Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 55132 |
|---|---|
| ensemblid | ENSG00000138709.20 |
| hgncid | 24704 |
| symbol | LARP1B |
| name | La ribonucleoprotein 1B |
| refseq_nuc | NM_018078.4 |
| refseq_prot | NP_060548.2 |
| ensembl_nuc | ENST00000326639.11 |
| ensembl_prot | ENSP00000321997.6 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 128061312 |
| end | 128211988 |
| strand | + |
| ver | v1.2 |
| region | chr4:128061312-128211988 |
| region5000 | chr4:128056312-128216988 |
| regionname0 | LARP1B_chr4_128061312_128211988 |
| regionname5000 | LARP1B_chr4_128056312_128216988 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 914 | 174 | 25 | 40 | 77 | 9 | 23 | 51 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0002 | 1/1 | 914 | 137 | 43 | 20 | 59 | 5 | 8 | 42 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0003 | 0/0 | 914 | 5 | 0 | 3 | 0 | 0 | 2 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0004 | 0/0 | 914 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0005 | 0/0 | 914 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0006 | 0/0 | 914 | 3 | 2 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0007 | 0/0 | 914 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0008 | 0/0 | 914 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0009 | 0/0 | 914 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0010 | 0/0 | 914 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0011 | 0/0 | 914 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0012 | 0/0 | 914 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0013 | 0/0 | 914 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0014 | 0/0 | 914 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| 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 | 0/0 | 2745 | 173 | 25 | 40 | 77 | 8 | 23 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| c0002 | 1/1 | 2745 | 122 | 29 | 20 | 59 | 5 | 7 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| c0003 | 0/0 | 2745 | 12 | 12 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| c0004 | 0/0 | 2745 | 5 | 0 | 3 | 0 | 0 | 2 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| c0005 | 0/0 | 2745 | 3 | 3 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| c0006 | 0/0 | 2745 | 3 | 2 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| c0007 | 0/0 | 2745 | 3 | 2 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| c0008 | 0/0 | 2745 | 3 | 3 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| c0009 | 0/0 | 2745 | 2 | 2 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| c0010 | 0/0 | 2745 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| c0011 | 0/0 | 2745 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| c0012 | 0/0 | 2745 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| c0013 | 0/0 | 2745 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| c0014 | 0/0 | 2745 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| c0015 | 0/0 | 2745 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| c0016 | 0/0 | 2745 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| c0017 | 0/0 | 2745 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| c0018 | 0/0 | 2745 | 1 | 0 | 0 | 0 | 1 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| c0019 | 0/0 | 2745 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| 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 | 2103 | 109 | 27 | 29 | 34 | 4 | 15 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| t0002 | 1/1 | 2103 | 108 | 24 | 14 | 55 | 5 | 8 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| t0003 | 0/0 | 2103 | 55 | 1 | 13 | 25 | 5 | 11 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| t0004 | 0/0 | 2103 | 23 | 0 | 1 | 22 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| t0005 | 0/0 | 2103 | 10 | 9 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| t0006 | 0/0 | 2100 | 8 | 8 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| t0007 | 0/0 | 2103 | 4 | 4 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| t0008 | 0/0 | 2103 | 4 | 0 | 4 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| t0009 | 0/0 | 2103 | 3 | 3 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| t0010 | 0/0 | 2100 | 3 | 2 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| t0011 | 0/0 | 2103 | 2 | 0 | 0 | 2 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| t0012 | 0/0 | 2103 | 2 | 0 | 0 | 2 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| t0013 | 0/0 | 2103 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| t0014 | 0/0 | 2103 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| t0015 | 0/0 | 2103 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| t0016 | 0/0 | 2103 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| t0017 | 0/0 | 2103 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0091 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0115 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| 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 | 0/0 | 2745 | 173 | 25 | 40 | 77 | 8 | 23 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0001c0018 | 0/0 | 2745 | 1 | 0 | 0 | 0 | 1 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0002c0002 | 1/1 | 2745 | 122 | 29 | 20 | 59 | 5 | 7 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0002c0003 | 0/0 | 2745 | 12 | 12 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0002c0012 | 0/0 | 2745 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0002c0017 | 0/0 | 2745 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0002c0019 | 0/0 | 2745 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0003c0004 | 0/0 | 2745 | 5 | 0 | 3 | 0 | 0 | 2 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0004c0005 | 0/0 | 2745 | 3 | 3 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0005c0006 | 0/0 | 2745 | 3 | 2 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0006c0007 | 0/0 | 2745 | 3 | 2 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0007c0008 | 0/0 | 2745 | 3 | 3 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0008c0009 | 0/0 | 2745 | 2 | 2 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0009c0010 | 0/0 | 2745 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0010c0011 | 0/0 | 2745 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0011c0016 | 0/0 | 2745 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0012c0013 | 0/0 | 2745 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0013c0014 | 0/0 | 2745 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0014c0015 | 0/0 | 2745 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4847 | 95 | 19 | 25 | 34 | 4 | 13 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0001c0001t0003 | 0/0 | 4847 | 51 | 1 | 13 | 23 | 4 | 10 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0001c0001t0004 | 0/0 | 4847 | 21 | 0 | 1 | 20 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0001c0001t0007 | 0/0 | 4847 | 4 | 4 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0001c0001t0014 | 0/0 | 4847 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0001c0001t0017 | 0/0 | 4847 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0001c0018t0003 | 0/0 | 4847 | 1 | 0 | 0 | 0 | 1 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0002c0002t0002 | 1/1 | 4847 | 106 | 23 | 14 | 55 | 5 | 7 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0002c0002t0005 | 0/0 | 4847 | 2 | 1 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0002c0002t0008 | 0/0 | 4847 | 4 | 0 | 4 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0002c0002t0010 | 0/0 | 4844 | 3 | 2 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0002c0002t0011 | 0/0 | 4847 | 2 | 0 | 0 | 2 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0002c0002t0012 | 0/0 | 4847 | 2 | 0 | 0 | 2 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0002c0002t0013 | 0/0 | 4847 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0002c0002t0015 | 0/0 | 4847 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0002c0002t0016 | 0/0 | 4847 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0002c0003t0001 | 0/0 | 4847 | 2 | 2 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0002c0003t0005 | 0/0 | 4847 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0002c0003t0006 | 0/0 | 4844 | 8 | 8 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0002c0003t0009 | 0/0 | 4847 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0002c0012t0005 | 0/0 | 4847 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0002c0017t0002 | 0/0 | 4847 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0002c0019t0002 | 0/0 | 4847 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0003c0004t0001 | 0/0 | 4847 | 5 | 0 | 3 | 0 | 0 | 2 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0004c0005t0005 | 0/0 | 4847 | 3 | 3 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0005c0006t0001 | 0/0 | 4847 | 3 | 2 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0006c0007t0004 | 0/0 | 4847 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0006c0007t0009 | 0/0 | 4847 | 2 | 2 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0007c0008t0001 | 0/0 | 4847 | 3 | 3 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0008c0009t0005 | 0/0 | 4847 | 2 | 2 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0009c0010t0003 | 0/0 | 4847 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0010c0011t0005 | 0/0 | 4847 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0011c0016t0003 | 0/0 | 4847 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0012c0013t0004 | 0/0 | 4847 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0013c0014t0003 | 0/0 | 4847 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| a0014c0015t0001 | 0/0 | 4847 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | copy fasta | chr4 | 128056312 | 128216988 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0003g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0004g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0004g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0004g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0004g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0004g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0004g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0004g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0004g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0004g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0004g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0004g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0004g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0004g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0004g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0004g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0004g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0004g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0004g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0004g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0004g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0004g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0007g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0007g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0007g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0007g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0014g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0001t0017g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0001c0018t0003g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0091 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0115 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0002g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0005g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0005g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0008g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0008g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0008g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0008g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0010g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0010g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0010g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0011g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0011g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0012g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0012g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0013g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0015g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0002t0016g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0003t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0003t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0003t0005g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0003t0006g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0003t0006g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0003t0006g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0003t0006g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0003t0006g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0003t0006g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0003t0006g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0003t0006g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0003t0009g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0012t0005g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0017t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0002c0019t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0003c0004t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0003c0004t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0003c0004t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0003c0004t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0003c0004t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0004c0005t0005g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0004c0005t0005g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0004c0005t0005g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0005c0006t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0005c0006t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0005c0006t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0006c0007t0004g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0006c0007t0009g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0006c0007t0009g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0007c0008t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0007c0008t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0007c0008t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0008c0009t0005g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0008c0009t0005g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0009c0010t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0010c0011t0005g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0011c0016t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0012c0013t0004g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0013c0014t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| a0014c0015t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0002 | g0039 | EUR | GBR | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG00099 | hp2 | a0001 | c0018 | t0003 | g0254 | EUR | GBR | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0237 | EUR | GBR | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0191 | EUR | GBR | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0193 | EUR | FIN | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0246 | EUR | FIN | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG00408 | hp1 | a0002 | c0002 | t0002 | g0056 | EAS | CHS | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0215 | EAS | CHS | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG00423 | hp1 | a0002 | c0002 | t0002 | g0294 | EAS | CHS | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | CHS | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | CHS | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG00438 | hp2 | a0002 | c0002 | t0002 | g0332 | EAS | CHS | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG00544 | hp1 | a0002 | c0002 | t0002 | g0297 | EAS | CHS | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | CHS | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0233 | EAS | CHS | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG00558 | hp2 | a0001 | c0001 | t0004 | g0318 | EAS | CHS | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG00597 | hp1 | a0002 | c0002 | t0002 | g0037 | EAS | CHS | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG00597 | hp2 | a0001 | c0001 | t0004 | g0320 | EAS | CHS | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG00609 | hp1 | a0001 | c0001 | t0004 | g0324 | EAS | CHS | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG00609 | hp2 | a0006 | c0007 | t0004 | g0234 | EAS | CHS | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG00639 | hp1 | a0002 | c0002 | t0002 | g0057 | AMR | PUR | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0243 | EAS | CHS | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG00735 | hp1 | a0002 | c0002 | t0002 | g0024 | AMR | PUR | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG00735 | hp2 | a0002 | c0002 | t0002 | g0067 | AMR | PUR | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG00738 | hp2 | a0001 | c0001 | t0004 | g0317 | AMR | PUR | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG00741 | hp2 | a0002 | c0002 | t0005 | g0059 | AMR | PUR | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01070 | hp2 | a0002 | c0002 | t0002 | g0082 | AMR | PUR | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01074 | hp2 | a0002 | c0002 | t0002 | g0062 | AMR | PUR | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01081 | hp2 | a0002 | c0002 | t0008 | g0304 | AMR | PUR | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01106 | hp1 | a0002 | c0002 | t0002 | g0080 | AMR | PUR | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0242 | AMR | PUR | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01109 | hp1 | a0002 | c0002 | t0002 | g0130 | AMR | PUR | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01109 | hp2 | a0003 | c0004 | t0001 | g0172 | AMR | PUR | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01167 | hp2 | a0003 | c0004 | t0001 | g0182 | AMR | PUR | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01168 | hp1 | a0005 | c0006 | t0001 | g0100 | AMR | PUR | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0257 | AMR | PUR | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01169 | hp1 | a0003 | c0004 | t0001 | g0183 | AMR | PUR | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0256 | AMR | PUR | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01175 | hp1 | a0002 | c0002 | t0002 | g0014 | AMR | PUR | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0102 | AMR | PUR | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0247 | AMR | PUR | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01243 | hp2 | a0002 | c0002 | t0010 | g0048 | AMR | PUR | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01256 | hp2 | a0002 | c0002 | t0002 | g0075 | AMR | CLM | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01258 | hp1 | a0002 | c0002 | t0002 | g0076 | AMR | CLM | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0103 | AMR | CLM | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01433 | hp1 | a0002 | c0002 | t0002 | g0287 | AMR | CLM | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01496 | hp1 | a0002 | c0002 | t0002 | g0028 | AMR | CLM | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0245 | AMR | CLM | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01515 | hp1 | a0002 | c0002 | t0002 | g0060 | EUR | IBS | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0125 | EUR | IBS | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01516 | hp1 | a0002 | c0002 | t0002 | g0073 | EUR | IBS | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0207 | EUR | IBS | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01517 | hp1 | a0002 | c0002 | t0002 | g0072 | EUR | IBS | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0212 | EUR | IBS | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0217 | AFR | ACB | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01884 | hp2 | a0002 | c0002 | t0002 | g0070 | AFR | ACB | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01891 | hp1 | a0001 | c0001 | t0007 | g0258 | AFR | ACB | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0255 | AMR | PEL | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0251 | AMR | PEL | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01952 | hp1 | a0001 | c0001 | t0014 | g0151 | AMR | PEL | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0231 | AMR | PEL | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0127 | AMR | PEL | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PEL | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01981 | hp1 | a0002 | c0002 | t0002 | g0044 | AMR | PEL | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01981 | hp2 | a0002 | c0002 | t0008 | g0293 | AMR | PEL | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0218 | AMR | PEL | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02004 | hp1 | a0002 | c0002 | t0002 | g0121 | AMR | PEL | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0224 | AMR | PEL | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02015 | hp1 | a0002 | c0002 | t0002 | g0058 | EAS | KHV | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0252 | EAS | KHV | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02027 | hp1 | a0002 | c0002 | t0002 | g0112 | EAS | KHV | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0239 | EAS | KHV | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0033 | EAS | KHV | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02055 | hp1 | a0004 | c0005 | t0005 | g0282 | AFR | ACB | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02055 | hp2 | a0002 | c0002 | t0002 | g0095 | AFR | ACB | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0235 | EAS | KHV | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02056 | hp2 | a0001 | c0001 | t0004 | g0325 | EAS | KHV | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02071 | hp2 | a0002 | c0002 | t0002 | g0117 | EAS | KHV | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02074 | hp2 | a0002 | c0002 | t0002 | g0330 | EAS | KHV | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02080 | hp1 | a0002 | c0002 | t0012 | g0065 | EAS | KHV | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02083 | hp1 | a0002 | c0002 | t0002 | g0035 | EAS | KHV | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02129 | hp1 | a0002 | c0002 | t0002 | g0302 | EAS | KHV | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02129 | hp2 | a0001 | c0001 | t0004 | g0335 | EAS | KHV | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0220 | EAS | KHV | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02132 | hp2 | a0001 | c0001 | t0004 | g0315 | EAS | KHV | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02145 | hp1 | a0002 | c0003 | t0001 | g0104 | AFR | ACB | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02145 | hp2 | a0002 | c0003 | t0006 | g0005 | AFR | ACB | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | CDX | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02155 | hp2 | a0002 | c0002 | t0002 | g0043 | EAS | CDX | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02165 | hp1 | a0002 | c0002 | t0002 | g0063 | EAS | CDX | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | CDX | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02257 | hp1 | a0002 | c0003 | t0006 | g0285 | AFR | ACB | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02273 | hp1 | a0002 | c0002 | t0008 | g0305 | AMR | PEL | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02280 | hp1 | a0002 | c0002 | t0002 | g0118 | AFR | ACB | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02280 | hp2 | a0010 | c0011 | t0005 | g0123 | AFR | ACB | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02300 | hp2 | a0002 | c0002 | t0008 | g0300 | AMR | PEL | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02451 | hp1 | a0002 | c0012 | t0005 | g0098 | AFR | ACB | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02451 | hp2 | a0002 | c0003 | t0001 | g0105 | AFR | ACB | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | KHV | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02523 | hp2 | a0002 | c0002 | t0002 | g0334 | EAS | KHV | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02572 | hp1 | a0008 | c0009 | t0005 | g0119 | AFR | GWD | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02602 | hp2 | a0002 | c0002 | t0002 | g0061 | SAS | PJL | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02622 | hp1 | a0002 | c0002 | t0002 | g0015 | AFR | GWD | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02622 | hp2 | a0001 | c0001 | t0007 | g0132 | AFR | GWD | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02630 | hp1 | a0002 | c0003 | t0009 | g0008 | AFR | GWD | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02647 | hp2 | a0002 | c0002 | t0002 | g0068 | AFR | GWD | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02723 | hp1 | a0002 | c0002 | t0002 | g0026 | AFR | GWD | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02723 | hp2 | a0008 | c0009 | t0005 | g0113 | AFR | GWD | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02735 | hp1 | a0003 | c0004 | t0001 | g0189 | SAS | PJL | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0250 | SAS | PJL | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0276 | SAS | PJL | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02809 | hp2 | a0002 | c0002 | t0002 | g0021 | AFR | GWD | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02818 | hp1 | a0002 | c0002 | t0002 | g0092 | AFR | GWD | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02818 | hp2 | a0002 | c0003 | t0006 | g0003 | AFR | GWD | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02896 | hp1 | a0002 | c0002 | t0002 | g0049 | AFR | GWD | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02896 | hp2 | a0002 | c0002 | t0002 | g0050 | AFR | GWD | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ESN | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | ESN | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02965 | hp2 | a0005 | c0006 | t0001 | g0101 | AFR | ESN | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02970 | hp1 | a0002 | c0003 | t0005 | g0122 | AFR | ESN | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02970 | hp2 | a0002 | c0003 | t0006 | g0006 | AFR | ESN | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02976 | hp1 | a0002 | c0002 | t0002 | g0022 | AFR | ESN | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02976 | hp2 | a0004 | c0005 | t0005 | g0281 | AFR | ESN | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0219 | SAS | PJL | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG03041 | hp1 | a0002 | c0002 | t0016 | g0064 | AFR | GWD | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG03041 | hp2 | a0002 | c0002 | t0002 | g0029 | AFR | GWD | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG03098 | hp1 | a0002 | c0002 | t0002 | g0094 | AFR | MSL | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | MSL | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ESN | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG03130 | hp2 | a0002 | c0017 | t0002 | g0074 | AFR | ESN | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG03139 | hp1 | a0006 | c0007 | t0009 | g0192 | AFR | ESN | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | ESN | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG03195 | hp1 | a0014 | c0015 | t0001 | g0206 | AFR | ESN | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG03195 | hp2 | a0002 | c0002 | t0002 | g0085 | AFR | ESN | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG03209 | hp1 | a0002 | c0002 | t0010 | g0036 | AFR | MSL | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG03209 | hp2 | a0004 | c0005 | t0005 | g0283 | AFR | MSL | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | MSL | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG03225 | hp2 | a0001 | c0001 | t0007 | g0131 | AFR | MSL | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG03486 | hp1 | a0002 | c0002 | t0002 | g0019 | AFR | MSL | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG03486 | hp2 | a0007 | c0008 | t0001 | g0139 | AFR | MSL | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0222 | SAS | PJL | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG03492 | hp1 | a0003 | c0004 | t0001 | g0264 | SAS | PJL | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0221 | SAS | PJL | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG03516 | hp2 | a0005 | c0006 | t0001 | g0099 | AFR | ESN | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG03540 | hp1 | a0002 | c0003 | t0006 | g0004 | AFR | GWD | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG03540 | hp2 | a0002 | c0002 | t0002 | g0025 | AFR | GWD | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0253 | SAS | PJL | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG03669 | hp2 | a0002 | c0002 | t0002 | g0013 | SAS | PJL | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | STU | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG03688 | hp2 | a0002 | c0002 | t0002 | g0120 | SAS | STU | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG03704 | hp1 | a0002 | c0019 | t0002 | g0083 | SAS | PJL | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG03710 | hp1 | a0002 | c0002 | t0002 | g0045 | SAS | PJL | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG03710 | hp2 | a0013 | c0014 | t0003 | g0226 | SAS | PJL | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | BEB | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0240 | SAS | BEB | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG03834 | hp1 | a0002 | c0002 | t0002 | g0284 | SAS | BEB | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | BEB | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0111 | SAS | STU | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | STU | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG04184 | hp1 | a0002 | c0002 | t0002 | g0031 | SAS | BEB | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0210 | SAS | BEB | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG04199 | hp1 | a0002 | c0002 | t0002 | g0016 | SAS | STU | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0266 | SAS | STU | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | STU | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0244 | SAS | STU | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18522 | hp1 | a0002 | c0002 | t0005 | g0097 | AFR | YRI | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18522 | hp2 | a0002 | c0002 | t0015 | g0020 | AFR | YRI | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18747 | hp1 | a0002 | c0002 | t0002 | g0291 | EAS | CHB | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | CHB | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18906 | hp1 | a0002 | c0003 | t0006 | g0009 | AFR | YRI | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18906 | hp2 | a0002 | c0002 | t0013 | g0093 | AFR | YRI | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18941 | hp1 | a0002 | c0002 | t0002 | g0071 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18942 | hp1 | a0002 | c0002 | t0002 | g0303 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18943 | hp1 | a0002 | c0002 | t0002 | g0329 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18945 | hp2 | a0002 | c0002 | t0011 | g0030 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18946 | hp2 | a0001 | c0001 | t0004 | g0322 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18949 | hp1 | a0002 | c0002 | t0002 | g0046 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0228 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18950 | hp2 | a0002 | c0002 | t0002 | g0032 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18951 | hp1 | a0002 | c0002 | t0002 | g0290 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18954 | hp1 | a0001 | c0001 | t0004 | g0327 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18954 | hp2 | a0002 | c0002 | t0002 | g0055 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18957 | hp1 | a0001 | c0001 | t0004 | g0321 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18957 | hp2 | a0002 | c0002 | t0002 | g0054 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18959 | hp2 | a0002 | c0002 | t0011 | g0042 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18962 | hp2 | a0002 | c0002 | t0002 | g0306 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0278 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18969 | hp1 | a0002 | c0002 | t0002 | g0078 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0280 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0216 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18973 | hp2 | a0002 | c0002 | t0002 | g0116 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0248 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18974 | hp2 | a0002 | c0002 | t0002 | g0295 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18979 | hp1 | a0002 | c0002 | t0002 | g0051 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18979 | hp2 | a0002 | c0002 | t0002 | g0047 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18980 | hp2 | a0002 | c0002 | t0002 | g0086 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18982 | hp1 | a0002 | c0002 | t0002 | g0079 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18982 | hp2 | a0002 | c0002 | t0012 | g0096 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18983 | hp1 | a0002 | c0002 | t0002 | g0298 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18984 | hp1 | a0001 | c0001 | t0004 | g0311 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0225 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18985 | hp1 | a0001 | c0001 | t0003 | g0279 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18985 | hp2 | a0002 | c0002 | t0002 | g0053 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18986 | hp1 | a0002 | c0002 | t0002 | g0289 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18989 | hp2 | a0002 | c0002 | t0002 | g0333 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18990 | hp1 | a0002 | c0002 | t0002 | g0299 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18990 | hp2 | a0001 | c0001 | t0004 | g0309 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18991 | hp1 | a0002 | c0002 | t0002 | g0087 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0214 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18998 | hp2 | a0002 | c0002 | t0002 | g0034 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA19000 | hp2 | a0002 | c0002 | t0002 | g0292 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA19002 | hp1 | a0002 | c0002 | t0002 | g0066 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA19002 | hp2 | a0001 | c0001 | t0004 | g0328 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA19004 | hp2 | a0011 | c0016 | t0003 | g0277 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA19005 | hp1 | a0001 | c0001 | t0004 | g0314 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA19005 | hp2 | a0002 | c0002 | t0002 | g0084 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA19007 | hp1 | a0002 | c0002 | t0002 | g0331 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA19011 | hp1 | a0002 | c0002 | t0002 | g0069 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA19011 | hp2 | a0001 | c0001 | t0004 | g0313 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA19012 | hp2 | a0002 | c0002 | t0002 | g0114 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA19054 | hp2 | a0002 | c0002 | t0002 | g0301 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA19056 | hp2 | a0002 | c0002 | t0002 | g0307 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA19057 | hp2 | a0002 | c0002 | t0002 | g0090 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0238 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA19062 | hp2 | a0002 | c0002 | t0002 | g0040 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA19064 | hp1 | a0012 | c0013 | t0004 | g0316 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA19064 | hp2 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA19066 | hp2 | a0001 | c0001 | t0004 | g0310 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA19068 | hp1 | a0002 | c0002 | t0002 | g0288 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA19068 | hp2 | a0009 | c0010 | t0003 | g0223 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA19070 | hp1 | a0001 | c0001 | t0004 | g0319 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA19070 | hp2 | a0002 | c0002 | t0002 | g0089 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA19074 | hp1 | a0002 | c0002 | t0002 | g0088 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA19078 | hp1 | a0001 | c0001 | t0003 | g0213 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA19078 | hp2 | a0001 | c0001 | t0004 | g0308 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA19081 | hp1 | a0002 | c0002 | t0002 | g0296 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA19081 | hp2 | a0001 | c0001 | t0004 | g0323 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA19085 | hp2 | a0001 | c0001 | t0004 | g0326 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA19240 | hp1 | a0002 | c0002 | t0002 | g0041 | AFR | YRI | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA19240 | hp2 | a0007 | c0008 | t0001 | g0158 | AFR | YRI | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA20129 | hp1 | a0002 | c0002 | t0010 | g0077 | AFR | ASW | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA20129 | hp2 | a0006 | c0007 | t0009 | g0204 | AFR | ASW | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA20752 | hp1 | a0002 | c0002 | t0002 | g0336 | EUR | TSI | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0142 | EUR | TSI | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02109 | hp1 | a0002 | c0003 | t0006 | g0007 | AFR | ACB | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02109 | hp2 | a0002 | c0002 | t0002 | g0081 | AFR | ACB | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02486 | hp1 | a0001 | c0001 | t0007 | g0133 | AFR | ACB | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02486 | hp2 | a0001 | c0001 | t0017 | g0106 | AFR | ACB | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02559 | hp1 | a0002 | c0002 | t0002 | g0038 | AFR | ACB | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG02559 | hp2 | a0002 | c0002 | t0002 | g0017 | AFR | ACB | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG03471 | hp1 | a0002 | c0002 | t0002 | g0023 | AFR | MSL | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG03471 | hp2 | a0002 | c0002 | t0002 | g0052 | AFR | MSL | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG06807 | hp1 | a0002 | c0003 | t0006 | g0286 | AFR | USA | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | USA | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18955 | hp1 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA18955 | hp2 | a0001 | c0001 | t0004 | g0312 | EAS | JPT | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA20300 | hp1 | a0007 | c0008 | t0001 | g0138 | AFR | USA | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | USA | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | LWK | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| NA21309 | hp2 | a0002 | c0002 | t0002 | g0027 | AFR | LWK | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0002 | g0115 | REF | REF | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| homoSapiens_grch38 | hp1 | a0002 | c0002 | t0002 | g0091 | REF | REF | LARP1B_chr4_128056312_128216988 | LARP1B | chr4 | 128056312 | 128216988 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:128077920
|
G | A | 1 | a0009 | 1 | NA19068.hp2 | missense_variant | MODERATE | c.175G>A | p.Val59Ile | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 4/20 | 342/4847 | 175/2745 | 59/914 | chr4 | 128077920 | ||
| chr4:128091463
|
G | A | 1 | a0010 | 1 | HG02280.hp2 | missense_variant | MODERATE | c.619G>A | p.Val207Met | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/20 | 786/4847 | 619/2745 | 207/914 | chr4 | 128091463 | ||
| chr4:128121940
|
A | C | 1 | a0011 | 1 | NA19004.hp2 | missense_variant | MODERATE | c.1276A>C | p.Asn426His | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/20 | 1443/4847 | 1276/2745 | 426/914 | chr4 | 128121940 | ||
| chr4:128122049
|
C | G | 10 | a0001a0003a0005others(7): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
missense_variant | MODERATE | c.1385C>G | p.Pro462Arg | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/20 | 1552/4847 | 1385/2745 | 462/914 | chr4 | 128122049 | ||
| chr4:128122174
|
C | T | 1 | a0004 | 3 | HG02055.hp1 HG02976.hp2 HG03209.hp2 |
missense_variant | MODERATE | c.1510C>T | p.His504Tyr | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/20 | 1677/4847 | 1510/2745 | 504/914 | chr4 | 128122174 | ||
| chr4:128178456
|
G | T | 1 | a0007 | 3 | HG03486.hp2 NA19240.hp2 NA20300.hp1 |
missense_variant | MODERATE | c.1710G>T | p.Lys570Asn | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 14/20 | 1877/4847 | 1710/2745 | 570/914 | chr4 | 128178456 | ||
| chr4:128178490
|
A | G | 1 | a0003 | 5 | HG01109.hp2 HG01167.hp2 HG01169.hp1 others(2): Show |
missense_variant | MODERATE | c.1744A>G | p.Met582Val | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 14/20 | 1911/4847 | 1744/2745 | 582/914 | chr4 | 128178490 | ||
| chr4:128179488
|
G | A | 9 | a0001a0003a0007others(6): Show | 188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
missense_variant | MODERATE | c.1979G>A | p.Arg660His | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/20 | 2146/4847 | 1979/2745 | 660/914 | chr4 | 128179488 | ||
| chr4:128199582
|
G | A | 1 | a0012 | 1 | NA19064.hp1 | missense_variant | MODERATE | c.2147G>A | p.Arg716His | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 16/20 | 2314/4847 | 2147/2745 | 716/914 | chr4 | 128199582 | ||
| chr4:128200655
|
G | A | 1 | a0014 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.2299G>A | p.Glu767Lys | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/20 | 2466/4847 | 2299/2745 | 767/914 | chr4 | 128200655 | ||
| chr4:128209920
|
G | A | 2 | a0005a0008 | 5 | HG01168.hp1 HG02572.hp1 HG02723.hp2 others(2): Show |
missense_variant | MODERATE | c.2612G>A | p.Arg871His | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 20/20 | 2779/4847 | 2612/2745 | 871/914 | chr4 | 128209920 | ||
| chr4:128209998
|
C | T | 1 | a0013 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.2690C>T | p.Pro897Leu | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 20/20 | 2857/4847 | 2690/2745 | 897/914 | chr4 | 128209998 | ||
| chr4:128210007
|
C | T | 1 | a0013 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.2699C>T | p.Ser900Phe | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 20/20 | 2866/4847 | 2699/2745 | 900/914 | chr4 | 128210007 | ||
| chr4:128210009
|
C | T | 1 | a0013 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.2701C>T | p.Pro901Ser | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 20/20 | 2868/4847 | 2701/2745 | 901/914 | chr4 | 128210009 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:128082220
|
A | G | 2 | a0001c0018a0002c0019 | 2 | HG00099.hp2 HG03704.hp1 |
synonymous_variant | LOW | c.273A>G | p.Gln91Gln | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/20 | 440/4847 | 273/2745 | 91/914 | chr4 | 128082220 | ||
| chr4:128091026
|
G | A | 15 | a0001c0001a0001c0018a0002c0003others(12): Show | 210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
synonymous_variant | LOW | c.384G>A | p.Arg128Arg | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 6/20 | 551/4847 | 384/2745 | 128/914 | chr4 | 128091026 | ||
| chr4:128091128
|
C | T | 1 | a0002c0017 | 1 | HG03130.hp2 | synonymous_variant | LOW | c.486C>T | p.Gly162Gly | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 6/20 | 653/4847 | 486/2745 | 162/914 | chr4 | 128091128 | ||
| chr4:128091483
|
A | G | 15 | a0001c0001a0001c0018a0002c0003others(12): Show | 210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
synonymous_variant | LOW | c.639A>G | p.Ala213Ala | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/20 | 806/4847 | 639/2745 | 213/914 | chr4 | 128091483 | ||
| chr4:128114634
|
T | C | 1 | a0004c0005 | 3 | HG02055.hp1 HG02976.hp2 HG03209.hp2 |
synonymous_variant | LOW | c.1053T>C | p.Ser351Ser | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/20 | 1220/4847 | 1053/2745 | 351/914 | chr4 | 128114634 | ||
| chr4:128122131
|
C | T | 11 | a0001c0001a0001c0018a0003c0004others(8): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
synonymous_variant | LOW | c.1467C>T | p.Tyr489Tyr | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/20 | 1634/4847 | 1467/2745 | 489/914 | chr4 | 128122131 | ||
| chr4:128162250
|
C | T | 1 | a0014c0015 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.1581C>T | p.Asn527Asn | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/20 | 1748/4847 | 1581/2745 | 527/914 | chr4 | 128162250 | ||
| chr4:128199475
|
A | G | 1 | a0002c0012 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.2040A>G | p.Leu680Leu | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 16/20 | 2207/4847 | 2040/2745 | 680/914 | chr4 | 128199475 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:128061332
|
C | T | 1 | a0001c0001t0017 | 1 | HG02486.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-147C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/20 | chr4 | 128061332 | ||||||
| chr4:128061349
|
G | A | 1 | a0002c0002t0013 | 1 | NA18906.hp2 | 5_prime_UTR_variant | MODIFIER | c.-130G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/20 | 13603 | chr4 | 128061349 | |||||
| chr4:128074485
|
G | A | 20 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(17): Show | 204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
5_prime_UTR_variant | MODIFIER | c.-52G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 2/20 | 467 | chr4 | 128074485 | |||||
| chr4:128210392
|
AAAC | A | 1 | a0002c0003t0006 | 8 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*342_*344delCAA | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 20/20 | 342 | INFO_REALIGN_3_PRIME | chr4 | 128210392 | ||||
| chr4:128210546
|
G | A | 1 | a0002c0002t0008 | 4 | HG01081.hp2 HG01981.hp2 HG02273.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*493G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 20/20 | 493 | chr4 | 128210546 | |||||
| chr4:128210587
|
C | A | 5 | a0001c0001t0004a0001c0001t0007a0002c0002t0011others(2): Show | 29 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*534C>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 20/20 | 534 | chr4 | 128210587 | |||||
| chr4:128210623
|
ACTT | A | 1 | a0002c0002t0010 | 3 | HG01243.hp2 HG03209.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*571_*573delCTT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 20/20 | 571 | chr4 | 128210623 | |||||
| chr4:128210938
|
A | G | 1 | a0001c0001t0007 | 4 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*885A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 20/20 | 885 | chr4 | 128210938 | |||||
| chr4:128211255
|
T | C | 26 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(23): Show | 215 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*1202T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 20/20 | 1202 | chr4 | 128211255 | |||||
| chr4:128211302
|
C | G | 1 | a0002c0002t0016 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1249C>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 20/20 | 1249 | chr4 | 128211302 | |||||
| chr4:128211433
|
A | G | 1 | a0002c0002t0015 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1380A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 20/20 | 1380 | chr4 | 128211433 | |||||
| chr4:128211774
|
C | T | 6 | a0001c0001t0003a0001c0018t0003a0002c0002t0012others(3): Show | 57 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*1721C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 20/20 | 1721 | chr4 | 128211774 | |||||
| chr4:128211980
|
A | G | 1 | a0001c0001t0014 | 1 | HG01952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1927A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 20/20 | 1927 | chr4 | 128211980 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:128061495
|
C | T | 1 | a0002c0002t0002g0336 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-78+94C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128061495 | ||||||
| chr4:128061635
|
G | T | 48 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(45): Show | 48 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.-78+234G>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128061635 | ||||||
| chr4:128061646
|
C | T | 1 | a0002c0002t0002g0287 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-78+245C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128061646 | ||||||
| chr4:128061656
|
G | A | 1 | a0001c0001t0001g0001 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-78+255G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128061656 | ||||||
| chr4:128061664
|
C | G | 2 | a0002c0003t0006g0285a0002c0003t0006g0286 | 2 | HG02257.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-78+263C>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128061664 | ||||||
| chr4:128061708
|
C | T | 2 | a0002c0002t0002g0284a0002c0002t0002g0287 | 2 | HG01433.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-78+307C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128061708 | ||||||
| chr4:128062294
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-78+893G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128062294 | ||||||
| chr4:128062399
|
G | A | 11 | a0001c0001t0001g0010a0001c0001t0001g0011a0002c0003t0006g0003others(8): Show | 11 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.-78+998G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128062399 | ||||||
| chr4:128062456
|
G | A | 1 | a0002c0002t0002g0012 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-78+1055G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128062456 | ||||||
| chr4:128062592
|
C | CT | 11 | a0002c0002t0002g0112a0002c0002t0002g0114a0002c0002t0002g0115others(8): Show | 11 | HG02004.hp1 HG02027.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.-78+1209dupT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128062592 | |||||
| chr4:128062592
|
C | CTTT | 6 | a0001c0001t0001g0124a0001c0001t0001g0126a0001c0001t0003g0125others(3): Show | 6 | HG01515.hp2 HG01975.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-78+1207_-78+1209d others(5): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128062592 | |||||
| chr4:128062592
|
C | CTTTT | 130 | a0001c0001t0001g0002a0001c0001t0001g0129a0001c0001t0001g0134others(127): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.-78+1206_-78+1209d others(6): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128062592 | |||||
| chr4:128062592
|
C | CTTTTT | 25 | a0001c0001t0001g0001a0001c0001t0001g0259a0001c0001t0001g0260others(22): Show | 25 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.-78+1205_-78+1209d others(7): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128062592 | |||||
| chr4:128062592
|
C | CTTTTTTT others(2): Show |
38 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(35): Show | 38 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.-78+1201_-78+1209d others(11): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128062592 | |||||
| chr4:128062592
|
C | CTTTTTTT others(3): Show |
6 | a0001c0001t0004g0335a0002c0002t0002g0330a0002c0002t0002g0331others(3): Show | 6 | HG00438.hp2 HG02074.hp2 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.-78+1200_-78+1209d others(12): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128062592 | |||||
| chr4:128062592
|
C | CTTTTTTT others(8): Show |
1 | a0004c0005t0005g0281 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-78+1195_-78+1209d others(17): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128062592 | |||||
| chr4:128062592
|
C | CTTTTTTT others(9): Show |
1 | a0004c0005t0005g0282 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-78+1194_-78+1209d others(18): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128062592 | |||||
| chr4:128062592
|
C | CTTTTTTT others(10): Show |
1 | a0004c0005t0005g0283 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-78+1193_-78+1209d others(19): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128062592 | |||||
| chr4:128062770
|
G | T | 173 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(170): Show | 173 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.-78+1369G>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128062770 | ||||||
| chr4:128062810
|
TGTTAAAT others(5): Show |
T | 2 | a0002c0002t0002g0290a0002c0002t0002g0329 | 2 | NA18943.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.-78+1413_-78+1424d others(14): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128062810 | |||||
| chr4:128062864
|
A | G | 2 | a0001c0001t0003g0256a0001c0001t0003g0257 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-78+1463A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128062864 | ||||||
| chr4:128063130
|
TAAG | T | 3 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136 | 3 | HG01070.hp1 HG01071.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.-78+1732_-78+1734d others(5): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128063130 | |||||
| chr4:128063198
|
G | A | 14 | a0002c0003t0001g0104a0002c0003t0001g0105a0002c0003t0006g0003others(11): Show | 14 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.-78+1797G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128063198 | ||||||
| chr4:128063321
|
A | G | 203 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(200): Show | 203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.-78+1920A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128063321 | ||||||
| chr4:128063400
|
C | CCTGGTCG others(1): Show |
60 | a0001c0001t0001g0126a0001c0001t0001g0211a0001c0001t0001g0236others(57): Show | 60 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.-78+2001_-78+2008d others(10): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128063400 | |||||
| chr4:128063427
|
C | CA | 113 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(110): Show | 113 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.-78+2056dupA | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128063427 | |||||
| chr4:128063427
|
C | CAA | 26 | a0001c0001t0001g0137a0001c0001t0001g0211a0001c0001t0003g0210others(23): Show | 26 | HG00408.hp2 HG00735.hp1 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.-78+2055_-78+2056d others(4): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128063427 | |||||
| chr4:128063427
|
CA | C | 12 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0275others(9): Show | 12 | HG01099.hp1 HG01099.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.-78+2056delA | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128063427 | |||||
| chr4:128063427
|
CAAAA | C | 19 | a0001c0001t0001g0209a0001c0001t0004g0312a0001c0001t0004g0313others(16): Show | 19 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(16): Show |
intron_variant | MODIFIER | c.-78+2053_-78+2056d others(6): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128063427 | |||||
| chr4:128063427
|
CAAAAAAA others(3): Show |
C | 11 | a0002c0003t0001g0104a0002c0003t0001g0105a0002c0003t0006g0003others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.-78+2047_-78+2056d others(12): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128063427 | |||||
| chr4:128063427
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0003g0255 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-78+2045_-78+2056d others(14): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128063427 | |||||
| chr4:128063914
|
CAA | C | 16 | a0002c0002t0002g0019a0002c0002t0002g0021a0002c0002t0002g0022others(13): Show | 16 | HG00735.hp1 HG01109.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.-78+2514_-78+2515d others(4): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128063914 | ||||||
| chr4:128063949
|
G | C | 11 | a0002c0003t0001g0104a0002c0003t0001g0105a0002c0003t0006g0003others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.-78+2548G>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128063949 | ||||||
| chr4:128063997
|
C | T | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(189): Show | 192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.-78+2596C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128063997 | ||||||
| chr4:128064155
|
C | A | 11 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(8): Show | 11 | HG01192.hp1 HG02486.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.-78+2754C>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128064155 | ||||||
| chr4:128064271
|
C | CAAAA | 40 | a0001c0001t0004g0311a0001c0001t0004g0325a0001c0001t0004g0326others(37): Show | 40 | HG00735.hp1 HG01109.hp1 HG02056.hp2 others(37): Show |
intron_variant | MODIFIER | c.-78+2886_-78+2889d others(6): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128064271 | |||||
| chr4:128064271
|
C | CAAAAA | 132 | a0001c0001t0001g0124a0001c0001t0001g0129a0001c0001t0001g0156others(129): Show | 132 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.-78+2885_-78+2889d others(7): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128064271 | |||||
| chr4:128064271
|
C | CAAAAAA | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(148): Show | 151 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.-78+2884_-78+2889d others(8): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128064271 | |||||
| chr4:128064271
|
C | CAAAAAAA | 9 | a0001c0001t0001g0010a0001c0001t0001g0141a0001c0001t0001g0162others(6): Show | 9 | HG00438.hp1 HG01175.hp2 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.-78+2883_-78+2889d others(9): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128064271 | |||||
| chr4:128064609
|
A | AGCAAAGA others(8): Show |
1 | a0001c0001t0003g0216 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-78+3209_-78+3223d others(17): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128064609 | |||||
| chr4:128064794
|
G | A | 11 | a0002c0003t0001g0104a0002c0003t0001g0105a0002c0003t0006g0003others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.-78+3393G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128064794 | ||||||
| chr4:128064887
|
