Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 113251 |
|---|---|
| ensemblid | ENSG00000161813.23 |
| hgncid | 24320 |
| symbol | LARP4 |
| name | La ribonucleoprotein 4 |
| refseq_nuc | NM_052879.5 |
| refseq_prot | NP_443111.4 |
| ensembl_nuc | ENST00000398473.7 |
| ensembl_prot | ENSP00000381490.2 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 50400885 |
| end | 50480004 |
| strand | + |
| ver | v1.2 |
| region | chr12:50400885-50480004 |
| region5000 | chr12:50395885-50485004 |
| regionname0 | LARP4_chr12_50400885_50480004 |
| regionname5000 | LARP4_chr12_50395885_50485004 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 724 | 279 | 82 | 43 | 118 | 9 | 25 | 92 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| a0002 | 0/0 | 724 | 14 | 0 | 0 | 13 | 0 | 1 | 12 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| a0003 | 0/0 | 724 | 11 | 0 | 2 | 4 | 1 | 4 | 2 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| a0004 | 0/0 | 724 | 8 | 0 | 0 | 8 | 0 | 0 | 7 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| a0005 | 0/0 | 724 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| a0006 | 0/0 | 724 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| a0007 | 0/0 | 724 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2175 | 269 | 78 | 42 | 114 | 9 | 24 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| c0002 | 0/0 | 2175 | 14 | 0 | 0 | 13 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| c0003 | 0/0 | 2175 | 11 | 0 | 2 | 4 | 1 | 4 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| c0004 | 0/0 | 2175 | 8 | 0 | 0 | 8 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| c0005 | 0/0 | 2175 | 3 | 0 | 0 | 3 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| c0006 | 0/0 | 2175 | 3 | 2 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| c0007 | 0/0 | 2175 | 3 | 0 | 3 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| c0008 | 0/0 | 2175 | 2 | 2 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| c0009 | 0/0 | 2175 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| c0010 | 0/0 | 2175 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| c0011 | 0/0 | 2175 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| c0012 | 0/0 | 2175 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| c0013 | 0/0 | 2175 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| 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 | 4268 | 144 | 42 | 16 | 70 | 1 | 15 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| t0002 | 0/1 | 4268 | 124 | 9 | 24 | 67 | 9 | 14 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| t0003 | 1/0 | 4267 | 9 | 6 | 2 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| t0004 | 0/0 | 4270 | 7 | 4 | 0 | 3 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| t0005 | 0/0 | 4268 | 6 | 6 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| t0006 | 0/0 | 4268 | 5 | 5 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| t0007 | 0/0 | 4268 | 4 | 3 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| t0008 | 0/0 | 4268 | 3 | 3 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| t0009 | 0/0 | 4268 | 2 | 0 | 2 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| t0010 | 0/0 | 4267 | 2 | 2 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| t0011 | 0/0 | 4268 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| t0012 | 0/0 | 4268 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| t0013 | 0/0 | 4268 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| t0014 | 0/0 | 4268 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| t0015 | 0/0 | 4268 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| t0016 | 0/0 | 4267 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| t0017 | 0/0 | 4268 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| t0018 | 0/0 | 4268 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| t0019 | 0/0 | 4268 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| t0020 | 0/0 | 4268 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| t0021 | 0/0 | 4270 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| t0022 | 0/0 | 4268 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0027 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0083 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2175 | 269 | 78 | 42 | 114 | 9 | 24 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| a0001c0005 | 0/0 | 2175 | 3 | 0 | 0 | 3 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| a0001c0006 | 0/0 | 2175 | 3 | 2 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| a0001c0009 | 0/0 | 2175 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| a0001c0010 | 0/0 | 2175 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| a0001c0011 | 0/0 | 2175 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| a0001c0012 | 0/0 | 2175 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| a0002c0002 | 0/0 | 2175 | 14 | 0 | 0 | 13 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| a0003c0003 | 0/0 | 2175 | 11 | 0 | 2 | 4 | 1 | 4 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| a0004c0004 | 0/0 | 2175 | 8 | 0 | 0 | 8 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| a0005c0007 | 0/0 | 2175 | 3 | 0 | 3 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| a0006c0008 | 0/0 | 2175 | 2 | 2 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| a0007c0013 | 0/0 | 2175 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6442 | 107 | 42 | 14 | 41 | 0 | 10 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| a0001c0001t0002 | 0/1 | 6442 | 118 | 8 | 21 | 66 | 9 | 13 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| a0001c0001t0003 | 1/0 | 6441 | 9 | 6 | 2 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| a0001c0001t0004 | 0/0 | 6444 | 7 | 4 | 0 | 3 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| a0001c0001t0005 | 0/0 | 6442 | 4 | 4 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| a0001c0001t0006 | 0/0 | 6442 | 5 | 5 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| a0001c0001t0008 | 0/0 | 6442 | 3 | 3 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| a0001c0001t0009 | 0/0 | 6442 | 2 | 0 | 2 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| a0001c0001t0010 | 0/0 | 6441 | 2 | 2 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| a0001c0001t0011 | 0/0 | 6442 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| a0001c0001t0012 | 0/0 | 6442 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| a0001c0001t0013 | 0/0 | 6442 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| a0001c0001t0014 | 0/0 | 6442 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| a0001c0001t0015 | 0/0 | 6442 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| a0001c0001t0016 | 0/0 | 6441 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| a0001c0001t0017 | 0/0 | 6442 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| a0001c0001t0018 | 0/0 | 6442 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| a0001c0001t0019 | 0/0 | 6442 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| a0001c0001t0020 | 0/0 | 6442 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| a0001c0001t0021 | 0/0 | 6444 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| a0001c0001t0022 | 0/0 | 6442 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| a0001c0005t0001 | 0/0 | 6442 | 3 | 0 | 0 | 3 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| a0001c0006t0007 | 0/0 | 6442 | 3 | 2 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| a0001c0009t0001 | 0/0 | 6442 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| a0001c0010t0007 | 0/0 | 6442 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| a0001c0011t0002 | 0/0 | 6442 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| a0001c0012t0002 | 0/0 | 6442 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| a0002c0002t0001 | 0/0 | 6442 | 14 | 0 | 0 | 13 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| a0003c0003t0001 | 0/0 | 6442 | 11 | 0 | 2 | 4 | 1 | 4 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| a0004c0004t0001 | 0/0 | 6442 | 8 | 0 | 0 | 8 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| a0005c0007t0002 | 0/0 | 6442 | 3 | 0 | 3 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| a0006c0008t0005 | 0/0 | 6442 | 2 | 2 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| a0007c0013t0002 | 0/0 | 6442 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | copy fasta | chr12 | 50395885 | 50485004 |
| 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 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0083 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0003g0027 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0004g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0004g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0004g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0005g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0005g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0005g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0005g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0006g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0006g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0006g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0006g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0006g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0008g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0008g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0008g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0009g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0009g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0010g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0010g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0011g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0012g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0013g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0014g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0015g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0016g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0017g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0018g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0019g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0020g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0021g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0022g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0005t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0005t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0005t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0006t0007g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0006t0007g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0006t0007g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0009t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0010t0007g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0011t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0012t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0002c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0002c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0003c0003t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0003c0003t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0003c0003t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0003c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0003c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0003c0003t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0003c0003t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0003c0003t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0003c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0003c0003t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0003c0003t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0004c0004t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0004c0004t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0004c0004t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0004c0004t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0004c0004t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0004c0004t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0004c0004t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0004c0004t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0005c0007t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0005c0007t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0005c0007t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0006c0008t0005g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0006c0008t0005g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0007c0013t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0075 | EUR | GBR | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0308 | EUR | GBR | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0106 | EUR | GBR | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG00140 | hp2 | a0003 | c0003 | t0001 | g0162 | EUR | GBR | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | CHS | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG00438 | hp2 | a0004 | c0004 | t0001 | g0239 | EAS | CHS | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | CHS | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG00544 | hp2 | a0003 | c0003 | t0001 | g0153 | EAS | CHS | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | CHS | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG00642 | hp2 | a0005 | c0007 | t0002 | g0136 | AMR | PUR | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | CHS | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | CHS | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG00738 | hp1 | a0005 | c0007 | t0002 | g0119 | AMR | PUR | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG00738 | hp2 | a0001 | c0001 | t0022 | g0002 | AMR | PUR | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG00741 | hp1 | a0001 | c0001 | t0009 | g0059 | AMR | PUR | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0031 | AMR | PUR | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01069 | hp2 | a0005 | c0007 | t0002 | g0084 | AMR | PUR | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0030 | AMR | PUR | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0303 | AMR | PUR | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0070 | AMR | PUR | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01074 | hp2 | a0001 | c0001 | t0009 | g0048 | AMR | PUR | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0307 | AMR | PUR | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01106 | hp2 | a0003 | c0003 | t0001 | g0173 | AMR | PUR | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01109 | hp1 | a0001 | c0006 | t0007 | g0110 | AMR | PUR | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0061 | AMR | PUR | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0077 | AMR | PUR | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0097 | AMR | CLM | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0313 | AMR | CLM | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0096 | AMR | CLM | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0120 | AMR | CLM | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | CLM | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | CLM | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0310 | AMR | CLM | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | CLM | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | CLM | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0135 | AMR | CLM | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01433 | hp2 | a0001 | c0001 | t0019 | g0134 | AMR | CLM | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0312 | EUR | IBS | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0052 | EUR | IBS | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0311 | EUR | IBS | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0074 | EUR | IBS | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0297 | AFR | ACB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0170 | AFR | ACB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0122 | AFR | ACB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01928 | hp1 | a0001 | c0001 | t0012 | g0246 | AMR | PEL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | PEL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0080 | AMR | PEL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PEL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01975 | hp1 | a0003 | c0003 | t0001 | g0163 | AMR | PEL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PEL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0085 | AMR | PEL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PEL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | KHV | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | KHV | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02040 | hp1 | a0003 | c0003 | t0001 | g0180 | EAS | KHV | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02040 | hp2 | a0001 | c0001 | t0004 | g0208 | EAS | KHV | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0169 | AFR | ACB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0287 | EAS | KHV | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | KHV | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | KHV | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02074 | hp2 | a0001 | c0001 | t0013 | g0194 | EAS | KHV | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | KHV | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02083 | hp2 | a0001 | c0009 | t0001 | g0271 | EAS | KHV | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | KHV | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0133 | AMR | PEL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | CDX | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | CDX | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | CDX | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | CDX | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0150 | AFR | ACB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02258 | hp1 | a0001 | c0001 | t0020 | g0300 | AFR | ACB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0148 | AFR | ACB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0137 | AFR | ACB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0105 | AMR | PEL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02451 | hp1 | a0001 | c0012 | t0002 | g0066 | AFR | ACB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02451 | hp2 | a0001 | c0001 | t0008 | g0158 | AFR | ACB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | KHV | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02572 | hp1 | a0001 | c0006 | t0007 | g0109 | AFR | GWD | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0035 | AFR | GWD | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0065 | SAS | PJL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0068 | SAS | PJL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0309 | AFR | GWD | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0034 | AFR | GWD | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0126 | AFR | GWD | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | GWD | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02647 | hp2 | a0001 | c0001 | t0006 | g0273 | AFR | GWD | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0076 | SAS | PJL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02683 | hp2 | a0001 | c0011 | t0002 | g0191 | SAS | PJL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02809 | hp2 | a0001 | c0001 | t0015 | g0317 | AFR | GWD | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0029 | AFR | GWD | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | GWD | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | GWD | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02896 | hp1 | a0001 | c0001 | t0010 | g0033 | AFR | GWD | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0026 | AFR | GWD | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02897 | hp1 | a0001 | c0001 | t0010 | g0025 | AFR | GWD | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0145 | AFR | ESN | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | ESN | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02970 | hp1 | a0001 | c0001 | t0008 | g0183 | AFR | ESN | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | ESN | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ESN | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02976 | hp2 | a0006 | c0008 | t0005 | g0037 | AFR | ESN | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0082 | SAS | PJL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03017 | hp2 | a0003 | c0003 | t0001 | g0165 | SAS | PJL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | MSL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | MSL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03130 | hp1 | a0006 | c0008 | t0005 | g0038 | AFR | ESN | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0032 | AFR | ESN | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | MSL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0294 | AFR | MSL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03225 | hp1 | a0001 | c0001 | t0011 | g0314 | AFR | MSL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03225 | hp2 | a0001 | c0006 | t0007 | g0108 | AFR | MSL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | MSL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | MSL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03486 | hp1 | a0001 | c0001 | t0021 | g0301 | AFR | MSL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | MSL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0058 | SAS | PJL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0056 | SAS | PJL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | MSL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03579 | hp2 | a0001 | c0001 | t0008 | g0184 | AFR | MSL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0306 | SAS | PJL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0305 | SAS | PJL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0099 | SAS | STU | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | STU | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0053 | SAS | PJL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03834 | hp1 | a0003 | c0003 | t0001 | g0171 | SAS | BEB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0214 | SAS | BEB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03927 | hp1 | a0001 | c0001 | t0017 | g0304 | SAS | BEB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0283 | SAS | BEB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0286 | SAS | STU | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0140 | SAS | STU | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | STU | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0138 | SAS | STU | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | STU | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | STU | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG04228 | hp1 | a0003 | c0003 | t0001 | g0186 | SAS | STU | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | STU | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | CHB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | CHB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | CHB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | CHB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0103 | AFR | YRI | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0146 | AFR | YRI | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18942 | hp1 | a0001 | c0001 | t0004 | g0202 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18942 | hp2 | a0004 | c0004 | t0001 | g0200 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0288 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0255 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18946 | hp1 | a0001 | c0001 | t0004 | g0220 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18948 | hp1 | a0001 | c0001 | t0018 | g0012 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0212 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18969 | hp1 | a0003 | c0003 | t0001 | g0166 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0210 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18979 | hp1 | a0004 | c0004 | t0001 | g0265 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0253 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18980 | hp2 | a0004 | c0004 | t0001 | g0227 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18989 | hp2 | a0003 | c0003 | t0001 | g0187 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18990 | hp1 | a0004 | c0004 | t0001 | g0250 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18990 | hp2 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18991 | hp1 | a0001 | c0005 | t0001 | g0010 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18992 | hp2 | a0001 | c0001 | t0014 | g0238 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0281 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0254 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0217 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19009 | hp1 | a0004 | c0004 | t0001 | g0198 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | LWK | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | LWK | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0318 | AFR | LWK | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0147 | AFR | LWK | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19054 | hp1 | a0004 | c0004 | t0001 | g0241 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19057 | hp1 | a0001 | c0001 | t0016 | g0259 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19058 | hp1 | a0002 | c0002 | t0001 | g0207 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19063 | hp1 | a0002 | c0002 | t0001 | g0211 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0280 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19074 | hp1 | a0004 | c0004 | t0001 | g0240 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19078 | hp2 | a0007 | c0013 | t0002 | g0101 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19080 | hp1 | a0001 | c0005 | t0001 | g0008 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19090 | hp2 | a0001 | c0005 | t0001 | g0260 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0139 | AFR | YRI | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | YRI | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ASW | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | ASW | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0152 | EUR | TSI | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0151 | EUR | TSI | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA20905 | hp1 | a0003 | c0003 | t0001 | g0179 | SAS | GIH | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0057 | SAS | GIH | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02109 | hp1 | a0001 | c0001 | t0006 | g0275 | AFR | ACB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | ACB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ACB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0086 | AFR | ACB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02559 | hp2 | a0001 | c0001 | t0006 | g0276 | AFR | ACB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03471 | hp1 | a0001 | c0001 | t0006 | g0274 | AFR | MSL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0149 | AFR | MSL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | USA | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | USA | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | LWK | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA21309 | hp2 | a0001 | c0010 | t0007 | g0111 | AFR | LWK | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0083 | REF | REF | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0027 | REF | REF | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:50401022
|
C | A | 1 | a0006 | 2 | HG02976.hp2 HG03130.hp1 |
missense_variant | MODERATE | c.12C>A | p.Phe4Leu | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/16 | 138/6441 | 12/2175 | 4/724 | chr12 | 50401022 | ||
| chr12:50427768
|
G | T | 1 | a0005 | 3 | HG00642.hp2 HG00738.hp1 HG01069.hp2 |
missense_variant | MODERATE | c.25G>T | p.Ala9Ser | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 2/16 | 151/6441 | 25/2175 | 9/724 | chr12 | 50427768 | ||
| chr12:50427888
|
A | G | 1 | a0004 | 8 | HG00438.hp2 NA18942.hp2 NA18979.hp1 others(5): Show |
missense_variant | MODERATE | c.145A>G | p.Thr49Ala | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 2/16 | 271/6441 | 145/2175 | 49/724 | chr12 | 50427888 | ||
| chr12:50430518
|
A | G | 1 | a0007 | 1 | NA19078.hp2 | missense_variant | MODERATE | c.346A>G | p.Thr116Ala | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 4/16 | 472/6441 | 346/2175 | 116/724 | chr12 | 50430518 | ||
| chr12:50454349
|
T | A | 1 | a0003 | 11 | HG00140.hp2 HG00544.hp2 HG01106.hp2 others(8): Show |
missense_variant | MODERATE | c.1053T>A | p.Phe351Leu | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/16 | 1179/6441 | 1053/2175 | 351/724 | chr12 | 50454349 | ||
| chr12:50467080
|
A | C | 1 | a0002 | 14 | HG02071.hp1 HG03834.hp2 NA18943.hp1 others(11): Show |
missense_variant | MODERATE | c.1505A>C | p.Asn502Thr | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/16 | 1631/6441 | 1505/2175 | 502/724 | chr12 | 50467080 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:50453600
|
A | G | 1 | a0001c0012 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.945A>G | p.Gln315Gln | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 9/16 | 1071/6441 | 945/2175 | 315/724 | chr12 | 50453600 | ||
| chr12:50461216
|
C | T | 1 | a0001c0011 | 1 | HG02683.hp2 | synonymous_variant | LOW | c.1203C>T | p.Asn401Asn | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 11/16 | 1329/6441 | 1203/2175 | 401/724 | chr12 | 50461216 | ||
| chr12:50461336
|
T | C | 1 | a0001c0009 | 1 | HG02083.hp2 | synonymous_variant | LOW | c.1323T>C | p.Tyr441Tyr | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 11/16 | 1449/6441 | 1323/2175 | 441/724 | chr12 | 50461336 | ||
| chr12:50461342
|
G | A | 1 | a0001c0005 | 3 | NA18991.hp1 NA19080.hp1 NA19090.hp2 |
synonymous_variant | LOW | c.1329G>A | p.Arg443Arg | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 11/16 | 1455/6441 | 1329/2175 | 443/724 | chr12 | 50461342 | ||
| chr12:50475531
|
C | T | 1 | a0001c0010 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.1842C>T | p.Pro614Pro | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 16/16 | 1968/6441 | 1842/2175 | 614/724 | chr12 | 50475531 | ||
| chr12:50475735
|
T | C | 2 | a0001c0006a0001c0010 | 4 | HG01109.hp1 HG02572.hp1 HG03225.hp2 others(1): Show |
synonymous_variant | LOW | c.2046T>C | p.Asn682Asn | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 16/16 | 2172/6441 | 2046/2175 | 682/724 | chr12 | 50475735 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:50476032
|
C | G | 1 | a0001c0001t0022 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*168C>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 16/16 | 168 | chr12 | 50476032 | |||||
| chr12:50476075
|
A | AAT | 2 | a0001c0001t0004a0001c0001t0021 | 8 | HG01884.hp2 HG02040.hp2 HG02055.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*227_*228dupTA | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 16/16 | 229 | INFO_REALIGN_3_PRIME | chr12 | 50476075 | ||||
| chr12:50476091
|
T | C | 3 | a0001c0001t0011a0001c0006t0007a0001c0010t0007 | 5 | HG01109.hp1 HG02572.hp1 HG03225.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*227T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 16/16 | 227 | chr12 | 50476091 | |||||
| chr12:50476362
|
G | A | 32 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(29): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
3_prime_UTR_variant | MODIFIER | c.*498G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 16/16 | 498 | chr12 | 50476362 | |||||
| chr12:50476557
|
A | G | 1 | a0001c0001t0010 | 2 | HG02896.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*693A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 16/16 | 693 | chr12 | 50476557 | |||||
| chr12:50476646
|
A | C | 13 | a0001c0001t0002a0001c0001t0005a0001c0001t0009others(10): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*782A>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 16/16 | 782 | chr12 | 50476646 | |||||
| chr12:50476690
|
C | CT | 30 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(27): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
3_prime_UTR_variant | MODIFIER | c.*826_*827insT | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 16/16 | 827 | chr12 | 50476690 | |||||
| chr12:50476690
|
C | T | 1 | a0001c0001t0016 | 1 | NA19057.hp1 | 3_prime_UTR_variant | MODIFIER | c.*826C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 16/16 | 826 | chr12 | 50476690 | |||||
| chr12:50476765
|
C | T | 1 | a0001c0001t0008 | 3 | HG02451.hp2 HG02970.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*901C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 16/16 | 901 | chr12 | 50476765 | |||||
| chr12:50476872
|
G | A | 2 | a0001c0006t0007a0001c0010t0007 | 4 | HG01109.hp1 HG02572.hp1 HG03225.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1008G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 16/16 | 1008 | chr12 | 50476872 | |||||
| chr12:50477022
|
T | A | 1 | a0001c0001t0017 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1158T>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 16/16 | 1158 | chr12 | 50477022 | |||||
| chr12:50477232
|
C | T | 2 | a0001c0006t0007a0001c0010t0007 | 4 | HG01109.hp1 HG02572.hp1 HG03225.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1368C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 16/16 | 1368 | chr12 | 50477232 | |||||
| chr12:50477340
|
A | G | 2 | a0001c0001t0020a0001c0001t0021 | 2 | HG02258.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1476A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 16/16 | 1476 | chr12 | 50477340 | |||||
| chr12:50478032
|
T | A | 1 | a0001c0001t0012 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2168T>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 16/16 | 2168 | chr12 | 50478032 | |||||
| chr12:50478220
|
A | G | 1 | a0001c0001t0019 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2356A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 16/16 | 2356 | chr12 | 50478220 | |||||
| chr12:50478335
|
A | G | 1 | a0001c0001t0018 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2471A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 16/16 | 2471 | chr12 | 50478335 | |||||
| chr12:50478423
|
C | T | 1 | a0001c0001t0015 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2559C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 16/16 | 2559 | chr12 | 50478423 | |||||
| chr12:50478455
|
C | A | 1 | a0001c0001t0015 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2591C>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 16/16 | 2591 | chr12 | 50478455 | |||||
| chr12:50478598
|
G | T | 1 | a0001c0001t0014 | 1 | NA18992.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2734G>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 16/16 | 2734 | chr12 | 50478598 | |||||
| chr12:50478834
|
A | T | 4 | a0001c0001t0005a0001c0001t0020a0001c0001t0021others(1): Show | 8 | HG02258.hp1 HG02258.hp2 HG02922.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2970A>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 16/16 | 2970 | chr12 | 50478834 | |||||
| chr12:50479058
|
G | A | 1 | a0001c0001t0006 | 5 | HG02109.hp1 HG02559.hp2 HG02647.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3194G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 16/16 | 3194 | chr12 | 50479058 | |||||
| chr12:50479229
|
A | G | 2 | a0001c0001t0020a0001c0001t0021 | 2 | HG02258.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3365A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 16/16 | 3365 | chr12 | 50479229 | |||||
| chr12:50479762
|
G | T | 1 | a0001c0001t0009 | 2 | HG00741.hp1 HG01074.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3898G>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 16/16 | 3898 | chr12 | 50479762 | |||||
| chr12:50479874
|
T | C | 1 | a0001c0001t0013 | 1 | HG02074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4010T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 16/16 | 4010 | chr12 | 50479874 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:50401158
|
C | T | 1 | a0001c0001t0001g0318 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.18+130C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50401158 | ||||||
| chr12:50401342
|
G | A | 11 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(8): Show | 11 | HG00738.hp2 HG01261.hp1 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.18+314G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50401342 | ||||||
| chr12:50401892
|
C | T | 1 | a0001c0001t0015g0317 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.18+864C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50401892 | ||||||
| chr12:50401963
|
G | C | 1 | a0001c0001t0018g0012 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.18+935G>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50401963 | ||||||
| chr12:50402001
|
C | A | 1 | a0001c0001t0002g0013 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.18+973C>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50402001 | ||||||
| chr12:50402190
|
T | G | 5 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(2): Show | 5 | HG01361.hp2 HG01928.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+1162T>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50402190 | ||||||
| chr12:50402194
|
