | 3 | HG02895.hp1 HG02897.hp2 HG03195.hp2 |
synonymous_variant | LOW | c.414T>C | p.His138His | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 6/31 | 742/7147 | 414/4896 | 138/1631 | chr13 | 75796701 | ||
| chr13:75804311
|
G | A | 1 | a0001c0021 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.684G>A | p.Ser228Ser | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 8/31 | 1012/7147 | 684/4896 | 228/1631 | chr13 | 75804311 | ||
| chr13:75804323
|
T | C | 30 | a0001c0001a0001c0019a0001c0020others(27): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
synonymous_variant | LOW | c.696T>C | p.Phe232Phe | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 8/31 | 1024/7147 | 696/4896 | 232/1631 | chr13 | 75804323 | ||
| chr13:75834302
|
C | T | 1 | a0007c0016 | 3 | HG02895.hp1 HG02897.hp2 HG03195.hp2 |
synonymous_variant | LOW | c.3141C>T | p.Asn1047Asn | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 17/31 | 3469/7147 | 3141/4896 | 1047/1631 | chr13 | 75834302 | ||
| chr13:75835300
|
A | G | 7 | a0002c0003a0002c0011a0004c0027others(4): Show | 44 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(41): Show |
synonymous_variant | LOW | c.3294A>G | p.Leu1098Leu | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 18/31 | 3622/7147 | 3294/4896 | 1098/1631 | chr13 | 75835300 | ||
| chr13:75856529
|
C | T | 1 | a0001c0020 | 2 | HG00621.hp1 NA18960.hp1 |
synonymous_variant | LOW | c.4794C>T | p.Leu1598Leu | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 30/31 | 5122/7147 | 4794/4896 | 1598/1631 | chr13 | 75856529 | ||
| chr13:75857934
|
C | T | 1 | a0001c0019 | 2 | HG00673.hp2 NA18983.hp2 |
synonymous_variant | LOW | c.4887C>T | p.Thr1629Thr | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 31/31 | 5215/7147 | 4887/4896 | 1629/1631 | chr13 | 75857934 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:75636570
|
C | T | 1 | a0009c0010t0017 | 1 | HG00735.hp1 | 5_prime_UTR_variant | MODIFIER | c.-88C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/31 | 88 | chr13 | 75636570 | |||||
| chr13:75636581
|
C | T | 1 | a0003c0002t0016 | 1 | HG02165.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-77C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/31 | chr13 | 75636581 | ||||||
| chr13:75636606
|
A | C | 34 | a0001c0001t0001a0001c0001t0003a0001c0021t0001others(31): Show | 157 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(154): Show |
5_prime_UTR_variant | MODIFIER | c.-52A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/31 | 52 | chr13 | 75636606 | |||||
| chr13:75858037
|
C | CT | 15 | a0001c0001t0003a0002c0007t0003a0002c0007t0004others(12): Show | 40 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*103dupT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 31/31 | 104 | INFO_REALIGN_3_PRIME | chr13 | 75858037 | ||||
| chr13:75858046
|
T | A | 1 | a0007c0009t0009 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*103T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 31/31 | 103 | chr13 | 75858046 | |||||
| chr13:75858047
|
A | T | 2 | a0001c0001t0008a0005c0005t0015 | 2 | HG01192.hp1 HG03017.hp1 |
3_prime_UTR_variant | MODIFIER | c.*104A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 31/31 | 104 | chr13 | 75858047 | |||||
| chr13:75858137
|
G | A | 2 | a0004c0004t0006a0004c0004t0010 | 2 | HG02818.hp1 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*194G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 31/31 | 194 | chr13 | 75858137 | |||||
| chr13:75858298
|
A | T | 1 | a0004c0004t0013 | 1 | NA19054.hp1 | 3_prime_UTR_variant | MODIFIER | c.*355A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 31/31 | 355 | chr13 | 75858298 | |||||
| chr13:75858636
|
C | T | 2 | a0012c0014t0007a0012c0014t0014 | 2 | HG01081.hp1 HG01255.hp1 |
3_prime_UTR_variant | MODIFIER | c.*693C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 31/31 | 693 | chr13 | 75858636 | |||||
| chr13:75859451
|
T | G | 2 | a0002c0003t0005a0002c0003t0011 | 4 | HG01099.hp1 HG01257.hp1 HG01346.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1508T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 31/31 | 1508 | chr13 | 75859451 | |||||
| chr13:75859722
|
C | T | 1 | a0002c0007t0012 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1779C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 31/31 | 1779 | chr13 | 75859722 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:75636754
|
C | T | 12 | a0001c0001t0002g0265a0001c0019t0002g0267a0001c0019t0002g0268others(9): Show | 12 | HG00621.hp1 HG00621.hp2 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.69+28C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75636754 | ||||||
| chr13:75636854
|
C | T | 7 | a0002c0003t0001g0253a0002c0003t0001g0255a0002c0003t0001g0256others(4): Show | 7 | HG00673.hp1 HG02040.hp1 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.69+128C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75636854 | ||||||
| chr13:75636916
|
G | A | 3 | a0009c0010t0017g0004a0012c0014t0001g0002a0012c0014t0001g0003 | 3 | HG00735.hp1 HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.69+190G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75636916 | ||||||
| chr13:75636927
|
C | A | 2 | a0012c0014t0001g0002a0012c0014t0001g0003 | 2 | HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.69+201C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75636927 | ||||||
| chr13:75636995
|
C | G | 10 | a0002c0007t0003g0246a0006c0006t0001g0245a0007c0009t0009g0251others(7): Show | 11 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.69+269C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75636995 | ||||||
| chr13:75637102
|
G | A | 2 | a0003c0002t0001g0006a0008c0008t0003g0005 | 2 | NA19077.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.69+376G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75637102 | ||||||
| chr13:75637179
|
G | C | 3 | a0009c0010t0017g0004a0012c0014t0001g0002a0012c0014t0001g0003 | 3 | HG00735.hp1 HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.69+453G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75637179 | ||||||
| chr13:75637317
|
G | T | 68 | a0001c0001t0001g0184a0001c0001t0001g0201a0001c0001t0001g0207others(65): Show | 68 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.69+591G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75637317 | ||||||
| chr13:75637352
|
T | G | 10 | a0001c0001t0001g0184a0001c0021t0001g0182a0002c0007t0003g0176others(7): Show | 10 | HG00140.hp2 HG00639.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.69+626T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75637352 | ||||||
| chr13:75637487
|
C | A | 94 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(91): Show | 94 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(91): Show |
intron_variant | MODIFIER | c.69+761C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75637487 | ||||||
| chr13:75637860
|
A | G | 76 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(73): Show | 76 | HG00280.hp1 HG00438.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.69+1134A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75637860 | ||||||
| chr13:75638413
|
T | A | 11 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(8): Show | 11 | HG02698.hp2 HG02809.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.69+1687T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75638413 | ||||||
| chr13:75638535
|
C | T | 2 | a0006c0006t0001g0174a0006c0006t0001g0175 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.69+1809C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75638535 | ||||||
| chr13:75638659
|
T | G | 77 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(74): Show | 77 | HG00280.hp1 HG00438.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.69+1933T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75638659 | ||||||
| chr13:75639047
|
C | T | 10 | a0002c0007t0003g0246a0006c0006t0001g0245a0007c0009t0009g0251others(7): Show | 11 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.69+2321C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75639047 | ||||||
| chr13:75639395
|
C | T | 68 | a0001c0001t0001g0184a0001c0001t0001g0201a0001c0001t0001g0207others(65): Show | 68 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.69+2669C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75639395 | ||||||
| chr13:75639413
|
G | C | 77 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(74): Show | 77 | HG00280.hp1 HG00438.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.69+2687G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75639413 | ||||||
| chr13:75639499
|
A | C | 1 | a0002c0007t0003g0173 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.69+2773A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75639499 | ||||||
| chr13:75639507
|
C | G | 158 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(155): Show | 159 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.69+2781C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75639507 | ||||||
| chr13:75639567
|
G | GT | 77 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(74): Show | 77 | HG00280.hp1 HG00438.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.69+2842dupT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75639567 | |||||
| chr13:75639926
|
G | A | 71 | a0001c0001t0001g0184a0001c0001t0001g0201a0001c0001t0001g0207others(68): Show | 71 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.69+3200G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75639926 | ||||||
| chr13:75639978
|
G | T | 2 | a0006c0006t0001g0174a0006c0006t0001g0175 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.69+3252G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75639978 | ||||||
| chr13:75639986
|
C | T | 2 | a0007c0016t0001g0001a0007c0016t0001g0252 | 3 | HG02895.hp1 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.69+3260C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75639986 | ||||||
| chr13:75640012
|
C | T | 1 | a0006c0006t0001g0172 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.69+3286C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75640012 | ||||||
| chr13:75640085
|
A | G | 18 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(15): Show | 18 | HG02451.hp2 HG02698.hp2 HG02809.hp1 others(15): Show |
intron_variant | MODIFIER | c.69+3359A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75640085 | ||||||
| chr13:75640163
|
C | CTAGCTGC others(65): Show |
269 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(266): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.69+3444_69+3445ins others(72): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75640163 | |||||
| chr13:75640163
|
C | CTAGCTGC others(65): Show |
1 | a0003c0002t0001g0243 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.69+3444_69+3445ins others(72): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75640163 | |||||
| chr13:75640181
|
A | G | 158 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(155): Show | 159 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.69+3455A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75640181 | ||||||
| chr13:75640322
|
A | G | 158 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(155): Show | 159 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.69+3596A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75640322 | ||||||
| chr13:75640340
|
G | A | 1 | a0001c0001t0002g0007 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.69+3614G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75640340 | ||||||
| chr13:75640667
|
G | A | 1 | a0003c0002t0001g0186 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.69+3941G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75640667 | ||||||
| chr13:75640726
|
TAAC | T | 8 | a0002c0007t0003g0246a0006c0006t0001g0245a0007c0009t0009g0251others(5): Show | 8 | HG01891.hp2 HG03041.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.69+4005_69+4007del others(3): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75640726 | |||||
| chr13:75640779
|
C | T | 267 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(264): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.69+4053C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75640779 | ||||||
| chr13:75641029
|
G | A | 2 | a0007c0016t0001g0001a0007c0016t0001g0252 | 3 | HG02895.hp1 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.69+4303G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75641029 | ||||||
| chr13:75641094
|
A | C | 2 | a0001c0001t0002g0088a0008c0008t0004g0087 | 2 | HG02258.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.69+4368A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75641094 | ||||||
| chr13:75641123
|
C | A | 4 | a0004c0004t0001g0187a0004c0004t0001g0188a0004c0004t0001g0190others(1): Show | 4 | NA18949.hp2 NA18954.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.69+4397C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75641123 | ||||||
| chr13:75641301
|
G | A | 2 | a0007c0016t0001g0001a0007c0016t0001g0252 | 3 | HG02895.hp1 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.69+4575G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75641301 | ||||||
| chr13:75641389
|
C | T | 1 | a0005c0005t0015g0171 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.69+4663C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75641389 | ||||||
| chr13:75641476
|
A | G | 2 | a0001c0001t0002g0007a0016c0024t0002g0086 | 2 | NA18954.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.69+4750A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75641476 | ||||||
| chr13:75641501
|
A | G | 18 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(15): Show | 18 | HG02451.hp2 HG02698.hp2 HG02809.hp1 others(15): Show |
intron_variant | MODIFIER | c.69+4775A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75641501 | ||||||
| chr13:75641594
|
A | G | 1 | a0012c0014t0001g0003 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.69+4868A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75641594 | ||||||
| chr13:75641736
|
C | G | 76 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(73): Show | 76 | HG00280.hp1 HG00438.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.69+5010C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75641736 | ||||||
| chr13:75641938
|
G | A | 68 | a0001c0001t0001g0184a0001c0001t0001g0201a0001c0001t0001g0207others(65): Show | 68 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.69+5212G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75641938 | ||||||
| chr13:75642187
|
A | G | 1 | a0008c0008t0001g0089 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.69+5461A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75642187 | ||||||
| chr13:75642414
|
A | G | 148 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(145): Show | 148 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.69+5688A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75642414 | ||||||
| chr13:75642442
|
C | CA | 97 | a0001c0001t0002g0007a0001c0001t0002g0018a0001c0001t0002g0020others(94): Show | 97 | HG00140.hp1 HG00280.hp2 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.69+5739dupA | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75642442 | |||||
| chr13:75642442
|
C | CAA | 10 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0012others(7): Show | 10 | HG02074.hp1 HG02559.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.69+5738_69+5739dup others(2): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75642442 | |||||
| chr13:75642442
|
CA | C | 69 | a0001c0001t0001g0113a0001c0001t0001g0116a0001c0001t0001g0117others(66): Show | 69 | HG00438.hp2 HG00609.hp1 HG01070.hp2 others(66): Show |
intron_variant | MODIFIER | c.69+5739delA | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75642442 | |||||
| chr13:75642442
|
CAA | C | 11 | a0001c0001t0001g0184a0001c0021t0001g0182a0002c0007t0003g0176others(8): Show | 11 | HG00140.hp2 HG00639.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.69+5738_69+5739del others(2): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75642442 | |||||
| chr13:75642442
|
CAAAA | C | 8 | a0002c0007t0003g0246a0006c0006t0001g0245a0007c0009t0009g0251others(5): Show | 8 | HG01891.hp2 HG03041.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.69+5736_69+5739del others(4): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75642442 | |||||
| chr13:75642469
|
G | A | 68 | a0001c0001t0001g0184a0001c0001t0001g0201a0001c0001t0001g0207others(65): Show | 68 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.69+5743G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75642469 | ||||||
| chr13:75642789
|
A | G | 3 | a0002c0007t0003g0173a0007c0009t0001g0165a0007c0009t0001g0166 | 3 | HG01891.hp1 HG03139.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.69+6063A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75642789 | ||||||
| chr13:75642907
|
G | A | 77 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(74): Show | 77 | HG00280.hp1 HG00438.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.69+6181G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75642907 | ||||||
| chr13:75642949
|
C | T | 8 | a0001c0001t0002g0017a0001c0001t0002g0078a0001c0001t0002g0079others(5): Show | 8 | HG00735.hp2 HG01496.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.69+6223C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75642949 | ||||||
| chr13:75642969
|
A | G | 10 | a0002c0007t0003g0246a0006c0006t0001g0245a0007c0009t0009g0251others(7): Show | 11 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.69+6243A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75642969 | ||||||
| chr13:75643138
|
T | A | 3 | a0003c0002t0001g0191a0003c0002t0001g0195a0003c0002t0001g0196 | 3 | HG01928.hp1 HG01952.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.69+6412T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75643138 | ||||||
| chr13:75643292
|
C | G | 2 | a0012c0014t0001g0002a0012c0014t0001g0003 | 2 | HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.69+6566C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75643292 | ||||||
| chr13:75643370
|
C | A | 10 | a0002c0007t0003g0246a0006c0006t0001g0245a0007c0009t0009g0251others(7): Show | 11 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.69+6644C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75643370 | ||||||
| chr13:75643416
|
G | A | 8 | a0002c0007t0003g0246a0006c0006t0001g0245a0007c0009t0009g0251others(5): Show | 8 | HG01891.hp2 HG03041.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.69+6690G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75643416 | ||||||
| chr13:75643486
|
T | C | 158 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(155): Show | 159 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.69+6760T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75643486 | ||||||
| chr13:75643570
|
G | C | 1 | a0008c0008t0002g0077 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.69+6844G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75643570 | ||||||
| chr13:75643679
|
A | C | 1 | a0005c0005t0003g0164 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.69+6953A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75643679 | ||||||
| chr13:75643727
|
A | G | 1 | a0008c0008t0003g0241 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.69+7001A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75643727 | ||||||
| chr13:75643744
|
A | T | 1 | a0002c0003t0001g0240 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.69+7018A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75643744 | ||||||
| chr13:75643940
|
C | T | 76 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(73): Show | 76 | HG00280.hp1 HG00438.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.69+7214C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75643940 | ||||||
| chr13:75644093
|
A | G | 2 | a0002c0003t0001g0238a0002c0003t0001g0239 | 2 | HG03491.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.69+7367A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75644093 | ||||||
| chr13:75644652
|
A | G | 73 | a0001c0001t0001g0184a0001c0001t0001g0201a0001c0001t0001g0207others(70): Show | 73 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.69+7926A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75644652 | ||||||
| chr13:75644820
|
C | G | 2 | a0019c0034t0002g0073a0020c0033t0002g0074 | 2 | HG02698.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.69+8094C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75644820 | ||||||
| chr13:75644824
|
G | A | 3 | a0009c0010t0017g0004a0012c0014t0001g0002a0012c0014t0001g0003 | 3 | HG00735.hp1 HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.69+8098G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75644824 | ||||||
| chr13:75644898
|
T | C | 2 | a0007c0016t0001g0001a0007c0016t0001g0252 | 3 | HG02895.hp1 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.69+8172T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75644898 | ||||||
| chr13:75644956
|
C | T | 1 | a0008c0008t0001g0089 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.69+8230C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75644956 | ||||||
| chr13:75644959
|
C | A | 10 | a0002c0007t0003g0246a0006c0006t0001g0245a0007c0009t0009g0251others(7): Show | 11 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.69+8233C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75644959 | ||||||
| chr13:75644980
|
T | C | 3 | a0006c0006t0001g0132a0010c0012t0001g0130a0010c0012t0001g0131 | 3 | HG01109.hp1 HG06807.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.69+8254T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75644980 | ||||||
| chr13:75645066
|
AG | A | 3 | a0009c0010t0017g0004a0012c0014t0001g0002a0012c0014t0001g0003 | 3 | HG00735.hp1 HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.69+8341delG | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75645066 | ||||||
| chr13:75645106
|
A | G | 1 | a0001c0001t0002g0085 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.69+8380A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75645106 | ||||||
| chr13:75645181
|
G | A | 3 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0080 | 3 | HG01496.hp2 NA18522.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.69+8455G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75645181 | ||||||
| chr13:75645476
|
G | A | 68 | a0001c0001t0001g0184a0001c0001t0001g0201a0001c0001t0001g0207others(65): Show | 68 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.69+8750G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75645476 | ||||||
| chr13:75645698
|
T | C | 18 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(15): Show | 18 | HG02451.hp2 HG02698.hp2 HG02809.hp1 others(15): Show |
intron_variant | MODIFIER | c.69+8972T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75645698 | ||||||
| chr13:75645740
|
C | T | 7 | a0002c0007t0001g0234a0003c0002t0001g0233a0003c0002t0001g0237others(4): Show | 7 | HG01070.hp2 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.69+9014C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75645740 | ||||||
| chr13:75645936
|
G | A | 93 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(90): Show | 93 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.69+9210G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75645936 | ||||||
| chr13:75646134
|
C | A | 1 | a0009c0010t0003g0244 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.69+9408C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75646134 | ||||||
| chr13:75646317
|
G | A | 3 | a0001c0001t0001g0135a0002c0003t0002g0134a0018c0028t0004g0133 | 3 | HG00639.hp2 HG00738.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.69+9591G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75646317 | ||||||
| chr13:75646324
|
C | A | 1 | a0008c0008t0003g0111 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.69+9598C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75646324 | ||||||
| chr13:75646347
|
A | C | 76 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(73): Show | 76 | HG00280.hp1 HG00438.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.69+9621A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75646347 | ||||||
| chr13:75646387
|
C | T | 2 | a0002c0003t0001g0238a0002c0003t0001g0239 | 2 | HG03491.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.69+9661C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75646387 | ||||||
| chr13:75646393
|
T | A | 1 | a0006c0006t0001g0172 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.69+9667T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75646393 | ||||||
| chr13:75646487
|
G | C | 148 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(145): Show | 148 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.69+9761G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75646487 | ||||||
| chr13:75646508
|
C | T | 1 | a0001c0020t0002g0271 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.69+9782C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75646508 | ||||||
| chr13:75646512
|
C | G | 2 | a0007c0009t0001g0162a0007c0009t0001g0163 | 2 | HG02135.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.69+9786C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75646512 | ||||||
| chr13:75646519
|
C | T | 1 | a0001c0001t0002g0072 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.69+9793C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75646519 | ||||||
| chr13:75646574
|
ACTT | A | 15 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(12): Show | 15 | HG02451.hp2 HG02698.hp2 HG02809.hp1 others(12): Show |
intron_variant | MODIFIER | c.69+9849_69+9851del others(3): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75646574 | ||||||
| chr13:75646574
|
ACTTT | A | 3 | a0005c0005t0003g0112a0008c0008t0003g0005a0008c0008t0003g0111 | 3 | HG02922.hp2 NA18969.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.69+9849_69+9852del others(4): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75646574 | ||||||
| chr13:75646575
|
CT | C | 80 | a0001c0001t0001g0184a0001c0001t0001g0201a0001c0001t0001g0207others(77): Show | 81 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.69+9867delT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75646575 | |||||
| chr13:75646575
|
CTT | C | 53 | a0001c0001t0001g0135a0001c0001t0001g0143a0001c0001t0001g0150others(50): Show | 53 | HG00280.hp1 HG00438.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.69+9866_69+9867del others(2): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75646575 | |||||
| chr13:75646575
|
CTTT | C | 9 | a0002c0003t0001g0253a0002c0003t0001g0255a0002c0003t0001g0256others(6): Show | 9 | HG00673.hp1 HG01515.hp1 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.69+9865_69+9867del others(3): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75646575 | |||||
| chr13:75646593
|
T | A | 88 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(85): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.69+9867T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75646593 | ||||||
| chr13:75646593
|
T | TA | 5 | a0001c0019t0002g0267a0001c0019t0002g0268a0001c0020t0002g0269others(2): Show | 5 | HG00621.hp1 HG00621.hp2 HG00673.hp2 others(2): Show |
intron_variant | MODIFIER | c.69+9869dupA | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75646593 | |||||
| chr13:75646596
|
T | A | 1 | a0003c0002t0001g0229 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.69+9870T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75646596 | ||||||
| chr13:75646670
|
A | G | 4 | a0006c0006t0001g0172a0009c0010t0017g0004a0012c0014t0001g0002others(1): Show | 4 | HG00735.hp1 HG02818.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.69+9944A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75646670 | ||||||
| chr13:75646816
|
C | T | 1 | a0002c0011t0002g0071 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.69+10090C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75646816 | ||||||
| chr13:75647066
|
GGT | G | 156 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(153): Show | 156 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.69+10359_69+10360d others(4): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75647066 | |||||
| chr13:75647066
|
GGTGTGTG others(1): Show |
G | 2 | a0007c0016t0001g0001a0007c0016t0001g0252 | 3 | HG02895.hp1 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.69+10353_69+10360d others(10): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75647066 | |||||
| chr13:75647171
|
C | T | 1 | a0001c0001t0002g0016 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.69+10445C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75647171 | ||||||
| chr13:75647465
|
A | T | 76 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(73): Show | 76 | HG00280.hp1 HG00438.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.69+10739A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75647465 | ||||||
| chr13:75647621
|
T | C | 52 | a0001c0001t0001g0143a0001c0001t0001g0150a0001c0001t0001g0151others(49): Show | 52 | HG00280.hp1 HG00438.hp1 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.69+10895T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75647621 | ||||||
| chr13:75647635
|
C | T | 2 | a0007c0016t0001g0001a0007c0016t0001g0252 | 3 | HG02895.hp1 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.69+10909C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75647635 | ||||||
| chr13:75647696
|
TA | T | 72 | a0001c0001t0001g0184a0001c0001t0001g0201a0001c0001t0001g0207others(69): Show | 72 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.69+10979delA | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75647696 | |||||
| chr13:75647893
|
A | G | 4 | a0001c0001t0001g0135a0002c0003t0002g0134a0008c0008t0001g0089others(1): Show | 4 | HG00639.hp2 HG00738.hp1 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.69+11167A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75647893 | ||||||
| chr13:75647951
|
C | CTTTCTT | 50 | a0001c0001t0001g0135a0001c0001t0001g0143a0001c0001t0001g0150others(47): Show | 50 | HG00280.hp1 HG00438.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.69+11228_69+11229i others(8): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75647951 | |||||
| chr13:75647951
|
C | CTTTTTT | 87 | a0001c0001t0001g0109a0001c0001t0002g0007a0001c0001t0002g0008others(84): Show | 88 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(85): Show |
intron_variant | MODIFIER | c.69+11238_69+11243d others(8): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75647951 | |||||
| chr13:75647951
|
C | CTTTTTTT | 30 | a0001c0001t0001g0113a0001c0001t0001g0116a0001c0001t0001g0117others(27): Show | 30 | HG00609.hp1 HG01099.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.69+11237_69+11243d others(9): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75647951 | |||||
| chr13:75647951
|
C | CTTTTTTT others(1): Show |
5 | a0003c0002t0001g0006a0005c0005t0003g0112a0009c0030t0001g0170others(2): Show | 5 | HG02809.hp2 NA18941.hp2 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.69+11236_69+11243d others(10): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75647951 | |||||
| chr13:75647951
|
C | CTTTTTTT others(2): Show |
62 | a0001c0001t0001g0184a0001c0001t0001g0207a0001c0001t0001g0208others(59): Show | 62 | HG00140.hp2 HG00438.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.69+11235_69+11243d others(11): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75647951 | |||||
| chr13:75647951
|
C | CTTTTTTT others(3): Show |
3 | a0003c0002t0001g0186a0003c0002t0001g0229a0004c0004t0001g0190 | 3 | NA18946.hp1 NA18999.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.69+11234_69+11243d others(12): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75647951 | |||||
| chr13:75648463
|
A | G | 1 | a0012c0014t0014g0185 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.69+11737A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75648463 | ||||||
| chr13:75648565
|
G | A | 1 | a0001c0001t0002g0008 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.69+11839G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75648565 | ||||||
| chr13:75649277
|
A | G | 75 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(72): Show | 75 | HG00280.hp1 HG00438.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.69+12551A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75649277 | ||||||
| chr13:75649451
|
C | T | 3 | a0003c0002t0001g0006a0008c0008t0003g0005a0009c0030t0001g0170 | 3 | HG02809.hp2 NA19077.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.69+12725C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75649451 | ||||||
| chr13:75649592
|
G | A | 1 | a0006c0006t0002g0097 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.69+12866G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75649592 | ||||||
| chr13:75649635
|
G | A | 1 | a0012c0014t0014g0185 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.69+12909G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75649635 | ||||||
| chr13:75649664
|
T | C | 1 | a0004c0004t0001g0202 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.69+12938T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75649664 | ||||||
| chr13:75649717
|
C | T | 54 | a0001c0001t0001g0143a0001c0001t0001g0150a0001c0001t0001g0151others(51): Show | 54 | HG00280.hp1 HG00438.hp1 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.69+12991C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75649717 | ||||||
| chr13:75649810
|
C | T | 1 | a0004c0004t0010g0119 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.69+13084C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75649810 | ||||||
| chr13:75649980
|
T | C | 1 | a0008c0008t0001g0089 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.69+13254T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75649980 | ||||||
| chr13:75650034
|
A | G | 1 | a0001c0001t0002g0066 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.69+13308A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75650034 | ||||||
| chr13:75650103
|
A | C | 1 | a0002c0003t0001g0258 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.69+13377A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75650103 | ||||||
| chr13:75650255
|
G | A | 5 | a0002c0003t0001g0121a0002c0003t0001g0137a0002c0003t0001g0138others(2): Show | 5 | HG01168.hp1 HG01169.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.69+13529G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75650255 | ||||||
| chr13:75650355
|
C | G | 2 | a0007c0016t0001g0001a0007c0016t0001g0252 | 3 | HG02895.hp1 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.69+13629C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75650355 | ||||||
| chr13:75650449
|
C | T | 2 | a0012c0014t0001g0002a0012c0014t0001g0003 | 2 | HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.69+13723C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75650449 | ||||||
| chr13:75650731
|
T | G | 2 | a0007c0016t0001g0001a0007c0016t0001g0252 | 3 | HG02895.hp1 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.69+14005T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75650731 | ||||||
| chr13:75651019
|
A | G | 1 | a0003c0002t0001g0157 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.69+14293A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75651019 | ||||||
| chr13:75651043
|
A | T | 157 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(154): Show | 158 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.69+14317A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75651043 | ||||||
| chr13:75651309
|
C | CT | 5 | a0001c0001t0002g0014a0001c0001t0002g0063a0001c0001t0002g0065others(2): Show | 5 | HG01928.hp2 HG02258.hp2 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.69+14599dupT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75651309 | |||||
| chr13:75651309
|
CT | C | 147 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(144): Show | 147 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.69+14599delT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75651309 | |||||
| chr13:75651598
|
G | A | 2 | a0002c0003t0001g0192a0002c0003t0001g0203 | 2 | HG01106.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.69+14872G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75651598 | ||||||
| chr13:75651608
|
G | T | 8 | a0002c0007t0003g0246a0006c0006t0001g0245a0007c0009t0009g0251others(5): Show | 8 | HG01891.hp2 HG03041.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.69+14882G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75651608 | ||||||
| chr13:75651653
|
C | T | 2 | a0006c0006t0001g0174a0006c0006t0001g0175 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.69+14927C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75651653 | ||||||
| chr13:75651673
|
C | T | 157 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(154): Show | 158 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.69+14947C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75651673 | ||||||
| chr13:75652003
|
G | A | 68 | a0001c0001t0001g0184a0001c0001t0001g0201a0001c0001t0001g0207others(65): Show | 68 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.69+15277G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75652003 | ||||||
| chr13:75652025
|
G | A | 8 | a0002c0007t0003g0246a0006c0006t0001g0245a0007c0009t0009g0251others(5): Show | 8 | HG01891.hp2 HG03041.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.69+15299G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75652025 | ||||||
| chr13:75652030
|
A | G | 3 | a0005c0005t0015g0171a0008c0008t0003g0168a0008c0008t0003g0169 | 3 | HG03017.hp1 HG03669.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.69+15304A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75652030 | ||||||
| chr13:75652143
|
T | G | 1 | a0004c0004t0001g0231 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.69+15417T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75652143 | ||||||
| chr13:75652156
|
A | G | 6 | a0001c0001t0002g0099a0001c0001t0002g0106a0001c0001t0002g0107others(3): Show | 6 | HG01099.hp2 HG01884.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.69+15430A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75652156 | ||||||
| chr13:75652202
|
C | T | 17 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(14): Show | 17 | HG02451.hp2 HG02698.hp2 HG02809.hp1 others(14): Show |
intron_variant | MODIFIER | c.69+15476C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75652202 | ||||||
| chr13:75652254
|
A | G | 1 | a0006c0006t0001g0172 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.69+15528A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75652254 | ||||||
| chr13:75652321
|
T | C | 2 | a0012c0014t0001g0002a0012c0014t0001g0003 | 2 | HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.69+15595T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75652321 | ||||||
| chr13:75652614
|
A | AGT | 55 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0016others(52): Show | 55 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.69+15931_69+15932d others(4): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75652614 | |||||
| chr13:75652614
|
A | AGTGT | 34 | a0001c0001t0002g0013a0002c0003t0001g0126a0002c0003t0001g0256others(31): Show | 34 | HG00438.hp2 HG00673.hp1 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.69+15929_69+15932d others(6): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75652614 | |||||
| chr13:75652614
|
A | AGTGTGT | 6 | a0001c0001t0002g0079a0001c0001t0002g0080a0003c0002t0001g0228others(3): Show | 6 | HG02895.hp2 HG03041.hp2 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.69+15927_69+15932d others(8): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75652614 | |||||
| chr13:75652614
|
A | AGTGTGTG others(1): Show |
3 | a0001c0001t0002g0020a0001c0001t0002g0062a0001c0001t0002g0078 | 3 | HG01496.hp2 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.69+15925_69+15932d others(10): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75652614 | |||||
| chr13:75652614
|
AGT | A | 38 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(35): Show | 38 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.69+15931_69+15932d others(4): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75652614 | |||||
| chr13:75652614
|
AGTGT | A | 37 | a0001c0001t0001g0143a0001c0001t0001g0159a0001c0001t0002g0009others(34): Show | 38 | HG00438.hp1 HG00609.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.69+15929_69+15932d others(6): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75652614 | |||||
| chr13:75652614
|
AGTGTGTG others(3): Show |
A | 1 | a0021c0026t0001g0122 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.69+15923_69+15932d others(12): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75652614 | |||||
| chr13:75652614
|
AGTGTGTG others(5): Show |
A | 1 | a0001c0001t0002g0024 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.69+15921_69+15932d others(14): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75652614 | |||||
| chr13:75652614
|
AGTGTGTG others(7): Show |
A | 14 | a0001c0001t0001g0184a0001c0001t0002g0014a0001c0001t0002g0021others(11): Show | 14 | HG00140.hp2 HG00639.hp1 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.69+15919_69+15932d others(16): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75652614 | |||||
| chr13:75652614
|
AGTGTGTG others(11): Show |
A | 3 | a0003c0002t0001g0141a0003c0002t0001g0157a0003c0002t0001g0158 | 3 | HG00280.hp1 HG01070.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.69+15915_69+15932d others(20): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75652614 | |||||
| chr13:75652659
|
A | G | 3 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0080 | 3 | HG01496.hp2 NA18522.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.69+15933A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75652659 | ||||||
| chr13:75652719
|
A | G | 1 | a0003c0002t0001g0230 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.69+15993A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75652719 | ||||||
| chr13:75652747
|
GT | G | 4 | a0006c0006t0001g0172a0009c0010t0017g0004a0012c0014t0001g0002others(1): Show | 4 | HG00735.hp1 HG02818.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.69+16022delT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75652747 | ||||||
| chr13:75652823
|
T | C | 1 | a0009c0030t0001g0170 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.69+16097T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75652823 | ||||||
| chr13:75652957
|
G | C | 1 | a0002c0007t0004g0261 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.69+16231G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75652957 | ||||||
| chr13:75652974
|
C | T | 3 | a0005c0005t0015g0171a0008c0008t0003g0168a0008c0008t0003g0169 | 3 | HG03017.hp1 HG03669.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.69+16248C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75652974 | ||||||
| chr13:75653115
|
G | A | 1 | a0003c0002t0001g0230 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.69+16389G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75653115 | ||||||
| chr13:75653118
|
A | G | 1 | a0003c0002t0001g0230 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.69+16392A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75653118 | ||||||
| chr13:75653129
|
G | C | 1 | a0001c0001t0001g0135 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.69+16403G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75653129 | ||||||
| chr13:75653291
|
T | C | 146 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(143): Show | 146 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.69+16565T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75653291 | ||||||
| chr13:75653694
|
G | A | 7 | a0002c0007t0003g0176a0002c0007t0003g0178a0002c0007t0003g0180others(4): Show | 7 | HG00639.hp1 HG01081.hp1 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.69+16968G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75653694 | ||||||
| chr13:75653786
|
T | C | 1 | a0003c0002t0001g0233 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.69+17060T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75653786 | ||||||
| chr13:75654090
|
A | G | 1 | a0004c0013t0002g0019 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.69+17364A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75654090 | ||||||
| chr13:75654427
|
G | A | 1 | a0002c0007t0003g0246 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.69+17701G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75654427 | ||||||
| chr13:75654447
|
T | C | 3 | a0001c0001t0001g0135a0002c0003t0002g0134a0018c0028t0004g0133 | 3 | HG00639.hp2 HG00738.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.69+17721T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75654447 | ||||||
| chr13:75654488
|
AG | A | 142 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(139): Show | 142 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.69+17764delG | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75654488 | |||||
| chr13:75654533
|
G | T | 93 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(90): Show | 93 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.69+17807G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75654533 | ||||||
| chr13:75654645
|
G | A | 157 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(154): Show | 158 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.69+17919G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75654645 | ||||||
| chr13:75654752
|
G | A | 6 | a0006c0006t0001g0245a0007c0009t0009g0251a0009c0010t0001g0248others(3): Show | 6 | HG01891.hp2 HG03041.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.69+18026G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75654752 | ||||||
| chr13:75654856
|
C | T | 2 | a0002c0003t0001g0192a0002c0003t0001g0203 | 2 | HG01106.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.69+18130C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75654856 | ||||||
| chr13:75654870
|
T | C | 1 | a0008c0008t0001g0089 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.69+18144T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75654870 | ||||||
| chr13:75654876
|
C | CT | 5 | a0002c0007t0003g0246a0002c0007t0004g0261a0007c0016t0001g0001others(2): Show | 6 | HG02895.hp1 HG02897.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.69+18163dupT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75654876 | |||||
| chr13:75654876
|
C | CTTT | 143 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(140): Show | 143 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.69+18161_69+18163d others(5): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75654876 | |||||
| chr13:75654876
|
C | CTTTT | 7 | a0002c0003t0001g0220a0003c0002t0001g0157a0003c0002t0001g0229others(4): Show | 7 | HG01433.hp2 HG02135.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.69+18160_69+18163d others(6): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75654876 | |||||
| chr13:75654973
|
C | T | 9 | a0001c0001t0002g0101a0002c0007t0004g0098a0004c0004t0006g0103others(6): Show | 9 | HG01106.hp2 HG01256.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.69+18247C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75654973 | ||||||
| chr13:75655027
|
C | T | 3 | a0001c0001t0001g0135a0002c0003t0002g0134a0018c0028t0004g0133 | 3 | HG00639.hp2 HG00738.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.69+18301C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75655027 | ||||||
| chr13:75655114
|
G | A | 8 | a0002c0007t0003g0246a0006c0006t0001g0245a0007c0009t0009g0251others(5): Show | 8 | HG01891.hp2 HG03041.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.69+18388G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75655114 | ||||||
| chr13:75655284
|
G | A | 3 | a0001c0001t0001g0135a0002c0003t0002g0134a0018c0028t0004g0133 | 3 | HG00639.hp2 HG00738.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.69+18558G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75655284 | ||||||
| chr13:75655562
|
A | G | 250 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(247): Show | 251 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.69+18836A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75655562 | ||||||
| chr13:75655637
|
T | TTATATAT others(1): Show |
6 | a0001c0001t0002g0085a0001c0001t0002g0099a0001c0001t0002g0106others(3): Show | 6 | HG00099.hp1 HG01099.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.69+18957_69+18964d others(10): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75655637 | |||||
| chr13:75655637
|
T | TTATATAT others(3): Show |
1 | a0001c0001t0002g0101 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.69+18955_69+18964d others(12): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75655637 | |||||
| chr13:75655637
|
T | TTATATAT others(7): Show |
1 | a0006c0006t0002g0100 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.69+18951_69+18964d others(16): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75655637 | |||||
| chr13:75655637
|
T | TTATATAT others(9): Show |
1 | a0010c0012t0002g0105 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.69+18949_69+18964d others(18): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75655637 | |||||
| chr13:75655637
|
TTATATAT others(3): Show |
T | 1 | a0006c0006t0002g0095 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.69+18955_69+18964d others(12): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75655637 | |||||
| chr13:75655637
|
TTATATAT others(9): Show |
T | 2 | a0013c0018t0004g0010a0013c0018t0004g0011 | 2 | HG02723.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.69+18949_69+18964d others(18): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75655637 | |||||
| chr13:75655637
|
TTATATAT others(13): Show |
T | 3 | a0001c0001t0002g0007a0002c0007t0004g0261a0003c0002t0002g0064 | 3 | NA18954.hp1 NA18987.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.69+18945_69+18964d others(22): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75655637 | |||||
| chr13:75655637
|
TTATATAT others(15): Show |
T | 21 | a0001c0001t0002g0016a0001c0001t0002g0025a0001c0001t0002g0026others(18): Show | 21 | HG00140.hp1 HG00609.hp2 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.69+18943_69+18964d others(24): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75655637 | |||||
| chr13:75655637
|
TTATATAT others(17): Show |
T | 68 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0012others(65): Show | 69 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.69+18941_69+18964d others(26): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75655637 | |||||
| chr13:75655637
|
TTATATAT others(19): Show |
T | 2 | a0001c0001t0002g0058a0001c0001t0002g0083 | 2 | HG02056.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.69+18939_69+18964d others(28): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75655637 | |||||
| chr13:75655637
|
TTATATAT others(25): Show |
T | 2 | a0002c0003t0001g0203a0002c0003t0001g0238 | 2 | HG02280.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.69+18933_69+18964d others(34): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75655637 | |||||
| chr13:75655637
|
TTATATAT others(27): Show |
T | 148 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(145): Show | 148 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.69+18931_69+18964d others(36): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75655637 | |||||
| chr13:75655637
|
TTATATAT others(29): Show |
T | 2 | a0004c0004t0010g0119a0015c0029t0001g0118 | 2 | HG02809.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.69+18929_69+18964d others(38): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75655637 | |||||
| chr13:75656399
|
G | A | 1 | a0001c0001t0002g0013 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.69+19673G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75656399 | ||||||
| chr13:75656624
|
C | T | 1 | a0001c0001t0002g0018 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.69+19898C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75656624 | ||||||
| chr13:75656973
|
C | A | 2 | a0006c0006t0001g0172a0009c0010t0017g0004 | 2 | HG00735.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.69+20247C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75656973 | ||||||
| chr13:75657258
|
G | A | 4 | a0006c0006t0001g0172a0009c0010t0017g0004a0012c0014t0001g0002others(1): Show | 4 | HG00735.hp1 HG02818.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.69+20532G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75657258 | ||||||
| chr13:75657334
|
C | T | 91 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(88): Show | 92 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.69+20608C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75657334 | ||||||
| chr13:75657467
|
A | G | 1 | a0001c0001t0002g0012 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.69+20741A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75657467 | ||||||
| chr13:75657473
|
G | A | 2 | a0007c0016t0001g0001a0007c0016t0001g0252 | 3 | HG02895.hp1 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.69+20747G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75657473 | ||||||
| chr13:75657544
|
T | TC | 9 | a0001c0001t0001g0184a0002c0007t0003g0176a0002c0007t0003g0178others(6): Show | 9 | HG00140.hp2 HG00639.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.69+20820dupC | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75657544 | |||||
| chr13:75657561
|
T | C | 2 | a0001c0001t0003g0153a0007c0009t0001g0152 | 2 | HG01081.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.69+20835T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75657561 | ||||||
| chr13:75657811
|
G | A | 2 | a0012c0014t0001g0002a0012c0014t0001g0003 | 2 | HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.69+21085G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75657811 | ||||||
| chr13:75657936
|
T | C | 70 | a0001c0001t0001g0184a0001c0001t0001g0201a0001c0001t0001g0207others(67): Show | 71 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.69+21210T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75657936 | ||||||
| chr13:75657987
|
T | C | 91 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(88): Show | 92 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.69+21261T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75657987 | ||||||
| chr13:75658071
|
T | C | 12 | a0001c0001t0002g0265a0001c0019t0002g0267a0001c0019t0002g0268others(9): Show | 12 | HG00621.hp1 HG00621.hp2 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.69+21345T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75658071 | ||||||
| chr13:75658119
|
G | A | 4 | a0001c0019t0002g0267a0001c0019t0002g0268a0001c0020t0002g0269others(1): Show | 4 | HG00621.hp1 HG00673.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.69+21393G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75658119 | ||||||
| chr13:75658444
|
C | A | 1 | a0001c0001t0002g0041 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.69+21718C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75658444 | ||||||
| chr13:75658518
|
T | G | 91 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(88): Show | 92 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.69+21792T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75658518 | ||||||
| chr13:75658549
|
A | G | 70 | a0001c0001t0001g0184a0001c0001t0001g0201a0001c0001t0001g0207others(67): Show | 71 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.69+21823A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75658549 | ||||||
| chr13:75658581
|
C | CTTATTT | 20 | a0001c0001t0001g0207a0001c0001t0001g0208a0002c0007t0001g0234others(17): Show | 20 | HG01070.hp2 HG01123.hp1 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.69+21870_69+21875d others(8): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75658581 | |||||
| chr13:75658635
|
G | A | 8 | a0002c0007t0003g0246a0006c0006t0001g0245a0007c0009t0009g0251others(5): Show | 8 | HG01891.hp2 HG03041.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.69+21909G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75658635 | ||||||
| chr13:75658646
|
C | T | 1 | a0002c0007t0001g0129 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.69+21920C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75658646 | ||||||
| chr13:75658791
|
G | A | 6 | a0003c0002t0001g0194a0003c0002t0001g0222a0003c0002t0001g0224others(3): Show | 6 | HG00438.hp2 HG02056.hp2 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.69+22065G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75658791 | ||||||
| chr13:75658873
|
G | A | 1 | a0007c0016t0001g0252 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.69+22147G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75658873 | ||||||
| chr13:75658942
|
T | C | 2 | a0012c0014t0001g0002a0012c0014t0001g0003 | 2 | HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.69+22216T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75658942 | ||||||
| chr13:75659028
|
G | C | 1 | a0001c0001t0002g0085 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.69+22302G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75659028 | ||||||
| chr13:75659047
|
A | ACTCT | 157 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(154): Show | 158 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.69+22324_69+22325i others(6): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75659047 | |||||
| chr13:75659360
|
C | G | 19 | a0001c0001t0002g0016a0002c0003t0005g0030a0002c0003t0005g0070others(16): Show | 19 | HG00099.hp2 HG00140.hp1 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.69+22634C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75659360 | ||||||
| chr13:75659401
|
A | G | 1 | a0009c0010t0017g0004 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.69+22675A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75659401 | ||||||
| chr13:75659409
|
G | C | 1 | a0002c0011t0002g0071 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.69+22683G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75659409 | ||||||
| chr13:75659504
|
G | A | 68 | a0001c0001t0001g0184a0001c0001t0001g0201a0001c0001t0001g0207others(65): Show | 68 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.69+22778G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75659504 | ||||||
| chr13:75659580
|
AC | A | 68 | a0001c0001t0001g0184a0001c0001t0001g0201a0001c0001t0001g0207others(65): Show | 68 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.69+22855delC | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75659580 | ||||||
| chr13:75659612
|
A | G | 1 | a0001c0001t0002g0023 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.69+22886A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75659612 | ||||||
| chr13:75659795
|
G | A | 1 | a0009c0010t0017g0004 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.69+23069G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75659795 | ||||||
| chr13:75659955
|
TA | T | 58 | a0001c0001t0001g0135a0001c0001t0001g0143a0001c0001t0001g0150others(55): Show | 58 | HG00280.hp1 HG00438.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.69+23230delA | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75659955 | ||||||
| chr13:75660089
|
G | T | 99 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(96): Show | 100 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.69+23363G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75660089 | ||||||
| chr13:75660174
|
A | G | 1 | a0001c0001t0002g0026 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.69+23448A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75660174 | ||||||
| chr13:75660470
|
C | T | 7 | a0001c0001t0002g0017a0001c0001t0002g0078a0001c0001t0002g0079others(4): Show | 7 | HG00735.hp2 HG01496.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+23744C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75660470 | ||||||
| chr13:75660489
|
C | T | 2 | a0001c0001t0001g0184a0006c0006t0001g0183 | 2 | HG00140.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.69+23763C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75660489 | ||||||
| chr13:75660515
|
G | A | 2 | a0007c0016t0001g0001a0007c0016t0001g0252 | 3 | HG02895.hp1 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.69+23789G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75660515 | ||||||
| chr13:75660516
|
C | G | 1 | a0004c0004t0010g0119 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.69+23790C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75660516 | ||||||
| chr13:75660955
|
A | G | 268 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(265): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.69+24229A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75660955 | ||||||
| chr13:75661324
|
T | C | 99 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(96): Show | 100 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.69+24598T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75661324 | ||||||
| chr13:75661524
|
AAT | A | 4 | a0006c0006t0001g0172a0009c0010t0017g0004a0012c0014t0001g0002others(1): Show | 4 | HG00735.hp1 HG02818.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.69+24801_69+24802d others(4): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75661524 | |||||
| chr13:75661562
|
G | A | 1 | a0002c0007t0003g0173 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.69+24836G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75661562 | ||||||
| chr13:75661650
|
C | G | 99 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(96): Show | 100 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.69+24924C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75661650 | ||||||
| chr13:75661832
|
T | C | 1 | a0001c0001t0002g0014 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.69+25106T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75661832 | ||||||
| chr13:75661936
|
A | T | 4 | a0006c0006t0001g0172a0009c0010t0017g0004a0012c0014t0001g0002others(1): Show | 4 | HG00735.hp1 HG02818.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.69+25210A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75661936 | ||||||
| chr13:75662343
|
G | A | 70 | a0001c0001t0001g0184a0001c0001t0001g0201a0001c0001t0001g0207others(67): Show | 71 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.69+25617G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75662343 | ||||||
| chr13:75662508
|
G | A | 58 | a0001c0001t0001g0135a0001c0001t0001g0143a0001c0001t0001g0150others(55): Show | 58 | HG00280.hp1 HG00438.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.69+25782G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75662508 | ||||||
| chr13:75662632
|
T | TAATGTGA others(12): Show |
10 | a0001c0001t0001g0184a0001c0021t0001g0182a0002c0007t0003g0176others(7): Show | 10 | HG00140.hp2 HG00639.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.69+25912_69+25913i others(21): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75662632 | |||||
| chr13:75663080
|
T | C | 2 | a0006c0006t0001g0172a0009c0010t0017g0004 | 2 | HG00735.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.69+26354T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75663080 | ||||||
| chr13:75663124
|
G | GT | 5 | a0001c0001t0002g0007a0001c0001t0002g0063a0001c0001t0002g0065others(2): Show | 5 | HG01928.hp2 HG02273.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.69+26409dupT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75663124 | |||||
| chr13:75663207
|
T | C | 2 | a0006c0006t0001g0172a0009c0010t0017g0004 | 2 | HG00735.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.69+26481T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75663207 | ||||||
| chr13:75663331
|
T | A | 91 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(88): Show | 92 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.69+26605T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75663331 | ||||||
| chr13:75663332
|
T | A | 252 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(249): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.69+26606T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75663332 | ||||||
| chr13:75663337
|
A | G | 1 | a0003c0002t0001g0219 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.69+26611A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75663337 | ||||||
| chr13:75663408
|
T | TTTTCTTT others(5): Show |
35 | a0001c0001t0002g0007a0001c0001t0002g0016a0001c0001t0002g0017others(32): Show | 35 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.69+26698_69+26709d others(14): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75663408 | |||||
| chr13:75663408
|
T | TTTTCTTT others(9): Show |
44 | a0001c0001t0002g0008a0001c0001t0002g0012a0001c0001t0002g0013others(41): Show | 44 | HG00280.hp2 HG00621.hp2 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.69+26694_69+26709d others(18): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75663408 | |||||
| chr13:75663408
|
T | TTTTCTTT others(13): Show |
8 | a0001c0001t0002g0025a0001c0001t0002g0039a0001c0001t0002g0043others(5): Show | 8 | HG00609.hp2 HG01192.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.69+26690_69+26709d others(22): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75663408 | |||||
| chr13:75663408
|
T | TTTTCTTT others(21): Show |
2 | a0001c0001t0002g0042a0004c0004t0002g0032 | 2 | NA18970.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.69+26709_69+26710i others(30): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75663408 | |||||
| chr13:75663408
|
TTTTC | T | 14 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(11): Show | 14 | HG02698.hp2 HG02809.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.69+26706_69+26709d others(6): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75663408 | |||||
| chr13:75663427
|
TCTTTC | T | 3 | a0001c0001t0001g0167a0004c0004t0010g0119a0008c0008t0003g0005 | 3 | HG02451.hp2 HG02970.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.69+26702_69+26706d others(7): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75663427 | ||||||
| chr13:75663432
|
C | CTT | 56 | a0001c0001t0001g0201a0001c0001t0001g0207a0001c0001t0001g0208others(53): Show | 56 | HG00438.hp2 HG00609.hp1 HG01070.hp2 others(53): Show |
intron_variant | MODIFIER | c.69+26721_69+26722d others(4): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75663432 | |||||
| chr13:75663432
|
C | CTTTCTTT | 61 | a0001c0001t0001g0143a0001c0001t0001g0150a0001c0001t0001g0151others(58): Show | 61 | HG00280.hp1 HG00438.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.69+26709_69+26710i others(9): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75663432 | |||||
| chr13:75663432
|
C | CTTTCTTT others(4): Show |
1 | a0008c0008t0001g0089 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.69+26709_69+26710i others(13): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75663432 | |||||
| chr13:75663432
|
C | CTTTCTTT others(6): Show |
1 | a0004c0013t0002g0061 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.69+26709_69+26710i others(15): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75663432 | |||||
| chr13:75663432
|
C | CTTTCTTT others(18): Show |
1 | a0001c0001t0002g0009 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.69+26709_69+26710i others(27): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75663432 | |||||
| chr13:75663432
|
C | CTTTCTTT others(27): Show |
2 | a0007c0016t0001g0001a0007c0016t0001g0252 | 3 | HG02895.hp1 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.69+26709_69+26710i others(36): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75663432 | |||||