C | T | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(163): Show | 166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.-78+3486C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128064887 | ||||||
| chr4:128064924
|
T | C | 11 | a0002c0003t0001g0104a0002c0003t0001g0105a0002c0003t0006g0003others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.-78+3523T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128064924 | ||||||
| chr4:128064958
|
G | C | 2 | a0001c0001t0001g0163a0001c0001t0001g0164 | 2 | HG00639.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.-78+3557G>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128064958 | ||||||
| chr4:128065130
|
A | G | 1 | a0001c0001t0001g0201 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-78+3729A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065130 | ||||||
| chr4:128065193
|
C | CATAGTGT others(4): Show |
334 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(331): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.-78+3794_-78+3804d others(13): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128065193 | |||||
| chr4:128065194
|
A | ATAGTGTA others(4): Show |
1 | a0001c0001t0004g0313 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-78+3803_-78+3804i others(13): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128065194 | |||||
| chr4:128065247
|
CAATT | C | 23 | a0001c0001t0001g0011a0001c0001t0001g0153a0001c0001t0001g0196others(20): Show | 23 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(20): Show |
intron_variant | MODIFIER | c.-78+3851_-78+3854d others(6): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128065247 | |||||
| chr4:128065249
|
A | ATTTCTTT others(5): Show |
1 | a0001c0001t0017g0106 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-78+3850_-78+3851i others(14): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128065249 | |||||
| chr4:128065249
|
A | ATTTCTTT others(9): Show |
1 | a0001c0001t0001g0161 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-78+3850_-78+3851i others(18): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128065249 | |||||
| chr4:128065249
|
ATTAATTT others(1): Show |
A | 19 | a0001c0001t0001g0010a0001c0001t0001g0126a0001c0001t0001g0157others(16): Show | 19 | HG00423.hp2 HG01168.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-78+3851_-78+3858d others(10): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128065249 | |||||
| chr4:128065249
|
ATTAATTT others(5): Show |
A | 13 | a0001c0001t0001g0002a0001c0001t0001g0194a0001c0001t0001g0195others(10): Show | 13 | HG00673.hp2 HG01975.hp1 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.-78+3851_-78+3862d others(14): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128065249 | |||||
| chr4:128065249
|
ATTAATTT others(9): Show |
A | 8 | a0001c0001t0001g0108a0001c0001t0001g0124a0001c0001t0001g0259others(5): Show | 8 | HG00438.hp1 HG02165.hp2 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.-78+3851_-78+3866d others(18): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128065249 | |||||
| chr4:128065249
|
ATTAATTT others(13): Show |
A | 2 | a0001c0001t0003g0125a0001c0001t0003g0212 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-78+3851_-78+3870d others(22): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128065249 | |||||
| chr4:128065249
|
ATTAATTT others(17): Show |
A | 2 | a0001c0001t0003g0102a0001c0001t0003g0103 | 2 | HG01175.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.-78+3851_-78+3874d others(26): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128065249 | |||||
| chr4:128065252
|
A | T | 111 | a0001c0001t0001g0001a0001c0001t0001g0107a0001c0001t0001g0109others(108): Show | 111 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.-78+3851A>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065252 | ||||||
| chr4:128065253
|
A | ATTTC | 14 | a0002c0002t0002g0026a0002c0002t0002g0047a0002c0002t0002g0049others(11): Show | 14 | HG01070.hp2 HG01106.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.-78+3914_-78+3917d others(6): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128065253 | |||||
| chr4:128065253
|
A | ATTTCTTT others(1): Show |
8 | a0002c0002t0002g0018a0002c0002t0002g0052a0002c0002t0002g0084others(5): Show | 8 | HG02071.hp2 HG03098.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.-78+3910_-78+3917d others(10): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128065253 | |||||
| chr4:128065253
|
A | ATTTCTTT others(5): Show |
3 | a0002c0002t0002g0053a0002c0002t0002g0087a0002c0002t0002g0095 | 3 | HG02055.hp2 NA18985.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.-78+3906_-78+3917d others(14): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128065253 | |||||
| chr4:128065253
|
A | ATTTCTTT others(9): Show |
2 | a0002c0002t0002g0027a0002c0002t0002g0032 | 2 | NA18950.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-78+3902_-78+3917d others(18): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128065253 | |||||
| chr4:128065253
|
A | C | 46 | a0001c0001t0001g0109a0001c0001t0001g0134a0001c0001t0001g0135others(43): Show | 46 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.-78+3852A>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065253 | ||||||
| chr4:128065253
|
ATTTC | A | 15 | a0002c0002t0002g0014a0002c0002t0002g0040a0002c0002t0002g0041others(12): Show | 15 | HG00735.hp2 HG01081.hp2 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.-78+3914_-78+3917d others(6): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128065253 | |||||
| chr4:128065253
|
ATTTCTTT others(1): Show |
A | 16 | a0002c0002t0002g0035a0002c0002t0002g0060a0002c0002t0002g0061others(13): Show | 16 | HG00741.hp2 HG01074.hp2 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.-78+3910_-78+3917d others(10): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128065253 | |||||
| chr4:128065253
|
ATTTCTTT others(5): Show |
A | 6 | a0001c0001t0004g0313a0001c0001t0004g0314a0002c0002t0002g0034others(3): Show | 6 | HG02280.hp1 NA18747.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.-78+3906_-78+3917d others(14): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128065253 | |||||
| chr4:128065253
|
ATTTCTTT others(9): Show |
A | 3 | a0002c0002t0002g0058a0002c0002t0002g0296a0002c0003t0005g0122 | 3 | HG02015.hp1 HG02970.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.-78+3902_-78+3917d others(18): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128065253 | |||||
| chr4:128065253
|
ATTTCTTT others(13): Show |
A | 4 | a0002c0002t0002g0307a0002c0002t0002g0331a0002c0002t0002g0333others(1): Show | 4 | HG02523.hp2 NA18989.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.-78+3898_-78+3917d others(22): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128065253 | |||||
| chr4:128065256
|
T | A | 26 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(23): Show | 26 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.-78+3855T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065256 | ||||||
| chr4:128065257
|
C | A | 64 | a0001c0001t0001g0001a0001c0001t0001g0107a0001c0001t0001g0129others(61): Show | 64 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.-78+3856C>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065257 | ||||||
| chr4:128065260
|
T | A | 1 | a0001c0001t0004g0308 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-78+3859T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065260 | ||||||
| chr4:128065261
|
C | A | 8 | a0001c0001t0001g0137a0001c0001t0001g0142a0001c0001t0001g0166others(5): Show | 8 | HG01346.hp2 HG02572.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.-78+3860C>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065261 | ||||||
| chr4:128065264
|
T | A | 1 | a0008c0009t0005g0113 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-78+3863T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065264 | ||||||
| chr4:128065265
|
C | A | 4 | a0001c0001t0001g0211a0007c0008t0001g0138a0008c0009t0005g0113others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-78+3864C>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065265 | ||||||
| chr4:128065268
|
T | A | 2 | a0001c0001t0004g0313a0001c0001t0004g0314 | 2 | NA19005.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.-78+3867T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065268 | ||||||
| chr4:128065269
|
C | A | 3 | a0001c0001t0001g0211a0001c0001t0004g0313a0001c0001t0004g0314 | 3 | HG02572.hp2 NA19005.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.-78+3868C>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065269 | ||||||
| chr4:128065272
|
T | A | 1 | a0002c0003t0005g0122 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-78+3871T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065272 | ||||||
| chr4:128065273
|
C | A | 2 | a0001c0001t0001g0211a0002c0003t0005g0122 | 2 | HG02572.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-78+3872C>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065273 | ||||||
| chr4:128065277
|
C | A | 1 | a0001c0001t0001g0211 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-78+3876C>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065277 | ||||||
| chr4:128065293
|
CTTTCTTT others(15): Show |
C | 1 | a0001c0001t0001g0249 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-78+3894_-78+3915d others(24): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128065293 | |||||
| chr4:128065297
|
CTTTCTTT others(3): Show |
C | 2 | a0001c0001t0004g0335a0002c0002t0002g0057 | 2 | HG00639.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.-78+3898_-78+3907d others(12): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128065297 | |||||
| chr4:128065297
|
CTTTCTTT others(11): Show |
C | 1 | a0001c0001t0001g0167 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-78+3898_-78+3915d others(20): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128065297 | |||||
| chr4:128065299
|
T | C | 1 | a0001c0001t0001g0149 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-78+3898T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065299 | ||||||
| chr4:128065301
|
CTTTCTT | C | 5 | a0001c0001t0004g0309a0001c0001t0004g0315a0001c0001t0004g0317others(2): Show | 5 | HG00738.hp2 HG02056.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.-78+3902_-78+3907d others(8): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128065301 | |||||
| chr4:128065301
|
CTTTCTTT others(3): Show |
C | 3 | a0002c0002t0002g0054a0002c0002t0002g0055a0010c0011t0005g0123 | 3 | HG02280.hp2 NA18954.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.-78+3902_-78+3911d others(12): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128065301 | |||||
| chr4:128065301
|
CTTTCTTT others(7): Show |
C | 3 | a0001c0001t0001g0265a0003c0004t0001g0182a0003c0004t0001g0183 | 3 | HG01167.hp2 HG01169.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.-78+3902_-78+3915d others(16): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128065301 | |||||
| chr4:128065303
|
T | C | 5 | a0001c0001t0001g0149a0001c0001t0004g0311a0001c0001t0004g0318others(2): Show | 5 | HG00544.hp1 HG00558.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.-78+3902T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065303 | ||||||
| chr4:128065303
|
TTCTTTCT others(9): Show |
T | 5 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0169others(2): Show | 5 | HG01346.hp2 HG03654.hp2 NA18942.hp2 others(2): Show |
intron_variant | MODIFIER | c.-78+3906_-78+3921d others(18): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128065303 | |||||
| chr4:128065307
|
T | C | 23 | a0001c0001t0001g0137a0001c0001t0001g0141a0001c0001t0001g0143others(20): Show | 23 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.-78+3906T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065307 | ||||||
| chr4:128065307
|
TTCTTTCT others(5): Show |
T | 3 | a0001c0001t0001g0107a0002c0002t0002g0038a0007c0008t0001g0138 | 3 | HG02559.hp1 HG03130.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-78+3910_-78+3921d others(14): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128065307 | |||||
| chr4:128065309
|
CTTTCTT | C | 4 | a0001c0001t0001g0171a0001c0001t0001g0184a0001c0001t0003g0250others(1): Show | 4 | HG00738.hp1 HG02735.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.-78+3910_-78+3915d others(8): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128065309 | |||||
| chr4:128065311
|
T | C | 67 | a0001c0001t0001g0124a0001c0001t0001g0129a0001c0001t0001g0137others(64): Show | 67 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.-78+3910T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065311 | ||||||
| chr4:128065311
|
TTCTTTCT others(1): Show |
T | 4 | a0001c0001t0001g0146a0001c0001t0001g0176a0001c0001t0001g0186others(1): Show | 4 | HG01943.hp1 HG02071.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-78+3914_-78+3921d others(10): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128065311 | |||||
| chr4:128065312
|
T | C | 1 | a0001c0001t0001g0149 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-78+3911T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065312 | ||||||
| chr4:128065313
|
C | CTCT | 3 | a0001c0001t0001g0141a0001c0001t0001g0143a0001c0001t0001g0144 | 3 | HG01243.hp1 HG01256.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.-78+3913_-78+3914i others(5): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128065313 | |||||
| chr4:128065315
|
T | C | 111 | a0001c0001t0001g0110a0001c0001t0001g0124a0001c0001t0001g0126others(108): Show | 111 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.-78+3914T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065315 | ||||||
| chr4:128065316
|
T | C | 3 | a0001c0001t0001g0141a0001c0001t0001g0143a0001c0001t0001g0144 | 3 | HG01243.hp1 HG01256.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.-78+3915T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065316 | ||||||
| chr4:128065317
|
C | CTTTCTT | 3 | a0001c0001t0003g0248a0002c0002t0002g0031a0002c0002t0002g0090 | 3 | HG04184.hp1 NA18974.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.-78+3917_-78+3918i others(8): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128065317 | |||||
| chr4:128065317
|
C | CTTTCTTT others(3): Show |
1 | a0002c0002t0002g0088 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-78+3917_-78+3918i others(12): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128065317 | |||||
| chr4:128065317
|
C | T | 5 | a0001c0001t0001g0137a0001c0001t0001g0170a0001c0001t0001g0201others(2): Show | 5 | HG00544.hp1 HG01071.hp2 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.-78+3916C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065317 | ||||||
| chr4:128065319
|
C | T | 51 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(48): Show | 51 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.-78+3918C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065319 | ||||||
| chr4:128065319
|
CTCTCT | C | 4 | a0001c0001t0001g0137a0001c0001t0001g0170a0001c0001t0001g0201others(1): Show | 4 | HG00544.hp1 HG01071.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.-78+3919_-78+3923d others(7): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065319 | ||||||
| chr4:128065320
|
T | TTTC | 7 | a0001c0001t0001g0129a0001c0001t0001g0173a0001c0001t0001g0174others(4): Show | 7 | HG00558.hp2 HG00642.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-78+3919_-78+3920i others(5): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065320 | ||||||
| chr4:128065321
|
C | CT | 3 | a0001c0001t0001g0141a0001c0001t0001g0143a0001c0001t0001g0144 | 3 | HG01243.hp1 HG01256.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.-78+3921dupT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128065321 | |||||
| chr4:128065321
|
C | T | 15 | a0001c0001t0001g0145a0001c0001t0001g0150a0001c0001t0001g0163others(12): Show | 15 | HG00639.hp2 HG01099.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-78+3920C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065321 | ||||||
| chr4:128065323
|
C | CCTTTCTT others(6): Show |
1 | a0001c0001t0001g0145 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-78+3922_-78+3923i others(15): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065323 | ||||||
| chr4:128065323
|
C | T | 17 | a0001c0001t0001g0129a0001c0001t0001g0141a0001c0001t0001g0143others(14): Show | 17 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(14): Show |
intron_variant | MODIFIER | c.-78+3922C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065323 | ||||||
| chr4:128065323
|
CT | C | 10 | a0001c0001t0001g0150a0001c0001t0001g0164a0001c0001t0001g0185others(7): Show | 10 | HG01099.hp1 HG01109.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.-78+3923delT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065323 | ||||||
| chr4:128065323
|
CTCTCTCT others(16): Show |
C | 1 | a0005c0006t0001g0101 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-78+3924_-78+3946d others(25): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128065323 | |||||
| chr4:128065324
|
T | TTTC | 13 | a0001c0001t0001g0152a0001c0001t0001g0162a0001c0001t0001g0179others(10): Show | 13 | HG00140.hp2 HG00609.hp2 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.-78+3923_-78+3924i others(5): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065324 | ||||||
| chr4:128065325
|
C | T | 48 | a0001c0001t0001g0110a0001c0001t0001g0124a0001c0001t0001g0126others(45): Show | 48 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.-78+3924C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065325 | ||||||
| chr4:128065326
|
TCTCTCTT others(2): Show |
T | 5 | a0001c0001t0003g0128a0001c0001t0003g0214a0001c0001t0003g0225others(2): Show | 5 | HG03195.hp1 HG03486.hp2 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.-78+3928_-78+3936d others(11): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128065326 | |||||
| chr4:128065327
|
C | T | 62 | a0001c0001t0001g0129a0001c0001t0001g0137a0001c0001t0001g0141others(59): Show | 62 | HG00140.hp2 HG00544.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.-78+3926C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065327 | ||||||
| chr4:128065327
|
CTCT | C | 45 | a0001c0001t0001g0110a0001c0001t0001g0124a0001c0001t0001g0126others(42): Show | 45 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.-78+3927_-78+3929d others(5): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065327 | ||||||
| chr4:128065327
|
CTCTCTTT others(7): Show |
C | 4 | a0001c0001t0003g0127a0001c0001t0003g0210a0001c0001t0003g0218others(1): Show | 4 | HG01934.hp2 HG01975.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.-78+3928_-78+3941d others(16): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128065327 | |||||
| chr4:128065327
|
CTCTCTTT others(9): Show |
C | 1 | a0001c0001t0001g0236 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-78+3930_-78+3945d others(18): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128065327 | |||||
| chr4:128065327
|
CTCTCTTT others(17): Show |
C | 1 | a0002c0002t0002g0039 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-78+3928_-78+3951d others(26): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128065327 | |||||
| chr4:128065329
|
C | T | 49 | a0001c0001t0001g0001a0001c0001t0001g0129a0001c0001t0001g0134others(46): Show | 49 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.-78+3928C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065329 | ||||||
| chr4:128065329
|
CT | C | 19 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0001t0001g0184others(16): Show | 19 | HG00639.hp1 HG00738.hp1 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.-78+3929delT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065329 | ||||||
| chr4:128065330
|
T | C | 12 | a0001c0001t0001g0129a0001c0001t0001g0141a0001c0001t0001g0143others(9): Show | 12 | HG00558.hp2 HG00642.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.-78+3929T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065330 | ||||||
| chr4:128065330
|
T | TC | 23 | a0001c0001t0001g0142a0001c0001t0001g0153a0001c0001t0001g0154others(20): Show | 23 | HG00280.hp1 HG00558.hp1 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.-78+3930dupC | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128065330 | |||||
| chr4:128065330
|
T | TTTTC | 6 | a0001c0001t0001g0152a0001c0001t0001g0191a0001c0001t0004g0323others(3): Show | 6 | HG00140.hp2 HG02074.hp2 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.-78+3929_-78+3930i others(6): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065330 | ||||||
| chr4:128065330
|
TC | T | 26 | a0001c0001t0001g0137a0001c0001t0001g0149a0001c0001t0001g0150others(23): Show | 26 | HG00544.hp1 HG00609.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.-78+3930delC | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065330 | ||||||
| chr4:128065331
|
C | CCTTTCT | 9 | a0001c0001t0001g0001a0001c0001t0001g0135a0001c0001t0001g0136others(6): Show | 9 | HG00408.hp2 HG00673.hp1 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.-78+3930_-78+3931i others(8): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065331 | ||||||
| chr4:128065331
|
C | CCTTTCTT others(4): Show |
2 | a0001c0001t0001g0200a0001c0001t0004g0312 | 2 | NA18955.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-78+3930_-78+3931i others(13): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065331 | ||||||
| chr4:128065331
|
C | CCTTTCTT others(9): Show |
1 | a0001c0001t0001g0208 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-78+3930_-78+3931i others(18): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065331 | ||||||
| chr4:128065331
|
C | T | 19 | a0001c0001t0001g0129a0001c0001t0001g0134a0001c0001t0001g0141others(16): Show | 19 | HG00140.hp2 HG00558.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.-78+3930C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065331 | ||||||
| chr4:128065332
|
TTTC | T | 7 | a0002c0003t0001g0105a0002c0003t0006g0003a0002c0003t0006g0004others(4): Show | 7 | HG02145.hp2 HG02257.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-78+3932_-78+3934d others(5): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065332 | ||||||
| chr4:128065333
|
T | C | 7 | a0001c0001t0003g0245a0001c0001t0003g0246a0001c0001t0007g0133others(4): Show | 7 | HG00280.hp2 HG01496.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.-78+3932T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065333 | ||||||
| chr4:128065335
|
C | CT | 4 | a0002c0002t0002g0031a0002c0002t0002g0088a0002c0003t0006g0007others(1): Show | 4 | HG02109.hp1 HG02630.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.-78+3934_-78+3935i others(3): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065335 | ||||||
| chr4:128065336
|
C | CTTTCT | 18 | a0001c0001t0001g0108a0001c0001t0001g0155a0002c0002t0002g0017others(15): Show | 18 | HG00735.hp1 HG01496.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.-78+3978_-78+3982d others(7): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128065336 | |||||
| chr4:128065336
|
C | CTTTCTTT others(3): Show |
8 | a0001c0001t0001g0109a0001c0001t0001g0148a0001c0001t0001g0181others(5): Show | 8 | HG01256.hp2 HG01258.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-78+3973_-78+3982d others(12): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128065336 | |||||
| chr4:128065336
|
C | T | 147 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0124others(144): Show | 147 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.-78+3935C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065336 | ||||||
| chr4:128065336
|
CTTTCT | C | 14 | a0001c0001t0001g0159a0001c0001t0003g0252a0002c0002t0002g0034others(11): Show | 14 | HG00741.hp2 HG01884.hp2 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.-78+3978_-78+3982d others(7): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128065336 | |||||
| chr4:128065336
|
CTTTCTTT others(3): Show |
C | 6 | a0001c0001t0003g0253a0002c0002t0002g0066a0002c0002t0002g0284others(3): Show | 6 | HG01433.hp1 HG02055.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-78+3973_-78+3982d others(12): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128065336 | |||||
| chr4:128065336
|
CTTTCTTT others(8): Show |
C | 2 | a0005c0006t0001g0099a0005c0006t0001g0100 | 2 | HG01168.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-78+3968_-78+3982d others(17): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128065336 | |||||
| chr4:128065337
|
T | C | 1 | a0002c0002t0002g0068 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-78+3936T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065337 | ||||||
| chr4:128065341
|
T | C | 20 | a0001c0001t0003g0128a0001c0001t0003g0214a0001c0001t0003g0225others(17): Show | 20 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.-78+3940T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065341 | ||||||
| chr4:128065346
|
T | C | 7 | a0001c0001t0001g0236a0001c0001t0003g0127a0001c0001t0003g0210others(4): Show | 7 | HG00280.hp2 HG01496.hp2 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.-78+3945T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065346 | ||||||
| chr4:128065351
|
T | C | 1 | a0005c0006t0001g0101 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-78+3950T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065351 | ||||||
| chr4:128065356
|
T | C | 1 | a0002c0002t0002g0039 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-78+3955T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065356 | ||||||
| chr4:128065512
|
A | G | 1 | a0001c0001t0001g0169 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-78+4111A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065512 | ||||||
| chr4:128065577
|
C | A | 5 | a0001c0001t0004g0315a0001c0001t0004g0319a0001c0001t0004g0321others(2): Show | 5 | HG02056.hp2 HG02129.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.-78+4176C>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065577 | ||||||
| chr4:128065719
|
C | T | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(207): Show | 210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.-78+4318C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065719 | ||||||
| chr4:128065815
|
C | T | 3 | a0002c0002t0002g0114a0002c0002t0012g0065a0002c0002t0012g0096 | 3 | HG02080.hp1 NA18982.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.-78+4414C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065815 | ||||||
| chr4:128065940
|
C | G | 2 | a0008c0009t0005g0113a0008c0009t0005g0119 | 2 | HG02572.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-78+4539C>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065940 | ||||||
| chr4:128065987
|
A | G | 15 | a0002c0002t0002g0019a0002c0002t0002g0021a0002c0002t0002g0022others(12): Show | 15 | HG00735.hp1 HG01109.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.-78+4586A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128065987 | ||||||
| chr4:128066165
|
C | CT | 19 | a0002c0002t0002g0031a0002c0002t0002g0037a0002c0002t0002g0046others(16): Show | 19 | HG00597.hp1 HG00741.hp2 HG02074.hp2 others(16): Show |
intron_variant | MODIFIER | c.-78+4785dupT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128066165 | |||||
| chr4:128066165
|
C | CTT | 122 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(119): Show | 122 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.-78+4784_-78+4785d others(4): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128066165 | |||||
| chr4:128066165
|
C | CTTT | 48 | a0001c0001t0001g0001a0001c0001t0001g0108a0001c0001t0001g0129others(45): Show | 48 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.-78+4783_-78+4785d others(5): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128066165 | |||||
| chr4:128066165
|
C | CTTTT | 23 | a0001c0001t0001g0142a0001c0001t0001g0260a0001c0001t0003g0240others(20): Show | 23 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.-78+4782_-78+4785d others(6): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128066165 | |||||
| chr4:128066191
|
T | A | 1 | a0002c0002t0002g0090 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-78+4790T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128066191 | ||||||
| chr4:128066228
|
G | A | 164 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(161): Show | 164 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.-78+4827G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128066228 | ||||||
| chr4:128066257
|
A | G | 2 | a0008c0009t0005g0113a0008c0009t0005g0119 | 2 | HG02572.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-78+4856A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128066257 | ||||||
| chr4:128066297
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-78+4896C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128066297 | ||||||
| chr4:128066322
|
G | A | 3 | a0001c0001t0001g0167a0001c0001t0001g0170a0001c0001t0001g0173 | 3 | HG02257.hp2 HG03225.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-78+4921G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128066322 | ||||||
| chr4:128066369
|
G | A | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(163): Show | 166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.-78+4968G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128066369 | ||||||
| chr4:128066423
|
C | T | 1 | a0002c0002t0011g0030 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-78+5022C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128066423 | ||||||
| chr4:128066477
|
CT | C | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(185): Show | 188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.-78+5093delT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128066477 | |||||
| chr4:128066678
|
A | G | 8 | a0001c0001t0003g0213a0001c0001t0003g0214a0001c0001t0003g0225others(5): Show | 8 | HG02015.hp2 NA18950.hp1 NA18969.hp2 others(5): Show |
intron_variant | MODIFIER | c.-78+5277A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128066678 | ||||||
| chr4:128066797
|
A | AT | 6 | a0001c0001t0003g0279a0001c0001t0004g0314a0002c0002t0002g0046others(3): Show | 6 | HG02071.hp2 HG02818.hp1 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.-78+5413dupT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128066797 | |||||
| chr4:128066797
|
AT | A | 84 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(81): Show | 84 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.-78+5413delT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128066797 | |||||
| chr4:128066797
|
ATT | A | 86 | a0001c0001t0001g0001a0001c0001t0001g0108a0001c0001t0001g0109others(83): Show | 86 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.-78+5412_-78+5413d others(4): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128066797 | |||||
| chr4:128066854
|
T | A | 22 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(19): Show | 22 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.-78+5453T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128066854 | ||||||
| chr4:128066859
|
C | T | 2 | a0001c0001t0001g0178a0001c0001t0001g0191 | 2 | HG00140.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-78+5458C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128066859 | ||||||
| chr4:128066885
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-78+5484C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128066885 | ||||||
| chr4:128066942
|
C | CT | 3 | a0001c0001t0001g0108a0001c0001t0003g0248a0001c0001t0003g0279 | 3 | NA18974.hp1 NA18985.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.-78+5541_-78+5542i others(3): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128066942 | ||||||
| chr4:128066960
|
C | T | 3 | a0002c0003t0005g0122a0002c0012t0005g0098a0010c0011t0005g0123 | 3 | HG02280.hp2 HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-78+5559C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128066960 | ||||||
| chr4:128067044
|
T | C | 1 | a0002c0002t0002g0056 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-78+5643T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128067044 | ||||||
| chr4:128067710
|
CT | C | 207 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(204): Show | 207 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.-78+6322delT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128067710 | |||||
| chr4:128067735
|
A | T | 1 | a0001c0001t0001g0200 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-78+6334A>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128067735 | ||||||
| chr4:128067802
|
C | T | 2 | a0006c0007t0009g0192a0006c0007t0009g0204 | 2 | HG03139.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-78+6401C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128067802 | ||||||
| chr4:128067911
|
C | T | 1 | a0002c0002t0005g0059 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-78+6510C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128067911 | ||||||
| chr4:128067933
|
T | C | 1 | a0002c0002t0002g0084 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-77-6527T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128067933 | ||||||
| chr4:128068070
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-77-6390C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128068070 | ||||||
| chr4:128068101
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-77-6359C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128068101 | ||||||
| chr4:128068171
|
C | T | 4 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-77-6289C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128068171 | ||||||
| chr4:128068172
|
G | A | 163 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(160): Show | 163 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.-77-6288G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128068172 | ||||||
| chr4:128068256
|
G | C | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(189): Show | 192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.-77-6204G>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128068256 | ||||||
| chr4:128068531
|
C | T | 1 | a0001c0001t0004g0318 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-77-5929C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128068531 | ||||||
| chr4:128068551
|
G | A | 1 | a0001c0001t0004g0324 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-77-5909G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128068551 | ||||||
| chr4:128068814
|
CAA | C | 22 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(19): Show | 22 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.-77-5641_-77-5640d others(4): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128068814 | |||||
| chr4:128069269
|
C | T | 1 | a0002c0002t0002g0295 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-77-5191C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128069269 | ||||||
| chr4:128069287
|
T | C | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(164): Show | 167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.-77-5173T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128069287 | ||||||
| chr4:128069299
|
A | G | 1 | a0002c0019t0002g0083 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-77-5161A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128069299 | ||||||
| chr4:128069319
|
G | T | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(190): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.-77-5141G>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128069319 | ||||||
| chr4:128069405
|
A | C | 3 | a0002c0003t0005g0122a0002c0012t0005g0098a0010c0011t0005g0123 | 3 | HG02280.hp2 HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-77-5055A>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128069405 | ||||||
| chr4:128069409
|
G | A | 1 | a0001c0001t0004g0326 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-77-5051G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128069409 | ||||||
| chr4:128069424
|
C | A | 22 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(19): Show | 22 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.-77-5036C>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128069424 | ||||||
| chr4:128069430
|
G | A | 1 | a0002c0002t0002g0021 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-77-5030G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128069430 | ||||||
| chr4:128069795
|
T | A | 1 | a0001c0001t0001g0211 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-77-4665T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128069795 | ||||||
| chr4:128069816
|
T | C | 2 | a0002c0002t0002g0018a0002c0002t0002g0079 | 2 | NA18982.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.-77-4644T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128069816 | ||||||
| chr4:128070040
|
C | T | 3 | a0007c0008t0001g0138a0007c0008t0001g0139a0007c0008t0001g0158 | 3 | HG03486.hp2 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-77-4420C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128070040 | ||||||
| chr4:128070287
|
T | G | 164 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(161): Show | 164 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.-77-4173T>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128070287 | ||||||
| chr4:128070315
|
G | A | 2 | a0002c0003t0001g0104a0002c0003t0001g0105 | 2 | HG02145.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-77-4145G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128070315 | ||||||
| chr4:128070409
|
C | G | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(190): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.-77-4051C>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128070409 | ||||||
| chr4:128070437
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-77-4023G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128070437 | ||||||
| chr4:128070530
|
T | C | 226 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(223): Show | 226 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.-77-3930T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128070530 | ||||||
| chr4:128070626
|
A | G | 1 | a0002c0019t0002g0083 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-77-3834A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128070626 | ||||||
| chr4:128070799
|
TA | T | 12 | a0001c0001t0004g0308a0002c0003t0001g0104a0002c0003t0001g0105others(9): Show | 12 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-77-3650delA | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128070799 | |||||
| chr4:128070904
|
A | C | 1 | a0001c0001t0001g0273 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-77-3556A>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128070904 | ||||||
| chr4:128070992
|
G | C | 1 | a0001c0001t0001g0211 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-77-3468G>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128070992 | ||||||
| chr4:128070993
|
C | A | 1 | a0001c0001t0001g0211 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-77-3467C>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128070993 | ||||||
| chr4:128071157
|
C | T | 2 | a0006c0007t0009g0192a0006c0007t0009g0204 | 2 | HG03139.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-77-3303C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128071157 | ||||||
| chr4:128071303
|
C | G | 1 | a0002c0002t0005g0059 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-77-3157C>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128071303 | ||||||
| chr4:128071421
|
A | AT | 15 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0171others(12): Show | 15 | HG00735.hp2 HG00738.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.-77-3019dupT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128071421 | |||||
| chr4:128071421
|
AT | A | 35 | a0001c0001t0001g0135a0001c0001t0003g0216a0001c0001t0003g0230others(32): Show | 35 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.-77-3019delT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128071421 | |||||
| chr4:128071421
|
ATT | A | 11 | a0002c0003t0001g0104a0002c0003t0001g0105a0002c0003t0006g0003others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.-77-3020_-77-3019d others(4): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128071421 | |||||
| chr4:128071445
|
A | C | 1 | a0002c0002t0002g0130 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-77-3015A>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128071445 | ||||||
| chr4:128071560
|
T | A | 3 | a0002c0003t0005g0122a0002c0012t0005g0098a0010c0011t0005g0123 | 3 | HG02280.hp2 HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-77-2900T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128071560 | ||||||
| chr4:128071713
|
C | T | 1 | a0002c0012t0005g0098 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-77-2747C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128071713 | ||||||
| chr4:128071918
|
A | G | 1 | a0002c0002t0011g0030 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-77-2542A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128071918 | ||||||
| chr4:128071920
|
A | T | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(189): Show | 192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.-77-2540A>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128071920 | ||||||
| chr4:128072002
|
C | CTTTATTT others(1): Show |
225 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(222): Show | 225 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.-77-2450_-77-2443d others(10): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128072002 | |||||
| chr4:128072030
|
C | T | 3 | a0005c0006t0001g0099a0005c0006t0001g0100a0005c0006t0001g0101 | 3 | HG01168.hp1 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-77-2430C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128072030 | ||||||
| chr4:128072126
|
A | G | 1 | a0002c0002t0002g0038 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-77-2334A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128072126 | ||||||
| chr4:128072285
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-77-2175G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128072285 | ||||||
| chr4:128072394
|
A | G | 1 | a0002c0002t0002g0033 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-77-2066A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128072394 | ||||||
| chr4:128072435
|
G | A | 5 | a0002c0002t0002g0018a0002c0002t0002g0032a0002c0002t0002g0047others(2): Show | 5 | NA18950.hp2 NA18973.hp2 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.-77-2025G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128072435 | ||||||
| chr4:128072501
|
T | C | 1 | a0003c0004t0001g0264 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-77-1959T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128072501 | ||||||
| chr4:128072625
|
C | T | 59 | a0001c0001t0001g0211a0001c0001t0001g0236a0001c0001t0001g0249others(56): Show | 59 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.-77-1835C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128072625 | ||||||
| chr4:128072705
|
C | T | 1 | a0002c0002t0002g0053 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-77-1755C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128072705 | ||||||
| chr4:128072887
|
G | A | 11 | a0002c0003t0001g0104a0002c0003t0001g0105a0002c0003t0006g0003others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.-77-1573G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128072887 | ||||||
| chr4:128072942
|
T | C | 3 | a0005c0006t0001g0099a0005c0006t0001g0100a0005c0006t0001g0101 | 3 | HG01168.hp1 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-77-1518T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128072942 | ||||||
| chr4:128073090
|
A | G | 3 | a0005c0006t0001g0099a0005c0006t0001g0100a0005c0006t0001g0101 | 3 | HG01168.hp1 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-77-1370A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128073090 | ||||||
| chr4:128073157
|
T | C | 1 | a0002c0002t0002g0043 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-77-1303T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128073157 | ||||||
| chr4:128073268
|
T | C | 2 | a0001c0001t0003g0237a0001c0001t0003g0244 | 2 | HG00140.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-77-1192T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128073268 | ||||||
| chr4:128073341
|
C | T | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(164): Show | 167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.-77-1119C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128073341 | ||||||
| chr4:128073360
|
G | T | 22 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(19): Show | 22 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.-77-1100G>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128073360 | ||||||
| chr4:128073368
|
A | C | 1 | a0001c0001t0003g0231 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-77-1092A>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128073368 | ||||||
| chr4:128073418
|
CA | C | 15 | a0002c0002t0002g0019a0002c0002t0002g0021a0002c0002t0002g0028others(12): Show | 15 | HG00099.hp1 HG01243.hp2 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.-77-1013delA | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128073418 | |||||
| chr4:128073418
|
CAA | C | 38 | a0002c0002t0002g0014a0002c0002t0002g0015a0002c0002t0002g0017others(35): Show | 38 | HG00735.hp1 HG00735.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.-77-1014_-77-1013d others(4): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128073418 | |||||
| chr4:128073418
|
CAAA | C | 109 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(106): Show | 109 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.-77-1015_-77-1013d others(5): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128073418 | |||||
| chr4:128073418
|
CAAAA | C | 161 | a0001c0001t0001g0001a0001c0001t0001g0107a0001c0001t0001g0109others(158): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-77-1016_-77-1013d others(6): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128073418 | |||||
| chr4:128073441
|
A | G | 5 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0160others(2): Show | 5 | HG02486.hp2 HG02647.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-77-1019A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128073441 | ||||||
| chr4:128073444
|
A | G | 175 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(172): Show | 175 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.-77-1016A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128073444 | ||||||
| chr4:128073503
|
G | GAAAT | 163 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(160): Show | 163 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.-77-953_-77-950dup others(4): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128073503 | |||||
| chr4:128073523
|
CA | C | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(189): Show | 192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.-77-925delA | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128073523 | |||||
| chr4:128073572
|
G | GT | 14 | a0002c0002t0002g0028a0002c0002t0002g0038a0002c0002t0002g0041others(11): Show | 14 | HG01258.hp1 HG01496.hp1 HG01515.hp1 others(11): Show |
intron_variant | MODIFIER | c.-77-851dupT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128073572 | |||||
| chr4:128073572
|
G | GTT | 16 | a0002c0002t0002g0012a0002c0002t0002g0013a0002c0002t0002g0016others(13): Show | 16 | HG01074.hp2 HG01433.hp1 HG02083.hp1 others(13): Show |
intron_variant | MODIFIER | c.-77-852_-77-851dup others(2): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128073572 | |||||
| chr4:128073572
|
G | GTTT | 21 | a0001c0001t0001g0149a0002c0002t0002g0018a0002c0002t0002g0019others(18): Show | 21 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.-77-853_-77-851dup others(3): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128073572 | |||||
| chr4:128073572
|
G | GTTTT | 12 | a0001c0001t0001g0249a0002c0002t0002g0021a0002c0002t0002g0023others(9): Show | 12 | HG01106.hp1 HG02572.hp1 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.-77-854_-77-851dup others(4): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128073572 | |||||
| chr4:128073572
|
G | GTTTTT | 17 | a0002c0002t0002g0014a0002c0002t0002g0039a0002c0002t0002g0047others(14): Show | 17 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(14): Show |
intron_variant | MODIFIER | c.-77-855_-77-851dup others(5): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128073572 | |||||
| chr4:128073572
|
G | GTTTTTTT others(3): Show |
4 | a0002c0002t0002g0291a0002c0002t0002g0297a0002c0002t0002g0334others(1): Show | 4 | HG00544.hp1 HG01981.hp2 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.-77-860_-77-851dup others(10): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128073572 | |||||
| chr4:128073572
|
G | GTTTTTTT others(5): Show |
1 | a0002c0002t0008g0305 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-77-862_-77-851dup others(12): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128073572 | |||||
| chr4:128073572
|
G | GTTTTTTT others(16): Show |
1 | a0002c0002t0002g0292 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-77-873_-77-851dup others(23): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128073572 | |||||
| chr4:128073572
|
G | GTTTTTTT others(17): Show |
1 | a0001c0001t0001g0157 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-77-874_-77-851dup others(24): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128073572 | |||||
| chr4:128073572
|
GTTTTTTT others(7): Show |
G | 4 | a0001c0001t0001g0148a0001c0001t0001g0181a0002c0002t0002g0044others(1): Show | 4 | HG01981.hp1 NA18990.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.-77-864_-77-851del others(14): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128073572 | |||||
| chr4:128073572
|
GTTTTTTT others(8): Show |
G | 1 | a0002c0002t0005g0059 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-77-865_-77-851del others(15): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128073572 | |||||
| chr4:128073572
|
GTTTTTTT others(9): Show |
G | 1 | a0002c0002t0002g0033 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-77-866_-77-851del others(16): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128073572 | |||||
| chr4:128073572
|
GTTTTTTT others(10): Show |
G | 3 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133 | 3 | HG02486.hp1 HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-77-867_-77-851del others(17): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128073572 | |||||
| chr4:128073572
|
GTTTTTTT others(11): Show |
G | 4 | a0001c0001t0007g0258a0002c0002t0002g0024a0002c0002t0002g0095others(1): Show | 4 | HG00735.hp1 HG01891.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.-77-868_-77-851del others(18): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128073572 | |||||
| chr4:128073572
|
GTTTTTTT others(12): Show |
G | 7 | a0001c0001t0001g0170a0001c0001t0001g0275a0002c0002t0002g0026others(4): Show | 7 | HG01099.hp1 HG01109.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-77-869_-77-851del others(19): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128073572 | |||||
| chr4:128073572
|
GTTTTTTT others(14): Show |
G | 1 | a0002c0012t0005g0098 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-77-871_-77-851del others(21): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128073572 | |||||
| chr4:128073572
|
GTTTTTTT others(16): Show |
G | 1 | a0002c0002t0002g0330 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-77-873_-77-851del others(23): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128073572 | |||||
| chr4:128073585
|
T | TTG | 10 | a0001c0001t0001g0166a0002c0003t0001g0104a0002c0003t0001g0105others(7): Show | 10 | HG01346.hp2 HG02109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.-77-874_-77-873ins others(2): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128073585 | |||||
| chr4:128073586
|
T | G | 1 | a0001c0001t0003g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-77-874T>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128073586 | ||||||
| chr4:128073587
|
T | G | 2 | a0001c0001t0003g0252a0001c0001t0003g0253 | 2 | HG02015.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.-77-873T>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128073587 | ||||||
| chr4:128073587
|
T | TTG | 8 | a0001c0001t0003g0219a0001c0001t0003g0246a0001c0001t0003g0250others(5): Show | 8 | HG00280.hp2 HG01109.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.-77-872_-77-871ins others(2): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128073587 | |||||
| chr4:128073590
|
T | G | 3 | a0001c0001t0001g0109a0001c0001t0003g0252a0001c0001t0003g0276 | 3 | HG02015.hp2 HG02738.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-77-870T>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128073590 | ||||||
| chr4:128073590
|
T | TTTG | 23 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(20): Show | 23 | HG00544.hp2 HG00741.hp1 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.-77-868_-77-867ins others(3): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128073590 | |||||
| chr4:128073590
|
T | TTTTG | 10 | a0001c0001t0001g0129a0001c0001t0001g0167a0001c0001t0001g0185others(7): Show | 10 | HG01433.hp2 HG02074.hp1 HG02738.hp2 others(7): Show |
intron_variant | MODIFIER | c.-77-867_-77-866ins others(4): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128073590 | |||||
| chr4:128073591
|
T | G | 20 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0107others(17): Show | 20 | HG00140.hp2 HG00280.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.-77-869T>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128073591 | ||||||
| chr4:128073591
|
T | TTG | 72 | a0001c0001t0001g0124a0001c0001t0001g0126a0001c0001t0001g0134others(69): Show | 72 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.-77-868_-77-867ins others(2): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128073591 | |||||
| chr4:128073591
|
T | TTGTA | 12 | a0001c0001t0004g0308a0001c0001t0004g0310a0001c0001t0004g0311others(9): Show | 12 | HG00609.hp1 HG00738.hp2 HG02129.hp2 others(9): Show |
intron_variant | MODIFIER | c.-77-868_-77-867ins others(4): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128073591 | |||||
| chr4:128073591
|
T | TTTG | 30 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0108others(27): Show | 30 | HG00140.hp1 HG00673.hp1 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.-77-867_-77-866ins others(3): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128073591 | |||||
| chr4:128073591
|
T | TTTGTA | 7 | a0001c0001t0004g0309a0001c0001t0004g0312a0001c0001t0004g0315others(4): Show | 7 | HG00597.hp2 HG02056.hp2 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.-77-867_-77-866ins others(5): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr4 | 128073591 | |||||
| chr4:128073598
|
T | G | 1 | a0005c0006t0001g0099 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-77-862T>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128073598 | ||||||
| chr4:128073599
|
T | G | 2 | a0005c0006t0001g0100a0005c0006t0001g0101 | 2 | HG01168.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-77-861T>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128073599 | ||||||
| chr4:128073617
|
G | A | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(190): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.-77-843G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128073617 | ||||||
| chr4:128073863
|
T | A | 1 | a0010c0011t0005g0123 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-77-597T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128073863 | ||||||
| chr4:128074065
|
T | C | 204 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(201): Show | 204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.-77-395T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128074065 | ||||||
| chr4:128074096
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-77-364G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128074096 | ||||||
| chr4:128074308
|
G | A | 204 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(201): Show | 204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.-77-152G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 1/19 | chr4 | 128074308 | ||||||
| chr4:128074596
|
G | A | 164 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(161): Show | 164 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.-19+78G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 2/19 | chr4 | 128074596 | ||||||
| chr4:128074834
|
A | G | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(190): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.-18-100A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 2/19 | chr4 | 128074834 | ||||||
| chr4:128075075
|
A | G | 5 | a0001c0001t0001g0149a0001c0001t0001g0175a0001c0001t0001g0193others(2): Show | 5 | HG00280.hp1 HG00642.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.42+82A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 3/19 | chr4 | 128075075 | ||||||
| chr4:128075112
|
T | A | 11 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(8): Show | 11 | HG01192.hp1 HG02486.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.42+119T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 3/19 | chr4 | 128075112 | ||||||
| chr4:128075143
|
C | T | 36 | a0001c0001t0001g0108a0001c0001t0001g0124a0001c0001t0001g0129others(33): Show | 36 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.42+150C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 3/19 | chr4 | 128075143 | ||||||
| chr4:128075192
|
G | T | 1 | a0006c0007t0004g0234 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.42+199G>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 3/19 | chr4 | 128075192 | ||||||
| chr4:128075510
|
G | T | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(206): Show | 209 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.42+517G>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 3/19 | chr4 | 128075510 | ||||||
| chr4:128075511
|
A | T | 1 | a0001c0001t0003g0248 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.42+518A>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 3/19 | chr4 | 128075511 | ||||||
| chr4:128075698
|
C | A | 4 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.42+705C>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 3/19 | chr4 | 128075698 | ||||||
| chr4:128075758
|
G | A | 3 | a0001c0001t0001g0167a0001c0001t0001g0170a0001c0001t0001g0173 | 3 | HG02257.hp2 HG03225.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.42+765G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 3/19 | chr4 | 128075758 | ||||||
| chr4:128075819
|
T | C | 9 | a0002c0003t0006g0003a0002c0003t0006g0004a0002c0003t0006g0005others(6): Show | 9 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.42+826T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 3/19 | chr4 | 128075819 | ||||||
| chr4:128076106
|
C | T | 5 | a0002c0002t0010g0036a0002c0002t0010g0048a0002c0002t0010g0077others(2): Show | 5 | HG01243.hp2 HG03041.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.42+1113C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 3/19 | chr4 | 128076106 | ||||||