G | GT | 17 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0002g0302others(14): Show | 17 | HG00099.hp2 HG01071.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.18+1175dupT | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50402194 | |||||
| chr12:50402536
|
C | T | 122 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(119): Show | 122 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(119): Show |
intron_variant | MODIFIER | c.18+1508C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50402536 | ||||||
| chr12:50402548
|
A | G | 1 | a0001c0011t0002g0191 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.18+1520A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50402548 | ||||||
| chr12:50402640
|
C | G | 39 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(36): Show | 39 | HG00140.hp2 HG00544.hp2 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.18+1612C>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50402640 | ||||||
| chr12:50402772
|
A | T | 1 | a0001c0001t0002g0152 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.18+1744A>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50402772 | ||||||
| chr12:50402802
|
C | A | 2 | a0001c0001t0002g0018a0001c0001t0002g0019 | 2 | NA18747.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.18+1774C>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50402802 | ||||||
| chr12:50403023
|
A | G | 1 | a0001c0001t0002g0151 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.18+1995A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50403023 | ||||||
| chr12:50403447
|
A | G | 1 | a0001c0001t0015g0317 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.18+2419A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50403447 | ||||||
| chr12:50403647
|
A | G | 2 | a0001c0001t0004g0149a0001c0001t0004g0150 | 2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.18+2619A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50403647 | ||||||
| chr12:50403648
|
C | G | 259 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(256): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.18+2620C>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50403648 | ||||||
| chr12:50403717
|
C | T | 1 | a0001c0001t0001g0036 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.18+2689C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50403717 | ||||||
| chr12:50403724
|
T | A | 1 | a0001c0001t0004g0149 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.18+2696T>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50403724 | ||||||
| chr12:50403793
|
A | G | 4 | a0001c0001t0005g0145a0001c0001t0005g0146a0001c0001t0005g0147others(1): Show | 4 | HG02258.hp2 HG02922.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.18+2765A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50403793 | ||||||
| chr12:50403823
|
C | G | 3 | a0001c0001t0002g0311a0001c0001t0002g0312a0001c0001t0002g0313 | 3 | HG01255.hp2 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.18+2795C>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50403823 | ||||||
| chr12:50403863
|
C | T | 3 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0144 | 3 | HG02074.hp1 NA18747.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.18+2835C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50403863 | ||||||
| chr12:50403935
|
G | GGAAAC | 307 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(304): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.18+2907_18+2908ins others(5): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50403935 | ||||||
| chr12:50403998
|
T | C | 309 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(306): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.18+2970T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50403998 | ||||||
| chr12:50404318
|
C | T | 1 | a0001c0001t0001g0299 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.18+3290C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50404318 | ||||||
| chr12:50404552
|
A | G | 122 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(119): Show | 122 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(119): Show |
intron_variant | MODIFIER | c.18+3524A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50404552 | ||||||
| chr12:50404606
|
G | A | 7 | a0001c0001t0001g0192a0001c0001t0005g0145a0001c0001t0005g0146others(4): Show | 7 | HG00597.hp1 HG02258.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.18+3578G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50404606 | ||||||
| chr12:50404659
|
C | T | 1 | a0001c0001t0002g0143 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.18+3631C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50404659 | ||||||
| chr12:50404681
|
G | GT | 15 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0181others(12): Show | 15 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.18+3677dupT | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50404681 | |||||
| chr12:50404681
|
GT | G | 117 | a0001c0001t0001g0011a0001c0001t0001g0277a0001c0001t0001g0278others(114): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.18+3677delT | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50404681 | |||||
| chr12:50404681
|
GTT | G | 99 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(96): Show | 99 | HG00438.hp2 HG00597.hp1 HG00738.hp2 others(96): Show |
intron_variant | MODIFIER | c.18+3676_18+3677del others(2): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50404681 | |||||
| chr12:50404750
|
C | T | 2 | a0001c0001t0020g0300a0001c0001t0021g0301 | 2 | HG02258.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.18+3722C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50404750 | ||||||
| chr12:50404751
|
G | A | 1 | a0001c0001t0002g0039 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.18+3723G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50404751 | ||||||
| chr12:50404770
|
A | G | 1 | a0001c0001t0002g0107 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.18+3742A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50404770 | ||||||
| chr12:50404855
|
A | G | 2 | a0001c0001t0020g0300a0001c0001t0021g0301 | 2 | HG02258.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.18+3827A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50404855 | ||||||
| chr12:50404939
|
C | T | 5 | a0001c0001t0006g0273a0001c0001t0006g0274a0001c0001t0006g0275others(2): Show | 5 | HG02109.hp1 HG02559.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+3911C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50404939 | ||||||
| chr12:50404983
|
T | C | 1 | a0001c0001t0020g0300 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.18+3955T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50404983 | ||||||
| chr12:50404987
|
G | A | 2 | a0001c0001t0001g0193a0001c0001t0013g0194 | 2 | HG02074.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.18+3959G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50404987 | ||||||
| chr12:50405324
|
G | T | 302 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(299): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.18+4296G>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50405324 | ||||||
| chr12:50405423
|
A | T | 1 | a0003c0003t0001g0180 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.18+4395A>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50405423 | ||||||
| chr12:50405451
|
GT | G | 259 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(256): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.18+4433delT | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50405451 | |||||
| chr12:50405615
|
A | G | 131 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.18+4587A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50405615 | ||||||
| chr12:50405619
|
A | G | 1 | a0003c0003t0001g0179 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.18+4591A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50405619 | ||||||
| chr12:50405623
|
T | G | 1 | a0001c0001t0002g0302 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.18+4595T>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50405623 | ||||||
| chr12:50405752
|
T | C | 122 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(119): Show | 122 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(119): Show |
intron_variant | MODIFIER | c.18+4724T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50405752 | ||||||
| chr12:50405787
|
G | T | 1 | a0001c0001t0002g0106 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.18+4759G>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50405787 | ||||||
| chr12:50405928
|
G | A | 1 | a0003c0003t0001g0153 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.18+4900G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50405928 | ||||||
| chr12:50405951
|
T | C | 1 | a0001c0001t0002g0040 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.18+4923T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50405951 | ||||||
| chr12:50406384
|
A | G | 1 | a0001c0001t0001g0192 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.18+5356A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50406384 | ||||||
| chr12:50406458
|
A | G | 317 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(314): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.18+5430A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50406458 | ||||||
| chr12:50406486
|
A | T | 1 | a0001c0001t0001g0036 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.18+5458A>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50406486 | ||||||
| chr12:50406576
|
G | C | 125 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(122): Show | 125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): Show |
intron_variant | MODIFIER | c.18+5548G>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50406576 | ||||||
| chr12:50406914
|
C | T | 1 | a0001c0001t0010g0033 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.18+5886C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50406914 | ||||||
| chr12:50407004
|
C | T | 2 | a0001c0001t0001g0272a0001c0009t0001g0271 | 2 | HG02083.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.18+5976C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50407004 | ||||||
| chr12:50407065
|
G | A | 3 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197 | 3 | HG01891.hp1 HG06807.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.18+6037G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50407065 | ||||||
| chr12:50407109
|
T | G | 1 | a0001c0001t0001g0181 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.18+6081T>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50407109 | ||||||
| chr12:50407112
|
G | A | 2 | a0001c0001t0002g0041a0001c0001t0002g0112 | 2 | NA18995.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.18+6084G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50407112 | ||||||
| chr12:50407146
|
C | T | 1 | a0001c0001t0001g0036 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.18+6118C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50407146 | ||||||
| chr12:50407214
|
C | T | 2 | a0001c0001t0002g0041a0001c0001t0002g0112 | 2 | NA18995.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.18+6186C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50407214 | ||||||
| chr12:50407215
|
G | A | 2 | a0001c0001t0002g0107a0001c0001t0002g0113 | 2 | HG00597.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.18+6187G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50407215 | ||||||
| chr12:50407306
|
G | T | 3 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0144 | 3 | HG02074.hp1 NA18747.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.18+6278G>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50407306 | ||||||
| chr12:50407442
|
T | C | 9 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(6): Show | 9 | HG00544.hp1 HG02523.hp2 NA18953.hp2 others(6): Show |
intron_variant | MODIFIER | c.18+6414T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50407442 | ||||||
| chr12:50407700
|
C | A | 1 | a0004c0004t0001g0198 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.18+6672C>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50407700 | ||||||
| chr12:50407894
|
A | C | 122 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(119): Show | 122 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(119): Show |
intron_variant | MODIFIER | c.18+6866A>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50407894 | ||||||
| chr12:50408024
|
G | A | 10 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(7): Show | 10 | HG02257.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.18+6996G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50408024 | ||||||
| chr12:50408120
|
C | G | 2 | a0001c0001t0001g0270a0001c0001t0001g0293 | 2 | HG00673.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.18+7092C>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50408120 | ||||||
| chr12:50408187
|
C | CT | 160 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0020others(157): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.18+7185dupT | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50408187 | |||||
| chr12:50408187
|
C | CTT | 52 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0159others(49): Show | 52 | HG00140.hp1 HG00597.hp2 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.18+7184_18+7185dup others(2): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50408187 | |||||
| chr12:50408187
|
CT | C | 7 | a0001c0001t0001g0199a0001c0001t0001g0201a0001c0001t0001g0277others(4): Show | 7 | HG00642.hp1 HG01934.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.18+7185delT | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50408187 | |||||
| chr12:50408187
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0195 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.18+7176_18+7185del others(10): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50408187 | |||||
| chr12:50408187
|
CTTTTTTT others(4): Show |
C | 4 | a0001c0006t0007g0108a0001c0006t0007g0109a0001c0006t0007g0110others(1): Show | 4 | HG01109.hp1 HG02572.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.18+7175_18+7185del others(11): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50408187 | |||||
| chr12:50408290
|
C | T | 2 | a0001c0001t0004g0149a0001c0001t0004g0150 | 2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.18+7262C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50408290 | ||||||
| chr12:50408487
|
G | T | 1 | a0001c0010t0007g0111 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.18+7459G>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50408487 | ||||||
| chr12:50408490
|
C | T | 3 | a0001c0001t0006g0273a0001c0001t0006g0274a0001c0001t0006g0275 | 3 | HG02109.hp1 HG02647.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.18+7462C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50408490 | ||||||
| chr12:50408540
|
A | G | 8 | a0001c0001t0002g0039a0001c0001t0002g0093a0001c0001t0002g0094others(5): Show | 8 | HG00597.hp2 HG02083.hp1 NA18967.hp2 others(5): Show |
intron_variant | MODIFIER | c.18+7512A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50408540 | ||||||
| chr12:50408587
|
C | T | 131 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.18+7559C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50408587 | ||||||
| chr12:50408592
|
G | A | 2 | a0001c0001t0004g0149a0001c0001t0004g0150 | 2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.18+7564G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50408592 | ||||||
| chr12:50408680
|
G | A | 1 | a0003c0003t0001g0180 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.18+7652G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50408680 | ||||||
| chr12:50408820
|
G | A | 309 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(306): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.18+7792G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50408820 | ||||||
| chr12:50408827
|
G | A | 1 | a0001c0001t0002g0144 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.18+7799G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50408827 | ||||||
| chr12:50408844
|
T | C | 1 | a0001c0001t0001g0001 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.18+7816T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50408844 | ||||||
| chr12:50408910
|
A | G | 3 | a0001c0001t0002g0307a0001c0001t0002g0308a0001c0001t0002g0310 | 3 | HG00099.hp2 HG01106.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.18+7882A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50408910 | ||||||
| chr12:50408970
|
C | G | 4 | a0001c0006t0007g0108a0001c0006t0007g0109a0001c0006t0007g0110others(1): Show | 4 | HG01109.hp1 HG02572.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.18+7942C>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50408970 | ||||||
| chr12:50408993
|
T | A | 8 | a0001c0001t0002g0049a0001c0001t0005g0145a0001c0001t0005g0146others(5): Show | 8 | HG00741.hp2 HG01074.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.18+7965T>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50408993 | ||||||
| chr12:50409003
|
G | C | 5 | a0001c0001t0006g0273a0001c0001t0006g0274a0001c0001t0006g0275others(2): Show | 5 | HG02109.hp1 HG02559.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+7975G>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50409003 | ||||||
| chr12:50409142
|
A | G | 1 | a0001c0001t0002g0092 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.18+8114A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50409142 | ||||||
| chr12:50409412
|
G | A | 1 | a0001c0001t0002g0117 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.18+8384G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50409412 | ||||||
| chr12:50409731
|
C | T | 1 | a0001c0001t0011g0314 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.18+8703C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50409731 | ||||||
| chr12:50409779
|
A | G | 1 | a0001c0001t0004g0149 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.18+8751A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50409779 | ||||||
| chr12:50409808
|
A | T | 120 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(117): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.18+8780A>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50409808 | ||||||
| chr12:50409935
|
C | G | 259 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(256): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.18+8907C>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50409935 | ||||||
| chr12:50409980
|
C | T | 11 | a0001c0001t0001g0251a0001c0001t0002g0088a0001c0001t0002g0089others(8): Show | 11 | HG00438.hp1 NA18950.hp2 NA18953.hp1 others(8): Show |
intron_variant | MODIFIER | c.18+8952C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50409980 | ||||||
| chr12:50410090
|
C | CA | 6 | a0001c0001t0001g0023a0001c0001t0002g0039a0001c0001t0002g0050others(3): Show | 6 | HG00738.hp1 HG01346.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.18+9076dupA | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50410090 | |||||
| chr12:50410090
|
CA | C | 126 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(123): Show | 126 | HG00438.hp2 HG00597.hp1 HG00673.hp2 others(123): Show |
intron_variant | MODIFIER | c.18+9076delA | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50410090 | |||||
| chr12:50410351
|
G | A | 1 | a0003c0003t0001g0162 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.18+9323G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50410351 | ||||||
| chr12:50410408
|
C | CT | 10 | a0001c0001t0001g0011a0001c0001t0001g0193a0001c0001t0001g0247others(7): Show | 10 | HG01981.hp1 HG01981.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.18+9397dupT | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50410408 | |||||
| chr12:50410408
|
CT | C | 7 | a0001c0001t0001g0164a0001c0001t0001g0199a0001c0001t0002g0015others(4): Show | 7 | HG01169.hp2 HG01975.hp1 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.18+9397delT | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50410408 | |||||
| chr12:50410606
|
G | A | 5 | a0001c0001t0006g0273a0001c0001t0006g0274a0001c0001t0006g0275others(2): Show | 5 | HG02109.hp1 HG02559.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+9578G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50410606 | ||||||
| chr12:50410952
|
A | G | 3 | a0001c0001t0001g0201a0001c0001t0001g0277a0001c0001t0012g0246 | 3 | HG00642.hp1 HG01928.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.18+9924A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50410952 | ||||||
| chr12:50411070
|
C | G | 1 | a0001c0001t0003g0032 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.18+10042C>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50411070 | ||||||
| chr12:50411072
|
A | T | 1 | a0001c0001t0003g0032 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.18+10044A>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50411072 | ||||||
| chr12:50411157
|
T | C | 1 | a0001c0001t0001g0172 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.18+10129T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50411157 | ||||||
| chr12:50411187
|
C | CT | 124 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(121): Show | 124 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(121): Show |
intron_variant | MODIFIER | c.18+10174dupT | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50411187 | |||||
| chr12:50411247
|
G | A | 4 | a0001c0006t0007g0108a0001c0006t0007g0109a0001c0006t0007g0110others(1): Show | 4 | HG01109.hp1 HG02572.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.18+10219G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50411247 | ||||||
| chr12:50411305
|
C | T | 1 | a0001c0001t0002g0127 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.18+10277C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50411305 | ||||||
| chr12:50411348
|
A | C | 3 | a0001c0006t0007g0108a0001c0006t0007g0109a0001c0006t0007g0110 | 3 | HG01109.hp1 HG02572.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.18+10320A>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50411348 | ||||||
| chr12:50411435
|
T | C | 309 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(306): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.18+10407T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50411435 | ||||||
| chr12:50411442
|
C | A | 1 | a0003c0003t0001g0165 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.18+10414C>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50411442 | ||||||
| chr12:50411460
|
A | G | 309 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(306): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.18+10432A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50411460 | ||||||
| chr12:50411681
|
T | A | 2 | a0001c0001t0002g0052a0001c0001t0002g0097 | 2 | HG01255.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.18+10653T>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50411681 | ||||||
| chr12:50411683
|
C | G | 2 | a0001c0001t0001g0177a0001c0001t0001g0190 | 2 | HG04199.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.18+10655C>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50411683 | ||||||
| chr12:50412084
|
A | C | 2 | a0001c0001t0020g0300a0001c0001t0021g0301 | 2 | HG02258.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.18+11056A>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50412084 | ||||||
| chr12:50412202
|
CT | C | 4 | a0001c0006t0007g0108a0001c0006t0007g0109a0001c0006t0007g0110others(1): Show | 4 | HG01109.hp1 HG02572.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.18+11179delT | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50412202 | |||||
| chr12:50412279
|
T | C | 1 | a0001c0001t0002g0053 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.18+11251T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50412279 | ||||||
| chr12:50412478
|
T | C | 1 | a0001c0006t0007g0108 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.18+11450T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50412478 | ||||||
| chr12:50412583
|
C | T | 1 | a0003c0003t0001g0162 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.18+11555C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50412583 | ||||||
| chr12:50412692
|
A | C | 1 | a0001c0001t0001g0181 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.18+11664A>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50412692 | ||||||
| chr12:50412781
|
A | G | 5 | a0001c0001t0006g0273a0001c0001t0006g0274a0001c0001t0006g0275others(2): Show | 5 | HG02109.hp1 HG02559.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+11753A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50412781 | ||||||
| chr12:50412820
|
G | A | 118 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(115): Show | 118 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(115): Show |
intron_variant | MODIFIER | c.18+11792G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50412820 | ||||||
| chr12:50412879
|
G | A | 72 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(69): Show | 72 | HG00597.hp1 HG00642.hp1 HG00673.hp2 others(69): Show |
intron_variant | MODIFIER | c.18+11851G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50412879 | ||||||
| chr12:50412994
|
C | T | 1 | a0001c0001t0001g0299 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.18+11966C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50412994 | ||||||
| chr12:50413106
|
C | T | 1 | a0001c0001t0002g0116 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.18+12078C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50413106 | ||||||
| chr12:50413147
|
C | T | 113 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(110): Show | 113 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(110): Show |
intron_variant | MODIFIER | c.18+12119C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50413147 | ||||||
| chr12:50413202
|
G | A | 4 | a0001c0006t0007g0108a0001c0006t0007g0109a0001c0006t0007g0110others(1): Show | 4 | HG01109.hp1 HG02572.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.18+12174G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50413202 | ||||||
| chr12:50413222
|
CA | C | 128 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.18+12209delA | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50413222 | |||||
| chr12:50413222
|
CAA | C | 118 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(115): Show | 118 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(115): Show |
intron_variant | MODIFIER | c.18+12208_18+12209d others(4): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50413222 | |||||
| chr12:50413508
|
T | C | 4 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0278others(1): Show | 4 | NA18959.hp1 NA19010.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+12480T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50413508 | ||||||
| chr12:50413639
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.18+12611G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50413639 | ||||||
| chr12:50413787
|
G | A | 259 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(256): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.18+12759G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50413787 | ||||||
| chr12:50413899
|
A | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0160 | 2 | HG02280.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.18+12871A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50413899 | ||||||
| chr12:50413923
|
C | T | 1 | a0001c0001t0002g0087 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.18+12895C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50413923 | ||||||
| chr12:50413927
|
T | C | 3 | a0001c0006t0007g0108a0001c0006t0007g0109a0001c0006t0007g0110 | 3 | HG01109.hp1 HG02572.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.18+12899T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50413927 | ||||||
| chr12:50414772
|
C | G | 1 | a0003c0003t0001g0171 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.19-12990C>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50414772 | ||||||
| chr12:50414985
|
A | T | 117 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(114): Show | 117 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(114): Show |
intron_variant | MODIFIER | c.19-12777A>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50414985 | ||||||
| chr12:50414993
|
A | G | 2 | a0001c0001t0020g0300a0001c0001t0021g0301 | 2 | HG02258.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.19-12769A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50414993 | ||||||
| chr12:50415011
|
T | C | 1 | a0001c0006t0007g0109 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.19-12751T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50415011 | ||||||
| chr12:50415202
|
C | T | 2 | a0001c0001t0001g0226a0001c0001t0001g0283 | 2 | HG03710.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.19-12560C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50415202 | ||||||
| chr12:50415238
|
T | G | 4 | a0001c0006t0007g0108a0001c0006t0007g0109a0001c0006t0007g0110others(1): Show | 4 | HG01109.hp1 HG02572.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.19-12524T>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50415238 | ||||||
| chr12:50415304
|
G | C | 5 | a0001c0001t0006g0273a0001c0001t0006g0274a0001c0001t0006g0275others(2): Show | 5 | HG02109.hp1 HG02559.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.19-12458G>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50415304 | ||||||
| chr12:50415495
|
T | C | 1 | a0001c0001t0001g0185 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.19-12267T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50415495 | ||||||
| chr12:50415695
|
TG | T | 4 | a0001c0001t0002g0052a0001c0001t0002g0054a0001c0001t0002g0055others(1): Show | 4 | HG01515.hp2 HG02922.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.19-12066delG | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50415695 | ||||||
| chr12:50415696
|
G | T | 127 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(124): Show | 127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.19-12066G>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50415696 | ||||||
| chr12:50415732
|
C | T | 1 | a0001c0001t0002g0141 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.19-12030C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50415732 | ||||||
| chr12:50416048
|
C | A | 118 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(115): Show | 118 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(115): Show |
intron_variant | MODIFIER | c.19-11714C>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50416048 | ||||||
| chr12:50416108
|
T | A | 1 | a0001c0001t0001g0161 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.19-11654T>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50416108 | ||||||
| chr12:50416170
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.19-11592G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50416170 | ||||||
| chr12:50416413
|
G | A | 1 | a0001c0001t0002g0133 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.19-11349G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50416413 | ||||||
| chr12:50416422
|
A | T | 259 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(256): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.19-11340A>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50416422 | ||||||
| chr12:50416784
|
C | G | 2 | a0001c0001t0004g0169a0001c0001t0004g0170 | 2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.19-10978C>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50416784 | ||||||
| chr12:50417048
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.19-10714C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50417048 | ||||||
| chr12:50417114
|
A | G | 2 | a0001c0001t0004g0169a0001c0001t0004g0170 | 2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.19-10648A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50417114 | ||||||
| chr12:50417191
|
C | T | 1 | a0001c0001t0013g0194 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.19-10571C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50417191 | ||||||
| chr12:50417346
|
GC | G | 118 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(115): Show | 118 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(115): Show |
intron_variant | MODIFIER | c.19-10414delC | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50417346 | |||||
| chr12:50417395
|
A | G | 1 | a0001c0001t0001g0262 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.19-10367A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50417395 | ||||||
| chr12:50417465
|
G | A | 2 | a0006c0008t0005g0037a0006c0008t0005g0038 | 2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.19-10297G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50417465 | ||||||
| chr12:50417513
|
A | G | 1 | a0001c0001t0002g0140 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.19-10249A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50417513 | ||||||
| chr12:50417597
|
G | A | 4 | a0001c0006t0007g0108a0001c0006t0007g0109a0001c0006t0007g0110others(1): Show | 4 | HG01109.hp1 HG02572.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.19-10165G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50417597 | ||||||
| chr12:50417921
|
C | A | 1 | a0001c0001t0001g0036 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.19-9841C>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50417921 | ||||||
| chr12:50417930
|
G | A | 39 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(36): Show | 39 | HG00140.hp2 HG00544.hp2 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.19-9832G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50417930 | ||||||
| chr12:50418016
|
A | G | 2 | a0001c0001t0002g0052a0001c0001t0002g0097 | 2 | HG01255.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.19-9746A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50418016 | ||||||
| chr12:50418140
|
T | C | 5 | a0001c0001t0006g0273a0001c0001t0006g0274a0001c0001t0006g0275others(2): Show | 5 | HG02109.hp1 HG02559.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.19-9622T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50418140 | ||||||
| chr12:50418148
|
A | C | 2 | a0006c0008t0005g0037a0006c0008t0005g0038 | 2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.19-9614A>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50418148 | ||||||
| chr12:50418366
|
A | C | 1 | a0001c0001t0015g0317 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.19-9396A>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50418366 | ||||||
| chr12:50418622
|
C | T | 5 | a0001c0001t0006g0273a0001c0001t0006g0274a0001c0001t0006g0275others(2): Show | 5 | HG02109.hp1 HG02559.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.19-9140C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50418622 | ||||||
| chr12:50418658
|
C | T | 5 | a0001c0001t0006g0273a0001c0001t0006g0274a0001c0001t0006g0275others(2): Show | 5 | HG02109.hp1 HG02559.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.19-9104C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50418658 | ||||||
| chr12:50418711
|
A | T | 2 | a0001c0001t0020g0300a0001c0001t0021g0301 | 2 | HG02258.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.19-9051A>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50418711 | ||||||
| chr12:50418775
|
A | G | 2 | a0001c0001t0002g0086a0001c0001t0002g0139 | 2 | HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.19-8987A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50418775 | ||||||
| chr12:50418797
|
T | G | 1 | a0001c0001t0015g0317 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.19-8965T>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50418797 | ||||||
| chr12:50418900
|
T | G | 2 | a0001c0001t0004g0149a0001c0001t0004g0150 | 2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.19-8862T>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50418900 | ||||||
| chr12:50418920
|
C | T | 1 | a0001c0001t0001g0245 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.19-8842C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50418920 | ||||||
| chr12:50418922
|
A | G | 2 | a0001c0001t0002g0049a0001c0001t0009g0048 | 2 | HG00741.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.19-8840A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50418922 | ||||||
| chr12:50419267
|
G | T | 53 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(50): Show | 53 | HG00597.hp1 HG00642.hp1 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.19-8495G>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50419267 | ||||||
| chr12:50419580
|
A | G | 2 | a0001c0001t0001g0226a0001c0001t0001g0283 | 2 | HG03710.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.19-8182A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50419580 | ||||||
| chr12:50419647
|
C | G | 1 | a0003c0003t0001g0153 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.19-8115C>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50419647 | ||||||
| chr12:50419763
|
C | T | 1 | a0001c0001t0001g0262 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.19-7999C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50419763 | ||||||
| chr12:50419880
|
G | C | 1 | a0001c0001t0002g0042 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.19-7882G>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50419880 | ||||||
| chr12:50420003
|
G | A | 2 | a0001c0001t0020g0300a0001c0001t0021g0301 | 2 | HG02258.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.19-7759G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50420003 | ||||||
| chr12:50420108
|
G | C | 2 | a0001c0001t0004g0149a0001c0001t0004g0150 | 2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.19-7654G>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50420108 | ||||||
| chr12:50420284
|
C | T | 2 | a0002c0002t0001g0217a0003c0003t0001g0180 | 2 | HG02040.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.19-7478C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50420284 | ||||||