| chr13:75663432
|
C | CTTTCTTT others(10): Show |
2 | a0012c0014t0001g0002a0012c0014t0001g0003 | 2 | HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.69+26709_69+26710i others(19): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75663432 | |||||
| chr13:75663432
|
C | T | 15 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(12): Show | 15 | HG02698.hp2 HG02809.hp1 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.69+26706C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75663432 | ||||||
| chr13:75663433
|
T | TTTCTTTC others(4): Show |
1 | a0013c0018t0004g0056 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.69+26709_69+26710i others(13): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75663433 | |||||
| chr13:75663434
|
T | TTCTTTCT others(7): Show |
8 | a0001c0001t0001g0184a0001c0021t0001g0182a0002c0007t0003g0178others(5): Show | 8 | HG00639.hp1 HG01081.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.69+26709_69+26710i others(16): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75663434 | |||||
| chr13:75663434
|
T | TTCTTTCT others(11): Show |
2 | a0002c0007t0003g0176a0006c0006t0001g0183 | 2 | HG00140.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.69+26709_69+26710i others(20): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75663434 | |||||
| chr13:75663436
|
T | C | 2 | a0001c0001t0002g0085a0008c0008t0003g0111 | 2 | HG00099.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.69+26710T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75663436 | ||||||
| chr13:75663440
|
T | C | 2 | a0001c0001t0002g0085a0008c0008t0003g0111 | 2 | HG00099.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.69+26714T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75663440 | ||||||
| chr13:75663588
|
A | G | 157 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(154): Show | 158 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.69+26862A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75663588 | ||||||
| chr13:75663707
|
G | A | 17 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(14): Show | 17 | HG02451.hp2 HG02698.hp2 HG02809.hp1 others(14): Show |
intron_variant | MODIFIER | c.69+26981G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75663707 | ||||||
| chr13:75663722
|
G | A | 10 | a0001c0001t0001g0184a0001c0021t0001g0182a0002c0007t0003g0176others(7): Show | 10 | HG00140.hp2 HG00639.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.69+26996G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75663722 | ||||||
| chr13:75663729
|
C | T | 91 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(88): Show | 92 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.69+27003C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75663729 | ||||||
| chr13:75664037
|
T | G | 269 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(266): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.69+27311T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75664037 | ||||||
| chr13:75664043
|
A | C | 35 | a0001c0001t0001g0207a0001c0001t0001g0208a0002c0003t0001g0220others(32): Show | 35 | HG00438.hp2 HG01070.hp2 HG01123.hp1 others(32): Show |
intron_variant | MODIFIER | c.69+27317A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75664043 | ||||||
| chr13:75664044
|
A | G | 38 | a0001c0001t0001g0143a0001c0001t0001g0150a0001c0001t0001g0151others(35): Show | 38 | HG00280.hp1 HG00438.hp1 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.69+27318A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75664044 | ||||||
| chr13:75664240
|
A | G | 68 | a0001c0001t0001g0184a0001c0001t0001g0201a0001c0001t0001g0207others(65): Show | 68 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.69+27514A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75664240 | ||||||
| chr13:75664319
|
A | G | 1 | a0001c0001t0002g0025 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.69+27593A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75664319 | ||||||
| chr13:75664451
|
A | C | 1 | a0009c0010t0017g0004 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.69+27725A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75664451 | ||||||
| chr13:75664573
|
T | C | 1 | a0001c0001t0002g0045 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.69+27847T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75664573 | ||||||
| chr13:75664651
|
G | C | 2 | a0001c0001t0002g0085a0008c0008t0003g0111 | 2 | HG00099.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.69+27925G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75664651 | ||||||
| chr13:75664685
|
C | G | 4 | a0006c0006t0001g0172a0009c0010t0017g0004a0012c0014t0001g0002others(1): Show | 4 | HG00735.hp1 HG02818.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.69+27959C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75664685 | ||||||
| chr13:75664779
|
T | A | 8 | a0002c0007t0003g0246a0006c0006t0001g0245a0007c0009t0009g0251others(5): Show | 8 | HG01891.hp2 HG03041.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.69+28053T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75664779 | ||||||
| chr13:75664925
|
A | G | 1 | a0001c0001t0001g0218 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.69+28199A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75664925 | ||||||
| chr13:75664946
|
A | C | 91 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(88): Show | 92 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.69+28220A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75664946 | ||||||
| chr13:75664947
|
C | A | 91 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(88): Show | 92 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.69+28221C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75664947 | ||||||
| chr13:75665041
|
T | C | 1 | a0010c0012t0002g0105 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.69+28315T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75665041 | ||||||
| chr13:75665340
|
A | G | 91 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(88): Show | 92 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.69+28614A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75665340 | ||||||
| chr13:75665531
|
A | AT | 153 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(150): Show | 154 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.69+28817dupT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75665531 | |||||
| chr13:75665587
|
C | T | 1 | a0012c0014t0014g0185 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.69+28861C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75665587 | ||||||
| chr13:75665702
|
C | T | 250 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(247): Show | 251 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.69+28976C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75665702 | ||||||
| chr13:75666456
|
G | A | 91 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(88): Show | 92 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.69+29730G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75666456 | ||||||
| chr13:75666471
|
G | A | 1 | a0003c0002t0016g0223 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.69+29745G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75666471 | ||||||
| chr13:75666854
|
C | A | 1 | a0001c0001t0001g0184 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.69+30128C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75666854 | ||||||
| chr13:75666975
|
T | A | 9 | a0001c0001t0001g0184a0002c0007t0003g0176a0002c0007t0003g0178others(6): Show | 9 | HG00140.hp2 HG00639.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.69+30249T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75666975 | ||||||
| chr13:75667150
|
A | G | 1 | a0008c0008t0001g0089 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.69+30424A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75667150 | ||||||
| chr13:75667183
|
T | G | 52 | a0001c0001t0001g0143a0001c0001t0001g0150a0001c0001t0001g0151others(49): Show | 52 | HG00280.hp1 HG00438.hp1 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.69+30457T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75667183 | ||||||
| chr13:75667411
|
A | C | 2 | a0007c0016t0001g0001a0007c0016t0001g0252 | 3 | HG02895.hp1 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.69+30685A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75667411 | ||||||
| chr13:75667422
|
G | A | 1 | a0002c0003t0005g0033 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.69+30696G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75667422 | ||||||
| chr13:75667525
|
G | A | 1 | a0002c0003t0001g0137 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.69+30799G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75667525 | ||||||
| chr13:75667604
|
A | G | 68 | a0001c0001t0001g0184a0001c0001t0001g0201a0001c0001t0001g0207others(65): Show | 68 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.69+30878A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75667604 | ||||||
| chr13:75667643
|
A | T | 1 | a0001c0001t0008g0044 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.69+30917A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75667643 | ||||||
| chr13:75667855
|
G | A | 1 | a0019c0034t0002g0073 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.69+31129G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75667855 | ||||||
| chr13:75668141
|
C | G | 91 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(88): Show | 92 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.69+31415C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75668141 | ||||||
| chr13:75668651
|
C | A | 2 | a0007c0016t0001g0001a0007c0016t0001g0252 | 3 | HG02895.hp1 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.69+31925C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75668651 | ||||||
| chr13:75668652
|
C | T | 2 | a0002c0003t0001g0238a0002c0003t0001g0239 | 2 | HG03491.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.69+31926C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75668652 | ||||||
| chr13:75668656
|
A | G | 3 | a0001c0001t0001g0135a0002c0003t0002g0134a0018c0028t0004g0133 | 3 | HG00639.hp2 HG00738.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.69+31930A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75668656 | ||||||
| chr13:75668942
|
C | T | 1 | a0006c0006t0002g0093 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.69+32216C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75668942 | ||||||
| chr13:75669069
|
A | G | 9 | a0002c0007t0001g0129a0002c0007t0003g0246a0006c0006t0001g0245others(6): Show | 9 | HG01891.hp2 HG01952.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.69+32343A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75669069 | ||||||
| chr13:75669231
|
A | G | 3 | a0001c0001t0001g0135a0002c0003t0002g0134a0018c0028t0004g0133 | 3 | HG00639.hp2 HG00738.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.69+32505A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75669231 | ||||||
| chr13:75669259
|
G | C | 1 | a0001c0001t0001g0113 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.69+32533G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75669259 | ||||||
| chr13:75669294
|
C | T | 2 | a0012c0014t0001g0002a0012c0014t0001g0003 | 2 | HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.69+32568C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75669294 | ||||||
| chr13:75669370
|
AC | A | 9 | a0002c0007t0001g0129a0002c0007t0003g0246a0006c0006t0001g0245others(6): Show | 9 | HG01891.hp2 HG01952.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.69+32651delC | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75669370 | |||||
| chr13:75669395
|
G | C | 79 | a0001c0001t0001g0184a0001c0001t0001g0201a0001c0001t0001g0207others(76): Show | 80 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.69+32669G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75669395 | ||||||
| chr13:75669439
|
C | T | 199 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(196): Show | 200 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.69+32713C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75669439 | ||||||
| chr13:75669516
|
TC | T | 7 | a0002c0003t0001g0253a0002c0003t0001g0255a0002c0003t0001g0256others(4): Show | 7 | HG00673.hp1 HG02040.hp1 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.69+32791delC | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75669516 | ||||||
| chr13:75669562
|
T | C | 2 | a0007c0016t0001g0001a0007c0016t0001g0252 | 3 | HG02895.hp1 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.69+32836T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75669562 | ||||||
| chr13:75669920
|
A | G | 85 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(82): Show | 85 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.69+33194A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75669920 | ||||||
| chr13:75670145
|
A | C | 7 | a0002c0007t0003g0246a0006c0006t0001g0172a0006c0006t0001g0245others(4): Show | 7 | HG01891.hp2 HG03098.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.69+33419A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75670145 | ||||||
| chr13:75670182
|
A | G | 193 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(190): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.69+33456A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75670182 | ||||||
| chr13:75670274
|
A | C | 2 | a0008c0008t0003g0111a0008c0008t0004g0087 | 2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.69+33548A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75670274 | ||||||
| chr13:75670465
|
G | A | 2 | a0007c0016t0001g0001a0007c0016t0001g0252 | 3 | HG02895.hp1 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.69+33739G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75670465 | ||||||
| chr13:75670572
|
A | G | 1 | a0004c0027t0002g0092 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.69+33846A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75670572 | ||||||
| chr13:75670668
|
C | T | 1 | a0006c0006t0002g0097 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.69+33942C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75670668 | ||||||
| chr13:75670697
|
C | T | 6 | a0002c0007t0003g0246a0006c0006t0001g0172a0006c0006t0001g0245others(3): Show | 6 | HG03098.hp1 HG03098.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.69+33971C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75670697 | ||||||
| chr13:75670727
|
A | G | 2 | a0008c0008t0003g0111a0008c0008t0004g0087 | 2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.69+34001A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75670727 | ||||||
| chr13:75670770
|
C | A | 2 | a0002c0007t0001g0129a0008c0008t0002g0077 | 2 | HG01952.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.69+34044C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75670770 | ||||||
| chr13:75670904
|
G | A | 1 | a0006c0006t0002g0100 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.69+34178G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75670904 | ||||||
| chr13:75670954
|
T | C | 67 | a0001c0001t0001g0143a0001c0001t0001g0184a0001c0001t0002g0085others(64): Show | 67 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(64): Show |
intron_variant | MODIFIER | c.69+34228T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75670954 | ||||||
| chr13:75670966
|
C | CT | 40 | a0001c0001t0001g0135a0001c0001t0001g0159a0001c0001t0001g0201others(37): Show | 40 | HG00438.hp1 HG00609.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.69+34257dupT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75670966 | |||||
| chr13:75670966
|
C | CTT | 5 | a0002c0007t0004g0260a0002c0007t0004g0261a0005c0005t0003g0124others(2): Show | 5 | HG01515.hp2 NA18940.hp2 NA18987.hp2 others(2): Show |
intron_variant | MODIFIER | c.69+34256_69+34257d others(4): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75670966 | |||||
| chr13:75670966
|
C | CTTTTTTT | 28 | a0001c0001t0002g0085a0001c0021t0001g0182a0002c0003t0001g0138others(25): Show | 28 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(25): Show |
intron_variant | MODIFIER | c.69+34251_69+34257d others(9): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75670966 | |||||
| chr13:75670966
|
C | CTTTTTTT others(1): Show |
34 | a0001c0001t0001g0143a0001c0001t0001g0184a0001c0001t0003g0153others(31): Show | 34 | HG00140.hp2 HG00280.hp1 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.69+34250_69+34257d others(10): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75670966 | |||||
| chr13:75670996
|
T | G | 1 | a0001c0001t0002g0085 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.69+34270T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75670996 | ||||||
| chr13:75671083
|
A | G | 1 | a0009c0010t0003g0244 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.69+34357A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75671083 | ||||||
| chr13:75671103
|
G | A | 18 | a0001c0001t0001g0135a0002c0003t0002g0134a0002c0007t0003g0176others(15): Show | 19 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.69+34377G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75671103 | ||||||
| chr13:75671209
|
C | CT | 7 | a0002c0007t0003g0176a0002c0007t0003g0178a0002c0007t0003g0180others(4): Show | 7 | HG00639.hp1 HG01081.hp1 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.69+34495dupT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75671209 | |||||
| chr13:75671209
|
C | CTT | 31 | a0001c0001t0002g0085a0001c0021t0001g0182a0002c0003t0001g0138others(28): Show | 31 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(28): Show |
intron_variant | MODIFIER | c.69+34494_69+34495d others(4): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75671209 | |||||
| chr13:75671209
|
C | CTTT | 35 | a0001c0001t0001g0143a0001c0001t0001g0184a0001c0001t0003g0153others(32): Show | 35 | HG00140.hp2 HG00280.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.69+34493_69+34495d others(5): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75671209 | |||||
| chr13:75671209
|
CT | C | 5 | a0004c0004t0010g0119a0007c0016t0001g0001a0007c0016t0001g0252others(2): Show | 6 | HG02809.hp1 HG02809.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.69+34495delT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75671209 | |||||
| chr13:75671242
|
A | G | 16 | a0001c0001t0001g0159a0002c0003t0001g0146a0002c0003t0001g0154others(13): Show | 16 | HG00438.hp1 HG01884.hp1 HG03654.hp2 others(13): Show |
intron_variant | MODIFIER | c.69+34516A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75671242 | ||||||
| chr13:75671406
|
G | A | 67 | a0001c0001t0001g0143a0001c0001t0001g0184a0001c0001t0002g0085others(64): Show | 67 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(64): Show |
intron_variant | MODIFIER | c.69+34680G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75671406 | ||||||
| chr13:75671506
|
C | T | 2 | a0008c0008t0003g0168a0008c0008t0003g0169 | 2 | HG03669.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.69+34780C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75671506 | ||||||
| chr13:75671986
|
T | C | 1 | a0007c0009t0009g0251 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.69+35260T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75671986 | ||||||
| chr13:75672086
|
C | T | 1 | a0004c0004t0001g0187 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.69+35360C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75672086 | ||||||
| chr13:75672240
|
AT | A | 43 | a0001c0001t0001g0143a0001c0001t0001g0184a0001c0001t0002g0054others(40): Show | 43 | HG00140.hp2 HG00280.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.69+35532delT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75672240 | |||||
| chr13:75672240
|
ATT | A | 27 | a0001c0001t0002g0085a0001c0021t0001g0182a0002c0003t0001g0253others(24): Show | 27 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(24): Show |
intron_variant | MODIFIER | c.69+35531_69+35532d others(4): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75672240 | |||||
| chr13:75672324
|
C | G | 1 | a0003c0002t0001g0198 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.69+35598C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75672324 | ||||||
| chr13:75672365
|
C | T | 1 | a0001c0001t0002g0082 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.69+35639C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75672365 | ||||||
| chr13:75672447
|
G | A | 38 | a0001c0001t0001g0143a0001c0001t0001g0184a0001c0001t0003g0153others(35): Show | 38 | HG00140.hp2 HG00280.hp1 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.69+35721G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75672447 | ||||||
| chr13:75672461
|
G | A | 1 | a0022c0025t0003g0177 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.69+35735G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75672461 | ||||||
| chr13:75672463
|
A | G | 1 | a0003c0002t0001g0219 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.69+35737A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75672463 | ||||||
| chr13:75672729
|
T | C | 2 | a0012c0014t0001g0002a0012c0014t0001g0003 | 2 | HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.69+36003T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75672729 | ||||||
| chr13:75672803
|
T | TGA | 67 | a0001c0001t0001g0143a0001c0001t0001g0184a0001c0001t0002g0085others(64): Show | 67 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(64): Show |
intron_variant | MODIFIER | c.69+36078_69+36079i others(4): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75672803 | |||||
| chr13:75672829
|
T | G | 1 | a0002c0007t0001g0129 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.69+36103T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75672829 | ||||||
| chr13:75672919
|
ATG | A | 100 | a0001c0001t0001g0135a0001c0001t0001g0143a0001c0001t0001g0159others(97): Show | 101 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(98): Show |
intron_variant | MODIFIER | c.69+36205_69+36206d others(4): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75672919 | |||||
| chr13:75672953
|
A | T | 1 | a0006c0006t0001g0172 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.69+36227A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75672953 | ||||||
| chr13:75672972
|
T | C | 7 | a0002c0007t0003g0176a0002c0007t0003g0178a0002c0007t0003g0180others(4): Show | 7 | HG00639.hp1 HG01081.hp1 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.69+36246T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75672972 | ||||||
| chr13:75673043
|
A | G | 67 | a0001c0001t0001g0143a0001c0001t0001g0184a0001c0001t0002g0085others(64): Show | 67 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(64): Show |
intron_variant | MODIFIER | c.69+36317A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75673043 | ||||||
| chr13:75673251
|
A | G | 1 | a0001c0001t0002g0058 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.69+36525A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75673251 | ||||||
| chr13:75673958
|
GTAAATCA others(16): Show |
G | 27 | a0001c0001t0002g0085a0001c0021t0001g0182a0002c0003t0001g0253others(24): Show | 27 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(24): Show |
intron_variant | MODIFIER | c.69+37240_69+37262d others(25): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75673958 | |||||
| chr13:75674393
|
T | C | 67 | a0001c0001t0001g0143a0001c0001t0001g0184a0001c0001t0002g0085others(64): Show | 67 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(64): Show |
intron_variant | MODIFIER | c.69+37667T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75674393 | ||||||
| chr13:75674916
|
G | T | 1 | a0001c0021t0001g0182 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.69+38190G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75674916 | ||||||
| chr13:75674967
|
G | A | 18 | a0001c0001t0001g0135a0002c0003t0002g0134a0002c0007t0003g0176others(15): Show | 19 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.70-38215G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75674967 | ||||||
| chr13:75675083
|
C | CT | 67 | a0001c0001t0001g0143a0001c0001t0001g0184a0001c0001t0002g0085others(64): Show | 67 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(64): Show |
intron_variant | MODIFIER | c.70-38088dupT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75675083 | |||||
| chr13:75675139
|
T | C | 200 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(197): Show | 201 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(198): Show |
intron_variant | MODIFIER | c.70-38043T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75675139 | ||||||
| chr13:75675263
|
G | A | 1 | a0002c0003t0001g0211 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.70-37919G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75675263 | ||||||
| chr13:75675272
|
C | T | 1 | a0004c0013t0002g0104 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.70-37910C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75675272 | ||||||
| chr13:75675355
|
T | C | 29 | a0001c0001t0001g0143a0001c0001t0001g0184a0001c0001t0003g0153others(26): Show | 29 | HG00280.hp1 HG01070.hp1 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.70-37827T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75675355 | ||||||
| chr13:75675551
|
T | A | 22 | a0001c0001t0001g0135a0001c0019t0002g0267a0001c0019t0002g0268others(19): Show | 23 | HG00621.hp1 HG00639.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.70-37631T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75675551 | ||||||
| chr13:75675843
|
C | G | 1 | a0001c0001t0002g0007 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.70-37339C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75675843 | ||||||
| chr13:75675873
|
C | T | 26 | a0001c0001t0001g0143a0001c0001t0003g0153a0002c0003t0001g0121others(23): Show | 26 | HG00280.hp1 HG01070.hp1 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.70-37309C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75675873 | ||||||
| chr13:75675885
|
C | T | 35 | a0001c0001t0001g0143a0001c0001t0003g0153a0002c0003t0001g0121others(32): Show | 35 | HG00280.hp1 HG01070.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.70-37297C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75675885 | ||||||
| chr13:75675888
|
G | GCA | 19 | a0001c0001t0001g0135a0001c0001t0002g0101a0002c0007t0003g0176others(16): Show | 20 | HG00140.hp2 HG00639.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.70-37266_70-37265d others(4): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75675888 | |||||
| chr13:75675888
|
G | GCACA | 14 | a0001c0001t0001g0159a0002c0003t0001g0146a0002c0003t0001g0154others(11): Show | 14 | HG00438.hp1 HG01884.hp1 HG03654.hp2 others(11): Show |
intron_variant | MODIFIER | c.70-37268_70-37265d others(6): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75675888 | |||||
| chr13:75675888
|
GCA | G | 5 | a0002c0003t0001g0220a0005c0005t0003g0115a0005c0005t0003g0147others(2): Show | 5 | HG02698.hp2 HG03041.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.70-37266_70-37265d others(4): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75675888 | |||||
| chr13:75675888
|
GCACA | G | 67 | a0001c0001t0001g0201a0001c0001t0001g0207a0001c0001t0001g0208others(64): Show | 67 | HG00438.hp2 HG00609.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.70-37268_70-37265d others(6): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75675888 | |||||
| chr13:75675888
|
GCACACA | G | 13 | a0002c0011t0002g0031a0002c0011t0002g0038a0002c0011t0002g0071others(10): Show | 13 | HG00099.hp2 HG00140.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.70-37270_70-37265d others(8): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75675888 | |||||
| chr13:75675888
|
GCACACAC others(3): Show |
G | 16 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(13): Show | 16 | HG00099.hp1 HG00673.hp1 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.70-37274_70-37265d others(12): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75675888 | |||||
| chr13:75675888
|
GCACACAC others(5): Show |
G | 37 | a0001c0001t0001g0143a0001c0001t0003g0153a0002c0003t0001g0121others(34): Show | 37 | HG00280.hp1 HG01070.hp1 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.70-37276_70-37265d others(14): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75675888 | |||||
| chr13:75676002
|
C | T | 1 | a0001c0001t0002g0265 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.70-37180C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75676002 | ||||||
| chr13:75676018
|
T | C | 4 | a0001c0001t0002g0265a0014c0017t0002g0027a0014c0017t0002g0028others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.70-37164T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75676018 | ||||||
| chr13:75676377
|
G | A | 1 | a0008c0008t0001g0089 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.70-36805G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75676377 | ||||||
| chr13:75676440
|
A | C | 66 | a0001c0001t0001g0143a0001c0001t0001g0184a0001c0001t0002g0085others(63): Show | 66 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(63): Show |
intron_variant | MODIFIER | c.70-36742A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75676440 | ||||||
| chr13:75677070
|
T | TGGGTTCA others(8): Show |
1 | a0002c0003t0001g0146 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.70-36112_70-36111i others(17): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75677070 | ||||||
| chr13:75677071
|
C | A | 1 | a0002c0003t0001g0146 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.70-36111C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75677071 | ||||||
| chr13:75677433
|
G | T | 4 | a0006c0006t0001g0245a0009c0010t0001g0248a0009c0010t0001g0249others(1): Show | 4 | HG03098.hp2 HG03486.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-35749G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75677433 | ||||||
| chr13:75677537
|
A | G | 1 | a0003c0002t0001g0213 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.70-35645A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75677537 | ||||||
| chr13:75677615
|
A | G | 37 | a0001c0001t0001g0143a0001c0001t0003g0153a0002c0003t0001g0121others(34): Show | 37 | HG00280.hp1 HG01070.hp1 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.70-35567A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75677615 | ||||||
| chr13:75677642
|
C | CT | 84 | a0001c0001t0001g0109a0001c0001t0001g0116a0001c0001t0001g0117others(81): Show | 84 | HG00609.hp2 HG00735.hp2 HG01099.hp2 others(81): Show |
intron_variant | MODIFIER | c.70-35528dupT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75677642 | |||||
| chr13:75677642
|
C | CTT | 42 | a0001c0001t0001g0113a0001c0001t0001g0143a0001c0001t0002g0018others(39): Show | 42 | HG00280.hp1 HG00280.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.70-35529_70-35528d others(4): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75677642 | |||||
| chr13:75677642
|
C | CTTT | 25 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(22): Show | 25 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(22): Show |
intron_variant | MODIFIER | c.70-35530_70-35528d others(5): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75677642 | |||||
| chr13:75677817
|
G | A | 1 | a0004c0004t0001g0202 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.70-35365G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75677817 | ||||||
| chr13:75677837
|
T | C | 66 | a0001c0001t0001g0143a0001c0001t0001g0184a0001c0001t0002g0085others(63): Show | 66 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(63): Show |
intron_variant | MODIFIER | c.70-35345T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75677837 | ||||||
| chr13:75677856
|
T | C | 2 | a0001c0001t0002g0034a0001c0001t0002g0041 | 2 | NA18942.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.70-35326T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75677856 | ||||||
| chr13:75677911
|
C | T | 1 | a0001c0001t0002g0013 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.70-35271C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75677911 | ||||||
| chr13:75677913
|
A | T | 1 | a0001c0001t0002g0039 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.70-35269A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75677913 | ||||||
| chr13:75677989
|
T | C | 22 | a0001c0001t0001g0135a0001c0019t0002g0267a0001c0019t0002g0268others(19): Show | 23 | HG00621.hp1 HG00639.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.70-35193T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75677989 | ||||||
| chr13:75678040
|
C | G | 1 | a0009c0010t0017g0004 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.70-35142C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75678040 | ||||||
| chr13:75678169
|
T | G | 22 | a0001c0001t0001g0135a0001c0019t0002g0267a0001c0019t0002g0268others(19): Show | 23 | HG00621.hp1 HG00639.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.70-35013T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75678169 | ||||||
| chr13:75678183
|
A | G | 7 | a0002c0007t0003g0176a0002c0007t0003g0178a0002c0007t0003g0180others(4): Show | 7 | HG00639.hp1 HG01081.hp1 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.70-34999A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75678183 | ||||||
| chr13:75678201
|
C | T | 1 | a0015c0029t0001g0118 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.70-34981C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75678201 | ||||||
| chr13:75678212
|
C | T | 13 | a0001c0001t0001g0135a0001c0019t0002g0267a0001c0019t0002g0268others(10): Show | 13 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.70-34970C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75678212 | ||||||
| chr13:75678547
|
C | T | 9 | a0002c0007t0003g0176a0002c0007t0003g0178a0002c0007t0003g0180others(6): Show | 10 | HG00639.hp1 HG01081.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.70-34635C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75678547 | ||||||
| chr13:75678714
|
T | A | 2 | a0002c0011t0002g0075a0002c0011t0002g0076 | 2 | HG00140.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.70-34468T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75678714 | ||||||
| chr13:75678722
|
G | T | 66 | a0001c0001t0001g0143a0001c0001t0001g0184a0001c0001t0002g0085others(63): Show | 66 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(63): Show |
intron_variant | MODIFIER | c.70-34460G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75678722 | ||||||
| chr13:75678726
|
T | C | 2 | a0010c0012t0001g0130a0010c0012t0001g0131 | 2 | HG06807.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.70-34456T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75678726 | ||||||
| chr13:75678743
|
T | C | 1 | a0009c0010t0017g0004 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.70-34439T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75678743 | ||||||
| chr13:75678873
|
G | A | 1 | a0006c0006t0001g0172 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.70-34309G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75678873 | ||||||
| chr13:75679111
|
A | G | 66 | a0001c0001t0001g0143a0001c0001t0001g0184a0001c0001t0002g0085others(63): Show | 66 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(63): Show |
intron_variant | MODIFIER | c.70-34071A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75679111 | ||||||
| chr13:75679218
|
T | C | 66 | a0001c0001t0001g0143a0001c0001t0001g0184a0001c0001t0002g0085others(63): Show | 66 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(63): Show |
intron_variant | MODIFIER | c.70-33964T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75679218 | ||||||
| chr13:75679338
|
T | C | 1 | a0008c0008t0003g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.70-33844T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75679338 | ||||||
| chr13:75679411
|
C | T | 1 | a0010c0012t0001g0247 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.70-33771C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75679411 | ||||||
| chr13:75679907
|
T | A | 3 | a0003c0002t0001g0200a0003c0002t0001g0214a0003c0002t0002g0046 | 3 | NA18960.hp2 NA18979.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.70-33275T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75679907 | ||||||
| chr13:75680033
|
G | A | 1 | a0011c0015t0001g0155 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.70-33149G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75680033 | ||||||
| chr13:75680133
|
G | T | 26 | a0001c0001t0001g0184a0001c0001t0002g0085a0002c0003t0001g0253others(23): Show | 26 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(23): Show |
intron_variant | MODIFIER | c.70-33049G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75680133 | ||||||
| chr13:75680189
|
G | T | 3 | a0002c0011t0002g0031a0002c0011t0002g0038a0002c0011t0002g0084 | 3 | HG00099.hp2 HG01168.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.70-32993G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75680189 | ||||||
| chr13:75680297
|
A | G | 66 | a0001c0001t0001g0143a0001c0001t0001g0184a0001c0001t0002g0085others(63): Show | 66 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(63): Show |
intron_variant | MODIFIER | c.70-32885A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75680297 | ||||||
| chr13:75680409
|
G | T | 66 | a0001c0001t0001g0143a0001c0001t0001g0184a0001c0001t0002g0085others(63): Show | 66 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(63): Show |
intron_variant | MODIFIER | c.70-32773G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75680409 | ||||||
| chr13:75680571
|
C | CT | 65 | a0001c0001t0001g0143a0001c0001t0001g0184a0001c0001t0002g0085others(62): Show | 65 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(62): Show |
intron_variant | MODIFIER | c.70-32599dupT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75680571 | |||||
| chr13:75680778
|
A | T | 189 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(186): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.70-32404A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75680778 | ||||||
| chr13:75680906
|
C | T | 18 | a0001c0001t0001g0135a0002c0003t0002g0134a0002c0007t0003g0176others(15): Show | 19 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.70-32276C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75680906 | ||||||
| chr13:75680942
|
T | C | 28 | a0001c0001t0001g0143a0001c0001t0003g0153a0002c0003t0001g0121others(25): Show | 28 | HG00280.hp1 HG01070.hp1 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.70-32240T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75680942 | ||||||
| chr13:75681010
|
G | GT | 7 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0002g0051others(4): Show | 7 | HG02132.hp2 HG02165.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.70-32162dupT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75681010 | |||||
| chr13:75681031
|
T | G | 2 | a0001c0021t0001g0182a0009c0010t0017g0004 | 2 | HG00735.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.70-32151T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75681031 | ||||||
| chr13:75681054
|
G | A | 9 | a0001c0001t0001g0135a0002c0003t0002g0134a0002c0007t0004g0260others(6): Show | 9 | HG00639.hp2 HG00738.hp1 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.70-32128G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75681054 | ||||||
| chr13:75681105
|
G | T | 3 | a0001c0001t0002g0018a0001c0001t0002g0052a0001c0001t0002g0053 | 3 | HG00280.hp2 HG01993.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.70-32077G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75681105 | ||||||
| chr13:75681561
|
A | G | 1 | a0002c0003t0001g0257 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.70-31621A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75681561 | ||||||
| chr13:75681696
|
GTATGTAT others(35): Show |
G | 1 | a0001c0001t0001g0143 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.70-31482_70-31441d others(44): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75681696 | |||||
| chr13:75681700
|
G | GTATGTGT others(23): Show |
1 | a0004c0004t0002g0032 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.70-31478_70-31449d others(32): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75681700 | |||||
| chr13:75681702
|
A | ATG | 4 | a0002c0007t0012g0156a0007c0009t0001g0162a0007c0009t0001g0166others(1): Show | 4 | HG01243.hp1 HG02258.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-31476_70-31475d others(4): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75681702 | |||||
| chr13:75681706
|
G | A | 1 | a0006c0006t0001g0172 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.70-31476G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75681706 | ||||||
| chr13:75681706
|
G | GTGTA | 13 | a0001c0001t0003g0153a0002c0003t0001g0121a0002c0003t0001g0138others(10): Show | 13 | HG00280.hp1 HG01070.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.70-31475_70-31474i others(6): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75681706 | |||||
| chr13:75681706
|
G | GTGTATA | 5 | a0002c0003t0001g0137a0002c0003t0005g0030a0002c0003t0011g0161others(2): Show | 5 | HG01257.hp1 HG01346.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.70-31475_70-31474i others(8): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75681706 | |||||
| chr13:75681706
|
G | GTGTGTAT others(7): Show |
2 | a0010c0012t0001g0130a0010c0012t0001g0131 | 2 | HG06807.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.70-31475_70-31474i others(16): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75681706 | |||||
| chr13:75681706
|
GTATATAT others(13): Show |
G | 1 | a0002c0003t0001g0126 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.70-31464_70-31445d others(22): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75681706 | |||||
| chr13:75681708
|
A | G | 2 | a0006c0006t0001g0172a0008c0008t0001g0089 | 2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.70-31474A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75681708 | ||||||
| chr13:75681710
|
A | G | 1 | a0006c0006t0001g0172 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.70-31472A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75681710 | ||||||
| chr13:75681718
|
G | A | 25 | a0001c0001t0003g0153a0002c0003t0001g0121a0002c0003t0001g0137others(22): Show | 25 | HG00280.hp1 HG01070.hp1 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.70-31464G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75681718 | ||||||
| chr13:75681718
|
G | GTA | 5 | a0001c0021t0001g0182a0002c0007t0004g0098a0006c0006t0001g0183others(2): Show | 5 | HG00140.hp2 HG03490.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.70-31434_70-31433d others(4): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75681718 | |||||
| chr13:75681718
|
G | GTATA | 10 | a0002c0007t0003g0173a0002c0011t0002g0075a0004c0013t0002g0059others(7): Show | 10 | HG00140.hp1 HG01109.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.70-31436_70-31433d others(6): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75681718 | |||||
| chr13:75681718
|
G | GTATATA | 6 | a0002c0011t0002g0076a0004c0013t0002g0057a0004c0013t0002g0104others(3): Show | 6 | HG00738.hp2 HG02698.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.70-31438_70-31433d others(8): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75681718 | |||||
| chr13:75681718
|
G | GTATATAT others(1): Show |
6 | a0001c0001t0001g0184a0001c0001t0001g0218a0003c0002t0001g0237others(3): Show | 6 | HG01255.hp2 HG01257.hp2 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.70-31440_70-31433d others(10): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75681718 | |||||
| chr13:75681718
|
G | GTATATAT others(3): Show |
4 | a0002c0011t0002g0071a0004c0004t0001g0231a0004c0004t0001g0236others(1): Show | 4 | HG01361.hp2 HG02273.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-31442_70-31433d others(12): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75681718 | |||||
| chr13:75681718
|
G | GTATATAT others(5): Show |
19 | a0001c0001t0001g0208a0002c0003t0001g0211a0002c0003t0001g0239others(16): Show | 19 | HG00099.hp2 HG01168.hp2 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.70-31444_70-31433d others(14): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75681718 | |||||
| chr13:75681718
|
G | GTATATAT others(7): Show |
16 | a0002c0003t0001g0238a0002c0007t0001g0234a0002c0007t0003g0246others(13): Show | 16 | HG00621.hp2 HG01070.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.70-31446_70-31433d others(16): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75681718 | |||||
| chr13:75681718
|
G | GTATATAT others(9): Show |
18 | a0001c0001t0001g0201a0001c0001t0002g0085a0003c0002t0001g0006others(15): Show | 18 | HG00099.hp1 HG00438.hp2 HG00609.hp1 others(15): Show |
intron_variant | MODIFIER | c.70-31448_70-31433d others(18): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75681718 | |||||
| chr13:75681718
|
G | GTATATAT others(11): Show |
1 | a0001c0001t0001g0207 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.70-31450_70-31433d others(20): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75681718 | |||||
| chr13:75681718
|
G | GTATATAT others(15): Show |
1 | a0003c0002t0002g0266 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.70-31454_70-31433d others(24): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75681718 | |||||
| chr13:75681718
|
G | GTATATAT others(19): Show |
1 | a0003c0002t0001g0195 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.70-31458_70-31433d others(28): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75681718 | |||||
| chr13:75681718
|
G | GTATATAT others(23): Show |
1 | a0003c0002t0001g0225 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.70-31462_70-31433d others(32): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75681718 | |||||
| chr13:75681718
|
G | GTATATAT others(21): Show |
1 | a0002c0003t0001g0220 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.70-31443_70-31442i others(30): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75681718 | |||||
| chr13:75681718
|
G | GTATATAT others(57): Show |
1 | a0008c0008t0003g0241 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.70-31443_70-31442i others(66): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75681718 | |||||
| chr13:75681718
|
G | GTATATGT others(11): Show |
1 | a0003c0002t0001g0230 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.70-31459_70-31458i others(20): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75681718 | |||||
| chr13:75681718
|
G | GTATATGT others(13): Show |
1 | a0003c0002t0001g0193 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.70-31459_70-31458i others(22): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75681718 | |||||
| chr13:75681718
|
G | GTATATGT others(15): Show |
3 | a0003c0002t0001g0204a0003c0002t0001g0205a0003c0002t0001g0229 | 3 | HG02040.hp2 HG02129.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.70-31459_70-31458i others(24): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75681718 | |||||
| chr13:75681718
|
G | GTGTATAT others(5): Show |
1 | a0004c0004t0001g0199 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.70-31463_70-31462i others(14): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75681718 | |||||
| chr13:75681718
|
G | GTGTATAT others(9): Show |
2 | a0003c0002t0001g0200a0011c0015t0001g0155 | 2 | NA19055.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.70-31463_70-31462i others(18): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75681718 | |||||
| chr13:75681718
|
GTATATA | G | 3 | a0003c0002t0001g0212a0006c0006t0002g0108a0007c0016t0001g0001 | 4 | HG02895.hp1 HG02897.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.70-31438_70-31433d others(8): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75681718 | |||||
| chr13:75681718
|
GTATATAT others(1): Show |
G | 10 | a0001c0001t0001g0135a0002c0003t0002g0134a0002c0007t0004g0260others(7): Show | 10 | HG00639.hp2 HG00738.hp1 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.70-31440_70-31433d others(10): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75681718 | |||||
| chr13:75681718
|
GTATATAT others(3): Show |
G | 7 | a0002c0007t0003g0176a0002c0007t0003g0178a0002c0007t0003g0180others(4): Show | 7 | HG00639.hp1 HG01081.hp1 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.70-31442_70-31433d others(12): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75681718 | |||||
| chr13:75681718
|
GTATATAT others(5): Show |
G | 15 | a0001c0001t0001g0159a0002c0003t0001g0146a0002c0003t0001g0154others(12): Show | 15 | HG00438.hp1 HG01884.hp1 HG03654.hp2 others(12): Show |
intron_variant | MODIFIER | c.70-31444_70-31433d others(14): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75681718 | |||||
| chr13:75681718
|
GTATATAT others(7): Show |
G | 7 | a0002c0003t0001g0253a0002c0003t0001g0255a0002c0003t0001g0256others(4): Show | 7 | HG00673.hp1 HG02040.hp1 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.70-31446_70-31433d others(16): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75681718 | |||||
| chr13:75681718
|
GTATATAT others(11): Show |
G | 1 | a0001c0001t0002g0025 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.70-31450_70-31433d others(20): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75681718 | |||||
| chr13:75681722
|
A | G | 1 | a0006c0006t0001g0172 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.70-31460A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75681722 | ||||||
| chr13:75681728
|
A | G | 1 | a0002c0003t0001g0126 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.70-31454A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75681728 | ||||||
| chr13:75681736
|
A | ATG | 8 | a0001c0001t0002g0078a0001c0001t0002g0088a0001c0001t0002g0099others(5): Show | 8 | HG01099.hp2 HG01496.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.70-31445_70-31444i others(4): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75681736 | |||||
| chr13:75681736
|
A | G | 81 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(78): Show | 81 | HG00280.hp2 HG00621.hp1 HG00673.hp2 others(78): Show |
intron_variant | MODIFIER | c.70-31446A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75681736 | ||||||
| chr13:75681837
|
A | G | 9 | a0001c0001t0001g0135a0002c0003t0002g0134a0002c0007t0004g0260others(6): Show | 9 | HG00639.hp2 HG00738.hp1 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.70-31345A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75681837 | ||||||
| chr13:75681879
|
C | T | 4 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0069others(1): Show | 4 | NA18979.hp2 NA18980.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.70-31303C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75681879 | ||||||
| chr13:75681909
|
T | G | 84 | a0001c0001t0001g0135a0001c0001t0001g0143a0001c0001t0001g0184others(81): Show | 85 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(82): Show |
intron_variant | MODIFIER | c.70-31273T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75681909 | ||||||
| chr13:75682013
|
G | A | 1 | a0008c0008t0001g0089 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.70-31169G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75682013 | ||||||
| chr13:75682230
|
A | G | 1 | a0006c0006t0001g0172 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.70-30952A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75682230 | ||||||
| chr13:75682693
|
G | C | 2 | a0007c0016t0001g0001a0007c0016t0001g0252 | 3 | HG02895.hp1 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.70-30489G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75682693 | ||||||
| chr13:75682933
|
G | A | 2 | a0008c0008t0003g0111a0008c0008t0004g0087 | 2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.70-30249G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75682933 | ||||||
| chr13:75683130
|
G | C | 66 | a0001c0001t0001g0143a0001c0001t0001g0184a0001c0001t0002g0085others(63): Show | 66 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(63): Show |
intron_variant | MODIFIER | c.70-30052G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75683130 | ||||||
| chr13:75683179
|
C | T | 4 | a0001c0001t0002g0013a0001c0001t0002g0034a0001c0001t0002g0041others(1): Show | 4 | HG01515.hp2 NA18941.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.70-30003C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75683179 | ||||||
| chr13:75683181
|
C | T | 1 | a0002c0011t0002g0071 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.70-30001C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75683181 | ||||||
| chr13:75683251
|
A | G | 22 | a0001c0001t0001g0135a0001c0019t0002g0267a0001c0019t0002g0268others(19): Show | 23 | HG00621.hp1 HG00639.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.70-29931A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75683251 | ||||||
| chr13:75683364
|
A | C | 1 | a0021c0026t0001g0122 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.70-29818A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75683364 | ||||||
| chr13:75683382
|
G | T | 15 | a0001c0001t0001g0159a0002c0003t0001g0146a0002c0003t0001g0154others(12): Show | 15 | HG00438.hp1 HG01884.hp1 HG03654.hp2 others(12): Show |
intron_variant | MODIFIER | c.70-29800G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75683382 | ||||||
| chr13:75684112
|
T | A | 1 | a0002c0003t0001g0121 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.70-29070T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75684112 | ||||||
| chr13:75684415
|
AT | A | 99 | a0001c0001t0001g0135a0001c0001t0001g0143a0001c0001t0001g0159others(96): Show | 100 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(97): Show |
intron_variant | MODIFIER | c.70-28759delT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75684415 | |||||
| chr13:75684489
|
C | T | 15 | a0001c0001t0001g0159a0002c0003t0001g0146a0002c0003t0001g0154others(12): Show | 15 | HG00438.hp1 HG01884.hp1 HG03654.hp2 others(12): Show |
intron_variant | MODIFIER | c.70-28693C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75684489 | ||||||
| chr13:75684536
|
C | G | 66 | a0001c0001t0001g0143a0001c0001t0001g0184a0001c0001t0002g0085others(63): Show | 66 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(63): Show |
intron_variant | MODIFIER | c.70-28646C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75684536 | ||||||
| chr13:75684547
|
C | CT | 56 | a0001c0001t0001g0143a0001c0001t0002g0085a0001c0001t0003g0153others(53): Show | 56 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(53): Show |
intron_variant | MODIFIER | c.70-28616dupT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75684547 | |||||
| chr13:75684579
|
C | T | 1 | a0002c0011t0002g0038 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.70-28603C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75684579 | ||||||
| chr13:75684584
|
A | G | 66 | a0001c0001t0001g0143a0001c0001t0001g0184a0001c0001t0002g0085others(63): Show | 66 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(63): Show |
intron_variant | MODIFIER | c.70-28598A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75684584 | ||||||
| chr13:75684622
|
C | T | 3 | a0001c0001t0002g0054a0001c0001t0002g0055a0004c0004t0002g0032 | 3 | NA18980.hp1 NA19012.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.70-28560C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75684622 | ||||||
| chr13:75684833
|
A | G | 4 | a0001c0001t0001g0159a0003c0002t0001g0123a0021c0026t0001g0122others(1): Show | 4 | NA18953.hp2 NA18986.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-28349A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75684833 | ||||||
| chr13:75684840
|
TACAC | T | 88 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(85): Show | 88 | HG00280.hp2 HG00609.hp2 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.70-28332_70-28329d others(6): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75684840 | |||||
| chr13:75684934
|
T | C | 66 | a0001c0001t0001g0143a0001c0001t0001g0184a0001c0001t0002g0085others(63): Show | 66 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(63): Show |
intron_variant | MODIFIER | c.70-28248T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75684934 | ||||||
| chr13:75684982
|
A | G | 66 | a0001c0001t0001g0143a0001c0001t0001g0184a0001c0001t0002g0085others(63): Show | 66 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(63): Show |
intron_variant | MODIFIER | c.70-28200A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75684982 | ||||||
| chr13:75685023
|
C | A | 1 | a0003c0002t0001g0212 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.70-28159C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75685023 | ||||||
| chr13:75685119
|
G | T | 66 | a0001c0001t0001g0143a0001c0001t0001g0184a0001c0001t0002g0085others(63): Show | 66 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(63): Show |
intron_variant | MODIFIER | c.70-28063G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75685119 | ||||||
| chr13:75685236
|
A | T | 2 | a0001c0001t0002g0020a0001c0001t0002g0062 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.70-27946A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75685236 | ||||||
| chr13:75685306
|
G | A | 66 | a0001c0001t0001g0143a0001c0001t0001g0184a0001c0001t0002g0085others(63): Show | 66 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(63): Show |
intron_variant | MODIFIER | c.70-27876G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75685306 | ||||||
| chr13:75685610
|
CA | C | 80 | a0001c0001t0001g0109a0001c0001t0001g0116a0001c0001t0001g0117others(77): Show | 80 | HG00280.hp2 HG00609.hp2 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.70-27568delA | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75685610 | |||||
| chr13:75685879
|
C | T | 66 | a0001c0001t0001g0143a0001c0001t0001g0184a0001c0001t0002g0085others(63): Show | 66 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(63): Show |
intron_variant | MODIFIER | c.70-27303C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75685879 | ||||||
| chr13:75685890
|
C | CT | 13 | a0001c0001t0001g0113a0001c0001t0002g0012a0001c0001t0002g0101others(10): Show | 13 | HG00438.hp2 HG00639.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.70-27269dupT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75685890 | |||||
| chr13:75685890
|
CT | C | 24 | a0001c0001t0001g0116a0001c0001t0001g0159a0001c0001t0002g0020others(21): Show | 24 | HG00438.hp1 HG00639.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.70-27269delT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75685890 | |||||
| chr13:75685890
|
CTT | C | 8 | a0001c0001t0001g0184a0001c0001t0002g0085a0005c0005t0003g0127others(5): Show | 8 | HG00099.hp1 HG00735.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.70-27270_70-27269d others(4): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75685890 | |||||
| chr13:75685890
|
CTTT | C | 56 | a0001c0001t0001g0143a0001c0001t0003g0153a0002c0003t0001g0121others(53): Show | 56 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(53): Show |
intron_variant | MODIFIER | c.70-27271_70-27269d others(5): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75685890 | |||||
| chr13:75685948
|
C | T | 7 | a0002c0003t0001g0253a0002c0003t0001g0255a0002c0003t0001g0256others(4): Show | 7 | HG00673.hp1 HG02040.hp1 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.70-27234C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75685948 | ||||||
| chr13:75686046
|
T | G | 5 | a0001c0001t0001g0135a0002c0003t0002g0134a0004c0004t0006g0103others(2): Show | 5 | HG00639.hp2 HG00738.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.70-27136T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75686046 | ||||||
| chr13:75686132
|
G | A | 2 | a0001c0001t0003g0153a0007c0009t0001g0152 | 2 | HG01081.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.70-27050G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75686132 | ||||||
| chr13:75686220
|
A | G | 66 | a0001c0001t0001g0143a0001c0001t0001g0184a0001c0001t0002g0085others(63): Show | 66 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(63): Show |
intron_variant | MODIFIER | c.70-26962A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75686220 | ||||||
| chr13:75686519
|
A | T | 1 | a0006c0006t0002g0102 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.70-26663A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75686519 | ||||||
| chr13:75686526
|
C | CT | 36 | a0001c0001t0001g0135a0001c0001t0001g0159a0001c0001t0002g0007others(33): Show | 37 | HG00438.hp1 HG00639.hp2 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.70-26638dupT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75686526 | |||||
| chr13:75686526
|
C | CTT | 27 | a0001c0001t0001g0184a0001c0001t0002g0085a0002c0003t0001g0139others(24): Show | 27 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(24): Show |
intron_variant | MODIFIER | c.70-26639_70-26638d others(4): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75686526 | |||||
| chr13:75686526
|
C | CTTT | 34 | a0001c0001t0001g0143a0001c0001t0003g0153a0001c0021t0001g0182others(31): Show | 34 | HG00280.hp1 HG00735.hp1 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.70-26640_70-26638d others(5): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75686526 | |||||
| chr13:75686526
|
CT | C | 6 | a0001c0001t0002g0026a0004c0004t0001g0148a0004c0004t0001g0149others(3): Show | 6 | NA18969.hp1 NA18969.hp2 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.70-26638delT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75686526 | |||||
| chr13:75686548
|
C | T | 2 | a0019c0034t0002g0073a0020c0033t0002g0074 | 2 | HG02698.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.70-26634C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75686548 | ||||||
| chr13:75687060
|
G | A | 18 | a0001c0001t0001g0135a0002c0003t0002g0134a0002c0007t0003g0176others(15): Show | 19 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.70-26122G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75687060 | ||||||
| chr13:75687347
|
A | G | 1 | a0006c0006t0001g0172 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.70-25835A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75687347 | ||||||
| chr13:75687821
|
A | C | 10 | a0001c0001t0001g0135a0001c0001t0002g0016a0002c0003t0002g0134others(7): Show | 11 | HG00639.hp2 HG00738.hp1 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.70-25361A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75687821 | ||||||
| chr13:75688046
|
C | A | 1 | a0008c0008t0002g0077 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.70-25136C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75688046 | ||||||
| chr13:75688071
|
C | T | 2 | a0002c0003t0001g0220a0008c0008t0003g0241 | 2 | HG03927.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.70-25111C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75688071 | ||||||
| chr13:75688073
|
C | T | 1 | a0009c0010t0002g0015 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.70-25109C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75688073 | ||||||
| chr13:75688142
|
T | C | 1 | a0002c0011t0002g0076 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.70-25040T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75688142 | ||||||
| chr13:75688201
|
C | T | 2 | a0006c0006t0001g0172a0008c0008t0003g0160 | 2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.70-24981C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75688201 | ||||||
| chr13:75688436
|
G | A | 5 | a0001c0001t0001g0159a0002c0003t0001g0146a0003c0002t0001g0123others(2): Show | 5 | HG00438.hp1 NA18953.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.70-24746G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75688436 | ||||||
| chr13:75688596
|
A | G | 2 | a0002c0007t0003g0173a0009c0010t0003g0244 | 2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.70-24586A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75688596 | ||||||
| chr13:75688795
|
AT | A | 14 | a0001c0001t0001g0184a0001c0001t0002g0085a0002c0007t0003g0246others(11): Show | 14 | HG00099.hp1 HG01257.hp2 HG02818.hp2 others(11): Show |
intron_variant | MODIFIER | c.70-24378delT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75688795 | |||||
| chr13:75688942
|
G | A | 1 | a0006c0006t0001g0132 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.70-24240G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75688942 | ||||||
| chr13:75689073
|
C | G | 1 | a0007c0009t0001g0162 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.70-24109C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75689073 | ||||||
| chr13:75689699
|
G | A | 22 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(19): Show | 22 | HG00099.hp1 HG01257.hp2 HG01952.hp2 others(19): Show |
intron_variant | MODIFIER | c.70-23483G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75689699 | ||||||
| chr13:75689771
|
C | G | 1 | a0014c0017t0002g0037 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.70-23411C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75689771 | ||||||
| chr13:75689839
|
G | A | 18 | a0001c0001t0001g0135a0002c0003t0002g0134a0002c0007t0003g0176others(15): Show | 19 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.70-23343G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75689839 | ||||||
| chr13:75689910
|
A | G | 1 | a0001c0001t0002g0088 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.70-23272A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75689910 | ||||||
| chr13:75689967
|
C | A | 2 | a0012c0014t0001g0002a0012c0014t0001g0003 | 2 | HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.70-23215C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75689967 | ||||||
| chr13:75689985
|
T | C | 1 | a0002c0007t0001g0129 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.70-23197T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75689985 | ||||||
| chr13:75690025
|
C | G | 2 | a0006c0006t0001g0174a0006c0006t0001g0175 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.70-23157C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75690025 | ||||||
| chr13:75690145
|
G | A | 1 | a0009c0010t0017g0004 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.70-23037G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75690145 | ||||||
| chr13:75690169
|
A | G | 2 | a0002c0003t0001g0220a0008c0008t0003g0241 | 2 | HG03927.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.70-23013A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75690169 | ||||||
| chr13:75690173
|
G | A | 32 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(29): Show | 32 | HG00099.hp1 HG01257.hp2 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.70-23009G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75690173 | ||||||
| chr13:75690228
|
T | C | 147 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(144): Show | 148 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.70-22954T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75690228 | ||||||
| chr13:75690240
|
C | T | 4 | a0001c0001t0001g0109a0001c0001t0001g0116a0001c0001t0001g0117others(1): Show | 4 | NA18944.hp1 NA18946.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.70-22942C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75690240 | ||||||
| chr13:75690354
|
G | A | 1 | a0001c0001t0002g0018 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.70-22828G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75690354 | ||||||
| chr13:75690360
|
C | T | 10 | a0002c0003t0001g0154a0004c0027t0002g0092a0005c0005t0001g0125others(7): Show | 10 | HG01884.hp1 HG03654.hp2 HG03831.hp2 others(7): Show |