| chr4:128076499
|
A | C | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(190): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.43-1289A>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 3/19 | chr4 | 128076499 | ||||||
| chr4:128076571
|
C | T | 1 | a0002c0002t0002g0092 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.43-1217C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 3/19 | chr4 | 128076571 | ||||||
| chr4:128077011
|
G | A | 1 | a0010c0011t0005g0123 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.43-777G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 3/19 | chr4 | 128077011 | ||||||
| chr4:128077232
|
G | C | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(207): Show | 210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.43-556G>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 3/19 | chr4 | 128077232 | ||||||
| chr4:128077336
|
T | TA | 6 | a0002c0002t0002g0019a0002c0002t0002g0021a0002c0002t0002g0022others(3): Show | 6 | HG02809.hp2 HG02818.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.43-440dupA | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr4 | 128077336 | |||||
| chr4:128077509
|
C | T | 3 | a0002c0002t0002g0015a0002c0002t0002g0017a0002c0002t0002g0049 | 3 | HG02559.hp2 HG02622.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.43-279C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 3/19 | chr4 | 128077509 | ||||||
| chr4:128077565
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.43-223C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 3/19 | chr4 | 128077565 | ||||||
| chr4:128077687
|
A | C | 1 | a0001c0001t0001g0273 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.43-101A>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 3/19 | chr4 | 128077687 | ||||||
| chr4:128077975
|
A | G | 1 | a0001c0001t0003g0248 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.217+13A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 4/19 | chr4 | 128077975 | ||||||
| chr4:128078036
|
C | T | 3 | a0004c0005t0005g0281a0004c0005t0005g0282a0004c0005t0005g0283 | 3 | HG02055.hp1 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.217+74C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 4/19 | chr4 | 128078036 | ||||||
| chr4:128078211
|
T | C | 2 | a0002c0002t0002g0284a0002c0002t0002g0287 | 2 | HG01433.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.217+249T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 4/19 | chr4 | 128078211 | ||||||
| chr4:128078464
|
C | T | 164 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(161): Show | 164 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.217+502C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 4/19 | chr4 | 128078464 | ||||||
| chr4:128078758
|
T | C | 1 | a0002c0002t0002g0085 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.217+796T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 4/19 | chr4 | 128078758 | ||||||
| chr4:128078924
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.217+962C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 4/19 | chr4 | 128078924 | ||||||
| chr4:128078969
|
A | G | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(164): Show | 167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.217+1007A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 4/19 | chr4 | 128078969 | ||||||
| chr4:128079061
|
C | T | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(190): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.217+1099C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 4/19 | chr4 | 128079061 | ||||||
| chr4:128079062
|
G | A | 1 | a0002c0002t0002g0031 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.217+1100G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 4/19 | chr4 | 128079062 | ||||||
| chr4:128079092
|
C | CT | 78 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(75): Show | 78 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.217+1148dupT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr4 | 128079092 | |||||
| chr4:128079092
|
CTTTTTTT others(3): Show |
C | 91 | a0001c0001t0001g0001a0001c0001t0001g0107a0001c0001t0001g0108others(88): Show | 91 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.217+1139_217+1148d others(12): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr4 | 128079092 | |||||
| chr4:128079110
|
T | A | 1 | a0002c0019t0002g0083 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.217+1148T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 4/19 | chr4 | 128079110 | ||||||
| chr4:128079110
|
T | C | 1 | a0002c0002t0002g0130 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.217+1148T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 4/19 | chr4 | 128079110 | ||||||
| chr4:128079159
|
G | A | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(207): Show | 210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.217+1197G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 4/19 | chr4 | 128079159 | ||||||
| chr4:128079188
|
G | A | 1 | a0002c0002t0002g0063 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.217+1226G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 4/19 | chr4 | 128079188 | ||||||
| chr4:128079384
|
C | A | 2 | a0001c0001t0004g0311a0001c0001t0004g0326 | 2 | NA18984.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.217+1422C>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 4/19 | chr4 | 128079384 | ||||||
| chr4:128079384
|
C | T | 1 | a0001c0001t0001g0110 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.217+1422C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 4/19 | chr4 | 128079384 | ||||||
| chr4:128079440
|
G | A | 333 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(330): Show | 333 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.217+1478G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 4/19 | chr4 | 128079440 | ||||||
| chr4:128079584
|
A | G | 1 | a0001c0001t0001g0249 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.217+1622A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 4/19 | chr4 | 128079584 | ||||||
| chr4:128079631
|
G | A | 11 | a0002c0003t0001g0104a0002c0003t0001g0105a0002c0003t0006g0003others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.217+1669G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 4/19 | chr4 | 128079631 | ||||||
| chr4:128079649
|
G | A | 22 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(19): Show | 22 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.217+1687G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 4/19 | chr4 | 128079649 | ||||||
| chr4:128079890
|
C | T | 1 | a0001c0001t0004g0317 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.217+1928C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 4/19 | chr4 | 128079890 | ||||||
| chr4:128079986
|
C | A | 54 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0126others(51): Show | 54 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.217+2024C>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 4/19 | chr4 | 128079986 | ||||||
| chr4:128079986
|
C | CT | 6 | a0001c0001t0001g0129a0001c0001t0004g0313a0001c0001t0004g0317others(3): Show | 6 | HG00738.hp2 HG02055.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.217+2039dupT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr4 | 128079986 | |||||
| chr4:128080028
|
C | T | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(190): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.217+2066C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 4/19 | chr4 | 128080028 | ||||||
| chr4:128080080
|
G | C | 4 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.218-2085G>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 4/19 | chr4 | 128080080 | ||||||
| chr4:128080230
|
G | T | 1 | a0002c0002t0002g0291 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.218-1935G>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 4/19 | chr4 | 128080230 | ||||||
| chr4:128080263
|
G | A | 3 | a0005c0006t0001g0099a0005c0006t0001g0100a0005c0006t0001g0101 | 3 | HG01168.hp1 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.218-1902G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 4/19 | chr4 | 128080263 | ||||||
| chr4:128080379
|
A | T | 1 | a0002c0002t0005g0059 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.218-1786A>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 4/19 | chr4 | 128080379 | ||||||
| chr4:128080447
|
TTATAG | T | 6 | a0002c0003t0005g0122a0002c0012t0005g0098a0004c0005t0005g0281others(3): Show | 6 | HG02055.hp1 HG02280.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.218-1713_218-1709d others(7): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr4 | 128080447 | |||||
| chr4:128080479
|
C | T | 2 | a0002c0002t0002g0068a0002c0002t0002g0070 | 2 | HG01884.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.218-1686C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 4/19 | chr4 | 128080479 | ||||||
| chr4:128080842
|
C | T | 1 | a0001c0001t0001g0263 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.218-1323C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 4/19 | chr4 | 128080842 | ||||||
| chr4:128081017
|
A | G | 204 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(201): Show | 204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.218-1148A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 4/19 | chr4 | 128081017 | ||||||
| chr4:128081029
|
A | T | 4 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.218-1136A>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 4/19 | chr4 | 128081029 | ||||||
| chr4:128081067
|
T | C | 1 | a0001c0001t0001g0137 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.218-1098T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 4/19 | chr4 | 128081067 | ||||||
| chr4:128081077
|
CTT | C | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(194): Show | 197 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.218-1071_218-1070d others(4): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr4 | 128081077 | |||||
| chr4:128081363
|
G | A | 2 | a0001c0001t0003g0247a0001c0018t0003g0254 | 2 | HG00099.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.218-802G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 4/19 | chr4 | 128081363 | ||||||
| chr4:128081365
|
C | T | 2 | a0001c0001t0003g0247a0001c0018t0003g0254 | 2 | HG00099.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.218-800C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 4/19 | chr4 | 128081365 | ||||||
| chr4:128081378
|
C | CT | 6 | a0002c0002t0002g0031a0002c0002t0010g0036a0002c0002t0010g0048others(3): Show | 6 | HG01243.hp2 HG03041.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.218-767dupT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr4 | 128081378 | |||||
| chr4:128081378
|
CT | C | 194 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(191): Show | 194 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.218-767delT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr4 | 128081378 | |||||
| chr4:128081378
|
CTT | C | 9 | a0001c0001t0001g0002a0001c0001t0001g0109a0001c0001t0001g0159others(6): Show | 9 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.218-768_218-767del others(2): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr4 | 128081378 | |||||
| chr4:128081380
|
T | G | 1 | a0002c0012t0005g0098 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.218-785T>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 4/19 | chr4 | 128081380 | ||||||
| chr4:128081401
|
G | C | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(164): Show | 167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.218-764G>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 4/19 | chr4 | 128081401 | ||||||
| chr4:128081477
|
A | T | 11 | a0002c0003t0001g0104a0002c0003t0001g0105a0002c0003t0006g0003others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.218-688A>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 4/19 | chr4 | 128081477 | ||||||
| chr4:128081608
|
T | C | 1 | a0001c0001t0001g0266 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.218-557T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 4/19 | chr4 | 128081608 | ||||||
| chr4:128081634
|
T | C | 2 | a0002c0003t0001g0104a0002c0003t0001g0105 | 2 | HG02145.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.218-531T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 4/19 | chr4 | 128081634 | ||||||
| chr4:128081718
|
G | C | 11 | a0002c0003t0001g0104a0002c0003t0001g0105a0002c0003t0006g0003others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.218-447G>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 4/19 | chr4 | 128081718 | ||||||
| chr4:128081808
|
C | T | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(164): Show | 167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.218-357C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 4/19 | chr4 | 128081808 | ||||||
| chr4:128081947
|
G | A | 1 | a0010c0011t0005g0123 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.218-218G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 4/19 | chr4 | 128081947 | ||||||
| chr4:128082420
|
T | C | 1 | a0001c0001t0003g0213 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.358+115T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128082420 | ||||||
| chr4:128082423
|
A | T | 1 | a0001c0001t0003g0213 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.358+118A>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128082423 | ||||||
| chr4:128082425
|
C | A | 1 | a0001c0001t0003g0213 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.358+120C>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128082425 | ||||||
| chr4:128082605
|
AT | A | 22 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(19): Show | 22 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.358+310delT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr4 | 128082605 | |||||
| chr4:128082668
|
T | C | 3 | a0002c0002t0002g0015a0002c0002t0002g0017a0002c0002t0002g0049 | 3 | HG02559.hp2 HG02622.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.358+363T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128082668 | ||||||
| chr4:128082804
|
CT | C | 56 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(53): Show | 56 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.358+514delT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr4 | 128082804 | |||||
| chr4:128082804
|
CTT | C | 175 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(172): Show | 175 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.358+513_358+514del others(2): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr4 | 128082804 | |||||
| chr4:128082807
|
T | A | 1 | a0003c0004t0001g0264 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.358+502T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128082807 | ||||||
| chr4:128082961
|
C | T | 3 | a0002c0003t0005g0122a0002c0012t0005g0098a0010c0011t0005g0123 | 3 | HG02280.hp2 HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.358+656C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128082961 | ||||||
| chr4:128082970
|
G | A | 4 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.358+665G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128082970 | ||||||
| chr4:128083130
|
G | T | 9 | a0002c0002t0002g0038a0002c0002t0002g0051a0002c0002t0002g0069others(6): Show | 9 | HG02080.hp1 HG02559.hp1 NA18941.hp1 others(6): Show |
intron_variant | MODIFIER | c.358+825G>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128083130 | ||||||
| chr4:128083174
|
A | T | 4 | a0001c0001t0003g0225a0001c0001t0003g0227a0001c0001t0003g0228others(1): Show | 4 | NA18950.hp1 NA18969.hp2 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.358+869A>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128083174 | ||||||
| chr4:128083215
|
A | T | 204 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(201): Show | 204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.358+910A>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128083215 | ||||||
| chr4:128083273
|
C | G | 12 | a0002c0002t0002g0295a0002c0003t0001g0104a0002c0003t0001g0105others(9): Show | 12 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.358+968C>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128083273 | ||||||
| chr4:128083302
|
A | G | 2 | a0002c0002t0002g0068a0002c0002t0002g0070 | 2 | HG01884.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.358+997A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128083302 | ||||||
| chr4:128083346
|
G | A | 1 | a0014c0015t0001g0206 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.358+1041G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128083346 | ||||||
| chr4:128083349
|
G | T | 1 | a0001c0001t0003g0247 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.358+1044G>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128083349 | ||||||
| chr4:128083390
|
C | T | 11 | a0002c0003t0001g0104a0002c0003t0001g0105a0002c0003t0006g0003others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.358+1085C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128083390 | ||||||
| chr4:128083418
|
C | T | 11 | a0002c0003t0001g0104a0002c0003t0001g0105a0002c0003t0006g0003others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.358+1113C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128083418 | ||||||
| chr4:128083422
|
C | T | 1 | a0002c0003t0005g0122 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.358+1117C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128083422 | ||||||
| chr4:128083435
|
C | T | 1 | a0007c0008t0001g0139 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.358+1130C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128083435 | ||||||
| chr4:128083452
|
C | G | 3 | a0004c0005t0005g0281a0004c0005t0005g0282a0004c0005t0005g0283 | 3 | HG02055.hp1 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.358+1147C>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128083452 | ||||||
| chr4:128083468
|
C | T | 22 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(19): Show | 22 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.358+1163C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128083468 | ||||||
| chr4:128083504
|
C | T | 5 | a0002c0002t0002g0290a0002c0002t0002g0295a0002c0002t0002g0298others(2): Show | 5 | NA18942.hp1 NA18943.hp1 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.358+1199C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128083504 | ||||||
| chr4:128083507
|
C | T | 1 | a0002c0002t0005g0059 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.358+1202C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128083507 | ||||||
| chr4:128083533
|
G | A | 1 | a0001c0001t0001g0273 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.358+1228G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128083533 | ||||||
| chr4:128083567
|
A | G | 227 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(224): Show | 227 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.358+1262A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128083567 | ||||||
| chr4:128083620
|
T | G | 2 | a0001c0001t0003g0246a0001c0001t0003g0253 | 2 | HG00280.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.358+1315T>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128083620 | ||||||
| chr4:128083634
|
C | A | 16 | a0002c0002t0002g0019a0002c0002t0002g0021a0002c0002t0002g0022others(13): Show | 16 | HG00735.hp1 HG01109.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.358+1329C>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128083634 | ||||||
| chr4:128083647
|
C | T | 1 | a0002c0002t0002g0038 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.358+1342C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128083647 | ||||||
| chr4:128083658
|
G | A | 3 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0177 | 3 | HG00741.hp1 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.358+1353G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128083658 | ||||||
| chr4:128083661
|
A | G | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(207): Show | 210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.358+1356A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128083661 | ||||||
| chr4:128083664
|
T | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(205): Show | 208 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.358+1359T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128083664 | ||||||
| chr4:128083664
|
T | G | 2 | a0001c0001t0001g0249a0001c0001t0003g0240 | 2 | HG02922.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.358+1359T>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128083664 | ||||||
| chr4:128083676
|
G | GC | 161 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(158): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.358+1378dupC | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr4 | 128083676 | |||||
| chr4:128083676
|
G | GCCCCCCC others(224): Show |
1 | a0001c0001t0003g0210 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.358+1378_358+1379i others(233): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr4 | 128083676 | |||||
| chr4:128083677
|
C | A | 1 | a0002c0002t0002g0044 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.358+1372C>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128083677 | ||||||
| chr4:128083691
|
T | G | 8 | a0002c0002t0002g0024a0002c0002t0002g0026a0002c0002t0002g0027others(5): Show | 8 | HG00735.hp1 HG01109.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.358+1386T>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128083691 | ||||||
| chr4:128083772
|
TGGACGGG others(42): Show |
T | 2 | a0002c0003t0001g0104a0002c0003t0001g0105 | 2 | HG02145.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.358+1482_358+1530d others(51): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr4 | 128083772 | |||||
| chr4:128083776
|
C | T | 5 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(2): Show | 5 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.358+1471C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128083776 | ||||||
| chr4:128083821
|
C | CAGACGGG others(221): Show |
2 | a0001c0001t0003g0237a0001c0001t0003g0244 | 2 | HG00140.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.358+1516_358+1517i others(230): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128083821 | ||||||
| chr4:128083821
|
C | T | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(188): Show | 191 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.358+1516C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128083821 | ||||||
| chr4:128083827
|
G | A | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(164): Show | 167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.358+1522G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128083827 | ||||||
| chr4:128083866
|
G | A | 3 | a0003c0004t0001g0182a0003c0004t0001g0183a0003c0004t0001g0189 | 3 | HG01167.hp2 HG01169.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.358+1561G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128083866 | ||||||
| chr4:128083906
|
G | A | 164 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(161): Show | 164 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.358+1601G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128083906 | ||||||
| chr4:128083910
|
C | T | 3 | a0001c0001t0001g0108a0001c0001t0001g0271a0002c0002t0002g0063 | 3 | HG02165.hp1 NA18983.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.358+1605C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128083910 | ||||||
| chr4:128083985
|
C | T | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(190): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.358+1680C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128083985 | ||||||
| chr4:128084022
|
C | T | 1 | a0002c0002t0002g0297 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.358+1717C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128084022 | ||||||
| chr4:128084023
|
G | A | 1 | a0014c0015t0001g0206 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.358+1718G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128084023 | ||||||
| chr4:128084033
|
C | T | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(190): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.358+1728C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128084033 | ||||||
| chr4:128084084
|
G | A | 3 | a0007c0008t0001g0138a0007c0008t0001g0139a0007c0008t0001g0158 | 3 | HG03486.hp2 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.358+1779G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128084084 | ||||||
| chr4:128084100
|
A | G | 2 | a0001c0001t0001g0124a0001c0001t0001g0267 | 2 | NA18951.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.358+1795A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128084100 | ||||||
| chr4:128084178
|
A | G | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(207): Show | 210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.358+1873A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128084178 | ||||||
| chr4:128084388
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.358+2083C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128084388 | ||||||
| chr4:128084540
|
A | T | 1 | a0002c0003t0005g0122 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.358+2235A>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128084540 | ||||||
| chr4:128084587
|
TTCGGC | T | 11 | a0002c0003t0001g0104a0002c0003t0001g0105a0002c0003t0006g0003others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.358+2288_358+2292d others(7): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr4 | 128084587 | |||||
| chr4:128084735
|
TACTA | T | 11 | a0002c0003t0001g0104a0002c0003t0001g0105a0002c0003t0006g0003others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.358+2434_358+2437d others(6): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr4 | 128084735 | |||||
| chr4:128084903
|
C | T | 21 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(18): Show | 21 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(18): Show |
intron_variant | MODIFIER | c.358+2598C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128084903 | ||||||
| chr4:128085192
|
T | C | 2 | a0001c0001t0001g0200a0001c0001t0001g0207 | 2 | HG01516.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.358+2887T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128085192 | ||||||
| chr4:128085344
|
C | A | 22 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(19): Show | 22 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.358+3039C>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128085344 | ||||||
| chr4:128085353
|
C | CT | 85 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(82): Show | 85 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.358+3072dupT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr4 | 128085353 | |||||
| chr4:128085353
|
C | CTT | 84 | a0001c0001t0001g0001a0001c0001t0001g0107a0001c0001t0001g0108others(81): Show | 84 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.358+3071_358+3072d others(4): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr4 | 128085353 | |||||
| chr4:128085353
|
CT | C | 38 | a0001c0001t0004g0311a0002c0002t0002g0012a0002c0002t0002g0013others(35): Show | 38 | HG00099.hp1 HG00735.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.358+3072delT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr4 | 128085353 | |||||
| chr4:128085377
|
T | TA | 4 | a0001c0001t0004g0313a0001c0001t0004g0314a0001c0001t0004g0320others(1): Show | 4 | HG00597.hp2 HG00609.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.358+3075dupA | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr4 | 128085377 | |||||
| chr4:128085451
|
G | A | 1 | a0001c0001t0004g0317 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.358+3146G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128085451 | ||||||
| chr4:128085513
|
G | A | 1 | a0001c0001t0003g0220 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.358+3208G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128085513 | ||||||
| chr4:128085599
|
C | T | 1 | a0002c0002t0002g0117 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.358+3294C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128085599 | ||||||
| chr4:128085962
|
T | C | 1 | a0001c0001t0003g0239 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.358+3657T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128085962 | ||||||
| chr4:128086009
|
C | CT | 9 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0017others(6): Show | 9 | HG00741.hp2 HG01433.hp1 HG02015.hp1 others(6): Show |
intron_variant | MODIFIER | c.358+3726dupT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr4 | 128086009 | |||||
| chr4:128086009
|
CT | C | 25 | a0001c0001t0001g0149a0001c0001t0001g0175a0001c0001t0003g0210others(22): Show | 25 | HG00639.hp1 HG00642.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.358+3726delT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr4 | 128086009 | |||||
| chr4:128086009
|
CTT | C | 181 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(178): Show | 181 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.358+3725_358+3726d others(4): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr4 | 128086009 | |||||
| chr4:128086052
|
C | T | 91 | a0001c0001t0001g0001a0001c0001t0001g0107a0001c0001t0001g0108others(88): Show | 91 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.358+3747C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128086052 | ||||||
| chr4:128086107
|
T | G | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(207): Show | 210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.358+3802T>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128086107 | ||||||
| chr4:128086160
|
C | T | 3 | a0001c0001t0003g0127a0001c0001t0003g0218a0001c0001t0003g0255 | 3 | HG01934.hp2 HG01975.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.358+3855C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128086160 | ||||||
| chr4:128086265
|
A | G | 2 | a0002c0002t0002g0058a0002c0002t0002g0089 | 2 | HG02015.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.358+3960A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128086265 | ||||||
| chr4:128086305
|
G | A | 11 | a0002c0003t0001g0104a0002c0003t0001g0105a0002c0003t0006g0003others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.358+4000G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128086305 | ||||||
| chr4:128086397
|
C | T | 3 | a0005c0006t0001g0099a0005c0006t0001g0100a0005c0006t0001g0101 | 3 | HG01168.hp1 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.358+4092C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128086397 | ||||||
| chr4:128086590
|
A | C | 3 | a0001c0001t0001g0166a0001c0001t0001g0178a0001c0001t0001g0191 | 3 | HG00140.hp2 HG01346.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.358+4285A>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128086590 | ||||||
| chr4:128087024
|
G | A | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(190): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.359-3977G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128087024 | ||||||
| chr4:128087129
|
C | T | 3 | a0002c0002t0002g0034a0002c0002t0002g0035a0002c0002t0002g0043 | 3 | HG02083.hp1 HG02155.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.359-3872C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128087129 | ||||||
| chr4:128087151
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.359-3850C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128087151 | ||||||
| chr4:128087845
|
G | C | 1 | a0002c0002t0002g0089 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.359-3156G>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128087845 | ||||||
| chr4:128087853
|
C | CAT | 3 | a0004c0005t0005g0281a0004c0005t0005g0282a0004c0005t0005g0283 | 3 | HG02055.hp1 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.359-3135_359-3134d others(4): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr4 | 128087853 | |||||
| chr4:128087907
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.359-3094T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128087907 | ||||||
| chr4:128087956
|
T | C | 2 | a0002c0002t0002g0063a0002c0002t0002g0112 | 2 | HG02027.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.359-3045T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128087956 | ||||||
| chr4:128088034
|
A | G | 1 | a0001c0001t0004g0313 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.359-2967A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128088034 | ||||||
| chr4:128088200
|
A | AATG | 164 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(161): Show | 164 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.359-2799_359-2798i others(5): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr4 | 128088200 | |||||
| chr4:128088203
|
A | AATG | 63 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(60): Show | 63 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.359-2781_359-2779d others(5): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr4 | 128088203 | |||||
| chr4:128088203
|
A | G | 164 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(161): Show | 164 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.359-2798A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128088203 | ||||||
| chr4:128088563
|
C | T | 4 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.359-2438C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128088563 | ||||||
| chr4:128088903
|
C | T | 2 | a0003c0004t0001g0172a0003c0004t0001g0264 | 2 | HG01109.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.359-2098C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128088903 | ||||||
| chr4:128089225
|
A | C | 1 | a0002c0002t0002g0086 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.359-1776A>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128089225 | ||||||
| chr4:128089248
|
G | A | 3 | a0005c0006t0001g0099a0005c0006t0001g0100a0005c0006t0001g0101 | 3 | HG01168.hp1 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.359-1753G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128089248 | ||||||
| chr4:128089472
|
A | G | 2 | a0006c0007t0009g0192a0006c0007t0009g0204 | 2 | HG03139.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.359-1529A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128089472 | ||||||
| chr4:128089480
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.359-1521C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128089480 | ||||||
| chr4:128089512
|
T | C | 1 | a0002c0002t0002g0037 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.359-1489T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128089512 | ||||||
| chr4:128089629
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.359-1372C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128089629 | ||||||
| chr4:128089722
|
T | TCTTAATT others(320): Show |
1 | a0001c0001t0001g0167 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.359-1262_359-1261i others(329): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr4 | 128089722 | |||||
| chr4:128089722
|
T | TCTTAATT others(342): Show |
1 | a0001c0001t0001g0173 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.359-1262_359-1261i others(351): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr4 | 128089722 | |||||
| chr4:128089722
|
T | TCTTAATT others(343): Show |
1 | a0001c0001t0001g0170 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.359-1262_359-1261i others(352): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr4 | 128089722 | |||||
| chr4:128089758
|
C | T | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(190): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.359-1243C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128089758 | ||||||
| chr4:128089906
|
G | A | 3 | a0002c0002t0002g0115a0002c0002t0002g0120a0002c0002t0002g0121 | 3 | HG02004.hp1 HG03688.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.359-1095G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128089906 | ||||||
| chr4:128089970
|
G | A | 4 | a0001c0001t0003g0230a0001c0001t0003g0235a0001c0001t0003g0243others(1): Show | 4 | HG00609.hp2 HG00673.hp1 HG02056.hp1 others(1): Show |
intron_variant | MODIFIER | c.359-1031G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128089970 | ||||||
| chr4:128090116
|
A | G | 1 | a0002c0002t0016g0064 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.359-885A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128090116 | ||||||
| chr4:128090362
|
C | T | 5 | a0001c0001t0001g0146a0001c0001t0001g0166a0001c0001t0001g0178others(2): Show | 5 | HG00140.hp2 HG01346.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.359-639C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128090362 | ||||||
| chr4:128090369
|
G | A | 1 | a0002c0002t0002g0040 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.359-632G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128090369 | ||||||
| chr4:128090520
|
A | G | 1 | a0001c0001t0001g0137 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.359-481A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128090520 | ||||||
| chr4:128090659
|
T | C | 1 | a0001c0001t0001g0196 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.359-342T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128090659 | ||||||
| chr4:128090703
|
T | C | 1 | a0001c0001t0001g0157 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.359-298T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 5/19 | chr4 | 128090703 | ||||||
| chr4:128091618
|
A | G | 1 | a0002c0002t0002g0023 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.668+106A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128091618 | ||||||
| chr4:128091659
|
C | T | 1 | a0002c0002t0002g0087 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.668+147C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128091659 | ||||||
| chr4:128091709
|
G | A | 4 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.668+197G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128091709 | ||||||
| chr4:128091723
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.668+211G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128091723 | ||||||
| chr4:128092029
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.668+517A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128092029 | ||||||
| chr4:128092632
|
A | G | 8 | a0002c0002t0002g0024a0002c0002t0002g0026a0002c0002t0002g0027others(5): Show | 8 | HG00735.hp1 HG01109.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.668+1120A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128092632 | ||||||
| chr4:128092869
|
G | C | 1 | a0010c0011t0005g0123 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.668+1357G>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128092869 | ||||||
| chr4:128092974
|
G | T | 1 | a0013c0014t0003g0226 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.668+1462G>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128092974 | ||||||
| chr4:128093075
|
A | G | 1 | a0014c0015t0001g0206 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.668+1563A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128093075 | ||||||
| chr4:128093378
|
C | T | 1 | a0001c0001t0001g0187 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.668+1866C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128093378 | ||||||
| chr4:128093422
|
C | T | 22 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(19): Show | 22 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.668+1910C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128093422 | ||||||
| chr4:128093436
|
A | G | 1 | a0001c0001t0007g0258 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.668+1924A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128093436 | ||||||
| chr4:128093485
|
A | C | 3 | a0002c0002t0002g0115a0002c0002t0002g0120a0002c0002t0002g0121 | 3 | HG02004.hp1 HG03688.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.668+1973A>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128093485 | ||||||
| chr4:128093512
|
T | C | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(207): Show | 210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.668+2000T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128093512 | ||||||
| chr4:128093533
|
G | T | 3 | a0007c0008t0001g0138a0007c0008t0001g0139a0007c0008t0001g0158 | 3 | HG03486.hp2 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.668+2021G>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128093533 | ||||||
| chr4:128093709
|
CT | C | 203 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(200): Show | 203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.668+2215delT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr4 | 128093709 | |||||
| chr4:128093709
|
CTTTTTTT | C | 16 | a0002c0002t0002g0019a0002c0002t0002g0021a0002c0002t0002g0022others(13): Show | 16 | HG00735.hp1 HG01109.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.668+2209_668+2215d others(9): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr4 | 128093709 | |||||
| chr4:128093924
|
T | C | 3 | a0003c0004t0001g0182a0003c0004t0001g0183a0003c0004t0001g0189 | 3 | HG01167.hp2 HG01169.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.668+2412T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128093924 | ||||||
| chr4:128093956
|
C | T | 1 | a0007c0008t0001g0138 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.668+2444C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128093956 | ||||||
| chr4:128093964
|
G | A | 2 | a0002c0002t0002g0024a0002c0002t0002g0027 | 2 | HG00735.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.668+2452G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128093964 | ||||||
| chr4:128094066
|
C | G | 1 | a0002c0002t0002g0052 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.668+2554C>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128094066 | ||||||
| chr4:128094146
|
C | T | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(190): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.668+2634C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128094146 | ||||||
| chr4:128094187
|
A | G | 1 | a0001c0001t0004g0324 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.668+2675A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128094187 | ||||||
| chr4:128094204
|
C | T | 2 | a0001c0001t0003g0125a0001c0001t0003g0212 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.668+2692C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128094204 | ||||||
| chr4:128094400
|
C | CT | 36 | a0001c0001t0001g0160a0001c0001t0001g0168a0001c0001t0003g0128others(33): Show | 36 | HG00408.hp2 HG00558.hp1 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.668+2906dupT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr4 | 128094400 | |||||
| chr4:128094400
|
CT | C | 8 | a0001c0001t0001g0124a0001c0001t0001g0143a0001c0001t0001g0185others(5): Show | 8 | HG01167.hp1 HG01256.hp1 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.668+2906delT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr4 | 128094400 | |||||
| chr4:128094494
|
G | A | 1 | a0002c0002t0002g0026 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.668+2982G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128094494 | ||||||
| chr4:128094521
|
C | G | 2 | a0003c0004t0001g0182a0003c0004t0001g0183 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.668+3009C>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128094521 | ||||||
| chr4:128094523
|
T | G | 22 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(19): Show | 22 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.668+3011T>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128094523 | ||||||
| chr4:128094617
|
A | G | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(207): Show | 210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.668+3105A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128094617 | ||||||
| chr4:128094784
|
T | C | 1 | a0001c0001t0007g0133 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.668+3272T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128094784 | ||||||
| chr4:128095066
|
T | G | 4 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.669-3120T>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128095066 | ||||||
| chr4:128095179
|
C | T | 1 | a0001c0001t0001g0271 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.669-3007C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128095179 | ||||||
| chr4:128095317
|
C | T | 4 | a0002c0002t0002g0296a0002c0002t0002g0299a0002c0002t0002g0307others(1): Show | 4 | NA18990.hp1 NA19007.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.669-2869C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128095317 | ||||||
| chr4:128095440
|
G | T | 1 | a0002c0002t0002g0130 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.669-2746G>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128095440 | ||||||
| chr4:128095489
|
CA | C | 286 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(283): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.669-2675delA | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr4 | 128095489 | |||||
| chr4:128095489
|
CAA | C | 43 | a0001c0001t0001g0002a0001c0001t0001g0160a0001c0001t0001g0163others(40): Show | 43 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.669-2676_669-2675d others(4): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr4 | 128095489 | |||||
| chr4:128095528
|
T | C | 1 | a0002c0002t0002g0050 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.669-2658T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128095528 | ||||||
| chr4:128095717
|
T | TC | 11 | a0002c0003t0001g0104a0002c0003t0001g0105a0002c0003t0006g0003others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.669-2468dupC | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr4 | 128095717 | |||||
| chr4:128095720
|
A | G | 3 | a0005c0006t0001g0099a0005c0006t0001g0100a0005c0006t0001g0101 | 3 | HG01168.hp1 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.669-2466A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128095720 | ||||||
| chr4:128095722
|
G | A | 1 | a0002c0002t0008g0305 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.669-2464G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128095722 | ||||||
| chr4:128095796
|
G | T | 1 | a0001c0001t0004g0308 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.669-2390G>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128095796 | ||||||
| chr4:128095860
|
T | G | 1 | a0001c0001t0001g0259 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.669-2326T>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128095860 | ||||||
| chr4:128095975
|
C | T | 333 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(330): Show | 333 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.669-2211C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128095975 | ||||||
| chr4:128095992
|
A | AT | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(128): Show | 131 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.669-2175dupT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr4 | 128095992 | |||||
| chr4:128095992
|
A | ATT | 25 | a0001c0001t0001g0157a0001c0001t0001g0181a0001c0001t0001g0211others(22): Show | 25 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.669-2176_669-2175d others(4): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr4 | 128095992 | |||||
| chr4:128096024
|
C | T | 3 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196 | 3 | HG00673.hp2 HG02155.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.669-2162C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128096024 | ||||||
| chr4:128096039
|
G | A | 3 | a0005c0006t0001g0099a0005c0006t0001g0100a0005c0006t0001g0101 | 3 | HG01168.hp1 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.669-2147G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128096039 | ||||||
| chr4:128096057
|
G | C | 1 | a0001c0001t0001g0167 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.669-2129G>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128096057 | ||||||
| chr4:128096138
|
C | T | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(191): Show | 194 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.669-2048C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128096138 | ||||||
| chr4:128096186
|
G | C | 1 | a0002c0002t0002g0287 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.669-2000G>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128096186 | ||||||
| chr4:128096229
|
G | A | 1 | a0002c0002t0008g0293 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.669-1957G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128096229 | ||||||
| chr4:128096245
|
G | A | 11 | a0002c0003t0001g0104a0002c0003t0001g0105a0002c0003t0006g0003others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.669-1941G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128096245 | ||||||
| chr4:128096263
|
G | C | 1 | a0001c0001t0001g0196 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.669-1923G>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128096263 | ||||||
| chr4:128096282
|
C | T | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(190): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.669-1904C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128096282 | ||||||
| chr4:128096283
|
G | A | 10 | a0002c0002t0002g0015a0002c0002t0002g0017a0002c0002t0002g0049others(7): Show | 10 | HG01243.hp2 HG01884.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.669-1903G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128096283 | ||||||
| chr4:128096463
|
C | T | 1 | a0001c0001t0001g0110 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.669-1723C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128096463 | ||||||
| chr4:128096588
|
C | T | 2 | a0001c0001t0004g0311a0001c0001t0004g0326 | 2 | NA18984.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.669-1598C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128096588 | ||||||
| chr4:128096810
|
C | T | 1 | a0001c0001t0003g0279 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.669-1376C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128096810 | ||||||
| chr4:128096879
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.669-1307C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128096879 | ||||||
| chr4:128096902
|
C | T | 3 | a0004c0005t0005g0281a0004c0005t0005g0282a0004c0005t0005g0283 | 3 | HG02055.hp1 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.669-1284C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128096902 | ||||||
| chr4:128096950
|
G | T | 11 | a0001c0001t0001g0129a0001c0001t0001g0142a0001c0001t0001g0144others(8): Show | 11 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.669-1236G>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128096950 | ||||||
| chr4:128097048
|
G | A | 1 | a0001c0001t0003g0247 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.669-1138G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128097048 | ||||||
| chr4:128097254
|
G | A | 204 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(201): Show | 204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.669-932G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128097254 | ||||||
| chr4:128097320
|
T | G | 36 | a0001c0001t0001g0108a0001c0001t0001g0124a0001c0001t0001g0129others(33): Show | 36 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.669-866T>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128097320 | ||||||
| chr4:128097399
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.669-787C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128097399 | ||||||
| chr4:128097431
|
C | T | 2 | a0002c0002t0002g0054a0002c0002t0002g0055 | 2 | NA18954.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.669-755C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128097431 | ||||||
| chr4:128097463
|
A | G | 3 | a0002c0002t0002g0033a0002c0002t0002g0056a0002c0002t0002g0117 | 3 | HG00408.hp1 HG02040.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.669-723A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128097463 | ||||||
| chr4:128097512
|
G | A | 2 | a0003c0004t0001g0182a0003c0004t0001g0183 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.669-674G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128097512 | ||||||
| chr4:128097598
|
C | G | 1 | a0002c0002t0008g0304 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.669-588C>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128097598 | ||||||
| chr4:128097715
|
A | C | 22 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(19): Show | 22 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.669-471A>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128097715 | ||||||
| chr4:128097718
|
T | C | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(190): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.669-468T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128097718 | ||||||
| chr4:128097764
|
T | G | 1 | a0001c0001t0001g0200 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.669-422T>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128097764 | ||||||
| chr4:128097927
|
A | G | 1 | a0011c0016t0003g0277 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.669-259A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128097927 | ||||||
| chr4:128097978
|
TTTTAAG | T | 4 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.669-201_669-196del others(6): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr4 | 128097978 | |||||
| chr4:128098013
|
T | C | 22 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(19): Show | 22 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.669-173T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 7/19 | chr4 | 128098013 | ||||||
| chr4:128098413
|
A | G | 11 | a0002c0003t0001g0104a0002c0003t0001g0105a0002c0003t0006g0003others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.813+83A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128098413 | ||||||
| chr4:128098536
|
G | A | 335 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(332): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.813+206G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128098536 | ||||||
| chr4:128098743
|
A | ATGTG | 3 | a0001c0001t0001g0157a0001c0001t0001g0199a0001c0001t0001g0262 | 3 | HG02886.hp1 NA19004.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.813+415_813+418dup others(4): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098743 | |||||
| chr4:128098743
|
A | ATGTGTG | 3 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196 | 3 | HG00673.hp2 HG02155.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.813+418_813+419ins others(6): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098743 | |||||
| chr4:128098743
|
A | G | 2 | a0001c0001t0001g0165a0001c0001t0001g0176 | 2 | HG02040.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.813+413A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128098743 | ||||||
| chr4:128098747
|
G | GTATATAT others(5): Show |
7 | a0002c0002t0002g0041a0002c0002t0002g0050a0002c0002t0002g0061others(4): Show | 7 | HG00741.hp2 HG02572.hp1 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.813+427_813+438dup others(12): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098747 | |||||
| chr4:128098747
|
G | GTATATAT others(7): Show |
3 | a0002c0002t0002g0035a0002c0002t0002g0040a0002c0002t0002g0046 | 3 | HG02083.hp1 NA18949.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.813+425_813+438dup others(14): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098747 | |||||
| chr4:128098747
|
G | GTATATAT others(11): Show |
1 | a0002c0002t0002g0120 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.813+421_813+438dup others(18): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098747 | |||||
| chr4:128098747
|
G | GTATATAT others(13): Show |
2 | a0002c0002t0002g0070a0002c0002t0002g0115 | 2 | HG01884.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.813+419_813+438dup others(20): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098747 | |||||
| chr4:128098747
|
G | GTGTATAT others(7): Show |
4 | a0002c0002t0002g0019a0002c0002t0002g0021a0002c0002t0002g0063others(1): Show | 4 | HG02165.hp1 HG02809.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.813+418_813+419ins others(14): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098747 | |||||
| chr4:128098747
|
G | GTGTATAT others(9): Show |
1 | a0004c0005t0005g0282 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.813+418_813+419ins others(16): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098747 | |||||
| chr4:128098747
|
G | GTGTATAT others(15): Show |
1 | a0002c0012t0005g0098 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.813+418_813+419ins others(22): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098747 | |||||
| chr4:128098747
|
G | GTGTGTA | 16 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0188others(13): Show | 16 | HG00408.hp2 HG01074.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.813+418_813+419ins others(6): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098747 | |||||
| chr4:128098747
|
G | GTGTGTAT others(1): Show |
34 | a0001c0001t0001g0140a0001c0001t0001g0159a0001c0001t0001g0160others(31): Show | 34 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.813+418_813+419ins others(8): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098747 | |||||
| chr4:128098747
|
G | GTGTGTAT others(3): Show |
18 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0109others(15): Show | 18 | HG01106.hp2 HG01433.hp2 HG02015.hp2 others(15): Show |
intron_variant | MODIFIER | c.813+418_813+419ins others(10): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098747 | |||||
| chr4:128098747
|
G | GTGTGTAT others(5): Show |
2 | a0001c0001t0001g0161a0001c0001t0001g0249 | 2 | HG02647.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.813+418_813+419ins others(12): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098747 | |||||
| chr4:128098747
|
G | GTGTGTAT others(7): Show |
3 | a0001c0001t0003g0240a0001c0001t0003g0276a0002c0002t0002g0025 | 3 | HG02738.hp1 HG03540.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.813+418_813+419ins others(14): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098747 | |||||
| chr4:128098747
|
G | GTGTGTAT others(9): Show |
4 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.813+418_813+419ins others(16): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098747 | |||||
| chr4:128098747
|
G | GTGTGTAT others(13): Show |
2 | a0001c0001t0001g0167a0001c0001t0001g0236 | 2 | HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.813+418_813+419ins others(20): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098747 | |||||
| chr4:128098747
|
G | GTGTGTAT others(15): Show |