| chr12:50420503
|
T | A | 1 | a0003c0003t0001g0153 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.19-7259T>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50420503 | ||||||
| chr12:50420782
|
G | A | 131 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.19-6980G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50420782 | ||||||
| chr12:50420947
|
C | CTTTT | 116 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(113): Show | 116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
intron_variant | MODIFIER | c.19-6801_19-6798dup others(4): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50420947 | |||||
| chr12:50420947
|
C | CTTTTTTT | 104 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(101): Show | 104 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(101): Show |
intron_variant | MODIFIER | c.19-6804_19-6798dup others(7): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50420947 | |||||
| chr12:50420947
|
C | CTTTTTTT others(1): Show |
14 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0216others(11): Show | 14 | HG01167.hp1 HG01261.hp1 HG01981.hp2 others(11): Show |
intron_variant | MODIFIER | c.19-6805_19-6798dup others(8): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50420947 | |||||
| chr12:50420947
|
C | CTTTTTTT others(10): Show |
2 | a0001c0001t0020g0300a0001c0001t0021g0301 | 2 | HG02258.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.19-6814_19-6798dup others(17): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50420947 | |||||
| chr12:50420947
|
C | CTTTTTTT others(14): Show |
2 | a0001c0001t0005g0145a0001c0001t0005g0147 | 2 | HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.19-6798_19-6797ins others(21): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50420947 | |||||
| chr12:50420947
|
C | CTTTTTTT others(15): Show |
2 | a0001c0001t0005g0146a0001c0001t0005g0148 | 2 | HG02258.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.19-6798_19-6797ins others(22): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50420947 | |||||
| chr12:50421139
|
C | CAG | 309 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(306): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.19-6623_19-6622ins others(2): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50421139 | ||||||
| chr12:50421145
|
C | T | 1 | a0001c0001t0015g0317 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.19-6617C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50421145 | ||||||
| chr12:50421166
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.19-6596G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50421166 | ||||||
| chr12:50421229
|
G | A | 1 | a0001c0001t0001g0195 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.19-6533G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50421229 | ||||||
| chr12:50421238
|
C | T | 2 | a0001c0001t0001g0270a0001c0001t0001g0293 | 2 | HG00673.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.19-6524C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50421238 | ||||||
| chr12:50421248
|
C | T | 1 | a0001c0001t0001g0036 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.19-6514C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50421248 | ||||||
| chr12:50421375
|
G | A | 2 | a0001c0001t0004g0149a0001c0001t0004g0150 | 2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.19-6387G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50421375 | ||||||
| chr12:50421410
|
G | A | 125 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(122): Show | 125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): Show |
intron_variant | MODIFIER | c.19-6352G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50421410 | ||||||
| chr12:50421461
|
G | A | 1 | a0001c0001t0003g0028 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.19-6301G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50421461 | ||||||
| chr12:50421643
|
A | AAAAT | 22 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0023others(19): Show | 22 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.19-6076_19-6073dup others(4): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50421643 | |||||
| chr12:50421643
|
A | AAAATAAA others(1): Show |
13 | a0001c0001t0001g0024a0001c0001t0001g0036a0001c0001t0001g0185others(10): Show | 13 | HG00140.hp2 HG01106.hp2 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.19-6080_19-6073dup others(8): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50421643 | |||||
| chr12:50421643
|
A | AAAATAAA others(5): Show |
2 | a0001c0001t0003g0028a0001c0001t0003g0034 | 2 | HG02109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.19-6084_19-6073dup others(12): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50421643 | |||||
| chr12:50421643
|
AAAAT | A | 5 | a0001c0001t0001g0266a0001c0001t0001g0299a0001c0001t0015g0317others(2): Show | 5 | HG02258.hp1 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.19-6076_19-6073del others(4): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50421643 | |||||
| chr12:50421643
|
AAAATAAA others(1): Show |
A | 90 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(87): Show | 90 | HG00597.hp1 HG00642.hp1 HG00673.hp2 others(87): Show |
intron_variant | MODIFIER | c.19-6080_19-6073del others(8): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50421643 | |||||
| chr12:50421643
|
AAAATAAA others(5): Show |
A | 38 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0231others(35): Show | 38 | HG00438.hp2 HG01167.hp1 HG01884.hp1 others(35): Show |
intron_variant | MODIFIER | c.19-6084_19-6073del others(12): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50421643 | |||||
| chr12:50421643
|
AAAATAAA others(13): Show |
A | 126 | a0001c0001t0001g0022a0001c0001t0002g0013a0001c0001t0002g0014others(123): Show | 126 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(123): Show |
intron_variant | MODIFIER | c.19-6092_19-6073del others(20): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50421643 | |||||
| chr12:50421715
|
A | G | 122 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(119): Show | 122 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(119): Show |
intron_variant | MODIFIER | c.19-6047A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50421715 | ||||||
| chr12:50421967
|
G | A | 4 | a0001c0006t0007g0108a0001c0006t0007g0109a0001c0006t0007g0110others(1): Show | 4 | HG01109.hp1 HG02572.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.19-5795G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50421967 | ||||||
| chr12:50421972
|
A | AT | 122 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(119): Show | 122 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(119): Show |
intron_variant | MODIFIER | c.19-5775dupT | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50421972 | |||||
| chr12:50422513
|
C | T | 122 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(119): Show | 122 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(119): Show |
intron_variant | MODIFIER | c.19-5249C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50422513 | ||||||
| chr12:50422523
|
A | C | 1 | a0001c0001t0002g0115 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.19-5239A>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50422523 | ||||||
| chr12:50422781
|
A | ATAT | 11 | a0001c0001t0001g0231a0001c0001t0001g0263a0001c0001t0002g0041others(8): Show | 11 | HG01891.hp2 HG02622.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.19-4931_19-4929dup others(3): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50422781 | |||||
| chr12:50422781
|
A | ATATTAT | 5 | a0001c0001t0002g0127a0001c0001t0002g0303a0001c0001t0003g0026others(2): Show | 5 | HG00673.hp1 HG01071.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.19-4934_19-4929dup others(6): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50422781 | |||||
| chr12:50422781
|
ATAT | A | 87 | a0001c0001t0001g0195a0001c0001t0001g0197a0001c0001t0001g0232others(84): Show | 87 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(84): Show |
intron_variant | MODIFIER | c.19-4931_19-4929del others(3): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50422781 | |||||
| chr12:50422781
|
ATATTAT | A | 36 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0022others(33): Show | 36 | HG00140.hp2 HG00544.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.19-4934_19-4929del others(6): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50422781 | |||||
| chr12:50422781
|
ATATTATT others(2): Show |
A | 39 | a0001c0001t0001g0161a0001c0001t0001g0167a0001c0001t0001g0172others(36): Show | 39 | HG00438.hp2 HG00597.hp2 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.19-4937_19-4929del others(9): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50422781 | |||||
| chr12:50422781
|
ATATTATT others(5): Show |
A | 84 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(81): Show | 84 | HG00597.hp1 HG00642.hp1 HG00673.hp2 others(81): Show |
intron_variant | MODIFIER | c.19-4940_19-4929del others(12): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50422781 | |||||
| chr12:50422781
|
ATATTATT others(11): Show |
A | 2 | a0001c0001t0001g0181a0003c0003t0001g0179 | 2 | HG02818.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.19-4946_19-4929del others(18): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50422781 | |||||
| chr12:50422781
|
ATATTATT others(14): Show |
A | 3 | a0001c0001t0006g0273a0001c0001t0006g0274a0001c0001t0006g0275 | 3 | HG02109.hp1 HG02647.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.19-4949_19-4929del others(21): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50422781 | |||||
| chr12:50422781
|
ATATTATT others(23): Show |
A | 4 | a0001c0006t0007g0108a0001c0006t0007g0109a0001c0006t0007g0110others(1): Show | 4 | HG01109.hp1 HG02572.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.19-4958_19-4929del others(30): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50422781 | |||||
| chr12:50422836
|
T | G | 1 | a0001c0001t0006g0294 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.19-4926T>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50422836 | ||||||
| chr12:50422842
|
G | A | 6 | a0001c0001t0003g0028a0001c0001t0003g0029a0001c0001t0003g0032others(3): Show | 6 | HG02109.hp2 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.19-4920G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50422842 | ||||||
| chr12:50422895
|
G | T | 1 | a0001c0001t0002g0115 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.19-4867G>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50422895 | ||||||
| chr12:50422991
|
T | A | 2 | a0001c0001t0002g0267a0001c0001t0002g0268 | 2 | NA18945.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.19-4771T>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50422991 | ||||||
| chr12:50422993
|
T | G | 2 | a0001c0001t0002g0267a0001c0001t0002g0268 | 2 | NA18945.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.19-4769T>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50422993 | ||||||
| chr12:50423051
|
C | A | 2 | a0001c0001t0020g0300a0001c0001t0021g0301 | 2 | HG02258.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.19-4711C>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50423051 | ||||||
| chr12:50423067
|
G | A | 1 | a0001c0001t0020g0300 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.19-4695G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50423067 | ||||||
| chr12:50423100
|
G | A | 4 | a0001c0001t0005g0145a0001c0001t0005g0146a0001c0001t0005g0147others(1): Show | 4 | HG02258.hp2 HG02922.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.19-4662G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50423100 | ||||||
| chr12:50423110
|
G | A | 1 | a0001c0001t0021g0301 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.19-4652G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50423110 | ||||||
| chr12:50423231
|
T | C | 1 | a0001c0001t0002g0018 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.19-4531T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50423231 | ||||||
| chr12:50423302
|
A | G | 1 | a0001c0001t0003g0032 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.19-4460A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50423302 | ||||||
| chr12:50423366
|
C | T | 4 | a0001c0006t0007g0108a0001c0006t0007g0109a0001c0006t0007g0110others(1): Show | 4 | HG01109.hp1 HG02572.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.19-4396C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50423366 | ||||||
| chr12:50423367
|
G | A | 1 | a0001c0001t0002g0070 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.19-4395G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50423367 | ||||||
| chr12:50423409
|
G | A | 1 | a0001c0001t0002g0116 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.19-4353G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50423409 | ||||||
| chr12:50423471
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.19-4291C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50423471 | ||||||
| chr12:50423515
|
C | T | 2 | a0001c0001t0004g0149a0001c0001t0004g0150 | 2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.19-4247C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50423515 | ||||||
| chr12:50423554
|
T | G | 11 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(8): Show | 11 | HG02257.hp1 HG02280.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.19-4208T>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50423554 | ||||||
| chr12:50423607
|
C | T | 1 | a0001c0001t0002g0151 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.19-4155C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50423607 | ||||||
| chr12:50423737
|
G | A | 4 | a0001c0006t0007g0108a0001c0006t0007g0109a0001c0006t0007g0110others(1): Show | 4 | HG01109.hp1 HG02572.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.19-4025G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50423737 | ||||||
| chr12:50423751
|
A | AT | 11 | a0001c0001t0001g0256a0001c0001t0001g0282a0001c0001t0001g0286others(8): Show | 11 | HG02258.hp2 HG02922.hp2 HG04115.hp1 others(8): Show |
intron_variant | MODIFIER | c.19-3993dupT | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50423751 | |||||
| chr12:50423770
|
A | T | 1 | a0001c0001t0001g0261 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.19-3992A>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50423770 | ||||||
| chr12:50423905
|
C | T | 2 | a0001c0001t0004g0149a0001c0001t0004g0150 | 2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.19-3857C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50423905 | ||||||
| chr12:50423957
|
T | C | 3 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197 | 3 | HG01891.hp1 HG06807.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.19-3805T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50423957 | ||||||
| chr12:50424034
|
C | T | 2 | a0001c0001t0004g0169a0001c0001t0004g0170 | 2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.19-3728C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50424034 | ||||||
| chr12:50424182
|
A | G | 2 | a0003c0003t0001g0165a0003c0003t0001g0186 | 2 | HG03017.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.19-3580A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50424182 | ||||||
| chr12:50424209
|
A | T | 118 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(115): Show | 118 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(115): Show |
intron_variant | MODIFIER | c.19-3553A>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50424209 | ||||||
| chr12:50424360
|
C | CT | 11 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(8): Show | 11 | HG01346.hp1 HG01891.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.19-3387dupT | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50424360 | |||||
| chr12:50424361
|
T | C | 3 | a0001c0001t0002g0122a0001c0001t0002g0151a0001c0001t0009g0059 | 3 | HG00741.hp1 HG01891.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.19-3401T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50424361 | ||||||
| chr12:50424388
|
C | T | 4 | a0001c0006t0007g0108a0001c0006t0007g0109a0001c0006t0007g0110others(1): Show | 4 | HG01109.hp1 HG02572.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.19-3374C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50424388 | ||||||
| chr12:50424486
|
G | C | 1 | a0001c0001t0002g0309 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.19-3276G>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50424486 | ||||||
| chr12:50424641
|
A | C | 2 | a0001c0001t0020g0300a0001c0001t0021g0301 | 2 | HG02258.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.19-3121A>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50424641 | ||||||
| chr12:50424783
|
A | G | 1 | a0001c0001t0002g0306 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.19-2979A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50424783 | ||||||
| chr12:50425006
|
A | G | 118 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(115): Show | 118 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(115): Show |
intron_variant | MODIFIER | c.19-2756A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50425006 | ||||||
| chr12:50425040
|
A | G | 2 | a0006c0008t0005g0037a0006c0008t0005g0038 | 2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.19-2722A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50425040 | ||||||
| chr12:50425133
|
C | T | 3 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197 | 3 | HG01891.hp1 HG06807.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.19-2629C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50425133 | ||||||
| chr12:50425179
|
G | C | 1 | a0001c0001t0002g0013 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.19-2583G>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50425179 | ||||||
| chr12:50425492
|
A | G | 1 | a0001c0001t0002g0068 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.19-2270A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50425492 | ||||||
| chr12:50425552
|
A | G | 1 | a0001c0001t0002g0086 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.19-2210A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50425552 | ||||||
| chr12:50425604
|
G | A | 2 | a0001c0001t0002g0054a0001c0001t0002g0098 | 2 | NA18989.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.19-2158G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50425604 | ||||||
| chr12:50425651
|
C | T | 1 | a0004c0004t0001g0198 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.19-2111C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50425651 | ||||||
| chr12:50425725
|
A | G | 3 | a0001c0001t0006g0273a0001c0001t0006g0274a0001c0001t0006g0275 | 3 | HG02109.hp1 HG02647.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.19-2037A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50425725 | ||||||
| chr12:50425765
|
A | G | 1 | a0001c0001t0002g0081 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.19-1997A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50425765 | ||||||
| chr12:50425814
|
CAT | C | 3 | a0005c0007t0002g0084a0005c0007t0002g0119a0005c0007t0002g0136 | 3 | HG00642.hp2 HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.19-1946_19-1945del others(2): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50425814 | |||||
| chr12:50425959
|
C | T | 120 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(117): Show | 120 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(117): Show |
intron_variant | MODIFIER | c.19-1803C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50425959 | ||||||
| chr12:50426526
|
T | A | 2 | a0001c0001t0020g0300a0001c0001t0021g0301 | 2 | HG02258.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.19-1236T>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50426526 | ||||||
| chr12:50426530
|
G | A | 317 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(314): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.19-1232G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50426530 | ||||||
| chr12:50426605
|
T | C | 3 | a0001c0001t0001g0174a0001c0001t0001g0188a0001c0001t0001g0189 | 3 | HG03209.hp1 HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.19-1157T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50426605 | ||||||
| chr12:50426663
|
G | T | 1 | a0001c0001t0001g0299 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.19-1099G>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50426663 | ||||||
| chr12:50426681
|
T | TGG | 6 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0219others(3): Show | 6 | HG01891.hp1 HG02027.hp2 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.19-1078_19-1077dup others(2): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50426681 | |||||
| chr12:50426684
|
G | GGGGTGTG others(3): Show |
1 | a0001c0001t0001g0022 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.19-1077_19-1076ins others(10): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50426684 | |||||
| chr12:50426684
|
G | GGGGTGTG others(5): Show |
1 | a0001c0001t0002g0113 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.19-1077_19-1076ins others(12): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50426684 | |||||
| chr12:50426684
|
G | GGGGTGTG others(9): Show |
1 | a0001c0001t0002g0093 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.19-1077_19-1076ins others(16): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50426684 | |||||
| chr12:50426684
|
G | GGT | 71 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(68): Show | 71 | HG00738.hp1 HG01069.hp2 HG01346.hp1 others(68): Show |
intron_variant | MODIFIER | c.19-1032_19-1031dup others(2): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50426684 | |||||
| chr12:50426684
|
G | GGTGT | 34 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0222others(31): Show | 34 | HG00438.hp1 HG01255.hp1 HG01261.hp2 others(31): Show |
intron_variant | MODIFIER | c.19-1034_19-1031dup others(4): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50426684 | |||||
| chr12:50426684
|
G | GGTGTGT | 6 | a0001c0001t0002g0041a0001c0001t0002g0046a0001c0001t0002g0047others(3): Show | 6 | HG00544.hp1 HG00741.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.19-1036_19-1031dup others(6): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50426684 | |||||
| chr12:50426684
|
G | GGTGTGTG others(1): Show |
4 | a0001c0001t0002g0051a0001c0001t0002g0055a0001c0001t0002g0100others(1): Show | 4 | HG00642.hp2 NA18954.hp1 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.19-1038_19-1031dup others(8): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50426684 | |||||
| chr12:50426684
|
G | GGTGTGTG others(3): Show |
2 | a0001c0001t0002g0067a0001c0001t0009g0048 | 2 | HG01074.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.19-1040_19-1031dup others(10): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50426684 | |||||
| chr12:50426684
|
G | GGTGTGTG others(7): Show |
3 | a0001c0001t0002g0039a0001c0001t0002g0094a0001c0001t0002g0131 | 3 | NA18967.hp2 NA19001.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.19-1044_19-1031dup others(14): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50426684 | |||||
| chr12:50426684
|
G | GGTGTGTG others(11): Show |
2 | a0001c0001t0002g0107a0001c0001t0002g0127 | 2 | HG00673.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.19-1048_19-1031dup others(18): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50426684 | |||||
| chr12:50426684
|
G | GTGTGTGT others(4): Show |
1 | a0001c0001t0002g0303 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.19-1078_19-1077ins others(11): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50426684 | ||||||
| chr12:50426684
|
G | GTGTGTGT others(8): Show |
1 | a0001c0001t0002g0144 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.19-1078_19-1077ins others(15): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50426684 | ||||||
| chr12:50426684
|
GGT | G | 26 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0001g0204others(23): Show | 26 | HG00597.hp1 HG01106.hp1 HG01361.hp1 others(23): Show |
intron_variant | MODIFIER | c.19-1032_19-1031del others(2): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50426684 | |||||
| chr12:50426684
|
GGTGT | G | 11 | a0001c0001t0001g0174a0001c0001t0001g0188a0001c0001t0001g0226others(8): Show | 11 | HG01109.hp2 HG01167.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.19-1034_19-1031del others(4): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50426684 | |||||
| chr12:50426684
|
GGTGTGT | G | 16 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(13): Show | 16 | HG02257.hp1 HG02257.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.19-1036_19-1031del others(6): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50426684 | |||||
| chr12:50426684
|
GGTGTGTG others(1): Show |
G | 25 | a0001c0001t0001g0164a0001c0001t0001g0167a0001c0001t0001g0168others(22): Show | 25 | HG00140.hp2 HG00544.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.19-1038_19-1031del others(8): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50426684 | |||||
| chr12:50426684
|
GGTGTGTG others(3): Show |
G | 6 | a0001c0001t0001g0036a0001c0001t0005g0145a0001c0001t0005g0146others(3): Show | 6 | HG02258.hp2 HG02630.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.19-1040_19-1031del others(10): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50426684 | |||||
| chr12:50426684
|
GGTGTGTG others(5): Show |
G | 1 | a0001c0001t0001g0206 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.19-1042_19-1031del others(12): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50426684 | |||||
| chr12:50426684
|
GGTGTGTG others(7): Show |
G | 4 | a0001c0001t0002g0040a0001c0001t0002g0060a0001c0001t0002g0106others(1): Show | 4 | HG00140.hp1 HG02280.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.19-1044_19-1031del others(14): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50426684 | |||||
| chr12:50426684
|
GGTGTGTG others(9): Show |
G | 2 | a0001c0001t0001g0270a0001c0001t0001g0293 | 2 | HG00673.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.19-1046_19-1031del others(16): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50426684 | |||||
| chr12:50426684
|
GGTGTGTG others(13): Show |
G | 3 | a0001c0006t0007g0108a0001c0006t0007g0109a0001c0006t0007g0110 | 3 | HG01109.hp1 HG02572.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.19-1050_19-1031del others(20): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50426684 | |||||
| chr12:50426684
|
GGTGTGTG others(15): Show |
G | 1 | a0001c0001t0001g0228 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.19-1052_19-1031del others(22): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50426684 | |||||
| chr12:50426686
|
T | G | 4 | a0001c0001t0001g0195a0001c0001t0001g0242a0001c0001t0001g0286others(1): Show | 4 | HG04115.hp1 HG04204.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.19-1076T>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50426686 | ||||||
| chr12:50426688
|
T | G | 7 | a0001c0001t0001g0299a0001c0001t0003g0028a0001c0001t0003g0029others(4): Show | 7 | HG02109.hp2 HG02258.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.19-1074T>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50426688 | ||||||
| chr12:50426690
|
T | G | 1 | a0001c0001t0004g0149 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.19-1072T>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50426690 | ||||||
| chr12:50426692
|
T | G | 12 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(9): Show | 12 | HG02257.hp1 HG02257.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.19-1070T>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50426692 | ||||||
| chr12:50426694
|
T | G | 3 | a0001c0001t0004g0170a0006c0008t0005g0037a0006c0008t0005g0038 | 3 | HG01884.hp2 HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.19-1068T>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50426694 | ||||||
| chr12:50426696
|
T | G | 4 | a0001c0001t0005g0145a0001c0001t0005g0146a0001c0001t0005g0147others(1): Show | 4 | HG02258.hp2 HG02922.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.19-1066T>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50426696 | ||||||
| chr12:50426706
|
T | G | 2 | a0001c0006t0007g0108a0001c0006t0007g0109 | 2 | HG02572.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.19-1056T>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50426706 | ||||||
| chr12:50426713
|
GTGTGTGT others(13): Show |
G | 1 | a0001c0010t0007g0111 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.19-1047_19-1028del others(20): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50426713 | |||||
| chr12:50426717
|
GTGTGTGT others(6): Show |
G | 1 | a0001c0001t0002g0069 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.19-1044_19-1032del others(13): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50426717 | ||||||
| chr12:50426732
|
G | GT | 11 | a0001c0001t0002g0016a0001c0001t0002g0044a0001c0001t0002g0052others(8): Show | 11 | HG01361.hp2 HG01515.hp2 HG02074.hp1 others(8): Show |
intron_variant | MODIFIER | c.19-1011dupT | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50426732 | |||||
| chr12:50426732
|
G | T | 1 | a0001c0001t0002g0130 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.19-1030G>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50426732 | ||||||
| chr12:50426732
|
GT | G | 140 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(137): Show | 140 | HG00140.hp2 HG00544.hp2 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.19-1011delT | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50426732 | |||||
| chr12:50426734
|
T | G | 1 | a0001c0001t0001g0216 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.19-1028T>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50426734 | ||||||
| chr12:50426995
|
C | T | 1 | a0001c0001t0015g0317 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.19-767C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50426995 | ||||||
| chr12:50427003
|
A | G | 302 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(299): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.19-759A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50427003 | ||||||
| chr12:50427062
|
T | C | 6 | a0001c0001t0004g0149a0001c0001t0004g0150a0001c0001t0005g0145others(3): Show | 6 | HG02257.hp2 HG02258.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.19-700T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50427062 | ||||||
| chr12:50427300
|
AAGTTATG others(5): Show |
A | 4 | a0001c0006t0007g0108a0001c0006t0007g0109a0001c0006t0007g0110others(1): Show | 4 | HG01109.hp1 HG02572.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.19-457_19-446delAT others(10): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 50427300 | |||||
| chr12:50427357
|
C | T | 317 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(314): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.19-405C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50427357 | ||||||
| chr12:50427402
|
T | C | 317 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(314): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.19-360T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50427402 | ||||||
| chr12:50427555
|
C | T | 117 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(114): Show | 117 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(114): Show |
intron_variant | MODIFIER | c.19-207C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50427555 | ||||||
| chr12:50427600
|
C | T | 5 | a0001c0001t0002g0306a0001c0001t0002g0311a0001c0001t0002g0312others(2): Show | 5 | HG01255.hp2 HG01515.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.19-162C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50427600 | ||||||
| chr12:50427678
|
G | A | 2 | a0001c0001t0001g0177a0001c0001t0001g0190 | 2 | HG04199.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.19-84G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50427678 | ||||||
| chr12:50427725
|
T | C | 1 | a0001c0001t0002g0067 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.19-37T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50427725 | ||||||
| chr12:50427993
|
C | CT | 275 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(272): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.166+104dupT | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 50427993 | |||||
| chr12:50427993
|
C | CTT | 23 | a0001c0001t0001g0009a0001c0001t0001g0181a0001c0001t0001g0213others(20): Show | 23 | HG00140.hp1 HG01167.hp1 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.166+103_166+104dup others(2): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 50427993 | |||||
| chr12:50428175
|
C | T | 117 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(114): Show | 117 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(114): Show |
intron_variant | MODIFIER | c.166+266C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 2/15 | chr12 | 50428175 | ||||||
| chr12:50428220
|
G | T | 1 | a0001c0001t0002g0057 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.166+311G>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 2/15 | chr12 | 50428220 | ||||||
| chr12:50428326
|
C | T | 117 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(114): Show | 117 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(114): Show |
intron_variant | MODIFIER | c.166+417C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 2/15 | chr12 | 50428326 | ||||||
| chr12:50428333
|
A | G | 117 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(114): Show | 117 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(114): Show |
intron_variant | MODIFIER | c.166+424A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 2/15 | chr12 | 50428333 | ||||||
| chr12:50428516
|
A | G | 2 | a0001c0001t0002g0041a0001c0001t0002g0112 | 2 | NA18995.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.167-419A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 2/15 | chr12 | 50428516 | ||||||
| chr12:50428888
|
G | T | 5 | a0001c0001t0002g0051a0001c0001t0002g0055a0001c0001t0002g0072others(2): Show | 5 | NA18954.hp1 NA18959.hp2 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.167-47G>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 2/15 | chr12 | 50428888 | ||||||
| chr12:50429310
|
A | G | 39 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(36): Show | 39 | HG00140.hp2 HG00544.hp2 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.322+220A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 3/15 | chr12 | 50429310 | ||||||
| chr12:50429362
|
C | T | 1 | a0001c0001t0002g0081 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.322+272C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 3/15 | chr12 | 50429362 | ||||||
| chr12:50429442
|
C | T | 307 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(304): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.322+352C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 3/15 | chr12 | 50429442 | ||||||
| chr12:50429476
|
G | A | 117 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(114): Show | 117 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(114): Show |
intron_variant | MODIFIER | c.322+386G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 3/15 | chr12 | 50429476 | ||||||
| chr12:50429518
|
C | G | 1 | a0001c0001t0005g0146 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.322+428C>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 3/15 | chr12 | 50429518 | ||||||
| chr12:50429611
|
T | C | 1 | a0001c0010t0007g0111 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.322+521T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 3/15 | chr12 | 50429611 | ||||||
| chr12:50429643
|
T | G | 1 | a0001c0001t0002g0303 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.322+553T>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 3/15 | chr12 | 50429643 | ||||||
| chr12:50429702
|
G | C | 2 | a0001c0001t0002g0052a0001c0001t0002g0097 | 2 | HG01255.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.322+612G>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 3/15 | chr12 | 50429702 | ||||||
| chr12:50429826
|
A | G | 2 | a0001c0001t0020g0300a0001c0001t0021g0301 | 2 | HG02258.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.323-669A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 3/15 | chr12 | 50429826 | ||||||
| chr12:50429920
|
G | A | 4 | a0001c0006t0007g0108a0001c0006t0007g0109a0001c0006t0007g0110others(1): Show | 4 | HG01109.hp1 HG02572.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.323-575G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 3/15 | chr12 | 50429920 | ||||||
| chr12:50429983
|
G | A | 255 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(252): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.323-512G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 3/15 | chr12 | 50429983 | ||||||
| chr12:50430095
|
G | A | 67 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(64): Show | 67 | HG00438.hp1 HG00642.hp2 HG00673.hp1 others(64): Show |
intron_variant | MODIFIER | c.323-400G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 3/15 | chr12 | 50430095 | ||||||
| chr12:50430151
|
AG | A | 136 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.323-343delG | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 3/15 | chr12 | 50430151 | ||||||
| chr12:50430152
|
G | A | 4 | a0001c0006t0007g0108a0001c0006t0007g0109a0001c0006t0007g0110others(1): Show | 4 | HG01109.hp1 HG02572.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.323-343G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 3/15 | chr12 | 50430152 | ||||||
| chr12:50430255
|
T | C | 1 | a0001c0001t0001g0199 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.323-240T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 3/15 | chr12 | 50430255 | ||||||
| chr12:50430418
|
A | G | 17 | a0001c0001t0001g0231a0001c0001t0001g0233a0001c0001t0001g0234others(14): Show | 17 | HG00438.hp2 HG02155.hp1 HG03491.hp2 others(14): Show |