intron_variant | MODIFIER | c.70-22822C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75690360 | ||||||
| chr13:75690467
|
ATCTG | A | 3 | a0001c0021t0001g0182a0006c0006t0001g0174a0006c0006t0001g0175 | 3 | HG02896.hp1 HG02897.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.70-22710_70-22707d others(6): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75690467 | |||||
| chr13:75690720
|
A | G | 1 | a0001c0001t0002g0099 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.70-22462A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75690720 | ||||||
| chr13:75690745
|
G | C | 22 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(19): Show | 22 | HG00099.hp1 HG01257.hp2 HG01952.hp2 others(19): Show |
intron_variant | MODIFIER | c.70-22437G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75690745 | ||||||
| chr13:75690859
|
T | C | 7 | a0002c0003t0001g0253a0002c0003t0001g0255a0002c0003t0001g0256others(4): Show | 7 | HG00673.hp1 HG02040.hp1 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.70-22323T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75690859 | ||||||
| chr13:75690945
|
G | A | 22 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(19): Show | 22 | HG00099.hp1 HG01257.hp2 HG01952.hp2 others(19): Show |
intron_variant | MODIFIER | c.70-22237G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75690945 | ||||||
| chr13:75691073
|
G | A | 1 | a0007c0009t0009g0251 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.70-22109G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75691073 | ||||||
| chr13:75691115
|
T | G | 22 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(19): Show | 22 | HG00099.hp1 HG01257.hp2 HG01952.hp2 others(19): Show |
intron_variant | MODIFIER | c.70-22067T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75691115 | ||||||
| chr13:75691310
|
G | A | 1 | a0003c0002t0001g0213 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.70-21872G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75691310 | ||||||
| chr13:75691319
|
G | C | 14 | a0001c0001t0001g0184a0001c0001t0002g0085a0002c0007t0003g0246others(11): Show | 14 | HG00099.hp1 HG01257.hp2 HG02818.hp2 others(11): Show |
intron_variant | MODIFIER | c.70-21863G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75691319 | ||||||
| chr13:75691347
|
G | C | 2 | a0003c0002t0001g0193a0003c0002t0001g0230 | 2 | NA19060.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.70-21835G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75691347 | ||||||
| chr13:75691401
|
A | T | 1 | a0002c0007t0001g0129 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.70-21781A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75691401 | ||||||
| chr13:75691531
|
C | T | 3 | a0014c0017t0002g0027a0014c0017t0002g0028a0014c0017t0002g0037 | 3 | HG01167.hp1 HG01169.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.70-21651C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75691531 | ||||||
| chr13:75691570
|
A | G | 2 | a0006c0006t0001g0172a0008c0008t0003g0160 | 2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.70-21612A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75691570 | ||||||
| chr13:75691602
|
C | T | 2 | a0006c0006t0001g0172a0008c0008t0003g0160 | 2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.70-21580C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75691602 | ||||||
| chr13:75691646
|
A | C | 1 | a0007c0009t0009g0251 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.70-21536A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75691646 | ||||||
| chr13:75691735
|
G | A | 22 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(19): Show | 22 | HG00099.hp1 HG01257.hp2 HG01952.hp2 others(19): Show |
intron_variant | MODIFIER | c.70-21447G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75691735 | ||||||
| chr13:75691835
|
C | G | 1 | a0020c0033t0002g0074 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.70-21347C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75691835 | ||||||
| chr13:75691905
|
G | A | 18 | a0001c0001t0001g0135a0002c0003t0002g0134a0002c0007t0003g0176others(15): Show | 19 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.70-21277G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75691905 | ||||||
| chr13:75691911
|
C | A | 18 | a0001c0001t0001g0135a0002c0003t0002g0134a0002c0007t0003g0176others(15): Show | 19 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.70-21271C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75691911 | ||||||
| chr13:75691915
|
G | A | 6 | a0001c0001t0001g0184a0001c0001t0002g0085a0003c0002t0001g0006others(3): Show | 6 | HG00099.hp1 HG01257.hp2 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.70-21267G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75691915 | ||||||
| chr13:75692017
|
G | T | 2 | a0006c0006t0001g0172a0008c0008t0003g0160 | 2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.70-21165G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75692017 | ||||||
| chr13:75692395
|
C | CT | 20 | a0001c0001t0001g0135a0002c0003t0002g0134a0002c0007t0003g0176others(17): Show | 21 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.70-20774dupT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75692395 | |||||
| chr13:75692419
|
A | G | 3 | a0001c0021t0001g0182a0006c0006t0001g0174a0006c0006t0001g0175 | 3 | HG02896.hp1 HG02897.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.70-20763A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75692419 | ||||||
| chr13:75692481
|
A | G | 22 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(19): Show | 22 | HG00099.hp1 HG01257.hp2 HG01952.hp2 others(19): Show |
intron_variant | MODIFIER | c.70-20701A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75692481 | ||||||
| chr13:75692568
|
T | C | 1 | a0002c0007t0001g0129 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.70-20614T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75692568 | ||||||
| chr13:75692586
|
G | A | 18 | a0001c0001t0001g0135a0002c0003t0002g0134a0002c0007t0003g0176others(15): Show | 19 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.70-20596G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75692586 | ||||||
| chr13:75692717
|
C | G | 2 | a0008c0008t0003g0111a0008c0008t0004g0087 | 2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.70-20465C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75692717 | ||||||
| chr13:75693217
|
T | C | 22 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(19): Show | 22 | HG00099.hp1 HG01257.hp2 HG01952.hp2 others(19): Show |
intron_variant | MODIFIER | c.70-19965T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75693217 | ||||||
| chr13:75693316
|
T | A | 1 | a0003c0002t0001g0179 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.70-19866T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75693316 | ||||||
| chr13:75693331
|
C | T | 45 | a0001c0001t0001g0143a0002c0003t0001g0121a0002c0003t0001g0126others(42): Show | 45 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(42): Show |
intron_variant | MODIFIER | c.70-19851C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75693331 | ||||||
| chr13:75693501
|
C | G | 1 | a0004c0027t0002g0092 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.70-19681C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75693501 | ||||||
| chr13:75693555
|
C | T | 22 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(19): Show | 22 | HG00099.hp1 HG01257.hp2 HG01952.hp2 others(19): Show |
intron_variant | MODIFIER | c.70-19627C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75693555 | ||||||
| chr13:75693557
|
G | A | 1 | a0004c0004t0001g0148 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.70-19625G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75693557 | ||||||
| chr13:75693801
|
G | A | 1 | a0011c0015t0001g0155 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.70-19381G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75693801 | ||||||
| chr13:75693881
|
T | C | 4 | a0006c0006t0001g0245a0009c0010t0001g0248a0009c0010t0001g0249others(1): Show | 4 | HG03098.hp2 HG03486.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-19301T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75693881 | ||||||
| chr13:75693939
|
T | G | 1 | a0002c0007t0004g0260 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.70-19243T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75693939 | ||||||
| chr13:75693994
|
G | T | 10 | a0002c0003t0001g0154a0004c0027t0002g0092a0005c0005t0001g0125others(7): Show | 10 | HG01884.hp1 HG03654.hp2 HG03831.hp2 others(7): Show |
intron_variant | MODIFIER | c.70-19188G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75693994 | ||||||
| chr13:75694014
|
TA | T | 28 | a0001c0001t0001g0184a0001c0001t0002g0085a0002c0003t0001g0154others(25): Show | 28 | HG00099.hp1 HG01257.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.70-19157delA | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75694014 | |||||
| chr13:75694209
|
G | A | 2 | a0001c0001t0002g0026a0001c0001t0002g0029 | 2 | HG02523.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.70-18973G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75694209 | ||||||
| chr13:75694259
|
TG | T | 22 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(19): Show | 22 | HG00099.hp1 HG01257.hp2 HG01952.hp2 others(19): Show |
intron_variant | MODIFIER | c.70-18919delG | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75694259 | |||||
| chr13:75694279
|
C | T | 22 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(19): Show | 22 | HG00099.hp1 HG01257.hp2 HG01952.hp2 others(19): Show |
intron_variant | MODIFIER | c.70-18903C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75694279 | ||||||
| chr13:75694287
|
G | A | 22 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(19): Show | 22 | HG00099.hp1 HG01257.hp2 HG01952.hp2 others(19): Show |
intron_variant | MODIFIER | c.70-18895G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75694287 | ||||||
| chr13:75694368
|
C | T | 14 | a0001c0001t0001g0184a0001c0001t0002g0085a0002c0007t0003g0246others(11): Show | 14 | HG00099.hp1 HG01257.hp2 HG02818.hp2 others(11): Show |
intron_variant | MODIFIER | c.70-18814C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75694368 | ||||||
| chr13:75694371
|
A | C | 1 | a0003c0002t0001g0222 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.70-18811A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75694371 | ||||||
| chr13:75694498
|
G | A | 22 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(19): Show | 22 | HG00099.hp1 HG01257.hp2 HG01952.hp2 others(19): Show |
intron_variant | MODIFIER | c.70-18684G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75694498 | ||||||
| chr13:75694565
|
G | T | 1 | a0008c0008t0002g0077 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.70-18617G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75694565 | ||||||
| chr13:75694873
|
G | A | 2 | a0008c0008t0003g0111a0008c0008t0004g0087 | 2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.70-18309G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75694873 | ||||||
| chr13:75694971
|
C | T | 1 | a0006c0006t0001g0172 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.70-18211C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75694971 | ||||||
| chr13:75695089
|
T | A | 4 | a0002c0007t0004g0260a0002c0007t0004g0261a0005c0005t0004g0263others(1): Show | 4 | HG01515.hp2 NA18940.hp2 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-18093T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75695089 | ||||||
| chr13:75695278
|
A | G | 2 | a0004c0013t0002g0059a0004c0013t0002g0061 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.70-17904A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75695278 | ||||||
| chr13:75695318
|
C | G | 2 | a0006c0006t0001g0172a0008c0008t0003g0160 | 2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.70-17864C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75695318 | ||||||
| chr13:75695327
|
G | T | 14 | a0001c0001t0001g0184a0001c0001t0002g0085a0002c0007t0003g0246others(11): Show | 14 | HG00099.hp1 HG01257.hp2 HG02818.hp2 others(11): Show |
intron_variant | MODIFIER | c.70-17855G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75695327 | ||||||
| chr13:75695484
|
C | T | 1 | a0001c0001t0002g0023 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.70-17698C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75695484 | ||||||
| chr13:75695547
|
G | A | 1 | a0001c0001t0002g0023 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.70-17635G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75695547 | ||||||
| chr13:75695556
|
C | G | 27 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(24): Show | 28 | HG00099.hp1 HG01257.hp2 HG01952.hp2 others(25): Show |
intron_variant | MODIFIER | c.70-17626C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75695556 | ||||||
| chr13:75695557
|
A | G | 127 | a0001c0001t0001g0113a0001c0001t0001g0135a0001c0001t0001g0150others(124): Show | 128 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.70-17625A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75695557 | ||||||
| chr13:75695581
|
G | A | 2 | a0006c0006t0001g0174a0006c0006t0001g0175 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.70-17601G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75695581 | ||||||
| chr13:75695647
|
G | T | 3 | a0002c0007t0001g0129a0008c0008t0003g0111a0008c0008t0004g0087 | 3 | HG01952.hp2 HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.70-17535G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75695647 | ||||||
| chr13:75695759
|
A | C | 25 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(22): Show | 26 | HG00099.hp1 HG01257.hp2 HG01952.hp2 others(23): Show |
intron_variant | MODIFIER | c.70-17423A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75695759 | ||||||
| chr13:75695927
|
C | CTAGA | 25 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(22): Show | 26 | HG00099.hp1 HG01257.hp2 HG01952.hp2 others(23): Show |
intron_variant | MODIFIER | c.70-17253_70-17250d others(6): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75695927 | |||||
| chr13:75695997
|
G | A | 1 | a0003c0002t0002g0064 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.70-17185G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75695997 | ||||||
| chr13:75696023
|
G | A | 3 | a0001c0021t0001g0182a0006c0006t0001g0174a0006c0006t0001g0175 | 3 | HG02896.hp1 HG02897.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.70-17159G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75696023 | ||||||
| chr13:75696028
|
T | C | 1 | a0001c0001t0002g0007 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.70-17154T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75696028 | ||||||
| chr13:75696039
|
C | T | 1 | a0003c0002t0001g0224 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.70-17143C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75696039 | ||||||
| chr13:75696078
|
C | T | 2 | a0006c0006t0001g0174a0006c0006t0001g0175 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.70-17104C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75696078 | ||||||
| chr13:75696094
|
T | C | 151 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(148): Show | 152 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.70-17088T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75696094 | ||||||
| chr13:75696108
|
G | A | 7 | a0001c0001t0001g0184a0001c0001t0002g0085a0003c0002t0001g0006others(4): Show | 7 | HG00099.hp1 HG01257.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.70-17074G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75696108 | ||||||
| chr13:75696198
|
T | G | 4 | a0001c0001t0002g0008a0001c0001t0002g0020a0001c0001t0002g0036others(1): Show | 4 | HG03491.hp2 HG03492.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.70-16984T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75696198 | ||||||
| chr13:75696353
|
TCAAAAAA others(1): Show |
T | 3 | a0001c0001t0002g0065a0003c0002t0001g0006a0008c0008t0003g0005 | 3 | HG01928.hp2 NA19077.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.70-16824_70-16817d others(10): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75696353 | |||||
| chr13:75696354
|
CAAAA | C | 24 | a0001c0001t0001g0184a0001c0001t0002g0063a0001c0001t0002g0085others(21): Show | 25 | HG00099.hp1 HG01257.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.70-16824_70-16821d others(6): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75696354 | |||||
| chr13:75696358
|
A | C | 113 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(110): Show | 113 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.70-16824A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75696358 | ||||||
| chr13:75696358
|
AAAACAAA others(1): Show |
A | 60 | a0001c0001t0001g0201a0001c0001t0001g0207a0001c0001t0001g0208others(57): Show | 60 | HG00438.hp2 HG00609.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.70-16804_70-16797d others(10): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75696358 | |||||
| chr13:75696487
|
A | G | 2 | a0012c0014t0001g0002a0012c0014t0001g0003 | 2 | HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.70-16695A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75696487 | ||||||
| chr13:75696553
|
T | G | 2 | a0002c0003t0001g0211a0002c0003t0001g0240 | 2 | HG02735.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.70-16629T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75696553 | ||||||
| chr13:75696680
|
A | G | 1 | a0002c0007t0004g0260 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.70-16502A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75696680 | ||||||
| chr13:75696748
|
C | T | 1 | a0001c0001t0001g0113 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.70-16434C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75696748 | ||||||
| chr13:75696801
|
C | A | 23 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(20): Show | 24 | HG00099.hp1 HG01257.hp2 HG02818.hp2 others(21): Show |
intron_variant | MODIFIER | c.70-16381C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75696801 | ||||||
| chr13:75696899
|
C | A | 1 | a0003c0002t0001g0204 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.70-16283C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75696899 | ||||||
| chr13:75696935
|
G | A | 2 | a0002c0007t0001g0129a0008c0008t0003g0160 | 2 | HG01952.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.70-16247G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75696935 | ||||||
| chr13:75696995
|
C | T | 116 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(113): Show | 116 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.70-16187C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75696995 | ||||||
| chr13:75697004
|
A | G | 9 | a0002c0003t0001g0154a0005c0005t0001g0125a0005c0005t0003g0124others(6): Show | 9 | HG03654.hp2 HG03831.hp2 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.70-16178A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75697004 | ||||||
| chr13:75697110
|
C | T | 116 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(113): Show | 116 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.70-16072C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75697110 | ||||||
| chr13:75697157
|
C | T | 1 | a0009c0010t0017g0004 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.70-16025C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75697157 | ||||||
| chr13:75697193
|
C | A | 1 | a0002c0007t0001g0129 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.70-15989C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75697193 | ||||||
| chr13:75697245
|
C | T | 25 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(22): Show | 26 | HG00099.hp1 HG01257.hp2 HG01952.hp2 others(23): Show |
intron_variant | MODIFIER | c.70-15937C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75697245 | ||||||
| chr13:75697262
|
C | T | 20 | a0001c0001t0001g0184a0001c0001t0002g0085a0002c0007t0003g0173others(17): Show | 21 | HG00099.hp1 HG01257.hp2 HG02818.hp2 others(18): Show |
intron_variant | MODIFIER | c.70-15920C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75697262 | ||||||
| chr13:75697302
|
A | G | 2 | a0002c0007t0001g0129a0008c0008t0003g0160 | 2 | HG01952.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.70-15880A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75697302 | ||||||
| chr13:75697339
|
A | C | 1 | a0001c0001t0002g0051 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.70-15843A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75697339 | ||||||
| chr13:75697359
|
C | A | 1 | a0001c0021t0001g0182 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.70-15823C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75697359 | ||||||
| chr13:75697409
|
C | T | 2 | a0002c0007t0001g0129a0008c0008t0003g0160 | 2 | HG01952.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.70-15773C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75697409 | ||||||
| chr13:75697516
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.70-15666C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75697516 | ||||||
| chr13:75697612
|
A | C | 3 | a0001c0021t0001g0182a0006c0006t0001g0174a0006c0006t0001g0175 | 3 | HG02896.hp1 HG02897.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.70-15570A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75697612 | ||||||
| chr13:75697685
|
C | T | 1 | a0008c0008t0003g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.70-15497C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75697685 | ||||||
| chr13:75697781
|
C | G | 1 | a0003c0002t0001g0214 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.70-15401C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75697781 | ||||||
| chr13:75697786
|
T | C | 4 | a0002c0007t0004g0260a0002c0007t0004g0261a0005c0005t0004g0263others(1): Show | 4 | HG01515.hp2 NA18940.hp2 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-15396T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75697786 | ||||||
| chr13:75698114
|
C | T | 2 | a0001c0001t0002g0007a0001c0001t0002g0025 | 2 | HG00609.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.70-15068C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75698114 | ||||||
| chr13:75698147
|
A | C | 152 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(149): Show | 153 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.70-15035A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75698147 | ||||||
| chr13:75698156
|
G | A | 1 | a0003c0002t0001g0226 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.70-15026G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75698156 | ||||||
| chr13:75698300
|
ATATACT | A | 9 | a0002c0003t0001g0154a0005c0005t0001g0125a0005c0005t0003g0124others(6): Show | 9 | HG03654.hp2 HG03831.hp2 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.70-14877_70-14872d others(8): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75698300 | |||||
| chr13:75698512
|
A | G | 1 | a0008c0008t0003g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.70-14670A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75698512 | ||||||
| chr13:75698519
|
G | C | 3 | a0002c0011t0002g0031a0002c0011t0002g0038a0002c0011t0002g0084 | 3 | HG00099.hp2 HG01168.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.70-14663G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75698519 | ||||||
| chr13:75698528
|
G | T | 3 | a0001c0021t0001g0182a0006c0006t0001g0174a0006c0006t0001g0175 | 3 | HG02896.hp1 HG02897.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.70-14654G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75698528 | ||||||
| chr13:75698602
|
G | GT | 18 | a0001c0001t0002g0085a0002c0007t0003g0246a0003c0002t0001g0006others(15): Show | 18 | HG00099.hp1 HG02135.hp2 HG02818.hp2 others(15): Show |
intron_variant | MODIFIER | c.70-14564dupT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75698602 | |||||
| chr13:75698602
|
GT | G | 10 | a0002c0003t0001g0154a0004c0027t0002g0092a0005c0005t0001g0125others(7): Show | 10 | HG01884.hp1 HG03654.hp2 HG03831.hp2 others(7): Show |
intron_variant | MODIFIER | c.70-14564delT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75698602 | |||||
| chr13:75698627
|
G | A | 1 | a0003c0002t0001g0123 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.70-14555G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75698627 | ||||||
| chr13:75698633
|
C | T | 3 | a0003c0002t0002g0262a0003c0002t0002g0266a0003c0002t0002g0270 | 3 | HG00621.hp2 HG02132.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.70-14549C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75698633 | ||||||
| chr13:75698709
|
G | A | 1 | a0008c0008t0003g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.70-14473G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75698709 | ||||||
| chr13:75698897
|
C | T | 1 | a0003c0002t0001g0226 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.70-14285C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75698897 | ||||||
| chr13:75699126
|
A | G | 2 | a0003c0002t0001g0209a0004c0004t0001g0210 | 2 | NA18990.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.70-14056A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75699126 | ||||||
| chr13:75699296
|
A | G | 25 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(22): Show | 26 | HG00099.hp1 HG01257.hp2 HG01952.hp2 others(23): Show |
intron_variant | MODIFIER | c.70-13886A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75699296 | ||||||
| chr13:75699404
|
A | AT | 6 | a0002c0003t0005g0030a0002c0011t0002g0075a0002c0011t0002g0076others(3): Show | 6 | HG00140.hp1 HG00738.hp2 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.70-13760dupT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75699404 | |||||
| chr13:75699404
|
AT | A | 19 | a0001c0001t0002g0058a0002c0003t0001g0154a0002c0003t0001g0255others(16): Show | 19 | HG00673.hp1 HG01515.hp1 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.70-13760delT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75699404 | |||||
| chr13:75699404
|
ATT | A | 114 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(111): Show | 114 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.70-13761_70-13760d others(4): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75699404 | |||||
| chr13:75699414
|
T | TG | 5 | a0002c0007t0001g0129a0007c0016t0001g0001a0007c0016t0001g0252others(2): Show | 6 | HG01952.hp2 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.70-13768_70-13767i others(3): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75699414 | ||||||
| chr13:75699418
|
T | G | 5 | a0002c0007t0001g0129a0007c0016t0001g0001a0007c0016t0001g0252others(2): Show | 6 | HG01952.hp2 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.70-13764T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75699418 | ||||||
| chr13:75699418
|
T | TG | 16 | a0001c0001t0001g0184a0001c0001t0002g0085a0002c0007t0003g0173others(13): Show | 16 | HG00099.hp1 HG01257.hp2 HG02818.hp2 others(13): Show |
intron_variant | MODIFIER | c.70-13764_70-13763i others(3): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75699418 | ||||||
| chr13:75699449
|
C | T | 1 | a0001c0001t0001g0113 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.70-13733C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75699449 | ||||||
| chr13:75699468
|
A | C | 270 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(267): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.70-13714A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75699468 | ||||||
| chr13:75699491
|
G | A | 1 | a0005c0005t0003g0115 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.70-13691G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75699491 | ||||||
| chr13:75699535
|
G | C | 116 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(113): Show | 116 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.70-13647G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75699535 | ||||||
| chr13:75699558
|
G | A | 1 | a0009c0010t0001g0250 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.70-13624G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75699558 | ||||||
| chr13:75699599
|
A | T | 16 | a0001c0001t0001g0184a0001c0001t0002g0085a0002c0007t0003g0173others(13): Show | 16 | HG00099.hp1 HG01257.hp2 HG02818.hp2 others(13): Show |
intron_variant | MODIFIER | c.70-13583A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75699599 | ||||||
| chr13:75699622
|
GAGTGTA | G | 42 | a0002c0003t0001g0121a0002c0003t0001g0126a0002c0003t0001g0137others(39): Show | 42 | HG00099.hp2 HG00140.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.70-13559_70-13554d others(8): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75699622 | ||||||
| chr13:75699629
|
C | T | 29 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0001t0002g0265others(26): Show | 30 | HG00099.hp1 HG01167.hp1 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.70-13553C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75699629 | ||||||
| chr13:75699639
|
G | A | 16 | a0001c0001t0001g0184a0001c0001t0002g0085a0002c0007t0003g0173others(13): Show | 16 | HG00099.hp1 HG01257.hp2 HG02818.hp2 others(13): Show |
intron_variant | MODIFIER | c.70-13543G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75699639 | ||||||
| chr13:75699665
|
G | A | 255 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(252): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.70-13517G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75699665 | ||||||
| chr13:75699834
|
C | T | 1 | a0001c0001t0002g0101 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.70-13348C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75699834 | ||||||
| chr13:75699873
|
C | T | 1 | a0001c0001t0002g0055 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.70-13309C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75699873 | ||||||
| chr13:75699892
|
G | A | 1 | a0001c0001t0002g0008 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.70-13290G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75699892 | ||||||
| chr13:75699939
|
C | T | 16 | a0001c0001t0001g0184a0001c0001t0002g0085a0002c0007t0003g0173others(13): Show | 16 | HG00099.hp1 HG01257.hp2 HG02818.hp2 others(13): Show |
intron_variant | MODIFIER | c.70-13243C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75699939 | ||||||
| chr13:75699951
|
C | A | 25 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(22): Show | 26 | HG00099.hp1 HG01257.hp2 HG01952.hp2 others(23): Show |
intron_variant | MODIFIER | c.70-13231C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75699951 | ||||||
| chr13:75700118
|
C | T | 1 | a0008c0008t0003g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.70-13064C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75700118 | ||||||
| chr13:75700238
|
G | A | 1 | a0001c0001t0002g0017 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.70-12944G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75700238 | ||||||
| chr13:75700447
|
C | T | 1 | a0006c0006t0002g0100 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.70-12735C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75700447 | ||||||
| chr13:75700519
|
A | G | 10 | a0002c0003t0001g0154a0004c0027t0002g0092a0005c0005t0001g0125others(7): Show | 10 | HG01884.hp1 HG03654.hp2 HG03831.hp2 others(7): Show |
intron_variant | MODIFIER | c.70-12663A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75700519 | ||||||
| chr13:75700590
|
T | C | 2 | a0012c0014t0001g0002a0012c0014t0001g0003 | 2 | HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.70-12592T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75700590 | ||||||
| chr13:75700666
|
A | G | 20 | a0002c0003t0001g0253a0002c0003t0001g0255a0002c0003t0001g0256others(17): Show | 20 | HG00099.hp2 HG00140.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.70-12516A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75700666 | ||||||
| chr13:75700782
|
G | A | 16 | a0001c0001t0001g0184a0001c0001t0002g0085a0002c0007t0003g0173others(13): Show | 16 | HG00099.hp1 HG01257.hp2 HG02818.hp2 others(13): Show |
intron_variant | MODIFIER | c.70-12400G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75700782 | ||||||
| chr13:75700831
|
G | A | 1 | a0001c0001t0002g0036 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.70-12351G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75700831 | ||||||
| chr13:75700898
|
CTG | C | 3 | a0001c0021t0001g0182a0006c0006t0001g0174a0006c0006t0001g0175 | 3 | HG02896.hp1 HG02897.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.70-12281_70-12280d others(4): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75700898 | |||||
| chr13:75701008
|
G | A | 1 | a0001c0001t0002g0025 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.70-12174G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75701008 | ||||||
| chr13:75701130
|
TTGTAGTG others(26): Show |
T | 141 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(138): Show | 142 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.70-12018_70-11986d others(35): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75701130 | |||||
| chr13:75701441
|
T | C | 141 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(138): Show | 142 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.70-11741T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75701441 | ||||||
| chr13:75701821
|
A | G | 25 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(22): Show | 26 | HG00099.hp1 HG01257.hp2 HG01952.hp2 others(23): Show |
intron_variant | MODIFIER | c.70-11361A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75701821 | ||||||
| chr13:75701911
|
A | G | 1 | a0007c0009t0001g0163 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.70-11271A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75701911 | ||||||
| chr13:75701971
|
C | T | 3 | a0001c0021t0001g0182a0006c0006t0001g0174a0006c0006t0001g0175 | 3 | HG02896.hp1 HG02897.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.70-11211C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75701971 | ||||||
| chr13:75701977
|
G | T | 25 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(22): Show | 26 | HG00099.hp1 HG01257.hp2 HG01952.hp2 others(23): Show |
intron_variant | MODIFIER | c.70-11205G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75701977 | ||||||
| chr13:75702008
|
G | A | 116 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(113): Show | 116 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.70-11174G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75702008 | ||||||
| chr13:75702172
|
AG | A | 62 | a0001c0001t0001g0201a0001c0001t0001g0207a0001c0001t0001g0208others(59): Show | 62 | HG00438.hp2 HG00609.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.70-11009delG | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75702172 | ||||||
| chr13:75702178
|
T | G | 4 | a0007c0016t0001g0001a0007c0016t0001g0252a0008c0008t0003g0111others(1): Show | 5 | HG02895.hp1 HG02897.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.70-11004T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75702178 | ||||||
| chr13:75702364
|
G | T | 20 | a0001c0001t0001g0184a0001c0001t0002g0085a0002c0007t0003g0173others(17): Show | 21 | HG00099.hp1 HG01257.hp2 HG02818.hp2 others(18): Show |
intron_variant | MODIFIER | c.70-10818G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75702364 | ||||||
| chr13:75702464
|
G | A | 4 | a0007c0016t0001g0001a0007c0016t0001g0252a0008c0008t0003g0111others(1): Show | 5 | HG02895.hp1 HG02897.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.70-10718G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75702464 | ||||||
| chr13:75702466
|
G | A | 4 | a0007c0016t0001g0001a0007c0016t0001g0252a0008c0008t0003g0111others(1): Show | 5 | HG02895.hp1 HG02897.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.70-10716G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75702466 | ||||||
| chr13:75702872
|
G | A | 1 | a0010c0012t0001g0131 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.70-10310G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75702872 | ||||||
| chr13:75702969
|
C | G | 10 | a0002c0003t0001g0154a0004c0027t0002g0092a0005c0005t0001g0125others(7): Show | 10 | HG01884.hp1 HG03654.hp2 HG03831.hp2 others(7): Show |
intron_variant | MODIFIER | c.70-10213C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75702969 | ||||||
| chr13:75702986
|
A | G | 3 | a0001c0021t0001g0182a0006c0006t0001g0174a0006c0006t0001g0175 | 3 | HG02896.hp1 HG02897.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.70-10196A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75702986 | ||||||
| chr13:75703005
|
T | C | 1 | a0003c0002t0001g0006 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.70-10177T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75703005 | ||||||
| chr13:75703077
|
G | A | 1 | a0004c0013t0002g0019 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.70-10105G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75703077 | ||||||
| chr13:75703084
|
G | C | 3 | a0001c0001t0002g0101a0006c0006t0002g0094a0006c0006t0002g0102 | 3 | HG02647.hp2 HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.70-10098G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75703084 | ||||||
| chr13:75703261
|
G | A | 21 | a0001c0001t0001g0184a0001c0001t0002g0085a0002c0007t0001g0129others(18): Show | 22 | HG00099.hp1 HG01257.hp2 HG01952.hp2 others(19): Show |
intron_variant | MODIFIER | c.70-9921G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75703261 | ||||||
| chr13:75703265
|
T | A | 4 | a0006c0006t0001g0245a0009c0010t0001g0248a0009c0010t0001g0249others(1): Show | 4 | HG03098.hp2 HG03486.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-9917T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75703265 | ||||||
| chr13:75703374
|
G | A | 1 | a0003c0002t0001g0006 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.70-9808G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75703374 | ||||||
| chr13:75703381
|
C | T | 21 | a0001c0001t0001g0184a0001c0001t0002g0085a0002c0007t0001g0129others(18): Show | 22 | HG00099.hp1 HG01257.hp2 HG01952.hp2 others(19): Show |
intron_variant | MODIFIER | c.70-9801C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75703381 | ||||||
| chr13:75703382
|
A | G | 26 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(23): Show | 27 | HG00099.hp1 HG00735.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.70-9800A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75703382 | ||||||
| chr13:75703451
|
T | C | 4 | a0011c0015t0001g0155a0011c0015t0001g0197a0011c0015t0001g0221others(1): Show | 4 | NA18941.hp2 NA18986.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-9731T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75703451 | ||||||
| chr13:75703476
|
G | A | 2 | a0012c0014t0001g0002a0012c0014t0001g0003 | 2 | HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.70-9706G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75703476 | ||||||
| chr13:75703567
|
C | T | 1 | a0002c0007t0001g0129 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.70-9615C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75703567 | ||||||
| chr13:75703589
|
A | G | 3 | a0001c0021t0001g0182a0006c0006t0001g0174a0006c0006t0001g0175 | 3 | HG02896.hp1 HG02897.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.70-9593A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75703589 | ||||||
| chr13:75703714
|
T | TTG | 5 | a0001c0001t0002g0016a0002c0011t0002g0075a0002c0011t0002g0076others(2): Show | 5 | HG00140.hp1 HG00738.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.70-9443_70-9442dup others(2): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75703714 | |||||
| chr13:75703714
|
TTG | T | 4 | a0006c0006t0002g0096a0013c0018t0004g0010a0013c0018t0004g0011others(1): Show | 4 | HG02723.hp2 HG02896.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-9443_70-9442del others(2): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75703714 | |||||
| chr13:75703714
|
TTGTG | T | 3 | a0004c0013t0002g0059a0004c0013t0002g0061a0009c0010t0017g0004 | 3 | HG00735.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.70-9445_70-9442del others(4): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75703714 | |||||
| chr13:75703739
|
T | C | 2 | a0005c0005t0004g0263a0005c0005t0004g0264 | 2 | NA18940.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.70-9443T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75703739 | ||||||
| chr13:75703739
|
T | TGC | 3 | a0002c0003t0005g0030a0002c0003t0005g0070a0002c0003t0011g0161 | 3 | HG01099.hp1 HG01257.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.70-9442_70-9441dup others(2): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75703739 | |||||
| chr13:75703739
|
T | TGTGTGTG others(3): Show |
3 | a0001c0021t0001g0182a0008c0008t0003g0111a0008c0008t0004g0087 | 3 | HG02922.hp2 HG02970.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.70-9442_70-9441ins others(10): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75703739 | |||||
| chr13:75703739
|
T | TGTGTGTG others(5): Show |
2 | a0007c0016t0001g0001a0007c0016t0001g0252 | 3 | HG02895.hp1 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.70-9442_70-9441ins others(12): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75703739 | |||||
| chr13:75703739
|
T | TGTGTGTG others(7): Show |
8 | a0001c0001t0001g0184a0001c0001t0002g0085a0008c0008t0002g0077others(5): Show | 8 | HG00099.hp1 HG01257.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.70-9442_70-9441ins others(14): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75703739 | |||||
| chr13:75703739
|
T | TGTGTGTG others(7): Show |
1 | a0002c0007t0001g0129 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.70-9442_70-9441ins others(14): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75703739 | |||||
| chr13:75703739
|
T | TGTGTGTG others(9): Show |
6 | a0002c0007t0003g0246a0003c0002t0001g0006a0006c0006t0001g0245others(3): Show | 6 | HG03098.hp2 HG03486.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.70-9442_70-9441ins others(16): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75703739 | |||||
| chr13:75703739
|
T | TGTGTGTG others(11): Show |
1 | a0002c0007t0003g0173 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.70-9442_70-9441ins others(18): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75703739 | |||||
| chr13:75703739
|
T | TGTGTGTG others(11): Show |
1 | a0009c0010t0003g0244 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.70-9442_70-9441ins others(18): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75703739 | |||||
| chr13:75703849
|
G | A | 10 | a0002c0003t0001g0154a0004c0027t0002g0092a0005c0005t0001g0125others(7): Show | 10 | HG01884.hp1 HG03654.hp2 HG03831.hp2 others(7): Show |
intron_variant | MODIFIER | c.70-9333G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75703849 | ||||||
| chr13:75703938
|
G | T | 25 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(22): Show | 26 | HG00099.hp1 HG01257.hp2 HG01952.hp2 others(23): Show |
intron_variant | MODIFIER | c.70-9244G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75703938 | ||||||
| chr13:75704033
|
G | C | 10 | a0002c0003t0001g0154a0004c0027t0002g0092a0005c0005t0001g0125others(7): Show | 10 | HG01884.hp1 HG03654.hp2 HG03831.hp2 others(7): Show |
intron_variant | MODIFIER | c.70-9149G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75704033 | ||||||
| chr13:75704333
|
A | T | 25 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(22): Show | 26 | HG00099.hp1 HG01257.hp2 HG01952.hp2 others(23): Show |
intron_variant | MODIFIER | c.70-8849A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75704333 | ||||||
| chr13:75704749
|
G | A | 1 | a0002c0007t0001g0234 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.70-8433G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75704749 | ||||||
| chr13:75704922
|
T | C | 2 | a0006c0006t0001g0174a0006c0006t0001g0175 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.70-8260T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75704922 | ||||||
| chr13:75704993
|
C | T | 1 | a0007c0009t0001g0152 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.70-8189C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75704993 | ||||||
| chr13:75705056
|
G | A | 1 | a0008c0008t0003g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.70-8126G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75705056 | ||||||
| chr13:75705091
|
C | A | 1 | a0001c0001t0002g0016 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.70-8091C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75705091 | ||||||
| chr13:75705111
|
T | C | 2 | a0001c0001t0001g0184a0001c0001t0002g0085 | 2 | HG00099.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.70-8071T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75705111 | ||||||
| chr13:75705114
|
G | C | 1 | a0008c0008t0003g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.70-8068G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75705114 | ||||||
| chr13:75705130
|
C | T | 3 | a0001c0021t0001g0182a0006c0006t0001g0174a0006c0006t0001g0175 | 3 | HG02896.hp1 HG02897.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.70-8052C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75705130 | ||||||
| chr13:75705230
|
G | C | 26 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(23): Show | 27 | HG00099.hp1 HG01257.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.70-7952G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75705230 | ||||||
| chr13:75705474
|
A | T | 25 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(22): Show | 26 | HG00099.hp1 HG01257.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.70-7708A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75705474 | ||||||
| chr13:75705597
|
C | T | 3 | a0001c0021t0001g0182a0006c0006t0001g0174a0006c0006t0001g0175 | 3 | HG02896.hp1 HG02897.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.70-7585C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75705597 | ||||||
| chr13:75705610
|
C | A | 1 | a0003c0002t0001g0230 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.70-7572C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75705610 | ||||||
| chr13:75705912
|
T | TAAAGGAT others(306): Show |
3 | a0003c0002t0001g0141a0003c0002t0001g0157a0003c0002t0001g0158 | 3 | HG00280.hp1 HG01070.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.70-7258_70-7257ins others(313): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75705912 | |||||
| chr13:75705912
|
T | TAAAGGAT others(309): Show |
1 | a0018c0028t0004g0133 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.70-7258_70-7257ins others(316): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75705912 | |||||
| chr13:75705912
|
T | TAAAGGAT others(310): Show |
1 | a0002c0003t0002g0134 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.70-7258_70-7257ins others(317): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75705912 | |||||
| chr13:75705912
|
T | TAAAGGAT others(315): Show |
1 | a0002c0007t0004g0260 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.70-7258_70-7257ins others(322): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75705912 | |||||
| chr13:75705912
|
T | TAAAGGAT others(333): Show |
1 | a0005c0005t0004g0263 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.70-7258_70-7257ins others(340): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75705912 | |||||
| chr13:75705912
|
T | TAAAGGAT others(334): Show |
1 | a0005c0005t0004g0264 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.70-7258_70-7257ins others(341): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75705912 | |||||
| chr13:75705912
|
T | TAAAGGAT others(338): Show |
3 | a0001c0001t0001g0135a0002c0007t0004g0261a0004c0004t0006g0103 | 3 | HG00738.hp1 HG02818.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.70-7258_70-7257ins others(345): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75705912 | |||||
| chr13:75706043
|
A | G | 2 | a0001c0001t0001g0184a0001c0001t0002g0085 | 2 | HG00099.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.70-7139A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75706043 | ||||||
| chr13:75706118
|
A | G | 2 | a0002c0011t0002g0075a0002c0011t0002g0076 | 2 | HG00140.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.70-7064A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75706118 | ||||||
| chr13:75706210
|
A | G | 26 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(23): Show | 27 | HG00099.hp1 HG01257.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.70-6972A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75706210 | ||||||
| chr13:75706329
|
T | A | 10 | a0002c0003t0001g0154a0004c0027t0002g0092a0005c0005t0001g0125others(7): Show | 10 | HG01884.hp1 HG03654.hp2 HG03831.hp2 others(7): Show |
intron_variant | MODIFIER | c.70-6853T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75706329 | ||||||
| chr13:75706532
|
ACTTAT | A | 26 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(23): Show | 27 | HG00099.hp1 HG01257.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.70-6644_70-6640del others(5): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75706532 | |||||
| chr13:75706542
|
T | C | 4 | a0004c0004t0001g0187a0004c0004t0001g0188a0004c0004t0001g0190others(1): Show | 4 | NA18949.hp2 NA18954.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.70-6640T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75706542 | ||||||
| chr13:75706969
|
G | A | 11 | a0001c0001t0001g0135a0002c0003t0002g0134a0002c0007t0004g0260others(8): Show | 11 | HG00280.hp1 HG00639.hp2 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.70-6213G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75706969 | ||||||
| chr13:75707066
|
A | G | 1 | a0001c0001t0002g0069 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.70-6116A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75707066 | ||||||
| chr13:75707071
|
T | C | 26 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(23): Show | 27 | HG00099.hp1 HG01257.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.70-6111T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75707071 | ||||||
| chr13:75707138
|
T | C | 2 | a0002c0007t0003g0173a0009c0010t0003g0244 | 2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.70-6044T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75707138 | ||||||
| chr13:75707172
|
C | A | 1 | a0002c0011t0002g0071 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.70-6010C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75707172 | ||||||
| chr13:75707256
|
A | T | 1 | a0022c0025t0003g0177 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.70-5926A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75707256 | ||||||
| chr13:75707367
|
T | G | 2 | a0006c0006t0001g0174a0006c0006t0001g0175 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.70-5815T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75707367 | ||||||
| chr13:75707437
|
C | T | 3 | a0001c0021t0001g0182a0006c0006t0001g0174a0006c0006t0001g0175 | 3 | HG02896.hp1 HG02897.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.70-5745C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75707437 | ||||||
| chr13:75707455
|
A | G | 10 | a0002c0003t0001g0154a0004c0027t0002g0092a0005c0005t0001g0125others(7): Show | 10 | HG01884.hp1 HG03654.hp2 HG03831.hp2 others(7): Show |
intron_variant | MODIFIER | c.70-5727A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75707455 | ||||||
| chr13:75707508
|
C | T | 1 | a0006c0006t0001g0172 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.70-5674C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75707508 | ||||||
| chr13:75707517
|
A | G | 26 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(23): Show | 27 | HG00099.hp1 HG01257.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.70-5665A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75707517 | ||||||
| chr13:75707752
|
T | A | 1 | a0009c0010t0017g0004 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.70-5430T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75707752 | ||||||
| chr13:75707802
|
T | G | 5 | a0002c0003t0001g0126a0002c0007t0012g0156a0004c0004t0001g0120others(2): Show | 5 | HG01081.hp2 HG01175.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.70-5380T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75707802 | ||||||
| chr13:75707961
|
C | T | 10 | a0002c0003t0001g0154a0004c0027t0002g0092a0005c0005t0001g0125others(7): Show | 10 | HG01884.hp1 HG03654.hp2 HG03831.hp2 others(7): Show |
intron_variant | MODIFIER | c.70-5221C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75707961 | ||||||
| chr13:75707963
|
T | C | 1 | a0006c0006t0001g0132 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.70-5219T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75707963 | ||||||
| chr13:75708164
|
A | G | 10 | a0002c0003t0001g0154a0004c0027t0002g0092a0005c0005t0001g0125others(7): Show | 10 | HG01884.hp1 HG03654.hp2 HG03831.hp2 others(7): Show |
intron_variant | MODIFIER | c.70-5018A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75708164 | ||||||
| chr13:75708538
|
G | A | 1 | a0008c0008t0003g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.70-4644G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75708538 | ||||||
| chr13:75708749
|
C | A | 6 | a0001c0001t0001g0184a0001c0001t0002g0085a0003c0002t0001g0006others(3): Show | 6 | HG00099.hp1 HG01257.hp2 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.70-4433C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75708749 | ||||||
| chr13:75708794
|
T | A | 1 | a0001c0001t0001g0143 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.70-4388T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75708794 | ||||||
| chr13:75708855
|
G | A | 1 | a0003c0002t0001g0186 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.70-4327G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75708855 | ||||||
| chr13:75708876
|
A | C | 26 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(23): Show | 27 | HG00099.hp1 HG01257.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.70-4306A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75708876 | ||||||
| chr13:75708931
|
A | G | 22 | a0001c0001t0001g0184a0001c0001t0002g0085a0002c0007t0001g0129others(19): Show | 23 | HG00099.hp1 HG01257.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.70-4251A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75708931 | ||||||
| chr13:75708945
|
C | T | 18 | a0001c0001t0001g0184a0001c0001t0002g0085a0002c0007t0001g0129others(15): Show | 18 | HG00099.hp1 HG01257.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.70-4237C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75708945 | ||||||
| chr13:75708946
|
G | C | 1 | a0008c0008t0003g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.70-4236G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75708946 | ||||||
| chr13:75708954
|
C | A | 26 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(23): Show | 27 | HG00099.hp1 HG01257.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.70-4228C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75708954 | ||||||
| chr13:75708959
|
C | A | 10 | a0002c0003t0001g0154a0004c0027t0002g0092a0005c0005t0001g0125others(7): Show | 10 | HG01884.hp1 HG03654.hp2 HG03831.hp2 others(7): Show |
intron_variant | MODIFIER | c.70-4223C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75708959 | ||||||
| chr13:75708972
|
G | A | 1 | a0007c0009t0001g0152 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.70-4210G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75708972 | ||||||
| chr13:75708982
|
G | A | 5 | a0006c0006t0001g0245a0009c0010t0001g0248a0009c0010t0001g0249others(2): Show | 5 | HG01891.hp2 HG03098.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.70-4200G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75708982 | ||||||
| chr13:75709066
|
C | T | 6 | a0002c0007t0003g0246a0006c0006t0001g0245a0009c0010t0001g0248others(3): Show | 6 | HG01891.hp2 HG03098.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.70-4116C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75709066 | ||||||
| chr13:75709074
|
T | A | 1 | a0004c0004t0001g0236 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.70-4108T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75709074 | ||||||
| chr13:75709176
|
C | T | 26 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(23): Show | 27 | HG00099.hp1 HG01257.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.70-4006C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75709176 | ||||||
| chr13:75709195
|
G | C | 1 | a0002c0007t0003g0246 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.70-3987G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75709195 | ||||||
| chr13:75709242
|
G | T | 1 | a0008c0008t0003g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.70-3940G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75709242 | ||||||
| chr13:75709260
|
G | C | 22 | a0002c0003t0001g0121a0002c0003t0001g0126a0002c0003t0001g0137others(19): Show | 22 | HG01081.hp2 HG01099.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.70-3922G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75709260 | ||||||
| chr13:75709338
|
G | T | 14 | a0001c0001t0001g0201a0003c0002t0001g0191a0003c0002t0001g0193others(11): Show | 14 | HG00609.hp1 HG01167.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.70-3844G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75709338 | ||||||
| chr13:75709368
|
A | G | 1 | a0008c0008t0003g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.70-3814A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75709368 | ||||||
| chr13:75709414
|
C | A | 26 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(23): Show | 27 | HG00099.hp1 HG01257.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.70-3768C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75709414 | ||||||
| chr13:75709441
|
A | G | 1 | a0002c0003t0011g0161 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.70-3741A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75709441 | ||||||
| chr13:75709442
|
T | C | 142 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(139): Show | 143 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.70-3740T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75709442 | ||||||
| chr13:75709446
|
C | T | 17 | a0001c0001t0001g0184a0001c0001t0002g0085a0002c0007t0003g0173others(14): Show | 17 | HG00099.hp1 HG01257.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.70-3736C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75709446 | ||||||
| chr13:75709481
|
A | T | 25 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(22): Show | 26 | HG00099.hp1 HG01257.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.70-3701A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75709481 | ||||||
| chr13:75709511
|
C | G | 2 | a0007c0016t0001g0001a0007c0016t0001g0252 | 3 | HG02895.hp1 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.70-3671C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75709511 | ||||||
| chr13:75709645
|
G | A | 1 | a0001c0001t0002g0017 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.70-3537G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75709645 | ||||||
| chr13:75709664
|
G | A | 3 | a0002c0011t0002g0031a0002c0011t0002g0038a0002c0011t0002g0084 | 3 | HG00099.hp2 HG01168.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.70-3518G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75709664 | ||||||
| chr13:75709712
|
T | A | 2 | a0008c0008t0003g0111a0008c0008t0004g0087 | 2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.70-3470T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75709712 | ||||||
| chr13:75709785
|
A | C | 24 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(21): Show | 25 | HG00099.hp1 HG01257.hp2 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.70-3397A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75709785 | ||||||
| chr13:75709847
|
G | T | 1 | a0002c0003t0001g0255 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.70-3335G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75709847 | ||||||
| chr13:75709850
|
GT | G | 116 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(113): Show | 116 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.70-3328delT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75709850 | |||||
| chr13:75709872
|
T | C | 2 | a0008c0008t0003g0111a0008c0008t0004g0087 | 2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.70-3310T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75709872 | ||||||
| chr13:75709873
|
G | C | 2 | a0008c0008t0003g0111a0008c0008t0004g0087 | 2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.70-3309G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75709873 | ||||||
| chr13:75709895
|
T | A | 3 | a0002c0003t0001g0220a0008c0008t0003g0241a0009c0010t0003g0244 | 3 | HG03579.hp1 HG03927.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.70-3287T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75709895 | ||||||
| chr13:75709939
|
A | G | 2 | a0008c0008t0003g0111a0008c0008t0004g0087 | 2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.70-3243A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75709939 | ||||||
| chr13:75710065
|
T | C | 1 | a0002c0007t0003g0246 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.70-3117T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75710065 | ||||||
| chr13:75710117
|
G | A | 132 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(129): Show | 132 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.70-3065G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75710117 | ||||||
| chr13:75710129
|
G | C | 1 | a0008c0008t0003g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.70-3053G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75710129 | ||||||
| chr13:75710173
|
G | C | 26 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(23): Show | 27 | HG00099.hp1 HG01257.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.70-3009G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75710173 | ||||||
| chr13:75710191
|
G | GA | 12 | a0001c0001t0001g0135a0002c0003t0001g0240a0002c0003t0002g0134others(9): Show | 12 | HG00280.hp1 HG00639.hp2 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.70-2991_70-2990ins others(1): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75710191 | ||||||
| chr13:75710340
|
G | T | 2 | a0007c0016t0001g0001a0007c0016t0001g0252 | 3 | HG02895.hp1 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.70-2842G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75710340 | ||||||
| chr13:75710349
|
G | A | 1 | a0008c0008t0003g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.70-2833G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75710349 | ||||||
| chr13:75710472
|
A | C | 41 | a0002c0003t0001g0121a0002c0003t0001g0126a0002c0003t0001g0137others(38): Show | 41 | HG00099.hp2 HG00140.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.70-2710A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75710472 | ||||||
| chr13:75710618
|
G | A | 26 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(23): Show | 27 | HG00099.hp1 HG01257.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.70-2564G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75710618 | ||||||
| chr13:75710632
|
T | G | 1 | a0001c0001t0001g0135 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.70-2550T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75710632 | ||||||
| chr13:75710639
|
C | G | 2 | a0003c0002t0001g0209a0004c0004t0001g0210 | 2 | NA18990.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.70-2543C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75710639 | ||||||
| chr13:75710705
|
T | C | 4 | a0001c0001t0002g0072a0001c0021t0001g0182a0006c0006t0001g0174others(1): Show | 4 | HG02896.hp1 HG02897.hp1 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.70-2477T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75710705 | ||||||
| chr13:75710706
|
G | A | 4 | a0001c0001t0002g0072a0001c0021t0001g0182a0006c0006t0001g0174others(1): Show | 4 | HG02896.hp1 HG02897.hp1 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.70-2476G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75710706 | ||||||
| chr13:75710720
|
G | A | 1 | a0008c0008t0003g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.70-2462G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75710720 | ||||||
| chr13:75710831
|
C | T | 4 | a0002c0007t0004g0260a0002c0007t0004g0261a0005c0005t0004g0263others(1): Show | 4 | HG01515.hp2 NA18940.hp2 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-2351C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75710831 | ||||||
| chr13:75710859
|
G | T | 25 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(22): Show | 26 | HG00099.hp1 HG01257.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.70-2323G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75710859 | ||||||
| chr13:75710866
|
A | T | 26 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(23): Show | 27 | HG00099.hp1 HG01257.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.70-2316A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75710866 | ||||||
| chr13:75710883
|
T | C | 26 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(23): Show | 27 | HG00099.hp1 HG01257.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.70-2299T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75710883 | ||||||
| chr13:75710926
|
T | G | 127 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(124): Show | 127 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.70-2256T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75710926 | ||||||
| chr13:75710977
|
A | G | 3 | a0001c0021t0001g0182a0006c0006t0001g0174a0006c0006t0001g0175 | 3 | HG02896.hp1 HG02897.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.70-2205A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75710977 | ||||||
| chr13:75711010
|
C | G | 28 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(25): Show | 29 | HG00099.hp1 HG01257.hp2 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.70-2172C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75711010 | ||||||
| chr13:75711193
|
C | T | 4 | a0001c0019t0002g0267a0001c0019t0002g0268a0001c0020t0002g0269others(1): Show | 4 | HG00621.hp1 HG00673.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.70-1989C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75711193 | ||||||
| chr13:75711271
|
G | A | 1 | a0001c0001t0002g0036 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.70-1911G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75711271 | ||||||
| chr13:75711324
|
A | G | 1 | a0008c0008t0003g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.70-1858A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75711324 | ||||||
| chr13:75711505
|
A | G | 118 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(115): Show | 118 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.70-1677A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75711505 | ||||||
| chr13:75711543
|
T | A | 26 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(23): Show | 27 | HG00099.hp1 HG01257.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.70-1639T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75711543 | ||||||
| chr13:75711568
|
G | A | 1 | a0002c0003t0001g0146 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.70-1614G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75711568 | ||||||
| chr13:75711654
|