2 | a0001c0001t0001g0179a0001c0001t0001g0190 | 2 | HG02630.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.813+418_813+419ins others(22): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098747 | |||||
| chr4:128098747
|
G | GTGTGTAT others(17): Show |
2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | HG01099.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.813+418_813+419ins others(24): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098747 | |||||
| chr4:128098747
|
G | GTGTGTAT others(19): Show |
3 | a0001c0001t0001g0152a0001c0001t0001g0171a0001c0001t0001g0173 | 3 | HG00738.hp1 HG02257.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.813+418_813+419ins others(26): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098747 | |||||
| chr4:128098747
|
G | GTGTGTAT others(21): Show |
4 | a0001c0001t0001g0164a0001c0001t0001g0186a0001c0001t0001g0187others(1): Show | 4 | HG01109.hp2 HG01943.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.813+418_813+419ins others(28): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098747 | |||||
| chr4:128098747
|
G | GTGTGTAT others(23): Show |
12 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0162others(9): Show | 12 | HG00639.hp2 HG00741.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.813+418_813+419ins others(30): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098747 | |||||
| chr4:128098747
|
G | GTGTGTAT others(25): Show |
9 | a0001c0001t0001g0110a0001c0001t0001g0147a0001c0001t0001g0148others(6): Show | 9 | HG01071.hp2 HG02040.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.813+418_813+419ins others(32): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098747 | |||||
| chr4:128098747
|
G | GTGTGTAT others(27): Show |
2 | a0001c0001t0001g0150a0001c0001t0014g0151 | 2 | HG01952.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.813+418_813+419ins others(34): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098747 | |||||
| chr4:128098747
|
G | GTGTGTAT others(29): Show |
1 | a0001c0001t0001g0176 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.813+418_813+419ins others(36): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098747 | |||||
| chr4:128098747
|
G | GTGTGTAT others(31): Show |
3 | a0001c0001t0001g0144a0001c0001t0001g0149a0001c0001t0001g0193 | 3 | HG00280.hp1 HG01243.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.813+418_813+419ins others(38): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098747 | |||||
| chr4:128098747
|
G | GTGTGTAT others(33): Show |
2 | a0001c0001t0001g0180a0001c0001t0001g0275 | 2 | HG01099.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.813+418_813+419ins others(40): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098747 | |||||
| chr4:128098747
|
G | GTGTGTAT others(35): Show |
1 | a0001c0001t0001g0174 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.813+418_813+419ins others(42): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098747 | |||||
| chr4:128098747
|
G | GTGTGTAT others(37): Show |
1 | a0001c0001t0001g0129 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.813+418_813+419ins others(44): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098747 | |||||
| chr4:128098747
|
G | GTGTGTGT others(3): Show |
1 | a0001c0001t0001g0211 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.813+418_813+419ins others(10): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098747 | |||||
| chr4:128098747
|
G | GTGTGTGT others(5): Show |
1 | a0001c0001t0001g0002 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.813+418_813+419ins others(12): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098747 | |||||
| chr4:128098747
|
G | GTGTGTGT others(7): Show |
1 | a0007c0008t0001g0138 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.813+418_813+419ins others(14): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098747 | |||||
| chr4:128098747
|
G | GTGTGTGT others(15): Show |
2 | a0001c0001t0001g0170a0006c0007t0009g0204 | 2 | NA20129.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.813+418_813+419ins others(22): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098747 | |||||
| chr4:128098747
|
G | GTGTGTGT others(19): Show |
2 | a0001c0001t0001g0178a0001c0001t0001g0191 | 2 | HG00140.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.813+418_813+419ins others(26): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098747 | |||||
| chr4:128098747
|
G | GTGTGTGT others(21): Show |
1 | a0006c0007t0009g0192 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.813+418_813+419ins others(28): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098747 | |||||
| chr4:128098747
|
G | GTGTGTGT others(23): Show |
5 | a0001c0001t0001g0126a0001c0001t0001g0166a0001c0001t0001g0175others(2): Show | 5 | HG00642.hp1 HG01346.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.813+418_813+419ins others(30): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098747 | |||||
| chr4:128098747
|
G | GTGTGTGT others(25): Show |
2 | a0001c0001t0001g0153a0001c0001t0001g0266 | 2 | HG00642.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.813+418_813+419ins others(32): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098747 | |||||
| chr4:128098747
|
G | GTGTGTGT others(29): Show |
1 | a0001c0001t0001g0145 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.813+418_813+419ins others(36): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098747 | |||||
| chr4:128098747
|
G | GTGTGTGT others(31): Show |
2 | a0001c0001t0001g0146a0003c0004t0001g0189 | 2 | HG02735.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.813+418_813+419ins others(38): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098747 | |||||
| chr4:128098747
|
G | GTGTGTGT others(15): Show |
1 | a0001c0001t0007g0133 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.813+418_813+419ins others(22): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098747 | |||||
| chr4:128098747
|
G | GTGTGTGT others(19): Show |
1 | a0001c0001t0007g0132 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.813+418_813+419ins others(26): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098747 | |||||
| chr4:128098747
|
G | GTGTGTGT others(21): Show |
1 | a0001c0001t0001g0137 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.813+418_813+419ins others(28): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098747 | |||||
| chr4:128098747
|
G | GTGTGTGT others(31): Show |
1 | a0001c0001t0001g0001 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.813+418_813+419ins others(38): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098747 | |||||
| chr4:128098747
|
G | GTGTGTGT others(33): Show |
1 | a0001c0001t0007g0131 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.813+418_813+419ins others(40): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098747 | |||||
| chr4:128098747
|
G | GTGTGTGT others(23): Show |
1 | a0001c0001t0001g0203 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.813+418_813+419ins others(30): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098747 | |||||
| chr4:128098747
|
G | GTGTGTGT others(25): Show |
1 | a0001c0001t0001g0143 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.813+418_813+419ins others(32): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098747 | |||||
| chr4:128098747
|
G | GTGTGTGT others(29): Show |
1 | a0001c0001t0007g0258 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.813+418_813+419ins others(36): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098747 | |||||
| chr4:128098747
|
G | GTGTGTGT others(21): Show |
2 | a0001c0001t0001g0108a0001c0001t0001g0271 | 2 | NA18983.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.813+418_813+419ins others(28): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098747 | |||||
| chr4:128098747
|
G | GTGTGTGT others(33): Show |
1 | a0001c0001t0001g0259 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.813+418_813+419ins others(40): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098747 | |||||
| chr4:128098747
|
G | GTGTGTGT others(37): Show |
3 | a0001c0001t0001g0124a0001c0001t0001g0260a0001c0001t0001g0267 | 3 | NA18951.hp2 NA18986.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.813+418_813+419ins others(44): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098747 | |||||
| chr4:128098747
|
G | GTGTGTGT others(39): Show |
1 | a0001c0001t0001g0261 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.813+418_813+419ins others(46): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098747 | |||||
| chr4:128098747
|
G | GTGTGTGT others(41): Show |
1 | a0001c0001t0001g0268 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.813+418_813+419ins others(48): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098747 | |||||
| chr4:128098747
|
G | GTGTGTGT others(45): Show |
1 | a0001c0001t0001g0269 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.813+418_813+419ins others(52): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098747 | |||||
| chr4:128098747
|
G | GTGTGTGT others(41): Show |
1 | a0001c0001t0001g0270 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.813+418_813+419ins others(48): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098747 | |||||
| chr4:128098747
|
G | GTGTGTGT others(43): Show |
1 | a0001c0001t0001g0272 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.813+418_813+419ins others(50): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098747 | |||||
| chr4:128098749
|
A | G | 35 | a0001c0001t0001g0107a0001c0001t0001g0156a0001c0001t0001g0157others(32): Show | 35 | HG00099.hp2 HG00558.hp2 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.813+419A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128098749 | ||||||
| chr4:128098751
|
A | G | 9 | a0001c0001t0001g0107a0001c0001t0001g0156a0001c0001t0001g0200others(6): Show | 9 | HG00099.hp2 HG01167.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.813+421A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128098751 | ||||||
| chr4:128098753
|
A | G | 23 | a0001c0001t0001g0205a0001c0001t0004g0308a0001c0001t0004g0309others(20): Show | 23 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.813+423A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128098753 | ||||||
| chr4:128098765
|
A | G | 1 | a0001c0001t0007g0133 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.813+435A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128098765 | ||||||
| chr4:128098767
|
A | ATACATAT others(8): Show |
1 | a0002c0002t0012g0096 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.813+438_813+439ins others(15): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098767 | |||||
| chr4:128098767
|
A | ATACATAT others(10): Show |
1 | a0002c0002t0012g0065 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.813+438_813+439ins others(17): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098767 | |||||
| chr4:128098767
|
A | ATATATAT others(4): Show |
5 | a0002c0002t0002g0038a0002c0002t0002g0058a0002c0002t0002g0306others(2): Show | 5 | HG02015.hp1 HG02559.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.813+438_813+439ins others(11): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098767 | |||||
| chr4:128098767
|
A | ATATATAT others(6): Show |
6 | a0002c0002t0002g0015a0002c0002t0002g0044a0002c0002t0002g0045others(3): Show | 6 | HG01070.hp2 HG01981.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.813+438_813+439ins others(13): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098767 | |||||
| chr4:128098767
|
A | ATATATAT others(8): Show |
2 | a0002c0002t0002g0071a0002c0002t0002g0121 | 2 | HG02004.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.813+438_813+439ins others(15): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098767 | |||||
| chr4:128098767
|
A | ATATATAT others(11): Show |
3 | a0002c0002t0002g0047a0002c0002t0002g0085a0002c0002t0002g0291 | 3 | HG03195.hp2 NA18747.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.813+438_813+439ins others(18): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098767 | |||||
| chr4:128098767
|
A | ATATATAT others(9): Show |
1 | a0002c0002t0002g0012 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.813+438_813+439ins others(16): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098767 | |||||
| chr4:128098767
|
A | ATATATAT others(11): Show |
1 | a0002c0002t0002g0114 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.813+438_813+439ins others(18): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098767 | |||||
| chr4:128098767
|
A | ATATATAT others(12): Show |
1 | a0002c0002t0002g0043 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.813+438_813+439ins others(19): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098767 | |||||
| chr4:128098767
|
A | ATATATAT others(7): Show |
11 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0052others(8): Show | 11 | HG02027.hp1 HG02040.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.813+438_813+439ins others(14): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098767 | |||||
| chr4:128098767
|
A | ATATATAT others(8): Show |
2 | a0002c0002t0002g0078a0002c0002t0002g0080 | 2 | HG01106.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.813+438_813+439ins others(15): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098767 | |||||
| chr4:128098767
|
A | ATATATAT others(9): Show |
2 | a0002c0002t0002g0032a0002c0002t0002g0051 | 2 | NA18950.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.813+438_813+439ins others(16): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098767 | |||||
| chr4:128098767
|
A | ATATATAT others(10): Show |
1 | a0002c0002t0002g0288 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.813+438_813+439ins others(17): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098767 | |||||
| chr4:128098767
|
A | ATATATAT others(5): Show |
22 | a0002c0002t0002g0013a0002c0002t0002g0016a0002c0002t0002g0018others(19): Show | 22 | HG00438.hp2 HG01243.hp2 HG01256.hp2 others(19): Show |
intron_variant | MODIFIER | c.813+438_813+439ins others(12): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098767 | |||||
| chr4:128098767
|
A | ATATATAT others(6): Show |
6 | a0002c0002t0002g0017a0002c0002t0002g0055a0002c0002t0002g0072others(3): Show | 6 | HG00423.hp1 HG01516.hp1 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.813+438_813+439ins others(13): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098767 | |||||
| chr4:128098767
|
A | ATATATAT others(7): Show |
2 | a0002c0002t0002g0056a0002c0019t0002g0083 | 2 | HG00408.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.813+438_813+439ins others(14): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098767 | |||||
| chr4:128098767
|
A | ATATATAT others(8): Show |
2 | a0002c0002t0002g0084a0002c0002t0002g0284 | 2 | HG03834.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.813+438_813+439ins others(15): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098767 | |||||
| chr4:128098767
|
A | ATATATAT others(9): Show |
1 | a0002c0002t0002g0287 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.813+438_813+439ins others(16): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098767 | |||||
| chr4:128098767
|
A | ATATATAT others(4): Show |
6 | a0002c0002t0002g0028a0002c0002t0002g0290a0002c0002t0002g0296others(3): Show | 6 | HG01081.hp2 HG01496.hp1 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.813+438_813+439ins others(11): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098767 | |||||
| chr4:128098767
|
A | ATATATAT others(5): Show |
13 | a0002c0002t0002g0057a0002c0002t0002g0060a0002c0002t0002g0062others(10): Show | 13 | HG00544.hp1 HG00639.hp1 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.813+438_813+439ins others(12): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098767 | |||||
| chr4:128098767
|
A | ATATATAT others(6): Show |
1 | a0002c0002t0002g0330 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.813+438_813+439ins others(13): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098767 | |||||
| chr4:128098767
|
A | ATATATAT others(3): Show |
1 | a0002c0002t0002g0130 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.813+438_813+439ins others(10): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098767 | |||||
| chr4:128098767
|
A | ATATATAT others(4): Show |
1 | a0002c0002t0002g0087 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.813+438_813+439ins others(11): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098767 | |||||
| chr4:128098767
|
A | ATATATTT others(3): Show |
1 | a0002c0002t0002g0024 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.813+438_813+439ins others(10): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098767 | |||||
| chr4:128098767
|
A | ATATATTT others(5): Show |
1 | a0002c0002t0002g0053 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.813+438_813+439ins others(12): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098767 | |||||
| chr4:128098767
|
A | G | 1 | a0004c0005t0005g0282 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.813+437A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128098767 | ||||||
| chr4:128098767
|
A | T | 2 | a0002c0002t0002g0063a0002c0002t0015g0020 | 2 | HG02165.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.813+437A>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128098767 | ||||||
| chr4:128098767
|
ATTT | A | 22 | a0001c0001t0004g0309a0001c0001t0004g0310a0001c0001t0004g0312others(19): Show | 22 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.813+463_813+465del others(3): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098767 | |||||
| chr4:128098767
|
ATTTT | A | 6 | a0001c0001t0004g0311a0001c0001t0004g0328a0002c0003t0006g0004others(3): Show | 6 | HG02109.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.813+462_813+465del others(4): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098767 | |||||
| chr4:128098767
|
ATTTTTTT others(3): Show |
A | 1 | a0001c0018t0003g0254 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.813+456_813+465del others(10): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128098767 | |||||
| chr4:128098768
|
T | TA | 57 | a0001c0001t0001g0109a0001c0001t0001g0135a0001c0001t0001g0136others(54): Show | 57 | HG00140.hp2 HG00408.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.813+438_813+439ins others(1): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128098768 | ||||||
| chr4:128098768
|
T | TATATATA others(4): Show |
2 | a0002c0002t0002g0081a0008c0009t0005g0113 | 2 | HG02109.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.813+438_813+439ins others(11): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128098768 | ||||||
| chr4:128098768
|
T | TATATATA others(8): Show |
1 | a0002c0002t0002g0092 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.813+438_813+439ins others(15): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128098768 | ||||||
| chr4:128098768
|
T | TATATATA others(12): Show |
1 | a0002c0002t0002g0068 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.813+438_813+439ins others(19): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128098768 | ||||||
| chr4:128098768
|
T | TATATATA others(16): Show |
1 | a0010c0011t0005g0123 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.813+438_813+439ins others(23): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128098768 | ||||||
| chr4:128098768
|
T | TATATATA others(12): Show |
1 | a0004c0005t0005g0281 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.813+438_813+439ins others(19): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128098768 | ||||||
| chr4:128098768
|
T | TATATATA others(8): Show |
1 | a0004c0005t0005g0283 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.813+438_813+439ins others(15): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128098768 | ||||||
| chr4:128098769
|
T | A | 102 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(99): Show | 102 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.813+439T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128098769 | ||||||
| chr4:128098769
|
T | G | 2 | a0002c0003t0005g0122a0002c0012t0005g0098 | 2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.813+439T>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128098769 | ||||||
| chr4:128098770
|
T | A | 59 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0135others(56): Show | 59 | HG00408.hp2 HG00673.hp2 HG01070.hp1 others(56): Show |
intron_variant | MODIFIER | c.813+440T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128098770 | ||||||
| chr4:128098770
|
T | G | 1 | a0010c0011t0005g0123 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.813+440T>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128098770 | ||||||
| chr4:128098771
|
T | A | 100 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(97): Show | 100 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.813+441T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128098771 | ||||||
| chr4:128098772
|
T | A | 74 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0135others(71): Show | 74 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.813+442T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128098772 | ||||||
| chr4:128098773
|
T | A | 83 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(80): Show | 83 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.813+443T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128098773 | ||||||
| chr4:128098774
|
T | A | 38 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0135others(35): Show | 38 | HG00408.hp2 HG01070.hp1 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.813+444T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128098774 | ||||||
| chr4:128098775
|
T | A | 73 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(70): Show | 73 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.813+445T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128098775 | ||||||
| chr4:128098776
|
T | A | 32 | a0001c0001t0001g0107a0001c0001t0001g0135a0001c0001t0001g0136others(29): Show | 32 | HG00408.hp2 HG01070.hp1 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.813+446T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128098776 | ||||||
| chr4:128098777
|
T | A | 56 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(53): Show | 56 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.813+447T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128098777 | ||||||
| chr4:128098778
|
T | A | 10 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0159others(7): Show | 10 | HG00408.hp2 HG01167.hp1 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.813+448T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128098778 | ||||||
| chr4:128098779
|
T | A | 21 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(18): Show | 21 | HG00673.hp1 HG00741.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.813+449T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128098779 | ||||||
| chr4:128098780
|
T | A | 3 | a0001c0001t0001g0159a0001c0001t0001g0205a0007c0008t0001g0158 | 3 | HG01167.hp1 HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.813+450T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128098780 | ||||||
| chr4:128098781
|
T | A | 9 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(6): Show | 9 | HG01192.hp1 HG01515.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.813+451T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128098781 | ||||||
| chr4:128098782
|
T | A | 2 | a0001c0001t0001g0159a0007c0008t0001g0158 | 2 | HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.813+452T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128098782 | ||||||
| chr4:128098784
|
T | A | 1 | a0001c0001t0001g0159 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.813+454T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128098784 | ||||||
| chr4:128098860
|
A | G | 1 | a0001c0001t0001g0211 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.813+530A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128098860 | ||||||
| chr4:128099029
|
G | A | 11 | a0002c0003t0001g0104a0002c0003t0001g0105a0002c0003t0006g0003others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.813+699G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128099029 | ||||||
| chr4:128099131
|
C | T | 4 | a0002c0002t0002g0012a0002c0002t0002g0054a0002c0002t0002g0055others(1): Show | 4 | NA18954.hp2 NA18955.hp1 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.813+801C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128099131 | ||||||
| chr4:128099159
|
G | GA | 21 | a0001c0001t0001g0152a0001c0001t0001g0168a0001c0001t0003g0127others(18): Show | 21 | HG00408.hp2 HG00558.hp1 HG00609.hp2 others(18): Show |
intron_variant | MODIFIER | c.813+839dupA | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128099159 | |||||
| chr4:128099221
|
GCCAATTT others(4): Show |
G | 3 | a0002c0002t0002g0053a0002c0002t0002g0086a0002c0002t0002g0087 | 3 | NA18980.hp2 NA18985.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.813+894_813+904del others(11): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128099221 | |||||
| chr4:128099286
|
C | T | 22 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(19): Show | 22 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.813+956C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128099286 | ||||||
| chr4:128099290
|
C | CT | 27 | a0001c0001t0003g0242a0001c0001t0003g0247a0001c0001t0004g0309others(24): Show | 27 | HG00099.hp2 HG00558.hp2 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.813+975dupT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128099290 | |||||
| chr4:128099290
|
CT | C | 17 | a0001c0001t0001g0163a0001c0001t0001g0207a0001c0001t0003g0227others(14): Show | 17 | HG00639.hp2 HG01516.hp2 HG02015.hp2 others(14): Show |
intron_variant | MODIFIER | c.813+975delT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128099290 | |||||
| chr4:128099368
|
A | G | 1 | a0011c0016t0003g0277 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.813+1038A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128099368 | ||||||
| chr4:128099511
|
G | T | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(164): Show | 167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.813+1181G>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128099511 | ||||||
| chr4:128099715
|
T | C | 1 | a0002c0012t0005g0098 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.813+1385T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128099715 | ||||||
| chr4:128099715
|
T | TAC | 4 | a0002c0002t0002g0092a0002c0002t0008g0300a0008c0009t0005g0113others(1): Show | 4 | HG02300.hp2 HG02572.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.813+1405_813+1406d others(4): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128099715 | |||||
| chr4:128099717
|
C | T | 201 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(198): Show | 201 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.813+1387C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128099717 | ||||||
| chr4:128099828
|
T | C | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(190): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.813+1498T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128099828 | ||||||
| chr4:128099832
|
C | T | 1 | a0001c0001t0003g0240 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.813+1502C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128099832 | ||||||
| chr4:128099950
|
G | A | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(164): Show | 167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.813+1620G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128099950 | ||||||
| chr4:128099998
|
AG | A | 11 | a0002c0003t0001g0104a0002c0003t0001g0105a0002c0003t0006g0003others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.813+1670delG | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128099998 | |||||
| chr4:128100148
|
G | A | 11 | a0002c0003t0001g0104a0002c0003t0001g0105a0002c0003t0006g0003others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.813+1818G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128100148 | ||||||
| chr4:128100169
|
C | A | 1 | a0002c0003t0006g0009 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.813+1839C>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128100169 | ||||||
| chr4:128100243
|
A | G | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(190): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.813+1913A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128100243 | ||||||
| chr4:128100429
|
A | C | 204 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(201): Show | 204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.813+2099A>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128100429 | ||||||
| chr4:128100835
|
TGAGA | T | 22 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(19): Show | 22 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.813+2506_813+2509d others(6): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128100835 | ||||||
| chr4:128100899
|
C | G | 6 | a0001c0001t0001g0266a0003c0004t0001g0172a0003c0004t0001g0182others(3): Show | 6 | HG01109.hp2 HG01167.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.813+2569C>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128100899 | ||||||
| chr4:128100919
|
G | A | 1 | a0002c0002t0002g0053 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.813+2589G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128100919 | ||||||
| chr4:128101048
|
T | C | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(207): Show | 210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.813+2718T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128101048 | ||||||
| chr4:128101251
|
A | C | 1 | a0001c0001t0001g0010 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.813+2921A>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128101251 | ||||||
| chr4:128101298
|
ACT | A | 11 | a0002c0003t0001g0104a0002c0003t0001g0105a0002c0003t0006g0003others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.813+2971_813+2972d others(4): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128101298 | |||||
| chr4:128101449
|
A | G | 58 | a0001c0001t0001g0168a0001c0001t0001g0236a0001c0001t0003g0102others(55): Show | 58 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.813+3119A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128101449 | ||||||
| chr4:128101515
|
A | G | 1 | a0001c0001t0004g0319 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.813+3185A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128101515 | ||||||
| chr4:128101561
|
G | GT | 6 | a0001c0001t0001g0162a0001c0001t0001g0263a0001c0001t0001g0265others(3): Show | 6 | HG01934.hp1 HG02602.hp1 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.813+3246dupT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128101561 | |||||
| chr4:128101561
|
G | GTTT | 9 | a0002c0003t0001g0105a0002c0003t0006g0003a0002c0003t0006g0004others(6): Show | 9 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.813+3244_813+3246d others(5): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128101561 | |||||
| chr4:128101719
|
A | G | 11 | a0002c0003t0001g0104a0002c0003t0001g0105a0002c0003t0006g0003others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.813+3389A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128101719 | ||||||
| chr4:128101769
|
C | T | 8 | a0002c0002t0002g0051a0002c0002t0002g0069a0002c0002t0002g0071others(5): Show | 8 | HG02080.hp1 NA18941.hp1 NA18969.hp1 others(5): Show |
intron_variant | MODIFIER | c.813+3439C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128101769 | ||||||
| chr4:128101773
|
G | A | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(190): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.813+3443G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128101773 | ||||||
| chr4:128102056
|
A | G | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(164): Show | 167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.813+3726A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128102056 | ||||||
| chr4:128102437
|
C | T | 3 | a0002c0002t0002g0296a0002c0002t0002g0307a0002c0002t0002g0331 | 3 | NA19007.hp1 NA19056.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.813+4107C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128102437 | ||||||
| chr4:128102592
|
C | T | 1 | a0001c0001t0003g0242 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.813+4262C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128102592 | ||||||
| chr4:128102724
|
A | C | 1 | a0002c0012t0005g0098 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.813+4394A>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128102724 | ||||||
| chr4:128102725
|
TA | T | 22 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(19): Show | 22 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.813+4396delA | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128102725 | ||||||
| chr4:128103079
|
A | G | 9 | a0002c0003t0006g0003a0002c0003t0006g0004a0002c0003t0006g0005others(6): Show | 9 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.814-4060A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128103079 | ||||||
| chr4:128103118
|
C | T | 59 | a0001c0001t0001g0211a0001c0001t0001g0236a0001c0001t0001g0249others(56): Show | 59 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.814-4021C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128103118 | ||||||
| chr4:128103155
|
A | C | 3 | a0005c0006t0001g0099a0005c0006t0001g0100a0005c0006t0001g0101 | 3 | HG01168.hp1 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.814-3984A>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128103155 | ||||||
| chr4:128103403
|
T | A | 3 | a0002c0003t0005g0122a0002c0012t0005g0098a0010c0011t0005g0123 | 3 | HG02280.hp2 HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.814-3736T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128103403 | ||||||
| chr4:128103424
|
A | T | 1 | a0001c0001t0003g0240 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.814-3715A>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128103424 | ||||||
| chr4:128103431
|
A | G | 11 | a0002c0003t0001g0104a0002c0003t0001g0105a0002c0003t0006g0003others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.814-3708A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128103431 | ||||||
| chr4:128103466
|
T | C | 1 | a0001c0001t0004g0325 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.814-3673T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128103466 | ||||||
| chr4:128103561
|
C | CT | 11 | a0001c0001t0001g0110a0001c0001t0004g0308a0002c0002t0002g0053others(8): Show | 11 | HG02004.hp1 HG02572.hp1 HG02735.hp1 others(8): Show |
intron_variant | MODIFIER | c.814-3559dupT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128103561 | |||||
| chr4:128103561
|
C | CTT | 24 | a0001c0001t0004g0309a0001c0001t0004g0310a0001c0001t0004g0311others(21): Show | 24 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.814-3560_814-3559d others(4): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128103561 | |||||
| chr4:128103561
|
CT | C | 19 | a0001c0001t0001g0109a0001c0001t0001g0143a0001c0001t0001g0168others(16): Show | 19 | HG00408.hp1 HG01070.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.814-3559delT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128103561 | |||||
| chr4:128103618
|
G | C | 3 | a0001c0001t0003g0210a0001c0001t0003g0237a0001c0001t0003g0244 | 3 | HG00140.hp1 HG04184.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.814-3521G>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128103618 | ||||||
| chr4:128103708
|
G | A | 2 | a0002c0002t0002g0284a0002c0002t0002g0287 | 2 | HG01433.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.814-3431G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128103708 | ||||||
| chr4:128103719
|
C | T | 2 | a0002c0002t0002g0296a0002c0002t0002g0307 | 2 | NA19056.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.814-3420C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128103719 | ||||||
| chr4:128103804
|
C | T | 11 | a0002c0003t0001g0104a0002c0003t0001g0105a0002c0003t0006g0003others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.814-3335C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128103804 | ||||||
| chr4:128103805
|
G | A | 90 | a0001c0001t0001g0001a0001c0001t0001g0107a0001c0001t0001g0108others(87): Show | 90 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.814-3334G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128103805 | ||||||
| chr4:128103845
|
A | G | 1 | a0002c0002t0002g0053 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.814-3294A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128103845 | ||||||
| chr4:128103888
|
A | G | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(207): Show | 210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.814-3251A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128103888 | ||||||
| chr4:128103947
|
C | T | 1 | a0010c0011t0005g0123 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.814-3192C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128103947 | ||||||
| chr4:128103958
|
T | G | 1 | a0002c0002t0002g0016 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.814-3181T>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128103958 | ||||||
| chr4:128103967
|
T | G | 1 | a0002c0002t0002g0071 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.814-3172T>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128103967 | ||||||
| chr4:128104255
|
C | T | 2 | a0008c0009t0005g0113a0008c0009t0005g0119 | 2 | HG02572.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.814-2884C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128104255 | ||||||
| chr4:128104537
|
C | T | 9 | a0002c0003t0006g0003a0002c0003t0006g0004a0002c0003t0006g0005others(6): Show | 9 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.814-2602C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128104537 | ||||||
| chr4:128104599
|
C | T | 49 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0126others(46): Show | 49 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.814-2540C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128104599 | ||||||
| chr4:128104647
|
T | C | 1 | a0001c0001t0001g0144 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.814-2492T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128104647 | ||||||
| chr4:128104695
|
C | T | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(190): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.814-2444C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128104695 | ||||||
| chr4:128104912
|
G | A | 2 | a0008c0009t0005g0113a0008c0009t0005g0119 | 2 | HG02572.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.814-2227G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128104912 | ||||||
| chr4:128104929
|
T | C | 4 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.814-2210T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128104929 | ||||||
| chr4:128105071
|
T | G | 204 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(201): Show | 204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.814-2068T>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128105071 | ||||||
| chr4:128105077
|
G | GT | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(166): Show | 169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.814-2052dupT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128105077 | |||||
| chr4:128105246
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.814-1893C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128105246 | ||||||
| chr4:128105301
|
G | A | 3 | a0005c0006t0001g0099a0005c0006t0001g0100a0005c0006t0001g0101 | 3 | HG01168.hp1 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.814-1838G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128105301 | ||||||
| chr4:128105618
|
C | T | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.814-1521C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128105618 | ||||||
| chr4:128105749
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.814-1390G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128105749 | ||||||
| chr4:128105886
|
G | T | 5 | a0002c0002t0002g0018a0002c0002t0002g0032a0002c0002t0002g0047others(2): Show | 5 | NA18950.hp2 NA18973.hp2 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.814-1253G>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128105886 | ||||||
| chr4:128106030
|
C | CT | 16 | a0002c0002t0002g0051a0002c0002t0002g0069a0002c0002t0002g0071others(13): Show | 16 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.814-1097dupT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128106030 | |||||
| chr4:128106065
|
C | G | 3 | a0002c0002t0002g0032a0002c0002t0002g0047a0002c0002t0002g0116 | 3 | NA18950.hp2 NA18973.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.814-1074C>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128106065 | ||||||
| chr4:128106130
|
TCTC | T | 22 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(19): Show | 22 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.814-1006_814-1004d others(5): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | 128106130 | |||||
| chr4:128106274
|
G | A | 1 | a0002c0002t0002g0086 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.814-865G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128106274 | ||||||
| chr4:128106316
|
C | T | 1 | a0010c0011t0005g0123 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.814-823C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128106316 | ||||||
| chr4:128106317
|
G | A | 1 | a0001c0001t0003g0217 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.814-822G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128106317 | ||||||
| chr4:128106380
|
A | G | 1 | a0002c0002t0002g0063 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.814-759A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128106380 | ||||||
| chr4:128106718
|
A | G | 2 | a0008c0009t0005g0113a0008c0009t0005g0119 | 2 | HG02572.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.814-421A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128106718 | ||||||
| chr4:128106902
|
C | G | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(190): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.814-237C>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128106902 | ||||||
| chr4:128106966
|
C | A | 11 | a0002c0003t0001g0104a0002c0003t0001g0105a0002c0003t0006g0003others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.814-173C>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128106966 | ||||||
| chr4:128107048
|
A | G | 1 | a0002c0002t0010g0036 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.814-91A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | chr4 | 128107048 | ||||||
| chr4:128107364
|
C | A | 1 | a0001c0001t0003g0241 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.988+51C>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128107364 | ||||||
| chr4:128107524
|
T | C | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(190): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.988+211T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128107524 | ||||||
| chr4:128107604
|
A | G | 4 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.988+291A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128107604 | ||||||
| chr4:128107656
|
A | T | 11 | a0002c0003t0001g0104a0002c0003t0001g0105a0002c0003t0006g0003others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.988+343A>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128107656 | ||||||
| chr4:128107708
|
C | T | 1 | a0002c0002t0002g0112 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.988+395C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128107708 | ||||||
| chr4:128107718
|
T | C | 2 | a0001c0001t0003g0216a0001c0001t0003g0232 | 2 | NA18946.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.988+405T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128107718 | ||||||
| chr4:128107854
|
G | GA | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(190): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.988+547dupA | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr4 | 128107854 | |||||
| chr4:128108151
|
T | C | 1 | a0002c0002t0002g0032 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.988+838T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128108151 | ||||||
| chr4:128108235
|
G | A | 5 | a0002c0002t0002g0041a0002c0002t0002g0050a0002c0002t0002g0081others(2): Show | 5 | HG02109.hp2 HG02280.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.988+922G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128108235 | ||||||
| chr4:128108398
|
C | T | 1 | a0002c0012t0005g0098 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.988+1085C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128108398 | ||||||
| chr4:128108492
|
A | G | 1 | a0002c0003t0005g0122 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.988+1179A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128108492 | ||||||
| chr4:128108498
|
G | A | 1 | a0002c0002t0002g0023 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.988+1185G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128108498 | ||||||
| chr4:128108602
|
A | T | 22 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(19): Show | 22 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.988+1289A>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128108602 | ||||||
| chr4:128108666
|
A | T | 1 | a0002c0002t0002g0331 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.988+1353A>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128108666 | ||||||
| chr4:128108733
|
A | C | 1 | a0010c0011t0005g0123 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.988+1420A>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128108733 | ||||||
| chr4:128109059
|
G | A | 6 | a0002c0003t0005g0122a0002c0012t0005g0098a0004c0005t0005g0281others(3): Show | 6 | HG02055.hp1 HG02280.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.988+1746G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128109059 | ||||||
| chr4:128109075
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.988+1762A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128109075 | ||||||
| chr4:128109076
|
T | G | 2 | a0001c0001t0001g0211a0001c0001t0001g0249 | 2 | HG02572.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.988+1763T>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128109076 | ||||||
| chr4:128109386
|
C | A | 1 | a0001c0001t0001g0271 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.988+2073C>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128109386 | ||||||
| chr4:128109414
|
T | A | 22 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(19): Show | 22 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.988+2101T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128109414 | ||||||
| chr4:128109493
|
A | G | 1 | a0002c0002t0002g0090 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.988+2180A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128109493 | ||||||
| chr4:128109839
|
CA | C | 6 | a0002c0003t0005g0122a0002c0012t0005g0098a0004c0005t0005g0281others(3): Show | 6 | HG02055.hp1 HG02280.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.988+2536delA | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr4 | 128109839 | |||||
| chr4:128109869
|
T | A | 4 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.988+2556T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128109869 | ||||||
| chr4:128109910
|
T | G | 6 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(3): Show | 6 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.988+2597T>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128109910 | ||||||
| chr4:128109938
|
CTG | C | 11 | a0002c0003t0001g0104a0002c0003t0001g0105a0002c0003t0006g0003others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.988+2627_988+2628d others(4): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr4 | 128109938 | |||||
| chr4:128109942
|
C | T | 9 | a0002c0003t0006g0003a0002c0003t0006g0004a0002c0003t0006g0005others(6): Show | 9 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.988+2629C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128109942 | ||||||
| chr4:128110301
|
A | T | 1 | a0001c0001t0001g0001 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.988+2988A>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128110301 | ||||||
| chr4:128110347
|
C | T | 22 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(19): Show | 22 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.988+3034C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128110347 | ||||||
| chr4:128110415
|
T | TA | 25 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(22): Show | 25 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.988+3113dupA | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr4 | 128110415 | |||||
| chr4:128110416
|
A | T | 164 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(161): Show | 164 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.988+3103A>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128110416 | ||||||
| chr4:128110448
|
C | T | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(190): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.988+3135C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128110448 | ||||||
| chr4:128110491
|
A | T | 1 | a0010c0011t0005g0123 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.988+3178A>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128110491 | ||||||
| chr4:128110493
|
C | T | 1 | a0001c0001t0001g0185 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.988+3180C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128110493 | ||||||
| chr4:128110534
|
G | A | 1 | a0002c0017t0002g0074 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.988+3221G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128110534 | ||||||
| chr4:128110546
|
G | T | 4 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.988+3233G>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128110546 | ||||||
| chr4:128110633
|
C | T | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(164): Show | 167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.988+3320C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128110633 | ||||||
| chr4:128110658
|
CAGAGCGA others(27): Show |
C | 4 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.988+3349_988+3382d others(36): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr4 | 128110658 | |||||
| chr4:128110668
|
C | T | 22 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(19): Show | 22 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.988+3355C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128110668 | ||||||
| chr4:128110676
|
C | CAAA | 11 | a0002c0003t0001g0104a0002c0003t0001g0105a0002c0003t0006g0003others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.988+3378_988+3380d others(5): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr4 | 128110676 | |||||
| chr4:128110676
|
C | CAAAAAAA | 13 | a0001c0001t0001g0202a0001c0001t0003g0128a0001c0001t0003g0238others(10): Show | 13 | HG01168.hp1 HG01975.hp2 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.988+3374_988+3380d others(9): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr4 | 128110676 | |||||
| chr4:128110676
|
C | CAAAAAAA others(1): Show |
126 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0110others(123): Show | 126 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.988+3373_988+3380d others(10): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr4 | 128110676 | |||||
| chr4:128110676
|
C | CAAAAAAA others(2): Show |
28 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(25): Show | 28 | HG00544.hp2 HG01074.hp1 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.988+3372_988+3380d others(11): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr4 | 128110676 | |||||
| chr4:128110676
|
C | CAAAAAAA others(3): Show |
22 | a0001c0001t0001g0161a0001c0001t0004g0308a0001c0001t0004g0310others(19): Show | 22 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.988+3371_988+3380d others(12): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr4 | 128110676 | |||||
| chr4:128110676
|
C | CAAAAAAA others(4): Show |
4 | a0001c0001t0004g0309a0001c0001t0004g0312a0001c0001t0004g0313others(1): Show | 4 | NA18955.hp2 NA18990.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.988+3370_988+3380d others(13): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr4 | 128110676 | |||||
| chr4:128110676
|
C | CAAAAAAA others(6): Show |
3 | a0002c0002t0002g0296a0002c0002t0002g0307a0002c0002t0002g0331 | 3 | NA19007.hp1 NA19056.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.988+3368_988+3380d others(15): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr4 | 128110676 | |||||
| chr4:128110676
|
C | CAAAAAAA others(9): Show |
1 | a0002c0002t0002g0284 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.988+3365_988+3380d others(18): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr4 | 128110676 | |||||
| chr4:128110676
|
C | CAAAAAAA others(10): Show |
4 | a0002c0002t0002g0026a0002c0002t0002g0027a0002c0002t0002g0028others(1): Show | 4 | HG01496.hp1 HG02040.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.988+3364_988+3380d others(19): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr4 | 128110676 | |||||
| chr4:128110676
|
C | CAAAAAAA others(11): Show |
9 | a0002c0002t0002g0021a0002c0002t0002g0029a0002c0002t0002g0092others(6): Show | 9 | HG01109.hp1 HG01433.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.988+3380_988+3381i others(20): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr4 | 128110676 | |||||
| chr4:128110676
|
C | CAAAAAAA others(12): Show |
5 | a0002c0002t0002g0022a0002c0002t0002g0024a0002c0002t0002g0025others(2): Show | 5 | HG00735.hp1 HG02451.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.988+3380_988+3381i others(21): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr4 | 128110676 | |||||
| chr4:128110676
|
C | CAAAAAAA others(13): Show |
2 | a0002c0002t0002g0019a0010c0011t0005g0123 | 2 | HG02280.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.988+3380_988+3381i others(22): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr4 | 128110676 | |||||
| chr4:128110676
|
C | CAAAAAAA others(14): Show |
3 | a0002c0002t0002g0050a0002c0002t0005g0097a0002c0003t0005g0122 | 3 | HG02896.hp2 HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.988+3380_988+3381i others(23): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr4 | 128110676 | |||||
| chr4:128110676
|
C | CAAAAAAA others(15): Show |
6 | a0002c0002t0002g0023a0002c0002t0002g0041a0002c0002t0002g0052others(3): Show | 6 | HG01256.hp2 HG01258.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.988+3380_988+3381i others(24): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr4 | 128110676 | |||||
| chr4:128110676
|
C | CAAAAAAA others(16): Show |
10 | a0002c0002t0002g0038a0002c0002t0002g0071a0002c0002t0002g0081others(7): Show | 10 | HG02109.hp2 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.988+3380_988+3381i others(25): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr4 | 128110676 | |||||
| chr4:128110676
|
C | CAAAAAAA others(17): Show |
7 | a0002c0002t0002g0068a0002c0002t0002g0070a0002c0002t0002g0114others(4): Show | 7 | HG00741.hp2 HG01243.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.988+3380_988+3381i others(26): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr4 | 128110676 | |||||
| chr4:128110676
|
C | CAAAAAAA others(18): Show |
2 | a0002c0002t0002g0051a0008c0009t0005g0119 | 2 | HG02572.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.988+3380_988+3381i others(27): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr4 | 128110676 | |||||
| chr4:128110676
|
C | CAAAAAAA others(19): Show |
3 | a0002c0002t0002g0034a0002c0002t0002g0080a0002c0002t0012g0096 | 3 | HG01106.hp1 NA18982.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.988+3380_988+3381i others(28): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr4 | 128110676 | |||||
| chr4:128110676
|
C | CAAAAAAA others(20): Show |
11 | a0002c0002t0002g0015a0002c0002t0002g0035a0002c0002t0002g0037others(8): Show | 11 | HG00438.hp2 HG00597.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.988+3380_988+3381i others(29): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr4 | 128110676 | |||||
| chr4:128110676
|
C | CAAAAAAA others(21): Show |
21 | a0002c0002t0002g0032a0002c0002t0002g0040a0002c0002t0002g0043others(18): Show | 21 | HG00639.hp1 HG00735.hp2 HG02074.hp2 others(18): Show |
intron_variant | MODIFIER | c.988+3380_988+3381i others(30): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr4 | 128110676 | |||||
| chr4:128110676
|
C | CAAAAAAA others(22): Show |
7 | a0002c0002t0002g0045a0002c0002t0002g0053a0002c0002t0002g0054others(4): Show | 7 | HG02027.hp1 HG02273.hp1 HG03710.hp1 others(4): Show |
intron_variant | MODIFIER | c.988+3380_988+3381i others(31): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr4 | 128110676 | |||||
| chr4:128110676
|
C | CAAAAAAA others(23): Show |
2 | a0002c0002t0002g0087a0002c0002t0011g0030 | 2 | NA18945.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.988+3380_988+3381i others(32): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr4 | 128110676 | |||||
| chr4:128110676
|
C | CAAAAAAA others(24): Show |
1 | a0002c0002t0002g0047 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.988+3380_988+3381i others(33): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr4 | 128110676 | |||||
| chr4:128110676
|
C | CAAAAAAA others(26): Show |
3 | a0002c0002t0002g0063a0002c0002t0002g0089a0002c0002t0002g0291 | 3 | HG02165.hp1 NA18747.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.988+3380_988+3381i others(35): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr4 | 128110676 | |||||
| chr4:128110676
|
C | CAAAAAAA others(27): Show |
6 | a0002c0002t0002g0016a0002c0002t0002g0058a0002c0002t0002g0060others(3): Show | 6 | HG01070.hp2 HG01515.hp1 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.988+3380_988+3381i others(36): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr4 | 128110676 | |||||
| chr4:128110676
|
C | CAAAAAAA others(28): Show |
2 | a0002c0002t0002g0115a0002c0002t0002g0120 | 2 | HG03688.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.988+3380_988+3381i others(37): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr4 | 128110676 | |||||
| chr4:128110676
|
C | CAAAAAAA others(29): Show |
2 | a0002c0002t0002g0013a0002c0002t0002g0018 | 2 | HG03669.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.988+3380_988+3381i others(38): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr4 | 128110676 | |||||
| chr4:128110676
|
C | CAAAAAAA others(30): Show |
4 | a0002c0002t0002g0066a0002c0002t0002g0294a0002c0002t0002g0297others(1): Show | 4 | HG00423.hp1 HG00544.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.988+3380_988+3381i others(39): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr4 | 128110676 | |||||