intron_variant | MODIFIER | c.323-77A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 3/15 | chr12 | 50430418 | ||||||
| chr12:50430425
|
C | T | 2 | a0001c0001t0020g0300a0001c0001t0021g0301 | 2 | HG02258.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.323-70C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 3/15 | chr12 | 50430425 | ||||||
| chr12:50430449
|
A | G | 54 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(51): Show | 54 | HG00438.hp1 HG01109.hp2 HG01255.hp1 others(51): Show |
intron_variant | MODIFIER | c.323-46A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 3/15 | chr12 | 50430449 | ||||||
| chr12:50430492
|
C | G | 117 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(114): Show | 117 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(114): Show |
splice_region_variant&intron_variant | LOW | c.323-3C>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 3/15 | chr12 | 50430492 | ||||||
| chr12:50430492
|
C | T | 1 | a0001c0001t0002g0077 | 1 | HG01169.hp1 | splice_region_variant&intron_variant | LOW | c.323-3C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 3/15 | chr12 | 50430492 | ||||||
| chr12:50430693
|
ATGT | A | 4 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(1): Show | 4 | HG02055.hp1 HG02615.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.398+127_398+129del others(3): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 50430693 | |||||
| chr12:50430848
|
G | A | 1 | a0001c0001t0002g0144 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.398+278G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 4/15 | chr12 | 50430848 | ||||||
| chr12:50431029
|
A | G | 117 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(114): Show | 117 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(114): Show |
intron_variant | MODIFIER | c.398+459A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 4/15 | chr12 | 50431029 | ||||||
| chr12:50431157
|
A | T | 1 | a0001c0001t0001g0261 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.398+587A>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 4/15 | chr12 | 50431157 | ||||||
| chr12:50431172
|
G | A | 3 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0245 | 3 | HG01167.hp1 HG02965.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.398+602G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 4/15 | chr12 | 50431172 | ||||||
| chr12:50431199
|
C | T | 1 | a0001c0001t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.398+629C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 4/15 | chr12 | 50431199 | ||||||
| chr12:50431493
|
A | G | 117 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(114): Show | 117 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(114): Show |
intron_variant | MODIFIER | c.398+923A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 4/15 | chr12 | 50431493 | ||||||
| chr12:50431749
|
A | G | 2 | a0001c0001t0001g0213a0001c0001t0001g0256 | 2 | HG02129.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.398+1179A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 4/15 | chr12 | 50431749 | ||||||
| chr12:50431769
|
C | T | 1 | a0001c0001t0004g0170 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.398+1199C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 4/15 | chr12 | 50431769 | ||||||
| chr12:50431964
|
T | G | 259 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(256): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.398+1394T>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 4/15 | chr12 | 50431964 | ||||||
| chr12:50431976
|
G | A | 136 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.398+1406G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 4/15 | chr12 | 50431976 | ||||||
| chr12:50431985
|
A | G | 1 | a0001c0001t0015g0317 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.398+1415A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 4/15 | chr12 | 50431985 | ||||||
| chr12:50431997
|
G | A | 1 | a0001c0001t0015g0317 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.398+1427G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 4/15 | chr12 | 50431997 | ||||||
| chr12:50432052
|
C | A | 1 | a0001c0001t0001g0036 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.398+1482C>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 4/15 | chr12 | 50432052 | ||||||
| chr12:50432065
|
T | TG | 117 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(114): Show | 117 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(114): Show |
intron_variant | MODIFIER | c.398+1496dupG | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 50432065 | |||||
| chr12:50432671
|
C | G | 1 | a0001c0001t0002g0144 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.398+2101C>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 4/15 | chr12 | 50432671 | ||||||
| chr12:50432860
|
C | CA | 42 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(39): Show | 42 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.398+2307dupA | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 50432860 | |||||
| chr12:50432860
|
C | CAA | 123 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.398+2306_398+2307d others(4): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 50432860 | |||||
| chr12:50432860
|
C | CAAA | 7 | a0001c0001t0001g0177a0001c0001t0001g0190a0001c0001t0002g0042others(4): Show | 7 | HG02559.hp1 HG02559.hp2 HG04199.hp1 others(4): Show |
intron_variant | MODIFIER | c.398+2305_398+2307d others(5): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 50432860 | |||||
| chr12:50432916
|
G | A | 1 | a0001c0001t0003g0034 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.398+2346G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 4/15 | chr12 | 50432916 | ||||||
| chr12:50433146
|
A | G | 1 | a0001c0001t0001g0224 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.399-2342A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 4/15 | chr12 | 50433146 | ||||||
| chr12:50433265
|
C | T | 117 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(114): Show | 117 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(114): Show |
intron_variant | MODIFIER | c.399-2223C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 4/15 | chr12 | 50433265 | ||||||
| chr12:50433269
|
A | ATT | 93 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(90): Show | 93 | HG00597.hp1 HG00642.hp1 HG00673.hp2 others(90): Show |
intron_variant | MODIFIER | c.399-2200_399-2199d others(4): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 50433269 | |||||
| chr12:50433269
|
A | ATTT | 18 | a0001c0001t0001g0011a0001c0001t0001g0197a0001c0001t0001g0242others(15): Show | 18 | HG00438.hp2 HG01361.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.399-2201_399-2199d others(5): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 50433269 | |||||
| chr12:50433269
|
AT | A | 23 | a0001c0001t0001g0164a0001c0001t0001g0174a0001c0001t0001g0188others(20): Show | 23 | HG00438.hp1 HG01109.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.399-2199delT | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 50433269 | |||||
| chr12:50433269
|
ATT | A | 117 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(114): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.399-2200_399-2199d others(4): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 50433269 | |||||
| chr12:50433437
|
G | T | 1 | a0001c0001t0002g0268 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.399-2051G>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 4/15 | chr12 | 50433437 | ||||||
| chr12:50433640
|
CT | C | 105 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0192others(102): Show | 105 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(102): Show |
intron_variant | MODIFIER | c.399-1832delT | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 50433640 | |||||
| chr12:50433708
|
C | T | 2 | a0001c0001t0002g0107a0001c0001t0002g0113 | 2 | HG00597.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.399-1780C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 4/15 | chr12 | 50433708 | ||||||
| chr12:50433786
|
C | T | 119 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(116): Show | 119 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(116): Show |
intron_variant | MODIFIER | c.399-1702C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 4/15 | chr12 | 50433786 | ||||||
| chr12:50433869
|
A | G | 136 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.399-1619A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 4/15 | chr12 | 50433869 | ||||||
| chr12:50433898
|
C | G | 1 | a0001c0001t0001g0237 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.399-1590C>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 4/15 | chr12 | 50433898 | ||||||
| chr12:50434405
|
A | C | 1 | a0001c0001t0001g0223 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.399-1083A>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 4/15 | chr12 | 50434405 | ||||||
| chr12:50434543
|
C | T | 1 | a0001c0001t0014g0238 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.399-945C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 4/15 | chr12 | 50434543 | ||||||
| chr12:50434590
|
A | G | 1 | a0001c0006t0007g0110 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.399-898A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 4/15 | chr12 | 50434590 | ||||||
| chr12:50434721
|
T | C | 1 | a0001c0006t0007g0108 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.399-767T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 4/15 | chr12 | 50434721 | ||||||
| chr12:50434941
|
G | A | 2 | a0001c0001t0001g0247a0001c0001t0001g0291 | 2 | NA19079.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.399-547G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 4/15 | chr12 | 50434941 | ||||||
| chr12:50435269
|
G | A | 110 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(107): Show | 110 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(107): Show |
intron_variant | MODIFIER | c.399-219G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 4/15 | chr12 | 50435269 | ||||||
| chr12:50435480
|
T | TTATTC | 262 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(259): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
splice_region_variant&intron_variant | LOW | c.399-7_399-6insATTC others(1): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 50435480 | |||||
| chr12:50435637
|
A | G | 2 | a0006c0008t0005g0037a0006c0008t0005g0038 | 2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.535+13A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 5/15 | chr12 | 50435637 | ||||||
| chr12:50435655
|
T | A | 1 | a0001c0001t0002g0042 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.535+31T>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 5/15 | chr12 | 50435655 | ||||||
| chr12:50435671
|
A | C | 1 | a0001c0001t0002g0129 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.535+47A>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 5/15 | chr12 | 50435671 | ||||||
| chr12:50435689
|
G | C | 1 | a0001c0001t0015g0317 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.535+65G>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 5/15 | chr12 | 50435689 | ||||||
| chr12:50435768
|
T | A | 4 | a0001c0006t0007g0108a0001c0006t0007g0109a0001c0006t0007g0110others(1): Show | 4 | HG01109.hp1 HG02572.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.535+144T>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 5/15 | chr12 | 50435768 | ||||||
| chr12:50435922
|
C | T | 1 | a0001c0001t0002g0085 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.535+298C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 5/15 | chr12 | 50435922 | ||||||
| chr12:50435968
|
G | A | 1 | a0002c0002t0001g0207 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.535+344G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 5/15 | chr12 | 50435968 | ||||||
| chr12:50435998
|
T | TA | 259 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(256): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.535+374_535+375ins others(1): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 5/15 | chr12 | 50435998 | ||||||
| chr12:50435999
|
T | A | 259 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(256): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.535+375T>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 5/15 | chr12 | 50435999 | ||||||
| chr12:50436051
|
C | CTG | 8 | a0001c0001t0003g0026a0001c0001t0003g0028a0001c0001t0003g0029others(5): Show | 8 | HG01069.hp1 HG01071.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.535+467_535+468dup others(2): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 50436051 | |||||
| chr12:50436051
|
C | G | 2 | a0001c0001t0020g0300a0001c0001t0021g0301 | 2 | HG02258.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.535+427C>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 5/15 | chr12 | 50436051 | ||||||
| chr12:50436051
|
CTG | C | 7 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0023others(4): Show | 7 | HG02055.hp1 HG02630.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.535+467_535+468del others(2): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 50436051 | |||||
| chr12:50436051
|
CTGTG | C | 7 | a0001c0001t0001g0022a0001c0001t0001g0156a0001c0001t0001g0157others(4): Show | 7 | HG02257.hp1 HG02257.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.535+465_535+468del others(4): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 50436051 | |||||
| chr12:50436051
|
CTGTGTG | C | 12 | a0001c0001t0001g0155a0001c0001t0001g0159a0001c0001t0001g0160others(9): Show | 12 | HG01167.hp1 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.535+463_535+468del others(6): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 50436051 | |||||
| chr12:50436051
|
CTGTGTGT others(1): Show |
C | 40 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0161others(37): Show | 40 | HG00140.hp2 HG00544.hp2 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.535+461_535+468del others(8): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 50436051 | |||||
| chr12:50436051
|
CTGTGTGT others(3): Show |
C | 74 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(71): Show | 74 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.535+459_535+468del others(10): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 50436051 | |||||
| chr12:50436051
|
CTGTGTGT others(5): Show |
C | 27 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(24): Show | 27 | HG01109.hp1 HG01361.hp1 HG01361.hp2 others(24): Show |
intron_variant | MODIFIER | c.535+457_535+468del others(12): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 50436051 | |||||
| chr12:50436051
|
CTGTGTGT others(7): Show |
C | 12 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(9): Show | 12 | HG01928.hp2 HG01943.hp2 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.535+455_535+468del others(14): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 50436051 | |||||
| chr12:50436051
|
CTGTGTGT others(9): Show |
C | 121 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0039others(118): Show | 121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.535+453_535+468del others(16): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 50436051 | |||||
| chr12:50436051
|
CTGTGTGT others(11): Show |
C | 2 | a0001c0001t0002g0121a0001c0001t0002g0125 | 2 | NA18975.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.535+451_535+468del others(18): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 50436051 | |||||
| chr12:50436051
|
CTGTGTGT others(17): Show |
C | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | NA18948.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.535+445_535+468del others(24): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 50436051 | |||||
| chr12:50436068
|
TGTGTGTG others(26): Show |
T | 1 | a0001c0001t0021g0301 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.535+464_535+496del others(33): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 50436068 | |||||
| chr12:50436070
|
TGTGTGTG others(24): Show |
T | 1 | a0001c0001t0020g0300 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.535+466_535+496del others(31): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 50436070 | |||||
| chr12:50436101
|
G | GGT | 291 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(288): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.535+495_535+496dup others(2): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 50436101 | |||||
| chr12:50436101
|
G | GGTGT | 5 | a0001c0001t0001g0161a0001c0001t0002g0052a0001c0001t0002g0086others(2): Show | 5 | HG01255.hp1 HG01515.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.535+493_535+496dup others(4): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 50436101 | |||||
| chr12:50436101
|
GGTGTGTG others(16): Show |
G | 1 | a0001c0001t0001g0199 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.535+494_535+516del others(23): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 50436101 | |||||
| chr12:50436108
|
GTGTGTGT others(8): Show |
G | 2 | a0001c0006t0007g0110a0001c0010t0007g0111 | 2 | HG01109.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.535+497_535+511del others(15): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 50436108 | |||||
| chr12:50436110
|
GTGTGTGT others(6): Show |
G | 2 | a0001c0006t0007g0108a0001c0006t0007g0109 | 2 | HG02572.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.535+497_535+509del others(13): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 50436110 | |||||
| chr12:50436121
|
A | T | 1 | a0001c0001t0001g0258 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.535+497A>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 5/15 | chr12 | 50436121 | ||||||
| chr12:50436122
|
T | G | 1 | a0001c0001t0001g0258 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.535+498T>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 5/15 | chr12 | 50436122 | ||||||
| chr12:50436123
|
A | G | 6 | a0001c0001t0001g0219a0001c0001t0002g0094a0001c0001t0006g0273others(3): Show | 6 | HG02109.hp1 HG02647.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.535+499A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 5/15 | chr12 | 50436123 | ||||||
| chr12:50436127
|
G | A | 1 | a0001c0001t0001g0258 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.535+503G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 5/15 | chr12 | 50436127 | ||||||
| chr12:50436139
|
GTAT | G | 4 | a0001c0006t0007g0108a0001c0006t0007g0109a0001c0006t0007g0110others(1): Show | 4 | HG01109.hp1 HG02572.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.535+516_535+518del others(3): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 5/15 | chr12 | 50436139 | ||||||
| chr12:50436145
|
ATCCCGCT others(4): Show |
A | 4 | a0001c0006t0007g0108a0001c0006t0007g0109a0001c0006t0007g0110others(1): Show | 4 | HG01109.hp1 HG02572.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.535+523_535+533del others(11): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 50436145 | |||||
| chr12:50436169
|
T | A | 1 | a0001c0001t0003g0034 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.535+545T>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 5/15 | chr12 | 50436169 | ||||||
| chr12:50436174
|
G | GTA | 6 | a0001c0001t0005g0145a0001c0001t0005g0146a0001c0001t0005g0147others(3): Show | 6 | HG02258.hp2 HG02922.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.535+570_535+571dup others(2): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 50436174 | |||||
| chr12:50436174
|
GTA | G | 225 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(222): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.535+570_535+571del others(2): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 50436174 | |||||
| chr12:50436194
|
A | C | 3 | a0001c0006t0007g0109a0001c0006t0007g0110a0001c0010t0007g0111 | 3 | HG01109.hp1 HG02572.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.535+570A>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 5/15 | chr12 | 50436194 | ||||||
| chr12:50436217
|
G | A | 1 | a0001c0001t0005g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.535+593G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 5/15 | chr12 | 50436217 | ||||||
| chr12:50436221
|
T | G | 1 | a0001c0001t0001g0277 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.535+597T>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 5/15 | chr12 | 50436221 | ||||||
| chr12:50436264
|
T | C | 261 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(258): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.535+640T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 5/15 | chr12 | 50436264 | ||||||
| chr12:50436356
|
T | G | 4 | a0001c0001t0006g0273a0001c0001t0006g0274a0001c0001t0006g0275others(1): Show | 4 | HG02109.hp1 HG02647.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.535+732T>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 5/15 | chr12 | 50436356 | ||||||
| chr12:50436463
|
T | A | 2 | a0001c0001t0004g0149a0001c0001t0004g0150 | 2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.535+839T>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 5/15 | chr12 | 50436463 | ||||||
| chr12:50436468
|
C | T | 2 | a0001c0001t0003g0030a0001c0001t0003g0031 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.535+844C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 5/15 | chr12 | 50436468 | ||||||
| chr12:50436874
|
A | G | 3 | a0001c0001t0002g0100a0001c0001t0020g0300a0001c0001t0021g0301 | 3 | HG02258.hp1 HG03486.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.536-861A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 5/15 | chr12 | 50436874 | ||||||
| chr12:50437111
|
T | C | 255 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(252): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.536-624T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 5/15 | chr12 | 50437111 | ||||||
| chr12:50437366
|
A | G | 1 | a0001c0001t0015g0317 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.536-369A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 5/15 | chr12 | 50437366 | ||||||
| chr12:50437433
|
A | G | 3 | a0001c0001t0001g0174a0001c0001t0001g0188a0001c0001t0001g0189 | 3 | HG03209.hp1 HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.536-302A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 5/15 | chr12 | 50437433 | ||||||
| chr12:50437524
|
A | G | 2 | a0001c0001t0003g0028a0001c0001t0003g0029 | 2 | HG02109.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.536-211A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 5/15 | chr12 | 50437524 | ||||||
| chr12:50437548
|
T | C | 3 | a0001c0006t0007g0108a0001c0006t0007g0109a0001c0006t0007g0110 | 3 | HG01109.hp1 HG02572.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.536-187T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 5/15 | chr12 | 50437548 | ||||||
| chr12:50437618
|
T | C | 121 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(118): Show | 121 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(118): Show |
intron_variant | MODIFIER | c.536-117T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 5/15 | chr12 | 50437618 | ||||||
| chr12:50437973
|
C | T | 4 | a0001c0006t0007g0108a0001c0006t0007g0109a0001c0006t0007g0110others(1): Show | 4 | HG01109.hp1 HG02572.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.639+135C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 6/15 | chr12 | 50437973 | ||||||
| chr12:50438006
|
A | C | 1 | a0003c0003t0001g0153 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.639+168A>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 6/15 | chr12 | 50438006 | ||||||
| chr12:50438047
|
T | C | 1 | a0001c0001t0015g0317 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.639+209T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 6/15 | chr12 | 50438047 | ||||||
| chr12:50438223
|
G | A | 5 | a0001c0001t0001g0164a0001c0001t0001g0167a0001c0001t0001g0168others(2): Show | 5 | HG01167.hp2 HG01169.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.639+385G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 6/15 | chr12 | 50438223 | ||||||
| chr12:50438283
|
G | C | 4 | a0001c0001t0005g0145a0001c0001t0005g0146a0001c0001t0005g0147others(1): Show | 4 | HG02258.hp2 HG02922.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.639+445G>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 6/15 | chr12 | 50438283 | ||||||
| chr12:50438492
|
C | CA | 124 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(121): Show | 124 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.639+666dupA | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 50438492 | |||||
| chr12:50438492
|
C | CAA | 7 | a0001c0001t0002g0086a0001c0001t0002g0090a0001c0001t0002g0106others(4): Show | 7 | HG00140.hp1 HG01346.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.639+665_639+666dup others(2): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 50438492 | |||||
| chr12:50438589
|
C | T | 1 | a0001c0001t0002g0085 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.639+751C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 6/15 | chr12 | 50438589 | ||||||
| chr12:50438788
|
A | G | 2 | a0001c0001t0002g0060a0001c0001t0002g0069 | 2 | NA18997.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.639+950A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 6/15 | chr12 | 50438788 | ||||||
| chr12:50438838
|
G | A | 7 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(4): Show | 7 | HG01361.hp2 HG01928.hp2 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.639+1000G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 6/15 | chr12 | 50438838 | ||||||
| chr12:50439037
|
A | C | 1 | a0001c0001t0004g0202 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.639+1199A>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 6/15 | chr12 | 50439037 | ||||||
| chr12:50439169
|
G | A | 2 | a0006c0008t0005g0037a0006c0008t0005g0038 | 2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.640-1270G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 6/15 | chr12 | 50439169 | ||||||
| chr12:50439178
|
A | G | 121 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(118): Show | 121 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(118): Show |
intron_variant | MODIFIER | c.640-1261A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 6/15 | chr12 | 50439178 | ||||||
| chr12:50439198
|
C | T | 1 | a0001c0010t0007g0111 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.640-1241C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 6/15 | chr12 | 50439198 | ||||||
| chr12:50439296
|
C | G | 1 | a0001c0001t0001g0225 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.640-1143C>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 6/15 | chr12 | 50439296 | ||||||
| chr12:50439308
|
A | T | 2 | a0001c0001t0020g0300a0001c0001t0021g0301 | 2 | HG02258.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.640-1131A>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 6/15 | chr12 | 50439308 | ||||||
| chr12:50439361
|
T | G | 1 | a0001c0001t0006g0294 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.640-1078T>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 6/15 | chr12 | 50439361 | ||||||
| chr12:50439410
|
C | A | 1 | a0001c0001t0019g0134 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.640-1029C>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 6/15 | chr12 | 50439410 | ||||||
| chr12:50439460
|
TG | T | 4 | a0001c0006t0007g0108a0001c0006t0007g0109a0001c0006t0007g0110others(1): Show | 4 | HG01109.hp1 HG02572.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.640-977delG | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 50439460 | |||||
| chr12:50439802
|
A | G | 2 | a0001c0001t0002g0103a0001c0001t0002g0120 | 2 | HG01346.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.640-637A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 6/15 | chr12 | 50439802 | ||||||
| chr12:50439954
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.640-485C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 6/15 | chr12 | 50439954 | ||||||
| chr12:50440225
|
C | T | 4 | a0001c0006t0007g0108a0001c0006t0007g0109a0001c0006t0007g0110others(1): Show | 4 | HG01109.hp1 HG02572.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.640-214C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 6/15 | chr12 | 50440225 | ||||||
| chr12:50440251
|
A | G | 2 | a0001c0001t0002g0068a0001c0001t0002g0099 | 2 | HG02602.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.640-188A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 6/15 | chr12 | 50440251 | ||||||
| chr12:50440385
|
A | T | 1 | a0001c0001t0001g0279 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.640-54A>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 6/15 | chr12 | 50440385 | ||||||
| chr12:50440593
|
A | G | 4 | a0001c0006t0007g0108a0001c0006t0007g0109a0001c0006t0007g0110others(1): Show | 4 | HG01109.hp1 HG02572.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.750+44A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 7/15 | chr12 | 50440593 | ||||||
| chr12:50440887
|
C | CT | 6 | a0001c0001t0002g0043a0001c0001t0002g0302a0001c0006t0007g0110others(3): Show | 6 | HG01109.hp1 HG02976.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.750+352dupT | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr12 | 50440887 | |||||
| chr12:50440922
|
C | T | 4 | a0001c0006t0007g0108a0001c0006t0007g0109a0001c0006t0007g0110others(1): Show | 4 | HG01109.hp1 HG02572.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.750+373C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 7/15 | chr12 | 50440922 | ||||||
| chr12:50440944
|
C | T | 1 | a0001c0001t0002g0071 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.750+395C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 7/15 | chr12 | 50440944 | ||||||
| chr12:50440948
|
A | G | 2 | a0001c0001t0020g0300a0001c0001t0021g0301 | 2 | HG02258.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.750+399A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 7/15 | chr12 | 50440948 | ||||||
| chr12:50440966
|
C | T | 1 | a0001c0001t0001g0292 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.750+417C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 7/15 | chr12 | 50440966 | ||||||
| chr12:50441179
|
G | A | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | NA18948.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.751-411G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 7/15 | chr12 | 50441179 | ||||||
| chr12:50441233
|
A | C | 1 | a0001c0001t0002g0100 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.751-357A>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 7/15 | chr12 | 50441233 | ||||||
| chr12:50441277
|
A | G | 262 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(259): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.751-313A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 7/15 | chr12 | 50441277 | ||||||
| chr12:50441702
|
T | A | 1 | a0001c0001t0002g0152 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.804+59T>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50441702 | ||||||
| chr12:50441775
|
G | T | 4 | a0001c0001t0001g0242a0001c0001t0001g0286a0001c0001t0001g0292others(1): Show | 4 | HG04115.hp1 HG04204.hp1 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.804+132G>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50441775 | ||||||
| chr12:50441808
|
G | A | 1 | a0001c0001t0001g0318 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.804+165G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50441808 | ||||||
| chr12:50441906
|
C | T | 1 | a0001c0001t0015g0317 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.804+263C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50441906 | ||||||
| chr12:50442306
|
C | T | 3 | a0001c0001t0008g0158a0001c0001t0008g0183a0001c0001t0008g0184 | 3 | HG02451.hp2 HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.804+663C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50442306 | ||||||
| chr12:50442386
|
T | G | 4 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0264others(1): Show | 4 | HG02155.hp1 NA18957.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.804+743T>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50442386 | ||||||
| chr12:50442477
|
T | C | 8 | a0001c0001t0002g0089a0001c0001t0002g0090a0001c0001t0002g0091others(5): Show | 8 | HG00438.hp1 NA18961.hp2 NA18984.hp1 others(5): Show |
intron_variant | MODIFIER | c.804+834T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50442477 | ||||||
| chr12:50442620
|
ATTC | A | 4 | a0001c0001t0001g0006a0001c0001t0001g0218a0001c0001t0001g0219others(1): Show | 4 | NA18612.hp2 NA18964.hp2 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.804+980_804+982del others(3): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50442620 | |||||
| chr12:50443303
|
C | G | 6 | a0001c0001t0005g0145a0001c0001t0005g0146a0001c0001t0005g0147others(3): Show | 6 | HG02258.hp2 HG02922.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.804+1660C>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50443303 | ||||||
| chr12:50443320
|
G | A | 2 | a0001c0001t0002g0086a0001c0001t0002g0139 | 2 | HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.804+1677G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50443320 | ||||||
| chr12:50443408
|
C | A | 117 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(114): Show | 117 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(114): Show |
intron_variant | MODIFIER | c.804+1765C>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50443408 | ||||||
| chr12:50443467
|
A | G | 2 | a0001c0001t0004g0149a0001c0001t0004g0150 | 2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.804+1824A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50443467 | ||||||
| chr12:50443506
|
G | A | 300 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(297): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.804+1863G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50443506 | ||||||
| chr12:50443654
|
C | G | 1 | a0001c0001t0002g0142 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.804+2011C>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50443654 | ||||||
| chr12:50443779
|
A | G | 1 | a0001c0001t0002g0102 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.804+2136A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50443779 | ||||||
| chr12:50443851
|
G | A | 3 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0144 | 3 | HG02074.hp1 NA18747.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.804+2208G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50443851 | ||||||
| chr12:50443852
|
A | T | 3 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0144 | 3 | HG02074.hp1 NA18747.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.804+2209A>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50443852 | ||||||
| chr12:50444032
|
A | G | 1 | a0001c0001t0001g0270 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.804+2389A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50444032 | ||||||
| chr12:50444062
|
C | A | 1 | a0001c0001t0002g0040 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.804+2419C>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50444062 | ||||||
| chr12:50444255
|
AT | A | 132 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.804+2620delT | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50444255 | |||||
| chr12:50444288
|
C | A | 1 | a0001c0001t0002g0046 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.804+2645C>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50444288 | ||||||
| chr12:50444785
|
G | A | 2 | a0001c0001t0004g0149a0001c0001t0004g0150 | 2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.804+3142G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50444785 | ||||||
| chr12:50444794
|
A | G | 133 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.804+3151A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50444794 | ||||||
| chr12:50444980
|
A | G | 1 | a0001c0001t0006g0276 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.804+3337A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50444980 | ||||||
| chr12:50445530
|
C | G | 1 | a0001c0001t0001g0266 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.804+3887C>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50445530 | ||||||
| chr12:50446003
|
C | CT | 32 | a0001c0001t0001g0036a0001c0001t0001g0174a0001c0001t0001g0209others(29): Show | 32 | HG00099.hp1 HG01071.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.804+4377dupT | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446003 | |||||
| chr12:50446009
|
T | C | 1 | a0001c0001t0001g0279 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.804+4366T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50446009 | ||||||
| chr12:50446089
|
G | A | 2 | a0001c0001t0002g0056a0001c0001t0002g0057 | 2 | HG03492.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.804+4446G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50446089 | ||||||
| chr12:50446157
|
C | T | 3 | a0001c0001t0002g0045a0001c0001t0002g0047a0001c0001t0002g0115 | 3 | HG00544.hp1 NA18980.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.804+4514C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50446157 | ||||||
| chr12:50446208
|
A | G | 257 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(254): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.804+4565A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50446208 | ||||||
| chr12:50446243
|
T | A | 4 | a0001c0006t0007g0108a0001c0006t0007g0109a0001c0006t0007g0110others(1): Show | 4 | HG01109.hp1 HG02572.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.804+4600T>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50446243 | ||||||
| chr12:50446300
|
C | T | 1 | a0001c0001t0001g0232 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.804+4657C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50446300 | ||||||