C | T | 1 | a0008c0008t0003g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.70-1528C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75711654 | ||||||
| chr13:75711658
|
T | C | 7 | a0002c0007t0003g0176a0002c0007t0003g0178a0002c0007t0003g0180others(4): Show | 7 | HG00639.hp1 HG01081.hp1 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.70-1524T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75711658 | ||||||
| chr13:75711759
|
T | C | 1 | a0002c0003t0001g0146 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.70-1423T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75711759 | ||||||
| chr13:75711763
|
T | G | 1 | a0008c0008t0003g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.70-1419T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75711763 | ||||||
| chr13:75711824
|
T | A | 2 | a0008c0008t0003g0111a0008c0008t0004g0087 | 2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.70-1358T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75711824 | ||||||
| chr13:75712175
|
C | T | 1 | a0001c0021t0001g0182 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.70-1007C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75712175 | ||||||
| chr13:75712263
|
T | C | 17 | a0001c0001t0001g0184a0001c0001t0002g0085a0002c0007t0003g0173others(14): Show | 17 | HG00099.hp1 HG01257.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.70-919T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75712263 | ||||||
| chr13:75712312
|
A | C | 1 | a0009c0010t0017g0004 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.70-870A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75712312 | ||||||
| chr13:75712424
|
A | G | 22 | a0001c0001t0001g0184a0001c0001t0002g0085a0002c0007t0001g0129others(19): Show | 23 | HG00099.hp1 HG01257.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.70-758A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75712424 | ||||||
| chr13:75712679
|
A | G | 26 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(23): Show | 27 | HG00099.hp1 HG01257.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.70-503A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75712679 | ||||||
| chr13:75712703
|
A | G | 2 | a0001c0001t0002g0054a0001c0001t0002g0055 | 2 | NA18980.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.70-479A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75712703 | ||||||
| chr13:75712794
|
G | A | 1 | a0007c0009t0001g0152 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.70-388G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75712794 | ||||||
| chr13:75712925
|
A | T | 23 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(20): Show | 23 | HG00099.hp1 HG01257.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.70-257A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75712925 | ||||||
| chr13:75712926
|
A | C | 25 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(22): Show | 26 | HG00099.hp1 HG01257.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.70-256A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75712926 | ||||||
| chr13:75712927
|
T | A | 25 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(22): Show | 26 | HG00099.hp1 HG01257.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.70-255T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75712927 | ||||||
| chr13:75712928
|
GATTA | G | 25 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(22): Show | 26 | HG00099.hp1 HG01257.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.70-253_70-250delAT others(2): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75712928 | ||||||
| chr13:75713057
|
TAACAGTC others(10): Show |
T | 25 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(22): Show | 26 | HG00099.hp1 HG01257.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.70-122_70-106delCA others(15): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr13 | 75713057 | |||||
| chr13:75713075
|
A | G | 1 | a0012c0014t0014g0185 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.70-107A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75713075 | ||||||
| chr13:75713107
|
A | G | 1 | a0008c0008t0003g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.70-75A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75713107 | ||||||
| chr13:75713150
|
A | G | 2 | a0007c0016t0001g0001a0007c0016t0001g0252 | 3 | HG02895.hp1 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.70-32A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 1/30 | chr13 | 75713150 | ||||||
| chr13:75713296
|
ATG | A | 115 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(112): Show | 115 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.140+55_140+56delTG | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr13 | 75713296 | |||||
| chr13:75713565
|
A | C | 25 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(22): Show | 26 | HG00099.hp1 HG01257.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.140+313A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75713565 | ||||||
| chr13:75713583
|
A | G | 1 | a0009c0010t0017g0004 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.140+331A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75713583 | ||||||
| chr13:75713829
|
A | G | 116 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(113): Show | 116 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.140+577A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75713829 | ||||||
| chr13:75713877
|
C | T | 2 | a0001c0001t0002g0023a0001c0001t0002g0024 | 2 | NA19058.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.140+625C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75713877 | ||||||
| chr13:75714282
|
G | A | 25 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(22): Show | 26 | HG00099.hp1 HG01257.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.140+1030G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75714282 | ||||||
| chr13:75714545
|
G | A | 1 | a0006c0006t0002g0096 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.140+1293G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75714545 | ||||||
| chr13:75714561
|
C | T | 1 | a0004c0004t0002g0032 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.140+1309C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75714561 | ||||||
| chr13:75714675
|
A | G | 7 | a0001c0001t0001g0135a0002c0003t0002g0134a0003c0002t0001g0141others(4): Show | 7 | HG00280.hp1 HG00639.hp2 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.140+1423A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75714675 | ||||||
| chr13:75714804
|
T | A | 26 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(23): Show | 27 | HG00099.hp1 HG01257.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.140+1552T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75714804 | ||||||
| chr13:75714890
|
A | G | 1 | a0017c0023t0002g0050 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.140+1638A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75714890 | ||||||
| chr13:75714904
|
A | G | 1 | a0012c0014t0014g0185 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.140+1652A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75714904 | ||||||
| chr13:75714922
|
A | G | 2 | a0008c0008t0003g0111a0008c0008t0004g0087 | 2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.140+1670A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75714922 | ||||||
| chr13:75715184
|
C | T | 1 | a0009c0010t0002g0015 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.140+1932C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75715184 | ||||||
| chr13:75715233
|
C | T | 1 | a0008c0008t0003g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.140+1981C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75715233 | ||||||
| chr13:75715343
|
A | G | 1 | a0001c0001t0001g0117 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.140+2091A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75715343 | ||||||
| chr13:75715659
|
C | T | 25 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(22): Show | 26 | HG00099.hp1 HG01257.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.140+2407C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75715659 | ||||||
| chr13:75715743
|
A | G | 26 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(23): Show | 27 | HG00099.hp1 HG01257.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.140+2491A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75715743 | ||||||
| chr13:75715844
|
G | C | 116 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(113): Show | 116 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.140+2592G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75715844 | ||||||
| chr13:75715960
|
A | G | 1 | a0004c0013t0002g0104 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.140+2708A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75715960 | ||||||
| chr13:75715980
|
T | A | 4 | a0007c0016t0001g0001a0007c0016t0001g0252a0008c0008t0003g0111others(1): Show | 5 | HG02895.hp1 HG02897.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.140+2728T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75715980 | ||||||
| chr13:75716033
|
A | G | 22 | a0001c0001t0001g0184a0001c0001t0002g0085a0002c0007t0001g0129others(19): Show | 23 | HG00099.hp1 HG01257.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.140+2781A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75716033 | ||||||
| chr13:75716221
|
A | G | 25 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(22): Show | 26 | HG00099.hp1 HG01257.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.140+2969A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75716221 | ||||||
| chr13:75716461
|
A | T | 1 | a0001c0001t0002g0080 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.140+3209A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75716461 | ||||||
| chr13:75716894
|
C | CT | 114 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0117others(111): Show | 114 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.140+3658dupT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr13 | 75716894 | |||||
| chr13:75716894
|
CT | C | 114 | a0001c0001t0001g0201a0001c0001t0001g0207a0001c0001t0001g0208others(111): Show | 115 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.140+3658delT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr13 | 75716894 | |||||
| chr13:75716894
|
CTT | C | 20 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(17): Show | 20 | HG00099.hp1 HG01257.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.140+3657_140+3658d others(4): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr13 | 75716894 | |||||
| chr13:75716910
|
T | C | 4 | a0011c0015t0001g0155a0011c0015t0001g0197a0011c0015t0001g0221others(1): Show | 4 | NA18941.hp2 NA18986.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.140+3658T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75716910 | ||||||
| chr13:75716917
|
T | A | 1 | a0011c0015t0001g0155 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.140+3665T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75716917 | ||||||
| chr13:75716974
|
T | C | 7 | a0001c0001t0001g0135a0002c0003t0002g0134a0003c0002t0001g0141others(4): Show | 7 | HG00280.hp1 HG00639.hp2 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.140+3722T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75716974 | ||||||
| chr13:75717069
|
G | C | 1 | a0003c0002t0001g0219 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.140+3817G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75717069 | ||||||
| chr13:75717082
|
G | C | 24 | a0001c0001t0001g0184a0001c0001t0002g0085a0001c0021t0001g0182others(21): Show | 25 | HG00099.hp1 HG01257.hp2 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.140+3830G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75717082 | ||||||
| chr13:75717198
|
T | C | 152 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(149): Show | 153 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.140+3946T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75717198 | ||||||
| chr13:75717232
|
G | A | 1 | a0008c0008t0003g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.140+3980G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75717232 | ||||||
| chr13:75717256
|
G | A | 10 | a0002c0003t0001g0154a0004c0027t0002g0092a0005c0005t0001g0125others(7): Show | 10 | HG01884.hp1 HG03654.hp2 HG03831.hp2 others(7): Show |
intron_variant | MODIFIER | c.140+4004G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75717256 | ||||||
| chr13:75717294
|
C | T | 1 | a0001c0001t0001g0201 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.140+4042C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75717294 | ||||||
| chr13:75717362
|
C | CA | 22 | a0002c0003t0001g0154a0003c0002t0001g0191a0003c0002t0001g0194others(19): Show | 22 | HG00438.hp2 HG00621.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.140+4129dupA | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr13 | 75717362 | |||||
| chr13:75717362
|
CA | C | 117 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(114): Show | 118 | HG00280.hp1 HG00280.hp2 HG00609.hp2 others(115): Show |
intron_variant | MODIFIER | c.140+4129delA | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr13 | 75717362 | |||||
| chr13:75717380
|
A | AC | 4 | a0003c0002t0001g0006a0008c0008t0003g0005a0008c0008t0003g0168others(1): Show | 4 | HG03669.hp1 HG03704.hp1 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.140+4128_140+4129i others(3): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75717380 | ||||||
| chr13:75717380
|
A | C | 3 | a0001c0001t0001g0184a0001c0001t0002g0085a0008c0008t0002g0077 | 3 | HG00099.hp1 HG01257.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.140+4128A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75717380 | ||||||
| chr13:75717385
|
A | C | 3 | a0001c0021t0001g0182a0006c0006t0001g0174a0006c0006t0001g0175 | 3 | HG02896.hp1 HG02897.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.140+4133A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75717385 | ||||||
| chr13:75717472
|
C | A | 10 | a0002c0003t0001g0154a0004c0027t0002g0092a0005c0005t0001g0125others(7): Show | 10 | HG01884.hp1 HG03654.hp2 HG03831.hp2 others(7): Show |
intron_variant | MODIFIER | c.140+4220C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75717472 | ||||||
| chr13:75717584
|
A | T | 1 | a0001c0001t0001g0201 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.140+4332A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75717584 | ||||||
| chr13:75717703
|
T | C | 1 | a0003c0002t0001g0186 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.140+4451T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75717703 | ||||||
| chr13:75717824
|
G | A | 114 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(111): Show | 114 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.140+4572G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75717824 | ||||||
| chr13:75717932
|
C | T | 3 | a0001c0001t0001g0109a0001c0001t0001g0116a0001c0001t0001g0117 | 3 | NA18944.hp1 NA18946.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.140+4680C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75717932 | ||||||
| chr13:75717944
|
T | C | 2 | a0012c0014t0001g0002a0012c0014t0001g0003 | 2 | HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.140+4692T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75717944 | ||||||
| chr13:75717955
|
G | A | 5 | a0001c0001t0002g0035a0001c0001t0002g0047a0001c0001t0002g0048others(2): Show | 5 | HG01981.hp1 HG02647.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.140+4703G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75717955 | ||||||
| chr13:75717961
|
C | T | 1 | a0008c0008t0002g0077 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.140+4709C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75717961 | ||||||
| chr13:75718092
|
C | A | 6 | a0002c0007t0003g0176a0002c0007t0003g0178a0002c0007t0003g0180others(3): Show | 6 | HG00639.hp1 HG01109.hp2 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.140+4840C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75718092 | ||||||
| chr13:75718194
|
A | G | 1 | a0001c0001t0001g0218 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.140+4942A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75718194 | ||||||
| chr13:75718276
|
A | T | 1 | a0014c0017t0002g0037 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.140+5024A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75718276 | ||||||
| chr13:75718297
|
G | A | 1 | a0001c0001t0002g0088 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.140+5045G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75718297 | ||||||
| chr13:75718383
|
G | A | 1 | a0008c0008t0003g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.140+5131G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75718383 | ||||||
| chr13:75718608
|
A | G | 7 | a0002c0003t0001g0220a0003c0002t0001g0006a0008c0008t0002g0077others(4): Show | 7 | HG03195.hp1 HG03669.hp1 HG03704.hp1 others(4): Show |
intron_variant | MODIFIER | c.140+5356A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75718608 | ||||||
| chr13:75718711
|
T | C | 3 | a0001c0001t0002g0052a0001c0001t0002g0053a0001c0001t0003g0153 | 3 | HG00280.hp2 HG01123.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.140+5459T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75718711 | ||||||
| chr13:75719043
|
G | A | 1 | a0002c0007t0004g0098 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.140+5791G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75719043 | ||||||
| chr13:75719048
|
C | T | 2 | a0005c0005t0001g0114a0008c0008t0003g0110 | 2 | NA19054.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.140+5796C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75719048 | ||||||
| chr13:75719213
|
C | G | 1 | a0008c0008t0003g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.140+5961C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75719213 | ||||||
| chr13:75719261
|
T | TG | 139 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(136): Show | 139 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.140+6010dupG | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr13 | 75719261 | |||||
| chr13:75719366
|
C | T | 3 | a0001c0021t0001g0182a0006c0006t0001g0174a0006c0006t0001g0175 | 3 | HG02896.hp1 HG02897.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.140+6114C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75719366 | ||||||
| chr13:75719422
|
T | C | 7 | a0002c0003t0001g0220a0003c0002t0001g0006a0008c0008t0002g0077others(4): Show | 7 | HG03195.hp1 HG03669.hp1 HG03704.hp1 others(4): Show |
intron_variant | MODIFIER | c.140+6170T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75719422 | ||||||
| chr13:75719526
|
C | T | 30 | a0002c0003t0001g0154a0002c0003t0001g0220a0002c0007t0001g0129others(27): Show | 30 | HG01884.hp1 HG01891.hp2 HG01952.hp2 others(27): Show |
intron_variant | MODIFIER | c.140+6274C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75719526 | ||||||
| chr13:75719628
|
G | A | 121 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(118): Show | 121 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.140+6376G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75719628 | ||||||
| chr13:75719636
|
C | T | 155 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(152): Show | 156 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.140+6384C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75719636 | ||||||
| chr13:75719653
|
C | T | 117 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(114): Show | 117 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.140+6401C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75719653 | ||||||
| chr13:75719688
|
C | T | 5 | a0006c0006t0001g0245a0009c0010t0001g0248a0009c0010t0001g0249others(2): Show | 5 | HG01891.hp2 HG03098.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.140+6436C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75719688 | ||||||
| chr13:75720226
|
A | G | 1 | a0007c0016t0001g0252 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.141-6803A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75720226 | ||||||
| chr13:75720459
|
G | A | 117 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0117others(114): Show | 117 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.141-6570G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75720459 | ||||||
| chr13:75720460
|
T | A | 1 | a0001c0001t0001g0116 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.141-6569T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75720460 | ||||||
| chr13:75720518
|
A | G | 1 | a0001c0001t0002g0025 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.141-6511A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75720518 | ||||||
| chr13:75720537
|
C | T | 1 | a0009c0010t0017g0004 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.141-6492C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75720537 | ||||||
| chr13:75720574
|
A | G | 1 | a0001c0001t0002g0058 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.141-6455A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75720574 | ||||||
| chr13:75720747
|
T | G | 2 | a0002c0011t0002g0075a0002c0011t0002g0076 | 2 | HG00140.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.141-6282T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75720747 | ||||||
| chr13:75720751
|
G | A | 29 | a0002c0003t0001g0154a0002c0003t0001g0220a0002c0007t0003g0173others(26): Show | 29 | HG01884.hp1 HG01891.hp2 HG02818.hp2 others(26): Show |
intron_variant | MODIFIER | c.141-6278G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75720751 | ||||||
| chr13:75720962
|
C | T | 1 | a0001c0001t0001g0113 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.141-6067C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75720962 | ||||||
| chr13:75721006
|
T | C | 1 | a0001c0001t0002g0042 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.141-6023T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75721006 | ||||||
| chr13:75721042
|
G | A | 1 | a0005c0005t0003g0147 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.141-5987G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75721042 | ||||||
| chr13:75721429
|
C | T | 1 | a0001c0001t0002g0008 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.141-5600C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75721429 | ||||||
| chr13:75721677
|
A | G | 1 | a0004c0004t0002g0060 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.141-5352A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75721677 | ||||||
| chr13:75721765
|
A | G | 258 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(255): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.141-5264A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75721765 | ||||||
| chr13:75721846
|
G | A | 1 | a0008c0008t0003g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.141-5183G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75721846 | ||||||
| chr13:75722290
|
G | A | 5 | a0002c0007t0001g0129a0007c0016t0001g0001a0007c0016t0001g0252others(2): Show | 6 | HG01952.hp2 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.141-4739G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75722290 | ||||||
| chr13:75722436
|
T | C | 20 | a0002c0003t0001g0121a0002c0003t0001g0126a0002c0003t0001g0137others(17): Show | 20 | HG01081.hp2 HG01099.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.141-4593T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75722436 | ||||||
| chr13:75722489
|
G | A | 156 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(153): Show | 157 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.141-4540G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75722489 | ||||||
| chr13:75722613
|
C | T | 1 | a0001c0001t0002g0018 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.141-4416C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75722613 | ||||||
| chr13:75722642
|
C | G | 1 | a0003c0002t0001g0212 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.141-4387C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75722642 | ||||||
| chr13:75722731
|
G | A | 3 | a0001c0021t0001g0182a0006c0006t0001g0174a0006c0006t0001g0175 | 3 | HG02896.hp1 HG02897.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.141-4298G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75722731 | ||||||
| chr13:75722820
|
C | A | 29 | a0002c0003t0001g0154a0002c0003t0001g0220a0002c0007t0003g0173others(26): Show | 29 | HG01884.hp1 HG01891.hp2 HG02818.hp2 others(26): Show |
intron_variant | MODIFIER | c.141-4209C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75722820 | ||||||
| chr13:75722888
|
A | G | 4 | a0002c0007t0004g0260a0002c0007t0004g0261a0005c0005t0004g0263others(1): Show | 4 | HG01515.hp2 NA18940.hp2 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.141-4141A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75722888 | ||||||
| chr13:75723059
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.141-3970G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75723059 | ||||||
| chr13:75723219
|
CT | C | 106 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(103): Show | 106 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.141-3809delT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75723219 | ||||||
| chr13:75723361
|
T | TAATAA | 154 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(151): Show | 155 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.141-3666_141-3662d others(7): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr13 | 75723361 | |||||
| chr13:75723382
|
G | C | 1 | a0007c0009t0009g0251 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.141-3647G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75723382 | ||||||
| chr13:75723474
|
T | C | 1 | a0009c0030t0001g0170 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.141-3555T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75723474 | ||||||
| chr13:75723499
|
C | T | 2 | a0004c0004t0001g0148a0004c0004t0001g0149 | 2 | NA19007.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.141-3530C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75723499 | ||||||
| chr13:75723702
|
G | C | 29 | a0002c0003t0001g0154a0002c0003t0001g0220a0002c0007t0003g0173others(26): Show | 29 | HG01884.hp1 HG01891.hp2 HG02818.hp2 others(26): Show |
intron_variant | MODIFIER | c.141-3327G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75723702 | ||||||
| chr13:75723751
|
A | G | 156 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(153): Show | 157 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.141-3278A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75723751 | ||||||
| chr13:75723754
|
G | C | 1 | a0006c0006t0001g0183 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.141-3275G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75723754 | ||||||
| chr13:75723872
|
T | C | 1 | a0002c0003t0001g0211 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.141-3157T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75723872 | ||||||
| chr13:75724225
|
C | G | 2 | a0001c0001t0002g0088a0007c0009t0001g0166 | 2 | HG02258.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.141-2804C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75724225 | ||||||
| chr13:75724378
|
G | C | 34 | a0002c0003t0001g0154a0002c0003t0001g0220a0002c0007t0001g0129others(31): Show | 35 | HG01884.hp1 HG01891.hp2 HG01952.hp2 others(32): Show |
intron_variant | MODIFIER | c.141-2651G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75724378 | ||||||
| chr13:75724423
|
A | G | 7 | a0001c0001t0001g0109a0001c0001t0001g0116a0001c0001t0001g0117others(4): Show | 7 | HG02698.hp2 HG03017.hp1 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.141-2606A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75724423 | ||||||
| chr13:75724621
|
T | A | 1 | a0010c0012t0002g0105 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.141-2408T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75724621 | ||||||
| chr13:75724753
|
T | G | 3 | a0001c0021t0001g0182a0006c0006t0001g0174a0006c0006t0001g0175 | 3 | HG02896.hp1 HG02897.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.141-2276T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75724753 | ||||||
| chr13:75724799
|
G | A | 5 | a0006c0006t0001g0245a0009c0010t0001g0248a0009c0010t0001g0249others(2): Show | 5 | HG01891.hp2 HG03098.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.141-2230G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75724799 | ||||||
| chr13:75724810
|
C | G | 28 | a0002c0003t0001g0154a0002c0003t0001g0220a0002c0007t0003g0173others(25): Show | 28 | HG01884.hp1 HG01891.hp2 HG02818.hp2 others(25): Show |
intron_variant | MODIFIER | c.141-2219C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75724810 | ||||||
| chr13:75724825
|
A | G | 5 | a0002c0007t0001g0129a0007c0016t0001g0001a0007c0016t0001g0252others(2): Show | 6 | HG01952.hp2 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.141-2204A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75724825 | ||||||
| chr13:75724856
|
T | G | 3 | a0013c0018t0004g0010a0013c0018t0004g0011a0013c0018t0004g0056 | 3 | HG02723.hp2 HG02896.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.141-2173T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75724856 | ||||||
| chr13:75724922
|
C | T | 1 | a0008c0008t0003g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.141-2107C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75724922 | ||||||
| chr13:75724966
|
C | T | 7 | a0001c0001t0001g0135a0002c0003t0002g0134a0003c0002t0001g0141others(4): Show | 7 | HG00280.hp1 HG00639.hp2 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.141-2063C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75724966 | ||||||
| chr13:75725554
|
G | T | 4 | a0001c0001t0001g0159a0001c0001t0002g0012a0003c0002t0001g0123others(1): Show | 4 | NA18953.hp2 NA18986.hp1 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.141-1475G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75725554 | ||||||
| chr13:75725566
|
A | G | 1 | a0004c0004t0001g0236 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.141-1463A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75725566 | ||||||
| chr13:75725761
|
C | G | 1 | a0008c0008t0001g0089 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.141-1268C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75725761 | ||||||
| chr13:75725949
|
C | G | 116 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(113): Show | 116 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.141-1080C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75725949 | ||||||
| chr13:75725988
|
A | AT | 6 | a0002c0003t0001g0126a0002c0007t0001g0129a0006c0006t0001g0172others(3): Show | 7 | HG01175.hp2 HG01952.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.141-1026dupT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr13 | 75725988 | |||||
| chr13:75726090
|
G | A | 1 | a0004c0004t0001g0199 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.141-939G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75726090 | ||||||
| chr13:75726135
|
T | C | 154 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(151): Show | 155 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.141-894T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75726135 | ||||||
| chr13:75726227
|
C | T | 1 | a0004c0027t0002g0092 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.141-802C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75726227 | ||||||
| chr13:75726429
|
A | G | 2 | a0001c0001t0002g0034a0001c0001t0002g0041 | 2 | NA18942.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.141-600A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75726429 | ||||||
| chr13:75726546
|
C | G | 256 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(253): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.141-483C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75726546 | ||||||
| chr13:75726728
|
G | C | 1 | a0009c0010t0017g0004 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.141-301G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75726728 | ||||||
| chr13:75726806
|
C | A | 154 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(151): Show | 155 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.141-223C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75726806 | ||||||
| chr13:75726848
|
G | A | 1 | a0009c0010t0017g0004 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.141-181G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75726848 | ||||||
| chr13:75726965
|
G | C | 2 | a0001c0001t0002g0088a0007c0009t0001g0166 | 2 | HG02258.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.141-64G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 2/30 | chr13 | 75726965 | ||||||
| chr13:75727188
|
C | T | 1 | a0002c0003t0001g0203 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.210+90C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75727188 | ||||||
| chr13:75727190
|
C | A | 1 | a0008c0008t0001g0089 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.210+92C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75727190 | ||||||
| chr13:75727225
|
G | C | 2 | a0003c0002t0001g0225a0003c0002t0001g0226 | 2 | NA18980.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.210+127G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75727225 | ||||||
| chr13:75727495
|
A | G | 1 | a0001c0001t0002g0029 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.210+397A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75727495 | ||||||
| chr13:75727792
|
C | T | 7 | a0001c0001t0001g0135a0002c0003t0002g0134a0003c0002t0001g0141others(4): Show | 7 | HG00280.hp1 HG00639.hp2 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.210+694C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75727792 | ||||||
| chr13:75727860
|
G | C | 1 | a0006c0006t0001g0183 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.210+762G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75727860 | ||||||
| chr13:75727895
|
G | A | 120 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(117): Show | 120 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.210+797G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75727895 | ||||||
| chr13:75727903
|
A | G | 10 | a0002c0003t0001g0154a0005c0005t0001g0125a0005c0005t0003g0112others(7): Show | 10 | HG03654.hp2 HG03831.hp2 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.210+805A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75727903 | ||||||
| chr13:75727955
|
G | T | 1 | a0003c0002t0001g0141 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.210+857G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75727955 | ||||||
| chr13:75727985
|
C | G | 154 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(151): Show | 155 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.210+887C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75727985 | ||||||
| chr13:75728060
|
G | A | 154 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(151): Show | 155 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.210+962G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75728060 | ||||||
| chr13:75728125
|
T | C | 65 | a0001c0001t0001g0113a0001c0001t0001g0143a0001c0001t0001g0150others(62): Show | 65 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.210+1027T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75728125 | ||||||
| chr13:75728172
|
C | A | 11 | a0002c0003t0001g0154a0004c0027t0002g0092a0005c0005t0001g0125others(8): Show | 11 | HG01884.hp1 HG03654.hp2 HG03831.hp2 others(8): Show |
intron_variant | MODIFIER | c.210+1074C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75728172 | ||||||
| chr13:75728238
|
C | G | 3 | a0001c0021t0001g0182a0006c0006t0001g0174a0006c0006t0001g0175 | 3 | HG02896.hp1 HG02897.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.210+1140C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75728238 | ||||||
| chr13:75728311
|
C | T | 1 | a0001c0001t0001g0208 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.210+1213C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75728311 | ||||||
| chr13:75728364
|
G | C | 1 | a0008c0008t0003g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.210+1266G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75728364 | ||||||
| chr13:75728469
|
T | C | 7 | a0001c0001t0001g0167a0001c0001t0002g0017a0001c0001t0002g0078others(4): Show | 7 | HG00735.hp2 HG01496.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.210+1371T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75728469 | ||||||
| chr13:75728475
|
GT | G | 154 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(151): Show | 155 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.210+1385delT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75728475 | |||||
| chr13:75728487
|
G | A | 256 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(253): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.210+1389G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75728487 | ||||||
| chr13:75728552
|
A | C | 1 | a0006c0006t0002g0093 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.210+1454A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75728552 | ||||||
| chr13:75728595
|
A | G | 2 | a0007c0016t0001g0001a0007c0016t0001g0252 | 3 | HG02895.hp1 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.210+1497A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75728595 | ||||||
| chr13:75728631
|
T | G | 18 | a0002c0003t0001g0121a0002c0003t0001g0126a0002c0003t0001g0137others(15): Show | 18 | HG01081.hp2 HG01099.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.210+1533T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75728631 | ||||||
| chr13:75728653
|
G | T | 20 | a0002c0003t0001g0121a0002c0003t0001g0126a0002c0003t0001g0137others(17): Show | 20 | HG01081.hp2 HG01099.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.210+1555G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75728653 | ||||||
| chr13:75728675
|
G | A | 1 | a0001c0001t0002g0043 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.210+1577G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75728675 | ||||||
| chr13:75728709
|
A | G | 156 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(153): Show | 157 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.210+1611A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75728709 | ||||||
| chr13:75728766
|
G | A | 5 | a0002c0007t0001g0129a0007c0016t0001g0001a0007c0016t0001g0252others(2): Show | 6 | HG01952.hp2 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.210+1668G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75728766 | ||||||
| chr13:75728768
|
T | G | 5 | a0002c0007t0001g0129a0007c0016t0001g0001a0007c0016t0001g0252others(2): Show | 6 | HG01952.hp2 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.210+1670T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75728768 | ||||||
| chr13:75728897
|
G | T | 1 | a0009c0010t0017g0004 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.210+1799G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75728897 | ||||||
| chr13:75728907
|
C | G | 29 | a0002c0003t0001g0154a0002c0003t0001g0220a0002c0007t0003g0173others(26): Show | 29 | HG01884.hp1 HG01891.hp2 HG02818.hp2 others(26): Show |
intron_variant | MODIFIER | c.210+1809C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75728907 | ||||||
| chr13:75728956
|
C | G | 154 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(151): Show | 155 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.210+1858C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75728956 | ||||||
| chr13:75728968
|
C | G | 8 | a0003c0002t0001g0142a0003c0002t0001g0194a0003c0002t0001g0222others(5): Show | 8 | HG00438.hp2 HG02056.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.210+1870C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75728968 | ||||||
| chr13:75729059
|
G | C | 2 | a0006c0006t0002g0096a0006c0006t0002g0108 | 2 | HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.210+1961G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75729059 | ||||||
| chr13:75729059
|
G | T | 1 | a0007c0009t0009g0251 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.210+1961G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75729059 | ||||||
| chr13:75729076
|
G | T | 4 | a0001c0001t0002g0036a0001c0021t0001g0182a0006c0006t0001g0174others(1): Show | 4 | HG02896.hp1 HG02897.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.210+1978G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75729076 | ||||||
| chr13:75729102
|
T | C | 3 | a0014c0017t0002g0027a0014c0017t0002g0028a0014c0017t0002g0037 | 3 | HG01167.hp1 HG01169.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.210+2004T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75729102 | ||||||
| chr13:75729151
|
C | T | 1 | a0001c0001t0002g0040 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.210+2053C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75729151 | ||||||
| chr13:75729168
|
T | G | 1 | a0001c0001t0002g0040 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.210+2070T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75729168 | ||||||
| chr13:75729187
|
G | T | 1 | a0008c0008t0003g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.210+2089G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75729187 | ||||||
| chr13:75729291
|
C | G | 2 | a0002c0011t0002g0075a0002c0011t0002g0076 | 2 | HG00140.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.210+2193C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75729291 | ||||||
| chr13:75729447
|
A | G | 1 | a0006c0006t0002g0095 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.210+2349A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75729447 | ||||||
| chr13:75729549
|
A | C | 1 | a0001c0001t0002g0088 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.210+2451A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75729549 | ||||||
| chr13:75729597
|
T | G | 2 | a0001c0001t0002g0054a0001c0001t0002g0055 | 2 | NA18980.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.210+2499T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75729597 | ||||||
| chr13:75729603
|
A | G | 1 | a0001c0001t0002g0088 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.210+2505A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75729603 | ||||||
| chr13:75729611
|
C | T | 2 | a0001c0001t0002g0054a0001c0001t0002g0055 | 2 | NA18980.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.210+2513C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75729611 | ||||||
| chr13:75729701
|
C | G | 154 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(151): Show | 155 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.210+2603C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75729701 | ||||||
| chr13:75729796
|
T | C | 154 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(151): Show | 155 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.210+2698T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75729796 | ||||||
| chr13:75729950
|
A | C | 1 | a0001c0001t0001g0218 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.210+2852A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75729950 | ||||||
| chr13:75729991
|
G | C | 1 | a0001c0001t0002g0085 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.210+2893G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75729991 | ||||||
| chr13:75729993
|
G | A | 40 | a0002c0003t0001g0121a0002c0003t0001g0126a0002c0003t0001g0137others(37): Show | 40 | HG00099.hp2 HG00140.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.210+2895G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75729993 | ||||||
| chr13:75730059
|
C | T | 4 | a0007c0016t0001g0001a0007c0016t0001g0252a0008c0008t0003g0111others(1): Show | 5 | HG02895.hp1 HG02897.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.210+2961C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75730059 | ||||||
| chr13:75730120
|
T | A | 1 | a0002c0003t0001g0154 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.210+3022T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75730120 | ||||||
| chr13:75730126
|
G | A | 5 | a0006c0006t0001g0245a0009c0010t0001g0248a0009c0010t0001g0249others(2): Show | 5 | HG01891.hp2 HG03098.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.210+3028G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75730126 | ||||||
| chr13:75730143
|
C | A | 154 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(151): Show | 155 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.210+3045C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75730143 | ||||||
| chr13:75730163
|
C | A | 4 | a0007c0016t0001g0001a0007c0016t0001g0252a0008c0008t0003g0111others(1): Show | 5 | HG02895.hp1 HG02897.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.210+3065C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75730163 | ||||||
| chr13:75730175
|
G | A | 1 | a0003c0002t0001g0229 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.210+3077G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75730175 | ||||||
| chr13:75730264
|
C | G | 154 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(151): Show | 155 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.210+3166C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75730264 | ||||||
| chr13:75730327
|
A | G | 59 | a0001c0001t0001g0201a0001c0001t0001g0207a0001c0001t0001g0208others(56): Show | 59 | HG00438.hp2 HG00609.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.210+3229A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75730327 | ||||||
| chr13:75730335
|
C | A | 1 | a0004c0004t0001g0187 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.210+3237C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75730335 | ||||||
| chr13:75730375
|
G | C | 117 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(114): Show | 117 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.210+3277G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75730375 | ||||||
| chr13:75730418
|
AG | A | 3 | a0002c0003t0005g0030a0002c0003t0005g0070a0002c0003t0011g0161 | 3 | HG01099.hp1 HG01257.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.210+3323delG | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75730418 | |||||
| chr13:75730462
|
A | T | 1 | a0015c0029t0001g0118 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.210+3364A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75730462 | ||||||
| chr13:75730465
|
A | G | 118 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(115): Show | 118 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.210+3367A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75730465 | ||||||
| chr13:75730543
|
C | T | 1 | a0008c0008t0003g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.210+3445C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75730543 | ||||||
| chr13:75730544
|
G | A | 1 | a0006c0006t0002g0100 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.210+3446G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75730544 | ||||||
| chr13:75730624
|
T | C | 1 | a0003c0002t0001g0193 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.210+3526T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75730624 | ||||||
| chr13:75730807
|
T | C | 154 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(151): Show | 155 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.210+3709T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75730807 | ||||||
| chr13:75730840
|
G | A | 1 | a0021c0026t0001g0122 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.210+3742G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75730840 | ||||||
| chr13:75730943
|
G | A | 29 | a0002c0003t0001g0154a0002c0003t0001g0220a0002c0007t0003g0173others(26): Show | 29 | HG01884.hp1 HG01891.hp2 HG02818.hp2 others(26): Show |
intron_variant | MODIFIER | c.210+3845G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75730943 | ||||||
| chr13:75731128
|
G | A | 1 | a0002c0011t0002g0071 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.210+4030G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75731128 | ||||||
| chr13:75731138
|
A | G | 1 | a0002c0003t0001g0154 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.210+4040A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75731138 | ||||||
| chr13:75731149
|
C | T | 1 | a0005c0005t0003g0147 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.210+4051C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75731149 | ||||||
| chr13:75731404
|
G | A | 1 | a0008c0008t0003g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.210+4306G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75731404 | ||||||
| chr13:75731409
|
G | T | 2 | a0002c0007t0003g0173a0009c0010t0003g0244 | 2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.210+4311G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75731409 | ||||||
| chr13:75731466
|
G | A | 1 | a0001c0001t0002g0069 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.210+4368G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75731466 | ||||||
| chr13:75731511
|
G | A | 5 | a0001c0001t0002g0035a0001c0001t0002g0047a0001c0001t0002g0048others(2): Show | 5 | HG01981.hp1 HG02647.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.210+4413G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75731511 | ||||||
| chr13:75731589
|
C | A | 1 | a0001c0001t0002g0058 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.210+4491C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75731589 | ||||||
| chr13:75731596
|
G | A | 1 | a0001c0001t0002g0068 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.210+4498G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75731596 | ||||||
| chr13:75731651
|
T | C | 1 | a0001c0020t0002g0269 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.210+4553T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75731651 | ||||||
| chr13:75731725
|
C | A | 1 | a0006c0006t0001g0183 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.210+4627C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75731725 | ||||||
| chr13:75731725
|
C | T | 1 | a0004c0004t0001g0199 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.210+4627C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75731725 | ||||||
| chr13:75731766
|
A | G | 1 | a0003c0002t0001g0216 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.210+4668A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75731766 | ||||||
| chr13:75731792
|
G | A | 8 | a0002c0007t0003g0176a0002c0007t0003g0178a0002c0007t0003g0180others(5): Show | 8 | HG00639.hp1 HG01081.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.210+4694G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75731792 | ||||||
| chr13:75731823
|
T | C | 1 | a0008c0008t0003g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.210+4725T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75731823 | ||||||
| chr13:75731832
|
C | T | 2 | a0002c0007t0003g0176a0022c0025t0003g0177 | 2 | HG03669.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.210+4734C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75731832 | ||||||
| chr13:75731833
|
A | G | 1 | a0008c0008t0003g0005 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.210+4735A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75731833 | ||||||
| chr13:75731881
|
G | A | 154 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(151): Show | 155 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.210+4783G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75731881 | ||||||
| chr13:75732080
|
A | G | 155 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(152): Show | 156 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.210+4982A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75732080 | ||||||
| chr13:75732127
|
A | G | 2 | a0010c0012t0001g0130a0010c0012t0001g0131 | 2 | HG06807.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.210+5029A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75732127 | ||||||
| chr13:75732131
|
CTG | C | 7 | a0002c0003t0001g0253a0002c0003t0001g0255a0002c0003t0001g0256others(4): Show | 7 | HG00673.hp1 HG02040.hp1 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.210+5036_210+5037d others(4): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75732131 | |||||
| chr13:75732140
|
C | T | 1 | a0007c0009t0001g0163 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.210+5042C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75732140 | ||||||
| chr13:75732204
|
A | G | 3 | a0001c0001t0002g0101a0006c0006t0002g0094a0006c0006t0002g0102 | 3 | HG02647.hp2 HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.210+5106A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75732204 | ||||||
| chr13:75732245
|
G | A | 1 | a0001c0001t0002g0013 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.210+5147G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75732245 | ||||||
| chr13:75732247
|
C | G | 2 | a0005c0005t0001g0114a0008c0008t0003g0110 | 2 | NA19054.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.210+5149C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75732247 | ||||||
| chr13:75732259
|
C | T | 1 | a0001c0001t0002g0018 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.210+5161C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75732259 | ||||||
| chr13:75732359
|
CTTCATTT others(2): Show |
C | 117 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(114): Show | 117 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.210+5272_210+5280d others(11): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75732359 | |||||
| chr13:75732439
|
C | T | 5 | a0007c0016t0001g0001a0007c0016t0001g0252a0008c0008t0002g0077others(2): Show | 6 | HG02895.hp1 HG02897.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.210+5341C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75732439 | ||||||
| chr13:75732486
|
A | G | 1 | a0003c0002t0001g0186 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.210+5388A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75732486 | ||||||
| chr13:75732524
|
G | T | 21 | a0002c0003t0001g0154a0002c0007t0003g0173a0002c0007t0003g0246others(18): Show | 21 | HG01884.hp1 HG01891.hp2 HG02818.hp2 others(18): Show |
intron_variant | MODIFIER | c.210+5426G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75732524 | ||||||
| chr13:75732570
|
C | A | 3 | a0001c0021t0001g0182a0006c0006t0001g0174a0006c0006t0001g0175 | 3 | HG02896.hp1 HG02897.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.210+5472C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75732570 | ||||||
| chr13:75732625
|
C | T | 1 | a0004c0004t0001g0231 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.210+5527C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75732625 | ||||||
| chr13:75732641
|
T | C | 2 | a0007c0016t0001g0001a0007c0016t0001g0252 | 3 | HG02895.hp1 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.210+5543T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75732641 | ||||||
| chr13:75732642
|
G | A | 2 | a0007c0016t0001g0001a0007c0016t0001g0252 | 3 | HG02895.hp1 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.210+5544G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75732642 | ||||||
| chr13:75732698
|
G | A | 1 | a0003c0002t0001g0227 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.210+5600G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75732698 | ||||||
| chr13:75732748
|
G | T | 1 | a0001c0001t0002g0045 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.210+5650G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75732748 | ||||||
| chr13:75732759
|
G | A | 1 | a0001c0001t0002g0008 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.210+5661G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75732759 | ||||||
| chr13:75732812
|
C | T | 1 | a0003c0002t0001g0212 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.210+5714C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75732812 | ||||||
| chr13:75732933
|
C | T | 1 | a0002c0003t0001g0238 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.210+5835C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75732933 | ||||||
| chr13:75733056
|
A | G | 155 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(152): Show | 156 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.210+5958A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75733056 | ||||||
| chr13:75733096
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.210+5998C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75733096 | ||||||
| chr13:75733244
|
G | T | 5 | a0001c0001t0002g0035a0001c0001t0002g0047a0001c0001t0002g0048others(2): Show | 5 | HG01981.hp1 HG02647.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.210+6146G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75733244 | ||||||
| chr13:75733285
|
T | G | 2 | a0002c0007t0003g0173a0009c0010t0003g0244 | 2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.210+6187T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75733285 | ||||||
| chr13:75733332
|
G | A | 1 | a0011c0015t0001g0155 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.210+6234G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75733332 | ||||||
| chr13:75733332
|
G | C | 1 | a0004c0027t0002g0092 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.210+6234G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75733332 | ||||||
| chr13:75733396
|
C | A | 117 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(114): Show | 117 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.210+6298C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75733396 | ||||||
| chr13:75733400
|
A | G | 2 | a0001c0001t0001g0135a0004c0004t0006g0103 | 2 | HG00738.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.210+6302A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75733400 | ||||||
| chr13:75733407
|
C | T | 1 | a0002c0007t0003g0246 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.210+6309C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75733407 | ||||||
| chr13:75733456
|
C | T | 154 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(151): Show | 155 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.210+6358C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75733456 | ||||||
| chr13:75733506
|
C | G | 29 | a0002c0003t0001g0154a0002c0003t0001g0220a0002c0007t0001g0129others(26): Show | 29 | HG01884.hp1 HG01891.hp2 HG01952.hp2 others(26): Show |
intron_variant | MODIFIER | c.210+6408C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75733506 | ||||||
| chr13:75733638
|
CTGCGCCC others(7): Show |
C | 117 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(114): Show | 117 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.210+6541_210+6554d others(16): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75733638 | ||||||
| chr13:75733641
|
C | T | 1 | a0006c0006t0001g0183 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.210+6543C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75733641 | ||||||
| chr13:75733675
|
A | C | 1 | a0002c0007t0004g0260 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.210+6577A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75733675 | ||||||
| chr13:75733682
|
T | C | 1 | a0002c0007t0004g0260 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.210+6584T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75733682 | ||||||
| chr13:75733683
|
G | T | 1 | a0002c0007t0004g0260 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.210+6585G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75733683 | ||||||
| chr13:75733826
|
A | C | 1 | a0001c0001t0002g0035 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.210+6728A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75733826 | ||||||
| chr13:75733845
|
C | T | 154 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(151): Show | 155 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.210+6747C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75733845 | ||||||
| chr13:75733864
|
A | G | 2 | a0001c0001t0002g0020a0001c0001t0002g0062 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.210+6766A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75733864 | ||||||
| chr13:75733960
|
G | C | 3 | a0001c0001t0002g0101a0006c0006t0002g0094a0006c0006t0002g0102 | 3 | HG02647.hp2 HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.210+6862G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75733960 | ||||||
| chr13:75733967
|
T | C | 1 | a0007c0016t0001g0252 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.210+6869T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75733967 | ||||||
| chr13:75734224
|
C | T | 154 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(151): Show | 155 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.210+7126C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75734224 | ||||||
| chr13:75734242
|
C | T | 1 | a0002c0003t0001g0126 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.210+7144C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75734242 | ||||||
| chr13:75734325
|
A | G | 2 | a0010c0012t0001g0130a0010c0012t0001g0131 | 2 | HG06807.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.210+7227A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75734325 | ||||||
| chr13:75734445
|
A | G | 3 | a0004c0004t0001g0188a0004c0004t0001g0190a0004c0004t0013g0189 | 3 | NA18949.hp2 NA18999.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.210+7347A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75734445 | ||||||
| chr13:75734486
|
C | G | 2 | a0002c0003t0001g0220a0008c0008t0003g0241 | 2 | HG03927.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.210+7388C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75734486 | ||||||
| chr13:75734520
|
A | G | 3 | a0001c0021t0001g0182a0006c0006t0001g0174a0006c0006t0001g0175 | 3 | HG02896.hp1 HG02897.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.210+7422A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75734520 | ||||||
| chr13:75734752
|
C | A | 11 | a0002c0003t0001g0154a0004c0027t0002g0092a0005c0005t0001g0125others(8): Show | 11 | HG01884.hp1 HG03654.hp2 HG03831.hp2 others(8): Show |
intron_variant | MODIFIER | c.210+7654C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75734752 | ||||||
| chr13:75734762
|
A | G | 4 | a0002c0011t0002g0031a0002c0011t0002g0038a0002c0011t0002g0071others(1): Show | 4 | HG00099.hp2 HG01168.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.210+7664A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75734762 | ||||||
| chr13:75734803
|
G | T | 2 | a0008c0008t0003g0111a0008c0008t0004g0087 | 2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.210+7705G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75734803 | ||||||
| chr13:75734821
|
C | T | 1 | a0002c0007t0003g0181 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.210+7723C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75734821 | ||||||
| chr13:75734887
|
C | T | 147 | a0001c0001t0001g0113a0001c0001t0001g0135a0001c0001t0001g0143others(144): Show | 148 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.210+7789C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75734887 | ||||||
| chr13:75734895
|
G | C | 144 | a0001c0001t0001g0113a0001c0001t0001g0135a0001c0001t0001g0143others(141): Show | 145 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.210+7797G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75734895 | ||||||
| chr13:75734915
|
C | T | 1 | a0008c0008t0003g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.210+7817C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75734915 | ||||||
| chr13:75735029
|
T | C | 7 | a0002c0003t0001g0253a0002c0003t0001g0255a0002c0003t0001g0256others(4): Show | 7 | HG00673.hp1 HG02040.hp1 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.210+7931T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75735029 | ||||||
| chr13:75735092
|
C | T | 123 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(120): Show | 123 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.210+7994C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75735092 | ||||||
| chr13:75735093
|
G | A | 1 | a0008c0008t0003g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.210+7995G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75735093 | ||||||
| chr13:75735116
|
C | CGT | 9 | a0001c0001t0002g0040a0001c0001t0002g0042a0002c0003t0005g0033others(6): Show | 9 | HG00735.hp1 HG01891.hp2 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.210+8043_210+8044d others(4): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75735116 | |||||
| chr13:75735116
|
CGT | C | 109 | a0001c0001t0001g0201a0001c0001t0001g0207a0001c0001t0001g0208others(106): Show | 109 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.210+8043_210+8044d others(4): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75735116 | |||||
| chr13:75735116
|
CGTGT | C | 6 | a0002c0007t0001g0129a0006c0006t0001g0172a0007c0016t0001g0001others(3): Show | 7 | HG01952.hp2 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.210+8041_210+8044d others(6): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75735116 | |||||
| chr13:75735141
|
GTA | G | 5 | a0001c0001t0001g0135a0002c0003t0002g0134a0003c0002t0001g0141others(2): Show | 5 | HG00280.hp1 HG00639.hp2 HG00738.hp1 others(2): Show |
intron_variant | MODIFIER | c.210+8045_210+8046d others(4): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75735141 | |||||
| chr13:75735143
|
A | G | 110 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(107): Show | 110 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.210+8045A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75735143 | ||||||
| chr13:75735154
|
T | A | 4 | a0007c0016t0001g0001a0007c0016t0001g0252a0008c0008t0003g0111others(1): Show | 5 | HG02895.hp1 HG02897.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.210+8056T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75735154 | ||||||
| chr13:75735208
|
C | T | 155 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(152): Show | 156 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.210+8110C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75735208 | ||||||
| chr13:75735229
|
T | A | 3 | a0001c0021t0001g0182a0006c0006t0001g0174a0006c0006t0001g0175 | 3 | HG02896.hp1 HG02897.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.210+8131T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75735229 | ||||||
| chr13:75735252
|
C | A | 3 | a0001c0021t0001g0182a0006c0006t0001g0174a0006c0006t0001g0175 | 3 | HG02896.hp1 HG02897.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.210+8154C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75735252 | ||||||
| chr13:75735364
|
T | TAC | 6 | a0001c0001t0001g0218a0001c0001t0002g0009a0001c0001t0002g0039others(3): Show | 6 | HG01346.hp2 HG02074.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.210+8284_210+8285d others(4): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75735364 | |||||
| chr13:75735501
|
C | A | 117 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(114): Show | 117 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.210+8403C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75735501 | ||||||
| chr13:75735535
|
C | G | 6 | a0002c0003t0001g0220a0008c0008t0001g0089a0008c0008t0003g0005others(3): Show | 6 | HG01243.hp1 HG03669.hp1 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.210+8437C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75735535 | ||||||
| chr13:75735548
|
G | T | 1 | a0001c0001t0002g0041 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.210+8450G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75735548 | ||||||