| chr4:128110676
|
C | CAAAAAAA others(31): Show |
1 | a0002c0002t0002g0061 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.988+3380_988+3381i others(40): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr4 | 128110676 | |||||
| chr4:128110676
|
C | CAAAAAAA others(32): Show |
1 | a0002c0002t0002g0056 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.988+3380_988+3381i others(41): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr4 | 128110676 | |||||
| chr4:128110676
|
C | CAAAAAAA others(34): Show |
1 | a0002c0002t0002g0012 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.988+3380_988+3381i others(43): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr4 | 128110676 | |||||
| chr4:128110676
|
C | CAAAAAAA others(35): Show |
1 | a0002c0002t0002g0336 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.988+3380_988+3381i others(44): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr4 | 128110676 | |||||
| chr4:128110676
|
C | CAAAAAAA others(48): Show |
1 | a0002c0002t0002g0017 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.988+3380_988+3381i others(57): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr4 | 128110676 | |||||
| chr4:128110707
|
A | G | 57 | a0001c0001t0001g0168a0001c0001t0003g0102a0001c0001t0003g0103others(54): Show | 57 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.988+3394A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128110707 | ||||||
| chr4:128110722
|
G | A | 204 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(201): Show | 204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.988+3409G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128110722 | ||||||
| chr4:128110803
|
T | C | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(164): Show | 167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.988+3490T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128110803 | ||||||
| chr4:128111043
|
A | AT | 15 | a0001c0001t0001g0263a0002c0002t0002g0080a0002c0002t0002g0087others(12): Show | 15 | HG01106.hp1 HG02109.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.989-3508dupT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr4 | 128111043 | |||||
| chr4:128111043
|
A | ATT | 9 | a0001c0001t0003g0213a0001c0001t0003g0214a0001c0001t0003g0225others(6): Show | 9 | HG02015.hp2 HG02145.hp1 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.989-3509_989-3508d others(4): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr4 | 128111043 | |||||
| chr4:128111043
|
AT | A | 10 | a0001c0001t0003g0127a0001c0001t0003g0278a0002c0002t0002g0071others(7): Show | 10 | HG01975.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.989-3508delT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr4 | 128111043 | |||||
| chr4:128111082
|
C | T | 4 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.989-3488C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128111082 | ||||||
| chr4:128111200
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.989-3370C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128111200 | ||||||
| chr4:128111393
|
A | G | 2 | a0008c0009t0005g0113a0008c0009t0005g0119 | 2 | HG02572.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.989-3177A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128111393 | ||||||
| chr4:128111532
|
A | G | 3 | a0002c0002t0002g0015a0002c0002t0002g0017a0002c0002t0002g0049 | 3 | HG02559.hp2 HG02622.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.989-3038A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128111532 | ||||||
| chr4:128111582
|
A | G | 11 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(8): Show | 11 | HG01192.hp1 HG02486.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.989-2988A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128111582 | ||||||
| chr4:128111626
|
G | A | 4 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.989-2944G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128111626 | ||||||
| chr4:128111690
|
CTT | C | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(190): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.989-2873_989-2872d others(4): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr4 | 128111690 | |||||
| chr4:128111723
|
G | T | 3 | a0002c0002t0002g0296a0002c0002t0002g0307a0002c0002t0002g0331 | 3 | NA19007.hp1 NA19056.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.989-2847G>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128111723 | ||||||
| chr4:128111734
|
C | G | 1 | a0001c0001t0001g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.989-2836C>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128111734 | ||||||
| chr4:128111838
|
C | T | 4 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.989-2732C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128111838 | ||||||
| chr4:128111856
|
AT | A | 22 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(19): Show | 22 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.989-2700delT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr4 | 128111856 | |||||
| chr4:128111941
|
C | T | 1 | a0002c0012t0005g0098 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.989-2629C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128111941 | ||||||
| chr4:128111989
|
C | T | 1 | a0002c0002t0005g0059 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.989-2581C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128111989 | ||||||
| chr4:128112061
|
T | G | 1 | a0002c0002t0002g0061 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.989-2509T>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128112061 | ||||||
| chr4:128112092
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.989-2478G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128112092 | ||||||
| chr4:128112235
|
A | T | 1 | a0002c0002t0002g0085 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.989-2335A>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128112235 | ||||||
| chr4:128112330
|
G | A | 1 | a0001c0001t0001g0211 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.989-2240G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128112330 | ||||||
| chr4:128112448
|
A | T | 1 | a0001c0001t0001g0109 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.989-2122A>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128112448 | ||||||
| chr4:128112466
|
A | AT | 122 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(119): Show | 122 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.989-2079dupT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr4 | 128112466 | |||||
| chr4:128112466
|
A | ATT | 20 | a0001c0001t0001g0124a0001c0001t0001g0178a0001c0001t0001g0194others(17): Show | 20 | HG00673.hp2 HG01169.hp2 HG01515.hp2 others(17): Show |
intron_variant | MODIFIER | c.989-2080_989-2079d others(4): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr4 | 128112466 | |||||
| chr4:128112466
|
A | ATTT | 45 | a0001c0001t0001g0168a0001c0001t0003g0102a0001c0001t0003g0111others(42): Show | 45 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(42): Show |
intron_variant | MODIFIER | c.989-2081_989-2079d others(5): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr4 | 128112466 | |||||
| chr4:128112466
|
A | ATTTT | 7 | a0001c0001t0003g0103a0001c0001t0003g0228a0001c0001t0003g0229others(4): Show | 7 | HG00609.hp2 HG01346.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.989-2082_989-2079d others(6): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr4 | 128112466 | |||||
| chr4:128112466
|
AT | A | 24 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(21): Show | 24 | HG00597.hp1 HG01074.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.989-2079delT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr4 | 128112466 | |||||
| chr4:128112565
|
C | G | 1 | a0002c0002t0002g0061 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.989-2005C>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128112565 | ||||||
| chr4:128112717
|
G | A | 22 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(19): Show | 22 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.989-1853G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128112717 | ||||||
| chr4:128112726
|
G | A | 1 | a0002c0002t0002g0086 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.989-1844G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128112726 | ||||||
| chr4:128112856
|
T | C | 2 | a0001c0001t0001g0199a0001c0001t0001g0262 | 2 | NA19004.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.989-1714T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128112856 | ||||||
| chr4:128112895
|
G | A | 1 | a0002c0002t0002g0299 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.989-1675G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128112895 | ||||||
| chr4:128113032
|
G | T | 1 | a0001c0018t0003g0254 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.989-1538G>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128113032 | ||||||
| chr4:128113086
|
G | A | 203 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(200): Show | 203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.989-1484G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128113086 | ||||||
| chr4:128113218
|
T | C | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(207): Show | 210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.989-1352T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128113218 | ||||||
| chr4:128113309
|
A | G | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(164): Show | 167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.989-1261A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128113309 | ||||||
| chr4:128113322
|
G | T | 4 | a0002c0003t0006g0003a0002c0003t0006g0005a0002c0003t0006g0285others(1): Show | 4 | HG02145.hp2 HG02257.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.989-1248G>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128113322 | ||||||
| chr4:128113351
|
CT | C | 6 | a0001c0001t0003g0125a0001c0001t0003g0220a0001c0001t0003g0256others(3): Show | 6 | HG01168.hp1 HG01169.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.989-1204delT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr4 | 128113351 | |||||
| chr4:128113485
|
T | C | 227 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(224): Show | 227 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.989-1085T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128113485 | ||||||
| chr4:128113632
|
C | T | 58 | a0001c0001t0001g0168a0001c0001t0001g0236a0001c0001t0003g0102others(55): Show | 58 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.989-938C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128113632 | ||||||
| chr4:128113752
|
C | T | 11 | a0002c0003t0001g0104a0002c0003t0001g0105a0002c0003t0006g0003others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.989-818C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128113752 | ||||||
| chr4:128113781
|
C | CT | 20 | a0001c0001t0001g0166a0001c0001t0001g0176a0001c0001t0001g0180others(17): Show | 20 | HG00408.hp2 HG01346.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.989-767dupT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr4 | 128113781 | |||||
| chr4:128113781
|
CT | C | 47 | a0001c0001t0001g0126a0001c0001t0001g0185a0001c0001t0001g0263others(44): Show | 47 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.989-767delT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr4 | 128113781 | |||||
| chr4:128113781
|
CTT | C | 11 | a0002c0003t0001g0104a0002c0003t0001g0105a0002c0003t0006g0003others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.989-768_989-767del others(2): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr4 | 128113781 | |||||
| chr4:128113781
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0137 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.989-777_989-767del others(11): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr4 | 128113781 | |||||
| chr4:128113822
|
T | C | 4 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.989-748T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128113822 | ||||||
| chr4:128113893
|
TCTCCTGC others(6): Show |
T | 1 | a0002c0002t0002g0061 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.989-670_989-658del others(13): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr4 | 128113893 | |||||
| chr4:128113896
|
C | T | 1 | a0001c0018t0003g0254 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.989-674C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128113896 | ||||||
| chr4:128113985
|
C | T | 1 | a0002c0003t0006g0004 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.989-585C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128113985 | ||||||
| chr4:128114000
|
A | G | 204 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(201): Show | 204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.989-570A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128114000 | ||||||
| chr4:128114098
|
A | T | 3 | a0002c0002t0002g0114a0002c0002t0012g0065a0002c0002t0012g0096 | 3 | HG02080.hp1 NA18982.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.989-472A>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128114098 | ||||||
| chr4:128114138
|
C | T | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(190): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.989-432C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128114138 | ||||||
| chr4:128114359
|
C | G | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(190): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.989-211C>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 9/19 | chr4 | 128114359 | ||||||
| chr4:128114946
|
T | A | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(162): Show | 165 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.1161+204T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128114946 | ||||||
| chr4:128114973
|
T | C | 1 | a0001c0001t0001g0180 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1161+231T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128114973 | ||||||
| chr4:128114998
|
C | T | 56 | a0001c0001t0003g0102a0001c0001t0003g0103a0001c0001t0003g0111others(53): Show | 56 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.1161+256C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128114998 | ||||||
| chr4:128115162
|
T | A | 1 | a0001c0001t0004g0314 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1161+420T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128115162 | ||||||
| chr4:128115200
|
T | C | 12 | a0001c0001t0003g0213a0001c0001t0003g0214a0001c0001t0003g0216others(9): Show | 12 | HG02015.hp2 HG03831.hp2 NA18946.hp1 others(9): Show |
intron_variant | MODIFIER | c.1161+458T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128115200 | ||||||
| chr4:128115320
|
C | T | 213 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(210): Show | 213 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.1161+578C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128115320 | ||||||
| chr4:128115562
|
C | T | 16 | a0002c0002t0002g0019a0002c0002t0002g0021a0002c0002t0002g0022others(13): Show | 16 | HG00735.hp1 HG01109.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.1161+820C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128115562 | ||||||
| chr4:128115658
|
T | C | 1 | a0001c0001t0001g0184 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1161+916T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128115658 | ||||||
| chr4:128115706
|
G | A | 1 | a0001c0001t0004g0315 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1161+964G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128115706 | ||||||
| chr4:128115984
|
A | T | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(166): Show | 169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.1161+1242A>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128115984 | ||||||
| chr4:128116089
|
A | G | 1 | a0002c0003t0009g0008 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1161+1347A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128116089 | ||||||
| chr4:128116207
|
A | G | 17 | a0002c0002t0002g0019a0002c0002t0002g0021a0002c0002t0002g0022others(14): Show | 17 | HG00735.hp1 HG01109.hp1 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.1161+1465A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128116207 | ||||||
| chr4:128116218
|
G | C | 1 | a0001c0001t0004g0310 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1161+1476G>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128116218 | ||||||
| chr4:128116321
|
A | C | 7 | a0002c0002t0005g0097a0002c0003t0005g0122a0002c0012t0005g0098others(4): Show | 7 | HG02055.hp1 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1161+1579A>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128116321 | ||||||
| chr4:128116338
|
T | C | 11 | a0002c0003t0001g0104a0002c0003t0001g0105a0002c0003t0006g0003others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1161+1596T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128116338 | ||||||
| chr4:128116500
|
G | A | 12 | a0001c0001t0003g0213a0001c0001t0003g0214a0001c0001t0003g0216others(9): Show | 12 | HG02015.hp2 HG03831.hp2 NA18946.hp1 others(9): Show |
intron_variant | MODIFIER | c.1161+1758G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128116500 | ||||||
| chr4:128116879
|
C | T | 4 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1161+2137C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128116879 | ||||||
| chr4:128116921
|
G | GT | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(148): Show | 151 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.1161+2193dupT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr4 | 128116921 | |||||
| chr4:128116921
|
G | GTT | 13 | a0001c0001t0001g0108a0001c0001t0001g0124a0001c0001t0001g0137others(10): Show | 13 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(10): Show |
intron_variant | MODIFIER | c.1161+2192_1161+219 others(6): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr4 | 128116921 | |||||
| chr4:128116976
|
G | A | 211 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(208): Show | 211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.1161+2234G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128116976 | ||||||
| chr4:128117145
|
G | T | 1 | a0002c0002t0002g0035 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1161+2403G>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128117145 | ||||||
| chr4:128117197
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1161+2455C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128117197 | ||||||
| chr4:128117206
|
A | AT | 14 | a0001c0001t0001g0129a0001c0001t0003g0103a0002c0002t0002g0053others(11): Show | 14 | HG00639.hp1 HG00735.hp2 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.1161+2479dupT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr4 | 128117206 | |||||
| chr4:128117278
|
T | C | 1 | a0001c0001t0004g0312 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1161+2536T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128117278 | ||||||
| chr4:128117290
|
A | G | 1 | a0002c0002t0002g0067 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1161+2548A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128117290 | ||||||
| chr4:128117319
|
C | T | 22 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(19): Show | 22 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.1161+2577C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128117319 | ||||||
| chr4:128117330
|
T | C | 211 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(208): Show | 211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.1161+2588T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128117330 | ||||||
| chr4:128117454
|
C | T | 1 | a0010c0011t0005g0123 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1161+2712C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128117454 | ||||||
| chr4:128117480
|
G | A | 22 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(19): Show | 22 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.1161+2738G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128117480 | ||||||
| chr4:128117509
|
C | T | 1 | a0002c0003t0006g0004 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1161+2767C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128117509 | ||||||
| chr4:128117524
|
T | G | 4 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1161+2782T>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128117524 | ||||||
| chr4:128117591
|
C | T | 22 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(19): Show | 22 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.1161+2849C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128117591 | ||||||
| chr4:128117660
|
AG | A | 4 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1161+2920delG | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr4 | 128117660 | |||||
| chr4:128117762
|
C | T | 1 | a0002c0002t0002g0303 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1161+3020C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128117762 | ||||||
| chr4:128117913
|
C | CT | 18 | a0002c0002t0002g0014a0002c0002t0002g0019a0002c0002t0002g0024others(15): Show | 18 | HG00423.hp1 HG00597.hp1 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.1161+3190dupT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr4 | 128117913 | |||||
| chr4:128117913
|
CT | C | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(183): Show | 186 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.1161+3190delT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr4 | 128117913 | |||||
| chr4:128118025
|
C | T | 1 | a0001c0001t0003g0224 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1161+3283C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128118025 | ||||||
| chr4:128118082
|
A | AT | 29 | a0001c0001t0001g0203a0001c0001t0003g0229a0001c0001t0003g0278others(26): Show | 29 | HG00423.hp1 HG00741.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.1161+3364dupT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr4 | 128118082 | |||||
| chr4:128118082
|
A | ATT | 154 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(151): Show | 154 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1161+3363_1161+336 others(6): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr4 | 128118082 | |||||
| chr4:128118082
|
A | ATTT | 34 | a0001c0001t0001g0001a0001c0001t0001g0129a0001c0001t0001g0140others(31): Show | 34 | HG00438.hp1 HG00597.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.1161+3362_1161+336 others(7): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr4 | 128118082 | |||||
| chr4:128118232
|
A | AT | 59 | a0001c0001t0001g0110a0001c0001t0001g0273a0001c0001t0004g0308others(56): Show | 59 | HG00558.hp2 HG00609.hp1 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.1161+3508dupT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr4 | 128118232 | |||||
| chr4:128118232
|
AT | A | 14 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(11): Show | 14 | HG01175.hp1 HG01192.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.1161+3508delT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr4 | 128118232 | |||||
| chr4:128118295
|
G | A | 3 | a0005c0006t0001g0099a0005c0006t0001g0100a0005c0006t0001g0101 | 3 | HG01168.hp1 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1162-3531G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128118295 | ||||||
| chr4:128118324
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1162-3502C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128118324 | ||||||
| chr4:128118351
|
C | T | 4 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1162-3475C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128118351 | ||||||
| chr4:128118847
|
C | A | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1162-2979C>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128118847 | ||||||
| chr4:128118881
|
CT | C | 203 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(200): Show | 203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.1162-2932delT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr4 | 128118881 | |||||
| chr4:128118919
|
C | A | 1 | a0002c0002t0002g0289 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1162-2907C>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128118919 | ||||||
| chr4:128118948
|
T | A | 1 | a0001c0001t0003g0210 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1162-2878T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128118948 | ||||||
| chr4:128119003
|
C | G | 1 | a0002c0002t0002g0052 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1162-2823C>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128119003 | ||||||
| chr4:128119029
|
C | T | 1 | a0001c0001t0003g0215 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1162-2797C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128119029 | ||||||
| chr4:128119032
|
C | T | 2 | a0002c0002t0002g0302a0002c0002t0002g0330 | 2 | HG02074.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.1162-2794C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128119032 | ||||||
| chr4:128119289
|
C | G | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(190): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.1162-2537C>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128119289 | ||||||
| chr4:128119373
|
A | G | 5 | a0001c0001t0004g0308a0001c0001t0004g0310a0004c0005t0005g0281others(2): Show | 5 | HG02055.hp1 HG02976.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1162-2453A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128119373 | ||||||
| chr4:128119415
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1162-2411G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128119415 | ||||||
| chr4:128119676
|
C | T | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(190): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.1162-2150C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128119676 | ||||||
| chr4:128119899
|
C | A | 1 | a0001c0001t0003g0210 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1162-1927C>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128119899 | ||||||
| chr4:128120095
|
G | A | 9 | a0002c0003t0006g0003a0002c0003t0006g0004a0002c0003t0006g0005others(6): Show | 9 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1162-1731G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128120095 | ||||||
| chr4:128120246
|
A | T | 1 | a0001c0001t0003g0255 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1162-1580A>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128120246 | ||||||
| chr4:128120331
|
G | T | 5 | a0002c0002t0002g0018a0002c0002t0002g0032a0002c0002t0002g0047others(2): Show | 5 | NA18950.hp2 NA18973.hp2 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.1162-1495G>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128120331 | ||||||
| chr4:128120452
|
C | CT | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(188): Show | 191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.1162-1360dupT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr4 | 128120452 | |||||
| chr4:128120491
|
C | T | 1 | a0014c0015t0001g0206 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1162-1335C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128120491 | ||||||
| chr4:128120768
|
C | T | 1 | a0001c0001t0003g0215 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1162-1058C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128120768 | ||||||
| chr4:128120803
|
A | AT | 14 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(11): Show | 14 | HG00544.hp1 HG01109.hp1 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.1162-1001dupT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr4 | 128120803 | |||||
| chr4:128120803
|
AT | A | 20 | a0001c0001t0004g0311a0002c0002t0002g0303a0002c0002t0002g0307others(17): Show | 20 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.1162-1001delT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr4 | 128120803 | |||||
| chr4:128120803
|
ATTTTTTT | A | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(162): Show | 165 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.1162-1007_1162-100 others(11): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr4 | 128120803 | |||||
| chr4:128120890
|
A | C | 3 | a0005c0006t0001g0099a0005c0006t0001g0100a0005c0006t0001g0101 | 3 | HG01168.hp1 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1162-936A>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128120890 | ||||||
| chr4:128121088
|
T | C | 1 | a0001c0001t0001g0157 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1162-738T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128121088 | ||||||
| chr4:128121168
|
G | A | 1 | a0002c0002t0002g0039 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1162-658G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128121168 | ||||||
| chr4:128121249
|
G | A | 1 | a0002c0002t0002g0066 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1162-577G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128121249 | ||||||
| chr4:128121356
|
C | T | 1 | a0001c0001t0001g0265 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1162-470C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128121356 | ||||||
| chr4:128121357
|
G | A | 1 | a0006c0007t0009g0204 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1162-469G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128121357 | ||||||
| chr4:128121377
|
G | A | 1 | a0002c0002t0002g0330 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1162-449G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128121377 | ||||||
| chr4:128121380
|
C | T | 1 | a0002c0003t0006g0005 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1162-446C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128121380 | ||||||
| chr4:128121597
|
C | T | 9 | a0002c0003t0006g0003a0002c0003t0006g0004a0002c0003t0006g0005others(6): Show | 9 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1162-229C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128121597 | ||||||
| chr4:128121612
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1162-214A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128121612 | ||||||
| chr4:128121614
|
G | A | 4 | a0002c0003t0006g0004a0002c0003t0006g0006a0002c0003t0006g0009others(1): Show | 4 | HG02630.hp1 HG02970.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1162-212G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128121614 | ||||||
| chr4:128121637
|
T | C | 1 | a0001c0001t0004g0314 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1162-189T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 10/19 | chr4 | 128121637 | ||||||
| chr4:128122438
|
G | GT | 20 | a0002c0002t0002g0031a0002c0002t0002g0046a0002c0002t0005g0097others(17): Show | 20 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1524+265dupT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128122438 | |||||
| chr4:128122446
|
T | G | 4 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1524+258T>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128122446 | ||||||
| chr4:128122446
|
T | TG | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(186): Show | 189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.1524+258_1524+259i others(3): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128122446 | ||||||
| chr4:128122449
|
T | G | 3 | a0002c0002t0002g0041a0002c0002t0002g0081a0002c0002t0002g0118 | 3 | HG02109.hp2 HG02280.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1524+261T>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128122449 | ||||||
| chr4:128122459
|
G | GT | 12 | a0002c0002t0011g0030a0002c0003t0001g0104a0002c0003t0001g0105others(9): Show | 12 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1524+280dupT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128122459 | |||||
| chr4:128122459
|
G | T | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(189): Show | 192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.1524+271G>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128122459 | ||||||
| chr4:128122462
|
T | G | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(163): Show | 166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.1524+274T>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128122462 | ||||||
| chr4:128122463
|
T | G | 1 | a0001c0001t0001g0184 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1524+275T>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128122463 | ||||||
| chr4:128122589
|
A | G | 1 | a0001c0001t0001g0208 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1524+401A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128122589 | ||||||
| chr4:128122654
|
G | A | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(190): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.1524+466G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128122654 | ||||||
| chr4:128122732
|
C | T | 2 | a0002c0003t0001g0104a0002c0003t0001g0105 | 2 | HG02145.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1524+544C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128122732 | ||||||
| chr4:128123343
|
G | A | 1 | a0002c0002t0002g0014 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1524+1155G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128123343 | ||||||
| chr4:128123590
|
AT | A | 22 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(19): Show | 22 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.1524+1409delT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128123590 | |||||
| chr4:128123838
|
C | G | 11 | a0002c0003t0001g0104a0002c0003t0001g0105a0002c0003t0006g0003others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1524+1650C>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128123838 | ||||||
| chr4:128123886
|
A | G | 4 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1524+1698A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128123886 | ||||||
| chr4:128123922
|
T | C | 38 | a0002c0002t0002g0034a0002c0002t0002g0035a0002c0002t0002g0037others(35): Show | 38 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.1524+1734T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128123922 | ||||||
| chr4:128124162
|
G | A | 230 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(227): Show | 230 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.1524+1974G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128124162 | ||||||
| chr4:128124198
|
G | A | 3 | a0004c0005t0005g0281a0004c0005t0005g0282a0004c0005t0005g0283 | 3 | HG02055.hp1 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1524+2010G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128124198 | ||||||
| chr4:128124253
|
T | G | 2 | a0001c0001t0004g0311a0001c0001t0004g0326 | 2 | NA18984.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1524+2065T>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128124253 | ||||||
| chr4:128124262
|
A | G | 11 | a0002c0003t0001g0104a0002c0003t0001g0105a0002c0003t0006g0003others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1524+2074A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128124262 | ||||||
| chr4:128124358
|
ACATAACC others(53): Show |
A | 1 | a0002c0002t0002g0120 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1524+2171_1524+223 others(64): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128124358 | ||||||
| chr4:128124360
|
A | G | 11 | a0002c0003t0001g0104a0002c0003t0001g0105a0002c0003t0006g0003others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1524+2172A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128124360 | ||||||
| chr4:128124656
|
A | G | 2 | a0002c0002t0002g0051a0002c0002t0002g0078 | 2 | NA18969.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.1524+2468A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128124656 | ||||||
| chr4:128124691
|
G | C | 1 | a0001c0001t0001g0109 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1524+2503G>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128124691 | ||||||
| chr4:128124725
|
C | T | 1 | a0002c0002t0002g0013 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1524+2537C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128124725 | ||||||
| chr4:128124925
|
T | C | 1 | a0001c0001t0004g0318 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1524+2737T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128124925 | ||||||
| chr4:128124962
|
A | G | 2 | a0001c0001t0001g0149a0001c0001t0001g0175 | 2 | HG00642.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1524+2774A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128124962 | ||||||
| chr4:128124983
|
A | G | 4 | a0001c0001t0001g0249a0005c0006t0001g0099a0005c0006t0001g0100others(1): Show | 4 | HG01168.hp1 HG02922.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1524+2795A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128124983 | ||||||
| chr4:128125115
|
T | C | 11 | a0002c0003t0001g0104a0002c0003t0001g0105a0002c0003t0006g0003others(8): Show | 11 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1524+2927T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128125115 | ||||||
| chr4:128125209
|
CGGGTAAA others(2): Show |
C | 5 | a0002c0002t0002g0041a0002c0002t0002g0050a0002c0002t0002g0081others(2): Show | 5 | HG02109.hp2 HG02280.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1524+3022_1524+303 others(13): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128125209 | ||||||
| chr4:128125232
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1524+3044G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128125232 | ||||||
| chr4:128125302
|
A | T | 1 | a0014c0015t0001g0206 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1524+3114A>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128125302 | ||||||
| chr4:128125367
|
A | G | 1 | a0014c0015t0001g0206 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1524+3179A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128125367 | ||||||
| chr4:128125506
|
G | A | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1524+3318G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128125506 | ||||||
| chr4:128125570
|
C | A | 2 | a0001c0001t0003g0102a0001c0001t0003g0103 | 2 | HG01175.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1524+3382C>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128125570 | ||||||
| chr4:128125699
|
T | G | 3 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136 | 3 | HG01070.hp1 HG01071.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1524+3511T>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128125699 | ||||||
| chr4:128125809
|
A | G | 206 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(203): Show | 206 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.1524+3621A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128125809 | ||||||
| chr4:128126006
|
C | T | 1 | a0002c0002t0002g0112 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1524+3818C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128126006 | ||||||
| chr4:128126066
|
G | C | 1 | a0001c0018t0003g0254 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1524+3878G>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128126066 | ||||||
| chr4:128126113
|
C | CT | 18 | a0002c0002t0002g0016a0002c0002t0002g0038a0002c0002t0002g0051others(15): Show | 18 | HG00438.hp2 HG02027.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1524+3951dupT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128126113 | |||||
| chr4:128126113
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0003g0213 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1524+3941_1524+395 others(15): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128126113 | |||||
| chr4:128126113
|
CTTTTTTT others(5): Show |
C | 55 | a0001c0001t0001g0168a0001c0001t0001g0211a0001c0001t0001g0249others(52): Show | 55 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.1524+3940_1524+395 others(16): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128126113 | |||||
| chr4:128126113
|
CTTTTTTT others(6): Show |
C | 121 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(118): Show | 121 | HG00140.hp2 HG00280.hp1 HG00558.hp2 others(118): Show |
intron_variant | MODIFIER | c.1524+3939_1524+395 others(17): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128126113 | |||||
| chr4:128126113
|
CTTTTTTT others(7): Show |
C | 12 | a0001c0001t0001g0011a0001c0001t0001g0108a0001c0001t0001g0124others(9): Show | 12 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(9): Show |
intron_variant | MODIFIER | c.1524+3938_1524+395 others(18): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128126113 | |||||
| chr4:128126153
|
T | G | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(186): Show | 189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.1524+3965T>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128126153 | ||||||
| chr4:128126198
|
T | C | 1 | a0002c0002t0002g0061 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1524+4010T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128126198 | ||||||
| chr4:128126310
|
A | C | 58 | a0002c0002t0002g0018a0002c0002t0002g0031a0002c0002t0002g0032others(55): Show | 58 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.1524+4122A>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128126310 | ||||||
| chr4:128126324
|
C | T | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(186): Show | 189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.1524+4136C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128126324 | ||||||
| chr4:128126363
|
T | C | 2 | a0008c0009t0005g0113a0008c0009t0005g0119 | 2 | HG02572.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1524+4175T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128126363 | ||||||
| chr4:128126375
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1524+4187G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128126375 | ||||||
| chr4:128126382
|
G | A | 57 | a0001c0001t0001g0168a0001c0001t0001g0236a0001c0001t0003g0102others(54): Show | 57 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.1524+4194G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128126382 | ||||||
| chr4:128126435
|
T | C | 2 | a0003c0004t0001g0182a0003c0004t0001g0183 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1524+4247T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128126435 | ||||||
| chr4:128126567
|
A | C | 57 | a0001c0001t0001g0168a0001c0001t0001g0236a0001c0001t0003g0102others(54): Show | 57 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.1524+4379A>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128126567 | ||||||
| chr4:128126713
|
A | G | 1 | a0002c0002t0002g0056 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1524+4525A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128126713 | ||||||
| chr4:128126715
|
G | A | 17 | a0002c0002t0002g0019a0002c0002t0002g0021a0002c0002t0002g0022others(14): Show | 17 | HG00735.hp1 HG01109.hp1 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.1524+4527G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128126715 | ||||||
| chr4:128126811
|
TG | T | 184 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(181): Show | 184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.1524+4624delG | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128126811 | ||||||
| chr4:128126812
|
G | A | 2 | a0002c0003t0001g0104a0002c0003t0001g0105 | 2 | HG02145.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1524+4624G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128126812 | ||||||
| chr4:128126812
|
G | T | 3 | a0001c0001t0001g0198a0001c0001t0004g0311a0001c0001t0004g0326 | 3 | HG02074.hp1 NA18984.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1524+4624G>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128126812 | ||||||
| chr4:128126820
|
T | A | 7 | a0001c0001t0004g0309a0001c0001t0004g0318a0001c0001t0007g0131others(4): Show | 7 | HG00558.hp2 HG01891.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1524+4632T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128126820 | ||||||
| chr4:128126821
|
T | A | 25 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(22): Show | 25 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.1524+4633T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128126821 | ||||||
| chr4:128126822
|
T | A | 29 | a0001c0001t0003g0242a0001c0001t0004g0308a0001c0001t0004g0309others(26): Show | 29 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.1524+4634T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128126822 | ||||||
| chr4:128127072
|
A | G | 1 | a0001c0001t0001g0211 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1524+4884A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128127072 | ||||||
| chr4:128127227
|
T | G | 1 | a0002c0002t0002g0050 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1524+5039T>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128127227 | ||||||
| chr4:128127245
|
C | T | 91 | a0001c0001t0001g0001a0001c0001t0001g0107a0001c0001t0001g0108others(88): Show | 91 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.1524+5057C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128127245 | ||||||
| chr4:128127257
|
CAG | C | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(186): Show | 189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.1524+5072_1524+507 others(6): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128127257 | |||||
| chr4:128127552
|
G | A | 22 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(19): Show | 22 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.1524+5364G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128127552 | ||||||
| chr4:128127590
|
T | C | 1 | a0002c0002t0002g0090 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1524+5402T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128127590 | ||||||
| chr4:128127591
|
C | G | 1 | a0002c0002t0002g0090 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1524+5403C>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128127591 | ||||||
| chr4:128127593
|
G | A | 1 | a0002c0002t0002g0090 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1524+5405G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128127593 | ||||||
| chr4:128127595
|
A | G | 1 | a0002c0002t0002g0090 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1524+5407A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128127595 | ||||||
| chr4:128127641
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1524+5453C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128127641 | ||||||
| chr4:128127685
|
T | A | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(186): Show | 189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.1524+5497T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128127685 | ||||||
| chr4:128127719
|
G | C | 1 | a0011c0016t0003g0277 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1524+5531G>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128127719 | ||||||
| chr4:128127790
|
C | T | 1 | a0001c0001t0001g0110 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1524+5602C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128127790 | ||||||
| chr4:128127873
|
A | G | 3 | a0005c0006t0001g0099a0005c0006t0001g0100a0005c0006t0001g0101 | 3 | HG01168.hp1 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1524+5685A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128127873 | ||||||
| chr4:128128071
|
T | C | 22 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(19): Show | 22 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.1524+5883T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128128071 | ||||||
| chr4:128128289
|
A | T | 1 | a0002c0002t0002g0090 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1524+6101A>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128128289 | ||||||
| chr4:128128314
|
T | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(206): Show | 209 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.1524+6126T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128128314 | ||||||
| chr4:128128341
|
A | T | 4 | a0002c0002t0005g0097a0002c0003t0005g0122a0002c0012t0005g0098others(1): Show | 4 | HG02280.hp2 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1524+6153A>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128128341 | ||||||
| chr4:128128567
|
A | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(206): Show | 209 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.1524+6379A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128128567 | ||||||
| chr4:128128594
|
A | G | 1 | a0001c0001t0001g0273 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1524+6406A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128128594 | ||||||
| chr4:128128687
|
G | C | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(186): Show | 189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.1524+6499G>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128128687 | ||||||
| chr4:128128787
|
A | G | 2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | HG01099.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.1524+6599A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128128787 | ||||||
| chr4:128128960
|
C | G | 1 | a0002c0002t0002g0112 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1524+6772C>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128128960 | ||||||
| chr4:128129022
|
A | G | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(186): Show | 189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.1524+6834A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128129022 | ||||||
| chr4:128129047
|
C | T | 1 | a0002c0002t0002g0295 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1524+6859C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128129047 | ||||||
| chr4:128129121
|
C | T | 3 | a0004c0005t0005g0281a0004c0005t0005g0282a0004c0005t0005g0283 | 3 | HG02055.hp1 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1524+6933C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128129121 | ||||||
| chr4:128129157
|
T | A | 1 | a0002c0002t0015g0020 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1524+6969T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128129157 | ||||||
| chr4:128129164
|
C | CA | 25 | a0002c0002t0002g0016a0002c0002t0002g0018a0002c0002t0002g0031others(22): Show | 25 | HG00438.hp2 HG00544.hp1 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.1524+7016dupA | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128129164 | |||||
| chr4:128129164
|
C | CAA | 14 | a0002c0002t0002g0014a0002c0002t0002g0022a0002c0002t0002g0033others(11): Show | 14 | HG00423.hp1 HG01175.hp1 HG01981.hp2 others(11): Show |
intron_variant | MODIFIER | c.1524+7015_1524+701 others(6): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128129164 | |||||
| chr4:128129164
|
C | CAAA | 6 | a0002c0002t0002g0012a0002c0002t0002g0057a0002c0002t0002g0058others(3): Show | 6 | HG00639.hp1 HG02015.hp1 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.1524+7014_1524+701 others(7): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128129164 | |||||
| chr4:128129164
|
C | CAAAAAAA | 8 | a0002c0002t0002g0024a0002c0002t0002g0026a0002c0002t0002g0027others(5): Show | 8 | HG00735.hp1 HG00735.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1524+7010_1524+701 others(11): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128129164 | |||||
| chr4:128129164
|
C | CAAAAAAA others(3): Show |
3 | a0002c0002t0002g0025a0002c0002t0002g0052a0002c0002t0002g0292 | 3 | HG03471.hp2 HG03540.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1524+7007_1524+701 others(14): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128129164 | |||||
| chr4:128129164
|
C | CAAAAAAA others(4): Show |
2 | a0002c0002t0002g0037a0002c0002t0015g0020 | 2 | HG00597.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1524+7006_1524+701 others(15): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128129164 | |||||
| chr4:128129164
|
C | CAAAAAAA others(5): Show |
2 | a0002c0002t0002g0019a0002c0003t0009g0008 | 2 | HG02630.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1524+7005_1524+701 others(16): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128129164 | |||||
| chr4:128129164
|
C | CAAAAAAA others(6): Show |
2 | a0002c0002t0002g0090a0002c0002t0002g0284 | 2 | HG03834.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1524+7004_1524+701 others(17): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128129164 | |||||
| chr4:128129164
|
C | CAAAAAAA others(7): Show |
2 | a0002c0002t0002g0070a0002c0002t0002g0094 | 2 | HG01884.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1524+7003_1524+701 others(18): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128129164 | |||||
| chr4:128129164
|
C | CAAAAAAA others(9): Show |
1 | a0002c0002t0002g0049 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1524+7001_1524+701 others(20): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128129164 | |||||
| chr4:128129164
|
C | CAAAAAAA others(10): Show |
3 | a0002c0002t0002g0015a0002c0002t0002g0084a0002c0002t0013g0093 | 3 | HG02622.hp1 NA18906.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1524+7000_1524+701 others(21): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128129164 | |||||
| chr4:128129164
|
C | CAAAAAAA others(15): Show |
1 | a0002c0002t0011g0042 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1524+6995_1524+701 others(26): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128129164 | |||||
| chr4:128129164
|
C | CAAAAAAA others(18): Show |
1 | a0002c0002t0002g0068 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1524+6992_1524+701 others(29): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128129164 | |||||
| chr4:128129164
|
C | CAAAAAAA others(21): Show |
1 | a0002c0002t0002g0017 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1524+6989_1524+701 others(32): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128129164 | |||||
| chr4:128129164
|
CA | C | 12 | a0001c0001t0004g0308a0001c0001t0004g0310a0001c0001t0004g0313others(9): Show | 12 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(9): Show |
intron_variant | MODIFIER | c.1524+7016delA | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128129164 | |||||
| chr4:128129164
|
CAA | C | 6 | a0001c0001t0004g0309a0001c0001t0004g0311a0001c0001t0004g0314others(3): Show | 6 | NA18984.hp1 NA18990.hp2 NA19005.hp1 others(3): Show |
intron_variant | MODIFIER | c.1524+7015_1524+701 others(6): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128129164 | |||||
| chr4:128129164
|
CAAAAAAA others(1): Show |
C | 9 | a0002c0002t0002g0296a0002c0003t0001g0105a0002c0003t0006g0003others(6): Show | 9 | HG02145.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1524+7009_1524+701 others(12): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128129164 | |||||
| chr4:128129164
|
CAAAAAAA others(2): Show |
C | 8 | a0002c0002t0002g0021a0002c0002t0002g0329a0002c0002t0005g0097others(5): Show | 8 | HG01168.hp1 HG02109.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1524+7008_1524+701 others(13): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128129164 | |||||
| chr4:128129164
|
CAAAAAAA others(3): Show |
C | 5 | a0001c0001t0007g0132a0002c0002t0002g0028a0002c0002t0002g0290others(2): Show | 5 | HG01496.hp1 HG02622.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1524+7007_1524+701 others(14): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128129164 | |||||
| chr4:128129164
|
CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0007g0131a0001c0001t0007g0133 | 2 | HG02486.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1524+7006_1524+701 others(15): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128129164 | |||||
| chr4:128129164
|
CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0007g0258a0002c0002t0002g0044 | 2 | HG01891.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.1524+7005_1524+701 others(16): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128129164 | |||||
| chr4:128129164
|
CAAAAAAA others(6): Show |
C | 2 | a0002c0002t0002g0047a0002c0002t0002g0116 | 2 | NA18973.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.1524+7004_1524+701 others(17): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128129164 | |||||
| chr4:128129164
|
CAAAAAAA others(7): Show |
C | 1 | a0002c0002t0002g0032 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1524+7003_1524+701 others(18): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128129164 | |||||
| chr4:128129164
|
CAAAAAAA others(9): Show |
C | 2 | a0001c0001t0001g0273a0001c0001t0004g0317 | 2 | HG00738.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1524+7001_1524+701 others(20): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128129164 | |||||
| chr4:128129164
|
CAAAAAAA others(10): Show |
C | 16 | a0001c0001t0001g0149a0001c0001t0001g0173a0001c0001t0001g0176others(13): Show | 16 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.1524+7000_1524+701 others(21): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128129164 | |||||
| chr4:128129164
|
CAAAAAAA others(11): Show |
C | 135 | a0001c0001t0001g0001a0001c0001t0001g0107a0001c0001t0001g0108others(132): Show | 135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.1524+6999_1524+701 others(22): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128129164 | |||||
| chr4:128129164
|
CAAAAAAA others(12): Show |
C | 13 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(10): Show | 13 | HG01070.hp1 HG01192.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1524+6998_1524+701 others(23): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128129164 | |||||
| chr4:128129164
|
CAAAAAAA others(13): Show |
C | 3 | a0002c0002t0002g0041a0002c0002t0002g0081a0002c0002t0002g0118 | 3 | HG02109.hp2 HG02280.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1524+6997_1524+701 others(24): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128129164 | |||||
| chr4:128129164
|
CAAAAAAA others(15): Show |
C | 1 | a0002c0017t0002g0074 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1524+6995_1524+701 others(26): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128129164 | |||||
| chr4:128129164
|
CAAAAAAA others(18): Show |
C | 1 | a0001c0001t0004g0315 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1524+6992_1524+701 others(29): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128129164 | |||||
| chr4:128129207
|
C | T | 3 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0177 | 3 | HG00741.hp1 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1524+7019C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128129207 | ||||||
| chr4:128129228
|
G | C | 1 | a0002c0002t0002g0035 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1524+7040G>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128129228 | ||||||
| chr4:128129286
|