| chr12:50446329
|
GTCTCTCT others(7): Show |
G | 1 | a0001c0001t0006g0273 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.804+4699_804+4712d others(16): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446329 | |||||
| chr12:50446336
|
T | TCTCTCTC others(65): Show |
1 | a0001c0001t0001g0229 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.804+4698_804+4699i others(74): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446336 | |||||
| chr12:50446340
|
T | TCTCTCTC others(56): Show |
1 | a0001c0001t0001g0197 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.804+4698_804+4699i others(65): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446340 | |||||
| chr12:50446342
|
C | T | 253 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(250): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.804+4699C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50446342 | ||||||
| chr12:50446346
|
T | TCTCTCTC others(63): Show |
1 | a0001c0001t0001g0251 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.804+4730_804+4731i others(72): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446346 | |||||
| chr12:50446348
|
T | C | 1 | a0001c0001t0001g0197 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.804+4705T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50446348 | ||||||
| chr12:50446348
|
T | TCTCTCTC others(48): Show |
1 | a0003c0003t0001g0171 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.804+4728_804+4729i others(57): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446348 | |||||
| chr12:50446348
|
T | TCTCTCTC others(60): Show |
1 | a0002c0002t0001g0212 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.804+4730_804+4731i others(69): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446348 | |||||
| chr12:50446350
|
T | C | 1 | a0001c0010t0007g0111 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.804+4707T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50446350 | ||||||
| chr12:50446350
|
T | TCTCTCTC others(56): Show |
1 | a0001c0001t0001g0266 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.804+4726_804+4727i others(65): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446350 | |||||
| chr12:50446350
|
T | TCTCTCTC others(58): Show |
1 | a0001c0001t0002g0252 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.804+4728_804+4729i others(67): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446350 | |||||
| chr12:50446350
|
T | TCTCTCTC others(56): Show |
1 | a0001c0001t0001g0242 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.804+4728_804+4729i others(65): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446350 | |||||
| chr12:50446350
|
T | TCTCTCTC others(59): Show |
1 | a0002c0002t0001g0255 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.804+4730_804+4731i others(68): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446350 | |||||
| chr12:50446352
|
T | TCTCTCTC others(48): Show |
1 | a0001c0001t0001g0036 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.804+4722_804+4723i others(57): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446352 | |||||
| chr12:50446352
|
T | TCTCTCTC others(47): Show |
1 | a0001c0001t0004g0220 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.804+4726_804+4727i others(56): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446352 | |||||
| chr12:50446352
|
T | TCTCTCTC others(53): Show |
2 | a0001c0001t0001g0196a0001c0001t0001g0228 | 2 | HG02976.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.804+4726_804+4727i others(62): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446352 | |||||
| chr12:50446352
|
T | TCTCTCTC others(42): Show |
1 | a0003c0003t0001g0153 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.804+4728_804+4729i others(51): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446352 | |||||
| chr12:50446352
|
T | TCTCTCTC others(56): Show |
1 | a0001c0001t0001g0283 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.804+4730_804+4731i others(65): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446352 | |||||
| chr12:50446352
|
T | TCTCTCTC others(64): Show |
1 | a0001c0001t0001g0316 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.804+4736_804+4737i others(73): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446352 | |||||
| chr12:50446352
|
T | TCTCTCTC others(64): Show |
1 | a0001c0001t0001g0235 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.804+4736_804+4737i others(73): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446352 | |||||
| chr12:50446354
|
T | TCCCCCCC others(36): Show |
2 | a0001c0001t0020g0300a0001c0001t0021g0301 | 2 | HG02258.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.804+4712_804+4713i others(45): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446354 | |||||
| chr12:50446354
|
T | TCTCTCTC others(44): Show |
1 | a0001c0001t0006g0275 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.804+4722_804+4723i others(53): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446354 | |||||
| chr12:50446354
|
T | TCTCTCTC others(48): Show |
1 | a0001c0001t0001g0218 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.804+4722_804+4723i others(57): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446354 | |||||
| chr12:50446354
|
T | TCTCTCTC others(50): Show |
1 | a0002c0002t0001g0280 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.804+4724_804+4725i others(59): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446354 | |||||
| chr12:50446354
|
T | TCTCTCTC others(49): Show |
1 | a0004c0004t0001g0200 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.804+4724_804+4725i others(58): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446354 | |||||
| chr12:50446354
|
T | TCTCTCTC others(52): Show |
1 | a0001c0001t0001g0292 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.804+4726_804+4727i others(61): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446354 | |||||
| chr12:50446354
|
T | TCTCTCTC others(39): Show |
1 | a0003c0003t0001g0179 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.804+4726_804+4727i others(48): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446354 | |||||
| chr12:50446354
|
T | TCTCTCTC others(49): Show |
2 | a0001c0001t0001g0022a0001c0001t0001g0023 | 2 | HG02055.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.804+4728_804+4729i others(58): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446354 | |||||
| chr12:50446354
|
T | TCTCTCTC others(47): Show |
1 | a0001c0001t0001g0216 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.804+4728_804+4729i others(56): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446354 | |||||
| chr12:50446354
|
T | TCTCTCTC others(62): Show |
1 | a0001c0001t0001g0192 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.804+4736_804+4737i others(71): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446354 | |||||
| chr12:50446354
|
T | TCTCTCTC others(63): Show |
1 | a0001c0001t0004g0149 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.804+4740_804+4741i others(72): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446354 | |||||
| chr12:50446356
|
T | TCTCTCTC others(44): Show |
2 | a0001c0001t0001g0296a0001c0001t0001g0318 | 2 | NA18948.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.804+4720_804+4721i others(53): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446356 | |||||
| chr12:50446356
|
T | TCTCTCTC others(48): Show |
1 | a0004c0004t0001g0250 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.804+4724_804+4725i others(57): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446356 | |||||
| chr12:50446356
|
T | TCTCTCTC others(46): Show |
1 | a0001c0001t0001g0021 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.804+4728_804+4729i others(55): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446356 | |||||
| chr12:50446356
|
T | TCTCTCTC others(40): Show |
1 | a0001c0001t0001g0190 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.804+4728_804+4729i others(49): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446356 | |||||
| chr12:50446356
|
T | TCTCTCTC others(51): Show |
1 | a0002c0002t0001g0217 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.804+4728_804+4729i others(60): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446356 | |||||
| chr12:50446356
|
T | TCTCTCTC others(39): Show |
1 | a0001c0001t0001g0181 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.804+4728_804+4729i others(48): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446356 | |||||
| chr12:50446356
|
T | TCTCTCTC others(53): Show |
1 | a0001c0001t0001g0230 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.804+4730_804+4731i others(62): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446356 | |||||
| chr12:50446356
|
T | TCTCTCTC others(40): Show |
1 | a0003c0003t0001g0180 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.804+4730_804+4731i others(49): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446356 | |||||
| chr12:50446358
|
T | TCTCTCTC others(41): Show |
1 | a0001c0001t0006g0274 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.804+4722_804+4723i others(50): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446358 | |||||
| chr12:50446358
|
T | TCTCTCTC others(40): Show |
1 | a0001c0001t0006g0294 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.804+4722_804+4723i others(49): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446358 | |||||
| chr12:50446358
|
T | TCTCTCTC others(46): Show |
1 | a0004c0004t0001g0227 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.804+4724_804+4725i others(55): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446358 | |||||
| chr12:50446358
|
T | TCTCTCTC others(50): Show |
1 | a0002c0002t0001g0214 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.804+4728_804+4729i others(59): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446358 | |||||
| chr12:50446358
|
T | TCTCTCTC others(44): Show |
1 | a0001c0001t0001g0020 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.804+4728_804+4729i others(53): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446358 | |||||
| chr12:50446358
|
T | TCTCTCTC others(49): Show |
1 | a0001c0001t0001g0284 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.804+4728_804+4729i others(58): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446358 | |||||
| chr12:50446358
|
T | TCTCTCTC others(36): Show |
1 | a0001c0001t0004g0170 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.804+4728_804+4729i others(45): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446358 | |||||
| chr12:50446358
|
T | TCTCTCTC others(37): Show |
1 | a0003c0003t0001g0163 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.804+4728_804+4729i others(46): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446358 | |||||
| chr12:50446358
|
T | TCTCTCTC others(35): Show |
1 | a0001c0001t0008g0158 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.804+4728_804+4729i others(44): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446358 | |||||
| chr12:50446358
|
T | TCTCTCTC others(52): Show |
1 | a0001c0001t0022g0002 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.804+4730_804+4731i others(61): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446358 | |||||
| chr12:50446358
|
T | TCTCTCTC others(50): Show |
1 | a0001c0001t0002g0267 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.804+4730_804+4731i others(59): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446358 | |||||
| chr12:50446358
|
T | TCTCTCTC others(51): Show |
1 | a0002c0002t0001g0288 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.804+4730_804+4731i others(60): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446358 | |||||
| chr12:50446358
|
T | TCTCTCTC others(40): Show |
1 | a0001c0001t0001g0177 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.804+4730_804+4731i others(49): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446358 | |||||
| chr12:50446358
|
T | TCTCTCTC others(60): Show |
1 | a0001c0001t0001g0236 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.804+4738_804+4739i others(69): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446358 | |||||
| chr12:50446360
|
T | C | 2 | a0001c0001t0020g0300a0001c0001t0021g0301 | 2 | HG02258.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.804+4717T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50446360 | ||||||
| chr12:50446360
|
T | TCTCCCCC others(40): Show |
1 | a0001c0001t0001g0295 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.804+4720_804+4721i others(49): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446360 | |||||
| chr12:50446360
|
T | TCTCTCCC others(30): Show |
1 | a0003c0003t0001g0162 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.804+4722_804+4723i others(39): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446360 | |||||
| chr12:50446360
|
T | TCTCTCTC others(44): Show |
1 | a0004c0004t0001g0240 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.804+4724_804+4725i others(53): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446360 | |||||
| chr12:50446360
|
T | TCTCTCTC others(44): Show |
1 | a0001c0001t0003g0030 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.804+4724_804+4725i others(53): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446360 | |||||
| chr12:50446360
|
T | TCTCTCTC others(43): Show |
1 | a0001c0001t0001g0245 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.804+4724_804+4725i others(52): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446360 | |||||
| chr12:50446360
|
T | TCTCTCTC others(43): Show |
1 | a0001c0001t0003g0031 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.804+4724_804+4725i others(52): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446360 | |||||
| chr12:50446360
|
T | TCTCTCTC others(51): Show |
1 | a0001c0001t0001g0234 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.804+4728_804+4729i others(60): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446360 | |||||
| chr12:50446360
|
T | TCTCTCTC others(44): Show |
1 | a0001c0001t0001g0262 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.804+4728_804+4729i others(53): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446360 | |||||
| chr12:50446360
|
T | TCTCTCTC others(49): Show |
1 | a0002c0002t0001g0287 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.804+4728_804+4729i others(58): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446360 | |||||
| chr12:50446360
|
T | TCTCTCTC others(48): Show |
1 | a0001c0001t0012g0246 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.804+4728_804+4729i others(57): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446360 | |||||
| chr12:50446360
|
T | TCTCTCTC others(36): Show |
1 | a0001c0001t0011g0314 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.804+4728_804+4729i others(45): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446360 | |||||
| chr12:50446360
|
T | TCTCTCTC others(47): Show |
2 | a0001c0001t0001g0315a0002c0002t0001g0207 | 2 | NA19055.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.804+4728_804+4729i others(56): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446360 | |||||
| chr12:50446360
|
T | TCTCTCTC others(47): Show |
1 | a0003c0003t0001g0165 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.804+4728_804+4729i others(56): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446360 | |||||
| chr12:50446360
|
T | TCTCTCTC others(33): Show |
2 | a0001c0001t0008g0184a0003c0003t0001g0166 | 2 | HG03579.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.804+4728_804+4729i others(42): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446360 | |||||
| chr12:50446360
|
T | TCTCTCTC others(34): Show |
2 | a0001c0001t0001g0159a0001c0001t0008g0183 | 2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.804+4728_804+4729i others(43): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446360 | |||||
| chr12:50446360
|
T | TCTCTCTC others(49): Show |
2 | a0001c0001t0002g0268a0002c0002t0001g0253 | 2 | NA18979.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.804+4730_804+4731i others(58): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446360 | |||||
| chr12:50446360
|
T | TCTCTCTC others(52): Show |
1 | a0001c0001t0016g0259 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.804+4732_804+4733i others(61): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446360 | |||||
| chr12:50446360
|
T | TCTCTCTC others(51): Show |
1 | a0001c0001t0001g0225 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.804+4732_804+4733i others(60): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446360 | |||||
| chr12:50446360
|
T | TCTCTCTC others(105): Show |
1 | a0001c0010t0007g0111 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.804+4734_804+4735i others(114): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446360 | |||||
| chr12:50446360
|
T | TCTCTCTC others(56): Show |
1 | a0001c0001t0001g0232 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.804+4736_804+4737i others(65): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446360 | |||||
| chr12:50446360
|
T | TCTCTCTC others(58): Show |
1 | a0001c0001t0004g0150 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.804+4740_804+4741i others(67): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446360 | |||||
| chr12:50446362
|
T | TCTCTCCC others(42): Show |
1 | a0001c0001t0001g0256 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.804+4724_804+4725i others(51): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446362 | |||||
| chr12:50446362
|
T | TCTCTCCC others(42): Show |
1 | a0004c0004t0001g0198 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.804+4724_804+4725i others(51): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446362 | |||||
| chr12:50446362
|
T | TCTCTCTC others(47): Show |
1 | a0002c0002t0001g0210 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.804+4728_804+4729i others(56): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446362 | |||||
| chr12:50446362
|
T | TCTCTCTC others(46): Show |
1 | a0002c0002t0001g0281 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.804+4728_804+4729i others(55): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446362 | |||||
| chr12:50446362
|
T | TCTCTCTC others(48): Show |
1 | a0001c0001t0001g0201 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.804+4728_804+4729i others(57): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446362 | |||||
| chr12:50446362
|
T | TCTCTCTC others(34): Show |
1 | a0001c0001t0001g0172 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.804+4728_804+4729i others(43): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446362 | |||||
| chr12:50446362
|
T | TCTCTCTC others(45): Show |
1 | a0001c0001t0001g0233 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.804+4728_804+4729i others(54): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446362 | |||||
| chr12:50446362
|
T | TCTCTCTC others(45): Show |
1 | a0003c0003t0001g0186 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.804+4728_804+4729i others(54): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446362 | |||||
| chr12:50446362
|
T | TCTCTCTC others(48): Show |
1 | a0001c0001t0001g0285 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.804+4730_804+4731i others(57): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446362 | |||||
| chr12:50446362
|
T | TCTCTCTC others(48): Show |
1 | a0001c0001t0001g0024 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.804+4730_804+4731i others(57): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446362 | |||||
| chr12:50446362
|
T | TCTCTCTC others(36): Show |
1 | a0001c0001t0001g0176 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.804+4730_804+4731i others(45): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446362 | |||||
| chr12:50446362
|
T | TCTCTCTC others(47): Show |
3 | a0001c0001t0001g0007a0001c0001t0001g0278a0002c0002t0001g0254 | 3 | NA19004.hp1 NA19004.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.804+4730_804+4731i others(56): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446362 | |||||
| chr12:50446362
|
T | TCTCTCTC others(34): Show |
1 | a0003c0003t0001g0187 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.804+4730_804+4731i others(43): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446362 | |||||
| chr12:50446362
|
T | TCTCTCTC others(50): Show |
1 | a0001c0001t0001g0011 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.804+4732_804+4733i others(59): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446362 | |||||
| chr12:50446362
|
T | TCTCTCTC others(49): Show |
2 | a0001c0001t0001g0261a0001c0001t0001g0282 | 2 | HG01358.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.804+4732_804+4733i others(58): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446362 | |||||
| chr12:50446362
|
T | TCTCTCTC others(48): Show |
1 | a0001c0001t0001g0289 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.804+4732_804+4733i others(57): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446362 | |||||
| chr12:50446362
|
T | TCTCTCTC others(150): Show |
1 | a0001c0006t0007g0108 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.804+4732_804+4733i others(159): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446362 | |||||
| chr12:50446362
|
T | TCTCTCTC others(53): Show |
1 | a0001c0001t0001g0203 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.804+4736_804+4737i others(62): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446362 | |||||
| chr12:50446362
|
T | TCTCTCTC others(56): Show |
1 | a0001c0001t0001g0290 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.804+4738_804+4739i others(65): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446362 | |||||
| chr12:50446364
|
T | TCTCCCCC others(41): Show |
1 | a0004c0004t0001g0239 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.804+4724_804+4725i others(50): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446364 | |||||
| chr12:50446364
|
T | TCTCCCCC others(34): Show |
2 | a0001c0001t0001g0231a0001c0001t0001g0237 | 2 | HG03491.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.804+4724_804+4725i others(43): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446364 | |||||
| chr12:50446364
|
T | TCTCCCCC others(40): Show |
1 | a0004c0004t0001g0265 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.804+4724_804+4725i others(49): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446364 | |||||
| chr12:50446364
|
T | TCTCCCCC others(39): Show |
3 | a0001c0001t0001g0243a0001c0001t0001g0244a0004c0004t0001g0241 | 3 | HG01167.hp1 NA19054.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.804+4724_804+4725i others(48): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446364 | |||||
| chr12:50446364
|
T | TCTCTCCC others(41): Show |
1 | a0001c0001t0003g0032 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.804+4726_804+4727i others(50): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446364 | |||||
| chr12:50446364
|
T | TCTCTCTC others(44): Show |
1 | a0001c0001t0001g0264 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.804+4728_804+4729i others(53): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446364 | |||||
| chr12:50446364
|
T | TCTCTCTC others(33): Show |
1 | a0001c0001t0004g0169 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.804+4728_804+4729i others(42): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446364 | |||||
| chr12:50446364
|
T | TCTCTCTC others(43): Show |
1 | a0001c0001t0002g0269 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.804+4728_804+4729i others(52): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446364 | |||||
| chr12:50446364
|
T | TCTCTCTC others(31): Show |
1 | a0001c0001t0001g0188 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.804+4728_804+4729i others(40): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446364 | |||||
| chr12:50446364
|
T | TCTCTCTC others(29): Show |
1 | a0001c0001t0001g0154 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.804+4728_804+4729i others(38): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446364 | |||||
| chr12:50446364
|
T | TCTCTCTC others(46): Show |
1 | a0001c0001t0001g0279 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.804+4730_804+4731i others(55): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446364 | |||||
| chr12:50446364
|
T | TCTCTCTC others(44): Show |
1 | a0001c0001t0001g0277 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.804+4730_804+4731i others(53): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446364 | |||||
| chr12:50446364
|
T | TCTCTCTC others(45): Show |
3 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0226 | 3 | HG01978.hp2 HG03710.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.804+4730_804+4731i others(54): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446364 | |||||
| chr12:50446364
|
T | TCTCTCTC others(45): Show |
1 | a0001c0001t0001g0206 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.804+4730_804+4731i others(54): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446364 | |||||
| chr12:50446364
|
T | TCTCTCTC others(33): Show |
1 | a0001c0001t0001g0164 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.804+4730_804+4731i others(42): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446364 | |||||
| chr12:50446364
|
T | TCTCTCTC others(47): Show |
1 | a0001c0001t0001g0222 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.804+4732_804+4733i others(56): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446364 | |||||
| chr12:50446366
|
T | TCCCCCCC others(32): Show |
1 | a0001c0001t0001g0263 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.804+4724_804+4725i others(41): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446366 | |||||
| chr12:50446366
|
T | TCCCCCCC others(25): Show |
1 | a0001c0001t0001g0299 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.804+4724_804+4725i others(34): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446366 | |||||
| chr12:50446366
|
T | TCCCCCCC others(31): Show |
2 | a0001c0001t0001g0213a0001c0001t0004g0202 | 2 | HG02129.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.804+4724_804+4725i others(40): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446366 | |||||
| chr12:50446366
|
T | TCCCCCCC others(37): Show |
1 | a0001c0001t0015g0317 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.804+4724_804+4725i others(46): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446366 | |||||
| chr12:50446366
|
T | TCTCCCCC others(41): Show |
1 | a0001c0001t0003g0028 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.804+4726_804+4727i others(50): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446366 | |||||
| chr12:50446366
|
T | TCTCCCCC others(40): Show |
1 | a0001c0001t0003g0035 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.804+4726_804+4727i others(49): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446366 | |||||
| chr12:50446366
|
T | TCTCCCCC others(28): Show |
2 | a0001c0001t0003g0026a0001c0001t0010g0033 | 2 | HG02896.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.804+4726_804+4727i others(37): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446366 | |||||
| chr12:50446366
|
T | TCTCCCCC others(39): Show |
2 | a0001c0001t0003g0029a0001c0001t0003g0034 | 2 | HG02622.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.804+4726_804+4727i others(48): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446366 | |||||
| chr12:50446366
|
T | TCTCCCCC others(27): Show |
1 | a0001c0001t0010g0025 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.804+4726_804+4727i others(36): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446366 | |||||
| chr12:50446366
|
T | TCTCTCCC others(43): Show |
1 | a0001c0001t0001g0298 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.804+4728_804+4729i others(52): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446366 | |||||
| chr12:50446366
|
T | TCTCTCCC others(42): Show |
1 | a0001c0001t0001g0221 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.804+4728_804+4729i others(51): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446366 | |||||
| chr12:50446366
|
T | TCTCTCCC others(30): Show |
1 | a0001c0001t0001g0174 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.804+4728_804+4729i others(39): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446366 | |||||
| chr12:50446366
|
T | TCTCTCCC others(41): Show |
2 | a0001c0001t0001g0195a0001c0001t0004g0208 | 2 | HG02040.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.804+4728_804+4729i others(50): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446366 | |||||
| chr12:50446366
|
T | TCTCTCCC others(28): Show |
3 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0182 | 3 | HG02257.hp1 HG02895.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.804+4728_804+4729i others(37): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446366 | |||||
| chr12:50446366
|
T | TCTCTCTC others(42): Show |
1 | a0001c0001t0001g0272 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.804+4730_804+4731i others(51): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446366 | |||||
| chr12:50446366
|
T | TCTCTCTC others(43): Show |
4 | a0001c0001t0001g0199a0001c0001t0001g0219a0001c0001t0001g0223others(1): Show | 4 | HG03688.hp2 NA18968.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.804+4730_804+4731i others(52): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446366 | |||||
| chr12:50446366
|
T | TCTCTCTC others(31): Show |
1 | a0001c0001t0001g0168 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.804+4730_804+4731i others(40): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446366 | |||||
| chr12:50446366
|
T | TCTCTCTC others(47): Show |
1 | a0001c0001t0001g0249 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.804+4732_804+4733i others(56): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446366 | |||||
| chr12:50446366
|
T | TCTCTCTC others(46): Show |
1 | a0001c0001t0001g0247 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.804+4732_804+4733i others(55): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446366 | |||||
| chr12:50446366
|
T | TCTCTCTC others(45): Show |
1 | a0002c0002t0001g0215 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.804+4732_804+4733i others(54): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446366 | |||||
| chr12:50446366
|
T | TCTCTCTC others(33): Show |
1 | a0001c0001t0001g0178 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.804+4732_804+4733i others(42): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446366 | |||||
| chr12:50446366
|
T | TCTCTCTC others(37): Show |
1 | a0003c0003t0001g0173 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.804+4736_804+4737i others(46): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446366 | |||||
| chr12:50446366
|
T | TCTCTCTC others(130): Show |
1 | a0001c0006t0007g0110 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.804+4736_804+4737i others(139): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446366 | |||||
| chr12:50446366
|
T | TCTCTCTC others(69): Show |
1 | a0001c0001t0002g0090 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.804+4744_804+4745i others(78): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446366 | |||||
| chr12:50446366
|
T | TCTCTCTC others(71): Show |
1 | a0001c0001t0002g0123 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.804+4744_804+4745i others(80): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446366 | |||||
| chr12:50446366
|
T | TCTCTCTC others(72): Show |
1 | a0001c0001t0002g0089 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.804+4748_804+4749i others(81): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446366 | |||||
| chr12:50446368
|
T | TCCCCCCC others(28): Show |
1 | a0001c0001t0001g0009 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.804+4726_804+4727i others(37): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446368 | |||||
| chr12:50446368
|
T | TCCCCCCC others(36): Show |
1 | a0001c0001t0014g0238 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.804+4726_804+4727i others(45): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446368 | |||||
| chr12:50446368
|
T | TCTCCCCC others(34): Show |
2 | a0001c0001t0001g0248a0001c0001t0001g0257 | 2 | HG02165.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.804+4728_804+4729i others(43): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446368 | |||||
| chr12:50446368
|
T | TCTCCCCC others(40): Show |
1 | a0001c0001t0001g0224 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.804+4728_804+4729i others(49): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446368 | |||||
| chr12:50446368
|
T | TCTCCCCC others(39): Show |
1 | a0001c0001t0001g0003 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.804+4728_804+4729i others(48): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446368 | |||||
| chr12:50446368
|
T | TCTCCCCC others(32): Show |
1 | a0001c0001t0001g0193 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.804+4728_804+4729i others(41): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446368 | |||||
| chr12:50446368
|
T | TCTCCCCC others(38): Show |
2 | a0001c0001t0001g0258a0001c0001t0001g0286 | 2 | HG02027.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.804+4728_804+4729i others(47): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446368 | |||||
| chr12:50446368
|
T | TCTCCCCC others(26): Show |
3 | a0001c0001t0001g0155a0001c0001t0001g0160a0001c0001t0001g0161 | 3 | HG02280.hp1 HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.804+4728_804+4729i others(35): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446368 | |||||
| chr12:50446368
|
T | TCTCCCTC others(48): Show |
1 | a0001c0001t0002g0050 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.804+4728_804+4729i others(57): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446368 | |||||
| chr12:50446368
|
T | TCTCTCCC others(42): Show |
1 | a0001c0001t0001g0270 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.804+4730_804+4731i others(51): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446368 | |||||
| chr12:50446368
|
T | TCTCTCCC others(41): Show |
3 | a0001c0001t0001g0005a0001c0001t0001g0205a0001c0001t0001g0291 | 3 | HG01261.hp1 NA19066.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.804+4730_804+4731i others(50): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446368 | |||||
| chr12:50446368
|
T | TCTCTCCC others(29): Show |
1 | a0001c0001t0001g0167 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.804+4730_804+4731i others(38): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446368 | |||||
| chr12:50446368
|
T | TCTCTCTC others(42): Show |
1 | a0001c0001t0001g0293 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.804+4732_804+4733i others(51): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446368 | |||||
| chr12:50446368
|
T | TCTCTCTC others(59): Show |
1 | a0001c0001t0002g0064 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.804+4732_804+4733i others(68): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446368 | |||||
| chr12:50446368
|
T | TCTCTCTC others(65): Show |
1 | a0001c0001t0002g0122 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.804+4744_804+4745i others(74): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446368 | |||||
| chr12:50446368
|
T | TCTCTCTC others(67): Show |
1 | a0001c0001t0002g0069 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.804+4744_804+4745i others(76): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446368 | |||||
| chr12:50446368
|
T | TCTCTCTC others(66): Show |
1 | a0001c0001t0002g0060 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.804+4744_804+4745i others(75): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446368 | |||||
| chr12:50446368
|
T | TCTCTCTC others(72): Show |
1 | a0001c0001t0002g0063 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.804+4744_804+4745i others(81): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446368 | |||||
| chr12:50446368
|
T | TCTCTCTC others(71): Show |
1 | a0001c0001t0002g0102 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.804+4744_804+4745i others(80): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446368 | |||||
| chr12:50446368
|
T | TCTCTCTC others(74): Show |
1 | a0001c0001t0002g0115 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.804+4746_804+4747i others(83): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446368 | |||||
| chr12:50446368
|
T | TCTCTCTC others(70): Show |
1 | a0001c0001t0002g0142 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.804+4746_804+4747i others(79): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446368 | |||||
| chr12:50446368
|
T | TCTCTCTC others(69): Show |
1 | a0001c0001t0002g0103 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.804+4746_804+4747i others(78): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446368 | |||||
| chr12:50446368
|
T | TCTCTCTC others(73): Show |
1 | a0001c0001t0002g0091 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.804+4750_804+4751i others(82): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446368 | |||||
| chr12:50446368
|
T | TCTCTCTC others(72): Show |
1 | a0001c0001t0002g0013 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.804+4750_804+4751i others(81): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446368 | |||||
| chr12:50446368
|
T | TCTCTCTC others(71): Show |
1 | a0001c0001t0002g0128 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.804+4750_804+4751i others(80): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446368 | |||||
| chr12:50446370
|
T | C | 3 | a0001c0001t0001g0231a0001c0001t0001g0237a0001c0001t0001g0299 | 3 | HG02886.hp2 HG03491.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.804+4727T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50446370 | ||||||
| chr12:50446370
|
T | TCCCCCCC others(35): Show |
1 | a0001c0001t0001g0209 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.804+4728_804+4729i others(44): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446370 | |||||