| chr13:75735564
|
C | T | 1 | a0010c0012t0002g0105 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.210+8466C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75735564 | ||||||
| chr13:75735565
|
G | A | 1 | a0003c0002t0001g0222 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.210+8467G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75735565 | ||||||
| chr13:75735610
|
C | T | 122 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(119): Show | 122 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.210+8512C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75735610 | ||||||
| chr13:75735612
|
G | T | 2 | a0012c0014t0001g0002a0012c0014t0001g0003 | 2 | HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.210+8514G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75735612 | ||||||
| chr13:75735628
|
A | AT | 4 | a0005c0005t0003g0128a0007c0016t0001g0001a0007c0016t0001g0252others(1): Show | 5 | HG02895.hp1 HG02897.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.210+8545dupT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75735628 | |||||
| chr13:75735678
|
G | A | 4 | a0007c0016t0001g0001a0007c0016t0001g0252a0008c0008t0003g0111others(1): Show | 5 | HG02895.hp1 HG02897.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.210+8580G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75735678 | ||||||
| chr13:75735737
|
G | A | 1 | a0004c0027t0002g0092 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.210+8639G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75735737 | ||||||
| chr13:75735787
|
A | G | 7 | a0001c0001t0002g0101a0006c0006t0001g0183a0006c0006t0002g0094others(4): Show | 7 | HG00140.hp2 HG01106.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.210+8689A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75735787 | ||||||
| chr13:75736116
|
A | G | 1 | a0002c0007t0001g0129 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.210+9018A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75736116 | ||||||
| chr13:75736255
|
A | G | 1 | a0004c0013t0002g0104 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.210+9157A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75736255 | ||||||
| chr13:75736585
|
C | T | 2 | a0002c0011t0002g0031a0002c0011t0002g0038 | 2 | HG01168.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.210+9487C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75736585 | ||||||
| chr13:75736646
|
A | T | 5 | a0001c0001t0002g0088a0001c0001t0002g0099a0001c0001t0002g0106others(2): Show | 5 | HG01099.hp2 HG01884.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.210+9548A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75736646 | ||||||
| chr13:75736697
|
G | T | 1 | a0001c0001t0001g0167 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.210+9599G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75736697 | ||||||
| chr13:75736714
|
C | T | 127 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(124): Show | 128 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.210+9616C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75736714 | ||||||
| chr13:75737093
|
T | C | 1 | a0001c0001t0002g0082 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.210+9995T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75737093 | ||||||
| chr13:75737406
|
C | T | 3 | a0002c0003t0001g0255a0002c0003t0001g0257a0002c0003t0001g0259 | 3 | HG02040.hp1 NA18747.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.210+10308C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75737406 | ||||||
| chr13:75737455
|
T | A | 2 | a0012c0014t0001g0002a0012c0014t0001g0003 | 2 | HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.210+10357T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75737455 | ||||||
| chr13:75737456
|
A | T | 127 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(124): Show | 128 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.210+10358A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75737456 | ||||||
| chr13:75737457
|
A | T | 2 | a0001c0019t0002g0267a0001c0019t0002g0268 | 2 | HG00673.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.210+10359A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75737457 | ||||||
| chr13:75737491
|
C | T | 11 | a0002c0003t0001g0154a0004c0027t0002g0092a0005c0005t0001g0125others(8): Show | 11 | HG01884.hp1 HG03654.hp2 HG03831.hp2 others(8): Show |
intron_variant | MODIFIER | c.210+10393C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75737491 | ||||||
| chr13:75737510
|
C | T | 1 | a0004c0004t0001g0236 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.210+10412C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75737510 | ||||||
| chr13:75737528
|
C | T | 1 | a0006c0006t0002g0095 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.210+10430C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75737528 | ||||||
| chr13:75737635
|
C | T | 60 | a0001c0001t0001g0201a0001c0001t0001g0207a0001c0001t0001g0208others(57): Show | 60 | HG00438.hp2 HG00609.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.210+10537C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75737635 | ||||||
| chr13:75737664
|
G | A | 127 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(124): Show | 128 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.210+10566G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75737664 | ||||||
| chr13:75737677
|
T | C | 1 | a0003c0002t0001g0224 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.210+10579T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75737677 | ||||||
| chr13:75737708
|
G | A | 4 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0069others(1): Show | 4 | NA18979.hp2 NA18980.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.210+10610G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75737708 | ||||||
| chr13:75737731
|
C | A | 5 | a0002c0007t0001g0129a0007c0016t0001g0001a0007c0016t0001g0252others(2): Show | 6 | HG01952.hp2 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.210+10633C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75737731 | ||||||
| chr13:75737747
|
C | T | 127 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(124): Show | 128 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.210+10649C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75737747 | ||||||
| chr13:75737752
|
C | CAAA | 109 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(106): Show | 109 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.210+10666_210+1066 others(7): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75737752 | |||||
| chr13:75737752
|
CA | C | 97 | a0001c0001t0001g0201a0001c0001t0001g0207a0001c0001t0001g0208others(94): Show | 97 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.210+10668delA | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75737752 | |||||
| chr13:75737761
|
A | T | 11 | a0002c0003t0001g0154a0004c0027t0002g0092a0005c0005t0001g0125others(8): Show | 11 | HG01884.hp1 HG03654.hp2 HG03831.hp2 others(8): Show |
intron_variant | MODIFIER | c.210+10663A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75737761 | ||||||
| chr13:75737762
|
A | T | 1 | a0003c0002t0001g0216 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.210+10664A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75737762 | ||||||
| chr13:75737766
|
AT | A | 28 | a0002c0003t0001g0121a0002c0003t0001g0126a0002c0003t0001g0137others(25): Show | 28 | HG00673.hp1 HG01081.hp2 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.210+10669delT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75737766 | ||||||
| chr13:75737767
|
T | A | 2 | a0005c0005t0004g0264a0016c0024t0002g0086 | 2 | NA18940.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.210+10669T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75737767 | ||||||
| chr13:75737767
|
TA | T | 3 | a0007c0009t0001g0165a0007c0009t0001g0166a0007c0009t0009g0251 | 3 | HG01891.hp1 HG03041.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.210+10673delA | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75737767 | |||||
| chr13:75737768
|
A | AATAAAAT others(1): Show |
4 | a0007c0016t0001g0001a0007c0016t0001g0252a0008c0008t0003g0111others(1): Show | 5 | HG02895.hp1 HG02897.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.210+10671_210+1067 others(12): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75737768 | |||||
| chr13:75737773
|
A | G | 123 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(120): Show | 123 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.210+10675A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75737773 | ||||||
| chr13:75737776
|
A | AT | 6 | a0002c0007t0003g0173a0002c0007t0003g0246a0005c0005t0003g0127others(3): Show | 6 | HG03579.hp1 HG03579.hp2 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.210+10679dupT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75737776 | |||||
| chr13:75737777
|
T | TA | 39 | a0001c0001t0001g0113a0001c0001t0001g0143a0001c0001t0001g0150others(36): Show | 39 | HG00099.hp1 HG00438.hp1 HG01168.hp2 others(36): Show |
intron_variant | MODIFIER | c.210+10683dupA | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75737777 | |||||
| chr13:75737777
|
T | TAA | 60 | a0001c0001t0001g0159a0001c0001t0001g0167a0001c0001t0001g0201others(57): Show | 60 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.210+10682_210+1068 others(6): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75737777 | |||||
| chr13:75737777
|
T | TAAA | 10 | a0001c0001t0002g0017a0001c0001t0002g0024a0001c0001t0002g0082others(7): Show | 10 | HG00673.hp1 HG00735.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.210+10681_210+1068 others(7): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75737777 | |||||
| chr13:75737777
|
T | TTA | 13 | a0002c0003t0001g0154a0004c0027t0002g0092a0005c0005t0001g0125others(10): Show | 13 | HG01884.hp1 HG01891.hp2 HG03098.hp2 others(10): Show |
intron_variant | MODIFIER | c.210+10679_210+1068 others(6): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75737777 | ||||||
| chr13:75737778
|
A | T | 9 | a0002c0003t0001g0220a0008c0008t0001g0089a0008c0008t0002g0077others(6): Show | 9 | HG01243.hp1 HG02818.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.210+10680A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75737778 | ||||||
| chr13:75737781
|
AT | A | 4 | a0001c0001t0002g0007a0001c0001t0002g0026a0008c0008t0003g0160others(1): Show | 4 | HG03704.hp1 NA18522.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.210+10684delT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75737781 | ||||||
| chr13:75737782
|
T | A | 168 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(165): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.210+10684T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75737782 | ||||||
| chr13:75737782
|
T | TAA | 65 | a0001c0001t0001g0135a0001c0001t0001g0207a0001c0001t0001g0218others(62): Show | 65 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.210+10702_210+1070 others(6): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75737782 | |||||
| chr13:75737782
|
T | TAAA | 6 | a0001c0001t0001g0208a0003c0002t0001g0194a0003c0002t0001g0196others(3): Show | 6 | HG02135.hp1 HG02293.hp2 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.210+10701_210+1070 others(7): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75737782 | |||||
| chr13:75737785
|
A | AAT | 16 | a0002c0003t0001g0121a0002c0003t0001g0137a0002c0003t0001g0138others(13): Show | 16 | HG00140.hp1 HG00738.hp2 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.210+10688_210+1068 others(6): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75737785 | |||||
| chr13:75737786
|
A | ATT | 3 | a0007c0009t0001g0162a0007c0009t0001g0163a0007c0009t0002g0067 | 3 | HG02135.hp2 HG03017.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.210+10688_210+1068 others(6): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75737786 | ||||||
| chr13:75737787
|
A | C | 1 | a0002c0003t0001g0154 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.210+10689A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75737787 | ||||||
| chr13:75737789
|
A | C | 4 | a0007c0016t0001g0001a0007c0016t0001g0252a0008c0008t0003g0111others(1): Show | 5 | HG02895.hp1 HG02897.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.210+10691A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75737789 | ||||||
| chr13:75737792
|
A | C | 1 | a0017c0023t0002g0050 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.210+10694A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75737792 | ||||||
| chr13:75737795
|
A | AAAC | 6 | a0002c0007t0003g0176a0002c0007t0003g0178a0002c0007t0003g0180others(3): Show | 6 | HG00639.hp1 HG01109.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.210+10699_210+1070 others(7): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75737795 | |||||
| chr13:75737795
|
A | C | 1 | a0002c0007t0003g0181 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.210+10697A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75737795 | ||||||
| chr13:75737842
|
C | CA | 63 | a0001c0001t0002g0026a0001c0001t0002g0058a0001c0001t0002g0079others(60): Show | 63 | HG00438.hp2 HG01070.hp2 HG01081.hp1 others(60): Show |
intron_variant | MODIFIER | c.210+10766dupA | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75737842 | |||||
| chr13:75737842
|
C | CAA | 106 | a0001c0001t0001g0135a0001c0001t0001g0143a0001c0001t0001g0151others(103): Show | 106 | HG00280.hp1 HG00280.hp2 HG00609.hp1 others(103): Show |
intron_variant | MODIFIER | c.210+10765_210+1076 others(6): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75737842 | |||||
| chr13:75737842
|
C | CAAA | 43 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(40): Show | 43 | HG00099.hp1 HG00438.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.210+10764_210+1076 others(7): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75737842 | |||||
| chr13:75737842
|
C | CAAAAAAA others(3): Show |
1 | a0008c0008t0003g0111 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.210+10757_210+1076 others(14): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75737842 | |||||
| chr13:75738078
|
G | GT | 5 | a0001c0001t0002g0099a0001c0001t0002g0106a0001c0001t0002g0107others(2): Show | 5 | HG01099.hp2 HG01884.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.210+10990dupT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75738078 | |||||
| chr13:75738637
|
G | A | 127 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(124): Show | 128 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.210+11539G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75738637 | ||||||
| chr13:75738940
|
T | C | 1 | a0009c0010t0002g0015 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.210+11842T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75738940 | ||||||
| chr13:75739043
|
A | G | 1 | a0001c0001t0002g0066 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.210+11945A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75739043 | ||||||
| chr13:75739079
|
G | A | 28 | a0002c0003t0001g0154a0002c0003t0001g0220a0002c0007t0003g0173others(25): Show | 28 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.210+11981G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75739079 | ||||||
| chr13:75739327
|
G | A | 1 | a0004c0004t0001g0187 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.210+12229G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75739327 | ||||||
| chr13:75739388
|
G | A | 20 | a0002c0003t0001g0253a0002c0003t0001g0255a0002c0003t0001g0256others(17): Show | 20 | HG00099.hp2 HG00140.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.210+12290G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75739388 | ||||||
| chr13:75739547
|
C | T | 1 | a0001c0001t0002g0009 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.210+12449C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75739547 | ||||||
| chr13:75739855
|
C | T | 1 | a0008c0008t0001g0089 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.210+12757C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75739855 | ||||||
| chr13:75740011
|
A | G | 1 | a0017c0023t0002g0050 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.210+12913A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75740011 | ||||||
| chr13:75740231
|
G | T | 1 | a0001c0021t0001g0182 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.210+13133G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75740231 | ||||||
| chr13:75740746
|
C | G | 1 | a0004c0004t0004g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.210+13648C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75740746 | ||||||
| chr13:75740774
|
G | C | 1 | a0002c0003t0005g0070 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.210+13676G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75740774 | ||||||
| chr13:75741226
|
A | G | 1 | a0008c0008t0003g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.210+14128A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75741226 | ||||||
| chr13:75741286
|
G | A | 2 | a0004c0013t0002g0059a0004c0013t0002g0061 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.210+14188G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75741286 | ||||||
| chr13:75741368
|
A | T | 1 | a0013c0018t0004g0056 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.210+14270A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75741368 | ||||||
| chr13:75741513
|
C | T | 1 | a0001c0021t0001g0182 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.210+14415C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75741513 | ||||||
| chr13:75741674
|
T | C | 2 | a0001c0001t0002g0063a0001c0001t0002g0065 | 2 | HG01928.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.210+14576T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75741674 | ||||||
| chr13:75741777
|
C | A | 1 | a0002c0003t0001g0203 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.210+14679C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75741777 | ||||||
| chr13:75742029
|
A | T | 125 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(122): Show | 126 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.210+14931A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75742029 | ||||||
| chr13:75742073
|
C | A | 7 | a0003c0002t0001g0191a0003c0002t0001g0195a0003c0002t0001g0196others(4): Show | 7 | HG00639.hp2 HG01255.hp2 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.210+14975C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75742073 | ||||||
| chr13:75742074
|
G | A | 11 | a0002c0003t0001g0154a0004c0027t0002g0092a0005c0005t0001g0125others(8): Show | 11 | HG01884.hp1 HG03654.hp2 HG03831.hp2 others(8): Show |
intron_variant | MODIFIER | c.210+14976G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75742074 | ||||||
| chr13:75742149
|
G | A | 1 | a0009c0010t0017g0004 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.210+15051G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75742149 | ||||||
| chr13:75742172
|
C | A | 6 | a0002c0007t0001g0234a0003c0002t0001g0233a0004c0004t0001g0231others(3): Show | 6 | HG01070.hp2 HG01123.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.210+15074C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75742172 | ||||||
| chr13:75742292
|
T | C | 5 | a0001c0001t0002g0043a0001c0001t0002g0045a0001c0001t0008g0044others(2): Show | 5 | HG01192.hp1 HG01243.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.210+15194T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75742292 | ||||||
| chr13:75742323
|
A | G | 19 | a0002c0003t0001g0121a0002c0003t0001g0126a0002c0003t0001g0137others(16): Show | 19 | HG01081.hp2 HG01099.hp1 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.210+15225A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75742323 | ||||||
| chr13:75742613
|
A | G | 268 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(265): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.210+15515A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75742613 | ||||||
| chr13:75742619
|
AG | A | 7 | a0002c0003t0001g0220a0008c0008t0001g0089a0008c0008t0002g0077others(4): Show | 7 | HG01243.hp1 HG03195.hp1 HG03669.hp1 others(4): Show |
intron_variant | MODIFIER | c.210+15523delG | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75742619 | |||||
| chr13:75742759
|
C | G | 1 | a0002c0011t0002g0075 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.210+15661C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75742759 | ||||||
| chr13:75742797
|
C | A | 117 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(114): Show | 117 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.210+15699C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75742797 | ||||||
| chr13:75742800
|
G | A | 2 | a0002c0007t0003g0173a0009c0010t0003g0244 | 2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.210+15702G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75742800 | ||||||
| chr13:75742986
|
C | T | 4 | a0007c0016t0001g0001a0007c0016t0001g0252a0008c0008t0003g0111others(1): Show | 5 | HG02895.hp1 HG02897.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.210+15888C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75742986 | ||||||
| chr13:75743217
|
T | G | 1 | a0008c0008t0003g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.210+16119T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75743217 | ||||||
| chr13:75743323
|
T | G | 118 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(115): Show | 118 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.210+16225T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75743323 | ||||||
| chr13:75743496
|
A | G | 126 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(123): Show | 127 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.210+16398A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75743496 | ||||||
| chr13:75743502
|
T | C | 5 | a0002c0007t0001g0129a0007c0016t0001g0001a0007c0016t0001g0252others(2): Show | 6 | HG01952.hp2 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.210+16404T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75743502 | ||||||
| chr13:75743658
|
G | A | 126 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(123): Show | 127 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.210+16560G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75743658 | ||||||
| chr13:75743826
|
G | A | 6 | a0002c0007t0001g0129a0007c0016t0001g0001a0007c0016t0001g0252others(3): Show | 7 | HG01952.hp2 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.210+16728G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75743826 | ||||||
| chr13:75743837
|
G | A | 126 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(123): Show | 127 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.210+16739G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75743837 | ||||||
| chr13:75743900
|
A | G | 4 | a0001c0001t0002g0035a0001c0001t0002g0047a0001c0001t0002g0048others(1): Show | 4 | HG01981.hp1 HG02647.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.210+16802A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75743900 | ||||||
| chr13:75744071
|
G | A | 1 | a0009c0010t0017g0004 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.211-16861G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75744071 | ||||||
| chr13:75744284
|
A | G | 7 | a0002c0003t0001g0220a0008c0008t0001g0089a0008c0008t0002g0077others(4): Show | 7 | HG01243.hp1 HG03195.hp1 HG03669.hp1 others(4): Show |
intron_variant | MODIFIER | c.211-16648A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75744284 | ||||||
| chr13:75744317
|
A | G | 126 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(123): Show | 127 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.211-16615A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75744317 | ||||||
| chr13:75744862
|
G | T | 1 | a0008c0008t0003g0169 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.211-16070G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75744862 | ||||||
| chr13:75744866
|
A | G | 1 | a0009c0010t0017g0004 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.211-16066A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75744866 | ||||||
| chr13:75744900
|
G | A | 1 | a0015c0029t0001g0118 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.211-16032G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75744900 | ||||||
| chr13:75745088
|
G | A | 1 | a0001c0001t0001g0159 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.211-15844G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75745088 | ||||||
| chr13:75745235
|
G | A | 1 | a0002c0003t0001g0238 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.211-15697G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75745235 | ||||||
| chr13:75745324
|
T | C | 126 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(123): Show | 127 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.211-15608T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75745324 | ||||||
| chr13:75745542
|
A | G | 1 | a0009c0010t0017g0004 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.211-15390A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75745542 | ||||||
| chr13:75745554
|
G | T | 4 | a0002c0007t0004g0260a0002c0007t0004g0261a0005c0005t0004g0263others(1): Show | 4 | HG01515.hp2 NA18940.hp2 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.211-15378G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75745554 | ||||||
| chr13:75745767
|
T | C | 1 | a0006c0006t0001g0183 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.211-15165T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75745767 | ||||||
| chr13:75745768
|
G | A | 1 | a0008c0008t0003g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.211-15164G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75745768 | ||||||
| chr13:75745871
|
G | A | 3 | a0001c0021t0001g0182a0006c0006t0001g0174a0006c0006t0001g0175 | 3 | HG02896.hp1 HG02897.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.211-15061G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75745871 | ||||||
| chr13:75745973
|
A | G | 1 | a0008c0008t0003g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.211-14959A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75745973 | ||||||
| chr13:75745978
|
T | C | 152 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(149): Show | 153 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.211-14954T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75745978 | ||||||
| chr13:75746084
|
A | G | 130 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(127): Show | 131 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.211-14848A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75746084 | ||||||
| chr13:75746362
|
A | C | 5 | a0002c0007t0001g0129a0007c0016t0001g0001a0007c0016t0001g0252others(2): Show | 6 | HG01952.hp2 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.211-14570A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75746362 | ||||||
| chr13:75746646
|
G | A | 6 | a0001c0001t0001g0201a0003c0002t0001g0193a0003c0002t0001g0204others(3): Show | 6 | HG00609.hp1 HG02040.hp2 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.211-14286G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75746646 | ||||||
| chr13:75747027
|
C | T | 16 | a0001c0001t0001g0207a0001c0001t0001g0208a0002c0007t0001g0234others(13): Show | 16 | HG01070.hp2 HG01123.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.211-13905C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75747027 | ||||||
| chr13:75747254
|
A | G | 1 | a0003c0002t0001g0186 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.211-13678A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75747254 | ||||||
| chr13:75747361
|
G | A | 120 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(117): Show | 121 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.211-13571G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75747361 | ||||||
| chr13:75747615
|
T | C | 1 | a0001c0001t0002g0040 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.211-13317T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75747615 | ||||||
| chr13:75747796
|
G | C | 1 | a0008c0008t0001g0089 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.211-13136G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75747796 | ||||||
| chr13:75747929
|
G | T | 106 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(103): Show | 106 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.211-13003G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75747929 | ||||||
| chr13:75747931
|
A | C | 1 | a0001c0021t0001g0182 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.211-13001A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75747931 | ||||||
| chr13:75748335
|
T | C | 1 | a0001c0001t0002g0078 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.211-12597T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75748335 | ||||||
| chr13:75748657
|
G | A | 64 | a0001c0001t0001g0201a0001c0001t0001g0207a0001c0001t0001g0208others(61): Show | 65 | HG00438.hp2 HG00609.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.211-12275G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75748657 | ||||||
| chr13:75748694
|
G | T | 1 | a0004c0027t0002g0092 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.211-12238G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75748694 | ||||||
| chr13:75748810
|
TC | T | 10 | a0001c0001t0001g0135a0002c0003t0001g0211a0002c0003t0001g0238others(7): Show | 10 | HG00738.hp1 HG01515.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.211-12121delC | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75748810 | ||||||
| chr13:75748815
|
C | CT | 39 | a0002c0003t0001g0121a0002c0003t0001g0126a0002c0003t0001g0137others(36): Show | 39 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.211-12104dupT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75748815 | |||||
| chr13:75748815
|
C | T | 10 | a0001c0001t0001g0135a0002c0003t0001g0211a0002c0003t0001g0238others(7): Show | 10 | HG00738.hp1 HG01515.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.211-12117C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75748815 | ||||||
| chr13:75748841
|
G | A | 132 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(129): Show | 132 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(129): Show |
intron_variant | MODIFIER | c.211-12091G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75748841 | ||||||
| chr13:75748996
|
G | A | 1 | a0001c0001t0001g0135 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.211-11936G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75748996 | ||||||
| chr13:75749177
|
A | G | 1 | a0001c0001t0002g0017 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.211-11755A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75749177 | ||||||
| chr13:75749183
|
C | T | 2 | a0005c0005t0001g0114a0008c0008t0003g0110 | 2 | NA19054.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.211-11749C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75749183 | ||||||
| chr13:75749229
|
T | C | 1 | a0002c0007t0001g0129 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.211-11703T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75749229 | ||||||
| chr13:75749291
|
T | C | 1 | a0002c0007t0001g0129 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.211-11641T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75749291 | ||||||
| chr13:75749349
|
T | A | 113 | a0001c0001t0001g0135a0001c0001t0001g0201a0001c0001t0001g0207others(110): Show | 114 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(111): Show |
intron_variant | MODIFIER | c.211-11583T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75749349 | ||||||
| chr13:75749371
|
G | A | 21 | a0002c0003t0001g0146a0002c0003t0001g0253a0002c0003t0001g0255others(18): Show | 21 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(18): Show |
intron_variant | MODIFIER | c.211-11561G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75749371 | ||||||
| chr13:75749568
|
C | A | 2 | a0008c0008t0003g0168a0008c0008t0003g0169 | 2 | HG03669.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.211-11364C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75749568 | ||||||
| chr13:75749638
|
T | C | 102 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(99): Show | 102 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.211-11294T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75749638 | ||||||
| chr13:75750058
|
T | TA | 12 | a0001c0021t0001g0182a0002c0003t0001g0154a0004c0027t0002g0092others(9): Show | 12 | HG01884.hp1 HG03654.hp2 HG03831.hp2 others(9): Show |
intron_variant | MODIFIER | c.211-10864dupA | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75750058 | |||||
| chr13:75750174
|
C | A | 10 | a0001c0001t0001g0135a0002c0003t0001g0211a0002c0003t0001g0238others(7): Show | 10 | HG00738.hp1 HG01515.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.211-10758C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75750174 | ||||||
| chr13:75750268
|
T | TCACCC | 4 | a0011c0015t0001g0155a0011c0015t0001g0197a0011c0015t0001g0221others(1): Show | 4 | NA18941.hp2 NA18986.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.211-10664_211-1066 others(9): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75750268 | ||||||
| chr13:75750269
|
G | A | 4 | a0011c0015t0001g0155a0011c0015t0001g0197a0011c0015t0001g0221others(1): Show | 4 | NA18941.hp2 NA18986.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.211-10663G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75750269 | ||||||
| chr13:75750270
|
C | G | 4 | a0011c0015t0001g0155a0011c0015t0001g0197a0011c0015t0001g0221others(1): Show | 4 | NA18941.hp2 NA18986.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.211-10662C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75750270 | ||||||
| chr13:75750296
|
G | A | 1 | a0004c0004t0001g0202 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.211-10636G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75750296 | ||||||
| chr13:75750373
|
G | A | 1 | a0015c0029t0001g0118 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.211-10559G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75750373 | ||||||
| chr13:75750377
|
C | CT | 59 | a0001c0001t0001g0201a0001c0001t0001g0208a0001c0001t0001g0218others(56): Show | 59 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.211-10533dupT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75750377 | |||||
| chr13:75750377
|
CT | C | 184 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(181): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.211-10533delT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75750377 | |||||
| chr13:75750377
|
CTT | C | 8 | a0001c0001t0002g0020a0002c0007t0003g0176a0002c0007t0003g0178others(5): Show | 8 | HG00639.hp1 HG01081.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.211-10534_211-1053 others(6): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75750377 | |||||
| chr13:75750547
|
A | T | 3 | a0011c0015t0001g0197a0011c0015t0001g0221a0011c0015t0001g0242 | 3 | NA18941.hp2 NA18986.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.211-10385A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75750547 | ||||||
| chr13:75750574
|
G | A | 1 | a0002c0003t0001g0192 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.211-10358G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75750574 | ||||||
| chr13:75750665
|
G | T | 1 | a0001c0001t0002g0034 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.211-10267G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75750665 | ||||||
| chr13:75750770
|
C | T | 1 | a0002c0007t0001g0129 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.211-10162C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75750770 | ||||||
| chr13:75750984
|
G | A | 7 | a0002c0003t0001g0220a0005c0005t0001g0114a0008c0008t0003g0005others(4): Show | 7 | HG03669.hp1 HG03704.hp1 HG03927.hp2 others(4): Show |
intron_variant | MODIFIER | c.211-9948G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75750984 | ||||||
| chr13:75751108
|
A | T | 2 | a0002c0011t0002g0075a0002c0011t0002g0076 | 2 | HG00140.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.211-9824A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75751108 | ||||||
| chr13:75751149
|
C | CT | 21 | a0002c0003t0001g0137a0002c0003t0001g0138a0002c0003t0001g0139others(18): Show | 21 | HG01081.hp2 HG01099.hp1 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.211-9754dupT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75751149 | |||||
| chr13:75751149
|
C | CTT | 19 | a0001c0001t0002g0101a0002c0003t0001g0121a0002c0003t0001g0126others(16): Show | 19 | HG00140.hp1 HG00140.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.211-9755_211-9754d others(4): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75751149 | |||||
| chr13:75751149
|
C | CTTT | 10 | a0002c0003t0001g0146a0002c0003t0001g0257a0002c0003t0001g0259others(7): Show | 10 | HG00438.hp1 HG01496.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.211-9756_211-9754d others(5): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75751149 | |||||
| chr13:75751149
|
C | CTTTT | 6 | a0002c0003t0001g0253a0002c0003t0001g0255a0002c0003t0001g0256others(3): Show | 6 | HG00673.hp1 HG02523.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.211-9757_211-9754d others(6): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75751149 | |||||
| chr13:75751149
|
CTT | C | 14 | a0001c0001t0002g0009a0001c0001t0002g0023a0001c0001t0002g0039others(11): Show | 14 | HG01109.hp2 HG01255.hp1 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.211-9755_211-9754d others(4): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75751149 | |||||
| chr13:75751149
|
CTTT | C | 95 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(92): Show | 95 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.211-9756_211-9754d others(5): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75751149 | |||||
| chr13:75751149
|
CTTTT | C | 52 | a0001c0001t0001g0201a0001c0001t0001g0218a0001c0001t0002g0040others(49): Show | 53 | HG00280.hp1 HG00609.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.211-9757_211-9754d others(6): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75751149 | |||||
| chr13:75751149
|
CTTTTTT | C | 34 | a0001c0001t0001g0159a0001c0001t0002g0012a0002c0003t0001g0154others(31): Show | 34 | HG00735.hp1 HG01243.hp1 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.211-9759_211-9754d others(8): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75751149 | |||||
| chr13:75751149
|
CTTTTTTT others(7): Show |
C | 2 | a0001c0001t0002g0034a0001c0001t0002g0041 | 2 | NA18942.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.211-9767_211-9754d others(16): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75751149 | |||||
| chr13:75751149
|
CTTTTTTT others(11): Show |
C | 2 | a0002c0007t0003g0173a0009c0010t0003g0244 | 2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.211-9771_211-9754d others(20): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75751149 | |||||
| chr13:75751191
|
C | T | 102 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(99): Show | 102 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.211-9741C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75751191 | ||||||
| chr13:75751442
|
G | T | 1 | a0008c0008t0003g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.211-9490G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75751442 | ||||||
| chr13:75751732
|
A | G | 11 | a0002c0003t0001g0154a0004c0027t0002g0092a0005c0005t0001g0125others(8): Show | 11 | HG01884.hp1 HG03654.hp2 HG03831.hp2 others(8): Show |
intron_variant | MODIFIER | c.211-9200A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75751732 | ||||||
| chr13:75751836
|
C | T | 63 | a0001c0001t0001g0201a0001c0001t0001g0207a0001c0001t0001g0208others(60): Show | 63 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.211-9096C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75751836 | ||||||
| chr13:75752032
|
G | C | 2 | a0005c0005t0003g0127a0005c0005t0003g0128 | 2 | NA18942.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.211-8900G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75752032 | ||||||
| chr13:75752038
|
A | G | 2 | a0002c0007t0003g0173a0009c0010t0003g0244 | 2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.211-8894A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75752038 | ||||||
| chr13:75752083
|
ACT | A | 68 | a0001c0001t0001g0201a0001c0001t0001g0207a0001c0001t0001g0208others(65): Show | 69 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.211-8840_211-8839d others(4): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75752083 | |||||
| chr13:75752092
|
C | A | 1 | a0008c0008t0003g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.211-8840C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75752092 | ||||||
| chr13:75752146
|
A | T | 215 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(212): Show | 216 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.211-8786A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75752146 | ||||||
| chr13:75752349
|
T | G | 5 | a0001c0001t0002g0035a0001c0001t0002g0047a0001c0001t0002g0048others(2): Show | 5 | HG01981.hp1 HG02647.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.211-8583T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75752349 | ||||||
| chr13:75752388
|
C | T | 1 | a0008c0008t0003g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.211-8544C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75752388 | ||||||
| chr13:75752564
|
C | T | 1 | a0002c0003t0002g0134 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.211-8368C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75752564 | ||||||
| chr13:75752565
|
G | A | 215 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(212): Show | 216 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.211-8367G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75752565 | ||||||
| chr13:75752756
|
G | A | 2 | a0004c0004t0001g0148a0004c0004t0001g0149 | 2 | NA19007.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.211-8176G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75752756 | ||||||
| chr13:75752825
|
G | C | 10 | a0001c0001t0001g0135a0002c0003t0001g0211a0002c0003t0001g0238others(7): Show | 10 | HG00738.hp1 HG01515.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.211-8107G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75752825 | ||||||
| chr13:75752833
|
T | C | 32 | a0002c0003t0001g0154a0002c0003t0001g0220a0002c0007t0001g0129others(29): Show | 32 | HG00735.hp1 HG01243.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.211-8099T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75752833 | ||||||
| chr13:75752844
|
T | G | 1 | a0002c0007t0004g0260 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.211-8088T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75752844 | ||||||
| chr13:75752868
|
A | G | 3 | a0001c0021t0001g0182a0006c0006t0001g0174a0006c0006t0001g0175 | 3 | HG02896.hp1 HG02897.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.211-8064A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75752868 | ||||||
| chr13:75753039
|
C | T | 1 | a0008c0008t0003g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.211-7893C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75753039 | ||||||
| chr13:75753761
|
C | A | 2 | a0007c0016t0001g0001a0007c0016t0001g0252 | 3 | HG02895.hp1 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.211-7171C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75753761 | ||||||
| chr13:75753854
|
C | T | 1 | a0008c0008t0004g0087 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.211-7078C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75753854 | ||||||
| chr13:75754224
|
G | T | 1 | a0006c0006t0002g0102 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.211-6708G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75754224 | ||||||
| chr13:75754522
|
C | T | 2 | a0002c0007t0003g0173a0009c0010t0003g0244 | 2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.211-6410C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75754522 | ||||||
| chr13:75754532
|
G | A | 11 | a0001c0001t0001g0135a0002c0003t0001g0211a0002c0003t0001g0238others(8): Show | 11 | HG00639.hp2 HG00738.hp1 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.211-6400G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75754532 | ||||||
| chr13:75754573
|
G | T | 1 | a0002c0003t0005g0030 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.211-6359G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75754573 | ||||||
| chr13:75754574
|
G | T | 1 | a0002c0003t0005g0030 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.211-6358G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75754574 | ||||||
| chr13:75754575
|
G | A | 1 | a0002c0003t0005g0030 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.211-6357G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75754575 | ||||||
| chr13:75754761
|
A | T | 5 | a0006c0006t0001g0245a0009c0010t0001g0248a0009c0010t0001g0249others(2): Show | 5 | HG01891.hp2 HG03098.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.211-6171A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75754761 | ||||||
| chr13:75755099
|
G | A | 2 | a0004c0004t0001g0120a0004c0004t0002g0060 | 2 | HG01515.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.211-5833G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75755099 | ||||||
| chr13:75755109
|
T | C | 102 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(99): Show | 102 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.211-5823T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75755109 | ||||||
| chr13:75755138
|
A | C | 1 | a0007c0009t0009g0251 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.211-5794A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75755138 | ||||||
| chr13:75755757
|
C | T | 44 | a0001c0001t0001g0135a0001c0021t0001g0182a0002c0003t0001g0154others(41): Show | 44 | HG00735.hp1 HG00738.hp1 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.211-5175C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75755757 | ||||||
| chr13:75755982
|
A | G | 1 | a0012c0014t0007g0049 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.211-4950A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75755982 | ||||||
| chr13:75756034
|
A | C | 10 | a0002c0007t0003g0173a0006c0006t0001g0245a0009c0010t0001g0248others(7): Show | 10 | HG00735.hp1 HG01891.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.211-4898A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75756034 | ||||||
| chr13:75756246
|
G | A | 3 | a0003c0002t0001g0217a0003c0002t0001g0233a0003c0002t0001g0237 | 3 | HG01123.hp1 HG01255.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.211-4686G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75756246 | ||||||
| chr13:75756418
|
A | G | 1 | a0002c0007t0003g0178 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.211-4514A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75756418 | ||||||
| chr13:75756679
|
T | G | 9 | a0002c0003t0001g0220a0005c0005t0001g0114a0008c0008t0001g0089others(6): Show | 9 | HG01243.hp1 HG03195.hp1 HG03669.hp1 others(6): Show |
intron_variant | MODIFIER | c.211-4253T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75756679 | ||||||
| chr13:75756715
|
G | C | 1 | a0003c0002t0001g0212 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.211-4217G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75756715 | ||||||
| chr13:75756744
|
G | A | 10 | a0001c0001t0001g0135a0002c0003t0001g0211a0002c0003t0001g0238others(7): Show | 10 | HG00738.hp1 HG01515.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.211-4188G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75756744 | ||||||
| chr13:75756756
|
A | C | 2 | a0004c0004t0001g0148a0004c0004t0001g0149 | 2 | NA19007.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.211-4176A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75756756 | ||||||
| chr13:75757082
|
T | C | 10 | a0001c0001t0001g0135a0002c0003t0001g0211a0002c0003t0001g0238others(7): Show | 10 | HG00738.hp1 HG01515.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.211-3850T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75757082 | ||||||
| chr13:75757123
|
C | T | 67 | a0001c0001t0001g0201a0001c0001t0001g0207a0001c0001t0001g0208others(64): Show | 68 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.211-3809C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75757123 | ||||||
| chr13:75757147
|
G | A | 5 | a0006c0006t0001g0245a0009c0010t0001g0248a0009c0010t0001g0249others(2): Show | 5 | HG01891.hp2 HG03098.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.211-3785G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75757147 | ||||||
| chr13:75757362
|
C | T | 3 | a0004c0004t0006g0103a0004c0004t0010g0119a0015c0029t0001g0118 | 3 | HG02809.hp1 HG02818.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.211-3570C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75757362 | ||||||
| chr13:75757790
|
CTG | C | 6 | a0002c0007t0004g0260a0002c0031t0002g0091a0006c0006t0001g0172others(3): Show | 6 | HG01515.hp2 HG01891.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.211-3092_211-3091d others(4): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75757790 | |||||
| chr13:75757790
|
CTGTG | C | 4 | a0001c0001t0001g0135a0002c0003t0005g0070a0002c0011t0002g0076others(1): Show | 4 | HG00738.hp1 HG00738.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.211-3094_211-3091d others(6): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75757790 | |||||
| chr13:75757790
|
CTGTGTG | C | 23 | a0002c0003t0001g0126a0002c0003t0001g0137a0002c0003t0001g0138others(20): Show | 23 | HG00140.hp1 HG00140.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.211-3096_211-3091d others(8): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75757790 | |||||
| chr13:75757790
|
CTGTGTGT others(1): Show |
C | 25 | a0001c0001t0002g0101a0002c0003t0001g0121a0002c0003t0001g0239others(22): Show | 25 | HG00099.hp2 HG00673.hp1 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.211-3098_211-3091d others(10): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75757790 | |||||
| chr13:75757790
|
CTGTGTGT others(3): Show |
C | 3 | a0002c0003t0001g0146a0007c0009t0001g0162a0007c0009t0002g0067 | 3 | HG00438.hp1 HG03017.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.211-3100_211-3091d others(12): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75757790 | |||||
| chr13:75757790
|
CTGTGTGT others(5): Show |
C | 3 | a0006c0006t0002g0097a0007c0009t0001g0163a0008c0008t0003g0111 | 3 | HG01256.hp1 HG02135.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.211-3102_211-3091d others(14): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75757790 | |||||
| chr13:75757790
|
CTGTGTGT others(7): Show |
C | 1 | a0008c0008t0004g0087 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.211-3104_211-3091d others(16): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75757790 | |||||
| chr13:75757790
|
CTGTGTGT others(9): Show |
C | 2 | a0007c0016t0001g0001a0007c0016t0001g0252 | 3 | HG02895.hp1 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.211-3106_211-3091d others(18): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75757790 | |||||
| chr13:75757790
|
CTGTGTGT others(11): Show |
C | 3 | a0001c0001t0001g0201a0002c0007t0001g0129a0018c0028t0004g0133 | 3 | HG00609.hp1 HG00639.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.211-3108_211-3091d others(20): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75757790 | |||||
| chr13:75757790
|
CTGTGTGT others(13): Show |
C | 20 | a0001c0001t0002g0069a0002c0007t0003g0173a0002c0007t0003g0246others(17): Show | 20 | HG00735.hp1 HG01123.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.211-3110_211-3091d others(22): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75757790 | |||||
| chr13:75757790
|
CTGTGTGT others(15): Show |
C | 84 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0218others(81): Show | 84 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(81): Show |
intron_variant | MODIFIER | c.211-3112_211-3091d others(24): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75757790 | |||||
| chr13:75757790
|
CTGTGTGT others(17): Show |
C | 94 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(91): Show | 94 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.211-3114_211-3091d others(26): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75757790 | |||||
| chr13:75757978
|
G | C | 1 | a0003c0002t0001g0243 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.211-2954G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75757978 | ||||||
| chr13:75757991
|
C | T | 1 | a0004c0027t0002g0092 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.211-2941C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75757991 | ||||||
| chr13:75758041
|
C | T | 67 | a0001c0001t0001g0201a0001c0001t0001g0207a0001c0001t0001g0208others(64): Show | 68 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.211-2891C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75758041 | ||||||
| chr13:75758194
|
T | C | 1 | a0003c0002t0001g0186 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.211-2738T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75758194 | ||||||
| chr13:75758416
|
A | G | 1 | a0002c0007t0003g0246 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.211-2516A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75758416 | ||||||
| chr13:75758553
|
A | G | 102 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(99): Show | 102 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.211-2379A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75758553 | ||||||
| chr13:75758723
|
A | G | 1 | a0008c0008t0003g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.211-2209A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75758723 | ||||||
| chr13:75758732
|
A | G | 102 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(99): Show | 102 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.211-2200A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75758732 | ||||||
| chr13:75758827
|
T | G | 10 | a0002c0007t0003g0173a0006c0006t0001g0245a0009c0010t0001g0248others(7): Show | 10 | HG00735.hp1 HG01891.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.211-2105T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75758827 | ||||||
| chr13:75759467
|
A | C | 1 | a0003c0002t0001g0186 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.211-1465A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75759467 | ||||||
| chr13:75759717
|
G | A | 34 | a0001c0021t0001g0182a0002c0003t0001g0154a0002c0003t0001g0220others(31): Show | 34 | HG00735.hp1 HG01243.hp1 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.211-1215G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75759717 | ||||||
| chr13:75759731
|
A | G | 68 | a0001c0001t0001g0201a0001c0001t0001g0207a0001c0001t0001g0208others(65): Show | 69 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.211-1201A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75759731 | ||||||
| chr13:75759795
|
C | G | 2 | a0019c0034t0002g0073a0020c0033t0002g0074 | 2 | HG02698.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.211-1137C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75759795 | ||||||
| chr13:75759815
|
A | G | 10 | a0001c0001t0001g0135a0002c0003t0001g0211a0002c0003t0001g0238others(7): Show | 10 | HG00738.hp1 HG01515.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.211-1117A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75759815 | ||||||
| chr13:75759925
|
G | A | 103 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(100): Show | 103 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(100): Show |
intron_variant | MODIFIER | c.211-1007G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75759925 | ||||||
| chr13:75760007
|
C | T | 10 | a0001c0001t0001g0135a0002c0003t0001g0211a0002c0003t0001g0238others(7): Show | 10 | HG00738.hp1 HG01515.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.211-925C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75760007 | ||||||
| chr13:75760050
|
TTTC | T | 31 | a0002c0003t0001g0154a0002c0003t0001g0220a0002c0007t0003g0173others(28): Show | 31 | HG00735.hp1 HG01243.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.211-873_211-871del others(3): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75760050 | |||||
| chr13:75760189
|
C | T | 3 | a0005c0005t0001g0114a0008c0008t0003g0005a0008c0008t0003g0110 | 3 | NA19054.hp2 NA19055.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.211-743C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75760189 | ||||||
| chr13:75760250
|
TGGAG | T | 10 | a0002c0003t0001g0154a0005c0005t0001g0125a0005c0005t0003g0112others(7): Show | 10 | HG03654.hp2 HG03831.hp2 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.211-675_211-672del others(4): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr13 | 75760250 | |||||
| chr13:75760275
|
T | A | 1 | a0008c0008t0003g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.211-657T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75760275 | ||||||
| chr13:75760293
|
G | A | 1 | a0003c0002t0001g0228 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.211-639G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75760293 | ||||||
| chr13:75760478
|
T | C | 2 | a0008c0008t0003g0111a0008c0008t0004g0087 | 2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.211-454T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75760478 | ||||||
| chr13:75760676
|
A | G | 1 | a0009c0010t0017g0004 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.211-256A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75760676 | ||||||
| chr13:75760682
|
C | T | 170 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(167): Show | 171 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.211-250C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75760682 | ||||||
| chr13:75760714
|
C | T | 1 | a0006c0006t0001g0183 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.211-218C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75760714 | ||||||
| chr13:75760757
|
A | G | 1 | a0012c0014t0014g0185 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.211-175A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 3/30 | chr13 | 75760757 | ||||||
| chr13:75761060
|
GAT | G | 195 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(192): Show | 196 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.317+37_317+38delAT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75761060 | |||||
| chr13:75761452
|
G | A | 10 | a0001c0001t0001g0135a0002c0003t0001g0211a0002c0003t0001g0238others(7): Show | 10 | HG00738.hp1 HG01515.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.317+414G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75761452 | ||||||
| chr13:75761569
|
G | A | 5 | a0006c0006t0001g0245a0009c0010t0001g0248a0009c0010t0001g0249others(2): Show | 5 | HG01891.hp2 HG03098.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.317+531G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75761569 | ||||||
| chr13:75762093
|
G | A | 4 | a0004c0004t0001g0187a0004c0004t0001g0188a0004c0004t0001g0190others(1): Show | 4 | NA18949.hp2 NA18954.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.317+1055G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75762093 | ||||||
| chr13:75762450
|
C | T | 1 | a0001c0001t0002g0083 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.317+1412C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75762450 | ||||||
| chr13:75762665
|
C | T | 1 | a0008c0008t0003g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.317+1627C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75762665 | ||||||
| chr13:75762951
|
C | T | 1 | a0008c0008t0001g0089 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.317+1913C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75762951 | ||||||
| chr13:75763066
|
G | T | 1 | a0002c0003t0001g0211 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.317+2028G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75763066 | ||||||
| chr13:75763317
|
G | A | 2 | a0002c0007t0004g0260a0002c0007t0004g0261 | 2 | HG01515.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.317+2279G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75763317 | ||||||
| chr13:75763644
|
A | C | 215 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(212): Show | 216 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.317+2606A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75763644 | ||||||
| chr13:75763902
|
GT | G | 33 | a0002c0003t0001g0154a0002c0003t0001g0220a0002c0007t0003g0173others(30): Show | 33 | HG00735.hp1 HG01243.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.317+2869delT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75763902 | |||||
| chr13:75763909
|
A | G | 9 | a0002c0003t0001g0220a0005c0005t0001g0114a0008c0008t0001g0089others(6): Show | 9 | HG01243.hp1 HG03195.hp1 HG03669.hp1 others(6): Show |
intron_variant | MODIFIER | c.317+2871A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75763909 | ||||||
| chr13:75764119
|
A | G | 3 | a0001c0021t0001g0182a0006c0006t0001g0174a0006c0006t0001g0175 | 3 | HG02896.hp1 HG02897.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.317+3081A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75764119 | ||||||
| chr13:75764234
|
A | G | 2 | a0012c0014t0001g0002a0012c0014t0001g0003 | 2 | HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.317+3196A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75764234 | ||||||
| chr13:75764255
|
A | T | 1 | a0010c0012t0001g0140 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.317+3217A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75764255 | ||||||
| chr13:75764402
|
G | A | 1 | a0003c0002t0002g0266 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.317+3364G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75764402 | ||||||
| chr13:75764472
|
G | A | 1 | a0001c0021t0001g0182 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.317+3434G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75764472 | ||||||
| chr13:75765002
|
C | T | 8 | a0002c0003t0001g0146a0002c0003t0001g0253a0002c0003t0001g0255others(5): Show | 8 | HG00438.hp1 HG00673.hp1 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.317+3964C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75765002 | ||||||
| chr13:75765316
|
C | CT | 8 | a0001c0021t0001g0182a0002c0011t0002g0031a0006c0006t0001g0132others(5): Show | 8 | HG01109.hp1 HG01168.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.317+4291dupT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75765316 | |||||
| chr13:75765371
|
CT | C | 4 | a0001c0001t0002g0072a0001c0001t0002g0085a0007c0016t0001g0001others(1): Show | 5 | HG00099.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.317+4349delT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75765371 | |||||
| chr13:75765431
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.317+4393A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75765431 | ||||||
| chr13:75765680
|
G | T | 1 | a0001c0001t0002g0051 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.317+4642G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75765680 | ||||||
| chr13:75765709
|
C | T | 1 | a0001c0021t0001g0182 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.317+4671C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75765709 | ||||||
| chr13:75765861
|
T | A | 1 | a0001c0001t0002g0023 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.317+4823T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75765861 | ||||||
| chr13:75766098
|
G | A | 1 | a0001c0001t0002g0065 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.317+5060G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75766098 | ||||||
| chr13:75766146
|
T | G | 1 | a0008c0008t0004g0087 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.317+5108T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75766146 | ||||||
| chr13:75766198
|
T | C | 2 | a0012c0014t0001g0002a0012c0014t0001g0003 | 2 | HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.317+5160T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75766198 | ||||||
| chr13:75766237
|
C | CT | 37 | a0002c0003t0001g0126a0002c0003t0001g0146a0002c0003t0001g0253others(34): Show | 37 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(34): Show |
intron_variant | MODIFIER | c.317+5219dupT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75766237 | |||||
| chr13:75766237
|
CT | C | 69 | a0001c0001t0001g0218a0002c0003t0001g0121a0002c0003t0001g0137others(66): Show | 69 | HG00438.hp2 HG00621.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.317+5219delT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75766237 | |||||
| chr13:75766237
|
CTT | C | 136 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(133): Show | 136 | HG00099.hp1 HG00280.hp2 HG00609.hp1 others(133): Show |
intron_variant | MODIFIER | c.317+5218_317+5219d others(4): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75766237 | |||||
| chr13:75766523
|
G | A | 8 | a0001c0001t0001g0167a0001c0001t0002g0017a0001c0001t0002g0078others(5): Show | 8 | HG00735.hp2 HG01496.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.317+5485G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75766523 | ||||||
| chr13:75766567
|
G | GGGAGATG others(16): Show |
224 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(221): Show | 225 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.317+5548_317+5549i others(25): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75766567 | |||||
| chr13:75766638
|
G | A | 1 | a0001c0001t0002g0058 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.317+5600G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75766638 | ||||||
| chr13:75766772
|
A | G | 1 | a0002c0007t0003g0173 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.317+5734A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75766772 | ||||||
| chr13:75766791
|
C | G | 1 | a0004c0013t0002g0019 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.317+5753C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75766791 | ||||||
| chr13:75766932
|
C | T | 1 | a0008c0008t0001g0089 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.317+5894C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75766932 | ||||||
| chr13:75766980
|
G | A | 124 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(121): Show | 124 | HG00099.hp1 HG00280.hp2 HG00609.hp1 others(121): Show |
intron_variant | MODIFIER | c.317+5942G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75766980 | ||||||
| chr13:75767001
|
T | C | 1 | a0001c0021t0001g0182 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.317+5963T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75767001 | ||||||
| chr13:75767019
|
A | G | 10 | a0002c0003t0001g0220a0008c0008t0001g0089a0008c0008t0002g0077others(7): Show | 10 | HG01243.hp1 HG02922.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.317+5981A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75767019 | ||||||
| chr13:75767083
|
G | A | 2 | a0004c0013t0002g0059a0004c0013t0002g0061 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.317+6045G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75767083 | ||||||
| chr13:75767245
|
A | G | 4 | a0002c0007t0001g0129a0007c0016t0001g0001a0007c0016t0001g0252others(1): Show | 5 | HG01952.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.317+6207A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75767245 | ||||||
| chr13:75767272
|