C | T | 1 | a0002c0002t0002g0114 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1524+7098C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128129286 | ||||||
| chr4:128129327
|
C | T | 3 | a0002c0002t0002g0015a0002c0002t0002g0017a0002c0002t0002g0049 | 3 | HG02559.hp2 HG02622.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1524+7139C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128129327 | ||||||
| chr4:128129344
|
G | A | 1 | a0001c0001t0004g0318 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1524+7156G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128129344 | ||||||
| chr4:128129348
|
C | CA | 10 | a0001c0001t0001g0157a0002c0003t0001g0105a0002c0003t0006g0003others(7): Show | 10 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1524+7176dupA | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128129348 | |||||
| chr4:128129348
|
C | CAA | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(179): Show | 182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.1524+7175_1524+717 others(6): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128129348 | |||||
| chr4:128129348
|
C | CAAA | 6 | a0001c0001t0001g0010a0001c0001t0001g0110a0001c0001t0001g0155others(3): Show | 6 | HG01943.hp2 HG02083.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.1524+7174_1524+717 others(7): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128129348 | |||||
| chr4:128129412
|
A | T | 1 | a0002c0002t0011g0030 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1524+7224A>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128129412 | ||||||
| chr4:128129490
|
A | G | 2 | a0002c0002t0002g0033a0002c0002t0002g0056 | 2 | HG00408.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.1524+7302A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128129490 | ||||||
| chr4:128129542
|
C | T | 3 | a0004c0005t0005g0281a0004c0005t0005g0282a0004c0005t0005g0283 | 3 | HG02055.hp1 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1524+7354C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128129542 | ||||||
| chr4:128129559
|
A | G | 5 | a0002c0002t0002g0041a0002c0002t0002g0050a0002c0002t0002g0081others(2): Show | 5 | HG02109.hp2 HG02280.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1524+7371A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128129559 | ||||||
| chr4:128129658
|
C | T | 1 | a0002c0002t0005g0097 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1524+7470C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128129658 | ||||||
| chr4:128129672
|
G | GAATAGAC others(38): Show |
1 | a0002c0002t0002g0291 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1524+7485_1524+752 others(49): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128129672 | |||||
| chr4:128129997
|
A | G | 2 | a0001c0001t0001g0163a0001c0001t0001g0164 | 2 | HG00639.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1524+7809A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128129997 | ||||||
| chr4:128130281
|
A | G | 2 | a0002c0002t0002g0068a0002c0002t0002g0070 | 2 | HG01884.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1524+8093A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128130281 | ||||||
| chr4:128130419
|
GCAAATAT others(23): Show |
G | 1 | a0001c0001t0003g0216 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1524+8239_1524+826 others(34): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128130419 | |||||
| chr4:128130637
|
T | C | 227 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(224): Show | 227 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.1524+8449T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128130637 | ||||||
| chr4:128130684
|
C | G | 2 | a0002c0002t0002g0080a0002c0002t0002g0082 | 2 | HG01070.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.1524+8496C>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128130684 | ||||||
| chr4:128130739
|
C | T | 3 | a0007c0008t0001g0138a0007c0008t0001g0139a0007c0008t0001g0158 | 3 | HG03486.hp2 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1524+8551C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128130739 | ||||||
| chr4:128130749
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1524+8561A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128130749 | ||||||
| chr4:128130828
|
A | G | 1 | a0014c0015t0001g0206 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1524+8640A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128130828 | ||||||
| chr4:128130859
|
G | A | 1 | a0014c0015t0001g0206 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1524+8671G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128130859 | ||||||
| chr4:128131053
|
A | C | 161 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(158): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.1524+8865A>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128131053 | ||||||
| chr4:128131053
|
A | T | 2 | a0001c0001t0001g0107a0001c0001t0003g0224 | 2 | HG02004.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1524+8865A>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128131053 | ||||||
| chr4:128131274
|
C | T | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(186): Show | 189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.1524+9086C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128131274 | ||||||
| chr4:128131425
|
G | T | 3 | a0004c0005t0005g0281a0004c0005t0005g0282a0004c0005t0005g0283 | 3 | HG02055.hp1 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1524+9237G>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128131425 | ||||||
| chr4:128131556
|
G | A | 1 | a0001c0001t0003g0102 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1524+9368G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128131556 | ||||||
| chr4:128131616
|
G | A | 2 | a0006c0007t0009g0192a0006c0007t0009g0204 | 2 | HG03139.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1524+9428G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128131616 | ||||||
| chr4:128132151
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1524+9963C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128132151 | ||||||
| chr4:128132307
|
C | T | 11 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(8): Show | 11 | HG01192.hp1 HG02486.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1524+10119C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128132307 | ||||||
| chr4:128132472
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1524+10284C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128132472 | ||||||
| chr4:128132495
|
A | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(206): Show | 209 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.1524+10307A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128132495 | ||||||
| chr4:128132905
|
A | G | 3 | a0002c0002t0002g0015a0002c0002t0002g0017a0002c0002t0002g0049 | 3 | HG02559.hp2 HG02622.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1524+10717A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128132905 | ||||||
| chr4:128133032
|
A | T | 5 | a0002c0002t0002g0041a0002c0002t0002g0050a0002c0002t0002g0081others(2): Show | 5 | HG02109.hp2 HG02280.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1524+10844A>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128133032 | ||||||
| chr4:128133034
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1524+10846T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128133034 | ||||||
| chr4:128133194
|
G | A | 1 | a0001c0001t0001g0268 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1524+11006G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128133194 | ||||||
| chr4:128133707
|
C | T | 1 | a0002c0002t0002g0295 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1524+11519C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128133707 | ||||||
| chr4:128133708
|
T | C | 1 | a0002c0002t0002g0295 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1524+11520T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128133708 | ||||||
| chr4:128133905
|
C | T | 1 | a0002c0002t0002g0025 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1524+11717C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128133905 | ||||||
| chr4:128133982
|
C | A | 1 | a0002c0002t0002g0061 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1524+11794C>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128133982 | ||||||
| chr4:128133999
|
A | AT | 9 | a0001c0001t0001g0191a0001c0001t0001g0236a0001c0001t0001g0267others(6): Show | 9 | HG00140.hp2 HG00558.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1524+11830dupT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128133999 | |||||
| chr4:128133999
|
A | ATT | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(152): Show | 155 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.1524+11829_1524+11 others(8): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128133999 | |||||
| chr4:128133999
|
A | ATTT | 28 | a0001c0001t0001g0142a0001c0001t0001g0188a0001c0001t0003g0102others(25): Show | 28 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.1524+11828_1524+11 others(9): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128133999 | |||||
| chr4:128133999
|
AT | A | 23 | a0002c0002t0002g0043a0002c0002t0002g0306a0002c0002t0002g0332others(20): Show | 23 | HG00438.hp2 HG01168.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.1524+11830delT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128133999 | |||||
| chr4:128134182
|
T | G | 2 | a0001c0001t0001g0209a0002c0002t0008g0300 | 2 | HG02300.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1524+11994T>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128134182 | ||||||
| chr4:128134200
|
G | A | 1 | a0001c0001t0007g0131 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1524+12012G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128134200 | ||||||
| chr4:128134295
|
C | T | 22 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(19): Show | 22 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.1524+12107C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128134295 | ||||||
| chr4:128134300
|
T | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(205): Show | 208 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.1524+12112T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128134300 | ||||||
| chr4:128134309
|
G | T | 1 | a0001c0001t0001g0193 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1524+12121G>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128134309 | ||||||
| chr4:128134319
|
A | G | 57 | a0001c0001t0001g0168a0001c0001t0001g0236a0001c0001t0003g0102others(54): Show | 57 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.1524+12131A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128134319 | ||||||
| chr4:128134571
|
A | G | 1 | a0002c0002t0002g0050 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1524+12383A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128134571 | ||||||
| chr4:128134621
|
A | G | 10 | a0002c0002t0002g0015a0002c0002t0002g0017a0002c0002t0002g0049others(7): Show | 10 | HG01243.hp2 HG01884.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1524+12433A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128134621 | ||||||
| chr4:128134933
|
C | T | 22 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(19): Show | 22 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.1524+12745C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128134933 | ||||||
| chr4:128135036
|
G | C | 1 | a0001c0001t0007g0133 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1524+12848G>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128135036 | ||||||
| chr4:128135056
|
C | T | 1 | a0002c0003t0005g0122 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1524+12868C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128135056 | ||||||
| chr4:128135098
|
A | AAAAT | 68 | a0001c0001t0001g0109a0001c0001t0001g0274a0001c0001t0003g0215others(65): Show | 68 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.1524+12954_1524+12 others(10): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128135098 | |||||
| chr4:128135098
|
A | AAAATAAA others(1): Show |
10 | a0002c0002t0002g0034a0002c0002t0002g0035a0002c0002t0002g0037others(7): Show | 10 | HG00597.hp1 HG01070.hp2 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.1524+12950_1524+12 others(14): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128135098 | |||||
| chr4:128135098
|
A | AAAATAAA others(5): Show |
1 | a0002c0002t0002g0053 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1524+12946_1524+12 others(18): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128135098 | |||||
| chr4:128135098
|
AAAAT | A | 100 | a0001c0001t0001g0001a0001c0001t0001g0107a0001c0001t0001g0110others(97): Show | 100 | HG00140.hp2 HG00558.hp2 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.1524+12954_1524+12 others(10): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128135098 | |||||
| chr4:128135098
|
AAAATAAA others(1): Show |
A | 38 | a0001c0001t0001g0124a0001c0001t0001g0126a0001c0001t0001g0129others(35): Show | 38 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.1524+12950_1524+12 others(14): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128135098 | |||||
| chr4:128135098
|
AAAATAAA others(5): Show |
A | 5 | a0001c0001t0001g0108a0001c0001t0001g0271a0005c0006t0001g0099others(2): Show | 5 | HG01168.hp1 HG02965.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1524+12946_1524+12 others(18): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128135098 | |||||
| chr4:128135218
|
G | C | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(186): Show | 189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.1524+13030G>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128135218 | ||||||
| chr4:128135310
|
C | T | 1 | a0001c0001t0003g0279 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1524+13122C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128135310 | ||||||
| chr4:128135311
|
G | T | 10 | a0002c0003t0001g0104a0002c0003t0001g0105a0002c0003t0006g0003others(7): Show | 10 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1524+13123G>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128135311 | ||||||
| chr4:128135692
|
A | G | 2 | a0001c0001t0001g0184a0001c0001t0001g0205 | 2 | HG01167.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1524+13504A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128135692 | ||||||
| chr4:128135854
|
G | A | 1 | a0002c0002t0002g0040 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1524+13666G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128135854 | ||||||
| chr4:128136091
|
G | C | 2 | a0001c0001t0001g0142a0001c0001t0001g0188 | 2 | HG01074.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1524+13903G>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128136091 | ||||||
| chr4:128136321
|
C | A | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(202): Show | 205 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.1524+14133C>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128136321 | ||||||
| chr4:128136329
|
C | A | 3 | a0004c0005t0005g0281a0004c0005t0005g0282a0004c0005t0005g0283 | 3 | HG02055.hp1 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1524+14141C>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128136329 | ||||||
| chr4:128136332
|
AAAAAC | A | 4 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1524+14154_1524+14 others(11): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128136332 | |||||
| chr4:128136355
|
A | G | 2 | a0001c0001t0003g0231a0001c0001t0003g0251 | 2 | HG01943.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.1524+14167A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128136355 | ||||||
| chr4:128136502
|
G | A | 1 | a0001c0001t0003g0250 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1524+14314G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128136502 | ||||||
| chr4:128136512
|
T | C | 4 | a0002c0002t0005g0097a0002c0003t0005g0122a0002c0012t0005g0098others(1): Show | 4 | HG02280.hp2 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1524+14324T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128136512 | ||||||
| chr4:128136970
|
T | C | 1 | a0001c0001t0003g0253 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1524+14782T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128136970 | ||||||
| chr4:128137058
|
G | A | 1 | a0013c0014t0003g0226 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1524+14870G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128137058 | ||||||
| chr4:128137207
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1524+15019C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128137207 | ||||||
| chr4:128137208
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1524+15020G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128137208 | ||||||
| chr4:128137459
|
T | C | 1 | a0002c0002t0002g0039 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1524+15271T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128137459 | ||||||
| chr4:128137494
|
A | C | 1 | a0001c0001t0003g0239 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1524+15306A>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128137494 | ||||||
| chr4:128137635
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1524+15447G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128137635 | ||||||
| chr4:128137753
|
A | G | 3 | a0004c0005t0005g0281a0004c0005t0005g0282a0004c0005t0005g0283 | 3 | HG02055.hp1 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1524+15565A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128137753 | ||||||
| chr4:128137770
|
C | CAT | 8 | a0002c0002t0002g0118a0002c0003t0006g0003a0002c0003t0006g0004others(5): Show | 8 | HG02109.hp1 HG02257.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1524+15603_1524+15 others(8): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128137770 | |||||
| chr4:128137770
|
C | CATAT | 4 | a0002c0002t0002g0041a0002c0002t0002g0081a0002c0003t0006g0009others(1): Show | 4 | HG02109.hp2 HG02280.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1524+15601_1524+15 others(10): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128137770 | |||||
| chr4:128137770
|
CAT | C | 8 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(5): Show | 8 | HG01256.hp2 HG01258.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.1524+15603_1524+15 others(8): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128137770 | |||||
| chr4:128137788
|
TATA | T | 11 | a0001c0001t0001g0157a0001c0001t0001g0166a0001c0001t0001g0176others(8): Show | 11 | HG01109.hp2 HG01167.hp1 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.1524+15601_1524+15 others(9): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128137788 | ||||||
| chr4:128137789
|
ATAT | A | 131 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(128): Show | 131 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.1524+15603_1524+15 others(9): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128137789 | |||||
| chr4:128137790
|
TA | T | 25 | a0001c0001t0001g0107a0001c0001t0001g0134a0001c0001t0001g0135others(22): Show | 25 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.1524+15603delA | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128137790 | ||||||
| chr4:128137791
|
A | T | 12 | a0001c0001t0004g0310a0001c0001t0007g0133a0001c0001t0007g0258others(9): Show | 12 | HG01433.hp1 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1524+15603A>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128137791 | ||||||
| chr4:128137791
|
ATTT | A | 11 | a0001c0001t0001g0129a0001c0001t0001g0144a0001c0001t0001g0149others(8): Show | 11 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.1524+15611_1524+15 others(9): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128137791 | |||||
| chr4:128137792
|
T | TA | 16 | a0001c0001t0001g0200a0002c0002t0002g0019a0002c0002t0002g0021others(13): Show | 16 | HG00735.hp1 HG01109.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.1524+15604_1524+15 others(7): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128137792 | ||||||
| chr4:128137793
|
T | A | 5 | a0002c0002t0002g0031a0002c0002t0002g0086a0002c0002t0002g0088others(2): Show | 5 | HG02280.hp2 HG04184.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.1524+15605T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128137793 | ||||||
| chr4:128137820
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1524+15632G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128137820 | ||||||
| chr4:128137880
|
C | T | 3 | a0001c0001t0001g0167a0001c0001t0001g0170a0001c0001t0001g0173 | 3 | HG02257.hp2 HG03225.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1524+15692C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128137880 | ||||||
| chr4:128138241
|
A | G | 1 | a0002c0002t0002g0023 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1524+16053A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128138241 | ||||||
| chr4:128138260
|
A | G | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(186): Show | 189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.1524+16072A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128138260 | ||||||
| chr4:128138502
|
A | T | 2 | a0001c0001t0001g0148a0001c0001t0001g0181 | 2 | NA19012.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1524+16314A>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128138502 | ||||||
| chr4:128138929
|
G | T | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(186): Show | 189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.1524+16741G>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128138929 | ||||||
| chr4:128139058
|
G | A | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(186): Show | 189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.1524+16870G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128139058 | ||||||
| chr4:128139169
|
A | G | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(186): Show | 189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.1524+16981A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128139169 | ||||||
| chr4:128139216
|
T | C | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(186): Show | 189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.1524+17028T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128139216 | ||||||
| chr4:128139275
|
A | G | 1 | a0001c0001t0001g0142 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1524+17087A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128139275 | ||||||
| chr4:128139305
|
C | T | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(164): Show | 167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.1524+17117C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128139305 | ||||||
| chr4:128139404
|
G | C | 8 | a0002c0003t0006g0003a0002c0003t0006g0004a0002c0003t0006g0005others(5): Show | 8 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1524+17216G>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128139404 | ||||||
| chr4:128139460
|
T | C | 1 | a0002c0003t0005g0122 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1524+17272T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128139460 | ||||||
| chr4:128139573
|
G | A | 1 | a0001c0001t0001g0211 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1524+17385G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128139573 | ||||||
| chr4:128139583
|
TA | T | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(185): Show | 188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.1524+17406delA | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128139583 | |||||
| chr4:128139654
|
T | TCA | 9 | a0001c0001t0003g0245a0001c0001t0003g0246a0001c0001t0003g0253others(6): Show | 9 | HG00280.hp2 HG01496.hp2 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.1524+17483_1524+17 others(8): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128139654 | |||||
| chr4:128139736
|
A | C | 1 | a0002c0019t0002g0083 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1524+17548A>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128139736 | ||||||
| chr4:128139878
|
A | ATCTG | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(186): Show | 189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.1524+17692_1524+17 others(10): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128139878 | |||||
| chr4:128139899
|
T | G | 1 | a0001c0001t0001g0178 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1524+17711T>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128139899 | ||||||
| chr4:128139900
|
A | AACCATTT others(10): Show |
1 | a0001c0001t0001g0178 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1524+17713_1524+17 others(23): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128139900 | |||||
| chr4:128139959
|
T | C | 1 | a0001c0001t0001g0236 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1524+17771T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128139959 | ||||||
| chr4:128140010
|
C | A | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(186): Show | 189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.1524+17822C>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128140010 | ||||||
| chr4:128140154
|
T | C | 1 | a0002c0002t0002g0288 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1524+17966T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128140154 | ||||||
| chr4:128140201
|
G | C | 163 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(160): Show | 163 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1524+18013G>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128140201 | ||||||
| chr4:128140604
|
A | G | 1 | a0002c0002t0002g0114 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1524+18416A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128140604 | ||||||
| chr4:128140824
|
G | GTTGTTTT others(3): Show |
158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(155): Show | 158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.1524+18638_1524+18 others(16): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128140824 | |||||
| chr4:128140824
|
G | GTTGTTTT others(4): Show |
5 | a0001c0001t0001g0265a0001c0001t0003g0214a0001c0001t0003g0220others(2): Show | 5 | HG02132.hp1 HG02602.hp1 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.1524+18638_1524+18 others(17): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128140824 | |||||
| chr4:128140824
|
G | GTTTTTTT | 23 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(20): Show | 23 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.1524+18641_1524+18 others(13): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128140824 | |||||
| chr4:128140837
|
G | T | 163 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(160): Show | 163 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1524+18649G>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128140837 | ||||||
| chr4:128140925
|
G | C | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(186): Show | 189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.1524+18737G>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128140925 | ||||||
| chr4:128140961
|
A | G | 2 | a0002c0003t0001g0104a0002c0003t0001g0105 | 2 | HG02145.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1524+18773A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128140961 | ||||||
| chr4:128141037
|
A | C | 1 | a0001c0001t0001g0001 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1524+18849A>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128141037 | ||||||
| chr4:128141289
|
C | T | 163 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(160): Show | 163 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1524+19101C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128141289 | ||||||
| chr4:128141454
|
T | C | 10 | a0002c0003t0001g0104a0002c0003t0001g0105a0002c0003t0006g0003others(7): Show | 10 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1524+19266T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128141454 | ||||||
| chr4:128141573
|
A | G | 1 | a0001c0001t0001g0249 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1524+19385A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128141573 | ||||||
| chr4:128141918
|
G | A | 1 | a0002c0002t0002g0057 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1524+19730G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128141918 | ||||||
| chr4:128141995
|
A | C | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(186): Show | 189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.1524+19807A>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128141995 | ||||||
| chr4:128142196
|
C | T | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(186): Show | 189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.1525-19998C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128142196 | ||||||
| chr4:128142629
|
C | G | 11 | a0001c0001t0001g0108a0001c0001t0001g0124a0001c0001t0001g0259others(8): Show | 11 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(8): Show |
intron_variant | MODIFIER | c.1525-19565C>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128142629 | ||||||
| chr4:128142695
|
A | C | 1 | a0001c0001t0003g0248 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1525-19499A>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128142695 | ||||||
| chr4:128142788
|
G | A | 1 | a0002c0002t0002g0115 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1525-19406G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128142788 | ||||||
| chr4:128142901
|
C | T | 3 | a0002c0002t0002g0015a0002c0002t0002g0017a0002c0002t0002g0049 | 3 | HG02559.hp2 HG02622.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1525-19293C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128142901 | ||||||
| chr4:128143022
|
C | G | 4 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1525-19172C>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128143022 | ||||||
| chr4:128143053
|
G | A | 1 | a0002c0003t0006g0285 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1525-19141G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128143053 | ||||||
| chr4:128143129
|
G | A | 227 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(224): Show | 227 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.1525-19065G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128143129 | ||||||
| chr4:128143159
|
G | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(206): Show | 209 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.1525-19035G>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128143159 | ||||||
| chr4:128143174
|
A | G | 1 | a0002c0002t0002g0291 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1525-19020A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128143174 | ||||||
| chr4:128143209
|
C | T | 1 | a0001c0001t0003g0224 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1525-18985C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128143209 | ||||||
| chr4:128143232
|
C | G | 1 | a0002c0012t0005g0098 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1525-18962C>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128143232 | ||||||
| chr4:128143272
|
C | T | 87 | a0002c0002t0002g0012a0002c0002t0002g0013a0002c0002t0002g0016others(84): Show | 87 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1525-18922C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128143272 | ||||||
| chr4:128143273
|
G | A | 4 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1525-18921G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128143273 | ||||||
| chr4:128143330
|
T | C | 4 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1525-18864T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128143330 | ||||||
| chr4:128143432
|
G | A | 4 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1525-18762G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128143432 | ||||||
| chr4:128143524
|
G | GAA | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(186): Show | 189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.1525-18670_1525-18 others(8): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128143524 | ||||||
| chr4:128143525
|
G | T | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(186): Show | 189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.1525-18669G>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128143525 | ||||||
| chr4:128143526
|
G | C | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(186): Show | 189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.1525-18668G>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128143526 | ||||||
| chr4:128143528
|
G | C | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(186): Show | 189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.1525-18666G>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128143528 | ||||||
| chr4:128143529
|
G | T | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(186): Show | 189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.1525-18665G>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128143529 | ||||||
| chr4:128143531
|
G | A | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(186): Show | 189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.1525-18663G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128143531 | ||||||
| chr4:128143532
|
C | A | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(186): Show | 189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.1525-18662C>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128143532 | ||||||
| chr4:128143537
|
T | TC | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(186): Show | 189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.1525-18657_1525-18 others(7): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128143537 | ||||||
| chr4:128143634
|
T | TA | 93 | a0001c0001t0001g0001a0001c0001t0001g0107a0001c0001t0001g0108others(90): Show | 93 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.1525-18559dupA | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128143634 | |||||
| chr4:128143664
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1525-18530G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128143664 | ||||||
| chr4:128143796
|
G | GGTGTGTG others(3): Show |
1 | a0001c0001t0007g0131 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1525-18385_1525-18 others(16): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128143796 | |||||
| chr4:128143796
|
G | GGTGTGTG others(5): Show |
3 | a0001c0001t0007g0132a0001c0001t0007g0133a0001c0001t0007g0258 | 3 | HG01891.hp1 HG02486.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1525-18387_1525-18 others(18): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128143796 | |||||
| chr4:128143796
|
G | GGTGTGTG others(7): Show |
22 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(19): Show | 22 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.1525-18389_1525-18 others(20): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128143796 | |||||
| chr4:128143796
|
G | GGTGTGTG others(9): Show |
15 | a0001c0001t0001g0134a0001c0001t0001g0142a0001c0001t0001g0152others(12): Show | 15 | HG00280.hp2 HG01168.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1525-18391_1525-18 others(22): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128143796 | |||||
| chr4:128143796
|
G | GGTGTGTG others(11): Show |
26 | a0001c0001t0001g0107a0001c0001t0001g0149a0001c0001t0001g0155others(23): Show | 26 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(23): Show |
intron_variant | MODIFIER | c.1525-18393_1525-18 others(24): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128143796 | |||||
| chr4:128143796
|
G | GGTGTGTG others(13): Show |
95 | a0001c0001t0001g0001a0001c0001t0001g0108a0001c0001t0001g0109others(92): Show | 95 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.1525-18395_1525-18 others(26): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128143796 | |||||
| chr4:128143796
|
G | GGTGTGTG others(15): Show |
17 | a0001c0001t0001g0002a0001c0001t0001g0110a0001c0001t0001g0143others(14): Show | 17 | HG00673.hp1 HG01074.hp1 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.1525-18397_1525-18 others(28): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128143796 | |||||
| chr4:128143796
|
G | GGTGTGTG others(17): Show |
1 | a0001c0001t0003g0125 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1525-18376_1525-18 others(30): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128143796 | |||||
| chr4:128143796
|
G | GGTGTGTG others(19): Show |
4 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0003g0212others(1): Show | 4 | HG01517.hp2 HG02809.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1525-18376_1525-18 others(32): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128143796 | |||||
| chr4:128143796
|
G | GTGTGTGT others(12): Show |
1 | a0001c0001t0003g0278 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1525-18398_1525-18 others(25): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128143796 | ||||||
| chr4:128143796
|
G | GTGTGTGT others(14): Show |
3 | a0001c0001t0001g0150a0001c0001t0001g0171a0001c0001t0001g0180 | 3 | HG00738.hp1 HG01993.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.1525-18398_1525-18 others(27): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128143796 | ||||||
| chr4:128143796
|
G | GTGTGTGT others(16): Show |
1 | a0001c0001t0017g0106 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1525-18398_1525-18 others(29): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128143796 | ||||||
| chr4:128143798
|
T | G | 5 | a0002c0002t0002g0018a0002c0002t0002g0032a0002c0002t0002g0047others(2): Show | 5 | NA18950.hp2 NA18973.hp2 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.1525-18396T>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128143798 | ||||||
| chr4:128143850
|
A | G | 11 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(8): Show | 11 | HG01192.hp1 HG02486.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1525-18344A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128143850 | ||||||
| chr4:128143868
|
A | G | 23 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(20): Show | 23 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.1525-18326A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128143868 | ||||||
| chr4:128144238
|
C | G | 4 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1525-17956C>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128144238 | ||||||
| chr4:128144434
|
A | AT | 4 | a0002c0002t0005g0097a0002c0003t0005g0122a0002c0012t0005g0098others(1): Show | 4 | HG02280.hp2 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1525-17754dupT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128144434 | |||||
| chr4:128144443
|
T | G | 3 | a0002c0002t0002g0115a0002c0002t0002g0120a0002c0002t0002g0121 | 3 | HG02004.hp1 HG03688.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1525-17751T>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128144443 | ||||||
| chr4:128144470
|
A | G | 4 | a0002c0003t0006g0003a0002c0003t0006g0005a0002c0003t0006g0285others(1): Show | 4 | HG02145.hp2 HG02257.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1525-17724A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128144470 | ||||||
| chr4:128144751
|
A | T | 244 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(241): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.1525-17443A>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128144751 | ||||||
| chr4:128144842
|
T | C | 4 | a0001c0001t0003g0128a0001c0001t0003g0238a0001c0001t0003g0280others(1): Show | 4 | NA18970.hp2 NA19004.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.1525-17352T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128144842 | ||||||
| chr4:128144991
|
AT | A | 20 | a0002c0002t0005g0097a0002c0003t0001g0104a0002c0003t0001g0105others(17): Show | 20 | HG01168.hp1 HG02055.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.1525-17199delT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128144991 | |||||
| chr4:128145068
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1525-17126C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128145068 | ||||||
| chr4:128145101
|
G | A | 1 | a0002c0002t0002g0089 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1525-17093G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128145101 | ||||||
| chr4:128145333
|
C | G | 244 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(241): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.1525-16861C>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128145333 | ||||||
| chr4:128145457
|
A | C | 22 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(19): Show | 22 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.1525-16737A>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128145457 | ||||||
| chr4:128145737
|
G | A | 1 | a0006c0007t0009g0204 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1525-16457G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128145737 | ||||||
| chr4:128146082
|
G | A | 1 | a0002c0002t0002g0045 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1525-16112G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128146082 | ||||||
| chr4:128146085
|
C | T | 1 | a0002c0002t0002g0058 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1525-16109C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128146085 | ||||||
| chr4:128146086
|
A | G | 3 | a0002c0002t0002g0015a0002c0002t0002g0017a0002c0002t0002g0049 | 3 | HG02559.hp2 HG02622.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1525-16108A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128146086 | ||||||
| chr4:128146136
|
G | A | 1 | a0001c0001t0001g0168 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1525-16058G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128146136 | ||||||
| chr4:128146140
|
A | G | 1 | a0001c0001t0001g0179 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1525-16054A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128146140 | ||||||
| chr4:128146149
|
C | T | 1 | a0001c0001t0003g0242 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1525-16045C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128146149 | ||||||
| chr4:128146439
|
C | G | 1 | a0001c0001t0001g0180 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1525-15755C>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128146439 | ||||||
| chr4:128146451
|
A | C | 146 | a0002c0002t0002g0012a0002c0002t0002g0013a0002c0002t0002g0014others(143): Show | 146 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.1525-15743A>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128146451 | ||||||
| chr4:128146540
|
A | G | 5 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0177others(2): Show | 5 | HG00741.hp1 HG01099.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.1525-15654A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128146540 | ||||||
| chr4:128146595
|
C | T | 1 | a0010c0011t0005g0123 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1525-15599C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128146595 | ||||||
| chr4:128146878
|
T | G | 17 | a0002c0002t0002g0019a0002c0002t0002g0021a0002c0002t0002g0022others(14): Show | 17 | HG00735.hp1 HG01109.hp1 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.1525-15316T>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128146878 | ||||||
| chr4:128147024
|
G | T | 172 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(169): Show | 172 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.1525-15170G>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128147024 | ||||||
| chr4:128147383
|
C | T | 1 | a0002c0002t0002g0066 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1525-14811C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128147383 | ||||||
| chr4:128147594
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1525-14600G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128147594 | ||||||
| chr4:128147702
|
A | C | 3 | a0005c0006t0001g0099a0005c0006t0001g0100a0005c0006t0001g0101 | 3 | HG01168.hp1 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1525-14492A>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128147702 | ||||||
| chr4:128147863
|
G | A | 3 | a0004c0005t0005g0281a0004c0005t0005g0282a0004c0005t0005g0283 | 3 | HG02055.hp1 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1525-14331G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128147863 | ||||||
| chr4:128147935
|
T | A | 2 | a0003c0004t0001g0172a0003c0004t0001g0264 | 2 | HG01109.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1525-14259T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128147935 | ||||||
| chr4:128148140
|
T | C | 5 | a0001c0001t0003g0256a0001c0001t0003g0257a0005c0006t0001g0099others(2): Show | 5 | HG01168.hp1 HG01168.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.1525-14054T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128148140 | ||||||
| chr4:128148158
|
C | T | 1 | a0002c0002t0002g0057 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1525-14036C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128148158 | ||||||
| chr4:128148292
|
G | A | 4 | a0002c0002t0005g0097a0002c0003t0005g0122a0002c0012t0005g0098others(1): Show | 4 | HG02280.hp2 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1525-13902G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128148292 | ||||||
| chr4:128148407
|
G | T | 10 | a0002c0003t0001g0104a0002c0003t0001g0105a0002c0003t0006g0003others(7): Show | 10 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1525-13787G>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128148407 | ||||||
| chr4:128148711
|
C | T | 2 | a0002c0002t0002g0295a0002c0002t0002g0298 | 2 | NA18974.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.1525-13483C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128148711 | ||||||
| chr4:128148987
|
A | G | 1 | a0001c0001t0004g0314 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1525-13207A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128148987 | ||||||
| chr4:128149043
|
T | C | 1 | a0002c0002t0002g0085 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1525-13151T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128149043 | ||||||
| chr4:128149044
|
G | A | 3 | a0004c0005t0005g0281a0004c0005t0005g0282a0004c0005t0005g0283 | 3 | HG02055.hp1 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1525-13150G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128149044 | ||||||
| chr4:128149156
|
G | A | 3 | a0004c0005t0005g0281a0004c0005t0005g0282a0004c0005t0005g0283 | 3 | HG02055.hp1 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1525-13038G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128149156 | ||||||
| chr4:128149270
|
A | G | 4 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1525-12924A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128149270 | ||||||
| chr4:128149423
|
G | A | 1 | a0001c0001t0003g0127 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1525-12771G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128149423 | ||||||
| chr4:128149425
|
TA | T | 146 | a0002c0002t0002g0012a0002c0002t0002g0013a0002c0002t0002g0014others(143): Show | 146 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.1525-12763delA | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128149425 | |||||
| chr4:128149832
|
A | G | 2 | a0001c0001t0003g0221a0001c0001t0003g0222 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1525-12362A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128149832 | ||||||
| chr4:128149951
|
G | T | 1 | a0002c0002t0002g0044 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1525-12243G>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128149951 | ||||||
| chr4:128150063
|
A | G | 2 | a0001c0001t0001g0108a0001c0001t0001g0271 | 2 | NA18983.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.1525-12131A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128150063 | ||||||
| chr4:128150083
|
G | A | 2 | a0002c0002t0002g0072a0002c0002t0002g0073 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1525-12111G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128150083 | ||||||
| chr4:128150164
|
A | G | 22 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(19): Show | 22 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.1525-12030A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128150164 | ||||||
| chr4:128150174
|
C | A | 1 | a0002c0002t0002g0057 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1525-12020C>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128150174 | ||||||
| chr4:128150248
|
C | A | 1 | a0001c0001t0004g0324 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1525-11946C>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128150248 | ||||||
| chr4:128150292
|
CT | C | 142 | a0001c0001t0001g0124a0001c0001t0003g0248a0002c0002t0002g0012others(139): Show | 142 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.1525-11886delT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128150292 | |||||
| chr4:128150359
|
CA | C | 10 | a0002c0003t0001g0104a0002c0003t0001g0105a0002c0003t0006g0003others(7): Show | 10 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1525-11834delA | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128150359 | ||||||
| chr4:128150526
|
C | T | 2 | a0002c0002t0002g0302a0002c0002t0002g0330 | 2 | HG02074.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.1525-11668C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128150526 | ||||||
| chr4:128150556
|
G | C | 2 | a0002c0002t0002g0284a0002c0002t0002g0287 | 2 | HG01433.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1525-11638G>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128150556 | ||||||
| chr4:128150969
|
A | G | 1 | a0001c0001t0003g0224 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1525-11225A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128150969 | ||||||
| chr4:128151136
|
A | C | 4 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1525-11058A>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128151136 | ||||||
| chr4:128151385
|
T | G | 3 | a0004c0005t0005g0281a0004c0005t0005g0282a0004c0005t0005g0283 | 3 | HG02055.hp1 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1525-10809T>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128151385 | ||||||
| chr4:128151415
|
A | G | 1 | a0002c0002t0002g0306 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1525-10779A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128151415 | ||||||
| chr4:128151695
|
C | T | 2 | a0008c0009t0005g0113a0008c0009t0005g0119 | 2 | HG02572.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1525-10499C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128151695 | ||||||
| chr4:128151894
|
G | A | 1 | a0001c0001t0001g0272 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1525-10300G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128151894 | ||||||
| chr4:128152040
|
T | C | 1 | a0002c0002t0002g0092 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1525-10154T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128152040 | ||||||
| chr4:128152207
|
A | AT | 6 | a0001c0001t0001g0109a0001c0001t0003g0225a0001c0001t0003g0242others(3): Show | 6 | HG00099.hp2 HG01106.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.1525-9972dupT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128152207 | |||||
| chr4:128152207
|
A | ATT | 22 | a0002c0002t0002g0078a0002c0002t0002g0295a0002c0002t0005g0097others(19): Show | 22 | HG01168.hp1 HG02055.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1525-9973_1525-997 others(6): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128152207 | |||||
| chr4:128152207
|
A | ATTT | 123 | a0001c0001t0001g0148a0001c0001t0001g0181a0002c0002t0002g0012others(120): Show | 123 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.1525-9974_1525-997 others(7): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128152207 | |||||
| chr4:128152293
|
T | G | 1 | a0002c0002t0002g0306 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1525-9901T>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128152293 | ||||||
| chr4:128152498
|
G | A | 22 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(19): Show | 22 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.1525-9696G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128152498 | ||||||
| chr4:128152720
|
A | G | 1 | a0001c0001t0003g0233 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1525-9474A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128152720 | ||||||
| chr4:128152973
|
C | CT | 17 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0198others(14): Show | 17 | HG01109.hp2 HG01175.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1525-9195dupT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128152973 | |||||
| chr4:128152973
|
CT | C | 87 | a0001c0001t0001g0002a0001c0001t0001g0110a0001c0001t0001g0126others(84): Show | 87 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.1525-9195delT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128152973 | |||||
| chr4:128152973
|
CTT | C | 13 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0157others(10): Show | 13 | HG02145.hp1 HG02809.hp1 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.1525-9196_1525-919 others(6): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128152973 | |||||
| chr4:128153070
|
C | T | 10 | a0002c0003t0001g0104a0002c0003t0001g0105a0002c0003t0006g0003others(7): Show | 10 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1525-9124C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128153070 | ||||||
| chr4:128153292
|
C | CATTT | 8 | a0001c0001t0001g0126a0001c0001t0001g0137a0001c0001t0001g0142others(5): Show | 8 | HG02273.hp2 HG03225.hp1 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.1525-8863_1525-886 others(8): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128153292 | |||||
| chr4:128153292
|
CATTT | C | 55 | a0001c0001t0001g0166a0001c0001t0001g0178a0001c0001t0001g0191others(52): Show | 55 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.1525-8863_1525-886 others(8): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128153292 | |||||
| chr4:128153292
|
CATTTATT others(1): Show |
C | 22 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(19): Show | 22 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.1525-8867_1525-886 others(12): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128153292 | |||||
| chr4:128153292
|
CATTTATT others(5): Show |
C | 5 | a0001c0018t0003g0254a0002c0002t0002g0121a0004c0005t0005g0281others(2): Show | 5 | HG00099.hp2 HG02004.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.1525-8871_1525-886 others(16): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128153292 | |||||
| chr4:128153292
|
CATTTATT others(9): Show |
C | 142 | a0002c0002t0002g0012a0002c0002t0002g0013a0002c0002t0002g0014others(139): Show | 142 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.1525-8875_1525-886 others(20): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128153292 | |||||
| chr4:128153412
|
A | G | 150 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(147): Show | 150 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.1525-8782A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128153412 | ||||||
| chr4:128153462
|
C | T | 2 | a0002c0002t0002g0307a0002c0002t0002g0331 | 2 | NA19007.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.1525-8732C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128153462 | ||||||
| chr4:128153492
|
G | A | 2 | a0001c0001t0004g0313a0001c0001t0004g0324 | 2 | HG00609.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1525-8702G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128153492 | ||||||
| chr4:128153766
|
A | G | 1 | a0001c0001t0001g0190 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1525-8428A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128153766 | ||||||
| chr4:128153958
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1525-8236G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128153958 | ||||||
| chr4:128154076
|
T | A | 1 | a0001c0001t0001g0163 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1525-8118T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128154076 | ||||||
| chr4:128154215
|
T | C | 2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | HG01099.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.1525-7979T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128154215 | ||||||
| chr4:128154577
|
A | G | 1 | a0001c0001t0004g0327 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1525-7617A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128154577 | ||||||
| chr4:128154654
|
C | T | 2 | a0002c0002t0002g0284a0002c0002t0002g0287 | 2 | HG01433.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1525-7540C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128154654 | ||||||
| chr4:128154766
|
T | C | 3 | a0005c0006t0001g0099a0005c0006t0001g0100a0005c0006t0001g0101 | 3 | HG01168.hp1 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1525-7428T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128154766 | ||||||
| chr4:128154826
|
T | A | 150 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(147): Show | 150 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.1525-7368T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128154826 | ||||||
| chr4:128154930
|
C | T | 1 | a0002c0002t0005g0059 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1525-7264C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128154930 | ||||||
| chr4:128155189
|
G | C | 1 | a0001c0001t0001g0193 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1525-7005G>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128155189 | ||||||
| chr4:128155417
|
C | T | 1 | a0001c0001t0003g0252 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1525-6777C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128155417 | ||||||
| chr4:128155603
|
A | G | 1 | a0002c0002t0002g0291 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1525-6591A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128155603 | ||||||
| chr4:128155643
|
C | T | 1 | a0002c0002t0013g0093 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1525-6551C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128155643 | ||||||
| chr4:128155663
|
T | G | 148 | a0001c0001t0001g0109a0002c0002t0002g0012a0002c0002t0002g0013others(145): Show | 148 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.1525-6531T>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128155663 | ||||||
| chr4:128155675
|
C | T | 1 | a0001c0001t0001g0110 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1525-6519C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128155675 | ||||||
| chr4:128155792
|
C | T | 1 | a0002c0002t0002g0060 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1525-6402C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128155792 | ||||||