| chr12:50446370
|
T | TCCCCCCC others(38): Show |
2 | a0001c0005t0001g0008a0002c0002t0001g0211 | 2 | NA19063.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.804+4728_804+4729i others(47): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446370 | |||||
| chr12:50446370
|
T | TCCCCCCC others(26): Show |
1 | a0001c0001t0001g0175 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.804+4728_804+4729i others(35): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446370 | |||||
| chr12:50446370
|
T | TCCCCCCC others(25): Show |
1 | a0001c0001t0001g0189 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.804+4728_804+4729i others(34): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446370 | |||||
| chr12:50446370
|
T | TCCCCCCC others(36): Show |
1 | a0001c0001t0013g0194 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.804+4728_804+4729i others(45): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446370 | |||||
| chr12:50446370
|
T | TCTCCCCC others(39): Show |
2 | a0001c0001t0001g0004a0001c0001t0001g0204 | 2 | HG02293.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.804+4730_804+4731i others(48): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446370 | |||||
| chr12:50446370
|
T | TCTCCCCC others(26): Show |
1 | a0001c0001t0001g0185 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.804+4730_804+4731i others(35): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446370 | |||||
| chr12:50446370
|
T | TCTCTCTC others(56): Show |
1 | a0001c0001t0002g0096 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.804+4736_804+4737i others(65): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446370 | |||||
| chr12:50446370
|
T | TCTCTCTC others(55): Show |
1 | a0001c0001t0002g0067 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.804+4736_804+4737i others(64): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446370 | |||||
| chr12:50446370
|
T | TCTCTCTC others(82): Show |
1 | a0001c0001t0002g0062 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.804+4740_804+4741i others(91): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446370 | |||||
| chr12:50446370
|
T | TCTCTCTC others(65): Show |
1 | a0001c0001t0002g0047 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.804+4742_804+4743i others(74): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446370 | |||||
| chr12:50446370
|
T | TCTCTCTC others(59): Show |
1 | a0001c0001t0002g0151 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.804+4742_804+4743i others(68): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446370 | |||||
| chr12:50446370
|
T | TCTCTCTC others(62): Show |
2 | a0001c0001t0002g0076a0001c0001t0002g0081 | 2 | HG02683.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.804+4742_804+4743i others(71): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446370 | |||||
| chr12:50446370
|
T | TCTCTCTC others(66): Show |
1 | a0001c0001t0002g0016 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.804+4744_804+4745i others(75): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446370 | |||||
| chr12:50446370
|
T | TCTCTCTC others(65): Show |
1 | a0001c0001t0002g0144 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.804+4744_804+4745i others(74): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446370 | |||||
| chr12:50446370
|
T | TCTCTCTC others(71): Show |
1 | a0001c0001t0002g0080 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.804+4744_804+4745i others(80): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446370 | |||||
| chr12:50446370
|
T | TCTCTCTC others(70): Show |
1 | a0001c0001t0002g0124 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.804+4746_804+4747i others(79): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446370 | |||||
| chr12:50446370
|
T | TCTCTCTC others(69): Show |
1 | a0001c0001t0002g0083 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.804+4748_804+4749i others(78): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446370 | |||||
| chr12:50446370
|
T | TCTCTCTC others(68): Show |
3 | a0001c0001t0002g0014a0001c0001t0002g0079a0001c0001t0002g0105 | 3 | HG01943.hp2 HG02293.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.804+4748_804+4749i others(77): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446370 | |||||
| chr12:50446370
|
T | TCTCTCTC others(67): Show |
1 | a0001c0001t0002g0077 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.804+4748_804+4749i others(76): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446370 | |||||
| chr12:50446370
|
T | TCTCTCTC others(73): Show |
1 | a0001c0001t0002g0061 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.804+4748_804+4749i others(82): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446370 | |||||
| chr12:50446370
|
T | TCTCTCTC others(77): Show |
1 | a0001c0001t0002g0112 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.804+4754_804+4755i others(86): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446370 | |||||
| chr12:50446372
|
T | C | 8 | a0001c0001t0001g0213a0001c0001t0001g0263a0001c0001t0001g0299others(5): Show | 8 | HG02129.hp2 HG02809.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.804+4729T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50446372 | ||||||
| chr12:50446372
|
T | TCCCCCCC others(48): Show |
1 | a0001c0005t0001g0010 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.804+4730_804+4731i others(57): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446372 | |||||
| chr12:50446372
|
T | TCCCCCCC others(43): Show |
1 | a0001c0001t0002g0107 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.804+4730_804+4731i others(52): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446372 | |||||
| chr12:50446372
|
T | TCCCCCCC others(48): Show |
1 | a0001c0001t0002g0113 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.804+4730_804+4731i others(57): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446372 | |||||
| chr12:50446372
|
T | TCTCTCCC others(55): Show |
1 | a0001c0001t0002g0045 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.804+4734_804+4735i others(64): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446372 | |||||
| chr12:50446372
|
T | TCTCTCTC others(57): Show |
1 | a0001c0001t0002g0039 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.804+4738_804+4739i others(66): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446372 | |||||
| chr12:50446372
|
T | TCTCTCTC others(56): Show |
2 | a0001c0001t0002g0071a0001c0001t0002g0093 | 2 | HG02155.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.804+4738_804+4739i others(65): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446372 | |||||
| chr12:50446372
|
T | TCTCTCTC others(59): Show |
1 | a0001c0001t0002g0088 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.804+4738_804+4739i others(68): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446372 | |||||
| chr12:50446372
|
T | TCTCTCTC others(59): Show |
1 | a0001c0001t0002g0104 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.804+4740_804+4741i others(68): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446372 | |||||
| chr12:50446372
|
T | TCTCTCTC others(57): Show |
1 | a0001c0001t0002g0058 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.804+4740_804+4741i others(66): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446372 | |||||
| chr12:50446372
|
T | TCTCTCTC others(50): Show |
1 | a0001c0009t0001g0271 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.804+4742_804+4743i others(59): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446372 | |||||
| chr12:50446372
|
T | TCTCTCTC others(59): Show |
1 | a0001c0001t0002g0099 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.804+4742_804+4743i others(68): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446372 | |||||
| chr12:50446372
|
T | TCTCTCTC others(60): Show |
4 | a0001c0001t0002g0053a0001c0001t0002g0086a0001c0001t0002g0106others(1): Show | 4 | HG00140.hp1 HG02559.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.804+4742_804+4743i others(69): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446372 | |||||
| chr12:50446372
|
T | TCTCTCTC others(72): Show |
1 | a0001c0001t0002g0141 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.804+4742_804+4743i others(81): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446372 | |||||
| chr12:50446372
|
T | TCTCTCTC others(64): Show |
1 | a0001c0001t0002g0092 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.804+4742_804+4743i others(73): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446372 | |||||
| chr12:50446372
|
T | TCTCTCTC others(65): Show |
2 | a0001c0001t0002g0051a0001c0001t0002g0055 | 2 | NA18954.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.804+4744_804+4745i others(74): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446372 | |||||
| chr12:50446372
|
T | TCTCTCTC others(63): Show |
2 | a0001c0001t0002g0114a0001c0001t0002g0130 | 2 | NA18953.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.804+4744_804+4745i others(72): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446372 | |||||
| chr12:50446372
|
T | TCTCTCTC others(63): Show |
1 | a0001c0001t0002g0127 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.804+4744_804+4745i others(72): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446372 | |||||
| chr12:50446372
|
T | TCTCTCTC others(62): Show |
4 | a0001c0001t0002g0098a0001c0001t0002g0120a0001c0001t0002g0137others(1): Show | 4 | HG01346.hp1 HG02280.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.804+4744_804+4745i others(71): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446372 | |||||
| chr12:50446372
|
T | TCTCTCTC others(61): Show |
1 | a0001c0001t0002g0049 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.804+4744_804+4745i others(70): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446372 | |||||
| chr12:50446372
|
T | TCTCTCTC others(60): Show |
1 | a0001c0001t0002g0307 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.804+4744_804+4745i others(69): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446372 | |||||
| chr12:50446372
|
T | TCTCTCTC others(65): Show |
1 | a0001c0001t0002g0129 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.804+4746_804+4747i others(74): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446372 | |||||
| chr12:50446372
|
T | TCTCTCTC others(65): Show |
1 | a0001c0001t0002g0117 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.804+4746_804+4747i others(74): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446372 | |||||
| chr12:50446372
|
T | TCTCTCTC others(64): Show |
4 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0116others(1): Show | 4 | HG01928.hp2 HG01975.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.804+4746_804+4747i others(73): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446372 | |||||
| chr12:50446372
|
T | TCTCTCTC others(65): Show |
2 | a0001c0001t0002g0135a0001c0001t0002g0311 | 2 | HG01433.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.804+4748_804+4749i others(74): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446372 | |||||
| chr12:50446372
|
T | TCTCTCTC others(66): Show |
2 | a0001c0001t0002g0054a0001c0001t0009g0048 | 2 | HG01074.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.804+4748_804+4749i others(75): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446372 | |||||
| chr12:50446372
|
T | TCTCTCTC others(70): Show |
1 | a0001c0001t0002g0138 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.804+4750_804+4751i others(79): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446372 | |||||
| chr12:50446372
|
T | TCTCTCTC others(70): Show |
1 | a0001c0001t0002g0305 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.804+4750_804+4751i others(79): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446372 | |||||
| chr12:50446372
|
T | TCTCTCTC others(67): Show |
1 | a0001c0001t0002g0312 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.804+4750_804+4751i others(76): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446372 | |||||
| chr12:50446372
|
T | TCTCTCTC others(68): Show |
3 | a0001c0001t0002g0075a0001c0001t0009g0059a0001c0001t0019g0134 | 3 | HG00099.hp1 HG00741.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.804+4750_804+4751i others(77): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446372 | |||||
| chr12:50446372
|
T | TCTCTCTC others(70): Show |
1 | a0001c0001t0018g0012 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.804+4752_804+4753i others(79): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446372 | |||||
| chr12:50446372
|
T | TCTCTCTC others(87): Show |
1 | a0001c0001t0002g0057 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.804+4752_804+4753i others(96): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446372 | |||||
| chr12:50446372
|
T | TCTCTCTC others(73): Show |
1 | a0001c0001t0002g0126 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.804+4754_804+4755i others(82): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446372 | |||||
| chr12:50446372
|
T | TCTCTCTC others(71): Show |
1 | a0001c0001t0002g0310 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.804+4754_804+4755i others(80): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446372 | |||||
| chr12:50446372
|
T | TCTCTCTC others(74): Show |
1 | a0001c0001t0002g0309 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.804+4756_804+4757i others(83): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446372 | |||||
| chr12:50446374
|
T | C | 5 | a0001c0001t0001g0009a0001c0001t0001g0193a0001c0001t0001g0248others(2): Show | 5 | HG02148.hp1 HG02165.hp2 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.804+4731T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50446374 | ||||||
| chr12:50446374
|
T | TCCCTCTC others(130): Show |
1 | a0001c0006t0007g0109 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.804+4732_804+4733i others(139): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446374 | |||||
| chr12:50446374
|
T | TCTCCCCC others(53): Show |
1 | a0001c0001t0002g0043 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.804+4734_804+4735i others(62): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446374 | |||||
| chr12:50446374
|
T | TCTCCCCC others(50): Show |
1 | a0001c0001t0002g0073 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.804+4734_804+4735i others(59): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446374 | |||||
| chr12:50446374
|
T | TCTCTCTC others(54): Show |
1 | a0001c0001t0002g0095 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.804+4738_804+4739i others(63): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446374 | |||||
| chr12:50446374
|
T | TCTCTCTC others(58): Show |
1 | a0001c0001t0002g0118 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.804+4738_804+4739i others(67): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446374 | |||||
| chr12:50446374
|
T | TCTCTCTC others(56): Show |
4 | a0001c0001t0002g0018a0001c0001t0002g0094a0001c0001t0002g0131others(1): Show | 4 | NA18747.hp1 NA19001.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.804+4740_804+4741i others(65): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446374 | |||||
| chr12:50446374
|
T | TCTCTCTC others(61): Show |
1 | a0001c0001t0002g0044 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.804+4742_804+4743i others(70): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446374 | |||||
| chr12:50446374
|
T | TCTCTCTC others(58): Show |
1 | a0001c0001t0002g0074 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.804+4742_804+4743i others(67): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446374 | |||||
| chr12:50446374
|
T | TCTCTCTC others(46): Show |
1 | a0006c0008t0005g0037 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.804+4742_804+4743i others(55): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446374 | |||||
| chr12:50446374
|
T | TCTCTCTC others(61): Show |
1 | a0001c0001t0002g0072 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.804+4744_804+4745i others(70): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446374 | |||||
| chr12:50446374
|
T | TCTCTCTC others(48): Show |
1 | a0006c0008t0005g0038 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.804+4744_804+4745i others(57): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446374 | |||||
| chr12:50446374
|
T | TCTCTCTC others(63): Show |
1 | a0001c0001t0002g0078 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.804+4746_804+4747i others(72): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446374 | |||||
| chr12:50446374
|
T | TCTCTCTC others(62): Show |
1 | a0001c0001t0002g0042 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.804+4746_804+4747i others(71): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446374 | |||||
| chr12:50446374
|
T | TCTCTCTC others(64): Show |
1 | a0001c0001t0002g0087 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.804+4746_804+4747i others(73): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446374 | |||||
| chr12:50446374
|
T | TCTCTCTC others(63): Show |
1 | a0001c0001t0002g0046 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.804+4746_804+4747i others(72): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446374 | |||||
| chr12:50446374
|
T | TCTCTCTC others(61): Show |
1 | a0005c0007t0002g0136 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.804+4746_804+4747i others(70): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446374 | |||||
| chr12:50446374
|
T | TCTCTCTC others(62): Show |
1 | a0001c0001t0002g0068 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.804+4746_804+4747i others(71): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446374 | |||||
| chr12:50446374
|
T | TCTCTCTC others(54): Show |
1 | a0001c0001t0006g0276 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.804+4746_804+4747i others(63): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446374 | |||||
| chr12:50446374
|
T | TCTCTCTC others(64): Show |
2 | a0001c0001t0002g0065a0001c0001t0002g0070 | 2 | HG01074.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.804+4748_804+4749i others(73): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446374 | |||||
| chr12:50446374
|
T | TCTCTCTC others(56): Show |
1 | a0001c0012t0002g0066 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.804+4748_804+4749i others(65): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446374 | |||||
| chr12:50446374
|
T | TCTCTCTC others(67): Show |
1 | a0001c0001t0002g0041 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.804+4748_804+4749i others(76): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446374 | |||||
| chr12:50446374
|
T | TCTCTCTC others(66): Show |
1 | a0005c0007t0002g0084 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.804+4750_804+4751i others(75): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446374 | |||||
| chr12:50446374
|
T | TCTCTCTC others(65): Show |
2 | a0001c0001t0002g0040a0001c0001t0002g0306 | 2 | HG02647.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.804+4750_804+4751i others(74): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446374 | |||||
| chr12:50446374
|
T | TCTCTCTC others(68): Show |
2 | a0001c0001t0002g0303a0007c0013t0002g0101 | 2 | HG01071.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.804+4752_804+4753i others(77): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446374 | |||||
| chr12:50446374
|
T | TCTCTCTC others(70): Show |
1 | a0001c0001t0017g0304 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.804+4754_804+4755i others(79): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446374 | |||||
| chr12:50446376
|
T | TCTCTCCC others(52): Show |
1 | a0001c0001t0002g0308 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.804+4738_804+4739i others(61): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446376 | |||||
| chr12:50446376
|
T | TCTCTCTC others(55): Show |
1 | a0001c0001t0002g0097 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.804+4740_804+4741i others(64): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446376 | |||||
| chr12:50446376
|
T | TCTCTCTC others(59): Show |
1 | a0001c0001t0002g0302 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.804+4742_804+4743i others(68): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446376 | |||||
| chr12:50446376
|
T | TCTCTCTC others(51): Show |
1 | a0001c0001t0002g0085 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.804+4742_804+4743i others(60): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446376 | |||||
| chr12:50446376
|
T | TCTCTCTC others(56): Show |
1 | a0001c0001t0002g0019 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.804+4742_804+4743i others(65): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446376 | |||||
| chr12:50446376
|
T | TCTCTCTC others(55): Show |
1 | a0005c0007t0002g0119 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.804+4742_804+4743i others(64): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446376 | |||||
| chr12:50446376
|
T | TCTCTCTC others(60): Show |
1 | a0001c0001t0002g0143 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.804+4742_804+4743i others(69): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446376 | |||||
| chr12:50446376
|
T | TCTCTCTC others(60): Show |
1 | a0001c0001t0002g0052 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.804+4746_804+4747i others(69): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446376 | |||||
| chr12:50446376
|
T | TCTCTCTC others(63): Show |
1 | a0001c0001t0002g0100 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.804+4748_804+4749i others(72): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446376 | |||||
| chr12:50446376
|
T | TCTCTCTC others(48): Show |
1 | a0001c0001t0005g0148 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.804+4748_804+4749i others(57): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446376 | |||||
| chr12:50446376
|
T | TCTCTCTC others(68): Show |
1 | a0001c0001t0002g0056 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.804+4754_804+4755i others(77): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446376 | |||||
| chr12:50446378
|
T | C | 2 | a0001c0001t0001g0299a0001c0001t0002g0107 | 2 | HG02083.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.804+4735T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50446378 | ||||||
| chr12:50446378
|
T | TCTCTCCC others(40): Show |
1 | a0001c0001t0005g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.804+4740_804+4741i others(49): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446378 | |||||
| chr12:50446378
|
T | TCTCTCTC others(43): Show |
1 | a0001c0001t0005g0146 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.804+4744_804+4745i others(52): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446378 | |||||
| chr12:50446378
|
T | TCTCTCTC others(45): Show |
1 | a0001c0001t0005g0145 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.804+4746_804+4747i others(54): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446378 | |||||
| chr12:50446378
|
T | TCTCTCTC others(66): Show |
2 | a0001c0001t0002g0121a0001c0001t0002g0152 | 2 | NA18975.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.804+4754_804+4755i others(75): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446378 | |||||
| chr12:50446378
|
T | TCTCTCTC others(70): Show |
1 | a0001c0001t0002g0313 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.804+4758_804+4759i others(79): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446378 | |||||
| chr12:50446380
|
T | TCTCTCCC others(42): Show |
1 | a0001c0001t0001g0297 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.804+4742_804+4743i others(51): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446380 | |||||
| chr12:50446380
|
T | TCTCTCTC others(57): Show |
1 | a0001c0001t0002g0140 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.804+4746_804+4747i others(66): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446380 | |||||
| chr12:50446380
|
T | TCTCTCTC others(56): Show |
1 | a0001c0001t0002g0082 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.804+4746_804+4747i others(65): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446380 | |||||
| chr12:50446380
|
T | TCTCTCTC others(60): Show |
1 | a0001c0001t0002g0125 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.804+4750_804+4751i others(69): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446380 | |||||
| chr12:50446393
|
C | A | 1 | a0001c0001t0021g0301 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.804+4750C>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50446393 | ||||||
| chr12:50446395
|
C | A | 1 | a0001c0001t0021g0301 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.804+4752C>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50446395 | ||||||
| chr12:50446397
|
C | A | 1 | a0001c0001t0021g0301 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.804+4754C>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50446397 | ||||||
| chr12:50446399
|
C | A | 1 | a0001c0001t0021g0301 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.804+4756C>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50446399 | ||||||
| chr12:50446401
|
C | A | 1 | a0001c0001t0021g0301 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.804+4758C>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50446401 | ||||||
| chr12:50446403
|
C | A | 1 | a0001c0001t0021g0301 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.804+4760C>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50446403 | ||||||
| chr12:50446405
|
C | A | 4 | a0001c0001t0004g0202a0001c0001t0006g0273a0001c0001t0015g0317others(1): Show | 4 | HG02647.hp2 HG02809.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.804+4762C>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50446405 | ||||||
| chr12:50446407
|
C | A | 12 | a0001c0001t0001g0159a0001c0001t0002g0086a0001c0001t0003g0028others(9): Show | 12 | HG00544.hp2 HG02109.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.804+4764C>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50446407 | ||||||
| chr12:50446409
|
C | A | 28 | a0001c0001t0001g0009a0001c0001t0001g0159a0001c0001t0001g0189others(25): Show | 28 | HG00544.hp2 HG00597.hp2 HG01261.hp2 others(25): Show |
intron_variant | MODIFIER | c.804+4766C>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50446409 | ||||||
| chr12:50446409
|
C | CTATATA | 5 | a0001c0001t0001g0177a0001c0001t0001g0190a0001c0001t0004g0169others(2): Show | 5 | HG00140.hp2 HG01106.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.804+4782_804+4787d others(8): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446409 | |||||
| chr12:50446409
|
C | CTATATAT others(1): Show |
6 | a0001c0001t0001g0175a0001c0001t0001g0188a0001c0001t0004g0150others(3): Show | 6 | HG02257.hp2 HG02258.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.804+4780_804+4787d others(10): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446409 | |||||
| chr12:50446409
|
C | CTATATAT others(3): Show |
7 | a0001c0001t0001g0154a0001c0001t0001g0157a0001c0001t0001g0174others(4): Show | 7 | HG02145.hp1 HG02451.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.804+4778_804+4787d others(12): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446409 | |||||
| chr12:50446409
|
C | CTATATAT others(5): Show |
7 | a0001c0001t0001g0155a0001c0001t0001g0161a0001c0001t0001g0181others(4): Show | 7 | HG02040.hp1 HG02818.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.804+4776_804+4787d others(14): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446409 | |||||
| chr12:50446409
|
C | CTATATAT others(7): Show |
8 | a0001c0001t0001g0036a0001c0001t0001g0156a0001c0001t0001g0160others(5): Show | 8 | HG01167.hp2 HG01169.hp2 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.804+4774_804+4787d others(16): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446409 | |||||
| chr12:50446409
|
C | CTATATAT others(9): Show |
2 | a0001c0001t0001g0167a0001c0001t0001g0185 | 2 | HG02622.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.804+4772_804+4787d others(18): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446409 | |||||
| chr12:50446409
|
C | CTATATAT others(11): Show |
1 | a0001c0001t0001g0219 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.804+4770_804+4787d others(20): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446409 | |||||
| chr12:50446409
|
C | CTATATAT others(17): Show |
1 | a0001c0001t0002g0269 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.804+4787_804+4788i others(26): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446409 | |||||
| chr12:50446409
|
C | CTATATAT others(21): Show |
1 | a0002c0002t0001g0288 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.804+4787_804+4788i others(30): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446409 | |||||
| chr12:50446411
|
A | C | 26 | a0001c0001t0001g0023a0001c0001t0001g0299a0001c0001t0002g0016others(23): Show | 26 | HG00099.hp2 HG00544.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.804+4768A>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50446411 | ||||||
| chr12:50446413
|
A | C | 7 | a0001c0001t0002g0016a0001c0001t0002g0070a0001c0001t0002g0074others(4): Show | 7 | HG00099.hp2 HG01074.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.804+4770A>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50446413 | ||||||
| chr12:50446428
|
TA | T | 11 | a0001c0001t0001g0022a0001c0001t0002g0045a0001c0001t0002g0047others(8): Show | 11 | HG00544.hp1 HG00741.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.804+4786delA | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50446428 | ||||||
| chr12:50446429
|
A | AT | 7 | a0001c0001t0001g0021a0001c0001t0002g0043a0001c0001t0002g0044others(4): Show | 7 | HG01433.hp1 HG02572.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.804+4801dupT | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446429 | |||||
| chr12:50446429
|
A | ATATATAT others(4): Show |
2 | a0001c0001t0001g0218a0001c0010t0007g0111 | 2 | NA18612.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.804+4787_804+4788i others(13): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446429 | |||||
| chr12:50446429
|
A | ATATATAT others(6): Show |
2 | a0001c0001t0001g0315a0001c0001t0022g0002 | 2 | HG00738.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.804+4787_804+4788i others(15): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446429 | |||||
| chr12:50446429
|
A | ATATATAT others(8): Show |
4 | a0001c0001t0001g0005a0001c0001t0001g0251a0001c0001t0001g0272others(1): Show | 4 | HG01261.hp1 HG03927.hp2 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.804+4787_804+4788i others(17): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446429 | |||||
| chr12:50446429
|
A | ATATATAT others(10): Show |
7 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0221others(4): Show | 7 | HG01981.hp2 NA18945.hp1 NA18945.hp2 others(4): Show |
intron_variant | MODIFIER | c.804+4787_804+4788i others(19): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446429 | |||||
| chr12:50446429
|
A | ATATATAT others(12): Show |
10 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0223others(7): Show | 10 | HG01978.hp2 HG02083.hp2 HG02148.hp1 others(7): Show |
intron_variant | MODIFIER | c.804+4787_804+4788i others(21): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446429 | |||||
| chr12:50446429
|
A | ATATATAT others(14): Show |
8 | a0001c0001t0001g0003a0001c0001t0001g0199a0001c0001t0001g0201others(5): Show | 8 | HG01934.hp1 HG01943.hp1 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.804+4787_804+4788i others(23): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446429 | |||||
| chr12:50446429
|
A | ATATATAT others(16): Show |
5 | a0001c0001t0001g0206a0001c0001t0012g0246a0001c0001t0016g0259others(2): Show | 5 | HG01928.hp1 HG02486.hp2 NA19057.hp1 others(2): Show |
intron_variant | MODIFIER | c.804+4787_804+4788i others(25): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446429 | |||||
| chr12:50446429
|
A | ATATATAT others(18): Show |
7 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0205others(4): Show | 7 | HG00673.hp2 HG02293.hp1 NA18747.hp2 others(4): Show |
intron_variant | MODIFIER | c.804+4787_804+4788i others(27): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446429 | |||||
| chr12:50446429
|
A | ATATATAT others(20): Show |
3 | a0001c0001t0001g0256a0001c0001t0001g0277a0002c0002t0001g0253 | 3 | HG00642.hp1 NA18967.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.804+4787_804+4788i others(29): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446429 | |||||
| chr12:50446429
|
A | ATATATAT others(22): Show |
1 | a0001c0001t0001g0248 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.804+4787_804+4788i others(31): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446429 | |||||
| chr12:50446429
|
A | ATATATAT others(24): Show |
2 | a0002c0002t0001g0210a0002c0002t0001g0280 | 2 | NA18975.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.804+4787_804+4788i others(33): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446429 | |||||
| chr12:50446429
|
A | ATATATAT others(26): Show |
1 | a0001c0001t0001g0213 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.804+4787_804+4788i others(35): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446429 | |||||
| chr12:50446429
|
A | ATATATAT others(21): Show |
1 | a0001c0005t0001g0010 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.804+4787_804+4788i others(30): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446429 | |||||
| chr12:50446429
|
A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0261 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.804+4787_804+4788i others(28): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446429 | |||||
| chr12:50446429
|
A | ATATATAT others(20): Show |
2 | a0001c0001t0001g0289a0001c0001t0001g0297 | 2 | HG01884.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.804+4787_804+4788i others(29): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446429 | |||||
| chr12:50446429
|
A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0279 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.804+4787_804+4788i others(28): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446429 | |||||
| chr12:50446429
|
A | ATATATAT others(13): Show |
1 | a0001c0001t0002g0252 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.804+4787_804+4788i others(22): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446429 | |||||
| chr12:50446429
|
A | ATATATAT others(14): Show |
4 | a0001c0001t0001g0231a0001c0001t0001g0236a0001c0001t0001g0263others(1): Show | 4 | HG03098.hp1 HG03486.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.804+4787_804+4788i others(23): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446429 | |||||
| chr12:50446429
|
A | ATATATAT others(15): Show |
1 | a0001c0001t0001g0225 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.804+4787_804+4788i others(24): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446429 | |||||
| chr12:50446429
|
A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0195 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.804+4787_804+4788i others(26): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446429 | |||||
| chr12:50446429
|
A | ATATATAT others(12): Show |
4 | a0001c0001t0001g0230a0001c0001t0001g0266a0001c0001t0001g0284others(1): Show | 4 | HG00438.hp2 HG02809.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.804+4787_804+4788i others(21): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446429 | |||||
| chr12:50446429
|
A | ATATATAT others(11): Show |
1 | a0001c0001t0004g0170 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.804+4787_804+4788i others(20): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446429 | |||||
| chr12:50446429
|
A | ATATATAT others(9): Show |
2 | a0001c0001t0001g0172a0001c0001t0001g0228 | 2 | HG02486.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.804+4787_804+4788i others(18): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446429 | |||||
| chr12:50446429
|
A | ATATATAT others(10): Show |
2 | a0001c0001t0001g0232a0001c0001t0001g0257 | 2 | HG03453.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.804+4787_804+4788i others(19): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446429 | |||||
| chr12:50446429
|
A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0237 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.804+4787_804+4788i others(20): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446429 | |||||
| chr12:50446429
|
A | ATATATAT others(7): Show |
1 | a0001c0001t0001g0285 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.804+4787_804+4788i others(16): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446429 | |||||
| chr12:50446429
|
A | ATATATAT others(8): Show |
2 | a0001c0001t0001g0235a0001c0001t0001g0316 | 2 | HG02970.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.804+4787_804+4788i others(17): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446429 | |||||
| chr12:50446429
|
A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0196 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.804+4787_804+4788i others(18): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446429 | |||||
| chr12:50446429
|
A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0264 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.804+4787_804+4788i others(14): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446429 | |||||
| chr12:50446429
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0229 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.804+4787_804+4788i others(15): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446429 | |||||
| chr12:50446429
|
A | ATATATAT others(7): Show |
2 | a0001c0001t0001g0233a0001c0001t0001g0318 | 2 | HG02155.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.804+4787_804+4788i others(16): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446429 | |||||
| chr12:50446429
|