T | G | 1 | a0001c0001t0002g0083 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.317+6234T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75767272 | ||||||
| chr13:75767473
|
G | C | 1 | a0008c0008t0002g0077 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.317+6435G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75767473 | ||||||
| chr13:75767574
|
C | CA | 22 | a0001c0001t0001g0135a0002c0003t0001g0121a0002c0003t0001g0137others(19): Show | 22 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.317+6545dupA | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75767574 | |||||
| chr13:75767730
|
C | T | 11 | a0002c0007t0003g0173a0002c0007t0003g0246a0009c0010t0001g0248others(8): Show | 11 | HG00735.hp1 HG01891.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.317+6692C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75767730 | ||||||
| chr13:75768014
|
C | A | 124 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(121): Show | 124 | HG00099.hp1 HG00280.hp2 HG00609.hp1 others(121): Show |
intron_variant | MODIFIER | c.317+6976C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75768014 | ||||||
| chr13:75768228
|
G | A | 1 | a0006c0006t0001g0183 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.317+7190G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75768228 | ||||||
| chr13:75768241
|
T | C | 22 | a0001c0001t0001g0135a0002c0003t0001g0121a0002c0003t0001g0137others(19): Show | 22 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.317+7203T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75768241 | ||||||
| chr13:75768305
|
T | A | 8 | a0002c0003t0001g0220a0008c0008t0003g0005a0008c0008t0003g0110others(5): Show | 8 | HG02922.hp2 HG02970.hp2 HG03669.hp1 others(5): Show |
intron_variant | MODIFIER | c.317+7267T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75768305 | ||||||
| chr13:75768503
|
C | CTG | 4 | a0009c0010t0001g0248a0009c0010t0001g0249a0009c0010t0001g0250others(1): Show | 4 | HG01891.hp2 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.317+7467_317+7468d others(4): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75768503 | |||||
| chr13:75768531
|
T | A | 12 | a0004c0027t0002g0092a0005c0005t0001g0125a0005c0005t0003g0112others(9): Show | 12 | HG01884.hp1 HG03831.hp2 NA18940.hp2 others(9): Show |
intron_variant | MODIFIER | c.317+7493T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75768531 | ||||||
| chr13:75768615
|
C | G | 130 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(127): Show | 130 | HG00099.hp1 HG00280.hp2 HG00609.hp1 others(127): Show |
intron_variant | MODIFIER | c.317+7577C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75768615 | ||||||
| chr13:75768664
|
T | G | 1 | a0001c0001t0002g0025 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.317+7626T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75768664 | ||||||
| chr13:75768754
|
C | G | 155 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(152): Show | 156 | HG00099.hp1 HG00280.hp2 HG00609.hp1 others(153): Show |
intron_variant | MODIFIER | c.317+7716C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75768754 | ||||||
| chr13:75768793
|
C | A | 1 | a0006c0006t0002g0096 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.317+7755C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75768793 | ||||||
| chr13:75768915
|
G | A | 83 | a0001c0001t0001g0113a0001c0001t0001g0143a0001c0001t0001g0150others(80): Show | 83 | HG00099.hp1 HG00280.hp2 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.317+7877G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75768915 | ||||||
| chr13:75768948
|
T | C | 1 | a0001c0001t0001g0218 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.317+7910T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75768948 | ||||||
| chr13:75769355
|
G | C | 1 | a0005c0005t0003g0112 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.317+8317G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75769355 | ||||||
| chr13:75769362
|
G | A | 22 | a0001c0001t0001g0135a0002c0003t0001g0121a0002c0003t0001g0137others(19): Show | 22 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.317+8324G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75769362 | ||||||
| chr13:75769482
|
T | TA | 11 | a0002c0007t0003g0173a0002c0007t0003g0246a0009c0010t0001g0248others(8): Show | 11 | HG00735.hp1 HG01891.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.317+8453dupA | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75769482 | |||||
| chr13:75769492
|
C | T | 1 | a0002c0007t0003g0178 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.317+8454C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75769492 | ||||||
| chr13:75769504
|
G | T | 1 | a0001c0021t0001g0182 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.317+8466G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75769504 | ||||||
| chr13:75769797
|
A | G | 212 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(209): Show | 213 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.317+8759A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75769797 | ||||||
| chr13:75770178
|
A | AT | 245 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(242): Show | 246 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.317+9152dupT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75770178 | |||||
| chr13:75770178
|
A | ATT | 7 | a0003c0002t0001g0193a0003c0002t0001g0204a0003c0002t0001g0205others(4): Show | 7 | HG02040.hp2 HG02129.hp2 HG04199.hp2 others(4): Show |
intron_variant | MODIFIER | c.317+9151_317+9152d others(4): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75770178 | |||||
| chr13:75770190
|
T | TC | 17 | a0002c0003t0001g0146a0002c0003t0001g0253a0002c0003t0001g0255others(14): Show | 17 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(14): Show |
intron_variant | MODIFIER | c.317+9156dupC | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75770190 | |||||
| chr13:75770359
|
A | C | 1 | a0004c0004t0004g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.317+9321A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75770359 | ||||||
| chr13:75770427
|
A | G | 1 | a0004c0004t0001g0236 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.317+9389A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75770427 | ||||||
| chr13:75770515
|
C | A | 41 | a0001c0001t0001g0218a0003c0002t0001g0123a0003c0002t0001g0141others(38): Show | 41 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.317+9477C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75770515 | ||||||
| chr13:75770692
|
C | T | 1 | a0006c0006t0001g0245 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.317+9654C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75770692 | ||||||
| chr13:75771078
|
A | G | 2 | a0002c0003t0001g0220a0008c0008t0003g0241 | 2 | HG03927.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.317+10040A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75771078 | ||||||
| chr13:75771115
|
C | A | 3 | a0007c0016t0001g0001a0007c0016t0001g0252a0008c0008t0003g0160 | 4 | HG02895.hp1 HG02897.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.317+10077C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75771115 | ||||||
| chr13:75771162
|
T | A | 224 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(221): Show | 225 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.317+10124T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75771162 | ||||||
| chr13:75771266
|
C | T | 2 | a0007c0016t0001g0001a0007c0016t0001g0252 | 3 | HG02895.hp1 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.317+10228C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75771266 | ||||||
| chr13:75771309
|
G | A | 4 | a0002c0007t0001g0129a0007c0016t0001g0001a0007c0016t0001g0252others(1): Show | 5 | HG01952.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.317+10271G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75771309 | ||||||
| chr13:75771545
|
T | TCTTTAAA others(17): Show |
56 | a0001c0001t0001g0218a0003c0002t0001g0006a0003c0002t0001g0123others(53): Show | 56 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.317+10516_317+1051 others(28): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75771545 | |||||
| chr13:75771545
|
T | TCTTTAAA others(41): Show |
23 | a0001c0001t0001g0135a0001c0001t0002g0055a0002c0003t0001g0121others(20): Show | 23 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.317+10516_317+1051 others(52): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75771545 | |||||
| chr13:75771545
|
T | TCTTTAAA others(65): Show |
131 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(128): Show | 131 | HG00099.hp1 HG00280.hp2 HG00609.hp1 others(128): Show |
intron_variant | MODIFIER | c.317+10516_317+1051 others(76): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75771545 | |||||
| chr13:75771545
|
T | TCTTTAAA others(89): Show |
2 | a0007c0016t0001g0001a0007c0016t0001g0252 | 3 | HG02895.hp1 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.317+10516_317+1051 others(100): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75771545 | |||||
| chr13:75771681
|
C | T | 1 | a0002c0007t0003g0180 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.317+10643C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75771681 | ||||||
| chr13:75771750
|
T | A | 1 | a0001c0001t0002g0016 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.317+10712T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75771750 | ||||||
| chr13:75771906
|
C | CAGGATTG others(5): Show |
268 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(265): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.317+10869_317+1087 others(16): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75771906 | |||||
| chr13:75772412
|
C | T | 1 | a0012c0014t0014g0185 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.317+11374C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75772412 | ||||||
| chr13:75772487
|
T | G | 133 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(130): Show | 133 | HG00099.hp1 HG00280.hp2 HG00609.hp1 others(130): Show |
intron_variant | MODIFIER | c.317+11449T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75772487 | ||||||
| chr13:75773005
|
A | G | 1 | a0006c0006t0002g0093 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.317+11967A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75773005 | ||||||
| chr13:75773244
|
G | A | 1 | a0006c0006t0002g0093 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.317+12206G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75773244 | ||||||
| chr13:75773680
|
G | T | 154 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(151): Show | 154 | HG00099.hp1 HG00280.hp2 HG00609.hp1 others(151): Show |
intron_variant | MODIFIER | c.317+12642G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75773680 | ||||||
| chr13:75773684
|
C | T | 2 | a0001c0001t0002g0054a0001c0001t0002g0055 | 2 | NA18980.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.317+12646C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75773684 | ||||||
| chr13:75773712
|
A | G | 1 | a0001c0001t0002g0088 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.317+12674A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75773712 | ||||||
| chr13:75773722
|
A | C | 1 | a0012c0014t0014g0185 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.317+12684A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75773722 | ||||||
| chr13:75773795
|
G | T | 1 | a0001c0001t0002g0082 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.317+12757G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75773795 | ||||||
| chr13:75773875
|
A | G | 42 | a0001c0001t0001g0218a0003c0002t0001g0123a0003c0002t0001g0141others(39): Show | 42 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.317+12837A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75773875 | ||||||
| chr13:75774172
|
C | T | 1 | a0006c0006t0002g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.317+13134C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75774172 | ||||||
| chr13:75774284
|
T | C | 1 | a0008c0008t0001g0089 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.317+13246T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75774284 | ||||||
| chr13:75774427
|
T | C | 1 | a0001c0001t0002g0082 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.317+13389T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75774427 | ||||||
| chr13:75774438
|
T | C | 134 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(131): Show | 134 | HG00099.hp1 HG00280.hp2 HG00609.hp1 others(131): Show |
intron_variant | MODIFIER | c.317+13400T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75774438 | ||||||
| chr13:75774450
|
G | A | 122 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(119): Show | 122 | HG00099.hp1 HG00280.hp2 HG00609.hp1 others(119): Show |
intron_variant | MODIFIER | c.317+13412G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75774450 | ||||||
| chr13:75774644
|
G | A | 6 | a0001c0001t0001g0109a0001c0001t0001g0116a0001c0001t0001g0117others(3): Show | 6 | HG02698.hp2 HG03017.hp1 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.317+13606G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75774644 | ||||||
| chr13:75774660
|
T | A | 1 | a0012c0014t0014g0185 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.317+13622T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75774660 | ||||||
| chr13:75774943
|
T | G | 1 | a0003c0002t0001g0205 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.317+13905T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75774943 | ||||||
| chr13:75775201
|
C | T | 1 | a0007c0009t0002g0067 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.317+14163C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75775201 | ||||||
| chr13:75775246
|
T | C | 3 | a0002c0007t0001g0129a0007c0016t0001g0001a0007c0016t0001g0252 | 4 | HG01952.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.317+14208T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75775246 | ||||||
| chr13:75775281
|
C | A | 1 | a0012c0014t0014g0185 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.317+14243C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75775281 | ||||||
| chr13:75775313
|
G | A | 224 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(221): Show | 225 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.317+14275G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75775313 | ||||||
| chr13:75775486
|
T | C | 1 | a0003c0002t0001g0216 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.317+14448T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75775486 | ||||||
| chr13:75775619
|
A | G | 12 | a0004c0027t0002g0092a0005c0005t0001g0125a0005c0005t0003g0112others(9): Show | 12 | HG01884.hp1 HG03831.hp2 NA18940.hp2 others(9): Show |
intron_variant | MODIFIER | c.317+14581A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75775619 | ||||||
| chr13:75775622
|
C | T | 22 | a0001c0001t0001g0135a0002c0003t0001g0121a0002c0003t0001g0137others(19): Show | 22 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.317+14584C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75775622 | ||||||
| chr13:75775696
|
G | A | 1 | a0011c0015t0001g0155 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.317+14658G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75775696 | ||||||
| chr13:75776094
|
GAT | G | 184 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(181): Show | 184 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.317+15074_317+1507 others(6): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75776094 | |||||
| chr13:75776112
|
T | TATATAC | 4 | a0002c0007t0001g0129a0007c0016t0001g0001a0007c0016t0001g0252others(1): Show | 5 | HG01952.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.317+15075_317+1507 others(10): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75776112 | |||||
| chr13:75776121
|
A | T | 1 | a0012c0014t0014g0185 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.317+15083A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75776121 | ||||||
| chr13:75776126
|
C | CAT | 27 | a0002c0003t0001g0126a0002c0003t0001g0146a0002c0003t0001g0255others(24): Show | 27 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(24): Show |
intron_variant | MODIFIER | c.317+15105_317+1510 others(6): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75776126 | |||||
| chr13:75776126
|
CAT | C | 59 | a0001c0001t0001g0159a0001c0001t0001g0218a0001c0001t0002g0009others(56): Show | 59 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.317+15105_317+1510 others(6): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75776126 | |||||
| chr13:75776128
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.317+15090T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75776128 | ||||||
| chr13:75776128
|
T | TAC | 22 | a0001c0001t0001g0135a0002c0003t0001g0121a0002c0003t0001g0137others(19): Show | 22 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.317+15091_317+1509 others(6): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75776128 | |||||
| chr13:75776143
|
ATGCCATG | A | 11 | a0005c0005t0001g0125a0005c0005t0003g0112a0005c0005t0003g0124others(8): Show | 11 | HG03831.hp2 NA18940.hp2 NA18942.hp2 others(8): Show |
intron_variant | MODIFIER | c.317+15107_317+1511 others(11): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75776143 | |||||
| chr13:75776144
|
T | G | 1 | a0001c0001t0002g0039 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.317+15106T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75776144 | ||||||
| chr13:75776150
|
G | GTATATAT others(18): Show |
2 | a0002c0003t0001g0253a0002c0003t0001g0257 | 2 | HG02040.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.317+15122_317+1514 others(29): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75776150 | |||||
| chr13:75776160
|
C | G | 11 | a0005c0005t0001g0125a0005c0005t0003g0112a0005c0005t0003g0124others(8): Show | 11 | HG03831.hp2 NA18940.hp2 NA18942.hp2 others(8): Show |
intron_variant | MODIFIER | c.317+15122C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75776160 | ||||||
| chr13:75776161
|
G | C | 11 | a0005c0005t0001g0125a0005c0005t0003g0112a0005c0005t0003g0124others(8): Show | 11 | HG03831.hp2 NA18940.hp2 NA18942.hp2 others(8): Show |
intron_variant | MODIFIER | c.317+15123G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75776161 | ||||||
| chr13:75776162
|
G | C | 11 | a0005c0005t0001g0125a0005c0005t0003g0112a0005c0005t0003g0124others(8): Show | 11 | HG03831.hp2 NA18940.hp2 NA18942.hp2 others(8): Show |
intron_variant | MODIFIER | c.317+15124G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75776162 | ||||||
| chr13:75776162
|
G | GAT | 14 | a0001c0001t0001g0208a0001c0001t0002g0082a0003c0002t0001g0212others(11): Show | 14 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.317+15166_317+1516 others(6): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75776162 | |||||
| chr13:75776162
|
G | GATAT | 17 | a0001c0001t0001g0151a0001c0001t0002g0039a0001c0001t0002g0042others(14): Show | 17 | HG01106.hp1 HG01123.hp1 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.317+15164_317+1516 others(8): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75776162 | |||||
| chr13:75776162
|
G | GATATAT | 12 | a0001c0001t0001g0150a0001c0001t0002g0045a0001c0001t0002g0083others(9): Show | 12 | HG00621.hp1 HG01256.hp2 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.317+15162_317+1516 others(10): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75776162 | |||||
| chr13:75776162
|
G | GATATATA others(1): Show |
9 | a0001c0001t0002g0023a0001c0001t0002g0035a0001c0001t0002g0079others(6): Show | 9 | HG01109.hp1 HG01993.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.317+15160_317+1516 others(12): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75776162 | |||||
| chr13:75776162
|
G | GATATATA others(3): Show |
11 | a0001c0001t0001g0159a0001c0001t0002g0040a0001c0001t0002g0051others(8): Show | 11 | HG00673.hp2 HG01175.hp2 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.317+15158_317+1516 others(14): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75776162 | |||||
| chr13:75776162
|
G | GATATATA others(5): Show |
18 | a0001c0001t0001g0113a0001c0001t0001g0116a0001c0001t0001g0117others(15): Show | 18 | HG01257.hp2 HG01952.hp2 HG02135.hp2 others(15): Show |
intron_variant | MODIFIER | c.317+15156_317+1516 others(16): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75776162 | |||||
| chr13:75776162
|
G | GATATATA others(7): Show |
20 | a0001c0001t0001g0143a0001c0001t0001g0167a0001c0001t0002g0007others(17): Show | 20 | HG00099.hp1 HG00280.hp2 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.317+15154_317+1516 others(18): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75776162 | |||||
| chr13:75776162
|
G | GATATATA others(9): Show |
9 | a0001c0001t0002g0014a0001c0001t0002g0020a0001c0001t0002g0036others(6): Show | 9 | HG01123.hp2 HG03491.hp2 HG03492.hp2 others(6): Show |
intron_variant | MODIFIER | c.317+15152_317+1516 others(20): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75776162 | |||||
| chr13:75776162
|
G | GATATATA others(11): Show |
6 | a0001c0001t0002g0018a0001c0001t0002g0034a0003c0002t0001g0142others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.317+15150_317+1516 others(22): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75776162 | |||||
| chr13:75776162
|
G | GATATATA others(13): Show |
6 | a0001c0001t0001g0109a0003c0002t0001g0194a0003c0002t0001g0198others(3): Show | 6 | HG02135.hp1 NA18953.hp1 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.317+15148_317+1516 others(24): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75776162 | |||||
| chr13:75776162
|
G | GATATATA others(15): Show |
7 | a0001c0001t0001g0218a0001c0001t0002g0013a0001c0001t0002g0022others(4): Show | 7 | HG01175.hp1 HG01346.hp2 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.317+15146_317+1516 others(26): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75776162 | |||||
| chr13:75776162
|
G | GATATATA others(17): Show |
3 | a0003c0002t0001g0123a0003c0002t0001g0206a0003c0002t0002g0270 | 3 | HG00621.hp2 NA18998.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.317+15144_317+1516 others(28): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75776162 | |||||
| chr13:75776162
|
G | GATATATA others(19): Show |
1 | a0003c0002t0001g0224 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.317+15142_317+1516 others(30): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75776162 | |||||
| chr13:75776162
|
G | GATATATA others(28): Show |
1 | a0002c0003t0005g0030 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.317+15148_317+1514 others(39): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75776162 | |||||
| chr13:75776162
|
G | GATATATA others(22): Show |
1 | a0002c0003t0005g0070 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.317+15148_317+1514 others(33): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75776162 | |||||
| chr13:75776162
|
G | GATATATA others(20): Show |
5 | a0002c0003t0001g0146a0002c0003t0001g0255a0002c0003t0001g0258others(2): Show | 5 | HG00438.hp1 HG02523.hp2 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.317+15146_317+1514 others(31): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75776162 | |||||
| chr13:75776162
|
G | GATATATA others(22): Show |
1 | a0002c0003t0001g0256 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.317+15146_317+1514 others(33): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75776162 | |||||
| chr13:75776162
|
G | GATATATA others(12): Show |
2 | a0004c0004t0001g0148a0004c0004t0001g0149 | 2 | NA19007.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.317+15136_317+1513 others(23): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75776162 | |||||
| chr13:75776162
|
GAT | G | 13 | a0001c0001t0001g0135a0001c0001t0002g0016a0004c0004t0001g0120others(10): Show | 13 | HG00738.hp1 HG01106.hp2 HG01515.hp1 others(10): Show |
intron_variant | MODIFIER | c.317+15166_317+1516 others(6): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75776162 | |||||
| chr13:75776162
|
GATAT | G | 6 | a0001c0001t0002g0043a0001c0001t0002g0054a0001c0001t0002g0055others(3): Show | 6 | HG01243.hp2 HG03225.hp1 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.317+15164_317+1516 others(8): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75776162 | |||||
| chr13:75776162
|
GATATATA others(1): Show |
G | 5 | a0002c0003t0001g0138a0002c0003t0001g0139a0002c0007t0004g0260others(2): Show | 5 | HG01168.hp1 HG01169.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.317+15160_317+1516 others(12): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75776162 | |||||
| chr13:75776162
|
GATATATA others(3): Show |
G | 12 | a0001c0001t0002g0021a0001c0001t0002g0041a0001c0001t0002g0265others(9): Show | 12 | HG00639.hp1 HG01261.hp1 HG02293.hp1 others(9): Show |
intron_variant | MODIFIER | c.317+15158_317+1516 others(14): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75776162 | |||||
| chr13:75776162
|
GATATATA others(5): Show |
G | 3 | a0001c0001t0002g0063a0003c0002t0001g0227a0008c0008t0004g0087 | 3 | HG02273.hp2 HG02970.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.317+15156_317+1516 others(16): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75776162 | |||||
| chr13:75776162
|
GATATATA others(7): Show |
G | 5 | a0004c0004t0001g0231a0004c0004t0001g0232a0004c0004t0001g0235others(2): Show | 5 | HG01070.hp2 HG01192.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.317+15154_317+1516 others(18): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75776162 | |||||
| chr13:75776162
|
GATATATA others(9): Show |
G | 3 | a0001c0001t0001g0201a0008c0008t0003g0169a0009c0010t0017g0004 | 3 | HG00609.hp1 HG00735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.317+15152_317+1516 others(20): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75776162 | |||||
| chr13:75776162
|
GATATATA others(11): Show |
G | 10 | a0002c0003t0001g0220a0003c0002t0002g0262a0008c0008t0001g0089others(7): Show | 10 | HG01243.hp1 HG02818.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.317+15150_317+1516 others(22): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75776162 | |||||
| chr13:75776162
|
GATATATA others(13): Show |
G | 8 | a0001c0001t0002g0088a0001c0001t0002g0099a0001c0001t0002g0106others(5): Show | 8 | HG01099.hp2 HG01884.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.317+15148_317+1516 others(24): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75776162 | |||||
| chr13:75776162
|
GATATATA others(15): Show |
G | 1 | a0003c0002t0001g0195 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.317+15146_317+1516 others(26): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75776162 | |||||
| chr13:75776162
|
GATATATA others(17): Show |
G | 11 | a0003c0002t0001g0141a0003c0002t0001g0157a0003c0002t0001g0158others(8): Show | 11 | HG00280.hp1 HG01070.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.317+15144_317+1516 others(28): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75776162 | |||||
| chr13:75776164
|
T | TATATATA others(18): Show |
1 | a0002c0003t0011g0161 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.317+15148_317+1514 others(29): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75776164 | |||||
| chr13:75776164
|
T | TATATATA others(45): Show |
1 | a0002c0011t0002g0071 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.317+15148_317+1514 others(56): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75776164 | |||||
| chr13:75776164
|
T | TATATATA others(43): Show |
2 | a0002c0011t0002g0075a0002c0011t0002g0076 | 2 | HG00140.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.317+15148_317+1514 others(54): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75776164 | |||||
| chr13:75776165
|
A | G | 11 | a0005c0005t0001g0125a0005c0005t0003g0112a0005c0005t0003g0124others(8): Show | 11 | HG03831.hp2 NA18940.hp2 NA18942.hp2 others(8): Show |
intron_variant | MODIFIER | c.317+15127A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75776165 | ||||||
| chr13:75776166
|
T | TATATATA others(43): Show |
2 | a0002c0011t0002g0031a0002c0011t0002g0084 | 2 | HG00099.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.317+15148_317+1514 others(54): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75776166 | |||||
| chr13:75776166
|
T | TATATATA others(97): Show |
1 | a0002c0011t0002g0038 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.317+15148_317+1514 others(108): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75776166 | |||||
| chr13:75776174
|
TATATA | T | 11 | a0005c0005t0001g0125a0005c0005t0003g0112a0005c0005t0003g0124others(8): Show | 11 | HG03831.hp2 NA18940.hp2 NA18942.hp2 others(8): Show |
intron_variant | MODIFIER | c.317+15137_317+1514 others(9): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75776174 | ||||||
| chr13:75776180
|
T | C | 11 | a0005c0005t0001g0125a0005c0005t0003g0112a0005c0005t0003g0124others(8): Show | 11 | HG03831.hp2 NA18940.hp2 NA18942.hp2 others(8): Show |
intron_variant | MODIFIER | c.317+15142T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75776180 | ||||||
| chr13:75776181
|
A | G | 11 | a0005c0005t0001g0125a0005c0005t0003g0112a0005c0005t0003g0124others(8): Show | 11 | HG03831.hp2 NA18940.hp2 NA18942.hp2 others(8): Show |
intron_variant | MODIFIER | c.317+15143A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75776181 | ||||||
| chr13:75776182
|
T | G | 11 | a0005c0005t0001g0125a0005c0005t0003g0112a0005c0005t0003g0124others(8): Show | 11 | HG03831.hp2 NA18940.hp2 NA18942.hp2 others(8): Show |
intron_variant | MODIFIER | c.317+15144T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75776182 | ||||||
| chr13:75776204
|
T | A | 1 | a0008c0008t0003g0111 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.317+15166T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75776204 | ||||||
| chr13:75776205
|
A | ATATATAT others(4): Show |
1 | a0005c0005t0001g0114 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.317+15167_317+1516 others(15): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75776205 | ||||||
| chr13:75776309
|
C | T | 12 | a0004c0027t0002g0092a0005c0005t0001g0125a0005c0005t0003g0112others(9): Show | 12 | HG01884.hp1 HG03831.hp2 NA18940.hp2 others(9): Show |
intron_variant | MODIFIER | c.317+15271C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75776309 | ||||||
| chr13:75776432
|
A | G | 2 | a0003c0002t0001g0224a0003c0002t0001g0228 | 2 | HG00438.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.317+15394A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75776432 | ||||||
| chr13:75776518
|
G | A | 41 | a0001c0001t0001g0218a0003c0002t0001g0123a0003c0002t0001g0141others(38): Show | 41 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.317+15480G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75776518 | ||||||
| chr13:75776685
|
C | A | 212 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(209): Show | 213 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.317+15647C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75776685 | ||||||
| chr13:75776749
|
C | G | 1 | a0003c0002t0001g0191 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.317+15711C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75776749 | ||||||
| chr13:75777031
|
C | T | 1 | a0004c0004t0001g0120 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.317+15993C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75777031 | ||||||
| chr13:75777150
|
A | G | 224 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(221): Show | 225 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.317+16112A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75777150 | ||||||
| chr13:75777156
|
TTTTA | T | 11 | a0002c0007t0003g0173a0002c0007t0003g0246a0009c0010t0001g0248others(8): Show | 11 | HG00735.hp1 HG01891.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.317+16122_317+1612 others(8): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75777156 | |||||
| chr13:75777257
|
C | T | 41 | a0001c0001t0001g0218a0003c0002t0001g0123a0003c0002t0001g0141others(38): Show | 41 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.317+16219C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75777257 | ||||||
| chr13:75777647
|
G | GT | 167 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(164): Show | 168 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.317+16625dupT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75777647 | |||||
| chr13:75777647
|
G | GTT | 33 | a0001c0001t0001g0135a0001c0001t0001g0208a0001c0001t0002g0099others(30): Show | 33 | HG00639.hp1 HG00639.hp2 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.317+16624_317+1662 others(6): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75777647 | |||||
| chr13:75777647
|
G | GTTT | 7 | a0002c0003t0001g0138a0002c0003t0001g0139a0002c0003t0001g0220others(4): Show | 7 | HG01168.hp1 HG01169.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.317+16623_317+1662 others(7): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75777647 | |||||
| chr13:75777740
|
G | A | 1 | a0002c0003t0005g0033 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.317+16702G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75777740 | ||||||
| chr13:75777799
|
C | T | 5 | a0002c0007t0003g0176a0002c0007t0003g0178a0002c0007t0003g0181others(2): Show | 5 | HG00639.hp1 HG01261.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.317+16761C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75777799 | ||||||
| chr13:75778001
|
T | G | 133 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(130): Show | 133 | HG00099.hp1 HG00280.hp2 HG00609.hp1 others(130): Show |
intron_variant | MODIFIER | c.317+16963T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75778001 | ||||||
| chr13:75778043
|
A | C | 10 | a0002c0003t0001g0220a0008c0008t0001g0089a0008c0008t0002g0077others(7): Show | 10 | HG01243.hp1 HG02922.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.317+17005A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75778043 | ||||||
| chr13:75778054
|
G | A | 44 | a0001c0001t0001g0218a0003c0002t0001g0006a0003c0002t0001g0123others(41): Show | 44 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.317+17016G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75778054 | ||||||
| chr13:75778056
|
A | G | 2 | a0001c0001t0002g0020a0001c0001t0002g0062 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.317+17018A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75778056 | ||||||
| chr13:75778478
|
C | T | 1 | a0002c0007t0003g0246 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.318-16923C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75778478 | ||||||
| chr13:75778653
|
C | A | 1 | a0004c0004t0001g0190 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.318-16748C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75778653 | ||||||
| chr13:75778694
|
T | C | 1 | a0008c0008t0001g0089 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.318-16707T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75778694 | ||||||
| chr13:75778716
|
T | C | 1 | a0001c0001t0002g0058 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.318-16685T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75778716 | ||||||
| chr13:75778826
|
A | G | 2 | a0005c0005t0003g0127a0005c0005t0003g0128 | 2 | NA18942.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.318-16575A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75778826 | ||||||
| chr13:75779020
|
C | T | 22 | a0001c0001t0001g0135a0002c0003t0001g0121a0002c0003t0001g0137others(19): Show | 22 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.318-16381C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75779020 | ||||||
| chr13:75779088
|
G | T | 1 | a0016c0024t0002g0086 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.318-16313G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75779088 | ||||||
| chr13:75779148
|
C | A | 1 | a0002c0007t0003g0173 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.318-16253C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75779148 | ||||||
| chr13:75779205
|
A | C | 1 | a0008c0008t0002g0077 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.318-16196A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75779205 | ||||||
| chr13:75779222
|
A | G | 1 | a0001c0001t0002g0055 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.318-16179A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75779222 | ||||||
| chr13:75779229
|
A | G | 1 | a0012c0014t0014g0185 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.318-16172A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75779229 | ||||||
| chr13:75779246
|
T | C | 4 | a0004c0004t0001g0187a0004c0004t0001g0188a0004c0004t0001g0190others(1): Show | 4 | NA18949.hp2 NA18954.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.318-16155T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75779246 | ||||||
| chr13:75779341
|
T | TG | 10 | a0002c0003t0001g0126a0002c0007t0012g0156a0007c0009t0001g0152others(7): Show | 10 | HG01081.hp2 HG01175.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.318-16054dupG | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75779341 | |||||
| chr13:75779386
|
A | T | 119 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(116): Show | 119 | HG00099.hp1 HG00280.hp2 HG00609.hp1 others(116): Show |
intron_variant | MODIFIER | c.318-16015A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75779386 | ||||||
| chr13:75779564
|
A | G | 36 | a0001c0001t0001g0109a0001c0001t0001g0116a0001c0001t0001g0117others(33): Show | 36 | HG01070.hp2 HG01192.hp2 HG01255.hp1 others(33): Show |
intron_variant | MODIFIER | c.318-15837A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75779564 | ||||||
| chr13:75779720
|
G | A | 5 | a0001c0001t0002g0021a0001c0001t0002g0039a0001c0001t0002g0042others(2): Show | 5 | NA18970.hp2 NA18980.hp1 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.318-15681G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75779720 | ||||||
| chr13:75779968
|
G | A | 12 | a0004c0027t0002g0092a0005c0005t0001g0125a0005c0005t0003g0112others(9): Show | 12 | HG01884.hp1 HG03831.hp2 NA18940.hp2 others(9): Show |
intron_variant | MODIFIER | c.318-15433G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75779968 | ||||||
| chr13:75779975
|
G | C | 1 | a0007c0016t0001g0001 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.318-15426G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75779975 | ||||||
| chr13:75780155
|
G | A | 129 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(126): Show | 129 | HG00099.hp1 HG00280.hp2 HG00609.hp1 others(126): Show |
intron_variant | MODIFIER | c.318-15246G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75780155 | ||||||
| chr13:75780159
|
A | G | 2 | a0007c0009t0001g0162a0007c0009t0002g0067 | 2 | HG03017.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.318-15242A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75780159 | ||||||
| chr13:75780163
|
A | G | 12 | a0004c0027t0002g0092a0005c0005t0001g0125a0005c0005t0003g0112others(9): Show | 12 | HG01884.hp1 HG03831.hp2 NA18940.hp2 others(9): Show |
intron_variant | MODIFIER | c.318-15238A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75780163 | ||||||
| chr13:75780289
|
G | A | 1 | a0008c0008t0003g0169 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.318-15112G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75780289 | ||||||
| chr13:75780363
|
C | T | 1 | a0006c0006t0002g0095 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.318-15038C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75780363 | ||||||
| chr13:75780439
|
A | G | 1 | a0009c0030t0001g0170 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.318-14962A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75780439 | ||||||
| chr13:75780451
|
C | T | 1 | a0003c0002t0001g0212 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.318-14950C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75780451 | ||||||
| chr13:75780456
|
G | A | 2 | a0002c0003t0001g0211a0002c0003t0001g0240 | 2 | HG02735.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.318-14945G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75780456 | ||||||
| chr13:75780680
|
T | G | 6 | a0009c0010t0001g0248a0009c0010t0001g0249a0009c0010t0001g0250others(3): Show | 6 | HG01891.hp2 HG03098.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.318-14721T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75780680 | ||||||
| chr13:75780860
|
C | T | 1 | a0001c0001t0008g0044 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.318-14541C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75780860 | ||||||
| chr13:75780940
|
C | T | 6 | a0009c0010t0001g0248a0009c0010t0001g0249a0009c0010t0001g0250others(3): Show | 6 | HG01891.hp2 HG03098.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.318-14461C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75780940 | ||||||
| chr13:75781031
|
A | G | 1 | a0007c0016t0001g0001 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.318-14370A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75781031 | ||||||
| chr13:75781087
|
T | G | 118 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(115): Show | 118 | HG00099.hp1 HG00280.hp2 HG00609.hp1 others(115): Show |
intron_variant | MODIFIER | c.318-14314T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75781087 | ||||||
| chr13:75781096
|
C | CT | 20 | a0001c0001t0001g0113a0001c0001t0001g0159a0001c0001t0001g0208others(17): Show | 21 | HG00438.hp1 HG00735.hp2 HG01952.hp2 others(18): Show |
intron_variant | MODIFIER | c.318-14282dupT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75781096 | |||||
| chr13:75781096
|
C | CTT | 40 | a0001c0001t0001g0218a0003c0002t0001g0006a0003c0002t0001g0123others(37): Show | 40 | HG00280.hp1 HG00621.hp2 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.318-14283_318-1428 others(6): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75781096 | |||||
| chr13:75781096
|
C | CTTT | 5 | a0003c0002t0001g0191a0003c0002t0001g0195a0003c0002t0001g0196others(2): Show | 5 | HG00438.hp2 HG01928.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.318-14284_318-1428 others(7): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75781096 | |||||
| chr13:75781096
|
CT | C | 17 | a0001c0001t0002g0034a0002c0003t0005g0033a0002c0011t0002g0038others(14): Show | 17 | HG01256.hp1 HG01496.hp1 HG03017.hp1 others(14): Show |
intron_variant | MODIFIER | c.318-14282delT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75781096 | |||||
| chr13:75781112
|
T | G | 1 | a0002c0007t0004g0260 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.318-14289T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75781112 | ||||||
| chr13:75781113
|
T | C | 1 | a0002c0007t0004g0260 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.318-14288T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75781113 | ||||||
| chr13:75781113
|
T | G | 21 | a0001c0001t0001g0135a0002c0003t0001g0121a0002c0003t0001g0137others(18): Show | 21 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.318-14288T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75781113 | ||||||
| chr13:75781114
|
T | C | 21 | a0001c0001t0001g0135a0002c0003t0001g0121a0002c0003t0001g0137others(18): Show | 21 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.318-14287T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75781114 | ||||||
| chr13:75781115
|
TTTTTGC | T | 21 | a0001c0001t0001g0135a0002c0003t0001g0121a0002c0003t0001g0137others(18): Show | 21 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.318-14281_318-1427 others(10): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75781115 | |||||
| chr13:75781120
|
GCTTTTTT others(4): Show |
G | 1 | a0011c0015t0001g0242 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.318-14275_318-1426 others(15): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75781120 | |||||
| chr13:75781234
|
G | A | 1 | a0001c0001t0002g0058 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.318-14167G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75781234 | ||||||
| chr13:75781261
|
A | G | 29 | a0001c0001t0001g0109a0001c0001t0001g0116a0001c0001t0001g0117others(26): Show | 30 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.318-14140A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75781261 | ||||||
| chr13:75781276
|
C | T | 3 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0002g0051 | 3 | HG02132.hp2 HG02165.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.318-14125C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75781276 | ||||||
| chr13:75781296
|
G | A | 1 | a0002c0007t0001g0129 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.318-14105G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75781296 | ||||||
| chr13:75781304
|
A | C | 4 | a0001c0001t0001g0159a0001c0001t0002g0012a0021c0026t0001g0122others(1): Show | 4 | NA18953.hp2 NA18986.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.318-14097A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75781304 | ||||||
| chr13:75781305
|
G | A | 129 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(126): Show | 129 | HG00099.hp1 HG00280.hp2 HG00609.hp1 others(126): Show |
intron_variant | MODIFIER | c.318-14096G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75781305 | ||||||
| chr13:75781395
|
G | A | 2 | a0002c0007t0003g0173a0008c0008t0003g0160 | 2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.318-14006G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75781395 | ||||||
| chr13:75781396
|
C | G | 2 | a0010c0012t0001g0130a0010c0012t0001g0131 | 2 | HG06807.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.318-14005C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75781396 | ||||||
| chr13:75781396
|
C | T | 2 | a0001c0001t0002g0045a0001c0001t0008g0044 | 2 | HG01192.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.318-14005C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75781396 | ||||||
| chr13:75781425
|
A | G | 1 | a0002c0007t0004g0261 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.318-13976A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75781425 | ||||||
| chr13:75781487
|
A | G | 2 | a0012c0014t0001g0002a0012c0014t0001g0003 | 2 | HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.318-13914A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75781487 | ||||||
| chr13:75781569
|
A | G | 1 | a0002c0007t0001g0129 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.318-13832A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75781569 | ||||||
| chr13:75781589
|
C | T | 1 | a0006c0006t0002g0097 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.318-13812C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75781589 | ||||||
| chr13:75781590
|
A | G | 3 | a0001c0001t0002g0058a0007c0009t0001g0162a0007c0009t0002g0067 | 3 | HG02056.hp1 HG03017.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.318-13811A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75781590 | ||||||
| chr13:75781654
|
G | T | 45 | a0001c0001t0001g0218a0003c0002t0001g0006a0003c0002t0001g0123others(42): Show | 45 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.318-13747G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75781654 | ||||||
| chr13:75781656
|
T | C | 45 | a0001c0001t0001g0218a0003c0002t0001g0006a0003c0002t0001g0123others(42): Show | 45 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.318-13745T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75781656 | ||||||
| chr13:75781677
|
G | C | 45 | a0001c0001t0001g0218a0003c0002t0001g0006a0003c0002t0001g0123others(42): Show | 45 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.318-13724G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75781677 | ||||||
| chr13:75781681
|
T | A | 45 | a0001c0001t0001g0218a0003c0002t0001g0006a0003c0002t0001g0123others(42): Show | 45 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.318-13720T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75781681 | ||||||
| chr13:75781698
|
G | A | 45 | a0001c0001t0001g0218a0003c0002t0001g0006a0003c0002t0001g0123others(42): Show | 45 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.318-13703G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75781698 | ||||||
| chr13:75781762
|
T | A | 1 | a0002c0007t0003g0173 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.318-13639T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75781762 | ||||||
| chr13:75781763
|
A | G | 4 | a0003c0002t0001g0006a0003c0002t0001g0200a0003c0002t0001g0214others(1): Show | 4 | NA18960.hp2 NA18979.hp1 NA19055.hp2 others(1): Show |
intron_variant | MODIFIER | c.318-13638A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75781763 | ||||||
| chr13:75782111
|
T | C | 1 | a0007c0016t0001g0001 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.318-13290T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75782111 | ||||||
| chr13:75782112
|
A | G | 1 | a0002c0007t0001g0129 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.318-13289A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75782112 | ||||||
| chr13:75782222
|
G | A | 10 | a0003c0002t0001g0194a0003c0002t0001g0222a0003c0002t0001g0224others(7): Show | 10 | HG00438.hp2 HG00621.hp2 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.318-13179G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75782222 | ||||||
| chr13:75782289
|
G | A | 1 | a0003c0002t0001g0219 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.318-13112G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75782289 | ||||||
| chr13:75782421
|
C | T | 45 | a0001c0001t0001g0218a0003c0002t0001g0006a0003c0002t0001g0123others(42): Show | 45 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.318-12980C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75782421 | ||||||
| chr13:75782545
|
C | T | 2 | a0004c0004t0001g0120a0004c0004t0002g0060 | 2 | HG01515.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.318-12856C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75782545 | ||||||
| chr13:75782549
|
A | G | 2 | a0002c0003t0001g0138a0002c0003t0001g0139 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.318-12852A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75782549 | ||||||
| chr13:75782807
|
C | T | 7 | a0002c0003t0001g0121a0002c0003t0001g0137a0002c0003t0001g0138others(4): Show | 7 | HG01106.hp1 HG01168.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.318-12594C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75782807 | ||||||
| chr13:75783081
|
A | G | 1 | a0001c0001t0002g0023 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.318-12320A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75783081 | ||||||
| chr13:75783156
|
C | T | 1 | a0002c0007t0003g0173 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.318-12245C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75783156 | ||||||
| chr13:75783330
|
C | T | 12 | a0004c0027t0002g0092a0005c0005t0001g0125a0005c0005t0003g0112others(9): Show | 12 | HG01884.hp1 HG03831.hp2 NA18940.hp2 others(9): Show |
intron_variant | MODIFIER | c.318-12071C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75783330 | ||||||
| chr13:75783352
|
G | A | 130 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(127): Show | 130 | HG00099.hp1 HG00280.hp2 HG00609.hp1 others(127): Show |
intron_variant | MODIFIER | c.318-12049G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75783352 | ||||||
| chr13:75783694
|
C | A | 44 | a0001c0001t0001g0218a0003c0002t0001g0006a0003c0002t0001g0123others(41): Show | 44 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.318-11707C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75783694 | ||||||
| chr13:75783745
|
C | G | 143 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(140): Show | 144 | HG00099.hp1 HG00280.hp2 HG00609.hp1 others(141): Show |
intron_variant | MODIFIER | c.318-11656C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75783745 | ||||||
| chr13:75783934
|
C | T | 1 | a0002c0007t0001g0129 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.318-11467C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75783934 | ||||||
| chr13:75784066
|
T | C | 10 | a0002c0003t0001g0220a0008c0008t0001g0089a0008c0008t0002g0077others(7): Show | 10 | HG01243.hp1 HG02922.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.318-11335T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75784066 | ||||||
| chr13:75784228
|
C | A | 118 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(115): Show | 118 | HG00099.hp1 HG00280.hp2 HG00609.hp1 others(115): Show |
intron_variant | MODIFIER | c.318-11173C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75784228 | ||||||
| chr13:75784691
|
C | T | 8 | a0002c0007t0003g0176a0002c0007t0003g0178a0002c0007t0003g0180others(5): Show | 8 | HG00639.hp1 HG01261.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.318-10710C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75784691 | ||||||
| chr13:75784734
|
C | T | 8 | a0002c0007t0003g0176a0002c0007t0003g0178a0002c0007t0003g0180others(5): Show | 8 | HG00639.hp1 HG01261.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.318-10667C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75784734 | ||||||
| chr13:75784888
|
A | T | 6 | a0002c0003t0001g0121a0002c0003t0001g0137a0002c0003t0001g0138others(3): Show | 6 | HG01106.hp1 HG01168.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.318-10513A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75784888 | ||||||
| chr13:75784969
|
T | C | 8 | a0002c0007t0003g0176a0002c0007t0003g0178a0002c0007t0003g0180others(5): Show | 8 | HG00639.hp1 HG01261.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.318-10432T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75784969 | ||||||
| chr13:75784997
|
A | G | 1 | a0009c0030t0001g0170 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.318-10404A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75784997 | ||||||
| chr13:75785150
|
A | T | 3 | a0002c0007t0001g0129a0007c0016t0001g0001a0007c0016t0001g0252 | 4 | HG01952.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.318-10251A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75785150 | ||||||
| chr13:75785448
|
G | T | 251 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(248): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.318-9953G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75785448 | ||||||
| chr13:75785643
|
T | G | 1 | a0001c0001t0001g0208 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.318-9758T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75785643 | ||||||
| chr13:75785688
|
A | G | 1 | a0003c0002t0001g0204 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.318-9713A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75785688 | ||||||
| chr13:75785902
|
C | G | 1 | a0002c0007t0003g0173 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.318-9499C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75785902 | ||||||
| chr13:75785942
|
A | G | 1 | a0002c0003t0005g0033 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.318-9459A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75785942 | ||||||
| chr13:75786137
|
C | G | 1 | a0005c0005t0001g0125 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.318-9264C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75786137 | ||||||
| chr13:75786162
|
T | TGTCA | 12 | a0004c0027t0002g0092a0005c0005t0001g0125a0005c0005t0003g0112others(9): Show | 12 | HG01884.hp1 HG03831.hp2 NA18940.hp2 others(9): Show |
intron_variant | MODIFIER | c.318-9238_318-9235d others(6): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75786162 | |||||
| chr13:75786418
|
A | G | 46 | a0001c0001t0001g0218a0003c0002t0001g0006a0003c0002t0001g0123others(43): Show | 46 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.318-8983A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75786418 | ||||||
| chr13:75786444
|
G | A | 1 | a0001c0021t0001g0182 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.318-8957G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75786444 | ||||||
| chr13:75786450
|
T | C | 1 | a0001c0020t0002g0269 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.318-8951T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75786450 | ||||||
| chr13:75786494
|
C | T | 1 | a0005c0005t0015g0171 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.318-8907C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75786494 | ||||||
| chr13:75786727
|
G | A | 1 | a0007c0009t0009g0251 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.318-8674G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75786727 | ||||||
| chr13:75786820
|
A | G | 1 | a0008c0008t0003g0169 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.318-8581A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75786820 | ||||||
| chr13:75786883
|
A | G | 3 | a0007c0009t0009g0251a0016c0024t0002g0086a0017c0023t0002g0050 | 3 | HG03041.hp2 NA18965.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.318-8518A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75786883 | ||||||
| chr13:75786927
|
C | T | 1 | a0008c0008t0001g0089 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.318-8474C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75786927 | ||||||
| chr13:75787159
|
G | A | 4 | a0001c0001t0002g0007a0001c0001t0002g0025a0001c0001t0002g0066others(1): Show | 4 | HG00609.hp2 NA18954.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.318-8242G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75787159 | ||||||
| chr13:75787177
|
A | G | 2 | a0002c0003t0001g0238a0002c0003t0001g0239 | 2 | HG03491.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.318-8224A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75787177 | ||||||
| chr13:75787219
|
G | A | 1 | a0002c0007t0003g0173 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.318-8182G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75787219 | ||||||
| chr13:75787265
|
A | G | 130 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(127): Show | 130 | HG00099.hp1 HG00280.hp2 HG00609.hp1 others(127): Show |
intron_variant | MODIFIER | c.318-8136A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75787265 | ||||||
| chr13:75787718
|
G | A | 1 | a0003c0002t0001g0193 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.318-7683G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75787718 | ||||||
| chr13:75787744
|
C | T | 2 | a0004c0013t0002g0019a0004c0013t0002g0057 | 2 | HG02735.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.318-7657C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75787744 | ||||||
| chr13:75787784
|
T | G | 1 | a0006c0006t0001g0132 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.318-7617T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75787784 | ||||||
| chr13:75787948
|
A | C | 6 | a0009c0010t0001g0248a0009c0010t0001g0249a0009c0010t0001g0250others(3): Show | 6 | HG01891.hp2 HG03098.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.318-7453A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75787948 | ||||||
| chr13:75788036
|
A | G | 4 | a0001c0001t0002g0035a0001c0001t0002g0047a0001c0001t0002g0048others(1): Show | 4 | HG01981.hp1 HG02647.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.318-7365A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75788036 | ||||||
| chr13:75788149
|
C | A | 1 | a0002c0007t0001g0129 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.318-7252C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75788149 | ||||||
| chr13:75788159
|
C | A | 1 | a0001c0001t0001g0218 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.318-7242C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75788159 | ||||||
| chr13:75788268
|
G | A | 2 | a0001c0001t0002g0020a0001c0001t0002g0062 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.318-7133G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75788268 | ||||||
| chr13:75788452
|
C | CA | 63 | a0001c0001t0001g0218a0001c0001t0002g0042a0001c0021t0001g0182others(60): Show | 63 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.318-6928dupA | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75788452 | |||||
| chr13:75788452
|
C | CAA | 10 | a0003c0002t0001g0123a0003c0002t0001g0209a0003c0002t0001g0215others(7): Show | 10 | HG00621.hp2 HG01175.hp1 HG03098.hp2 others(7): Show |
intron_variant | MODIFIER | c.318-6929_318-6928d others(4): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75788452 | |||||
| chr13:75788546
|
C | T | 47 | a0001c0001t0001g0218a0001c0001t0002g0045a0001c0001t0008g0044others(44): Show | 47 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.318-6855C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75788546 | ||||||
| chr13:75788581
|
C | T | 1 | a0004c0004t0004g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.318-6820C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75788581 | ||||||
| chr13:75788603
|
T | C | 130 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(127): Show | 130 | HG00099.hp1 HG00280.hp2 HG00609.hp1 others(127): Show |
intron_variant | MODIFIER | c.318-6798T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75788603 | ||||||
| chr13:75788651
|
A | AT | 12 | a0004c0027t0002g0092a0005c0005t0001g0125a0005c0005t0003g0112others(9): Show | 12 | HG01884.hp1 HG03831.hp2 NA18940.hp2 others(9): Show |
intron_variant | MODIFIER | c.318-6741dupT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75788651 | |||||
| chr13:75788767
|
A | G | 12 | a0004c0027t0002g0092a0005c0005t0001g0125a0005c0005t0003g0112others(9): Show | 12 | HG01884.hp1 HG03831.hp2 NA18940.hp2 others(9): Show |
intron_variant | MODIFIER | c.318-6634A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75788767 | ||||||
| chr13:75788883
|
T | G | 1 | a0001c0020t0002g0269 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.318-6518T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75788883 | ||||||
| chr13:75788944
|
CTGGGCAA others(5023): Show |
C | 1 | a0006c0006t0002g0096 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.318-6454_318-1425d others(2): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75788944 | |||||
| chr13:75789519
|
C | T | 130 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(127): Show | 130 | HG00099.hp1 HG00280.hp2 HG00609.hp1 others(127): Show |
intron_variant | MODIFIER | c.318-5882C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75789519 | ||||||
| chr13:75789585
|
G | A | 41 | a0001c0001t0001g0135a0002c0003t0001g0121a0002c0003t0001g0126others(38): Show | 41 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.318-5816G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75789585 | ||||||
| chr13:75789668
|
G | A | 1 | a0005c0005t0003g0164 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.318-5733G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75789668 | ||||||
| chr13:75789887
|
T | A | 12 | a0004c0027t0002g0092a0005c0005t0001g0125a0005c0005t0003g0112others(9): Show | 12 | HG01884.hp1 HG03831.hp2 NA18940.hp2 others(9): Show |
intron_variant | MODIFIER | c.318-5514T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75789887 | ||||||
| chr13:75790203
|
C | T | 3 | a0001c0001t0002g0035a0001c0001t0002g0047a0001c0001t0002g0048 | 3 | HG02647.hp1 HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.318-5198C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75790203 | ||||||
| chr13:75790266
|
A | G | 1 | a0012c0014t0007g0049 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.318-5135A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75790266 | ||||||
| chr13:75790333
|
A | G | 10 | a0008c0008t0001g0089a0008c0008t0002g0077a0008c0008t0003g0005others(7): Show | 10 | HG01243.hp1 HG02922.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.318-5068A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75790333 | ||||||
| chr13:75790430
|
G | A | 1 | a0001c0021t0001g0182 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.318-4971G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75790430 | ||||||
| chr13:75790633
|
G | A | 1 | a0002c0007t0004g0260 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.318-4768G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75790633 | ||||||
| chr13:75790724
|
G | A | 1 | a0009c0010t0017g0004 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.318-4677G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75790724 | ||||||
| chr13:75790946
|
AT | A | 199 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(196): Show | 200 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.318-4446delT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75790946 | |||||
| chr13:75790983
|
C | CT | 128 | a0001c0001t0001g0109a0001c0001t0001g0116a0001c0001t0001g0117others(125): Show | 128 | HG00099.hp1 HG00280.hp2 HG00609.hp1 others(125): Show |
intron_variant | MODIFIER | c.318-4406dupT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr13 | 75790983 | |||||
| chr13:75791007
|
T | C | 199 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(196): Show | 200 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.318-4394T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75791007 | ||||||
| chr13:75791043
|
C | G | 2 | a0003c0002t0001g0123a0003c0002t0001g0209 | 2 | NA18990.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.318-4358C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75791043 | ||||||
| chr13:75791407
|
T | C | 4 | a0003c0002t0001g0141a0003c0002t0001g0157a0003c0002t0001g0158others(1): Show | 4 | HG00280.hp1 HG01070.hp1 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.318-3994T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75791407 | ||||||
| chr13:75791505
|
C | T | 11 | a0002c0007t0003g0173a0002c0007t0003g0246a0009c0010t0001g0248others(8): Show | 11 | HG00735.hp1 HG01891.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.318-3896C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75791505 | ||||||
| chr13:75791690
|
G | A | 12 | a0004c0027t0002g0092a0005c0005t0001g0125a0005c0005t0003g0112others(9): Show | 12 | HG01884.hp1 HG03831.hp2 NA18940.hp2 others(9): Show |
intron_variant | MODIFIER | c.318-3711G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75791690 | ||||||
| chr13:75791693
|
C | T | 45 | a0001c0001t0001g0218a0003c0002t0001g0006a0003c0002t0001g0123others(42): Show | 45 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.318-3708C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75791693 | ||||||
| chr13:75791756
|
G | C | 9 | a0003c0002t0001g0194a0003c0002t0001g0222a0003c0002t0001g0224others(6): Show | 9 | HG00438.hp2 HG00621.hp2 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.318-3645G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75791756 | ||||||
| chr13:75792052
|
T | G | 1 | a0002c0007t0001g0129 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.318-3349T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75792052 | ||||||
| chr13:75792419
|
C | T | 1 | a0002c0003t0001g0220 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.318-2982C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75792419 | ||||||
| chr13:75792486
|
T | G | 8 | a0002c0007t0003g0176a0002c0007t0003g0178a0002c0007t0003g0180others(5): Show | 8 | HG00639.hp1 HG01261.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.318-2915T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75792486 | ||||||
| chr13:75792533
|
C | T | 1 | a0009c0010t0017g0004 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.318-2868C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75792533 | ||||||
| chr13:75792576
|
T | G | 4 | a0002c0007t0001g0129a0006c0006t0002g0097a0007c0016t0001g0001others(1): Show | 5 | HG01256.hp1 HG01952.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.318-2825T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75792576 | ||||||