| chr4:128156003
|
C | A | 1 | a0002c0002t0002g0079 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1525-6191C>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128156003 | ||||||
| chr4:128156298
|
C | A | 1 | a0002c0002t0002g0296 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1525-5896C>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128156298 | ||||||
| chr4:128156863
|
T | TA | 65 | a0001c0001t0001g0001a0001c0001t0001g0109a0001c0001t0001g0110others(62): Show | 65 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.1525-5306dupA | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128156863 | |||||
| chr4:128156863
|
TA | T | 56 | a0001c0001t0003g0128a0001c0001t0003g0256a0001c0001t0003g0257others(53): Show | 56 | HG00099.hp1 HG00558.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.1525-5306delA | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128156863 | |||||
| chr4:128156863
|
TAA | T | 102 | a0002c0002t0002g0012a0002c0002t0002g0013a0002c0002t0002g0018others(99): Show | 102 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.1525-5307_1525-530 others(6): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128156863 | |||||
| chr4:128157031
|
A | G | 1 | a0002c0012t0005g0098 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1525-5163A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128157031 | ||||||
| chr4:128157152
|
T | A | 3 | a0004c0005t0005g0281a0004c0005t0005g0282a0004c0005t0005g0283 | 3 | HG02055.hp1 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1525-5042T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128157152 | ||||||
| chr4:128157212
|
A | G | 1 | a0002c0002t0002g0038 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1525-4982A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128157212 | ||||||
| chr4:128157241
|
A | G | 1 | a0001c0001t0003g0230 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1525-4953A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128157241 | ||||||
| chr4:128157549
|
A | G | 1 | a0002c0002t0002g0022 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1525-4645A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128157549 | ||||||
| chr4:128157790
|
T | C | 22 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(19): Show | 22 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.1525-4404T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128157790 | ||||||
| chr4:128157949
|
A | G | 49 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0126others(46): Show | 49 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.1525-4245A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128157949 | ||||||
| chr4:128158189
|
G | C | 22 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(19): Show | 22 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.1525-4005G>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128158189 | ||||||
| chr4:128158295
|
G | A | 1 | a0002c0002t0002g0095 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1525-3899G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128158295 | ||||||
| chr4:128158310
|
A | G | 4 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1525-3884A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128158310 | ||||||
| chr4:128158540
|
A | G | 1 | a0002c0002t0002g0307 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1525-3654A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128158540 | ||||||
| chr4:128158741
|
G | A | 147 | a0002c0002t0002g0012a0002c0002t0002g0013a0002c0002t0002g0014others(144): Show | 147 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.1525-3453G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128158741 | ||||||
| chr4:128158875
|
A | T | 1 | a0002c0002t0002g0045 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1525-3319A>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128158875 | ||||||
| chr4:128159017
|
T | TA | 146 | a0002c0002t0002g0012a0002c0002t0002g0013a0002c0002t0002g0014others(143): Show | 146 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.1525-3166dupA | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128159017 | |||||
| chr4:128159367
|
T | C | 1 | a0002c0012t0005g0098 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1525-2827T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128159367 | ||||||
| chr4:128159460
|
T | C | 1 | a0001c0001t0001g0195 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1525-2734T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128159460 | ||||||
| chr4:128159485
|
C | T | 1 | a0001c0001t0003g0224 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1525-2709C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128159485 | ||||||
| chr4:128159558
|
A | G | 1 | a0002c0002t0002g0090 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1525-2636A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128159558 | ||||||
| chr4:128159571
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1525-2623G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128159571 | ||||||
| chr4:128159753
|
A | G | 1 | a0002c0002t0002g0121 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1525-2441A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128159753 | ||||||
| chr4:128159930
|
G | T | 22 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(19): Show | 22 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.1525-2264G>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128159930 | ||||||
| chr4:128160039
|
A | G | 3 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0177 | 3 | HG00741.hp1 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1525-2155A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128160039 | ||||||
| chr4:128160119
|
A | G | 1 | a0002c0002t0002g0039 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1525-2075A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128160119 | ||||||
| chr4:128160158
|
G | T | 147 | a0002c0002t0002g0012a0002c0002t0002g0013a0002c0002t0002g0014others(144): Show | 147 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.1525-2036G>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128160158 | ||||||
| chr4:128160274
|
C | T | 144 | a0002c0002t0002g0012a0002c0002t0002g0013a0002c0002t0002g0014others(141): Show | 144 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.1525-1920C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128160274 | ||||||
| chr4:128160305
|
G | A | 173 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(170): Show | 173 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.1525-1889G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128160305 | ||||||
| chr4:128160522
|
TTG | T | 3 | a0001c0001t0001g0249a0006c0007t0004g0234a0014c0015t0001g0206 | 3 | HG00609.hp2 HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1525-1654_1525-165 others(6): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr4 | 128160522 | |||||
| chr4:128160992
|
C | T | 1 | a0002c0002t0002g0013 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1525-1202C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128160992 | ||||||
| chr4:128161030
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1525-1164C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128161030 | ||||||
| chr4:128161336
|
T | C | 299 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(296): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1525-858T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128161336 | ||||||
| chr4:128161560
|
A | G | 4 | a0002c0002t0002g0012a0002c0002t0002g0054a0002c0002t0002g0055others(1): Show | 4 | NA18954.hp2 NA18955.hp1 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.1525-634A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128161560 | ||||||
| chr4:128161578
|
T | G | 147 | a0002c0002t0002g0012a0002c0002t0002g0013a0002c0002t0002g0014others(144): Show | 147 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.1525-616T>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128161578 | ||||||
| chr4:128161663
|
C | T | 3 | a0001c0001t0003g0210a0001c0001t0003g0237a0001c0001t0003g0244 | 3 | HG00140.hp1 HG04184.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1525-531C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128161663 | ||||||
| chr4:128161666
|
T | A | 173 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(170): Show | 173 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.1525-528T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128161666 | ||||||
| chr4:128161988
|
T | C | 151 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(148): Show | 151 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.1525-206T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128161988 | ||||||
| chr4:128162013
|
C | T | 2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | HG01099.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.1525-181C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128162013 | ||||||
| chr4:128162060
|
T | A | 1 | a0001c0001t0001g0109 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1525-134T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128162060 | ||||||
| chr4:128162185
|
C | T | 17 | a0002c0002t0002g0019a0002c0002t0002g0021a0002c0002t0002g0022others(14): Show | 17 | HG00735.hp1 HG01109.hp1 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.1525-9C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 11/19 | chr4 | 128162185 | ||||||
| chr4:128163227
|
G | C | 22 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(19): Show | 22 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.1648+910G>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128163227 | ||||||
| chr4:128163658
|
T | C | 57 | a0001c0001t0001g0168a0001c0001t0001g0236a0001c0001t0003g0102others(54): Show | 57 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.1648+1341T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128163658 | ||||||
| chr4:128163676
|
C | T | 151 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(148): Show | 151 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.1648+1359C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128163676 | ||||||
| chr4:128163765
|
GTTA | G | 5 | a0005c0006t0001g0099a0005c0006t0001g0100a0005c0006t0001g0101others(2): Show | 5 | HG01168.hp1 HG02572.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1648+1463_1648+146 others(7): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr4 | 128163765 | |||||
| chr4:128164019
|
G | A | 2 | a0002c0002t0005g0097a0002c0003t0005g0122 | 2 | HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1648+1702G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128164019 | ||||||
| chr4:128164057
|
T | C | 1 | a0002c0002t0002g0038 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1648+1740T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128164057 | ||||||
| chr4:128164072
|
A | G | 2 | a0001c0001t0001g0211a0001c0001t0001g0249 | 2 | HG02572.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1648+1755A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128164072 | ||||||
| chr4:128164305
|
G | A | 3 | a0004c0005t0005g0281a0004c0005t0005g0282a0004c0005t0005g0283 | 3 | HG02055.hp1 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1648+1988G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128164305 | ||||||
| chr4:128164348
|
T | C | 127 | a0001c0001t0001g0110a0002c0002t0002g0012a0002c0002t0002g0013others(124): Show | 127 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.1648+2031T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128164348 | ||||||
| chr4:128164468
|
C | T | 1 | a0001c0001t0003g0240 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1648+2151C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128164468 | ||||||
| chr4:128164471
|
A | G | 1 | a0001c0001t0003g0238 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1648+2154A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128164471 | ||||||
| chr4:128164821
|
A | G | 2 | a0002c0002t0002g0040a0002c0002t0002g0046 | 2 | NA18949.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.1648+2504A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128164821 | ||||||
| chr4:128164976
|
G | GAAAAAAT others(2): Show |
22 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(19): Show | 22 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.1648+2665_1648+267 others(13): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr4 | 128164976 | |||||
| chr4:128165001
|
A | G | 3 | a0004c0005t0005g0281a0004c0005t0005g0282a0004c0005t0005g0283 | 3 | HG02055.hp1 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1648+2684A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128165001 | ||||||
| chr4:128165010
|
A | G | 144 | a0002c0002t0002g0012a0002c0002t0002g0013a0002c0002t0002g0014others(141): Show | 144 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.1648+2693A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128165010 | ||||||
| chr4:128165219
|
G | A | 1 | a0001c0001t0001g0263 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1648+2902G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128165219 | ||||||
| chr4:128165307
|
A | G | 1 | a0001c0001t0001g0152 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1648+2990A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128165307 | ||||||
| chr4:128165309
|
G | C | 151 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(148): Show | 151 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.1648+2992G>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128165309 | ||||||
| chr4:128165460
|
TA | T | 126 | a0002c0002t0002g0012a0002c0002t0002g0013a0002c0002t0002g0014others(123): Show | 126 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.1648+3150delA | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr4 | 128165460 | |||||
| chr4:128165508
|
T | C | 3 | a0004c0005t0005g0281a0004c0005t0005g0282a0004c0005t0005g0283 | 3 | HG02055.hp1 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1648+3191T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128165508 | ||||||
| chr4:128165578
|
G | A | 4 | a0001c0001t0001g0011a0001c0001t0001g0160a0001c0001t0001g0161others(1): Show | 4 | HG02486.hp2 HG02647.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1648+3261G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128165578 | ||||||
| chr4:128165689
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1648+3372A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128165689 | ||||||
| chr4:128166056
|
A | G | 10 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0140others(7): Show | 10 | HG01192.hp1 HG02486.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1648+3739A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128166056 | ||||||
| chr4:128166445
|
G | A | 8 | a0002c0003t0006g0003a0002c0003t0006g0004a0002c0003t0006g0005others(5): Show | 8 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1648+4128G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128166445 | ||||||
| chr4:128166569
|
C | T | 1 | a0001c0001t0004g0321 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1648+4252C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128166569 | ||||||
| chr4:128166856
|
A | G | 3 | a0002c0002t0005g0097a0002c0003t0005g0122a0002c0012t0005g0098 | 3 | HG02451.hp1 HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1648+4539A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128166856 | ||||||
| chr4:128166930
|
T | TTC | 4 | a0001c0001t0001g0185a0001c0001t0001g0260a0001c0001t0001g0273others(1): Show | 4 | HG02451.hp1 HG02738.hp2 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.1648+4653_1648+465 others(6): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr4 | 128166930 | |||||
| chr4:128166930
|
TTC | T | 13 | a0001c0001t0001g0171a0001c0001t0001g0173a0001c0001t0001g0175others(10): Show | 13 | HG00099.hp2 HG00642.hp1 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.1648+4653_1648+465 others(6): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr4 | 128166930 | |||||
| chr4:128166930
|
TTCTC | T | 26 | a0001c0001t0001g0143a0001c0001t0001g0195a0001c0001t0003g0125others(23): Show | 26 | HG00140.hp1 HG00280.hp2 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.1648+4651_1648+465 others(8): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr4 | 128166930 | |||||
| chr4:128166930
|
TTCTCTC | T | 38 | a0001c0001t0001g0275a0001c0001t0003g0102a0001c0001t0003g0103others(35): Show | 38 | HG00408.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.1648+4649_1648+465 others(10): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr4 | 128166930 | |||||
| chr4:128166930
|
TTCTCTCT others(1): Show |
T | 48 | a0001c0001t0003g0220a0002c0002t0002g0012a0002c0002t0002g0013others(45): Show | 48 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.1648+4647_1648+465 others(12): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr4 | 128166930 | |||||
| chr4:128166930
|
TTCTCTCT others(3): Show |
T | 14 | a0001c0001t0004g0312a0001c0001t0004g0314a0001c0001t0004g0317others(11): Show | 14 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(11): Show |
intron_variant | MODIFIER | c.1648+4645_1648+465 others(14): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr4 | 128166930 | |||||
| chr4:128166930
|
TTCTCTCT others(5): Show |
T | 12 | a0001c0001t0007g0258a0002c0002t0002g0069a0002c0002t0005g0097others(9): Show | 12 | HG01891.hp1 HG02145.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1648+4643_1648+465 others(16): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr4 | 128166930 | |||||
| chr4:128166960
|
CTCTCTCT others(5): Show |
C | 3 | a0002c0002t0002g0114a0002c0002t0012g0065a0002c0003t0006g0007 | 3 | HG02080.hp1 HG02109.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.1648+4645_1648+465 others(16): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr4 | 128166960 | |||||
| chr4:128166962
|
CTCTCTCT others(3): Show |
C | 10 | a0001c0001t0004g0308a0001c0001t0004g0311a0001c0001t0004g0313others(7): Show | 10 | HG02056.hp2 HG02129.hp2 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.1648+4647_1648+465 others(14): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr4 | 128166962 | |||||
| chr4:128166962
|
CTCTCTCT others(5): Show |
C | 6 | a0002c0002t0002g0051a0002c0002t0002g0071a0002c0002t0002g0078others(3): Show | 6 | HG02970.hp1 HG03540.hp1 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.1648+4647_1648+465 others(16): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr4 | 128166962 | |||||
| chr4:128166964
|
C | A | 6 | a0001c0001t0001g0140a0001c0001t0003g0111a0001c0001t0003g0217others(3): Show | 6 | HG01192.hp1 HG01192.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.1648+4647C>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128166964 | ||||||
| chr4:128166964
|
CTCTCTCT others(1): Show |
C | 29 | a0001c0001t0001g0141a0001c0001t0001g0208a0001c0001t0003g0276others(26): Show | 29 | HG00639.hp1 HG00735.hp2 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.1648+4649_1648+465 others(12): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr4 | 128166964 | |||||
| chr4:128166964
|
CTCTCTCT others(3): Show |
C | 5 | a0001c0001t0004g0310a0001c0001t0004g0326a0001c0001t0004g0328others(2): Show | 5 | HG02486.hp1 NA19002.hp2 NA19064.hp1 others(2): Show |
intron_variant | MODIFIER | c.1648+4649_1648+465 others(14): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr4 | 128166964 | |||||
| chr4:128166966
|
C | A | 17 | a0001c0001t0001g0140a0001c0001t0003g0103a0001c0001t0003g0111others(14): Show | 17 | HG00099.hp2 HG00558.hp1 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.1648+4649C>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128166966 | ||||||
| chr4:128166966
|
CTCTCTA | C | 13 | a0001c0001t0001g0177a0001c0001t0001g0179a0001c0001t0003g0256others(10): Show | 13 | HG00741.hp1 HG01168.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.1648+4651_1648+465 others(10): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr4 | 128166966 | |||||
| chr4:128166966
|
CTCTCTAT others(1): Show |
C | 13 | a0001c0001t0001g0211a0002c0002t0002g0016a0002c0002t0002g0032others(10): Show | 13 | HG00438.hp2 HG01981.hp1 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.1648+4651_1648+465 others(12): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr4 | 128166966 | |||||
| chr4:128166968
|
C | A | 45 | a0001c0001t0001g0011a0001c0001t0001g0109a0001c0001t0001g0140others(42): Show | 45 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.1648+4651C>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128166968 | ||||||
| chr4:128166968
|
CTCTA | C | 19 | a0001c0001t0001g0002a0001c0001t0001g0110a0001c0001t0001g0134others(16): Show | 19 | HG00735.hp1 HG01258.hp2 HG01975.hp2 others(16): Show |
intron_variant | MODIFIER | c.1648+4653_1648+465 others(8): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr4 | 128166968 | |||||
| chr4:128166968
|
CTCTATAT others(1): Show |
C | 8 | a0001c0001t0001g0147a0001c0001t0001g0207a0001c0001t0003g0221others(5): Show | 8 | HG00609.hp2 HG01516.hp2 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.1648+4653_1648+466 others(12): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr4 | 128166968 | |||||
| chr4:128166970
|
C | A | 106 | a0001c0001t0001g0011a0001c0001t0001g0107a0001c0001t0001g0109others(103): Show | 106 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.1648+4653C>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128166970 | ||||||
| chr4:128166970
|
CTA | C | 6 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0142others(3): Show | 6 | HG00423.hp2 HG01070.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1648+4676_1648+467 others(6): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr4 | 128166970 | |||||
| chr4:128166970
|
CTATA | C | 24 | a0001c0001t0001g0001a0001c0001t0001g0126a0001c0001t0001g0148others(21): Show | 24 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.1648+4674_1648+467 others(8): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr4 | 128166970 | |||||
| chr4:128166970
|
CTATATA | C | 3 | a0001c0001t0001g0168a0001c0001t0001g0186a0001c0001t0001g0187 | 3 | HG01943.hp1 NA18942.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.1648+4672_1648+467 others(10): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr4 | 128166970 | |||||
| chr4:128166972
|
A | C | 12 | a0001c0001t0001g0010a0001c0001t0001g0108a0001c0001t0001g0157others(9): Show | 12 | HG00544.hp2 HG01109.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1648+4655A>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128166972 | ||||||
| chr4:128166974
|
A | C | 6 | a0001c0001t0001g0185a0001c0001t0001g0263a0001c0001t0001g0271others(3): Show | 6 | HG02280.hp1 HG02451.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.1648+4657A>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128166974 | ||||||
| chr4:128166976
|
A | C | 17 | a0001c0001t0001g0001a0001c0001t0001g0126a0001c0001t0001g0150others(14): Show | 17 | HG01433.hp2 HG01891.hp2 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.1648+4659A>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128166976 | ||||||
| chr4:128166978
|
A | C | 1 | a0001c0001t0001g0001 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1648+4661A>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128166978 | ||||||
| chr4:128166991
|
T | C | 127 | a0002c0002t0002g0012a0002c0002t0002g0013a0002c0002t0002g0014others(124): Show | 127 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.1648+4674T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128166991 | ||||||
| chr4:128166993
|
T | C | 153 | a0001c0001t0001g0178a0001c0001t0001g0191a0001c0001t0003g0276others(150): Show | 153 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.1648+4676T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128166993 | ||||||
| chr4:128167063
|
T | C | 1 | a0001c0001t0004g0310 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1648+4746T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128167063 | ||||||
| chr4:128167063
|
T | TAC | 3 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0258 | 3 | HG01891.hp1 HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1648+4760_1648+476 others(6): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr4 | 128167063 | |||||
| chr4:128167074
|
ACAC | A | 3 | a0004c0005t0005g0281a0004c0005t0005g0282a0004c0005t0005g0283 | 3 | HG02055.hp1 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1648+4758_1648+476 others(7): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128167074 | ||||||
| chr4:128167190
|
C | A | 4 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1648+4873C>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128167190 | ||||||
| chr4:128167196
|
A | G | 1 | a0001c0001t0001g0207 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1648+4879A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128167196 | ||||||
| chr4:128167199
|
G | A | 4 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1648+4882G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128167199 | ||||||
| chr4:128167324
|
C | T | 2 | a0001c0001t0003g0125a0001c0001t0003g0212 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1648+5007C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128167324 | ||||||
| chr4:128167399
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1648+5082A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128167399 | ||||||
| chr4:128167775
|
A | G | 1 | a0001c0001t0001g0155 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1648+5458A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128167775 | ||||||
| chr4:128167970
|
C | G | 4 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1648+5653C>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128167970 | ||||||
| chr4:128168015
|
T | C | 1 | a0001c0001t0001g0249 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1648+5698T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128168015 | ||||||
| chr4:128168119
|
G | C | 9 | a0001c0001t0001g0002a0001c0001t0001g0140a0001c0001t0001g0159others(6): Show | 9 | HG01192.hp1 HG02486.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1648+5802G>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128168119 | ||||||
| chr4:128168119
|
G | T | 1 | a0001c0001t0001g0011 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1648+5802G>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128168119 | ||||||
| chr4:128168174
|
A | G | 1 | a0001c0001t0003g0242 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1648+5857A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128168174 | ||||||
| chr4:128168278
|
G | T | 2 | a0008c0009t0005g0113a0008c0009t0005g0119 | 2 | HG02572.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1648+5961G>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128168278 | ||||||
| chr4:128168289
|
A | T | 170 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0162others(167): Show | 170 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.1648+5972A>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128168289 | ||||||
| chr4:128168290
|
A | T | 147 | a0002c0002t0002g0012a0002c0002t0002g0013a0002c0002t0002g0014others(144): Show | 147 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.1648+5973A>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128168290 | ||||||
| chr4:128168291
|
A | T | 19 | a0002c0002t0002g0019a0002c0002t0002g0021a0002c0002t0002g0022others(16): Show | 19 | HG00735.hp1 HG01109.hp1 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.1648+5974A>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128168291 | ||||||
| chr4:128168465
|
A | G | 10 | a0002c0003t0001g0104a0002c0003t0001g0105a0002c0003t0006g0003others(7): Show | 10 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1648+6148A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128168465 | ||||||
| chr4:128168586
|
G | T | 3 | a0002c0002t0002g0019a0002c0002t0015g0020a0002c0003t0009g0008 | 3 | HG02630.hp1 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1648+6269G>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128168586 | ||||||
| chr4:128168768
|
G | GT | 7 | a0002c0002t0002g0019a0002c0002t0002g0021a0002c0002t0002g0022others(4): Show | 7 | HG02630.hp1 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1648+6462dupT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr4 | 128168768 | |||||
| chr4:128168865
|
T | C | 126 | a0002c0002t0002g0012a0002c0002t0002g0013a0002c0002t0002g0014others(123): Show | 126 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.1648+6548T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128168865 | ||||||
| chr4:128168867
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1648+6550T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128168867 | ||||||
| chr4:128168912
|
A | T | 1 | a0001c0001t0007g0258 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1648+6595A>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128168912 | ||||||
| chr4:128168948
|
T | G | 1 | a0001c0001t0001g0109 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1648+6631T>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128168948 | ||||||
| chr4:128169041
|
A | G | 173 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(170): Show | 173 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.1648+6724A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128169041 | ||||||
| chr4:128169159
|
C | T | 1 | a0002c0003t0006g0004 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1648+6842C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128169159 | ||||||
| chr4:128169369
|
A | G | 173 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(170): Show | 173 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.1648+7052A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128169369 | ||||||
| chr4:128169573
|
T | G | 7 | a0002c0002t0002g0019a0002c0002t0002g0021a0002c0002t0002g0022others(4): Show | 7 | HG02630.hp1 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1648+7256T>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128169573 | ||||||
| chr4:128169947
|
G | A | 173 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(170): Show | 173 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.1649-6925G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128169947 | ||||||
| chr4:128170080
|
T | C | 1 | a0002c0002t0002g0088 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1649-6792T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128170080 | ||||||
| chr4:128170110
|
T | C | 3 | a0004c0005t0005g0281a0004c0005t0005g0282a0004c0005t0005g0283 | 3 | HG02055.hp1 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1649-6762T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128170110 | ||||||
| chr4:128170325
|
G | A | 4 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1649-6547G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128170325 | ||||||
| chr4:128170739
|
A | G | 1 | a0002c0002t0002g0015 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1649-6133A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128170739 | ||||||
| chr4:128170770
|
A | G | 8 | a0002c0003t0006g0003a0002c0003t0006g0004a0002c0003t0006g0005others(5): Show | 8 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1649-6102A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128170770 | ||||||
| chr4:128170781
|
A | G | 1 | a0001c0001t0001g0249 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1649-6091A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128170781 | ||||||
| chr4:128170852
|
A | T | 5 | a0001c0001t0003g0219a0001c0001t0003g0224a0001c0001t0003g0250others(2): Show | 5 | HG01168.hp2 HG01169.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.1649-6020A>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128170852 | ||||||
| chr4:128170872
|
C | CT | 30 | a0001c0001t0001g0001a0001c0001t0001g0260a0001c0001t0003g0222others(27): Show | 30 | HG00280.hp2 HG00558.hp2 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.1649-5983dupT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr4 | 128170872 | |||||
| chr4:128170872
|
CT | C | 118 | a0001c0001t0001g0186a0001c0001t0007g0131a0002c0002t0002g0012others(115): Show | 118 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.1649-5983delT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr4 | 128170872 | |||||
| chr4:128170872
|
CTT | C | 6 | a0002c0002t0002g0290a0002c0002t0002g0295a0002c0002t0002g0296others(3): Show | 6 | NA18942.hp1 NA18943.hp1 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.1649-5984_1649-598 others(6): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr4 | 128170872 | |||||
| chr4:128170878
|
T | C | 2 | a0006c0007t0009g0192a0006c0007t0009g0204 | 2 | HG03139.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1649-5994T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128170878 | ||||||
| chr4:128170909
|
G | A | 22 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(19): Show | 22 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.1649-5963G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128170909 | ||||||
| chr4:128170986
|
T | C | 3 | a0004c0005t0005g0281a0004c0005t0005g0282a0004c0005t0005g0283 | 3 | HG02055.hp1 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1649-5886T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128170986 | ||||||
| chr4:128171105
|
AT | A | 126 | a0002c0002t0002g0012a0002c0002t0002g0013a0002c0002t0002g0014others(123): Show | 126 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.1649-5755delT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr4 | 128171105 | |||||
| chr4:128171155
|
G | T | 3 | a0004c0005t0005g0281a0004c0005t0005g0282a0004c0005t0005g0283 | 3 | HG02055.hp1 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1649-5717G>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128171155 | ||||||
| chr4:128171193
|
G | A | 3 | a0002c0002t0002g0075a0002c0002t0002g0076a0002c0002t0002g0336 | 3 | HG01256.hp2 HG01258.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1649-5679G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128171193 | ||||||
| chr4:128171224
|
G | T | 22 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(19): Show | 22 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.1649-5648G>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128171224 | ||||||
| chr4:128171276
|
A | G | 2 | a0001c0001t0003g0221a0001c0001t0003g0222 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1649-5596A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128171276 | ||||||
| chr4:128171277
|
C | T | 5 | a0003c0004t0001g0172a0003c0004t0001g0182a0003c0004t0001g0183others(2): Show | 5 | HG01109.hp2 HG01167.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1649-5595C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128171277 | ||||||
| chr4:128171281
|
A | G | 1 | a0002c0002t0002g0031 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1649-5591A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128171281 | ||||||
| chr4:128171296
|
T | A | 4 | a0001c0001t0004g0312a0001c0001t0004g0318a0001c0001t0004g0322others(1): Show | 4 | HG00558.hp2 NA18946.hp2 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.1649-5576T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128171296 | ||||||
| chr4:128171310
|
G | T | 10 | a0002c0003t0001g0104a0002c0003t0001g0105a0002c0003t0006g0003others(7): Show | 10 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1649-5562G>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128171310 | ||||||
| chr4:128171671
|
A | C | 3 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0177 | 3 | HG00741.hp1 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1649-5201A>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128171671 | ||||||
| chr4:128171890
|
A | T | 1 | a0001c0001t0003g0224 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1649-4982A>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128171890 | ||||||
| chr4:128171914
|
A | AT | 7 | a0001c0001t0001g0208a0001c0001t0004g0335a0001c0001t0007g0131others(4): Show | 7 | HG01099.hp2 HG01891.hp1 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.1649-4944dupT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr4 | 128171914 | |||||
| chr4:128171948
|
A | G | 151 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(148): Show | 151 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.1649-4924A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128171948 | ||||||
| chr4:128172125
|
G | T | 144 | a0002c0002t0002g0012a0002c0002t0002g0013a0002c0002t0002g0014others(141): Show | 144 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.1649-4747G>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128172125 | ||||||
| chr4:128172174
|
G | C | 18 | a0002c0002t0002g0019a0002c0002t0002g0021a0002c0002t0002g0022others(15): Show | 18 | HG00735.hp1 HG01109.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.1649-4698G>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128172174 | ||||||
| chr4:128172177
|
G | A | 1 | a0002c0002t0002g0061 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1649-4695G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128172177 | ||||||
| chr4:128172397
|
T | C | 144 | a0002c0002t0002g0012a0002c0002t0002g0013a0002c0002t0002g0014others(141): Show | 144 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.1649-4475T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128172397 | ||||||
| chr4:128172437
|
A | T | 3 | a0004c0005t0005g0281a0004c0005t0005g0282a0004c0005t0005g0283 | 3 | HG02055.hp1 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1649-4435A>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128172437 | ||||||
| chr4:128172466
|
G | A | 1 | a0001c0001t0001g0211 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1649-4406G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128172466 | ||||||
| chr4:128172546
|
C | T | 22 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(19): Show | 22 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.1649-4326C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128172546 | ||||||
| chr4:128172618
|
G | A | 7 | a0002c0002t0002g0292a0002c0002t0002g0294a0002c0002t0002g0297others(4): Show | 7 | HG00423.hp1 HG00544.hp1 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.1649-4254G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128172618 | ||||||
| chr4:128172624
|
T | G | 3 | a0004c0005t0005g0281a0004c0005t0005g0282a0004c0005t0005g0283 | 3 | HG02055.hp1 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1649-4248T>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128172624 | ||||||
| chr4:128172634
|
G | A | 2 | a0002c0002t0002g0024a0002c0002t0002g0027 | 2 | HG00735.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1649-4238G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128172634 | ||||||
| chr4:128172831
|
G | T | 4 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1649-4041G>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128172831 | ||||||
| chr4:128172937
|
A | ATG | 10 | a0001c0001t0001g0001a0001c0001t0001g0109a0001c0001t0001g0196others(7): Show | 10 | HG01891.hp2 HG01993.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.1649-3901_1649-390 others(6): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr4 | 128172937 | |||||
| chr4:128172937
|
A | ATGTG | 9 | a0001c0001t0001g0141a0002c0002t0002g0023a0002c0002t0002g0034others(6): Show | 9 | HG02896.hp2 HG03471.hp1 HG03831.hp1 others(6): Show |
intron_variant | MODIFIER | c.1649-3903_1649-390 others(8): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr4 | 128172937 | |||||
| chr4:128172937
|
A | ATGTGTG | 89 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(86): Show | 89 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.1649-3905_1649-390 others(10): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr4 | 128172937 | |||||
| chr4:128172937
|
A | ATGTGTGT others(1): Show |
35 | a0002c0002t0002g0014a0002c0002t0002g0019a0002c0002t0002g0021others(32): Show | 35 | HG00099.hp1 HG00735.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.1649-3907_1649-390 others(12): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr4 | 128172937 | |||||
| chr4:128172937
|
A | ATGTGTGT others(3): Show |
24 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(21): Show | 24 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.1649-3909_1649-390 others(14): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr4 | 128172937 | |||||
| chr4:128172937
|
A | ATGTGTGT others(5): Show |
9 | a0001c0001t0004g0314a0001c0001t0004g0318a0002c0003t0006g0004others(6): Show | 9 | HG00558.hp2 HG02145.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1649-3911_1649-390 others(16): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr4 | 128172937 | |||||
| chr4:128172937
|
A | ATGTGTGT others(7): Show |
2 | a0002c0002t0005g0097a0002c0003t0005g0122 | 2 | HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1649-3913_1649-390 others(18): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr4 | 128172937 | |||||
| chr4:128172937
|
A | ATGTGTGT others(9): Show |
1 | a0002c0003t0006g0003 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1649-3915_1649-390 others(20): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr4 | 128172937 | |||||
| chr4:128172937
|
A | G | 1 | a0002c0002t0002g0016 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1649-3935A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128172937 | ||||||
| chr4:128172937
|
ATG | A | 4 | a0001c0001t0001g0171a0001c0001t0001g0211a0001c0001t0003g0220others(1): Show | 4 | HG00738.hp1 HG02004.hp2 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.1649-3901_1649-390 others(6): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr4 | 128172937 | |||||
| chr4:128172973
|
A | G | 4 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1649-3899A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128172973 | ||||||
| chr4:128172975
|
G | A | 3 | a0001c0001t0003g0245a0001c0001t0003g0246a0001c0001t0003g0253 | 3 | HG00280.hp2 HG01496.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1649-3897G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128172975 | ||||||
| chr4:128173145
|
A | C | 1 | a0001c0001t0001g0002 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1649-3727A>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128173145 | ||||||
| chr4:128173227
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1649-3645G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128173227 | ||||||
| chr4:128173242
|
C | T | 5 | a0002c0002t0002g0018a0002c0002t0002g0032a0002c0002t0002g0047others(2): Show | 5 | NA18950.hp2 NA18973.hp2 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.1649-3630C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128173242 | ||||||
| chr4:128173450
|
G | A | 22 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(19): Show | 22 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.1649-3422G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128173450 | ||||||
| chr4:128173964
|
T | A | 1 | a0002c0002t0002g0298 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1649-2908T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128173964 | ||||||
| chr4:128174234
|
G | A | 6 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0159others(3): Show | 6 | HG02486.hp2 HG02647.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1649-2638G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128174234 | ||||||
| chr4:128174276
|
A | G | 147 | a0002c0002t0002g0012a0002c0002t0002g0013a0002c0002t0002g0014others(144): Show | 147 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.1649-2596A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128174276 | ||||||
| chr4:128174308
|
CA | C | 21 | a0002c0002t0005g0097a0002c0003t0001g0104a0002c0003t0001g0105others(18): Show | 21 | HG01168.hp1 HG02055.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.1649-2558delA | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr4 | 128174308 | |||||
| chr4:128174815
|
C | T | 147 | a0002c0002t0002g0012a0002c0002t0002g0013a0002c0002t0002g0014others(144): Show | 147 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.1649-2057C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128174815 | ||||||
| chr4:128174931
|
C | T | 22 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(19): Show | 22 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.1649-1941C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128174931 | ||||||
| chr4:128175004
|
G | A | 4 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1649-1868G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128175004 | ||||||
| chr4:128175358
|
G | T | 1 | a0001c0001t0003g0242 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1649-1514G>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128175358 | ||||||
| chr4:128175724
|
A | G | 1 | a0001c0001t0001g0259 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1649-1148A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128175724 | ||||||
| chr4:128175987
|
G | C | 1 | a0001c0001t0004g0308 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1649-885G>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128175987 | ||||||
| chr4:128176019
|
G | T | 5 | a0005c0006t0001g0099a0005c0006t0001g0100a0005c0006t0001g0101others(2): Show | 5 | HG01168.hp1 HG02572.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1649-853G>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128176019 | ||||||
| chr4:128176109
|
C | T | 1 | a0002c0002t0008g0304 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1649-763C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128176109 | ||||||
| chr4:128176112
|
A | G | 10 | a0002c0003t0001g0104a0002c0003t0001g0105a0002c0003t0006g0003others(7): Show | 10 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1649-760A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128176112 | ||||||
| chr4:128176134
|
GTATATAT others(47): Show |
G | 1 | a0003c0004t0001g0189 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1649-732_1649-679d others(56): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr4 | 128176134 | |||||
| chr4:128176160
|
AAT | A | 19 | a0001c0001t0003g0235a0002c0002t0005g0097a0002c0003t0001g0104others(16): Show | 19 | HG01168.hp1 HG02056.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1649-703_1649-702d others(4): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr4 | 128176160 | |||||
| chr4:128176163
|
A | ATATATAT others(26): Show |
1 | a0002c0002t0002g0288 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1649-694_1649-662d others(35): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr4 | 128176163 | |||||
| chr4:128176169
|
ATT | A | 54 | a0001c0001t0001g0236a0001c0001t0003g0102a0001c0001t0003g0103others(51): Show | 54 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.1649-702_1649-701d others(4): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128176169 | ||||||
| chr4:128176170
|
T | A | 1 | a0001c0001t0003g0235 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1649-702T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128176170 | ||||||
| chr4:128176185
|
TA | T | 25 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(22): Show | 25 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.1649-684delA | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr4 | 128176185 | |||||
| chr4:128176211
|
T | A | 144 | a0002c0002t0002g0012a0002c0002t0002g0013a0002c0002t0002g0014others(141): Show | 144 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.1649-661T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128176211 | ||||||
| chr4:128176212
|
T | A | 144 | a0002c0002t0002g0012a0002c0002t0002g0013a0002c0002t0002g0014others(141): Show | 144 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.1649-660T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128176212 | ||||||
| chr4:128176220
|
A | C | 17 | a0002c0002t0002g0019a0002c0002t0002g0021a0002c0002t0002g0022others(14): Show | 17 | HG00735.hp1 HG01109.hp1 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.1649-652A>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128176220 | ||||||
| chr4:128176224
|
TATATATA others(11): Show |
T | 1 | a0002c0012t0005g0098 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1649-630_1649-613d others(20): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr4 | 128176224 | |||||
| chr4:128176266
|
C | CAT | 26 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(23): Show | 26 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.1649-603_1649-602d others(4): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr4 | 128176266 | |||||
| chr4:128176271
|
G | A | 146 | a0002c0002t0002g0012a0002c0002t0002g0013a0002c0002t0002g0014others(143): Show | 146 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.1649-601G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128176271 | ||||||
| chr4:128176285
|
G | A | 1 | a0001c0001t0001g0195 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1649-587G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128176285 | ||||||
| chr4:128176285
|
G | GTA | 4 | a0001c0001t0001g0011a0001c0001t0001g0160a0001c0001t0001g0161others(1): Show | 4 | HG02486.hp2 HG02647.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1649-571_1649-570d others(4): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr4 | 128176285 | |||||
| chr4:128176285
|
GTA | G | 136 | a0002c0002t0002g0012a0002c0002t0002g0013a0002c0002t0002g0014others(133): Show | 136 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.1649-571_1649-570d others(4): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr4 | 128176285 | |||||
| chr4:128176287
|
A | G | 2 | a0001c0001t0003g0217a0001c0001t0004g0311 | 2 | HG01884.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1649-585A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128176287 | ||||||
| chr4:128176301
|
A | T | 2 | a0002c0002t0002g0057a0002c0003t0006g0005 | 2 | HG00639.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1649-571A>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128176301 | ||||||
| chr4:128176301
|
ATT | A | 10 | a0002c0002t0002g0038a0002c0002t0002g0051a0002c0002t0002g0069others(7): Show | 10 | HG02080.hp1 HG02559.hp1 NA18941.hp1 others(7): Show |
intron_variant | MODIFIER | c.1649-562_1649-561d others(4): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr4 | 128176301 | |||||
| chr4:128176303
|
T | A | 59 | a0001c0001t0001g0129a0001c0001t0001g0144a0001c0001t0001g0146others(56): Show | 59 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.1649-569T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128176303 | ||||||
| chr4:128176305
|
T | A | 1 | a0001c0001t0003g0239 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1649-567T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128176305 | ||||||
| chr4:128176406
|
G | A | 22 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(19): Show | 22 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.1649-466G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128176406 | ||||||
| chr4:128176540
|
C | T | 2 | a0002c0002t0002g0018a0002c0002t0002g0079 | 2 | NA18982.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1649-332C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128176540 | ||||||
| chr4:128176614
|
A | G | 22 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(19): Show | 22 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.1649-258A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128176614 | ||||||
| chr4:128176746
|
A | G | 4 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1649-126A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128176746 | ||||||
| chr4:128176831
|
C | G | 1 | a0002c0002t0002g0085 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1649-41C>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 12/19 | chr4 | 128176831 | ||||||
| chr4:128177298
|
C | A | 2 | a0001c0001t0003g0102a0001c0001t0003g0103 | 2 | HG01175.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1684+391C>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 13/19 | chr4 | 128177298 | ||||||
| chr4:128177362
|
TTA | T | 3 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0258 | 3 | HG01891.hp1 HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1684+459_1684+460d others(4): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr4 | 128177362 | |||||
| chr4:128177513
|
G | A | 5 | a0005c0006t0001g0099a0005c0006t0001g0100a0005c0006t0001g0101others(2): Show | 5 | HG01168.hp1 HG02572.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1684+606G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 13/19 | chr4 | 128177513 | ||||||
| chr4:128177548
|
G | C | 1 | a0001c0001t0004g0317 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1684+641G>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 13/19 | chr4 | 128177548 | ||||||
| chr4:128177881
|
A | C | 1 | a0002c0019t0002g0083 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1685-550A>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 13/19 | chr4 | 128177881 | ||||||
| chr4:128178032
|
A | G | 8 | a0002c0002t0002g0034a0002c0002t0002g0035a0002c0002t0002g0037others(5): Show | 8 | HG00597.hp1 HG02083.hp1 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.1685-399A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 13/19 | chr4 | 128178032 | ||||||
| chr4:128178035
|
G | GAT | 73 | a0001c0001t0001g0146a0001c0001t0001g0149a0001c0001t0001g0166others(70): Show | 73 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(70): Show |
intron_variant | MODIFIER | c.1685-372_1685-371d others(4): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr4 | 128178035 | |||||
| chr4:128178035
|
G | GATAT | 8 | a0001c0001t0001g0002a0001c0001t0001g0236a0001c0001t0003g0210others(5): Show | 8 | HG02027.hp2 HG02735.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1685-374_1685-371d others(6): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr4 | 128178035 | |||||
| chr4:128178035
|
G | GATATATA others(5): Show |
1 | a0001c0001t0004g0308 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1685-382_1685-371d others(14): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr4 | 128178035 | |||||
| chr4:128178035
|
G | GATATATA others(7): Show |
11 | a0001c0001t0003g0242a0001c0001t0004g0310a0001c0001t0004g0313others(8): Show | 11 | HG00558.hp2 HG00609.hp1 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.1685-384_1685-371d others(16): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr4 | 128178035 | |||||
| chr4:128178035
|
G | GATATATA others(9): Show |
5 | a0001c0001t0004g0309a0001c0001t0004g0320a0001c0001t0004g0323others(2): Show | 5 | HG00597.hp2 NA18990.hp2 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.1685-386_1685-371d others(18): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr4 | 128178035 | |||||
| chr4:128178035
|
G | GATATATA others(11): Show |
1 | a0001c0001t0004g0317 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1685-388_1685-371d others(20): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr4 | 128178035 | |||||
| chr4:128178035
|
G | GATATATA others(13): Show |
1 | a0001c0001t0004g0314 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1685-390_1685-371d others(22): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr4 | 128178035 | |||||
| chr4:128178035
|
G | GATATATA others(15): Show |
1 | a0001c0001t0004g0312 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1685-392_1685-371d others(24): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr4 | 128178035 | |||||
| chr4:128178035
|
G | GATATATA others(17): Show |
1 | a0001c0001t0004g0322 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1685-394_1685-371d others(26): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr4 | 128178035 | |||||
| chr4:128178035
|
GAT | G | 23 | a0001c0001t0001g0011a0001c0001t0001g0140a0001c0001t0001g0159others(20): Show | 23 | HG00741.hp2 HG01192.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.1685-372_1685-371d others(4): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr4 | 128178035 | |||||
| chr4:128178035
|
GATAT | G | 14 | a0001c0001t0001g0107a0001c0001t0001g0124a0001c0001t0001g0267others(11): Show | 14 | HG01168.hp1 HG02055.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.1685-374_1685-371d others(6): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr4 | 128178035 | |||||
| chr4:128178035
|
GATATATA others(5): Show |
G | 2 | a0001c0001t0004g0311a0001c0001t0004g0326 | 2 | NA18984.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1685-382_1685-371d others(14): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr4 | 128178035 | |||||
| chr4:128178058
|
A | G | 3 | a0002c0002t0005g0097a0002c0003t0005g0122a0002c0012t0005g0098 | 3 | HG02451.hp1 HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1685-373A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 13/19 | chr4 | 128178058 | ||||||
| chr4:128178416
|
T | G | 1 | a0001c0001t0001g0107 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1685-15T>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 13/19 | chr4 | 128178416 | ||||||
| chr4:128178657
|
C | A | 7 | a0001c0001t0004g0309a0001c0001t0004g0315a0001c0001t0004g0319others(4): Show | 7 | HG02056.hp2 HG02129.hp2 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.1896+15C>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 14/19 | chr4 | 128178657 | ||||||
| chr4:128178811
|
C | T | 1 | a0001c0001t0003g0242 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1896+169C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 14/19 | chr4 | 128178811 | ||||||
| chr4:128178873
|
G | A | 1 | a0014c0015t0001g0206 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1896+231G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 14/19 | chr4 | 128178873 | ||||||
| chr4:128178896
|
G | T | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(185): Show | 188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.1896+254G>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 14/19 | chr4 | 128178896 | ||||||
| chr4:128179528
|
A | G | 1 | a0002c0002t0002g0284 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2003+16A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128179528 | ||||||
| chr4:128179622
|
T | C | 22 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(19): Show | 22 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.2003+110T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128179622 | ||||||
| chr4:128179662
|
A | G | 1 | a0002c0002t0002g0045 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2003+150A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128179662 | ||||||
| chr4:128179766
|
G | A | 8 | a0002c0003t0006g0003a0002c0003t0006g0004a0002c0003t0006g0005others(5): Show | 8 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.2003+254G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128179766 | ||||||
| chr4:128180123
|
T | A | 3 | a0001c0001t0003g0210a0001c0001t0003g0237a0001c0001t0003g0244 | 3 | HG00140.hp1 HG04184.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.2003+611T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128180123 | ||||||