A | ATATATAT others(4): Show |
2 | a0001c0001t0001g0234a0001c0001t0014g0238 | 2 | NA18992.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.804+4787_804+4788i others(13): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446429 | |||||
| chr12:50446429
|
A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0197 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.804+4787_804+4788i others(14): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446429 | |||||
| chr12:50446429
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0243 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.804+4787_804+4788i others(17): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446429 | |||||
| chr12:50446429
|
A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0244 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.804+4787_804+4788i others(18): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446429 | |||||
| chr12:50446429
|
A | ATATATAT others(3): Show |
1 | a0001c0001t0015g0317 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.804+4787_804+4788i others(12): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446429 | |||||
| chr12:50446429
|
A | ATATATTT others(4): Show |
1 | a0001c0001t0001g0245 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.804+4787_804+4788i others(13): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446429 | |||||
| chr12:50446429
|
A | T | 2 | a0001c0001t0001g0023a0001c0001t0001g0299 | 2 | HG02055.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.804+4786A>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50446429 | ||||||
| chr12:50446429
|
AT | A | 40 | a0001c0001t0002g0013a0001c0001t0002g0016a0001c0001t0002g0050others(37): Show | 40 | HG00099.hp1 HG00673.hp1 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.804+4801delT | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50446429 | |||||
| chr12:50446430
|
T | TA | 33 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0017others(30): Show | 33 | HG00438.hp1 HG00597.hp2 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.804+4787_804+4788i others(3): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50446430 | ||||||
| chr12:50446430
|
T | TATA | 11 | a0001c0001t0002g0019a0001c0001t0002g0052a0001c0001t0002g0056others(8): Show | 11 | HG00642.hp2 HG00738.hp1 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.804+4787_804+4788i others(5): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50446430 | ||||||
| chr12:50446430
|
T | TATATA | 8 | a0001c0001t0002g0073a0001c0001t0002g0100a0001c0001t0002g0107others(5): Show | 8 | HG02083.hp1 HG02165.hp1 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.804+4787_804+4788i others(7): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50446430 | ||||||
| chr12:50446430
|
T | TATATATA others(4): Show |
1 | a0003c0003t0001g0166 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.804+4787_804+4788i others(13): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50446430 | ||||||
| chr12:50446430
|
T | TATATATA others(6): Show |
1 | a0001c0001t0001g0216 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.804+4787_804+4788i others(15): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50446430 | ||||||
| chr12:50446430
|
T | TATATATA others(8): Show |
2 | a0001c0001t0001g0192a0001c0006t0007g0110 | 2 | HG00597.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.804+4787_804+4788i others(17): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50446430 | ||||||
| chr12:50446430
|
T | TATATATA others(16): Show |
2 | a0001c0001t0004g0208a0002c0002t0001g0281 | 2 | HG02040.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.804+4787_804+4788i others(25): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50446430 | ||||||
| chr12:50446430
|
T | TATATATA others(18): Show |
1 | a0001c0001t0001g0193 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.804+4787_804+4788i others(27): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50446430 | ||||||
| chr12:50446430
|
T | TATATATA others(20): Show |
4 | a0001c0001t0001g0203a0001c0001t0001g0222a0001c0001t0001g0282others(1): Show | 4 | HG02523.hp1 NA18999.hp2 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.804+4787_804+4788i others(29): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50446430 | ||||||
| chr12:50446430
|
T | TATATATA others(22): Show |
2 | a0001c0001t0001g0224a0001c0001t0001g0249 | 2 | NA18998.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.804+4787_804+4788i others(31): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50446430 | ||||||
| chr12:50446430
|
T | TATATATA others(24): Show |
1 | a0001c0001t0001g0247 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.804+4787_804+4788i others(33): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50446430 | ||||||
| chr12:50446430
|
T | TATATATA others(26): Show |
1 | a0001c0001t0013g0194 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.804+4787_804+4788i others(35): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50446430 | ||||||
| chr12:50446431
|
T | A | 47 | a0001c0001t0001g0036a0001c0001t0001g0154a0001c0001t0001g0155others(44): Show | 47 | HG00140.hp2 HG00544.hp2 HG01106.hp2 others(44): Show |
intron_variant | MODIFIER | c.804+4788T>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50446431 | ||||||
| chr12:50446432
|
T | A | 9 | a0001c0001t0001g0203a0001c0001t0001g0216a0001c0001t0001g0249others(6): Show | 9 | HG00597.hp2 HG01071.hp2 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.804+4789T>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50446432 | ||||||
| chr12:50446433
|
T | A | 12 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0159others(9): Show | 12 | HG02257.hp1 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.804+4790T>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50446433 | ||||||
| chr12:50446434
|
T | A | 2 | a0001c0001t0001g0203a0001c0001t0001g0216 | 2 | HG02523.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.804+4791T>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50446434 | ||||||
| chr12:50446443
|
T | A | 1 | a0001c0001t0001g0172 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.804+4800T>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50446443 | ||||||
| chr12:50446520
|
T | C | 125 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(122): Show | 125 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(122): Show |
intron_variant | MODIFIER | c.804+4877T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50446520 | ||||||
| chr12:50446523
|
G | T | 2 | a0001c0001t0020g0300a0001c0001t0021g0301 | 2 | HG02258.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.804+4880G>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50446523 | ||||||
| chr12:50446617
|
C | G | 1 | a0001c0001t0004g0150 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.804+4974C>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50446617 | ||||||
| chr12:50446638
|
A | T | 32 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(29): Show | 32 | HG00438.hp2 HG01346.hp2 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.804+4995A>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50446638 | ||||||
| chr12:50446664
|
T | G | 2 | a0001c0001t0008g0158a0001c0001t0008g0183 | 2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.804+5021T>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50446664 | ||||||
| chr12:50446679
|
A | G | 1 | a0001c0006t0007g0109 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.804+5036A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50446679 | ||||||
| chr12:50446706
|
C | T | 10 | a0001c0001t0002g0075a0001c0001t0002g0303a0001c0001t0002g0306others(7): Show | 10 | HG00099.hp1 HG01071.hp2 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.804+5063C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50446706 | ||||||
| chr12:50446798
|
G | A | 6 | a0001c0001t0005g0145a0001c0001t0005g0146a0001c0001t0005g0147others(3): Show | 6 | HG02258.hp2 HG02922.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.804+5155G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50446798 | ||||||
| chr12:50446884
|
G | A | 2 | a0001c0001t0020g0300a0001c0001t0021g0301 | 2 | HG02258.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.804+5241G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50446884 | ||||||
| chr12:50447041
|
A | G | 121 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(118): Show | 121 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(118): Show |
intron_variant | MODIFIER | c.804+5398A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50447041 | ||||||
| chr12:50447274
|
A | G | 126 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(123): Show | 126 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(123): Show |
intron_variant | MODIFIER | c.804+5631A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50447274 | ||||||
| chr12:50447326
|
AT | A | 5 | a0001c0001t0001g0006a0001c0001t0001g0218a0001c0001t0001g0219others(2): Show | 5 | NA18612.hp2 NA18964.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.804+5687delT | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50447326 | |||||
| chr12:50447502
|
G | A | 121 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(118): Show | 121 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(118): Show |
intron_variant | MODIFIER | c.804+5859G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50447502 | ||||||
| chr12:50447652
|
A | G | 1 | a0001c0001t0015g0317 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.805-5808A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50447652 | ||||||
| chr12:50447726
|
G | T | 1 | a0001c0001t0001g0192 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.805-5734G>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50447726 | ||||||
| chr12:50447790
|
C | T | 123 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(120): Show | 123 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(120): Show |
intron_variant | MODIFIER | c.805-5670C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50447790 | ||||||
| chr12:50447849
|
C | G | 27 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0233others(24): Show | 27 | HG00438.hp2 HG01884.hp1 HG02155.hp1 others(24): Show |
intron_variant | MODIFIER | c.805-5611C>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50447849 | ||||||
| chr12:50447858
|
T | A | 39 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(36): Show | 39 | HG00140.hp2 HG00544.hp2 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.805-5602T>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50447858 | ||||||
| chr12:50447858
|
T | TC | 16 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0203others(13): Show | 16 | HG00597.hp1 HG01109.hp2 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.805-5594dupC | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50447858 | |||||
| chr12:50447865
|
C | A | 39 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(36): Show | 39 | HG00140.hp2 HG00544.hp2 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.805-5595C>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50447865 | ||||||
| chr12:50447928
|
C | T | 132 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.805-5532C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50447928 | ||||||
| chr12:50447967
|
A | G | 2 | a0001c0001t0002g0103a0001c0001t0002g0120 | 2 | HG01346.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.805-5493A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50447967 | ||||||
| chr12:50448109
|
C | T | 132 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.805-5351C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50448109 | ||||||
| chr12:50448244
|
CT | C | 4 | a0001c0006t0007g0108a0001c0006t0007g0109a0001c0006t0007g0110others(1): Show | 4 | HG01109.hp1 HG02572.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.805-5211delT | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50448244 | |||||
| chr12:50448253
|
C | T | 121 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(118): Show | 121 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(118): Show |
intron_variant | MODIFIER | c.805-5207C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50448253 | ||||||
| chr12:50448268
|
C | T | 255 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(252): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.805-5192C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50448268 | ||||||
| chr12:50448284
|
A | G | 4 | a0001c0006t0007g0108a0001c0006t0007g0109a0001c0006t0007g0110others(1): Show | 4 | HG01109.hp1 HG02572.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.805-5176A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50448284 | ||||||
| chr12:50448328
|
A | G | 1 | a0001c0001t0002g0093 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.805-5132A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50448328 | ||||||
| chr12:50448389
|
GT | G | 4 | a0001c0006t0007g0108a0001c0006t0007g0109a0001c0006t0007g0110others(1): Show | 4 | HG01109.hp1 HG02572.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.805-5069delT | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50448389 | |||||
| chr12:50448512
|
A | G | 5 | a0001c0001t0001g0203a0001c0001t0001g0222a0001c0001t0001g0224others(2): Show | 5 | HG02523.hp1 NA18999.hp2 NA19001.hp2 others(2): Show |
intron_variant | MODIFIER | c.805-4948A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50448512 | ||||||
| chr12:50448514
|
C | A | 5 | a0001c0001t0001g0203a0001c0001t0001g0222a0001c0001t0001g0224others(2): Show | 5 | HG02523.hp1 NA18999.hp2 NA19001.hp2 others(2): Show |
intron_variant | MODIFIER | c.805-4946C>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50448514 | ||||||
| chr12:50448685
|
T | A | 1 | a0001c0001t0002g0058 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.805-4775T>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50448685 | ||||||
| chr12:50449021
|
C | T | 126 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(123): Show | 126 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(123): Show |
intron_variant | MODIFIER | c.805-4439C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50449021 | ||||||
| chr12:50449135
|
C | A | 1 | a0001c0001t0002g0305 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.805-4325C>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50449135 | ||||||
| chr12:50449229
|
G | A | 1 | a0003c0003t0001g0180 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.805-4231G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50449229 | ||||||
| chr12:50449400
|
A | G | 1 | a0001c0001t0001g0023 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.805-4060A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50449400 | ||||||
| chr12:50449434
|
C | T | 2 | a0001c0001t0004g0149a0001c0001t0004g0150 | 2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.805-4026C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50449434 | ||||||
| chr12:50449774
|
T | C | 1 | a0001c0001t0002g0127 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.805-3686T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50449774 | ||||||
| chr12:50449863
|
C | T | 27 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0233others(24): Show | 27 | HG00438.hp2 HG01884.hp1 HG02155.hp1 others(24): Show |
intron_variant | MODIFIER | c.805-3597C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50449863 | ||||||
| chr12:50449923
|
A | AT | 25 | a0001c0001t0001g0023a0001c0001t0001g0226a0001c0001t0001g0231others(22): Show | 25 | HG02055.hp1 HG02074.hp1 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.805-3508dupT | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50449923 | |||||
| chr12:50449923
|
A | ATT | 63 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(60): Show | 63 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.805-3509_805-3508d others(4): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50449923 | |||||
| chr12:50449923
|
A | ATTT | 24 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(21): Show | 24 | HG01346.hp2 HG01358.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.805-3510_805-3508d others(5): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50449923 | |||||
| chr12:50449923
|
A | ATTTT | 10 | a0001c0001t0001g0223a0001c0001t0001g0232a0001c0001t0001g0235others(7): Show | 10 | HG01167.hp1 HG02965.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.805-3511_805-3508d others(6): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50449923 | |||||
| chr12:50449923
|
AT | A | 148 | a0001c0001t0001g0021a0001c0001t0001g0036a0001c0001t0001g0154others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.805-3508delT | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50449923 | |||||
| chr12:50449923
|
ATT | A | 10 | a0001c0001t0001g0164a0001c0001t0001g0167a0001c0001t0001g0172others(7): Show | 10 | HG01169.hp2 HG01943.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.805-3509_805-3508d others(4): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50449923 | |||||
| chr12:50449978
|
G | C | 5 | a0001c0001t0001g0164a0001c0001t0001g0167a0001c0001t0001g0168others(2): Show | 5 | HG01167.hp2 HG01169.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.805-3482G>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50449978 | ||||||
| chr12:50450014
|
A | G | 4 | a0001c0001t0005g0145a0001c0001t0005g0146a0001c0001t0005g0147others(1): Show | 4 | HG02258.hp2 HG02922.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.805-3446A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50450014 | ||||||
| chr12:50450019
|
C | T | 132 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.805-3441C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50450019 | ||||||
| chr12:50450021
|
C | T | 126 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(123): Show | 126 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(123): Show |
intron_variant | MODIFIER | c.805-3439C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50450021 | ||||||
| chr12:50450140
|
G | A | 1 | a0001c0001t0002g0078 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.805-3320G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50450140 | ||||||
| chr12:50450177
|
G | A | 1 | a0004c0004t0001g0200 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.805-3283G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50450177 | ||||||
| chr12:50450463
|
T | G | 1 | a0003c0003t0001g0179 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.805-2997T>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50450463 | ||||||
| chr12:50450475
|
G | A | 259 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(256): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.805-2985G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50450475 | ||||||
| chr12:50450512
|
T | G | 117 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(114): Show | 117 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(114): Show |
intron_variant | MODIFIER | c.805-2948T>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50450512 | ||||||
| chr12:50450602
|
A | G | 1 | a0001c0001t0001g0218 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.805-2858A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50450602 | ||||||
| chr12:50450644
|
G | T | 1 | a0001c0001t0001g0286 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.805-2816G>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50450644 | ||||||
| chr12:50450779
|
G | A | 3 | a0001c0001t0001g0174a0001c0001t0001g0188a0001c0001t0001g0189 | 3 | HG03209.hp1 HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.805-2681G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50450779 | ||||||
| chr12:50451093
|
T | G | 121 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(118): Show | 121 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(118): Show |
intron_variant | MODIFIER | c.805-2367T>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50451093 | ||||||
| chr12:50451865
|
G | A | 4 | a0001c0006t0007g0108a0001c0006t0007g0109a0001c0006t0007g0110others(1): Show | 4 | HG01109.hp1 HG02572.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.805-1595G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50451865 | ||||||
| chr12:50452072
|
T | G | 121 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(118): Show | 121 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(118): Show |
intron_variant | MODIFIER | c.805-1388T>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50452072 | ||||||
| chr12:50452089
|
C | T | 259 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(256): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.805-1371C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50452089 | ||||||
| chr12:50452234
|
G | T | 1 | a0001c0001t0003g0026 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.805-1226G>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50452234 | ||||||
| chr12:50452235
|
A | G | 1 | a0001c0001t0003g0026 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.805-1225A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50452235 | ||||||
| chr12:50452236
|
C | A | 1 | a0001c0001t0003g0026 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.805-1224C>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50452236 | ||||||
| chr12:50452327
|
G | C | 4 | a0001c0001t0005g0145a0001c0001t0005g0146a0001c0001t0005g0147others(1): Show | 4 | HG02258.hp2 HG02922.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.805-1133G>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50452327 | ||||||
| chr12:50452407
|
C | T | 2 | a0001c0001t0010g0025a0001c0001t0010g0033 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.805-1053C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50452407 | ||||||
| chr12:50452417
|
A | C | 1 | a0001c0001t0001g0195 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.805-1043A>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50452417 | ||||||
| chr12:50452655
|
A | G | 1 | a0001c0001t0017g0304 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.805-805A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50452655 | ||||||
| chr12:50452790
|
G | A | 1 | a0001c0001t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.805-670G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50452790 | ||||||
| chr12:50452869
|
A | G | 2 | a0001c0001t0001g0270a0001c0001t0001g0293 | 2 | HG00673.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.805-591A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50452869 | ||||||
| chr12:50452973
|
G | A | 1 | a0001c0001t0002g0042 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.805-487G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50452973 | ||||||
| chr12:50453004
|
G | T | 1 | a0001c0001t0004g0202 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.805-456G>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50453004 | ||||||
| chr12:50453071
|
C | T | 136 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.805-389C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50453071 | ||||||
| chr12:50453074
|
C | CT | 6 | a0001c0001t0001g0001a0001c0001t0001g0190a0001c0001t0002g0129others(3): Show | 6 | HG00438.hp1 HG01978.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.805-369dupT | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 50453074 | |||||
| chr12:50453103
|
A | T | 4 | a0001c0006t0007g0108a0001c0006t0007g0109a0001c0006t0007g0110others(1): Show | 4 | HG01109.hp1 HG02572.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.805-357A>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50453103 | ||||||
| chr12:50453247
|
G | T | 1 | a0001c0001t0002g0107 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.805-213G>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50453247 | ||||||
| chr12:50453258
|
T | C | 1 | a0001c0001t0002g0070 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.805-202T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50453258 | ||||||
| chr12:50453265
|
T | C | 2 | a0001c0001t0001g0247a0001c0001t0001g0291 | 2 | NA19079.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.805-195T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50453265 | ||||||
| chr12:50453350
|
T | G | 1 | a0001c0010t0007g0111 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.805-110T>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50453350 | ||||||
| chr12:50453814
|
G | A | 1 | a0001c0001t0001g0204 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1017+142G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 9/15 | chr12 | 50453814 | ||||||
| chr12:50453820
|
A | G | 1 | a0001c0001t0001g0261 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1017+148A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 9/15 | chr12 | 50453820 | ||||||
| chr12:50453854
|
A | G | 117 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(114): Show | 117 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(114): Show |
intron_variant | MODIFIER | c.1017+182A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 9/15 | chr12 | 50453854 | ||||||
| chr12:50454027
|
A | G | 138 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(135): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.1018-287A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 9/15 | chr12 | 50454027 | ||||||
| chr12:50454113
|
C | T | 1 | a0001c0001t0004g0149 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1018-201C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 9/15 | chr12 | 50454113 | ||||||
| chr12:50454443
|
G | A | 1 | a0001c0001t0001g0289 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1121+26G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50454443 | ||||||
| chr12:50454724
|
A | T | 2 | a0001c0001t0002g0050a0001c0001t0002g0143 | 2 | NA19005.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.1121+307A>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50454724 | ||||||
| chr12:50454942
|
T | C | 4 | a0001c0001t0002g0071a0001c0001t0002g0073a0001c0001t0002g0081others(1): Show | 4 | HG02071.hp2 HG02155.hp2 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.1121+525T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50454942 | ||||||
| chr12:50454968
|
T | G | 1 | a0001c0001t0002g0305 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1121+551T>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50454968 | ||||||
| chr12:50455260
|
T | C | 259 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(256): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.1121+843T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50455260 | ||||||
| chr12:50455325
|
C | A | 1 | a0001c0001t0002g0077 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1121+908C>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50455325 | ||||||
| chr12:50455792
|
T | A | 1 | a0001c0001t0002g0077 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1121+1375T>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50455792 | ||||||
| chr12:50455807
|
C | G | 9 | a0001c0001t0001g0006a0001c0001t0001g0204a0001c0001t0001g0205others(6): Show | 9 | HG02027.hp1 NA18612.hp2 NA18959.hp1 others(6): Show |
intron_variant | MODIFIER | c.1121+1390C>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50455807 | ||||||
| chr12:50455809
|
G | A | 2 | a0003c0003t0001g0165a0003c0003t0001g0186 | 2 | HG03017.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1121+1392G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50455809 | ||||||
| chr12:50455836
|
C | T | 1 | a0001c0001t0002g0079 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1121+1419C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50455836 | ||||||
| chr12:50455906
|
G | T | 4 | a0001c0001t0005g0145a0001c0001t0005g0146a0001c0001t0005g0147others(1): Show | 4 | HG02258.hp2 HG02922.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1121+1489G>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50455906 | ||||||
| chr12:50455959
|
C | T | 1 | a0001c0001t0001g0024 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1121+1542C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50455959 | ||||||
| chr12:50456000
|
C | T | 1 | a0001c0001t0001g0277 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1121+1583C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50456000 | ||||||
| chr12:50456088
|
C | G | 1 | a0001c0001t0002g0306 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1121+1671C>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50456088 | ||||||
| chr12:50456247
|
C | G | 2 | a0001c0001t0004g0149a0001c0001t0004g0150 | 2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1121+1830C>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50456247 | ||||||
| chr12:50456389
|
T | A | 1 | a0001c0001t0001g0036 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1121+1972T>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50456389 | ||||||
| chr12:50456389
|
T | TA | 130 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.1121+1977dupA | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr12 | 50456389 | |||||
| chr12:50456433
|
T | C | 3 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0245 | 3 | HG01167.hp1 HG02965.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1121+2016T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50456433 | ||||||
| chr12:50456445
|
GCTTCTAA others(10): Show |
G | 1 | a0001c0001t0001g0024 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1121+2048_1121+206 others(21): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr12 | 50456445 | |||||
| chr12:50456517
|
T | A | 1 | a0001c0001t0002g0061 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1121+2100T>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50456517 | ||||||
| chr12:50456920
|
ATT | A | 135 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.1121+2513_1121+251 others(6): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr12 | 50456920 | |||||
| chr12:50456956
|
G | A | 1 | a0002c0002t0001g0211 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1121+2539G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50456956 | ||||||
| chr12:50456993
|
A | G | 118 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(115): Show | 118 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(115): Show |
intron_variant | MODIFIER | c.1121+2576A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50456993 | ||||||
| chr12:50457053
|
C | T | 1 | a0001c0001t0001g0006 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1121+2636C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50457053 | ||||||
| chr12:50457057
|
C | A | 1 | a0001c0001t0002g0124 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1121+2640C>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50457057 | ||||||
| chr12:50457201
|
C | CT | 18 | a0001c0001t0001g0023a0001c0001t0001g0176a0001c0001t0001g0221others(15): Show | 18 | HG00438.hp1 HG00642.hp2 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.1121+2805dupT | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr12 | 50457201 | |||||
| chr12:50457201
|
C | CTT | 100 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(97): Show | 100 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.1121+2804_1121+280 others(6): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr12 | 50457201 | |||||
| chr12:50457201
|
C | CTTT | 18 | a0001c0001t0001g0201a0001c0001t0001g0206a0001c0001t0001g0226others(15): Show | 18 | HG01361.hp1 HG01934.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.1121+2803_1121+280 others(7): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr12 | 50457201 | |||||
| chr12:50457222
|
TA | T | 6 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0167others(3): Show | 6 | HG02257.hp1 HG02895.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1121+2808delA | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr12 | 50457222 | |||||
| chr12:50457223
|
A | T | 296 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(293): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.1121+2806A>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50457223 | ||||||
| chr12:50457251
|
G | T | 117 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(114): Show | 117 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(114): Show |
intron_variant | MODIFIER | c.1121+2834G>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50457251 | ||||||
| chr12:50457276
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1121+2859G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50457276 | ||||||
| chr12:50457326
|
C | T | 1 | a0001c0001t0015g0317 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1121+2909C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50457326 | ||||||
| chr12:50457356
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1121+2939G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50457356 | ||||||
| chr12:50457505
|
C | T | 5 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(2): Show | 5 | HG01346.hp2 HG02809.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1121+3088C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50457505 | ||||||
| chr12:50457510
|
C | G | 261 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(258): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.1121+3093C>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50457510 | ||||||
| chr12:50457690
|
T | C | 1 | a0003c0003t0001g0163 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1121+3273T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50457690 | ||||||
| chr12:50457757
|
T | G | 1 | a0001c0001t0001g0197 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1121+3340T>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50457757 | ||||||
| chr12:50457812
|
C | CA | 52 | a0001c0001t0001g0036a0001c0001t0001g0155a0001c0001t0001g0156others(49): Show | 52 | HG00140.hp2 HG00544.hp2 HG01106.hp2 others(49): Show |
intron_variant | MODIFIER | c.1122-3309dupA | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr12 | 50457812 | |||||
| chr12:50457812
|
C | CAA | 129 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(126): Show | 129 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(126): Show |
intron_variant | MODIFIER | c.1122-3310_1122-330 others(6): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr12 | 50457812 | |||||
| chr12:50457812
|
C | CAAA | 109 | a0001c0001t0001g0236a0001c0001t0001g0289a0001c0001t0002g0013others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.1122-3311_1122-330 others(7): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr12 | 50457812 | |||||
| chr12:50457812
|
C | CAAAA | 7 | a0001c0001t0002g0051a0001c0001t0002g0055a0001c0001t0002g0069others(4): Show | 7 | HG01074.hp2 NA18954.hp1 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.1122-3312_1122-330 others(8): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr12 | 50457812 | |||||
| chr12:50457812
|
CA | C | 6 | a0001c0001t0003g0026a0001c0001t0003g0028a0001c0001t0003g0029others(3): Show | 6 | HG02109.hp2 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1122-3309delA | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr12 | 50457812 | |||||
| chr12:50457904
|
A | G | 1 | a0001c0001t0015g0317 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1122-3231A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50457904 | ||||||
| chr12:50457935
|
C | CT | 109 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(106): Show | 109 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(106): Show |
intron_variant | MODIFIER | c.1122-3184dupT | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr12 | 50457935 | |||||
| chr12:50457935
|
C | CTT | 8 | a0001c0001t0001g0249a0001c0001t0001g0282a0001c0001t0001g0289others(5): Show | 8 | HG02109.hp1 HG02559.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1122-3185_1122-318 others(6): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr12 | 50457935 | |||||
| chr12:50457935
|
CT | C | 6 | a0001c0001t0001g0036a0001c0001t0002g0077a0001c0006t0007g0108others(3): Show | 6 | HG01069.hp2 HG01169.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1122-3184delT | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr12 | 50457935 | |||||
| chr12:50458027
|
A | G | 1 | a0001c0001t0002g0103 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1122-3108A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50458027 | ||||||
| chr12:50458038
|
A | G | 80 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(77): Show | 80 | HG00597.hp1 HG00642.hp1 HG00673.hp2 others(77): Show |
intron_variant | MODIFIER | c.1122-3097A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50458038 | ||||||
| chr12:50458273
|
T | G | 1 | a0001c0001t0011g0314 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1122-2862T>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50458273 | ||||||
| chr12:50458365
|
C | T | 2 | a0001c0001t0001g0226a0001c0001t0001g0283 | 2 | HG03710.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1122-2770C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50458365 | ||||||
| chr12:50458498
|
G | A | 23 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0233others(20): Show | 23 | HG00438.hp2 HG01884.hp1 HG02155.hp1 others(20): Show |
intron_variant | MODIFIER | c.1122-2637G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50458498 | ||||||
| chr12:50458648
|
A | C | 1 | a0001c0001t0003g0034 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1122-2487A>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50458648 | ||||||
| chr12:50458744
|
C | T | 1 | a0001c0001t0001g0284 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1122-2391C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50458744 | ||||||
| chr12:50458833
|
C | G | 4 | a0001c0001t0006g0273a0001c0001t0006g0274a0001c0001t0006g0275others(1): Show | 4 | HG02109.hp1 HG02647.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1122-2302C>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50458833 | ||||||