| chr13:75792784
|
G | A | 2 | a0007c0009t0001g0165a0007c0009t0001g0166 | 2 | HG01891.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.318-2617G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75792784 | ||||||
| chr13:75792961
|
A | G | 3 | a0006c0006t0002g0097a0007c0016t0001g0001a0007c0016t0001g0252 | 4 | HG01256.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.318-2440A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75792961 | ||||||
| chr13:75793336
|
C | T | 1 | a0002c0011t0002g0084 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.318-2065C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75793336 | ||||||
| chr13:75793360
|
C | G | 3 | a0006c0006t0002g0094a0006c0006t0002g0097a0006c0006t0002g0102 | 3 | HG01256.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.318-2041C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75793360 | ||||||
| chr13:75793368
|
C | T | 1 | a0002c0003t0001g0220 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.318-2033C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75793368 | ||||||
| chr13:75793380
|
G | C | 1 | a0001c0021t0001g0182 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.318-2021G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75793380 | ||||||
| chr13:75793551
|
C | A | 8 | a0002c0007t0003g0176a0002c0007t0003g0178a0002c0007t0003g0180others(5): Show | 8 | HG00639.hp1 HG01261.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.318-1850C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75793551 | ||||||
| chr13:75793630
|
G | T | 3 | a0003c0002t0001g0123a0003c0002t0001g0209a0003c0002t0001g0227 | 3 | NA18990.hp1 NA19012.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.318-1771G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75793630 | ||||||
| chr13:75793979
|
G | T | 1 | a0002c0007t0003g0173 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.318-1422G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75793979 | ||||||
| chr13:75793996
|
G | T | 2 | a0012c0014t0001g0002a0012c0014t0001g0003 | 2 | HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.318-1405G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75793996 | ||||||
| chr13:75794027
|
C | T | 8 | a0002c0007t0003g0176a0002c0007t0003g0178a0002c0007t0003g0180others(5): Show | 8 | HG00639.hp1 HG01261.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.318-1374C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75794027 | ||||||
| chr13:75794063
|
G | A | 6 | a0002c0003t0001g0121a0002c0003t0001g0137a0002c0003t0001g0138others(3): Show | 6 | HG01106.hp1 HG01168.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.318-1338G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75794063 | ||||||
| chr13:75794093
|
C | A | 11 | a0002c0007t0003g0173a0002c0007t0003g0246a0009c0010t0001g0248others(8): Show | 11 | HG00735.hp1 HG01891.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.318-1308C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75794093 | ||||||
| chr13:75794101
|
A | C | 1 | a0005c0005t0001g0114 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.318-1300A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75794101 | ||||||
| chr13:75794204
|
A | G | 1 | a0001c0001t0002g0048 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.318-1197A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75794204 | ||||||
| chr13:75794317
|
T | C | 2 | a0010c0012t0001g0130a0010c0012t0001g0131 | 2 | HG06807.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.318-1084T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75794317 | ||||||
| chr13:75794327
|
T | C | 1 | a0004c0027t0002g0092 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.318-1074T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75794327 | ||||||
| chr13:75794391
|
G | A | 1 | a0002c0003t0001g0240 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.318-1010G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75794391 | ||||||
| chr13:75794490
|
T | C | 1 | a0003c0002t0001g0204 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.318-911T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75794490 | ||||||
| chr13:75794592
|
G | A | 2 | a0007c0016t0001g0001a0007c0016t0001g0252 | 3 | HG02895.hp1 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.318-809G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75794592 | ||||||
| chr13:75794740
|
C | T | 1 | a0003c0002t0001g0213 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.318-661C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75794740 | ||||||
| chr13:75794947
|
C | T | 8 | a0003c0002t0001g0191a0003c0002t0001g0195a0003c0002t0001g0196others(5): Show | 8 | HG00639.hp2 HG01123.hp1 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.318-454C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75794947 | ||||||
| chr13:75795050
|
C | T | 1 | a0001c0001t0002g0058 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.318-351C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75795050 | ||||||
| chr13:75795359
|
G | A | 1 | a0008c0008t0003g0111 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.318-42G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 4/30 | chr13 | 75795359 | ||||||
| chr13:75795566
|
A | C | 45 | a0001c0001t0001g0218a0003c0002t0001g0006a0003c0002t0001g0123others(42): Show | 45 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.348+135A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 5/30 | chr13 | 75795566 | ||||||
| chr13:75795610
|
C | T | 210 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(207): Show | 211 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.348+179C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 5/30 | chr13 | 75795610 | ||||||
| chr13:75796059
|
G | A | 129 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(126): Show | 129 | HG00099.hp1 HG00280.hp2 HG00609.hp1 others(126): Show |
intron_variant | MODIFIER | c.349-577G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 5/30 | chr13 | 75796059 | ||||||
| chr13:75796087
|
T | C | 1 | a0001c0001t0008g0044 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.349-549T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 5/30 | chr13 | 75796087 | ||||||
| chr13:75796113
|
C | A | 1 | a0002c0003t0001g0121 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.349-523C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 5/30 | chr13 | 75796113 | ||||||
| chr13:75796353
|
C | T | 1 | a0002c0011t0002g0076 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.349-283C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 5/30 | chr13 | 75796353 | ||||||
| chr13:75796401
|
A | G | 2 | a0007c0016t0001g0001a0007c0016t0001g0252 | 3 | HG02895.hp1 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.349-235A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 5/30 | chr13 | 75796401 | ||||||
| chr13:75796406
|
T | C | 2 | a0007c0016t0001g0001a0007c0016t0001g0252 | 3 | HG02895.hp1 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.349-230T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 5/30 | chr13 | 75796406 | ||||||
| chr13:75796428
|
G | A | 210 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(207): Show | 211 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.349-208G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 5/30 | chr13 | 75796428 | ||||||
| chr13:75796536
|
A | G | 1 | a0001c0021t0001g0182 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.349-100A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 5/30 | chr13 | 75796536 | ||||||
| chr13:75796619
|
A | AT | 4 | a0001c0021t0001g0182a0002c0007t0001g0129a0007c0016t0001g0001others(1): Show | 5 | HG01952.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.349-4dupT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 5/30 | INFO_REALIGN_3_PRIME | chr13 | 75796619 | |||||
| chr13:75796619
|
AT | A | 119 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(116): Show | 119 | HG00099.hp1 HG00280.hp2 HG00609.hp1 others(116): Show |
splice_region_variant&intron_variant | LOW | c.349-4delT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 5/30 | INFO_REALIGN_3_PRIME | chr13 | 75796619 | |||||
| chr13:75796828
|
TCTC | T | 2 | a0007c0016t0001g0001a0007c0016t0001g0252 | 3 | HG02895.hp1 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.462+82_462+84delCC others(1): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr13 | 75796828 | |||||
| chr13:75797039
|
C | T | 3 | a0002c0007t0001g0129a0007c0016t0001g0001a0007c0016t0001g0252 | 4 | HG01952.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.462+290C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 6/30 | chr13 | 75797039 | ||||||
| chr13:75797080
|
G | A | 1 | a0001c0021t0001g0182 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.462+331G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 6/30 | chr13 | 75797080 | ||||||
| chr13:75797097
|
T | C | 1 | a0008c0008t0003g0169 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.462+348T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 6/30 | chr13 | 75797097 | ||||||
| chr13:75797150
|
G | A | 12 | a0004c0027t0002g0092a0005c0005t0001g0125a0005c0005t0003g0112others(9): Show | 12 | HG01884.hp1 HG03831.hp2 NA18940.hp2 others(9): Show |
intron_variant | MODIFIER | c.462+401G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 6/30 | chr13 | 75797150 | ||||||
| chr13:75797223
|
C | T | 12 | a0004c0027t0002g0092a0005c0005t0001g0125a0005c0005t0003g0112others(9): Show | 12 | HG01884.hp1 HG03831.hp2 NA18940.hp2 others(9): Show |
intron_variant | MODIFIER | c.462+474C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 6/30 | chr13 | 75797223 | ||||||
| chr13:75797395
|
C | A | 45 | a0001c0001t0001g0218a0003c0002t0001g0006a0003c0002t0001g0123others(42): Show | 45 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.462+646C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 6/30 | chr13 | 75797395 | ||||||
| chr13:75797442
|
G | A | 1 | a0002c0007t0004g0098 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.462+693G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 6/30 | chr13 | 75797442 | ||||||
| chr13:75797502
|
T | A | 1 | a0002c0007t0003g0173 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.462+753T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 6/30 | chr13 | 75797502 | ||||||
| chr13:75797545
|
G | A | 4 | a0003c0002t0001g0141a0003c0002t0001g0157a0003c0002t0001g0158others(1): Show | 4 | HG00280.hp1 HG01070.hp1 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.462+796G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 6/30 | chr13 | 75797545 | ||||||
| chr13:75797740
|
A | G | 52 | a0001c0001t0001g0113a0001c0001t0001g0143a0001c0001t0001g0150others(49): Show | 52 | HG00099.hp1 HG00609.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.462+991A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 6/30 | chr13 | 75797740 | ||||||
| chr13:75797879
|
T | TATGTTA | 3 | a0002c0007t0001g0129a0007c0016t0001g0001a0007c0016t0001g0252 | 4 | HG01952.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.462+1131_462+1132i others(8): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr13 | 75797879 | |||||
| chr13:75797883
|
C | CTTAGTAC others(3): Show |
3 | a0002c0007t0001g0129a0007c0016t0001g0001a0007c0016t0001g0252 | 4 | HG01952.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.462+1134_462+1135i others(12): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 6/30 | chr13 | 75797883 | ||||||
| chr13:75797884
|
A | G | 3 | a0002c0007t0001g0129a0007c0016t0001g0001a0007c0016t0001g0252 | 4 | HG01952.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.462+1135A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 6/30 | chr13 | 75797884 | ||||||
| chr13:75797948
|
A | G | 12 | a0004c0027t0002g0092a0005c0005t0001g0125a0005c0005t0003g0112others(9): Show | 12 | HG01884.hp1 HG03831.hp2 NA18940.hp2 others(9): Show |
intron_variant | MODIFIER | c.462+1199A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 6/30 | chr13 | 75797948 | ||||||
| chr13:75797979
|
A | T | 3 | a0008c0008t0003g0160a0008c0008t0003g0168a0008c0008t0003g0169 | 3 | HG03669.hp1 HG03704.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.462+1230A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 6/30 | chr13 | 75797979 | ||||||
| chr13:75798278
|
G | T | 12 | a0004c0027t0002g0092a0005c0005t0001g0125a0005c0005t0003g0112others(9): Show | 12 | HG01884.hp1 HG03831.hp2 NA18940.hp2 others(9): Show |
intron_variant | MODIFIER | c.462+1529G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 6/30 | chr13 | 75798278 | ||||||
| chr13:75798565
|
G | T | 3 | a0007c0009t0009g0251a0016c0024t0002g0086a0017c0023t0002g0050 | 3 | HG03041.hp2 NA18965.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.462+1816G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 6/30 | chr13 | 75798565 | ||||||
| chr13:75798702
|
T | G | 8 | a0002c0007t0003g0176a0002c0007t0003g0178a0002c0007t0003g0180others(5): Show | 8 | HG00639.hp1 HG01261.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.462+1953T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 6/30 | chr13 | 75798702 | ||||||
| chr13:75798986
|
C | G | 1 | a0001c0001t0002g0099 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.463-1698C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 6/30 | chr13 | 75798986 | ||||||
| chr13:75799172
|
C | T | 1 | a0001c0020t0002g0269 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.463-1512C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 6/30 | chr13 | 75799172 | ||||||
| chr13:75799277
|
A | T | 210 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(207): Show | 211 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.463-1407A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 6/30 | chr13 | 75799277 | ||||||
| chr13:75799407
|
T | G | 3 | a0002c0007t0001g0129a0007c0016t0001g0001a0007c0016t0001g0252 | 4 | HG01952.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.463-1277T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 6/30 | chr13 | 75799407 | ||||||
| chr13:75799458
|
A | T | 25 | a0001c0001t0001g0207a0001c0001t0001g0208a0002c0007t0001g0234others(22): Show | 25 | HG01070.hp2 HG01192.hp2 HG01361.hp2 others(22): Show |
intron_variant | MODIFIER | c.463-1226A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 6/30 | chr13 | 75799458 | ||||||
| chr13:75799482
|
A | G | 45 | a0003c0002t0001g0006a0003c0002t0001g0123a0003c0002t0001g0141others(42): Show | 45 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.463-1202A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 6/30 | chr13 | 75799482 | ||||||
| chr13:75799540
|
C | T | 8 | a0002c0007t0003g0176a0002c0007t0003g0178a0002c0007t0003g0180others(5): Show | 8 | HG00639.hp1 HG01261.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.463-1144C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 6/30 | chr13 | 75799540 | ||||||
| chr13:75799690
|
T | G | 45 | a0003c0002t0001g0006a0003c0002t0001g0123a0003c0002t0001g0141others(42): Show | 45 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.463-994T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 6/30 | chr13 | 75799690 | ||||||
| chr13:75799788
|
G | A | 210 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(207): Show | 211 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.463-896G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 6/30 | chr13 | 75799788 | ||||||
| chr13:75799920
|
A | G | 2 | a0006c0006t0001g0183a0006c0006t0002g0095 | 2 | HG00140.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.463-764A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 6/30 | chr13 | 75799920 | ||||||
| chr13:75800108
|
T | G | 2 | a0003c0002t0001g0157a0003c0002t0001g0158 | 2 | HG01070.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.463-576T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 6/30 | chr13 | 75800108 | ||||||
| chr13:75800135
|
G | A | 3 | a0002c0007t0001g0129a0007c0016t0001g0001a0007c0016t0001g0252 | 4 | HG01952.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.463-549G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 6/30 | chr13 | 75800135 | ||||||
| chr13:75800482
|
A | G | 1 | a0004c0004t0001g0231 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.463-202A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 6/30 | chr13 | 75800482 | ||||||
| chr13:75800485
|
G | C | 1 | a0012c0014t0014g0185 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.463-199G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 6/30 | chr13 | 75800485 | ||||||
| chr13:75800516
|
A | G | 1 | a0004c0004t0004g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.463-168A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 6/30 | chr13 | 75800516 | ||||||
| chr13:75800586
|
C | T | 3 | a0002c0007t0001g0129a0007c0016t0001g0001a0007c0016t0001g0252 | 4 | HG01952.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.463-98C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 6/30 | chr13 | 75800586 | ||||||
| chr13:75800609
|
G | A | 2 | a0012c0014t0001g0002a0012c0014t0001g0003 | 2 | HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.463-75G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 6/30 | chr13 | 75800609 | ||||||
| chr13:75800610
|
C | A | 2 | a0012c0014t0001g0002a0012c0014t0001g0003 | 2 | HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.463-74C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 6/30 | chr13 | 75800610 | ||||||
| chr13:75800622
|
G | A | 1 | a0002c0003t0001g0258 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.463-62G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 6/30 | chr13 | 75800622 | ||||||
| chr13:75800659
|
A | G | 8 | a0002c0007t0003g0176a0002c0007t0003g0178a0002c0007t0003g0180others(5): Show | 8 | HG00639.hp1 HG01261.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.463-25A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 6/30 | chr13 | 75800659 | ||||||
| chr13:75800980
|
T | C | 2 | a0007c0016t0001g0001a0007c0016t0001g0252 | 3 | HG02895.hp1 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.661+98T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 7/30 | chr13 | 75800980 | ||||||
| chr13:75801038
|
T | G | 12 | a0004c0027t0002g0092a0005c0005t0001g0125a0005c0005t0003g0112others(9): Show | 12 | HG01884.hp1 HG03831.hp2 NA18940.hp2 others(9): Show |
intron_variant | MODIFIER | c.661+156T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 7/30 | chr13 | 75801038 | ||||||
| chr13:75801181
|
G | A | 8 | a0002c0007t0003g0176a0002c0007t0003g0178a0002c0007t0003g0180others(5): Show | 8 | HG00639.hp1 HG01261.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.661+299G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 7/30 | chr13 | 75801181 | ||||||
| chr13:75801237
|
C | CAA | 47 | a0002c0007t0001g0129a0003c0002t0001g0006a0003c0002t0001g0123others(44): Show | 48 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.661+369_661+370dup others(2): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr13 | 75801237 | |||||
| chr13:75801665
|
T | C | 11 | a0002c0003t0001g0146a0002c0003t0001g0253a0002c0003t0001g0255others(8): Show | 11 | HG00438.hp1 HG00673.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.661+783T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 7/30 | chr13 | 75801665 | ||||||
| chr13:75801927
|
A | G | 1 | a0001c0021t0001g0182 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.661+1045A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 7/30 | chr13 | 75801927 | ||||||
| chr13:75801959
|
CCT | C | 46 | a0001c0021t0001g0182a0003c0002t0001g0006a0003c0002t0001g0123others(43): Show | 46 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.661+1088_661+1089d others(4): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr13 | 75801959 | |||||
| chr13:75801959
|
CCTCT | C | 118 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(115): Show | 118 | HG00099.hp1 HG00280.hp2 HG00609.hp1 others(115): Show |
intron_variant | MODIFIER | c.661+1086_661+1089d others(6): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr13 | 75801959 | |||||
| chr13:75802061
|
C | T | 1 | a0002c0007t0003g0178 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.661+1179C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 7/30 | chr13 | 75802061 | ||||||
| chr13:75802248
|
C | T | 4 | a0011c0015t0001g0155a0011c0015t0001g0197a0011c0015t0001g0221others(1): Show | 4 | NA18941.hp2 NA18986.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.661+1366C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 7/30 | chr13 | 75802248 | ||||||
| chr13:75802285
|
C | G | 3 | a0002c0007t0001g0129a0007c0016t0001g0001a0007c0016t0001g0252 | 4 | HG01952.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.661+1403C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 7/30 | chr13 | 75802285 | ||||||
| chr13:75802338
|
T | A | 8 | a0002c0007t0003g0176a0002c0007t0003g0178a0002c0007t0003g0180others(5): Show | 8 | HG00639.hp1 HG01261.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.661+1456T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 7/30 | chr13 | 75802338 | ||||||
| chr13:75802343
|
T | C | 1 | a0001c0001t0002g0058 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.661+1461T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 7/30 | chr13 | 75802343 | ||||||
| chr13:75802554
|
T | C | 1 | a0002c0003t0001g0192 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.661+1672T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 7/30 | chr13 | 75802554 | ||||||
| chr13:75802557
|
C | G | 1 | a0002c0007t0003g0173 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.661+1675C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 7/30 | chr13 | 75802557 | ||||||
| chr13:75802594
|
A | T | 12 | a0004c0027t0002g0092a0005c0005t0001g0125a0005c0005t0003g0112others(9): Show | 12 | HG01884.hp1 HG03831.hp2 NA18940.hp2 others(9): Show |
intron_variant | MODIFIER | c.662-1695A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 7/30 | chr13 | 75802594 | ||||||
| chr13:75802736
|
A | T | 1 | a0004c0004t0004g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.662-1553A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 7/30 | chr13 | 75802736 | ||||||
| chr13:75802808
|
C | G | 1 | a0001c0001t0002g0007 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.662-1481C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 7/30 | chr13 | 75802808 | ||||||
| chr13:75802815
|
G | A | 1 | a0001c0001t0002g0085 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.662-1474G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 7/30 | chr13 | 75802815 | ||||||
| chr13:75802993
|
G | A | 210 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(207): Show | 211 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.662-1296G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 7/30 | chr13 | 75802993 | ||||||
| chr13:75803194
|
T | A | 1 | a0001c0001t0001g0143 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.662-1095T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 7/30 | chr13 | 75803194 | ||||||
| chr13:75803486
|
T | C | 12 | a0004c0027t0002g0092a0005c0005t0001g0125a0005c0005t0003g0112others(9): Show | 12 | HG01884.hp1 HG03831.hp2 NA18940.hp2 others(9): Show |
intron_variant | MODIFIER | c.662-803T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 7/30 | chr13 | 75803486 | ||||||
| chr13:75803578
|
C | G | 2 | a0010c0012t0001g0130a0010c0012t0001g0131 | 2 | HG06807.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.662-711C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 7/30 | chr13 | 75803578 | ||||||
| chr13:75803674
|
T | C | 3 | a0002c0007t0001g0129a0007c0016t0001g0001a0007c0016t0001g0252 | 4 | HG01952.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.662-615T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 7/30 | chr13 | 75803674 | ||||||
| chr13:75803822
|
T | G | 12 | a0004c0027t0002g0092a0005c0005t0001g0125a0005c0005t0003g0112others(9): Show | 12 | HG01884.hp1 HG03831.hp2 NA18940.hp2 others(9): Show |
intron_variant | MODIFIER | c.662-467T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 7/30 | chr13 | 75803822 | ||||||
| chr13:75803840
|
A | G | 1 | a0009c0010t0017g0004 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.662-449A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 7/30 | chr13 | 75803840 | ||||||
| chr13:75804203
|
G | A | 8 | a0002c0007t0003g0176a0002c0007t0003g0178a0002c0007t0003g0180others(5): Show | 8 | HG00639.hp1 HG01261.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.662-86G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 7/30 | chr13 | 75804203 | ||||||
| chr13:75804274
|
G | A | 6 | a0009c0010t0001g0248a0009c0010t0001g0249a0009c0010t0001g0250others(3): Show | 6 | HG01891.hp2 HG03098.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.662-15G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 7/30 | chr13 | 75804274 | ||||||
| chr13:75804285
|
A | T | 2 | a0001c0001t0002g0063a0001c0001t0002g0065 | 2 | HG01928.hp2 HG02273.hp2 |
splice_region_variant&intron_variant | LOW | c.662-4A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 7/30 | chr13 | 75804285 | ||||||
| chr13:75804601
|
A | T | 120 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(117): Show | 120 | HG00099.hp1 HG00280.hp2 HG00609.hp1 others(117): Show |
intron_variant | MODIFIER | c.914+60A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 8/30 | chr13 | 75804601 | ||||||
| chr13:75804865
|
G | C | 1 | a0001c0021t0001g0182 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.914+324G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 8/30 | chr13 | 75804865 | ||||||
| chr13:75804942
|
C | T | 5 | a0001c0001t0001g0113a0001c0001t0002g0014a0001c0001t0002g0022others(2): Show | 5 | NA18940.hp1 NA19001.hp1 NA19056.hp2 others(2): Show |
intron_variant | MODIFIER | c.914+401C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 8/30 | chr13 | 75804942 | ||||||
| chr13:75804973
|
C | T | 1 | a0004c0004t0004g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.914+432C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 8/30 | chr13 | 75804973 | ||||||
| chr13:75804987
|
G | A | 9 | a0008c0008t0001g0089a0008c0008t0003g0005a0008c0008t0003g0110others(6): Show | 9 | HG01243.hp1 HG02922.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.914+446G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 8/30 | chr13 | 75804987 | ||||||
| chr13:75805030
|
G | A | 6 | a0006c0006t0001g0183a0006c0006t0002g0094a0006c0006t0002g0095others(3): Show | 6 | HG00140.hp2 HG01106.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.915-449G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 8/30 | chr13 | 75805030 | ||||||
| chr13:75805052
|
G | GC | 8 | a0002c0007t0003g0176a0002c0007t0003g0178a0002c0007t0003g0180others(5): Show | 8 | HG00639.hp1 HG01261.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.915-423dupC | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 8/30 | INFO_REALIGN_3_PRIME | chr13 | 75805052 | |||||
| chr13:75805070
|
G | A | 1 | a0002c0003t0001g0258 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.915-409G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 8/30 | chr13 | 75805070 | ||||||
| chr13:75805128
|
A | T | 14 | a0004c0027t0002g0092a0005c0005t0001g0125a0005c0005t0003g0112others(11): Show | 14 | HG01884.hp1 HG03831.hp2 NA18940.hp2 others(11): Show |
intron_variant | MODIFIER | c.915-351A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 8/30 | chr13 | 75805128 | ||||||
| chr13:75805161
|
C | T | 8 | a0002c0007t0003g0176a0002c0007t0003g0178a0002c0007t0003g0180others(5): Show | 8 | HG00639.hp1 HG01261.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.915-318C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 8/30 | chr13 | 75805161 | ||||||
| chr13:75805186
|
A | G | 1 | a0004c0013t0002g0057 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.915-293A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 8/30 | chr13 | 75805186 | ||||||
| chr13:75805286
|
A | T | 2 | a0004c0004t0001g0148a0004c0004t0001g0149 | 2 | NA19007.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.915-193A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 8/30 | chr13 | 75805286 | ||||||
| chr13:75805460
|
G | A | 1 | a0006c0006t0002g0100 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.915-19G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 8/30 | chr13 | 75805460 | ||||||
| chr13:75805878
|
G | A | 1 | a0008c0008t0003g0168 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1196+118G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 9/30 | chr13 | 75805878 | ||||||
| chr13:75806040
|
T | C | 3 | a0002c0007t0001g0129a0007c0016t0001g0001a0007c0016t0001g0252 | 4 | HG01952.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1196+280T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 9/30 | chr13 | 75806040 | ||||||
| chr13:75806106
|
C | T | 44 | a0003c0002t0001g0006a0003c0002t0001g0123a0003c0002t0001g0141others(41): Show | 44 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.1196+346C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 9/30 | chr13 | 75806106 | ||||||
| chr13:75806113
|
G | A | 1 | a0007c0016t0001g0001 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1196+353G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 9/30 | chr13 | 75806113 | ||||||
| chr13:75806149
|
G | T | 12 | a0004c0027t0002g0092a0005c0005t0001g0125a0005c0005t0003g0112others(9): Show | 12 | HG01884.hp1 HG03831.hp2 NA18940.hp2 others(9): Show |
intron_variant | MODIFIER | c.1196+389G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 9/30 | chr13 | 75806149 | ||||||
| chr13:75806335
|
A | G | 1 | a0010c0012t0001g0140 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1196+575A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 9/30 | chr13 | 75806335 | ||||||
| chr13:75806520
|
T | C | 2 | a0004c0004t0001g0148a0004c0004t0001g0149 | 2 | NA19007.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1196+760T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 9/30 | chr13 | 75806520 | ||||||
| chr13:75806782
|
C | T | 1 | a0002c0007t0003g0246 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1197-698C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 9/30 | chr13 | 75806782 | ||||||
| chr13:75806858
|
C | T | 4 | a0001c0001t0002g0099a0001c0001t0002g0106a0001c0001t0002g0107others(1): Show | 4 | HG01099.hp2 HG01884.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1197-622C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 9/30 | chr13 | 75806858 | ||||||
| chr13:75806871
|
A | G | 1 | a0007c0009t0002g0067 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1197-609A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 9/30 | chr13 | 75806871 | ||||||
| chr13:75806946
|
C | T | 1 | a0001c0021t0001g0182 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1197-534C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 9/30 | chr13 | 75806946 | ||||||
| chr13:75807096
|
G | A | 8 | a0002c0007t0003g0176a0002c0007t0003g0178a0002c0007t0003g0180others(5): Show | 8 | HG00639.hp1 HG01261.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.1197-384G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 9/30 | chr13 | 75807096 | ||||||
| chr13:75807151
|
C | G | 8 | a0002c0007t0003g0176a0002c0007t0003g0178a0002c0007t0003g0180others(5): Show | 8 | HG00639.hp1 HG01261.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.1197-329C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 9/30 | chr13 | 75807151 | ||||||
| chr13:75807156
|
T | G | 3 | a0002c0007t0001g0129a0007c0016t0001g0001a0007c0016t0001g0252 | 4 | HG01952.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1197-324T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 9/30 | chr13 | 75807156 | ||||||
| chr13:75807394
|
A | G | 23 | a0001c0001t0001g0207a0001c0001t0001g0208a0002c0007t0001g0234others(20): Show | 23 | HG01070.hp2 HG01192.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.1197-86A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 9/30 | chr13 | 75807394 | ||||||
| chr13:75808286
|
C | T | 1 | a0007c0016t0001g0001 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1916+87C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 10/30 | chr13 | 75808286 | ||||||
| chr13:75808428
|
T | C | 2 | a0006c0006t0001g0174a0006c0006t0001g0175 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1916+229T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 10/30 | chr13 | 75808428 | ||||||
| chr13:75808636
|
T | A | 8 | a0002c0007t0003g0176a0002c0007t0003g0178a0002c0007t0003g0180others(5): Show | 8 | HG00639.hp1 HG01261.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.1916+437T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 10/30 | chr13 | 75808636 | ||||||
| chr13:75808696
|
T | C | 1 | a0001c0001t0002g0007 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1917-458T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 10/30 | chr13 | 75808696 | ||||||
| chr13:75808918
|
A | G | 6 | a0002c0007t0001g0234a0004c0004t0001g0231a0004c0004t0001g0232others(3): Show | 6 | HG01070.hp2 HG01192.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.1917-236A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 10/30 | chr13 | 75808918 | ||||||
| chr13:75809217
|
C | T | 8 | a0002c0003t0001g0126a0002c0007t0012g0156a0007c0009t0001g0152others(5): Show | 8 | HG01081.hp2 HG01175.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.1946+34C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75809217 | ||||||
| chr13:75809272
|
A | T | 2 | a0002c0003t0001g0238a0002c0003t0001g0239 | 2 | HG03491.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1946+89A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75809272 | ||||||
| chr13:75809277
|
G | T | 1 | a0001c0021t0001g0182 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1946+94G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75809277 | ||||||
| chr13:75809544
|
G | C | 1 | a0001c0001t0002g0026 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1946+361G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75809544 | ||||||
| chr13:75809603
|
A | G | 24 | a0001c0001t0001g0109a0001c0001t0001g0116a0001c0001t0001g0117others(21): Show | 24 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(21): Show |
intron_variant | MODIFIER | c.1946+420A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75809603 | ||||||
| chr13:75809657
|
C | T | 12 | a0005c0005t0001g0125a0005c0005t0003g0112a0005c0005t0003g0124others(9): Show | 12 | HG02523.hp2 HG03831.hp2 NA18940.hp2 others(9): Show |
intron_variant | MODIFIER | c.1946+474C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75809657 | ||||||
| chr13:75809669
|
T | C | 1 | a0004c0004t0010g0119 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1946+486T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75809669 | ||||||
| chr13:75809828
|
A | AT | 38 | a0001c0001t0001g0159a0001c0001t0002g0055a0002c0031t0002g0091others(35): Show | 38 | HG00140.hp2 HG00735.hp1 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.1946+666dupT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr13 | 75809828 | |||||
| chr13:75809828
|
AT | A | 48 | a0001c0001t0002g0034a0001c0001t0002g0085a0002c0007t0003g0173others(45): Show | 49 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.1946+666delT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr13 | 75809828 | |||||
| chr13:75809828
|
ATT | A | 12 | a0002c0007t0003g0176a0002c0007t0003g0178a0002c0007t0003g0180others(9): Show | 12 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.1946+665_1946+666d others(4): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr13 | 75809828 | |||||
| chr13:75809832
|
T | G | 8 | a0008c0008t0003g0005a0008c0008t0003g0110a0008c0008t0003g0111others(5): Show | 8 | HG02922.hp2 HG02970.hp2 HG03669.hp1 others(5): Show |
intron_variant | MODIFIER | c.1946+649T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75809832 | ||||||
| chr13:75810309
|
T | C | 269 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(266): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1946+1126T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75810309 | ||||||
| chr13:75810426
|
G | A | 9 | a0002c0007t0003g0176a0002c0007t0003g0178a0002c0007t0003g0180others(6): Show | 9 | HG00639.hp1 HG00639.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.1946+1243G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75810426 | ||||||
| chr13:75810524
|
A | G | 121 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(118): Show | 121 | HG00099.hp1 HG00280.hp2 HG00609.hp1 others(118): Show |
intron_variant | MODIFIER | c.1946+1341A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75810524 | ||||||
| chr13:75810833
|
G | A | 1 | a0004c0013t0002g0104 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1946+1650G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75810833 | ||||||
| chr13:75810917
|
T | G | 1 | a0010c0012t0002g0105 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1946+1734T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75810917 | ||||||
| chr13:75811136
|
T | A | 1 | a0003c0002t0001g0200 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1946+1953T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75811136 | ||||||
| chr13:75811194
|
CT | C | 44 | a0002c0007t0012g0156a0003c0002t0001g0006a0003c0002t0001g0123others(41): Show | 44 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.1946+2018delT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr13 | 75811194 | |||||
| chr13:75811204
|
T | TTC | 3 | a0009c0010t0001g0248a0009c0010t0001g0250a0009c0030t0001g0170 | 3 | HG02809.hp2 HG03098.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1946+2025_1946+202 others(6): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr13 | 75811204 | |||||
| chr13:75811208
|
C | CT | 98 | a0001c0001t0001g0135a0002c0003t0001g0121a0002c0003t0001g0126others(95): Show | 99 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.1946+2043dupT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr13 | 75811208 | |||||
| chr13:75811209
|
T | TC | 33 | a0001c0001t0001g0113a0001c0001t0002g0008a0001c0001t0002g0020others(30): Show | 33 | HG00140.hp2 HG01106.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.1946+2026_1946+202 others(5): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75811209 | ||||||
| chr13:75811210
|
T | C | 120 | a0001c0001t0001g0109a0001c0001t0001g0116a0001c0001t0001g0117others(117): Show | 120 | HG00099.hp1 HG00280.hp2 HG00609.hp1 others(117): Show |
intron_variant | MODIFIER | c.1946+2027T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75811210 | ||||||
| chr13:75811211
|
T | C | 1 | a0004c0004t0001g0232 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1946+2028T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75811211 | ||||||
| chr13:75811212
|
T | C | 1 | a0001c0001t0002g0036 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1946+2029T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75811212 | ||||||
| chr13:75811602
|
G | A | 256 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(253): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.1946+2419G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75811602 | ||||||
| chr13:75811939
|
T | G | 212 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(209): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.1946+2756T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75811939 | ||||||
| chr13:75811944
|
C | T | 1 | a0001c0001t0002g0039 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1946+2761C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75811944 | ||||||
| chr13:75811972
|
G | A | 1 | a0006c0006t0002g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1946+2789G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75811972 | ||||||
| chr13:75812019
|
A | G | 44 | a0002c0007t0012g0156a0003c0002t0001g0006a0003c0002t0001g0123others(41): Show | 44 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.1946+2836A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75812019 | ||||||
| chr13:75812118
|
T | C | 269 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(266): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1946+2935T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75812118 | ||||||
| chr13:75812158
|
TA | T | 212 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(209): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.1946+2978delA | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr13 | 75812158 | |||||
| chr13:75812731
|
T | A | 42 | a0001c0001t0001g0135a0002c0003t0001g0121a0002c0003t0001g0126others(39): Show | 43 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.1946+3548T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75812731 | ||||||
| chr13:75812795
|
G | A | 2 | a0001c0001t0002g0014a0001c0001t0002g0022 | 2 | NA19001.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.1946+3612G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75812795 | ||||||
| chr13:75812880
|
A | C | 5 | a0004c0004t0001g0120a0004c0004t0002g0060a0004c0013t0002g0019others(2): Show | 5 | HG01515.hp1 HG02735.hp1 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.1946+3697A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75812880 | ||||||
| chr13:75812943
|
T | G | 3 | a0013c0018t0004g0010a0013c0018t0004g0011a0013c0018t0004g0056 | 3 | HG02723.hp2 HG02896.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1946+3760T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75812943 | ||||||
| chr13:75812945
|
T | C | 1 | a0002c0003t0005g0033 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1946+3762T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75812945 | ||||||
| chr13:75812986
|
C | G | 1 | a0007c0009t0009g0251 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1946+3803C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75812986 | ||||||
| chr13:75813125
|
A | G | 1 | a0009c0010t0017g0004 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1946+3942A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75813125 | ||||||
| chr13:75813268
|
G | A | 1 | a0001c0001t0002g0021 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1947-3893G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75813268 | ||||||
| chr13:75813370
|
C | T | 44 | a0002c0007t0012g0156a0003c0002t0001g0006a0003c0002t0001g0123others(41): Show | 44 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.1947-3791C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75813370 | ||||||
| chr13:75813495
|
C | T | 1 | a0005c0005t0003g0112 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1947-3666C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75813495 | ||||||
| chr13:75813657
|
T | G | 44 | a0001c0001t0001g0135a0002c0003t0001g0121a0002c0003t0001g0126others(41): Show | 44 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.1947-3504T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75813657 | ||||||
| chr13:75813684
|
C | A | 1 | a0017c0023t0002g0050 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1947-3477C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75813684 | ||||||
| chr13:75813745
|
G | A | 1 | a0006c0006t0001g0245 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1947-3416G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75813745 | ||||||
| chr13:75814019
|
A | T | 2 | a0012c0014t0001g0002a0012c0014t0001g0003 | 2 | HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1947-3142A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75814019 | ||||||
| chr13:75814207
|
C | G | 2 | a0012c0014t0007g0049a0012c0014t0014g0185 | 2 | HG01081.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.1947-2954C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75814207 | ||||||
| chr13:75814287
|
G | A | 1 | a0009c0010t0017g0004 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1947-2874G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75814287 | ||||||
| chr13:75814406
|
G | A | 1 | a0002c0003t0001g0240 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1947-2755G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75814406 | ||||||
| chr13:75814491
|
G | A | 2 | a0004c0004t0001g0148a0004c0004t0001g0149 | 2 | NA19007.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1947-2670G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75814491 | ||||||
| chr13:75814768
|
T | A | 42 | a0001c0001t0001g0135a0002c0003t0001g0121a0002c0003t0001g0126others(39): Show | 43 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.1947-2393T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75814768 | ||||||
| chr13:75815319
|
T | C | 2 | a0003c0002t0001g0006a0003c0002t0002g0046 | 2 | NA18960.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1947-1842T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75815319 | ||||||
| chr13:75815898
|
C | T | 1 | a0003c0002t0001g0141 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1947-1263C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75815898 | ||||||
| chr13:75815939
|
T | C | 1 | a0001c0001t0002g0012 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1947-1222T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75815939 | ||||||
| chr13:75815940
|
C | T | 1 | a0001c0001t0002g0012 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1947-1221C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75815940 | ||||||
| chr13:75816013
|
C | A | 1 | a0001c0001t0002g0012 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1947-1148C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75816013 | ||||||
| chr13:75816090
|
C | T | 44 | a0002c0007t0012g0156a0003c0002t0001g0006a0003c0002t0001g0123others(41): Show | 44 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.1947-1071C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75816090 | ||||||
| chr13:75816197
|
A | G | 1 | a0001c0001t0002g0012 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1947-964A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75816197 | ||||||
| chr13:75816198
|
G | A | 1 | a0001c0001t0002g0012 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1947-963G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75816198 | ||||||
| chr13:75816203
|
A | G | 16 | a0002c0007t0001g0129a0002c0007t0003g0173a0002c0007t0003g0176others(13): Show | 16 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.1947-958A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75816203 | ||||||
| chr13:75816377
|
C | A | 1 | a0001c0001t0002g0012 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1947-784C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75816377 | ||||||
| chr13:75816473
|
T | A | 3 | a0002c0007t0001g0129a0002c0007t0003g0246a0002c0031t0002g0091 | 3 | HG01952.hp2 HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1947-688T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75816473 | ||||||
| chr13:75816562
|
A | G | 1 | a0009c0010t0017g0004 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1947-599A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75816562 | ||||||
| chr13:75816574
|
G | A | 3 | a0013c0018t0004g0010a0013c0018t0004g0011a0013c0018t0004g0056 | 3 | HG02723.hp2 HG02896.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1947-587G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75816574 | ||||||
| chr13:75816650
|
CGGATCTT others(3): Show |
C | 44 | a0002c0007t0012g0156a0003c0002t0001g0006a0003c0002t0001g0123others(41): Show | 44 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.1947-503_1947-494d others(12): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr13 | 75816650 | |||||
| chr13:75816807
|
T | G | 12 | a0006c0006t0001g0172a0006c0006t0001g0245a0008c0008t0001g0089others(9): Show | 12 | HG01243.hp1 HG02922.hp2 HG02970.hp2 others(9): Show |
intron_variant | MODIFIER | c.1947-354T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75816807 | ||||||
| chr13:75816921
|
T | G | 41 | a0002c0003t0001g0121a0002c0003t0001g0126a0002c0003t0001g0137others(38): Show | 42 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.1947-240T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75816921 | ||||||
| chr13:75817051
|
C | T | 1 | a0003c0002t0001g0213 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1947-110C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 11/30 | chr13 | 75817051 | ||||||
| chr13:75817485
|
C | A | 1 | a0004c0013t0002g0057 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2064+207C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 12/30 | chr13 | 75817485 | ||||||
| chr13:75817722
|
A | G | 1 | a0002c0031t0002g0091 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2064+444A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 12/30 | chr13 | 75817722 | ||||||
| chr13:75817746
|
T | C | 1 | a0001c0001t0001g0159 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2064+468T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 12/30 | chr13 | 75817746 | ||||||
| chr13:75817798
|
A | C | 3 | a0013c0018t0004g0010a0013c0018t0004g0011a0013c0018t0004g0056 | 3 | HG02723.hp2 HG02896.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2064+520A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 12/30 | chr13 | 75817798 | ||||||
| chr13:75817866
|
C | T | 1 | a0002c0031t0002g0091 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2064+588C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 12/30 | chr13 | 75817866 | ||||||
| chr13:75817900
|
G | C | 1 | a0006c0006t0001g0132 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2064+622G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 12/30 | chr13 | 75817900 | ||||||
| chr13:75817987
|
T | C | 2 | a0002c0007t0003g0173a0010c0012t0001g0140 | 2 | HG01981.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2064+709T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 12/30 | chr13 | 75817987 | ||||||
| chr13:75818264
|
T | A | 44 | a0002c0003t0001g0121a0002c0003t0001g0126a0002c0003t0001g0137others(41): Show | 44 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.2064+986T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 12/30 | chr13 | 75818264 | ||||||
| chr13:75818271
|
G | A | 3 | a0001c0001t0002g0043a0001c0001t0002g0265a0010c0012t0001g0140 | 3 | HG01243.hp2 HG01981.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.2064+993G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 12/30 | chr13 | 75818271 | ||||||
| chr13:75818396
|
C | T | 3 | a0007c0009t0001g0162a0007c0009t0001g0163a0007c0009t0002g0067 | 3 | HG02135.hp2 HG03017.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.2065-997C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 12/30 | chr13 | 75818396 | ||||||
| chr13:75818397
|
G | A | 2 | a0001c0001t0002g0045a0001c0001t0008g0044 | 2 | HG01192.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.2065-996G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 12/30 | chr13 | 75818397 | ||||||
| chr13:75818444
|
A | G | 1 | a0002c0007t0003g0246 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2065-949A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 12/30 | chr13 | 75818444 | ||||||
| chr13:75818468
|
A | G | 1 | a0001c0001t0001g0143 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2065-925A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 12/30 | chr13 | 75818468 | ||||||
| chr13:75818543
|
T | TG | 44 | a0002c0007t0012g0156a0003c0002t0001g0006a0003c0002t0001g0123others(41): Show | 44 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.2065-843dupG | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 12/30 | INFO_REALIGN_3_PRIME | chr13 | 75818543 | |||||
| chr13:75818703
|
A | G | 3 | a0013c0018t0004g0010a0013c0018t0004g0011a0013c0018t0004g0056 | 3 | HG02723.hp2 HG02896.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2065-690A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 12/30 | chr13 | 75818703 | ||||||
| chr13:75818775
|
G | A | 2 | a0003c0002t0001g0215a0003c0002t0001g0216 | 2 | HG01167.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.2065-618G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 12/30 | chr13 | 75818775 | ||||||
| chr13:75818988
|
C | T | 3 | a0003c0002t0001g0157a0003c0002t0001g0158a0003c0002t0001g0179 | 3 | HG01070.hp1 HG01109.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.2065-405C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 12/30 | chr13 | 75818988 | ||||||
| chr13:75818999
|
G | A | 1 | a0003c0002t0001g0186 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2065-394G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 12/30 | chr13 | 75818999 | ||||||
| chr13:75819150
|
G | A | 1 | a0002c0031t0002g0091 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2065-243G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 12/30 | chr13 | 75819150 | ||||||
| chr13:75819215
|
C | T | 1 | a0002c0003t0001g0256 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2065-178C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 12/30 | chr13 | 75819215 | ||||||
| chr13:75819220
|
G | A | 2 | a0012c0014t0007g0049a0012c0014t0014g0185 | 2 | HG01081.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.2065-173G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 12/30 | chr13 | 75819220 | ||||||
| chr13:75819557
|
C | T | 1 | a0002c0007t0001g0129 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2207+22C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 13/30 | chr13 | 75819557 | ||||||
| chr13:75819667
|
G | A | 1 | a0008c0008t0002g0077 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2207+132G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 13/30 | chr13 | 75819667 | ||||||
| chr13:75819686
|
G | A | 2 | a0016c0024t0002g0086a0017c0023t0002g0050 | 2 | NA18965.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.2207+151G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 13/30 | chr13 | 75819686 | ||||||
| chr13:75819714
|
G | T | 1 | a0002c0003t0001g0238 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2207+179G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 13/30 | chr13 | 75819714 | ||||||
| chr13:75819936
|
C | T | 1 | a0002c0003t0005g0033 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2207+401C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 13/30 | chr13 | 75819936 | ||||||
| chr13:75820015
|
A | C | 1 | a0013c0018t0004g0056 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2207+480A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 13/30 | chr13 | 75820015 | ||||||
| chr13:75820067
|
A | G | 6 | a0007c0009t0001g0152a0007c0009t0001g0162a0007c0009t0001g0163others(3): Show | 6 | HG01081.hp2 HG01891.hp1 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.2207+532A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 13/30 | chr13 | 75820067 | ||||||
| chr13:75820323
|
G | A | 41 | a0002c0003t0001g0121a0002c0003t0001g0126a0002c0003t0001g0137others(38): Show | 41 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.2207+788G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 13/30 | chr13 | 75820323 | ||||||
| chr13:75820668
|
A | G | 4 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0080others(1): Show | 4 | HG01496.hp2 NA18522.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.2208-509A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 13/30 | chr13 | 75820668 | ||||||
| chr13:75820672
|
T | A | 1 | a0005c0005t0001g0114 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2208-505T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 13/30 | chr13 | 75820672 | ||||||
| chr13:75820732
|
T | C | 1 | a0003c0002t0001g0186 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2208-445T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 13/30 | chr13 | 75820732 | ||||||
| chr13:75820898
|
G | T | 2 | a0008c0008t0003g0111a0008c0008t0004g0087 | 2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2208-279G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 13/30 | chr13 | 75820898 | ||||||
| chr13:75820934
|
T | G | 1 | a0001c0001t0001g0184 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2208-243T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 13/30 | chr13 | 75820934 | ||||||
| chr13:75820976
|
C | A | 1 | a0008c0008t0003g0169 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2208-201C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 13/30 | chr13 | 75820976 | ||||||
| chr13:75820976
|
C | T | 3 | a0001c0001t0002g0088a0012c0014t0007g0049a0012c0014t0014g0185 | 3 | HG01081.hp1 HG01255.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.2208-201C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 13/30 | chr13 | 75820976 | ||||||
| chr13:75820984
|
C | T | 1 | a0023c0022t0001g0136 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2208-193C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 13/30 | chr13 | 75820984 | ||||||
| chr13:75820991
|
C | T | 1 | a0001c0001t0002g0088 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2208-186C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 13/30 | chr13 | 75820991 | ||||||
| chr13:75820997
|
CA | C | 112 | a0002c0003t0001g0121a0002c0003t0001g0126a0002c0003t0001g0137others(109): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.2208-163delA | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 13/30 | INFO_REALIGN_3_PRIME | chr13 | 75820997 | |||||
| chr13:75820997
|
CAA | C | 18 | a0006c0006t0001g0132a0006c0006t0001g0172a0006c0006t0001g0174others(15): Show | 19 | HG00140.hp2 HG01106.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.2208-164_2208-163d others(4): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 13/30 | INFO_REALIGN_3_PRIME | chr13 | 75820997 | |||||
| chr13:75821142
|
G | A | 101 | a0002c0007t0001g0234a0004c0004t0001g0120a0004c0004t0001g0148others(98): Show | 102 | HG00140.hp2 HG00735.hp1 HG01070.hp2 others(99): Show |
intron_variant | MODIFIER | c.2208-35G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 13/30 | chr13 | 75821142 | ||||||
| chr13:75821167
|
C | T | 1 | a0004c0004t0004g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2208-10C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 13/30 | chr13 | 75821167 | ||||||
| chr13:75821889
|
T | C | 4 | a0001c0019t0002g0267a0001c0019t0002g0268a0001c0020t0002g0269others(1): Show | 4 | HG00621.hp1 HG00673.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.2640+280T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 14/30 | chr13 | 75821889 | ||||||
| chr13:75821948
|
T | G | 46 | a0002c0007t0001g0234a0002c0007t0012g0156a0002c0011t0002g0038others(43): Show | 46 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.2640+339T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 14/30 | chr13 | 75821948 | ||||||
| chr13:75821987
|
T | TATAA | 12 | a0008c0008t0001g0089a0008c0008t0002g0077a0008c0008t0003g0005others(9): Show | 12 | HG01081.hp1 HG01243.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.2640+379_2640+380i others(6): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 14/30 | INFO_REALIGN_3_PRIME | chr13 | 75821987 | |||||
| chr13:75822237
|
A | G | 1 | a0001c0001t0002g0022 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2640+628A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 14/30 | chr13 | 75822237 | ||||||
| chr13:75822679
|
A | G | 267 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(264): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.2641-886A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 14/30 | chr13 | 75822679 | ||||||
| chr13:75822762
|
C | CTA | 26 | a0001c0001t0001g0113a0001c0001t0001g0150a0001c0001t0001g0151others(23): Show | 26 | HG00609.hp1 HG00609.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.2641-770_2641-769d others(4): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 14/30 | INFO_REALIGN_3_PRIME | chr13 | 75822762 | |||||
| chr13:75822762
|
C | CTATA | 11 | a0001c0001t0002g0048a0002c0007t0003g0178a0002c0007t0003g0180others(8): Show | 11 | HG00639.hp1 HG00639.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.2641-772_2641-769d others(6): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 14/30 | INFO_REALIGN_3_PRIME | chr13 | 75822762 | |||||
| chr13:75822762
|
C | CTATATA | 8 | a0001c0001t0002g0013a0001c0001t0002g0055a0001c0001t0002g0088others(5): Show | 8 | HG00735.hp1 HG01261.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.2641-774_2641-769d others(8): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 14/30 | INFO_REALIGN_3_PRIME | chr13 | 75822762 | |||||
| chr13:75822762
|
C | CTATATAT others(1): Show |
13 | a0001c0001t0002g0054a0001c0001t0002g0106a0001c0001t0002g0107others(10): Show | 13 | HG01070.hp2 HG01361.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.2641-776_2641-769d others(10): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 14/30 | INFO_REALIGN_3_PRIME | chr13 | 75822762 | |||||
| chr13:75822762
|
C | CTATATAT others(3): Show |
5 | a0004c0004t0001g0235a0005c0005t0003g0115a0011c0015t0001g0155others(2): Show | 5 | HG01192.hp2 HG02698.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2641-778_2641-769d others(12): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 14/30 | INFO_REALIGN_3_PRIME | chr13 | 75822762 | |||||
| chr13:75822762
|
C | CTATATAT others(5): Show |
3 | a0001c0001t0002g0099a0004c0004t0001g0187a0011c0015t0001g0242 | 3 | HG01099.hp2 NA18954.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.2641-780_2641-769d others(14): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 14/30 | INFO_REALIGN_3_PRIME | chr13 | 75822762 | |||||
| chr13:75822762
|
C | CTATATAT others(7): Show |
5 | a0004c0004t0001g0190a0004c0004t0010g0119a0011c0015t0001g0197others(2): Show | 5 | HG02970.hp1 HG03225.hp2 NA18941.hp2 others(2): Show |
intron_variant | MODIFIER | c.2641-782_2641-769d others(16): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 14/30 | INFO_REALIGN_3_PRIME | chr13 | 75822762 | |||||
| chr13:75822762
|
C | CTATATAT others(9): Show |
2 | a0004c0004t0001g0188a0004c0004t0013g0189 | 2 | NA18949.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.2641-784_2641-769d others(18): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 14/30 | INFO_REALIGN_3_PRIME | chr13 | 75822762 | |||||
| chr13:75822762
|
CTA | C | 45 | a0001c0001t0001g0167a0001c0001t0002g0017a0001c0001t0002g0039others(42): Show | 46 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(43): Show |
intron_variant | MODIFIER | c.2641-770_2641-769d others(4): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 14/30 | INFO_REALIGN_3_PRIME | chr13 | 75822762 | |||||
| chr13:75822762
|
CTATA | C | 20 | a0001c0001t0002g0082a0001c0020t0002g0269a0002c0003t0001g0138others(17): Show | 20 | HG00621.hp1 HG00735.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.2641-772_2641-769d others(6): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 14/30 | INFO_REALIGN_3_PRIME | chr13 | 75822762 | |||||
| chr13:75822762
|
CTATATA | C | 6 | a0001c0001t0001g0184a0001c0001t0002g0085a0002c0003t0001g0220others(3): Show | 6 | HG00099.hp1 HG01257.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.2641-774_2641-769d others(8): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 14/30 | INFO_REALIGN_3_PRIME | chr13 | 75822762 | |||||
| chr13:75822762
|
CTATATAT others(3): Show |
C | 1 | a0009c0010t0003g0244 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2641-778_2641-769d others(12): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 14/30 | INFO_REALIGN_3_PRIME | chr13 | 75822762 | |||||
| chr13:75822762
|
CTATATAT others(7): Show |
C | 3 | a0002c0011t0002g0038a0004c0004t0001g0148a0004c0004t0001g0149 | 3 | HG01496.hp1 NA19007.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.2641-782_2641-769d others(16): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 14/30 | INFO_REALIGN_3_PRIME | chr13 | 75822762 | |||||
| chr13:75822762
|
CTATATAT others(9): Show |
C | 45 | a0002c0007t0001g0234a0002c0007t0012g0156a0003c0002t0001g0006others(42): Show | 45 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.2641-784_2641-769d others(18): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 14/30 | INFO_REALIGN_3_PRIME | chr13 | 75822762 | |||||
| chr13:75822762
|
CTATATAT others(11): Show |
C | 1 | a0002c0011t0002g0076 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2641-786_2641-769d others(20): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 14/30 | INFO_REALIGN_3_PRIME | chr13 | 75822762 | |||||
| chr13:75822771
|
T | C | 3 | a0006c0006t0002g0100a0012c0014t0007g0049a0012c0014t0014g0185 | 3 | HG01081.hp1 HG01255.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2641-794T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 14/30 | chr13 | 75822771 | ||||||
| chr13:75822773
|
T | C | 3 | a0008c0008t0001g0089a0008c0008t0002g0077a0008c0008t0003g0111 | 3 | HG01243.hp1 HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2641-792T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 14/30 | chr13 | 75822773 | ||||||
| chr13:75822775
|
T | C | 6 | a0008c0008t0003g0005a0008c0008t0003g0110a0008c0008t0003g0160others(3): Show | 6 | HG02970.hp2 HG03669.hp1 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.2641-790T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 14/30 | chr13 | 75822775 | ||||||
| chr13:75822798
|
T | C | 1 | a0007c0009t0009g0251 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2641-767T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 14/30 | chr13 | 75822798 | ||||||
| chr13:75822825
|
AAT | A | 187 | a0002c0003t0001g0121a0002c0003t0001g0126a0002c0003t0001g0137others(184): Show | 188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.2641-722_2641-721d others(4): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 14/30 | INFO_REALIGN_3_PRIME | chr13 | 75822825 | |||||
| chr13:75822827
|
T | TATATATA others(15): Show |
1 | a0007c0009t0001g0165 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2641-720_2641-719i others(24): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 14/30 | INFO_REALIGN_3_PRIME | chr13 | 75822827 | |||||
| chr13:75823013
|
A | G | 75 | a0004c0004t0001g0120a0004c0004t0001g0148a0004c0004t0001g0149others(72): Show | 75 | HG00140.hp2 HG00735.hp1 HG01070.hp2 others(72): Show |
intron_variant | MODIFIER | c.2641-552A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 14/30 | chr13 | 75823013 | ||||||
| chr13:75823378
|
A | G | 1 | a0008c0008t0003g0168 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2641-187A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 14/30 | chr13 | 75823378 | ||||||
| chr13:75823457
|
T | A | 75 | a0004c0004t0001g0120a0004c0004t0001g0148a0004c0004t0001g0149others(72): Show | 75 | HG00140.hp2 HG00735.hp1 HG01070.hp2 others(72): Show |
intron_variant | MODIFIER | c.2641-108T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 14/30 | chr13 | 75823457 | ||||||
| chr13:75823953
|
A | C | 75 | a0004c0004t0001g0120a0004c0004t0001g0148a0004c0004t0001g0149others(72): Show | 75 | HG00140.hp2 HG00735.hp1 HG01070.hp2 others(72): Show |
intron_variant | MODIFIER | c.2949+80A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75823953 | ||||||
| chr13:75824077
|
A | G | 1 | a0009c0010t0002g0015 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2949+204A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75824077 | ||||||
| chr13:75824281
|
G | A | 1 | a0006c0006t0001g0132 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2949+408G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75824281 | ||||||
| chr13:75824335
|
A | G | 1 | a0002c0007t0003g0173 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2949+462A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75824335 | ||||||
| chr13:75824366
|
T | C | 1 | a0002c0007t0004g0261 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.2949+493T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75824366 | ||||||
| chr13:75824396
|