| chr4:128180175
|
CT | C | 4 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.2003+665delT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr4 | 128180175 | |||||
| chr4:128180293
|
T | C | 1 | a0001c0001t0001g0137 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2003+781T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128180293 | ||||||
| chr4:128180493
|
T | C | 3 | a0004c0005t0005g0281a0004c0005t0005g0282a0004c0005t0005g0283 | 3 | HG02055.hp1 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2003+981T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128180493 | ||||||
| chr4:128180699
|
G | C | 3 | a0004c0005t0005g0281a0004c0005t0005g0282a0004c0005t0005g0283 | 3 | HG02055.hp1 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2003+1187G>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128180699 | ||||||
| chr4:128180712
|
A | G | 4 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.2003+1200A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128180712 | ||||||
| chr4:128180916
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2003+1404C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128180916 | ||||||
| chr4:128181030
|
A | C | 228 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(225): Show | 228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.2003+1518A>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128181030 | ||||||
| chr4:128181180
|
CT | C | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(185): Show | 188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.2003+1684delT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr4 | 128181180 | |||||
| chr4:128181342
|
T | G | 5 | a0005c0006t0001g0099a0005c0006t0001g0100a0005c0006t0001g0101others(2): Show | 5 | HG01168.hp1 HG02572.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2003+1830T>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128181342 | ||||||
| chr4:128181398
|
C | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(206): Show | 209 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.2003+1886C>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128181398 | ||||||
| chr4:128181441
|
G | T | 1 | a0001c0001t0001g0109 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2003+1929G>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128181441 | ||||||
| chr4:128181541
|
A | G | 2 | a0002c0002t0002g0080a0002c0002t0002g0082 | 2 | HG01070.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.2003+2029A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128181541 | ||||||
| chr4:128181570
|
T | A | 4 | a0002c0002t0008g0293a0002c0002t0008g0300a0002c0002t0008g0304others(1): Show | 4 | HG01081.hp2 HG01981.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.2003+2058T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128181570 | ||||||
| chr4:128181740
|
T | C | 1 | a0002c0002t0002g0013 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2003+2228T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128181740 | ||||||
| chr4:128181801
|
CT | C | 151 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(148): Show | 151 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.2003+2311delT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr4 | 128181801 | |||||
| chr4:128181801
|
CTT | C | 164 | a0001c0001t0001g0001a0001c0001t0001g0108a0001c0001t0001g0109others(161): Show | 164 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.2003+2310_2003+231 others(6): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr4 | 128181801 | |||||
| chr4:128181801
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0208 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2003+2298_2003+231 others(18): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr4 | 128181801 | |||||
| chr4:128181828
|
C | T | 3 | a0004c0005t0005g0281a0004c0005t0005g0282a0004c0005t0005g0283 | 3 | HG02055.hp1 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2003+2316C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128181828 | ||||||
| chr4:128181906
|
C | T | 2 | a0001c0001t0003g0247a0001c0018t0003g0254 | 2 | HG00099.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.2003+2394C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128181906 | ||||||
| chr4:128181954
|
C | T | 1 | a0007c0008t0001g0139 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2003+2442C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128181954 | ||||||
| chr4:128181957
|
C | T | 36 | a0001c0001t0001g0108a0001c0001t0001g0124a0001c0001t0001g0129others(33): Show | 36 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.2003+2445C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128181957 | ||||||
| chr4:128181963
|
G | A | 3 | a0002c0002t0002g0297a0002c0002t0002g0302a0002c0002t0002g0330 | 3 | HG00544.hp1 HG02074.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.2003+2451G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128181963 | ||||||
| chr4:128182021
|
C | A | 1 | a0001c0001t0003g0255 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2003+2509C>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128182021 | ||||||
| chr4:128182107
|
C | T | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(159): Show | 162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.2003+2595C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128182107 | ||||||
| chr4:128182111
|
C | CT | 180 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(177): Show | 180 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.2003+2619dupT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr4 | 128182111 | |||||
| chr4:128182111
|
C | CTT | 10 | a0001c0001t0001g0135a0001c0001t0001g0141a0001c0001t0001g0153others(7): Show | 10 | HG00280.hp1 HG00280.hp2 HG00642.hp2 others(7): Show |
intron_variant | MODIFIER | c.2003+2618_2003+261 others(6): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr4 | 128182111 | |||||
| chr4:128182175
|
A | G | 1 | a0002c0002t0002g0086 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2003+2663A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128182175 | ||||||
| chr4:128182192
|
C | T | 2 | a0002c0002t0002g0295a0002c0002t0002g0298 | 2 | NA18974.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.2003+2680C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128182192 | ||||||
| chr4:128182219
|
T | A | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(185): Show | 188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.2003+2707T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128182219 | ||||||
| chr4:128182621
|
G | A | 1 | a0002c0002t0002g0032 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2003+3109G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128182621 | ||||||
| chr4:128182719
|
C | T | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(185): Show | 188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.2003+3207C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128182719 | ||||||
| chr4:128182728
|
C | A | 1 | a0001c0001t0003g0214 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2003+3216C>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128182728 | ||||||
| chr4:128183382
|
G | A | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(206): Show | 209 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.2003+3870G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128183382 | ||||||
| chr4:128183738
|
T | C | 1 | a0001c0001t0001g0147 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2003+4226T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128183738 | ||||||
| chr4:128184031
|
C | T | 1 | a0002c0002t0008g0300 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2003+4519C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128184031 | ||||||
| chr4:128184317
|
G | A | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(185): Show | 188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.2003+4805G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128184317 | ||||||
| chr4:128184467
|
G | T | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(159): Show | 162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.2003+4955G>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128184467 | ||||||
| chr4:128184533
|
A | G | 1 | a0001c0001t0001g0273 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2003+5021A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128184533 | ||||||
| chr4:128184734
|
G | A | 22 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(19): Show | 22 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.2003+5222G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128184734 | ||||||
| chr4:128184791
|
A | G | 4 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.2003+5279A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128184791 | ||||||
| chr4:128184843
|
T | C | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(159): Show | 162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.2003+5331T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128184843 | ||||||
| chr4:128184946
|
A | G | 2 | a0001c0001t0001g0149a0001c0001t0001g0175 | 2 | HG00642.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.2003+5434A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128184946 | ||||||
| chr4:128184960
|
A | G | 10 | a0002c0003t0001g0104a0002c0003t0001g0105a0002c0003t0006g0003others(7): Show | 10 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.2003+5448A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128184960 | ||||||
| chr4:128185037
|
C | CAT | 5 | a0005c0006t0001g0099a0005c0006t0001g0100a0005c0006t0001g0101others(2): Show | 5 | HG01168.hp1 HG02572.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2003+5533_2003+553 others(6): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr4 | 128185037 | |||||
| chr4:128185134
|
A | C | 2 | a0001c0001t0001g0211a0001c0001t0001g0249 | 2 | HG02572.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2003+5622A>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128185134 | ||||||
| chr4:128185192
|
C | T | 2 | a0002c0002t0002g0018a0002c0002t0002g0079 | 2 | NA18982.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.2003+5680C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128185192 | ||||||
| chr4:128185193
|
A | C | 1 | a0002c0002t0002g0023 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2003+5681A>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128185193 | ||||||
| chr4:128185534
|
G | GT | 184 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(181): Show | 184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.2003+6033dupT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr4 | 128185534 | |||||
| chr4:128185605
|
G | A | 3 | a0002c0002t0002g0075a0002c0002t0002g0076a0002c0002t0002g0336 | 3 | HG01256.hp2 HG01258.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.2003+6093G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128185605 | ||||||
| chr4:128185692
|
A | G | 1 | a0004c0005t0005g0283 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2003+6180A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128185692 | ||||||
| chr4:128185736
|
G | A | 23 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(20): Show | 23 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.2003+6224G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128185736 | ||||||
| chr4:128185841
|
C | G | 8 | a0002c0003t0006g0003a0002c0003t0006g0004a0002c0003t0006g0005others(5): Show | 8 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.2003+6329C>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128185841 | ||||||
| chr4:128185894
|
T | C | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(186): Show | 189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.2003+6382T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128185894 | ||||||
| chr4:128185895
|
G | A | 1 | a0014c0015t0001g0206 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2003+6383G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128185895 | ||||||
| chr4:128185924
|
C | T | 185 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(182): Show | 185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.2003+6412C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128185924 | ||||||
| chr4:128186159
|
C | T | 2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | HG01099.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.2003+6647C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128186159 | ||||||
| chr4:128186176
|
G | A | 23 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(20): Show | 23 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.2003+6664G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128186176 | ||||||
| chr4:128186214
|
A | ATGTCATA others(3): Show |
189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(186): Show | 189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.2003+6702_2003+670 others(14): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128186214 | ||||||
| chr4:128186255
|
A | G | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(186): Show | 189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.2003+6743A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128186255 | ||||||
| chr4:128186319
|
C | T | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(207): Show | 210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.2003+6807C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128186319 | ||||||
| chr4:128186480
|
G | GT | 23 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(20): Show | 23 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.2003+6975dupT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr4 | 128186480 | |||||
| chr4:128186827
|
G | A | 1 | a0001c0001t0007g0132 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2003+7315G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128186827 | ||||||
| chr4:128186837
|
G | A | 1 | a0001c0001t0001g0142 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2003+7325G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128186837 | ||||||
| chr4:128186945
|
G | C | 77 | a0002c0002t0002g0012a0002c0002t0002g0013a0002c0002t0002g0016others(74): Show | 77 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.2003+7433G>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128186945 | ||||||
| chr4:128187000
|
G | T | 2 | a0002c0002t0002g0307a0002c0002t0002g0331 | 2 | NA19007.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.2003+7488G>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128187000 | ||||||
| chr4:128187218
|
A | G | 1 | a0002c0002t0002g0040 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2003+7706A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128187218 | ||||||
| chr4:128187219
|
C | G | 1 | a0001c0001t0001g0167 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2003+7707C>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128187219 | ||||||
| chr4:128187473
|
A | G | 1 | a0001c0001t0003g0219 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2003+7961A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128187473 | ||||||
| chr4:128187642
|
G | T | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(159): Show | 162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.2003+8130G>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128187642 | ||||||
| chr4:128187669
|
A | G | 23 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(20): Show | 23 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.2003+8157A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128187669 | ||||||
| chr4:128188076
|
A | AT | 29 | a0001c0001t0001g0109a0001c0001t0001g0166a0001c0001t0003g0215others(26): Show | 29 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.2003+8579dupT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr4 | 128188076 | |||||
| chr4:128188076
|
AT | A | 13 | a0002c0002t0012g0096a0002c0003t0006g0003a0002c0003t0006g0004others(10): Show | 13 | HG01168.hp1 HG02109.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.2003+8579delT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr4 | 128188076 | |||||
| chr4:128188160
|
C | T | 4 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.2003+8648C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128188160 | ||||||
| chr4:128188206
|
C | T | 1 | a0002c0002t0002g0022 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2003+8694C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128188206 | ||||||
| chr4:128188265
|
G | A | 9 | a0001c0001t0001g0124a0001c0001t0001g0259a0001c0001t0001g0260others(6): Show | 9 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(6): Show |
intron_variant | MODIFIER | c.2003+8753G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128188265 | ||||||
| chr4:128188318
|
G | A | 1 | a0002c0002t0002g0025 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2003+8806G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128188318 | ||||||
| chr4:128188366
|
C | T | 1 | a0002c0002t0011g0042 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2003+8854C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128188366 | ||||||
| chr4:128188420
|
T | C | 23 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(20): Show | 23 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.2003+8908T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128188420 | ||||||
| chr4:128188476
|
A | G | 1 | a0002c0002t0002g0121 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2003+8964A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128188476 | ||||||
| chr4:128188589
|
G | A | 7 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(4): Show | 7 | HG01891.hp1 HG02055.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2003+9077G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128188589 | ||||||
| chr4:128188644
|
A | C | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(189): Show | 192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.2003+9132A>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128188644 | ||||||
| chr4:128188645
|
T | G | 3 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196 | 3 | HG00673.hp2 HG02155.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.2003+9133T>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128188645 | ||||||
| chr4:128188698
|
C | T | 1 | a0002c0002t0011g0042 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2003+9186C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128188698 | ||||||
| chr4:128188883
|
T | A | 1 | a0001c0001t0001g0109 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2003+9371T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128188883 | ||||||
| chr4:128189245
|
C | G | 1 | a0001c0001t0001g0260 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2003+9733C>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128189245 | ||||||
| chr4:128189262
|
C | CT | 185 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(182): Show | 185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.2003+9767dupT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr4 | 128189262 | |||||
| chr4:128189262
|
CT | C | 20 | a0002c0002t0002g0025a0002c0002t0002g0060a0002c0002t0005g0097others(17): Show | 20 | HG01168.hp1 HG01515.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.2003+9767delT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr4 | 128189262 | |||||
| chr4:128189324
|
C | CT | 87 | a0001c0001t0001g0001a0001c0001t0001g0108a0001c0001t0001g0109others(84): Show | 87 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.2003+9838dupT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr4 | 128189324 | |||||
| chr4:128189324
|
C | CTT | 85 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(82): Show | 85 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.2003+9837_2003+983 others(6): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr4 | 128189324 | |||||
| chr4:128189324
|
C | CTTT | 7 | a0001c0001t0001g0176a0001c0001t0003g0228a0001c0001t0003g0239others(4): Show | 7 | HG02027.hp2 HG02071.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.2003+9836_2003+983 others(7): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr4 | 128189324 | |||||
| chr4:128189324
|
CT | C | 37 | a0001c0001t0004g0309a0001c0001t0004g0310a0001c0001t0004g0311others(34): Show | 37 | HG00099.hp1 HG00558.hp2 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.2003+9838delT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr4 | 128189324 | |||||
| chr4:128189400
|
G | C | 3 | a0004c0005t0005g0281a0004c0005t0005g0282a0004c0005t0005g0283 | 3 | HG02055.hp1 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2003+9888G>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128189400 | ||||||
| chr4:128189553
|
C | T | 3 | a0001c0001t0001g0167a0001c0001t0001g0170a0001c0001t0001g0173 | 3 | HG02257.hp2 HG03225.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2004-9886C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128189553 | ||||||
| chr4:128189725
|
A | C | 2 | a0003c0004t0001g0182a0003c0004t0001g0183 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.2004-9714A>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128189725 | ||||||
| chr4:128189950
|
A | T | 1 | a0001c0001t0003g0251 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2004-9489A>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128189950 | ||||||
| chr4:128190467
|
G | A | 1 | a0002c0002t0002g0022 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2004-8972G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128190467 | ||||||
| chr4:128190634
|
A | G | 1 | a0002c0019t0002g0083 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2004-8805A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128190634 | ||||||
| chr4:128190677
|
C | T | 3 | a0001c0001t0003g0210a0001c0001t0003g0237a0001c0001t0003g0244 | 3 | HG00140.hp1 HG04184.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.2004-8762C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128190677 | ||||||
| chr4:128191032
|
T | C | 3 | a0004c0005t0005g0281a0004c0005t0005g0282a0004c0005t0005g0283 | 3 | HG02055.hp1 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2004-8407T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128191032 | ||||||
| chr4:128191101
|
G | A | 5 | a0005c0006t0001g0099a0005c0006t0001g0100a0005c0006t0001g0101others(2): Show | 5 | HG01168.hp1 HG02572.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2004-8338G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128191101 | ||||||
| chr4:128191111
|
A | AT | 33 | a0001c0001t0001g0002a0001c0001t0001g0124a0001c0001t0001g0236others(30): Show | 33 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.2004-8317dupT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr4 | 128191111 | |||||
| chr4:128191111
|
A | ATT | 156 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(153): Show | 156 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.2004-8318_2004-831 others(6): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr4 | 128191111 | |||||
| chr4:128191122
|
T | A | 10 | a0002c0003t0001g0104a0002c0003t0001g0105a0002c0003t0006g0003others(7): Show | 10 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.2004-8317T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128191122 | ||||||
| chr4:128191145
|
A | G | 1 | a0002c0002t0002g0117 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2004-8294A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128191145 | ||||||
| chr4:128191214
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2004-8225T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128191214 | ||||||
| chr4:128191223
|
T | C | 1 | a0002c0002t0002g0112 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2004-8216T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128191223 | ||||||
| chr4:128191425
|
G | A | 23 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(20): Show | 23 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.2004-8014G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128191425 | ||||||
| chr4:128191633
|
A | G | 4 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.2004-7806A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128191633 | ||||||
| chr4:128191742
|
T | G | 1 | a0002c0002t0002g0334 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2004-7697T>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128191742 | ||||||
| chr4:128191930
|
A | G | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(207): Show | 210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.2004-7509A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128191930 | ||||||
| chr4:128192004
|
C | T | 9 | a0002c0002t0002g0038a0002c0002t0002g0051a0002c0002t0002g0069others(6): Show | 9 | HG02080.hp1 HG02559.hp1 NA18941.hp1 others(6): Show |
intron_variant | MODIFIER | c.2004-7435C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128192004 | ||||||
| chr4:128192102
|
G | A | 1 | a0013c0014t0003g0226 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2004-7337G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128192102 | ||||||
| chr4:128192340
|
A | G | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(189): Show | 192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.2004-7099A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128192340 | ||||||
| chr4:128192518
|
A | G | 1 | a0001c0001t0001g0163 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2004-6921A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128192518 | ||||||
| chr4:128192768
|
T | C | 1 | a0001c0001t0003g0213 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.2004-6671T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128192768 | ||||||
| chr4:128192794
|
T | C | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(189): Show | 192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.2004-6645T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128192794 | ||||||
| chr4:128192852
|
A | T | 185 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(182): Show | 185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.2004-6587A>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128192852 | ||||||
| chr4:128193020
|
G | A | 23 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(20): Show | 23 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.2004-6419G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128193020 | ||||||
| chr4:128193034
|
A | G | 2 | a0002c0002t0002g0054a0002c0002t0002g0055 | 2 | NA18954.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.2004-6405A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128193034 | ||||||
| chr4:128193045
|
G | C | 1 | a0001c0001t0001g0236 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2004-6394G>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128193045 | ||||||
| chr4:128193321
|
G | C | 3 | a0002c0003t0006g0004a0002c0003t0006g0006a0002c0003t0006g0009 | 3 | HG02970.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2004-6118G>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128193321 | ||||||
| chr4:128193363
|
T | C | 3 | a0002c0002t0005g0097a0002c0003t0005g0122a0002c0012t0005g0098 | 3 | HG02451.hp1 HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2004-6076T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128193363 | ||||||
| chr4:128193529
|
A | G | 1 | a0001c0018t0003g0254 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2004-5910A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128193529 | ||||||
| chr4:128193713
|
T | C | 1 | a0001c0001t0003g0218 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2004-5726T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128193713 | ||||||
| chr4:128193758
|
A | G | 3 | a0004c0005t0005g0281a0004c0005t0005g0282a0004c0005t0005g0283 | 3 | HG02055.hp1 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2004-5681A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128193758 | ||||||
| chr4:128193899
|
T | C | 23 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(20): Show | 23 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.2004-5540T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128193899 | ||||||
| chr4:128194030
|
T | C | 3 | a0005c0006t0001g0099a0005c0006t0001g0100a0005c0006t0001g0101 | 3 | HG01168.hp1 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2004-5409T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128194030 | ||||||
| chr4:128194053
|
T | G | 10 | a0002c0003t0001g0104a0002c0003t0001g0105a0002c0003t0006g0003others(7): Show | 10 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.2004-5386T>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128194053 | ||||||
| chr4:128194135
|
C | T | 11 | a0002c0002t0002g0031a0002c0002t0002g0038a0002c0002t0002g0051others(8): Show | 11 | HG02080.hp1 HG02559.hp1 HG04184.hp1 others(8): Show |
intron_variant | MODIFIER | c.2004-5304C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128194135 | ||||||
| chr4:128194203
|
G | T | 1 | a0002c0002t0002g0294 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2004-5236G>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128194203 | ||||||
| chr4:128194231
|
C | T | 1 | a0002c0002t0005g0097 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2004-5208C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128194231 | ||||||
| chr4:128194299
|
T | C | 56 | a0001c0001t0001g0168a0001c0001t0003g0102a0001c0001t0003g0103others(53): Show | 56 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.2004-5140T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128194299 | ||||||
| chr4:128194424
|
T | C | 1 | a0001c0001t0001g0002 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2004-5015T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128194424 | ||||||
| chr4:128194551
|
C | T | 30 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(27): Show | 30 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.2004-4888C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128194551 | ||||||
| chr4:128194600
|
G | C | 18 | a0002c0002t0005g0097a0002c0003t0001g0104a0002c0003t0001g0105others(15): Show | 18 | HG01168.hp1 HG02109.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.2004-4839G>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128194600 | ||||||
| chr4:128194682
|
C | CA | 11 | a0001c0001t0003g0216a0001c0001t0004g0309a0001c0001t0004g0321others(8): Show | 11 | HG00609.hp1 HG02055.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2004-4728dupA | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr4 | 128194682 | |||||
| chr4:128194682
|
CA | C | 170 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0108others(167): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.2004-4728delA | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr4 | 128194682 | |||||
| chr4:128194682
|
CAA | C | 77 | a0001c0001t0001g0001a0001c0001t0001g0107a0001c0001t0001g0110others(74): Show | 77 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.2004-4729_2004-472 others(6): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr4 | 128194682 | |||||
| chr4:128194682
|
CAAAAAAA others(4): Show |
C | 1 | a0002c0002t0002g0061 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2004-4738_2004-472 others(15): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr4 | 128194682 | |||||
| chr4:128194682
|
CAAAAAAA others(8): Show |
C | 1 | a0002c0003t0001g0105 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2004-4742_2004-472 others(19): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr4 | 128194682 | |||||
| chr4:128194742
|
T | C | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(207): Show | 210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.2004-4697T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128194742 | ||||||
| chr4:128194773
|
AGGAGAAT others(1): Show |
A | 23 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(20): Show | 23 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.2004-4664_2004-465 others(12): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr4 | 128194773 | |||||
| chr4:128195125
|
C | G | 1 | a0001c0001t0001g0141 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2004-4314C>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128195125 | ||||||
| chr4:128195406
|
C | T | 1 | a0001c0001t0001g0263 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2004-4033C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128195406 | ||||||
| chr4:128195486
|
T | G | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(159): Show | 162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.2004-3953T>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128195486 | ||||||
| chr4:128195663
|
A | G | 1 | a0002c0002t0002g0035 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2004-3776A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128195663 | ||||||
| chr4:128195844
|
G | A | 4 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.2004-3595G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128195844 | ||||||
| chr4:128195916
|
T | C | 1 | a0007c0008t0001g0158 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2004-3523T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128195916 | ||||||
| chr4:128196248
|
CA | C | 46 | a0001c0001t0001g0169a0001c0001t0004g0308a0001c0001t0004g0309others(43): Show | 46 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.2004-3172delA | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr4 | 128196248 | |||||
| chr4:128196248
|
CAA | C | 161 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(158): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.2004-3173_2004-317 others(6): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr4 | 128196248 | |||||
| chr4:128196593
|
T | C | 1 | a0002c0002t0002g0026 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2004-2846T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128196593 | ||||||
| chr4:128196594
|
T | C | 2 | a0007c0008t0001g0138a0007c0008t0001g0158 | 2 | NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2004-2845T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128196594 | ||||||
| chr4:128196825
|
TTAGA | T | 23 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(20): Show | 23 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.2004-2611_2004-260 others(8): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr4 | 128196825 | |||||
| chr4:128196997
|
A | G | 2 | a0002c0002t0002g0040a0002c0002t0002g0046 | 2 | NA18949.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.2004-2442A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128196997 | ||||||
| chr4:128197113
|
G | C | 41 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0126others(38): Show | 41 | HG00642.hp2 HG00741.hp1 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.2004-2326G>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128197113 | ||||||
| chr4:128197130
|
C | G | 5 | a0002c0002t0002g0018a0002c0002t0002g0032a0002c0002t0002g0047others(2): Show | 5 | NA18950.hp2 NA18973.hp2 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.2004-2309C>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128197130 | ||||||
| chr4:128197422
|
G | T | 1 | a0001c0001t0001g0273 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2004-2017G>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128197422 | ||||||
| chr4:128197680
|
G | A | 1 | a0002c0012t0005g0098 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2004-1759G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128197680 | ||||||
| chr4:128197807
|
A | T | 3 | a0004c0005t0005g0281a0004c0005t0005g0282a0004c0005t0005g0283 | 3 | HG02055.hp1 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2004-1632A>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128197807 | ||||||
| chr4:128197863
|
T | TAAGAAAA others(341): Show |
1 | a0004c0005t0005g0283 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2004-1563_2004-156 others(352): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr4 | 128197863 | |||||
| chr4:128197863
|
T | TAAGAAAA others(347): Show |
1 | a0004c0005t0005g0281 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2004-1563_2004-156 others(358): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr4 | 128197863 | |||||
| chr4:128197863
|
T | TAAGAAAA others(350): Show |
1 | a0004c0005t0005g0282 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2004-1563_2004-156 others(361): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr4 | 128197863 | |||||
| chr4:128197880
|
C | CT | 103 | a0001c0001t0001g0109a0001c0001t0001g0136a0001c0001t0001g0146others(100): Show | 103 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.2004-1536dupT | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr4 | 128197880 | |||||
| chr4:128197880
|
C | CTT | 9 | a0001c0001t0004g0313a0001c0001t0004g0314a0001c0001t0004g0318others(6): Show | 9 | HG00558.hp2 HG02486.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.2004-1537_2004-153 others(6): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr4 | 128197880 | |||||
| chr4:128197941
|
A | T | 1 | a0002c0002t0002g0013 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2004-1498A>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128197941 | ||||||
| chr4:128197971
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2004-1468G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128197971 | ||||||
| chr4:128197978
|
G | A | 23 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(20): Show | 23 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.2004-1461G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128197978 | ||||||
| chr4:128198015
|
G | A | 1 | a0001c0001t0001g0249 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2004-1424G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128198015 | ||||||
| chr4:128198059
|
A | G | 1 | a0001c0001t0003g0233 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2004-1380A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128198059 | ||||||
| chr4:128198520
|
C | T | 23 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(20): Show | 23 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.2004-919C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128198520 | ||||||
| chr4:128198568
|
A | G | 1 | a0013c0014t0003g0226 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2004-871A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128198568 | ||||||
| chr4:128198823
|
C | T | 1 | a0002c0019t0002g0083 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2004-616C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128198823 | ||||||
| chr4:128198974
|
A | T | 1 | a0002c0003t0006g0006 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2004-465A>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128198974 | ||||||
| chr4:128199392
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2004-47G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 15/19 | chr4 | 128199392 | ||||||
| chr4:128199601
|
T | C | 1 | a0002c0002t0002g0121 | 1 | HG02004.hp1 | splice_donor_variant&intron_variant | HIGH | c.2164+2T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 16/19 | chr4 | 128199601 | ||||||
| chr4:128199605
|
A | G | 1 | a0001c0001t0001g0236 | 1 | HG03139.hp2 | splice_region_variant&intron_variant | LOW | c.2164+6A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 16/19 | chr4 | 128199605 | ||||||
| chr4:128199695
|
T | A | 23 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(20): Show | 23 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.2164+96T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 16/19 | chr4 | 128199695 | ||||||
| chr4:128199889
|
C | T | 12 | a0001c0001t0003g0213a0001c0001t0003g0214a0001c0001t0003g0216others(9): Show | 12 | HG02015.hp2 HG03831.hp2 NA18946.hp1 others(9): Show |
intron_variant | MODIFIER | c.2164+290C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 16/19 | chr4 | 128199889 | ||||||
| chr4:128200041
|
G | A | 1 | a0002c0002t0002g0013 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2164+442G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 16/19 | chr4 | 128200041 | ||||||
| chr4:128200107
|
T | A | 27 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(24): Show | 27 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.2165-414T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 16/19 | chr4 | 128200107 | ||||||
| chr4:128200178
|
G | A | 23 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(20): Show | 23 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.2165-343G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 16/19 | chr4 | 128200178 | ||||||
| chr4:128200248
|
G | A | 1 | a0001c0001t0001g0249 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2165-273G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 16/19 | chr4 | 128200248 | ||||||
| chr4:128200707
|
T | A | 1 | a0002c0002t0002g0018 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2309+42T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | chr4 | 128200707 | ||||||
| chr4:128200836
|
C | G | 1 | a0010c0011t0005g0123 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2309+171C>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | chr4 | 128200836 | ||||||
| chr4:128200865
|
A | G | 5 | a0005c0006t0001g0099a0005c0006t0001g0100a0005c0006t0001g0101others(2): Show | 5 | HG01168.hp1 HG02572.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2309+200A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | chr4 | 128200865 | ||||||
| chr4:128200870
|
C | T | 1 | a0002c0012t0005g0098 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2309+205C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | chr4 | 128200870 | ||||||
| chr4:128201088
|
C | T | 23 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(20): Show | 23 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.2309+423C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | chr4 | 128201088 | ||||||
| chr4:128201261
|
G | A | 3 | a0004c0005t0005g0281a0004c0005t0005g0282a0004c0005t0005g0283 | 3 | HG02055.hp1 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2309+596G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | chr4 | 128201261 | ||||||
| chr4:128201310
|
A | G | 2 | a0004c0005t0005g0281a0004c0005t0005g0282 | 2 | HG02055.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2309+645A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | chr4 | 128201310 | ||||||
| chr4:128201468
|
A | C | 3 | a0001c0001t0001g0167a0001c0001t0001g0170a0001c0001t0001g0173 | 3 | HG02257.hp2 HG03225.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2309+803A>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | chr4 | 128201468 | ||||||
| chr4:128201500
|
T | G | 1 | a0009c0010t0003g0223 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2309+835T>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | chr4 | 128201500 | ||||||
| chr4:128201531
|
T | TA | 8 | a0002c0003t0006g0003a0002c0003t0006g0004a0002c0003t0006g0005others(5): Show | 8 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.2309+867dupA | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr4 | 128201531 | |||||
| chr4:128201611
|
C | G | 1 | a0014c0015t0001g0206 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2309+946C>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | chr4 | 128201611 | ||||||
| chr4:128201749
|
A | C | 1 | a0001c0001t0001g0010 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2309+1084A>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | chr4 | 128201749 | ||||||
| chr4:128201829
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2309+1164G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | chr4 | 128201829 | ||||||
| chr4:128202015
|
T | C | 4 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.2309+1350T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | chr4 | 128202015 | ||||||
| chr4:128202100
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2309+1435G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | chr4 | 128202100 | ||||||
| chr4:128202208
|
T | A | 1 | a0001c0001t0003g0242 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2309+1543T>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | chr4 | 128202208 | ||||||
| chr4:128202305
|
C | T | 1 | a0001c0001t0003g0250 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2309+1640C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | chr4 | 128202305 | ||||||
| chr4:128202410
|
A | C | 4 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.2309+1745A>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | chr4 | 128202410 | ||||||
| chr4:128202968
|
G | T | 1 | a0002c0002t0002g0092 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2309+2303G>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | chr4 | 128202968 | ||||||
| chr4:128202981
|
T | C | 4 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.2309+2316T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | chr4 | 128202981 | ||||||
| chr4:128203070
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2309+2405C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | chr4 | 128203070 | ||||||
| chr4:128203089
|
G | A | 1 | a0010c0011t0005g0123 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2309+2424G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | chr4 | 128203089 | ||||||
| chr4:128203194
|
C | CA | 5 | a0002c0002t0002g0044a0002c0002t0002g0075a0002c0002t0002g0076others(2): Show | 5 | HG01256.hp2 HG01258.hp1 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.2309+2538dupA | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr4 | 128203194 | |||||
| chr4:128203248
|
T | C | 1 | a0001c0001t0004g0324 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2309+2583T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | chr4 | 128203248 | ||||||
| chr4:128203268
|
G | A | 1 | a0002c0003t0009g0008 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2309+2603G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | chr4 | 128203268 | ||||||
| chr4:128203304
|
C | T | 1 | a0002c0002t0002g0052 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2309+2639C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | chr4 | 128203304 | ||||||
| chr4:128203318
|
TCTCC | T | 3 | a0004c0005t0005g0281a0004c0005t0005g0282a0004c0005t0005g0283 | 3 | HG02055.hp1 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2309+2677_2309+268 others(8): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr4 | 128203318 | |||||
| chr4:128203324
|
T | C | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(163): Show | 166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.2309+2659T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | chr4 | 128203324 | ||||||
| chr4:128203420
|
C | G | 1 | a0001c0001t0003g0239 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2309+2755C>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | chr4 | 128203420 | ||||||
| chr4:128203442
|
C | T | 1 | a0001c0001t0003g0239 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2309+2777C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | chr4 | 128203442 | ||||||
| chr4:128203477
|
A | G | 3 | a0007c0008t0001g0138a0007c0008t0001g0139a0007c0008t0001g0158 | 3 | HG03486.hp2 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2309+2812A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | chr4 | 128203477 | ||||||
| chr4:128203482
|
T | C | 3 | a0007c0008t0001g0138a0007c0008t0001g0139a0007c0008t0001g0158 | 3 | HG03486.hp2 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2309+2817T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | chr4 | 128203482 | ||||||
| chr4:128203483
|
T | C | 3 | a0007c0008t0001g0138a0007c0008t0001g0139a0007c0008t0001g0158 | 3 | HG03486.hp2 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2309+2818T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | chr4 | 128203483 | ||||||
| chr4:128203488
|
C | T | 5 | a0005c0006t0001g0099a0005c0006t0001g0100a0005c0006t0001g0101others(2): Show | 5 | HG01168.hp1 HG02572.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2309+2823C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | chr4 | 128203488 | ||||||
| chr4:128203878
|
A | G | 1 | a0001c0001t0001g0011 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2310-2550A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | chr4 | 128203878 | ||||||
| chr4:128204133
|
C | A | 2 | a0002c0003t0001g0104a0002c0003t0001g0105 | 2 | HG02145.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.2310-2295C>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | chr4 | 128204133 | ||||||
| chr4:128204203
|
ACTTCTCC others(23): Show |
A | 25 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(22): Show | 25 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.2310-2220_2310-219 others(34): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr4 | 128204203 | |||||
| chr4:128204218
|
A | G | 1 | a0003c0004t0001g0172 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2310-2210A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | chr4 | 128204218 | ||||||
| chr4:128204328
|
A | G | 59 | a0001c0001t0001g0168a0001c0001t0003g0102a0001c0001t0003g0103others(56): Show | 59 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.2310-2100A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | chr4 | 128204328 | ||||||
| chr4:128204455
|
G | A | 1 | a0001c0001t0003g0238 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2310-1973G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | chr4 | 128204455 | ||||||
| chr4:128204500
|
C | T | 1 | a0010c0011t0005g0123 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2310-1928C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | chr4 | 128204500 | ||||||
| chr4:128204604
|
G | A | 25 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(22): Show | 25 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.2310-1824G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | chr4 | 128204604 | ||||||
| chr4:128204676
|
TA | T | 8 | a0001c0001t0001g0146a0001c0001t0001g0163a0001c0001t0001g0164others(5): Show | 8 | HG00140.hp2 HG00639.hp2 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.2310-1746delA | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr4 | 128204676 | |||||
| chr4:128204709
|
A | G | 29 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(26): Show | 29 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.2310-1719A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | chr4 | 128204709 | ||||||
| chr4:128204813
|
C | T | 2 | a0001c0001t0004g0327a0002c0002t0011g0030 | 2 | NA18945.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.2310-1615C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | chr4 | 128204813 | ||||||
| chr4:128204867
|
T | TAAAA | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(159): Show | 162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.2310-1555_2310-155 others(8): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr4 | 128204867 | |||||
| chr4:128205170
|
G | A | 1 | a0001c0001t0003g0242 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2310-1258G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | chr4 | 128205170 | ||||||
| chr4:128205188
|
G | A | 4 | a0002c0002t0002g0015a0002c0002t0002g0017a0002c0002t0002g0050others(1): Show | 4 | HG02559.hp2 HG02622.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2310-1240G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | chr4 | 128205188 | ||||||
| chr4:128205690
|
CA | C | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(162): Show | 165 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.2310-737delA | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | chr4 | 128205690 | ||||||
| chr4:128205876
|
G | T | 1 | a0001c0001t0001g0137 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2310-552G>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | chr4 | 128205876 | ||||||
| chr4:128206008
|
C | T | 1 | a0001c0001t0004g0323 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.2310-420C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | chr4 | 128206008 | ||||||
| chr4:128206185
|
G | A | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(162): Show | 165 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.2310-243G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | chr4 | 128206185 | ||||||
| chr4:128206193
|
G | A | 1 | a0001c0001t0003g0230 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2310-235G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | chr4 | 128206193 | ||||||
| chr4:128206240
|
C | T | 1 | a0002c0002t0002g0057 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2310-188C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | chr4 | 128206240 | ||||||
| chr4:128206246
|
C | T | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(162): Show | 165 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.2310-182C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | chr4 | 128206246 | ||||||
| chr4:128206308
|
A | G | 37 | a0001c0001t0001g0108a0001c0001t0001g0124a0001c0001t0001g0129others(34): Show | 37 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.2310-120A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 17/19 | chr4 | 128206308 | ||||||
| chr4:128206789
|
C | T | 1 | a0001c0001t0001g0273 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2419+252C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 18/19 | chr4 | 128206789 | ||||||
| chr4:128206814
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2419+277A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 18/19 | chr4 | 128206814 | ||||||
| chr4:128206822
|
A | G | 1 | a0001c0001t0003g0278 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2419+285A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 18/19 | chr4 | 128206822 | ||||||
| chr4:128207174
|
T | C | 1 | a0001c0001t0001g0179 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2420-82T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 18/19 | chr4 | 128207174 | ||||||
| chr4:128207228
|
C | T | 29 | a0001c0001t0004g0308a0001c0001t0004g0309a0001c0001t0004g0310others(26): Show | 29 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.2420-28C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 18/19 | chr4 | 128207228 | ||||||
| chr4:128207486
|
T | C | 3 | a0002c0002t0005g0097a0002c0003t0005g0122a0002c0012t0005g0098 | 3 | HG02451.hp1 HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2547+103T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 19/19 | chr4 | 128207486 | ||||||
| chr4:128207594
|
A | G | 1 | a0002c0002t0002g0291 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2547+211A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 19/19 | chr4 | 128207594 | ||||||
| chr4:128207793
|
G | A | 7 | a0001c0001t0001g0124a0001c0001t0001g0259a0001c0001t0001g0260others(4): Show | 7 | HG00423.hp2 HG00438.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.2547+410G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 19/19 | chr4 | 128207793 | ||||||
| chr4:128207984
|
G | A | 1 | a0002c0002t0002g0090 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2547+601G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 19/19 | chr4 | 128207984 | ||||||
| chr4:128208083
|
T | C | 1 | a0002c0002t0002g0047 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2547+700T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 19/19 | chr4 | 128208083 | ||||||
| chr4:128208200
|
C | T | 4 | a0001c0001t0001g0109a0002c0002t0002g0015a0002c0002t0002g0017others(1): Show | 4 | HG02559.hp2 HG02622.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2547+817C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 19/19 | chr4 | 128208200 | ||||||
| chr4:128208477
|
A | G | 1 | a0002c0002t0002g0071 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2547+1094A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 19/19 | chr4 | 128208477 | ||||||
| chr4:128208867
|
C | T | 3 | a0002c0002t0010g0036a0002c0002t0010g0048a0002c0002t0010g0077 | 3 | HG01243.hp2 HG03209.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2548-989C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 19/19 | chr4 | 128208867 | ||||||
| chr4:128209208
|
T | C | 1 | a0001c0001t0001g0205 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2548-648T>C | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 19/19 | chr4 | 128209208 | ||||||
| chr4:128209282
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2548-574G>A | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 19/19 | chr4 | 128209282 | ||||||
| chr4:128209451
|
A | G | 1 | a0013c0014t0003g0226 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2548-405A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 19/19 | chr4 | 128209451 | ||||||
| chr4:128209504
|
C | T | 4 | a0001c0001t0007g0131a0001c0001t0007g0132a0001c0001t0007g0133others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.2548-352C>T | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 19/19 | chr4 | 128209504 | ||||||
| chr4:128209511
|
A | G | 8 | a0002c0003t0006g0003a0002c0003t0006g0004a0002c0003t0006g0005others(5): Show | 8 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.2548-345A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 19/19 | chr4 | 128209511 | ||||||
| chr4:128209522
|
A | G | 3 | a0004c0005t0005g0281a0004c0005t0005g0282a0004c0005t0005g0283 | 3 | HG02055.hp1 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2548-334A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 19/19 | chr4 | 128209522 | ||||||
| chr4:128209720
|
CA | C | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(183): Show | 186 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.2548-113delA | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr4 | 128209720 | |||||
| chr4:128209721
|
A | AG | 8 | a0001c0001t0004g0314a0002c0002t0002g0013a0002c0002t0002g0070others(5): Show | 8 | HG00544.hp1 HG01884.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.2548-135_2548-134i others(3): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 19/19 | chr4 | 128209721 | ||||||
| chr4:128209722
|
A | G | 131 | a0001c0001t0001g0142a0001c0001t0001g0266a0001c0001t0001g0270others(128): Show | 131 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.2548-134A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 19/19 | chr4 | 128209722 | ||||||
| chr4:128209723
|
A | G | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(183): Show | 186 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.2548-133A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 19/19 | chr4 | 128209723 | ||||||
| chr4:128209724
|
A | G | 2 | a0001c0001t0004g0311a0001c0001t0004g0315 | 2 | HG02132.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.2548-132A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 19/19 | chr4 | 128209724 | ||||||
| chr4:128209729
|
A | G | 3 | a0005c0006t0001g0099a0005c0006t0001g0100a0005c0006t0001g0101 | 3 | HG01168.hp1 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2548-127A>G | LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 19/19 | chr4 | 128209729 |