C | A | 1 | a0001c0001t0002g0063 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2949+523C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75824396 | ||||||
| chr13:75824487
|
C | A | 1 | a0002c0031t0002g0091 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2949+614C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75824487 | ||||||
| chr13:75824829
|
GTA | G | 15 | a0005c0005t0001g0114a0005c0005t0001g0125a0005c0005t0003g0112others(12): Show | 15 | HG02523.hp2 HG02698.hp2 HG03017.hp1 others(12): Show |
intron_variant | MODIFIER | c.2949+964_2949+965d others(4): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr13 | 75824829 | |||||
| chr13:75824831
|
A | G | 163 | a0002c0003t0001g0121a0002c0003t0001g0126a0002c0003t0001g0137others(160): Show | 164 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.2949+958A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75824831 | ||||||
| chr13:75825011
|
A | G | 75 | a0004c0004t0001g0120a0004c0004t0001g0148a0004c0004t0001g0149others(72): Show | 75 | HG00140.hp2 HG00735.hp1 HG01070.hp2 others(72): Show |
intron_variant | MODIFIER | c.2949+1138A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75825011 | ||||||
| chr13:75825163
|
A | T | 1 | a0002c0007t0003g0246 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2949+1290A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75825163 | ||||||
| chr13:75825190
|
A | G | 1 | a0002c0031t0002g0091 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2949+1317A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75825190 | ||||||
| chr13:75825197
|
AC | A | 3 | a0007c0009t0009g0251a0007c0016t0001g0001a0007c0016t0001g0252 | 4 | HG02895.hp1 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2949+1325delC | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75825197 | ||||||
| chr13:75825204
|
A | G | 1 | a0002c0007t0003g0246 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2949+1331A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75825204 | ||||||
| chr13:75825239
|
A | G | 1 | a0002c0007t0001g0129 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2949+1366A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75825239 | ||||||
| chr13:75825418
|
G | A | 1 | a0008c0008t0002g0077 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2949+1545G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75825418 | ||||||
| chr13:75825633
|
A | G | 1 | a0007c0016t0001g0252 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2949+1760A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75825633 | ||||||
| chr13:75825803
|
G | A | 1 | a0001c0001t0002g0009 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2949+1930G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75825803 | ||||||
| chr13:75825883
|
G | C | 1 | a0003c0002t0001g0195 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2949+2010G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75825883 | ||||||
| chr13:75826231
|
G | A | 3 | a0014c0017t0002g0027a0014c0017t0002g0028a0014c0017t0002g0037 | 3 | HG01167.hp1 HG01169.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.2949+2358G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75826231 | ||||||
| chr13:75826504
|
A | G | 178 | a0002c0003t0001g0121a0002c0003t0001g0126a0002c0003t0001g0137others(175): Show | 179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.2949+2631A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75826504 | ||||||
| chr13:75826803
|
C | A | 34 | a0004c0004t0001g0120a0004c0004t0001g0148a0004c0004t0001g0149others(31): Show | 34 | HG01070.hp2 HG01192.hp2 HG01361.hp2 others(31): Show |
intron_variant | MODIFIER | c.2949+2930C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75826803 | ||||||
| chr13:75826906
|
C | G | 45 | a0002c0007t0001g0234a0002c0007t0012g0156a0003c0002t0001g0006others(42): Show | 45 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.2949+3033C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75826906 | ||||||
| chr13:75827104
|
T | C | 3 | a0010c0012t0002g0105a0012c0014t0001g0002a0012c0014t0001g0003 | 3 | HG02818.hp2 HG02895.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2949+3231T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75827104 | ||||||
| chr13:75827176
|
G | A | 1 | a0002c0007t0001g0129 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2949+3303G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75827176 | ||||||
| chr13:75827401
|
G | A | 1 | a0001c0001t0002g0025 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2949+3528G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75827401 | ||||||
| chr13:75827468
|
G | T | 12 | a0002c0003t0001g0121a0002c0003t0001g0137a0002c0003t0001g0138others(9): Show | 12 | HG01106.hp1 HG01168.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.2949+3595G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75827468 | ||||||
| chr13:75827479
|
C | T | 45 | a0002c0007t0001g0234a0002c0007t0012g0156a0003c0002t0001g0006others(42): Show | 45 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.2949+3606C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75827479 | ||||||
| chr13:75827515
|
T | C | 178 | a0002c0003t0001g0121a0002c0003t0001g0126a0002c0003t0001g0137others(175): Show | 179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.2949+3642T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75827515 | ||||||
| chr13:75827522
|
A | G | 190 | a0002c0003t0001g0121a0002c0003t0001g0126a0002c0003t0001g0137others(187): Show | 191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.2949+3649A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75827522 | ||||||
| chr13:75827746
|
CTA | C | 45 | a0002c0007t0001g0234a0002c0007t0012g0156a0003c0002t0001g0006others(42): Show | 45 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.2949+3875_2949+387 others(6): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr13 | 75827746 | |||||
| chr13:75827748
|
A | G | 1 | a0001c0001t0001g0159 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2949+3875A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75827748 | ||||||
| chr13:75828003
|
A | G | 25 | a0006c0006t0001g0132a0006c0006t0001g0172a0006c0006t0001g0174others(22): Show | 25 | HG00140.hp2 HG00735.hp1 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.2949+4130A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75828003 | ||||||
| chr13:75828025
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2949+4152C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75828025 | ||||||
| chr13:75828026
|
G | A | 15 | a0005c0005t0001g0114a0005c0005t0001g0125a0005c0005t0003g0112others(12): Show | 15 | HG02523.hp2 HG02698.hp2 HG03017.hp1 others(12): Show |
intron_variant | MODIFIER | c.2949+4153G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75828026 | ||||||
| chr13:75828080
|
T | G | 4 | a0009c0010t0001g0248a0009c0010t0001g0249a0009c0010t0001g0250others(1): Show | 4 | HG03098.hp2 HG03486.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.2949+4207T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75828080 | ||||||
| chr13:75828082
|
G | T | 15 | a0005c0005t0001g0114a0005c0005t0001g0125a0005c0005t0003g0112others(12): Show | 15 | HG02523.hp2 HG02698.hp2 HG03017.hp1 others(12): Show |
intron_variant | MODIFIER | c.2949+4209G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75828082 | ||||||
| chr13:75828128
|
G | T | 1 | a0005c0005t0003g0115 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2949+4255G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75828128 | ||||||
| chr13:75828223
|
C | G | 1 | a0004c0013t0002g0104 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2949+4350C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75828223 | ||||||
| chr13:75828236
|
C | T | 1 | a0012c0014t0014g0185 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2949+4363C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75828236 | ||||||
| chr13:75828270
|
G | A | 12 | a0008c0008t0001g0089a0008c0008t0002g0077a0008c0008t0003g0005others(9): Show | 12 | HG01081.hp1 HG01243.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.2949+4397G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75828270 | ||||||
| chr13:75828275
|
A | G | 15 | a0006c0006t0001g0132a0006c0006t0001g0172a0006c0006t0001g0174others(12): Show | 15 | HG00140.hp2 HG01106.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.2949+4402A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75828275 | ||||||
| chr13:75828804
|
G | T | 1 | a0001c0001t0002g0066 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2950-4247G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75828804 | ||||||
| chr13:75829025
|
A | G | 1 | a0002c0007t0003g0173 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2950-4026A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75829025 | ||||||
| chr13:75829088
|
G | A | 9 | a0002c0007t0003g0176a0002c0007t0003g0178a0002c0007t0003g0180others(6): Show | 9 | HG00639.hp1 HG00639.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.2950-3963G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75829088 | ||||||
| chr13:75829092
|
C | T | 2 | a0002c0007t0003g0176a0022c0025t0003g0177 | 2 | HG03669.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2950-3959C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75829092 | ||||||
| chr13:75829105
|
A | G | 1 | a0004c0013t0002g0057 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2950-3946A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75829105 | ||||||
| chr13:75829165
|
A | C | 15 | a0005c0005t0001g0114a0005c0005t0001g0125a0005c0005t0003g0112others(12): Show | 15 | HG02523.hp2 HG02698.hp2 HG03017.hp1 others(12): Show |
intron_variant | MODIFIER | c.2950-3886A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75829165 | ||||||
| chr13:75829245
|
G | C | 1 | a0004c0004t0001g0232 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2950-3806G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75829245 | ||||||
| chr13:75829422
|
G | A | 1 | a0008c0008t0003g0169 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2950-3629G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75829422 | ||||||
| chr13:75829700
|
GT | G | 177 | a0002c0003t0001g0121a0002c0003t0001g0126a0002c0003t0001g0137others(174): Show | 178 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.2950-3340delT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr13 | 75829700 | |||||
| chr13:75829711
|
T | A | 45 | a0002c0007t0001g0234a0002c0007t0012g0156a0003c0002t0001g0006others(42): Show | 45 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.2950-3340T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75829711 | ||||||
| chr13:75830170
|
A | G | 2 | a0005c0005t0003g0127a0005c0005t0003g0128 | 2 | NA18942.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.2950-2881A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75830170 | ||||||
| chr13:75830174
|
A | G | 45 | a0002c0007t0001g0234a0002c0007t0012g0156a0003c0002t0001g0006others(42): Show | 45 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.2950-2877A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75830174 | ||||||
| chr13:75830277
|
A | G | 1 | a0004c0027t0002g0092 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2950-2774A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75830277 | ||||||
| chr13:75830287
|
G | A | 46 | a0004c0004t0001g0120a0004c0004t0001g0148a0004c0004t0001g0149others(43): Show | 46 | HG01070.hp2 HG01081.hp1 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.2950-2764G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75830287 | ||||||
| chr13:75830291
|
A | G | 9 | a0002c0007t0003g0176a0002c0007t0003g0178a0002c0007t0003g0180others(6): Show | 9 | HG00639.hp1 HG00639.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.2950-2760A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75830291 | ||||||
| chr13:75830341
|
C | A | 43 | a0002c0003t0001g0121a0002c0003t0001g0126a0002c0003t0001g0137others(40): Show | 44 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.2950-2710C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75830341 | ||||||
| chr13:75830386
|
A | C | 1 | a0005c0005t0015g0171 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2950-2665A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75830386 | ||||||
| chr13:75830450
|
G | C | 1 | a0006c0006t0002g0095 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2950-2601G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75830450 | ||||||
| chr13:75830500
|
A | T | 71 | a0004c0004t0001g0120a0004c0004t0001g0148a0004c0004t0001g0149others(68): Show | 71 | HG00140.hp2 HG00735.hp1 HG01070.hp2 others(68): Show |
intron_variant | MODIFIER | c.2950-2551A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75830500 | ||||||
| chr13:75830501
|
C | T | 1 | a0002c0007t0001g0129 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2950-2550C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75830501 | ||||||
| chr13:75830805
|
A | G | 2 | a0001c0001t0002g0014a0001c0001t0002g0022 | 2 | NA19001.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.2950-2246A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75830805 | ||||||
| chr13:75830865
|
A | G | 1 | a0010c0012t0001g0247 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2950-2186A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75830865 | ||||||
| chr13:75831163
|
A | G | 1 | a0009c0010t0017g0004 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2950-1888A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75831163 | ||||||
| chr13:75831165
|
C | T | 9 | a0002c0007t0003g0176a0002c0007t0003g0178a0002c0007t0003g0180others(6): Show | 9 | HG00639.hp1 HG00639.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.2950-1886C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75831165 | ||||||
| chr13:75831254
|
A | T | 45 | a0002c0007t0001g0234a0002c0007t0012g0156a0003c0002t0001g0006others(42): Show | 45 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.2950-1797A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75831254 | ||||||
| chr13:75831404
|
A | G | 1 | a0006c0006t0002g0097 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2950-1647A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75831404 | ||||||
| chr13:75831545
|
T | C | 1 | a0002c0031t0002g0091 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2950-1506T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75831545 | ||||||
| chr13:75831814
|
C | G | 1 | a0018c0028t0004g0133 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2950-1237C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75831814 | ||||||
| chr13:75831849
|
T | C | 1 | a0002c0007t0003g0246 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2950-1202T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75831849 | ||||||
| chr13:75832100
|
T | G | 3 | a0008c0008t0002g0077a0012c0014t0007g0049a0012c0014t0014g0185 | 3 | HG01081.hp1 HG01255.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2950-951T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75832100 | ||||||
| chr13:75832205
|
A | G | 1 | a0008c0008t0003g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2950-846A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75832205 | ||||||
| chr13:75832208
|
C | T | 1 | a0003c0002t0001g0224 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2950-843C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75832208 | ||||||
| chr13:75832398
|
A | C | 1 | a0002c0007t0003g0173 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2950-653A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75832398 | ||||||
| chr13:75832488
|
C | T | 43 | a0002c0003t0001g0121a0002c0003t0001g0126a0002c0003t0001g0137others(40): Show | 44 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.2950-563C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75832488 | ||||||
| chr13:75832606
|
G | A | 12 | a0008c0008t0001g0089a0008c0008t0002g0077a0008c0008t0003g0005others(9): Show | 12 | HG01081.hp1 HG01243.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.2950-445G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75832606 | ||||||
| chr13:75832646
|
G | A | 1 | a0006c0006t0001g0172 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2950-405G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75832646 | ||||||
| chr13:75832713
|
T | C | 45 | a0002c0007t0001g0234a0002c0007t0012g0156a0003c0002t0001g0006others(42): Show | 45 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.2950-338T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75832713 | ||||||
| chr13:75832759
|
C | T | 4 | a0009c0010t0001g0248a0009c0010t0001g0249a0009c0010t0001g0250others(1): Show | 4 | HG03098.hp2 HG03486.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.2950-292C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75832759 | ||||||
| chr13:75832845
|
C | T | 45 | a0002c0007t0001g0234a0002c0007t0012g0156a0003c0002t0001g0006others(42): Show | 45 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.2950-206C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75832845 | ||||||
| chr13:75832991
|
A | G | 9 | a0002c0007t0003g0176a0002c0007t0003g0178a0002c0007t0003g0180others(6): Show | 9 | HG00639.hp1 HG00639.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.2950-60A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75832991 | ||||||
| chr13:75833003
|
G | A | 15 | a0005c0005t0001g0114a0005c0005t0001g0125a0005c0005t0003g0112others(12): Show | 15 | HG02523.hp2 HG02698.hp2 HG03017.hp1 others(12): Show |
intron_variant | MODIFIER | c.2950-48G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 15/30 | chr13 | 75833003 | ||||||
| chr13:75833392
|
A | C | 1 | a0003c0002t0001g0191 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.3064+227A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 16/30 | chr13 | 75833392 | ||||||
| chr13:75833401
|
T | G | 1 | a0009c0030t0001g0170 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3064+236T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 16/30 | chr13 | 75833401 | ||||||
| chr13:75833464
|
A | G | 1 | a0003c0002t0001g0233 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.3064+299A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 16/30 | chr13 | 75833464 | ||||||
| chr13:75833532
|
T | C | 46 | a0004c0004t0001g0120a0004c0004t0001g0148a0004c0004t0001g0149others(43): Show | 46 | HG01070.hp2 HG01081.hp1 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.3064+367T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 16/30 | chr13 | 75833532 | ||||||
| chr13:75833602
|
A | G | 3 | a0010c0012t0002g0105a0012c0014t0001g0002a0012c0014t0001g0003 | 3 | HG02818.hp2 HG02895.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3064+437A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 16/30 | chr13 | 75833602 | ||||||
| chr13:75833993
|
G | T | 18 | a0006c0006t0001g0132a0006c0006t0001g0172a0006c0006t0001g0174others(15): Show | 18 | HG00140.hp2 HG01106.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.3065-233G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 16/30 | chr13 | 75833993 | ||||||
| chr13:75834022
|
A | G | 1 | a0007c0009t0009g0251 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3065-204A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 16/30 | chr13 | 75834022 | ||||||
| chr13:75834097
|
G | T | 2 | a0004c0004t0006g0103a0004c0004t0010g0119 | 2 | HG02818.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.3065-129G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 16/30 | chr13 | 75834097 | ||||||
| chr13:75834113
|
A | G | 30 | a0004c0004t0001g0120a0004c0004t0001g0148a0004c0004t0001g0149others(27): Show | 30 | HG01070.hp2 HG01192.hp2 HG01361.hp2 others(27): Show |
intron_variant | MODIFIER | c.3065-113A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 16/30 | chr13 | 75834113 | ||||||
| chr13:75834520
|
G | A | 12 | a0008c0008t0001g0089a0008c0008t0002g0077a0008c0008t0003g0005others(9): Show | 12 | HG01081.hp1 HG01243.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.3226+133G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 17/30 | chr13 | 75834520 | ||||||
| chr13:75834555
|
CTCTG | C | 45 | a0002c0007t0001g0234a0002c0007t0012g0156a0003c0002t0001g0006others(42): Show | 45 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.3226+173_3226+176d others(6): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr13 | 75834555 | |||||
| chr13:75834646
|
C | A | 1 | a0001c0001t0001g0113 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.3226+259C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 17/30 | chr13 | 75834646 | ||||||
| chr13:75835007
|
C | T | 2 | a0003c0002t0001g0142a0003c0002t0001g0229 | 2 | NA18946.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.3227-226C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 17/30 | chr13 | 75835007 | ||||||
| chr13:75835074
|
A | G | 1 | a0012c0014t0007g0049 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3227-159A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 17/30 | chr13 | 75835074 | ||||||
| chr13:75835687
|
C | T | 46 | a0004c0004t0001g0120a0004c0004t0001g0148a0004c0004t0001g0149others(43): Show | 46 | HG01070.hp2 HG01081.hp1 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.3333+348C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 18/30 | chr13 | 75835687 | ||||||
| chr13:75835734
|
G | A | 34 | a0004c0004t0001g0120a0004c0004t0001g0148a0004c0004t0001g0149others(31): Show | 34 | HG01070.hp2 HG01192.hp2 HG01361.hp2 others(31): Show |
intron_variant | MODIFIER | c.3333+395G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 18/30 | chr13 | 75835734 | ||||||
| chr13:75835882
|
G | A | 177 | a0002c0003t0001g0121a0002c0003t0001g0126a0002c0003t0001g0137others(174): Show | 178 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.3334-515G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 18/30 | chr13 | 75835882 | ||||||
| chr13:75836197
|
C | T | 2 | a0012c0014t0001g0002a0012c0014t0001g0003 | 2 | HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.3334-200C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 18/30 | chr13 | 75836197 | ||||||
| chr13:75836503
|
A | T | 1 | a0009c0030t0001g0170 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3394+46A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 19/30 | chr13 | 75836503 | ||||||
| chr13:75836589
|
A | G | 178 | a0002c0003t0001g0121a0002c0003t0001g0126a0002c0003t0001g0137others(175): Show | 179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.3394+132A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 19/30 | chr13 | 75836589 | ||||||
| chr13:75836622
|
C | T | 1 | a0008c0008t0003g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3394+165C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 19/30 | chr13 | 75836622 | ||||||
| chr13:75836623
|
G | A | 15 | a0005c0005t0001g0114a0005c0005t0001g0125a0005c0005t0003g0112others(12): Show | 15 | HG02523.hp2 HG02698.hp2 HG03017.hp1 others(12): Show |
intron_variant | MODIFIER | c.3394+166G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 19/30 | chr13 | 75836623 | ||||||
| chr13:75836970
|
G | C | 1 | a0002c0007t0003g0246 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3394+513G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 19/30 | chr13 | 75836970 | ||||||
| chr13:75837221
|
G | A | 1 | a0001c0001t0002g0065 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.3394+764G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 19/30 | chr13 | 75837221 | ||||||
| chr13:75837415
|
T | C | 1 | a0002c0007t0003g0173 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3395-725T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 19/30 | chr13 | 75837415 | ||||||
| chr13:75837941
|
A | C | 1 | a0010c0012t0002g0105 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3395-199A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 19/30 | chr13 | 75837941 | ||||||
| chr13:75838075
|
C | T | 12 | a0008c0008t0001g0089a0008c0008t0002g0077a0008c0008t0003g0005others(9): Show | 12 | HG01081.hp1 HG01243.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.3395-65C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 19/30 | chr13 | 75838075 | ||||||
| chr13:75838076
|
G | T | 1 | a0001c0001t0002g0012 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.3395-64G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 19/30 | chr13 | 75838076 | ||||||
| chr13:75838280
|
A | C | 1 | a0002c0007t0003g0173 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3451+84A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 20/30 | chr13 | 75838280 | ||||||
| chr13:75838407
|
T | C | 1 | a0005c0005t0003g0254 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.3451+211T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 20/30 | chr13 | 75838407 | ||||||
| chr13:75838453
|
T | TA | 8 | a0001c0001t0001g0207a0001c0001t0002g0012a0001c0001t0002g0014others(5): Show | 8 | HG00735.hp2 HG02735.hp1 HG03579.hp2 others(5): Show |
intron_variant | MODIFIER | c.3451+278dupA | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 20/30 | INFO_REALIGN_3_PRIME | chr13 | 75838453 | |||||
| chr13:75838453
|
TA | T | 91 | a0001c0001t0001g0150a0001c0001t0001g0184a0001c0001t0002g0013others(88): Show | 91 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.3451+278delA | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 20/30 | INFO_REALIGN_3_PRIME | chr13 | 75838453 | |||||
| chr13:75838453
|
TAA | T | 43 | a0002c0003t0001g0121a0002c0003t0001g0137a0002c0003t0001g0138others(40): Show | 44 | HG00099.hp2 HG00438.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.3451+277_3451+278d others(4): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 20/30 | INFO_REALIGN_3_PRIME | chr13 | 75838453 | |||||
| chr13:75838585
|
A | G | 1 | a0009c0010t0003g0244 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3451+389A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 20/30 | chr13 | 75838585 | ||||||
| chr13:75838654
|
G | A | 1 | a0003c0002t0001g0006 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.3451+458G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 20/30 | chr13 | 75838654 | ||||||
| chr13:75838760
|
G | A | 12 | a0002c0003t0001g0121a0002c0003t0001g0137a0002c0003t0001g0138others(9): Show | 12 | HG01106.hp1 HG01168.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.3451+564G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 20/30 | chr13 | 75838760 | ||||||
| chr13:75838764
|
G | A | 46 | a0002c0003t0001g0253a0002c0007t0001g0234a0002c0007t0012g0156others(43): Show | 46 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.3451+568G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 20/30 | chr13 | 75838764 | ||||||
| chr13:75838918
|
C | T | 1 | a0001c0001t0002g0101 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3451+722C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 20/30 | chr13 | 75838918 | ||||||
| chr13:75839566
|
A | G | 1 | a0002c0003t0001g0255 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.3452-519A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 20/30 | chr13 | 75839566 | ||||||
| chr13:75839702
|
G | C | 86 | a0004c0004t0001g0120a0004c0004t0001g0148a0004c0004t0001g0149others(83): Show | 86 | HG00140.hp2 HG00735.hp1 HG01070.hp2 others(83): Show |
intron_variant | MODIFIER | c.3452-383G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 20/30 | chr13 | 75839702 | ||||||
| chr13:75839727
|
C | CT | 11 | a0002c0007t0003g0173a0002c0007t0003g0176a0002c0007t0003g0178others(8): Show | 11 | HG00639.hp1 HG00639.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.3452-341dupT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 20/30 | INFO_REALIGN_3_PRIME | chr13 | 75839727 | |||||
| chr13:75839727
|
CT | C | 59 | a0002c0003t0001g0121a0002c0003t0001g0126a0002c0003t0001g0137others(56): Show | 60 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.3452-341delT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 20/30 | INFO_REALIGN_3_PRIME | chr13 | 75839727 | |||||
| chr13:75839727
|
CTT | C | 70 | a0004c0004t0001g0120a0004c0004t0001g0148a0004c0004t0001g0149others(67): Show | 70 | HG00140.hp2 HG00735.hp1 HG01070.hp2 others(67): Show |
intron_variant | MODIFIER | c.3452-342_3452-341d others(4): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 20/30 | INFO_REALIGN_3_PRIME | chr13 | 75839727 | |||||
| chr13:75840269
|
C | G | 1 | a0002c0003t0001g0146 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.3478-122C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 21/30 | chr13 | 75840269 | ||||||
| chr13:75840762
|
A | T | 2 | a0003c0002t0001g0157a0003c0002t0001g0158 | 2 | HG01070.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.3582+267A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 22/30 | chr13 | 75840762 | ||||||
| chr13:75840934
|
T | G | 1 | a0008c0008t0002g0077 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3583-175T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 22/30 | chr13 | 75840934 | ||||||
| chr13:75841243
|
C | G | 45 | a0002c0007t0001g0234a0002c0007t0012g0156a0003c0002t0001g0006others(42): Show | 45 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.3675+42C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 23/30 | chr13 | 75841243 | ||||||
| chr13:75841324
|
T | C | 4 | a0004c0004t0004g0081a0013c0018t0004g0010a0013c0018t0004g0011others(1): Show | 4 | HG02451.hp1 HG02723.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.3675+123T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 23/30 | chr13 | 75841324 | ||||||
| chr13:75841379
|
T | C | 1 | a0001c0001t0001g0159 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.3675+178T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 23/30 | chr13 | 75841379 | ||||||
| chr13:75841429
|
A | T | 1 | a0002c0007t0001g0129 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.3676-199A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 23/30 | chr13 | 75841429 | ||||||
| chr13:75842305
|
T | G | 43 | a0002c0003t0001g0121a0002c0003t0001g0126a0002c0003t0001g0137others(40): Show | 44 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.4031+322T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 24/30 | chr13 | 75842305 | ||||||
| chr13:75842502
|
G | A | 147 | a0002c0003t0001g0121a0002c0003t0001g0126a0002c0003t0001g0137others(144): Show | 148 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.4032-349G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 24/30 | chr13 | 75842502 | ||||||
| chr13:75842593
|
C | A | 15 | a0005c0005t0001g0114a0005c0005t0001g0125a0005c0005t0003g0112others(12): Show | 15 | HG02523.hp2 HG02698.hp2 HG03017.hp1 others(12): Show |
intron_variant | MODIFIER | c.4032-258C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 24/30 | chr13 | 75842593 | ||||||
| chr13:75842765
|
G | T | 3 | a0011c0015t0001g0197a0011c0015t0001g0221a0011c0015t0001g0242 | 3 | NA18941.hp2 NA18986.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.4032-86G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 24/30 | chr13 | 75842765 | ||||||
| chr13:75842824
|
A | G | 22 | a0006c0006t0001g0132a0006c0006t0001g0172a0006c0006t0001g0174others(19): Show | 22 | HG00140.hp2 HG00735.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.4032-27A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 24/30 | chr13 | 75842824 | ||||||
| chr13:75842965
|
C | T | 145 | a0002c0003t0001g0121a0002c0003t0001g0126a0002c0003t0001g0137others(142): Show | 146 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.4097+49C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 25/30 | chr13 | 75842965 | ||||||
| chr13:75842996
|
A | G | 1 | a0003c0002t0001g0179 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.4097+80A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 25/30 | chr13 | 75842996 | ||||||
| chr13:75843306
|
G | A | 1 | a0004c0004t0001g0190 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.4097+390G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 25/30 | chr13 | 75843306 | ||||||
| chr13:75843395
|
C | T | 2 | a0001c0001t0002g0007a0001c0001t0002g0025 | 2 | HG00609.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.4097+479C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 25/30 | chr13 | 75843395 | ||||||
| chr13:75843519
|
A | G | 1 | a0005c0005t0003g0254 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.4097+603A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 25/30 | chr13 | 75843519 | ||||||
| chr13:75843582
|
G | A | 1 | a0002c0003t0001g0121 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.4097+666G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 25/30 | chr13 | 75843582 | ||||||
| chr13:75843672
|
T | G | 1 | a0004c0004t0001g0187 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.4097+756T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 25/30 | chr13 | 75843672 | ||||||
| chr13:75843684
|
A | G | 4 | a0004c0004t0004g0081a0013c0018t0004g0010a0013c0018t0004g0011others(1): Show | 4 | HG02451.hp1 HG02723.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.4097+768A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 25/30 | chr13 | 75843684 | ||||||
| chr13:75843691
|
T | A | 2 | a0012c0014t0001g0002a0012c0014t0001g0003 | 2 | HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.4097+775T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 25/30 | chr13 | 75843691 | ||||||
| chr13:75843709
|
C | A | 26 | a0006c0006t0001g0132a0006c0006t0001g0172a0006c0006t0001g0174others(23): Show | 26 | HG00140.hp2 HG00735.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.4097+793C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 25/30 | chr13 | 75843709 | ||||||
| chr13:75843711
|
AT | A | 4 | a0004c0004t0004g0081a0013c0018t0004g0010a0013c0018t0004g0011others(1): Show | 4 | HG02451.hp1 HG02723.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.4097+800delT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 25/30 | INFO_REALIGN_3_PRIME | chr13 | 75843711 | |||||
| chr13:75843871
|
C | T | 1 | a0012c0014t0007g0049 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.4097+955C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 25/30 | chr13 | 75843871 | ||||||
| chr13:75843872
|
G | A | 15 | a0005c0005t0001g0114a0005c0005t0001g0125a0005c0005t0003g0112others(12): Show | 15 | HG02523.hp2 HG02698.hp2 HG03017.hp1 others(12): Show |
intron_variant | MODIFIER | c.4097+956G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 25/30 | chr13 | 75843872 | ||||||
| chr13:75843983
|
A | C | 4 | a0004c0004t0004g0081a0013c0018t0004g0010a0013c0018t0004g0011others(1): Show | 4 | HG02451.hp1 HG02723.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.4097+1067A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 25/30 | chr13 | 75843983 | ||||||
| chr13:75844050
|
A | G | 1 | a0006c0006t0002g0093 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4097+1134A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 25/30 | chr13 | 75844050 | ||||||
| chr13:75844062
|
A | G | 26 | a0006c0006t0001g0132a0006c0006t0001g0172a0006c0006t0001g0174others(23): Show | 26 | HG00140.hp2 HG00735.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.4097+1146A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 25/30 | chr13 | 75844062 | ||||||
| chr13:75844129
|
G | A | 1 | a0005c0005t0001g0114 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.4098-1198G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 25/30 | chr13 | 75844129 | ||||||
| chr13:75844156
|
A | G | 2 | a0012c0014t0001g0002a0012c0014t0001g0003 | 2 | HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.4098-1171A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 25/30 | chr13 | 75844156 | ||||||
| chr13:75844177
|
A | T | 1 | a0007c0009t0001g0162 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.4098-1150A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 25/30 | chr13 | 75844177 | ||||||
| chr13:75844203
|
A | G | 1 | a0001c0001t0001g0113 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.4098-1124A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 25/30 | chr13 | 75844203 | ||||||
| chr13:75844210
|
A | G | 3 | a0006c0006t0001g0174a0006c0006t0001g0175a0006c0006t0002g0096 | 3 | HG02896.hp1 HG02897.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.4098-1117A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 25/30 | chr13 | 75844210 | ||||||
| chr13:75844321
|
T | C | 1 | a0002c0031t0002g0091 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.4098-1006T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 25/30 | chr13 | 75844321 | ||||||
| chr13:75844336
|
A | G | 2 | a0001c0001t0002g0053a0002c0007t0003g0173 | 2 | HG00280.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.4098-991A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 25/30 | chr13 | 75844336 | ||||||
| chr13:75844415
|
C | T | 9 | a0002c0007t0003g0176a0002c0007t0003g0178a0002c0007t0003g0180others(6): Show | 9 | HG00639.hp1 HG00639.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.4098-912C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 25/30 | chr13 | 75844415 | ||||||
| chr13:75844417
|
T | C | 9 | a0002c0007t0003g0176a0002c0007t0003g0178a0002c0007t0003g0180others(6): Show | 9 | HG00639.hp1 HG00639.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.4098-910T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 25/30 | chr13 | 75844417 | ||||||
| chr13:75844433
|
G | A | 7 | a0001c0001t0001g0109a0001c0001t0001g0116a0001c0001t0001g0117others(4): Show | 7 | NA18944.hp1 NA18946.hp2 NA18953.hp2 others(4): Show |
intron_variant | MODIFIER | c.4098-894G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 25/30 | chr13 | 75844433 | ||||||
| chr13:75844440
|
C | T | 1 | a0004c0004t0004g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4098-887C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 25/30 | chr13 | 75844440 | ||||||
| chr13:75844448
|
C | T | 1 | a0002c0007t0003g0181 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.4098-879C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 25/30 | chr13 | 75844448 | ||||||
| chr13:75844449
|
G | A | 12 | a0008c0008t0001g0089a0008c0008t0002g0077a0008c0008t0003g0005others(9): Show | 12 | HG01081.hp1 HG01243.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.4098-878G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 25/30 | chr13 | 75844449 | ||||||
| chr13:75844536
|
A | G | 1 | a0008c0008t0002g0077 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.4098-791A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 25/30 | chr13 | 75844536 | ||||||
| chr13:75844584
|
A | G | 16 | a0004c0004t0004g0081a0008c0008t0001g0089a0008c0008t0002g0077others(13): Show | 16 | HG01081.hp1 HG01243.hp1 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.4098-743A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 25/30 | chr13 | 75844584 | ||||||
| chr13:75844909
|
T | C | 1 | a0001c0001t0002g0047 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4098-418T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 25/30 | chr13 | 75844909 | ||||||
| chr13:75844938
|
G | A | 1 | a0009c0030t0001g0170 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4098-389G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 25/30 | chr13 | 75844938 | ||||||
| chr13:75845097
|
G | A | 9 | a0002c0007t0003g0176a0002c0007t0003g0178a0002c0007t0003g0180others(6): Show | 9 | HG00639.hp1 HG00639.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.4098-230G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 25/30 | chr13 | 75845097 | ||||||
| chr13:75845285
|
AT | A | 190 | a0002c0003t0001g0121a0002c0003t0001g0126a0002c0003t0001g0137others(187): Show | 191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.4098-39delT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 25/30 | INFO_REALIGN_3_PRIME | chr13 | 75845285 | |||||
| chr13:75845308
|
A | G | 4 | a0009c0010t0001g0248a0009c0010t0001g0249a0009c0010t0001g0250others(1): Show | 4 | HG03098.hp2 HG03486.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.4098-19A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 25/30 | chr13 | 75845308 | ||||||
| chr13:75845386
|
G | A | 1 | a0006c0006t0001g0183 | 1 | HG00140.hp2 | splice_region_variant&intron_variant | LOW | c.4150+7G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 26/30 | chr13 | 75845386 | ||||||
| chr13:75845388
|
G | A | 1 | a0008c0008t0003g0169 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.4150+9G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 26/30 | chr13 | 75845388 | ||||||
| chr13:75845472
|
T | C | 7 | a0002c0003t0001g0146a0002c0003t0001g0253a0002c0003t0001g0255others(4): Show | 7 | HG00438.hp1 HG00673.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.4150+93T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 26/30 | chr13 | 75845472 | ||||||
| chr13:75845638
|
G | A | 45 | a0002c0007t0001g0234a0002c0007t0012g0156a0003c0002t0001g0006others(42): Show | 45 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.4150+259G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 26/30 | chr13 | 75845638 | ||||||
| chr13:75845779
|
C | A | 1 | a0008c0008t0004g0087 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.4150+400C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 26/30 | chr13 | 75845779 | ||||||
| chr13:75845966
|
A | G | 30 | a0004c0004t0001g0120a0004c0004t0001g0148a0004c0004t0001g0149others(27): Show | 30 | HG01070.hp2 HG01192.hp2 HG01361.hp2 others(27): Show |
intron_variant | MODIFIER | c.4150+587A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 26/30 | chr13 | 75845966 | ||||||
| chr13:75846015
|
T | C | 1 | a0001c0001t0002g0088 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4150+636T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 26/30 | chr13 | 75846015 | ||||||
| chr13:75846103
|
T | TA | 76 | a0001c0001t0002g0048a0002c0007t0001g0234a0002c0007t0003g0176others(73): Show | 76 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.4150+738dupA | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr13 | 75846103 | |||||
| chr13:75846103
|
TA | T | 21 | a0004c0004t0001g0232a0004c0013t0002g0019a0006c0006t0001g0132others(18): Show | 21 | HG00140.hp2 HG01070.hp2 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.4150+738delA | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr13 | 75846103 | |||||
| chr13:75846163
|
T | A | 15 | a0005c0005t0001g0114a0005c0005t0001g0125a0005c0005t0003g0112others(12): Show | 15 | HG02523.hp2 HG02698.hp2 HG03017.hp1 others(12): Show |
intron_variant | MODIFIER | c.4150+784T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 26/30 | chr13 | 75846163 | ||||||
| chr13:75846652
|
T | C | 15 | a0005c0005t0001g0114a0005c0005t0001g0125a0005c0005t0003g0112others(12): Show | 15 | HG02523.hp2 HG02698.hp2 HG03017.hp1 others(12): Show |
intron_variant | MODIFIER | c.4150+1273T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 26/30 | chr13 | 75846652 | ||||||
| chr13:75846672
|
C | T | 4 | a0001c0001t0002g0018a0001c0001t0002g0052a0001c0001t0002g0053others(1): Show | 4 | HG00280.hp2 HG01123.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.4150+1293C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 26/30 | chr13 | 75846672 | ||||||
| chr13:75846927
|
A | C | 26 | a0006c0006t0001g0132a0006c0006t0001g0172a0006c0006t0001g0174others(23): Show | 26 | HG00140.hp2 HG00735.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.4150+1548A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 26/30 | chr13 | 75846927 | ||||||
| chr13:75846956
|
G | A | 1 | a0010c0012t0001g0247 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.4150+1577G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 26/30 | chr13 | 75846956 | ||||||
| chr13:75846963
|
A | T | 1 | a0005c0005t0015g0171 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.4150+1584A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 26/30 | chr13 | 75846963 | ||||||
| chr13:75846972
|
A | G | 1 | a0002c0007t0001g0129 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.4150+1593A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 26/30 | chr13 | 75846972 | ||||||
| chr13:75847014
|
G | A | 1 | a0001c0001t0001g0113 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.4150+1635G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 26/30 | chr13 | 75847014 | ||||||
| chr13:75847029
|
C | CA | 20 | a0001c0001t0002g0058a0002c0007t0003g0173a0006c0006t0001g0172others(17): Show | 20 | HG00140.hp2 HG00735.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.4150+1668dupA | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr13 | 75847029 | |||||
| chr13:75847029
|
CA | C | 126 | a0001c0001t0002g0088a0002c0003t0001g0121a0002c0003t0001g0126others(123): Show | 127 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.4150+1668delA | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr13 | 75847029 | |||||
| chr13:75847339
|
C | T | 1 | a0002c0007t0003g0173 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4151-1740C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 26/30 | chr13 | 75847339 | ||||||
| chr13:75847395
|
T | A | 16 | a0004c0004t0004g0081a0008c0008t0001g0089a0008c0008t0002g0077others(13): Show | 16 | HG01081.hp1 HG01243.hp1 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.4151-1684T>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 26/30 | chr13 | 75847395 | ||||||
| chr13:75847399
|
C | T | 157 | a0002c0003t0001g0121a0002c0003t0001g0126a0002c0003t0001g0137others(154): Show | 158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.4151-1680C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 26/30 | chr13 | 75847399 | ||||||
| chr13:75847495
|
G | A | 157 | a0002c0003t0001g0121a0002c0003t0001g0126a0002c0003t0001g0137others(154): Show | 158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.4151-1584G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 26/30 | chr13 | 75847495 | ||||||
| chr13:75847546
|
G | C | 9 | a0002c0007t0003g0176a0002c0007t0003g0178a0002c0007t0003g0180others(6): Show | 9 | HG00639.hp1 HG00639.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.4151-1533G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 26/30 | chr13 | 75847546 | ||||||
| chr13:75847570
|
C | T | 1 | a0001c0001t0003g0153 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.4151-1509C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 26/30 | chr13 | 75847570 | ||||||
| chr13:75847594
|
A | G | 157 | a0002c0003t0001g0121a0002c0003t0001g0126a0002c0003t0001g0137others(154): Show | 158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.4151-1485A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 26/30 | chr13 | 75847594 | ||||||
| chr13:75847853
|
A | G | 2 | a0012c0014t0001g0002a0012c0014t0001g0003 | 2 | HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.4151-1226A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 26/30 | chr13 | 75847853 | ||||||
| chr13:75847961
|
C | CTATTTAT others(1): Show |
78 | a0002c0007t0001g0234a0002c0007t0012g0156a0003c0002t0001g0006others(75): Show | 78 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.4151-1109_4151-110 others(12): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr13 | 75847961 | |||||
| chr13:75848085
|
G | A | 1 | a0010c0012t0001g0140 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.4151-994G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 26/30 | chr13 | 75848085 | ||||||
| chr13:75848407
|
A | T | 1 | a0001c0001t0002g0058 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.4151-672A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 26/30 | chr13 | 75848407 | ||||||
| chr13:75848431
|
T | TCATCTAT others(1): Show |
9 | a0002c0003t0001g0121a0002c0003t0001g0137a0002c0003t0001g0138others(6): Show | 9 | HG00438.hp1 HG01106.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.4151-648_4151-647i others(10): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 26/30 | chr13 | 75848431 | ||||||
| chr13:75848431
|
T | TCATCTAT others(5): Show |
31 | a0002c0003t0001g0126a0002c0003t0001g0154a0002c0003t0001g0220others(28): Show | 32 | HG00099.hp2 HG00140.hp1 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.4151-648_4151-647i others(14): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 26/30 | chr13 | 75848431 | ||||||
| chr13:75848431
|
T | TCATCTAT others(9): Show |
1 | a0007c0009t0001g0162 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.4151-648_4151-647i others(18): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 26/30 | chr13 | 75848431 | ||||||
| chr13:75848431
|
T | TTATC | 97 | a0001c0001t0001g0113a0001c0001t0001g0143a0001c0001t0001g0167others(94): Show | 97 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.4151-613_4151-610d others(6): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr13 | 75848431 | |||||
| chr13:75848431
|
T | TTATCTAT others(1): Show |
66 | a0001c0001t0001g0109a0001c0001t0001g0116a0001c0001t0001g0117others(63): Show | 66 | HG00280.hp1 HG00609.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.4151-617_4151-610d others(10): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr13 | 75848431 | |||||
| chr13:75848431
|
T | TTATCTAT others(5): Show |
36 | a0001c0001t0001g0151a0001c0001t0001g0207a0001c0001t0001g0218others(33): Show | 36 | HG00280.hp2 HG00639.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.4151-621_4151-610d others(14): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr13 | 75848431 | |||||
| chr13:75848431
|
TTATCTAT others(1): Show |
T | 2 | a0002c0007t0001g0129a0002c0007t0003g0173 | 2 | HG01952.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.4151-617_4151-610d others(10): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr13 | 75848431 | |||||
| chr13:75848449
|
A | ATCTG | 8 | a0008c0008t0003g0005a0008c0008t0003g0110a0008c0008t0003g0111others(5): Show | 8 | HG02922.hp2 HG02970.hp2 HG03669.hp1 others(5): Show |
intron_variant | MODIFIER | c.4151-627_4151-626i others(6): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr13 | 75848449 | |||||
| chr13:75848470
|
A | T | 1 | a0001c0001t0002g0058 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.4151-609A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 26/30 | chr13 | 75848470 | ||||||
| chr13:75848583
|
A | G | 7 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0207others(4): Show | 7 | HG01346.hp2 HG02132.hp2 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.4151-496A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 26/30 | chr13 | 75848583 | ||||||
| chr13:75848619
|
GTA | G | 190 | a0002c0003t0001g0121a0002c0003t0001g0126a0002c0003t0001g0137others(187): Show | 191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.4151-446_4151-445d others(4): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr13 | 75848619 | |||||
| chr13:75848848
|
T | C | 1 | a0018c0028t0004g0133 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.4151-231T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 26/30 | chr13 | 75848848 | ||||||
| chr13:75848891
|
C | T | 1 | a0002c0007t0001g0129 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.4151-188C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 26/30 | chr13 | 75848891 | ||||||
| chr13:75849500
|
C | CT | 20 | a0006c0006t0001g0132a0006c0006t0001g0172a0006c0006t0001g0174others(17): Show | 20 | HG00140.hp2 HG01106.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.4364+218dupT | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 27/30 | INFO_REALIGN_3_PRIME | chr13 | 75849500 | |||||
| chr13:75849500
|
C | CTTT | 9 | a0002c0007t0003g0176a0002c0007t0003g0178a0002c0007t0003g0180others(6): Show | 9 | HG00639.hp1 HG00639.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.4364+216_4364+218d others(5): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 27/30 | INFO_REALIGN_3_PRIME | chr13 | 75849500 | |||||
| chr13:75849544
|
C | T | 1 | a0002c0003t0001g0192 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.4364+252C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 27/30 | chr13 | 75849544 | ||||||
| chr13:75849550
|
C | CA | 9 | a0003c0002t0001g0194a0003c0002t0001g0222a0003c0002t0001g0224others(6): Show | 9 | HG00438.hp2 HG00621.hp2 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.4364+262dupA | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 27/30 | INFO_REALIGN_3_PRIME | chr13 | 75849550 | |||||
| chr13:75849788
|
A | G | 2 | a0012c0014t0001g0002a0012c0014t0001g0003 | 2 | HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.4364+496A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 27/30 | chr13 | 75849788 | ||||||
| chr13:75850057
|
G | T | 1 | a0005c0005t0003g0115 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.4364+765G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 27/30 | chr13 | 75850057 | ||||||
| chr13:75850446
|
A | T | 1 | a0001c0001t0002g0039 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.4364+1154A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 27/30 | chr13 | 75850446 | ||||||
| chr13:75850721
|
C | A | 2 | a0012c0014t0001g0002a0012c0014t0001g0003 | 2 | HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.4364+1429C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 27/30 | chr13 | 75850721 | ||||||
| chr13:75850799
|
C | T | 158 | a0002c0003t0001g0121a0002c0003t0001g0126a0002c0003t0001g0137others(155): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.4364+1507C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 27/30 | chr13 | 75850799 | ||||||
| chr13:75851017
|
G | A | 73 | a0002c0007t0003g0173a0002c0007t0003g0176a0002c0007t0003g0178others(70): Show | 74 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.4364+1725G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 27/30 | chr13 | 75851017 | ||||||
| chr13:75851250
|
A | G | 31 | a0001c0001t0002g0066a0004c0004t0001g0120a0004c0004t0001g0148others(28): Show | 31 | HG01070.hp2 HG01192.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.4365-1842A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 27/30 | chr13 | 75851250 | ||||||
| chr13:75851283
|
G | C | 1 | a0003c0002t0001g0214 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.4365-1809G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 27/30 | chr13 | 75851283 | ||||||
| chr13:75851540
|
T | C | 26 | a0006c0006t0001g0132a0006c0006t0001g0172a0006c0006t0001g0174others(23): Show | 26 | HG00140.hp2 HG00735.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.4365-1552T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 27/30 | chr13 | 75851540 | ||||||
| chr13:75851560
|
G | A | 2 | a0004c0004t0001g0120a0004c0004t0002g0060 | 2 | HG01515.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.4365-1532G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 27/30 | chr13 | 75851560 | ||||||
| chr13:75851701
|
AAG | A | 26 | a0006c0006t0001g0132a0006c0006t0001g0172a0006c0006t0001g0174others(23): Show | 26 | HG00140.hp2 HG00735.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.4365-1385_4365-138 others(6): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 27/30 | INFO_REALIGN_3_PRIME | chr13 | 75851701 | |||||
| chr13:75851912
|
G | C | 70 | a0002c0003t0001g0121a0002c0003t0001g0126a0002c0003t0001g0137others(67): Show | 70 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.4365-1180G>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 27/30 | chr13 | 75851912 | ||||||
| chr13:75852306
|
C | T | 1 | a0002c0011t0002g0071 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.4365-786C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 27/30 | chr13 | 75852306 | ||||||
| chr13:75852366
|
G | A | 4 | a0004c0004t0004g0081a0013c0018t0004g0010a0013c0018t0004g0011others(1): Show | 4 | HG02451.hp1 HG02723.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.4365-726G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 27/30 | chr13 | 75852366 | ||||||
| chr13:75852526
|
T | C | 1 | a0002c0007t0003g0173 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4365-566T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 27/30 | chr13 | 75852526 | ||||||
| chr13:75852611
|
C | T | 1 | a0002c0011t0002g0071 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.4365-481C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 27/30 | chr13 | 75852611 | ||||||
| chr13:75853069
|
G | T | 2 | a0002c0007t0003g0176a0022c0025t0003g0177 | 2 | HG03669.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.4365-23G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 27/30 | chr13 | 75853069 | ||||||
| chr13:75853475
|
A | G | 3 | a0002c0007t0003g0173a0012c0014t0001g0002a0012c0014t0001g0003 | 3 | HG02818.hp2 HG02895.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.4661+87A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 28/30 | chr13 | 75853475 | ||||||
| chr13:75853526
|
A | G | 26 | a0006c0006t0001g0132a0006c0006t0001g0172a0006c0006t0001g0174others(23): Show | 26 | HG00140.hp2 HG00735.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.4661+138A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 28/30 | chr13 | 75853526 | ||||||
| chr13:75853632
|
T | C | 118 | a0002c0007t0001g0234a0002c0007t0003g0173a0002c0007t0003g0176others(115): Show | 119 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.4661+244T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 28/30 | chr13 | 75853632 | ||||||
| chr13:75853715
|
T | C | 61 | a0002c0007t0001g0234a0002c0007t0012g0156a0003c0002t0001g0006others(58): Show | 61 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.4661+327T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 28/30 | chr13 | 75853715 | ||||||
| chr13:75853716
|
A | G | 45 | a0002c0007t0001g0234a0002c0007t0012g0156a0003c0002t0001g0006others(42): Show | 45 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.4661+328A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 28/30 | chr13 | 75853716 | ||||||
| chr13:75853904
|
C | T | 1 | a0002c0003t0001g0239 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.4661+516C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 28/30 | chr13 | 75853904 | ||||||
| chr13:75853905
|
G | A | 1 | a0009c0010t0003g0244 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4661+517G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 28/30 | chr13 | 75853905 | ||||||
| chr13:75854052
|
T | C | 46 | a0002c0007t0001g0234a0002c0007t0012g0156a0003c0002t0001g0006others(43): Show | 46 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.4661+664T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 28/30 | chr13 | 75854052 | ||||||
| chr13:75854319
|
G | T | 190 | a0002c0003t0001g0121a0002c0003t0001g0126a0002c0003t0001g0137others(187): Show | 191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.4661+931G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 28/30 | chr13 | 75854319 | ||||||
| chr13:75854415
|
A | G | 5 | a0007c0009t0009g0251a0007c0016t0001g0001a0007c0016t0001g0252others(2): Show | 6 | HG02895.hp1 HG02897.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.4662-845A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 28/30 | chr13 | 75854415 | ||||||
| chr13:75854458
|
C | T | 46 | a0002c0007t0001g0234a0002c0007t0012g0156a0003c0002t0001g0006others(43): Show | 46 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.4662-802C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 28/30 | chr13 | 75854458 | ||||||
| chr13:75854508
|
A | C | 2 | a0012c0014t0001g0002a0012c0014t0001g0003 | 2 | HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.4662-752A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 28/30 | chr13 | 75854508 | ||||||
| chr13:75854829
|
G | A | 1 | a0003c0002t0001g0212 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.4662-431G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 28/30 | chr13 | 75854829 | ||||||
| chr13:75855110
|
T | C | 2 | a0012c0014t0001g0002a0012c0014t0001g0003 | 2 | HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.4662-150T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 28/30 | chr13 | 75855110 | ||||||
| chr13:75855175
|
G | A | 118 | a0002c0007t0001g0234a0002c0007t0003g0173a0002c0007t0003g0176others(115): Show | 119 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.4662-85G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 28/30 | chr13 | 75855175 | ||||||
| chr13:75855381
|
C | G | 2 | a0001c0001t0002g0063a0001c0001t0002g0065 | 2 | HG01928.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.4770+13C>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 29/30 | chr13 | 75855381 | ||||||
| chr13:75855483
|
C | A | 190 | a0002c0003t0001g0121a0002c0003t0001g0126a0002c0003t0001g0137others(187): Show | 191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.4770+115C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 29/30 | chr13 | 75855483 | ||||||
| chr13:75855577
|
A | G | 1 | a0008c0008t0003g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4770+209A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 29/30 | chr13 | 75855577 | ||||||
| chr13:75855600
|
A | G | 6 | a0009c0010t0001g0248a0009c0010t0001g0249a0009c0010t0001g0250others(3): Show | 6 | HG00735.hp1 HG02809.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.4770+232A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 29/30 | chr13 | 75855600 | ||||||
| chr13:75855666
|
T | C | 1 | a0003c0002t0001g0217 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.4770+298T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 29/30 | chr13 | 75855666 | ||||||
| chr13:75855712
|
C | T | 1 | a0002c0031t0002g0091 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.4770+344C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 29/30 | chr13 | 75855712 | ||||||
| chr13:75855874
|
T | G | 1 | a0009c0010t0003g0244 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4770+506T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 29/30 | chr13 | 75855874 | ||||||
| chr13:75856058
|
A | T | 3 | a0004c0004t0001g0188a0004c0004t0001g0190a0004c0004t0013g0189 | 3 | NA18949.hp2 NA18999.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.4771-448A>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 29/30 | chr13 | 75856058 | ||||||
| chr13:75856077
|
C | T | 2 | a0012c0014t0001g0002a0012c0014t0001g0003 | 2 | HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.4771-429C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 29/30 | chr13 | 75856077 | ||||||
| chr13:75856151
|
G | A | 1 | a0004c0004t0001g0190 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.4771-355G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 29/30 | chr13 | 75856151 | ||||||
| chr13:75856243
|
A | G | 1 | a0008c0008t0003g0168 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.4771-263A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 29/30 | chr13 | 75856243 | ||||||
| chr13:75856311
|
T | C | 1 | a0023c0022t0001g0136 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.4771-195T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 29/30 | chr13 | 75856311 | ||||||
| chr13:75856325
|
C | T | 45 | a0002c0007t0001g0234a0002c0007t0012g0156a0003c0002t0001g0006others(42): Show | 45 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.4771-181C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 29/30 | chr13 | 75856325 | ||||||
| chr13:75856340
|
T | G | 270 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0116others(267): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.4771-166T>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 29/30 | chr13 | 75856340 | ||||||
| chr13:75856794
|
G | A | 2 | a0007c0009t0001g0165a0007c0009t0001g0166 | 2 | HG01891.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.4873+186G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 30/30 | chr13 | 75856794 | ||||||
| chr13:75856795
|
C | A | 4 | a0007c0009t0009g0251a0007c0016t0001g0001a0007c0016t0001g0252others(1): Show | 5 | HG02895.hp1 HG02897.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.4873+187C>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 30/30 | chr13 | 75856795 | ||||||
| chr13:75856803
|
G | A | 1 | a0008c0008t0002g0077 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.4873+195G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 30/30 | chr13 | 75856803 | ||||||
| chr13:75856831
|
A | C | 4 | a0009c0010t0001g0248a0009c0010t0001g0249a0009c0010t0001g0250others(1): Show | 4 | HG03098.hp2 HG03486.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.4873+223A>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 30/30 | chr13 | 75856831 | ||||||
| chr13:75856844
|
A | G | 1 | a0002c0031t0002g0091 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.4873+236A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 30/30 | chr13 | 75856844 | ||||||
| chr13:75856884
|
G | A | 1 | a0003c0002t0002g0270 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.4873+276G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 30/30 | chr13 | 75856884 | ||||||
| chr13:75856884
|
G | T | 8 | a0002c0003t0001g0126a0002c0003t0001g0220a0002c0011t0002g0031others(5): Show | 8 | HG00099.hp2 HG00140.hp1 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.4873+276G>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 30/30 | chr13 | 75856884 | ||||||
| chr13:75856909
|
TACAA | T | 3 | a0001c0001t0001g0113a0001c0001t0002g0066a0001c0001t0002g0068 | 3 | NA18940.hp1 NA18993.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.4873+308_4873+311d others(6): Show |
LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr13 | 75856909 | |||||
| chr13:75857054
|
C | T | 156 | a0001c0001t0003g0153a0002c0003t0001g0121a0002c0003t0001g0126others(153): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.4873+446C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 30/30 | chr13 | 75857054 | ||||||
| chr13:75857103
|
T | C | 1 | a0003c0002t0001g0186 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.4873+495T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 30/30 | chr13 | 75857103 | ||||||
| chr13:75857368
|
T | C | 156 | a0001c0001t0003g0153a0002c0003t0001g0121a0002c0003t0001g0126others(153): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.4874-553T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 30/30 | chr13 | 75857368 | ||||||
| chr13:75857757
|
C | T | 1 | a0002c0007t0001g0129 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.4874-164C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 30/30 | chr13 | 75857757 | ||||||
| chr13:75857817
|
C | T | 41 | a0001c0001t0003g0153a0002c0007t0003g0173a0002c0007t0003g0176others(38): Show | 41 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.4874-104C>T | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 30/30 | chr13 | 75857817 | ||||||
| chr13:75857860
|
A | G | 41 | a0001c0001t0003g0153a0002c0007t0003g0173a0002c0007t0003g0176others(38): Show | 41 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.4874-61A>G | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 30/30 | chr13 | 75857860 | ||||||
| chr13:75857869
|
T | C | 1 | a0001c0001t0002g0068 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.4874-52T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 30/30 | chr13 | 75857869 | ||||||
| chr13:75857874
|
G | A | 41 | a0001c0001t0003g0153a0002c0007t0003g0173a0002c0007t0003g0176others(38): Show | 41 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.4874-47G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 30/30 | chr13 | 75857874 | ||||||
| chr13:75857893
|
T | C | 1 | a0008c0008t0002g0077 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.4874-28T>C | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 30/30 | chr13 | 75857893 | ||||||
| chr13:75857915
|
G | A | 4 | a0007c0009t0009g0251a0007c0016t0001g0001a0007c0016t0001g0252others(1): Show | 5 | HG02895.hp1 HG02897.hp2 HG03041.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.4874-6G>A | LMO7 | ENSG00000136153.20 | transcript | ENST00000377534.8 | protein_coding | 30/30 | chr13 | 75857915 |