| chr12:50458938
|
T | C | 1 | a0001c0001t0001g0011 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1122-2197T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50458938 | ||||||
| chr12:50459058
|
G | C | 2 | a0001c0001t0020g0300a0001c0001t0021g0301 | 2 | HG02258.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1122-2077G>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50459058 | ||||||
| chr12:50459428
|
C | T | 1 | a0001c0001t0001g0175 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1122-1707C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50459428 | ||||||
| chr12:50459499
|
G | A | 4 | a0001c0001t0001g0242a0001c0001t0001g0286a0001c0001t0001g0292others(1): Show | 4 | HG04115.hp1 HG04204.hp1 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.1122-1636G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50459499 | ||||||
| chr12:50459527
|
T | C | 5 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(2): Show | 5 | HG02055.hp1 HG02145.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1122-1608T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50459527 | ||||||
| chr12:50459631
|
G | A | 1 | a0001c0001t0002g0089 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1122-1504G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50459631 | ||||||
| chr12:50459716
|
C | T | 1 | a0002c0002t0001g0215 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1122-1419C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50459716 | ||||||
| chr12:50459780
|
C | T | 6 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(3): Show | 6 | HG02257.hp1 HG02280.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1122-1355C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50459780 | ||||||
| chr12:50459822
|
C | CA | 14 | a0001c0001t0001g0022a0001c0001t0001g0036a0001c0001t0001g0175others(11): Show | 14 | HG00544.hp2 HG01346.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1122-1289dupA | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr12 | 50459822 | |||||
| chr12:50459822
|
CA | C | 107 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(104): Show | 107 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(104): Show |
intron_variant | MODIFIER | c.1122-1289delA | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr12 | 50459822 | |||||
| chr12:50459822
|
CAAA | C | 12 | a0001c0001t0002g0053a0001c0001t0002g0063a0001c0001t0002g0064others(9): Show | 12 | HG00438.hp1 HG01358.hp2 HG02148.hp2 others(9): Show |
intron_variant | MODIFIER | c.1122-1291_1122-128 others(7): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr12 | 50459822 | |||||
| chr12:50459822
|
CAAAA | C | 93 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(90): Show | 93 | HG00099.hp1 HG00597.hp2 HG00642.hp2 others(90): Show |
intron_variant | MODIFIER | c.1122-1292_1122-128 others(8): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr12 | 50459822 | |||||
| chr12:50459822
|
CAAAAAAA others(8): Show |
C | 26 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0044others(23): Show | 26 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.1122-1303_1122-128 others(19): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr12 | 50459822 | |||||
| chr12:50459888
|
C | T | 5 | a0001c0001t0002g0306a0001c0001t0002g0311a0001c0001t0002g0312others(2): Show | 5 | HG01255.hp2 HG01515.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.1122-1247C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50459888 | ||||||
| chr12:50459907
|
G | A | 4 | a0001c0006t0007g0108a0001c0006t0007g0109a0001c0006t0007g0110others(1): Show | 4 | HG01109.hp1 HG02572.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1122-1228G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50459907 | ||||||
| chr12:50459962
|
C | G | 1 | a0001c0001t0015g0317 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1122-1173C>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50459962 | ||||||
| chr12:50460099
|
C | T | 1 | a0001c0001t0002g0127 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1122-1036C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50460099 | ||||||
| chr12:50460118
|
G | C | 1 | a0001c0001t0002g0082 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1122-1017G>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50460118 | ||||||
| chr12:50460137
|
CA | C | 118 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(115): Show | 118 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(115): Show |
intron_variant | MODIFIER | c.1122-984delA | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr12 | 50460137 | |||||
| chr12:50460149
|
A | G | 39 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(36): Show | 39 | HG00140.hp2 HG00544.hp2 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.1122-986A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50460149 | ||||||
| chr12:50460297
|
T | C | 1 | a0001c0001t0011g0314 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1122-838T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50460297 | ||||||
| chr12:50460413
|
A | T | 1 | a0007c0013t0002g0101 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1122-722A>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50460413 | ||||||
| chr12:50460477
|
ATACCACT others(16): Show |
A | 13 | a0001c0001t0001g0177a0001c0001t0001g0190a0003c0003t0001g0153others(10): Show | 13 | HG00140.hp2 HG00544.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.1122-656_1122-634d others(25): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr12 | 50460477 | |||||
| chr12:50460521
|
G | T | 1 | a0001c0001t0021g0301 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1122-614G>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50460521 | ||||||
| chr12:50460590
|
C | T | 2 | a0002c0002t0001g0214a0002c0002t0001g0217 | 2 | HG03834.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.1122-545C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50460590 | ||||||
| chr12:50460613
|
T | C | 4 | a0001c0006t0007g0108a0001c0006t0007g0109a0001c0006t0007g0110others(1): Show | 4 | HG01109.hp1 HG02572.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1122-522T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50460613 | ||||||
| chr12:50460671
|
T | C | 39 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(36): Show | 39 | HG00140.hp2 HG00544.hp2 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.1122-464T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50460671 | ||||||
| chr12:50460787
|
C | G | 4 | a0001c0001t0006g0273a0001c0001t0006g0274a0001c0001t0006g0275others(1): Show | 4 | HG02109.hp1 HG02647.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1122-348C>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50460787 | ||||||
| chr12:50460906
|
C | T | 2 | a0001c0001t0002g0074a0001c0001t0002g0308 | 2 | HG00099.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1122-229C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50460906 | ||||||
| chr12:50460907
|
G | A | 2 | a0006c0008t0005g0037a0006c0008t0005g0038 | 2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1122-228G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50460907 | ||||||
| chr12:50460928
|
C | T | 2 | a0001c0001t0004g0149a0001c0001t0004g0150 | 2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1122-207C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50460928 | ||||||
| chr12:50460959
|
T | C | 2 | a0001c0001t0004g0169a0001c0001t0004g0170 | 2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.1122-176T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50460959 | ||||||
| chr12:50460981
|
G | A | 4 | a0001c0001t0006g0273a0001c0001t0006g0274a0001c0001t0006g0275others(1): Show | 4 | HG02109.hp1 HG02647.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1122-154G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50460981 | ||||||
| chr12:50460987
|
G | C | 1 | a0001c0001t0019g0134 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1122-148G>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50460987 | ||||||
| chr12:50461108
|
G | A | 4 | a0001c0006t0007g0108a0001c0006t0007g0109a0001c0006t0007g0110others(1): Show | 4 | HG01109.hp1 HG02572.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1122-27G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50461108 | ||||||
| chr12:50461113
|
T | C | 1 | a0001c0001t0001g0195 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1122-22T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50461113 | ||||||
| chr12:50461412
|
A | G | 138 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(135): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.1334+65A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 11/15 | chr12 | 50461412 | ||||||
| chr12:50461474
|
C | T | 7 | a0002c0002t0001g0207a0002c0002t0001g0211a0002c0002t0001g0215others(4): Show | 7 | HG02071.hp1 NA18979.hp2 NA18990.hp2 others(4): Show |
intron_variant | MODIFIER | c.1334+127C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 11/15 | chr12 | 50461474 | ||||||
| chr12:50461492
|
A | G | 1 | a0001c0001t0002g0065 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1334+145A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 11/15 | chr12 | 50461492 | ||||||
| chr12:50461528
|
G | GCCCATAC others(7): Show |
1 | a0001c0001t0002g0130 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1334+182_1334+195d others(16): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr12 | 50461528 | |||||
| chr12:50461693
|
A | T | 1 | a0007c0013t0002g0101 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1334+346A>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 11/15 | chr12 | 50461693 | ||||||
| chr12:50461702
|
A | G | 14 | a0002c0002t0001g0207a0002c0002t0001g0210a0002c0002t0001g0211others(11): Show | 14 | HG02071.hp1 HG03834.hp2 NA18943.hp1 others(11): Show |
intron_variant | MODIFIER | c.1334+355A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 11/15 | chr12 | 50461702 | ||||||
| chr12:50461705
|
C | T | 1 | a0001c0001t0014g0238 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1334+358C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 11/15 | chr12 | 50461705 | ||||||
| chr12:50461945
|
G | A | 1 | a0001c0001t0002g0078 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1334+598G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 11/15 | chr12 | 50461945 | ||||||
| chr12:50461946
|
C | T | 1 | a0001c0001t0001g0036 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1334+599C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 11/15 | chr12 | 50461946 | ||||||
| chr12:50461968
|
T | C | 118 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(115): Show | 118 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(115): Show |
intron_variant | MODIFIER | c.1335-614T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 11/15 | chr12 | 50461968 | ||||||
| chr12:50462046
|
A | G | 1 | a0001c0001t0002g0309 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1335-536A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 11/15 | chr12 | 50462046 | ||||||
| chr12:50462339
|
G | A | 39 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(36): Show | 39 | HG00140.hp2 HG00544.hp2 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.1335-243G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 11/15 | chr12 | 50462339 | ||||||
| chr12:50462463
|
C | T | 1 | a0001c0001t0002g0102 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1335-119C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 11/15 | chr12 | 50462463 | ||||||
| chr12:50462476
|
C | CA | 252 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(249): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.1335-92dupA | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr12 | 50462476 | |||||
| chr12:50462476
|
C | CAA | 53 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(50): Show | 53 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.1335-93_1335-92dup others(2): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr12 | 50462476 | |||||
| chr12:50462696
|
C | T | 6 | a0001c0001t0001g0283a0001c0001t0006g0273a0001c0001t0006g0274others(3): Show | 6 | HG02109.hp1 HG02647.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1383+66C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 12/15 | chr12 | 50462696 | ||||||
| chr12:50462803
|
C | T | 1 | a0001c0001t0011g0314 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1383+173C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 12/15 | chr12 | 50462803 | ||||||
| chr12:50462809
|
A | G | 1 | a0001c0001t0002g0079 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1383+179A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 12/15 | chr12 | 50462809 | ||||||
| chr12:50462821
|
G | A | 5 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(2): Show | 5 | HG02055.hp1 HG02145.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1383+191G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 12/15 | chr12 | 50462821 | ||||||
| chr12:50462830
|
T | G | 138 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(135): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.1383+200T>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 12/15 | chr12 | 50462830 | ||||||
| chr12:50462999
|
C | T | 1 | a0001c0001t0002g0052 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1383+369C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 12/15 | chr12 | 50462999 | ||||||
| chr12:50463037
|
A | G | 1 | a0001c0001t0002g0151 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1383+407A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 12/15 | chr12 | 50463037 | ||||||
| chr12:50463142
|
C | T | 1 | a0001c0001t0001g0036 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1383+512C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 12/15 | chr12 | 50463142 | ||||||
| chr12:50463158
|
G | A | 1 | a0001c0001t0002g0143 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1383+528G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 12/15 | chr12 | 50463158 | ||||||
| chr12:50463359
|
G | A | 1 | a0001c0001t0002g0070 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1383+729G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 12/15 | chr12 | 50463359 | ||||||
| chr12:50463415
|
C | G | 2 | a0001c0001t0002g0040a0001c0012t0002g0066 | 2 | HG02451.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1383+785C>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 12/15 | chr12 | 50463415 | ||||||
| chr12:50463418
|
T | TA | 47 | a0001c0001t0001g0024a0001c0001t0001g0036a0001c0001t0001g0154others(44): Show | 47 | HG01361.hp1 HG01884.hp1 HG01975.hp1 others(44): Show |
intron_variant | MODIFIER | c.1383+788_1383+789i others(3): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 12/15 | chr12 | 50463418 | ||||||
| chr12:50463418
|
TCCAAAAA others(4): Show |
T | 1 | a0001c0001t0001g0262 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1383+789_1383+799d others(13): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 12/15 | chr12 | 50463418 | ||||||
| chr12:50463418
|
TCCAAAAA others(7): Show |
T | 2 | a0006c0008t0005g0037a0006c0008t0005g0038 | 2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1383+789_1383+802d others(16): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 12/15 | chr12 | 50463418 | ||||||
| chr12:50463419
|
C | A | 264 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(261): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1383+789C>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 12/15 | chr12 | 50463419 | ||||||
| chr12:50463420
|
C | A | 47 | a0001c0001t0001g0024a0001c0001t0001g0036a0001c0001t0001g0154others(44): Show | 47 | HG01361.hp1 HG01884.hp1 HG01975.hp1 others(44): Show |
intron_variant | MODIFIER | c.1383+790C>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 12/15 | chr12 | 50463420 | ||||||
| chr12:50463420
|
C | CAA | 20 | a0001c0001t0001g0156a0001c0001t0001g0161a0001c0001t0001g0164others(17): Show | 20 | HG00544.hp2 HG01106.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.1383+817_1383+818d others(4): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr12 | 50463420 | |||||
| chr12:50463420
|
CA | C | 142 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.1383+818delA | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr12 | 50463420 | |||||
| chr12:50463422
|
A | C | 2 | a0001c0001t0001g0006a0001c0001t0002g0043 | 2 | NA19057.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1383+792A>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 12/15 | chr12 | 50463422 | ||||||
| chr12:50463426
|
A | C | 1 | a0003c0003t0001g0162 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1383+796A>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 12/15 | chr12 | 50463426 | ||||||
| chr12:50463431
|
A | C | 1 | a0001c0001t0001g0262 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1383+801A>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 12/15 | chr12 | 50463431 | ||||||
| chr12:50463434
|
A | C | 2 | a0006c0008t0005g0037a0006c0008t0005g0038 | 2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1383+804A>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 12/15 | chr12 | 50463434 | ||||||
| chr12:50463600
|
A | G | 1 | a0004c0004t0001g0200 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1383+970A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 12/15 | chr12 | 50463600 | ||||||
| chr12:50463685
|
C | T | 1 | a0001c0001t0015g0317 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1383+1055C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 12/15 | chr12 | 50463685 | ||||||
| chr12:50464133
|
G | A | 2 | a0001c0001t0001g0196a0001c0001t0001g0197 | 2 | HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1383+1503G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 12/15 | chr12 | 50464133 | ||||||
| chr12:50464160
|
G | T | 2 | a0001c0001t0010g0025a0001c0001t0010g0033 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1383+1530G>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 12/15 | chr12 | 50464160 | ||||||
| chr12:50464486
|
G | A | 137 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.1383+1856G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 12/15 | chr12 | 50464486 | ||||||
| chr12:50464581
|
CG | C | 4 | a0001c0006t0007g0108a0001c0006t0007g0109a0001c0006t0007g0110others(1): Show | 4 | HG01109.hp1 HG02572.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1383+1953delG | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr12 | 50464581 | |||||
| chr12:50464846
|
G | A | 302 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(299): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.1384-2113G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 12/15 | chr12 | 50464846 | ||||||
| chr12:50465037
|
C | T | 135 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.1384-1922C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 12/15 | chr12 | 50465037 | ||||||
| chr12:50465098
|
G | A | 2 | a0001c0001t0004g0149a0001c0001t0004g0150 | 2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1384-1861G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 12/15 | chr12 | 50465098 | ||||||
| chr12:50465228
|
C | T | 113 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(110): Show | 113 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(110): Show |
intron_variant | MODIFIER | c.1384-1731C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 12/15 | chr12 | 50465228 | ||||||
| chr12:50465229
|
G | A | 1 | a0003c0003t0001g0180 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1384-1730G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 12/15 | chr12 | 50465229 | ||||||
| chr12:50465302
|
G | A | 117 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(114): Show | 117 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(114): Show |
intron_variant | MODIFIER | c.1384-1657G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 12/15 | chr12 | 50465302 | ||||||
| chr12:50465371
|
C | CA | 129 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0039others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.1384-1570dupA | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr12 | 50465371 | |||||
| chr12:50465371
|
C | CAA | 6 | a0001c0001t0002g0045a0001c0001t0002g0120a0001c0001t0002g0306others(3): Show | 6 | HG01346.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1384-1571_1384-157 others(6): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr12 | 50465371 | |||||
| chr12:50465371
|
C | CAAA | 7 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(4): Show | 7 | HG01361.hp2 HG01928.hp2 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.1384-1572_1384-157 others(7): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr12 | 50465371 | |||||
| chr12:50465380
|
A | G | 113 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(110): Show | 113 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(110): Show |
intron_variant | MODIFIER | c.1384-1579A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 12/15 | chr12 | 50465380 | ||||||
| chr12:50465394
|
G | A | 136 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.1384-1565G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 12/15 | chr12 | 50465394 | ||||||
| chr12:50465499
|
G | A | 117 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(114): Show | 117 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(114): Show |
intron_variant | MODIFIER | c.1384-1460G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 12/15 | chr12 | 50465499 | ||||||
| chr12:50466022
|
A | G | 1 | a0001c0001t0001g0230 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1384-937A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 12/15 | chr12 | 50466022 | ||||||
| chr12:50466085
|
A | T | 4 | a0001c0001t0006g0273a0001c0001t0006g0274a0001c0001t0006g0275others(1): Show | 4 | HG02109.hp1 HG02647.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1384-874A>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 12/15 | chr12 | 50466085 | ||||||
| chr12:50466336
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1384-623G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 12/15 | chr12 | 50466336 | ||||||
| chr12:50466429
|
C | T | 1 | a0001c0001t0001g0199 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1384-530C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 12/15 | chr12 | 50466429 | ||||||
| chr12:50466462
|
A | T | 138 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(135): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.1384-497A>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 12/15 | chr12 | 50466462 | ||||||
| chr12:50466534
|
A | G | 3 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0096 | 3 | HG01261.hp2 HG03492.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1384-425A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 12/15 | chr12 | 50466534 | ||||||
| chr12:50466548
|
A | G | 2 | a0001c0001t0004g0149a0001c0001t0004g0150 | 2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1384-411A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 12/15 | chr12 | 50466548 | ||||||
| chr12:50466549
|
G | A | 5 | a0001c0001t0001g0164a0001c0001t0001g0167a0001c0001t0001g0168others(2): Show | 5 | HG01167.hp2 HG01169.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.1384-410G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 12/15 | chr12 | 50466549 | ||||||
| chr12:50466867
|
T | G | 1 | a0001c0001t0004g0149 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1384-92T>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 12/15 | chr12 | 50466867 | ||||||
| chr12:50466914
|
G | T | 6 | a0001c0001t0003g0026a0001c0001t0003g0028a0001c0001t0003g0029others(3): Show | 6 | HG02109.hp2 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1384-45G>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 12/15 | chr12 | 50466914 | ||||||
| chr12:50467275
|
T | G | 1 | a0001c0001t0002g0013 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1545+155T>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | chr12 | 50467275 | ||||||
| chr12:50467447
|
T | A | 1 | a0001c0001t0001g0279 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1545+327T>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | chr12 | 50467447 | ||||||
| chr12:50467761
|
G | A | 302 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(299): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.1545+641G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | chr12 | 50467761 | ||||||
| chr12:50467857
|
G | GT | 136 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.1545+747dupT | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr12 | 50467857 | |||||
| chr12:50467867
|
T | TA | 113 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(110): Show | 113 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(110): Show |
intron_variant | MODIFIER | c.1545+749dupA | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr12 | 50467867 | |||||
| chr12:50468072
|
C | T | 137 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.1545+952C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | chr12 | 50468072 | ||||||
| chr12:50468172
|
G | T | 1 | a0001c0001t0004g0220 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1545+1052G>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | chr12 | 50468172 | ||||||
| chr12:50468229
|
C | T | 118 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(115): Show | 118 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(115): Show |
intron_variant | MODIFIER | c.1545+1109C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | chr12 | 50468229 | ||||||
| chr12:50468294
|
C | CT | 137 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.1545+1183dupT | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr12 | 50468294 | |||||
| chr12:50468356
|
C | T | 1 | a0005c0007t0002g0119 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1545+1236C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | chr12 | 50468356 | ||||||
| chr12:50468451
|
G | A | 129 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.1545+1331G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | chr12 | 50468451 | ||||||
| chr12:50468901
|
G | T | 1 | a0001c0001t0006g0274 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1545+1781G>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | chr12 | 50468901 | ||||||
| chr12:50468938
|
C | A | 302 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(299): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.1545+1818C>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | chr12 | 50468938 | ||||||
| chr12:50469264
|
T | C | 1 | a0001c0001t0001g0286 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1545+2144T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | chr12 | 50469264 | ||||||
| chr12:50469271
|
A | G | 2 | a0001c0001t0002g0311a0001c0001t0002g0312 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1545+2151A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | chr12 | 50469271 | ||||||
| chr12:50469400
|
C | T | 1 | a0007c0013t0002g0101 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1545+2280C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | chr12 | 50469400 | ||||||
| chr12:50469401
|
G | A | 1 | a0001c0001t0002g0082 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1545+2281G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | chr12 | 50469401 | ||||||
| chr12:50469458
|
G | A | 2 | a0001c0001t0004g0149a0001c0001t0004g0150 | 2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1545+2338G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | chr12 | 50469458 | ||||||
| chr12:50469493
|
T | C | 1 | a0001c0001t0001g0178 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1545+2373T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | chr12 | 50469493 | ||||||
| chr12:50469601
|
C | CA | 134 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0233others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.1545+2503dupA | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr12 | 50469601 | |||||
| chr12:50469601
|
C | CAA | 15 | a0001c0001t0001g0206a0001c0001t0002g0016a0001c0001t0002g0019others(12): Show | 15 | HG01261.hp2 HG01358.hp2 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.1545+2502_1545+250 others(6): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr12 | 50469601 | |||||
| chr12:50469601
|
CA | C | 9 | a0001c0001t0001g0155a0001c0001t0001g0157a0001c0001t0001g0219others(6): Show | 9 | HG00140.hp2 HG02258.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.1545+2503delA | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr12 | 50469601 | |||||
| chr12:50469772
|
G | A | 6 | a0001c0001t0002g0068a0001c0001t0002g0070a0001c0001t0002g0074others(3): Show | 6 | HG00099.hp2 HG01074.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.1545+2652G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | chr12 | 50469772 | ||||||
| chr12:50469831
|
C | T | 2 | a0001c0001t0002g0106a0001c0001t0002g0137 | 2 | HG00140.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1545+2711C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | chr12 | 50469831 | ||||||
| chr12:50469882
|
C | G | 1 | a0001c0001t0001g0161 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1545+2762C>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | chr12 | 50469882 | ||||||
| chr12:50469891
|
A | G | 1 | a0004c0004t0001g0200 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1545+2771A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | chr12 | 50469891 | ||||||
| chr12:50469928
|
A | G | 2 | a0001c0001t0009g0048a0001c0001t0009g0059 | 2 | HG00741.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.1545+2808A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | chr12 | 50469928 | ||||||
| chr12:50469937
|
TAGGC | T | 126 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(123): Show | 126 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(123): Show |
intron_variant | MODIFIER | c.1545+2823_1545+282 others(8): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr12 | 50469937 | |||||
| chr12:50470018
|
G | A | 1 | a0001c0001t0001g0318 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1545+2898G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | chr12 | 50470018 | ||||||
| chr12:50470048
|
C | T | 1 | a0001c0001t0015g0317 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1545+2928C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | chr12 | 50470048 | ||||||
| chr12:50470184
|
A | G | 8 | a0001c0001t0005g0145a0001c0001t0005g0146a0001c0001t0005g0147others(5): Show | 8 | HG02258.hp1 HG02258.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.1545+3064A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | chr12 | 50470184 | ||||||
| chr12:50470220
|
CA | C | 316 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(313): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.1545+3112delA | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr12 | 50470220 | |||||
| chr12:50470287
|
C | T | 2 | a0001c0001t0004g0169a0001c0001t0004g0170 | 2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.1546-3128C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | chr12 | 50470287 | ||||||
| chr12:50470412
|
A | T | 2 | a0001c0001t0010g0025a0001c0001t0010g0033 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1546-3003A>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | chr12 | 50470412 | ||||||
| chr12:50470415
|
T | C | 1 | a0001c0001t0012g0246 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1546-3000T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | chr12 | 50470415 | ||||||
| chr12:50470443
|
T | C | 3 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0284 | 3 | HG01346.hp2 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1546-2972T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | chr12 | 50470443 | ||||||
| chr12:50470558
|
C | T | 2 | a0001c0001t0002g0074a0001c0001t0002g0308 | 2 | HG00099.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1546-2857C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | chr12 | 50470558 | ||||||
| chr12:50470667
|
C | T | 1 | a0001c0001t0009g0059 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1546-2748C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | chr12 | 50470667 | ||||||
| chr12:50470686
|
G | C | 2 | a0001c0001t0010g0025a0001c0001t0010g0033 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1546-2729G>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | chr12 | 50470686 | ||||||
| chr12:50470844
|
T | C | 39 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(36): Show | 39 | HG00140.hp2 HG00544.hp2 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.1546-2571T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | chr12 | 50470844 | ||||||
| chr12:50470899
|
G | C | 1 | a0001c0001t0015g0317 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1546-2516G>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | chr12 | 50470899 | ||||||
| chr12:50470936
|
A | G | 1 | a0001c0001t0002g0087 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1546-2479A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | chr12 | 50470936 | ||||||
| chr12:50471516
|
G | A | 1 | a0001c0001t0001g0223 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1546-1899G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | chr12 | 50471516 | ||||||
| chr12:50471563
|
G | A | 1 | a0001c0001t0002g0269 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1546-1852G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | chr12 | 50471563 | ||||||
| chr12:50471564
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1546-1851C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | chr12 | 50471564 | ||||||
| chr12:50471626
|
C | T | 37 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(34): Show | 37 | HG00140.hp2 HG00544.hp2 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.1546-1789C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | chr12 | 50471626 | ||||||
| chr12:50471642
|
G | T | 1 | a0001c0001t0015g0317 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1546-1773G>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | chr12 | 50471642 | ||||||
| chr12:50471670
|
G | A | 3 | a0001c0001t0001g0199a0001c0001t0001g0270a0001c0001t0001g0293 | 3 | HG00673.hp2 NA18747.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.1546-1745G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | chr12 | 50471670 | ||||||
| chr12:50471989
|
A | G | 5 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(2): Show | 5 | HG02055.hp1 HG02145.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1546-1426A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | chr12 | 50471989 | ||||||
| chr12:50472404
|
A | G | 5 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(2): Show | 5 | HG02055.hp1 HG02145.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1546-1011A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | chr12 | 50472404 | ||||||
| chr12:50472500
|
A | AT | 117 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(114): Show | 117 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(114): Show |
intron_variant | MODIFIER | c.1546-906dupT | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr12 | 50472500 | |||||
| chr12:50472556
|
G | C | 2 | a0001c0001t0020g0300a0001c0001t0021g0301 | 2 | HG02258.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1546-859G>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | chr12 | 50472556 | ||||||
| chr12:50472559
|
C | T | 3 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023 | 3 | HG02055.hp1 HG02615.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1546-856C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | chr12 | 50472559 | ||||||
| chr12:50472560
|
C | T | 3 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023 | 3 | HG02055.hp1 HG02615.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1546-855C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | chr12 | 50472560 | ||||||
| chr12:50472574
|
C | T | 3 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197 | 3 | HG01891.hp1 HG06807.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1546-841C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | chr12 | 50472574 | ||||||
| chr12:50472721
|
A | G | 2 | a0001c0001t0001g0196a0001c0001t0001g0197 | 2 | HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1546-694A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | chr12 | 50472721 | ||||||
| chr12:50472835
|
T | G | 4 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0278others(1): Show | 4 | NA18959.hp1 NA19010.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.1546-580T>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | chr12 | 50472835 | ||||||
| chr12:50472896
|
T | G | 1 | a0001c0001t0001g0218 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1546-519T>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | chr12 | 50472896 | ||||||
| chr12:50473220
|
C | T | 1 | a0001c0006t0007g0110 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1546-195C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | chr12 | 50473220 | ||||||
| chr12:50473249
|
T | A | 129 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.1546-166T>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | chr12 | 50473249 | ||||||
| chr12:50473577
|
T | A | 2 | a0001c0001t0020g0300a0001c0001t0021g0301 | 2 | HG02258.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1667+41T>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 14/15 | chr12 | 50473577 | ||||||
| chr12:50473601
|
C | T | 2 | a0001c0001t0002g0060a0001c0001t0002g0069 | 2 | NA18997.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1667+65C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 14/15 | chr12 | 50473601 | ||||||
| chr12:50473708
|
A | G | 10 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(7): Show | 10 | HG02257.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1667+172A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 14/15 | chr12 | 50473708 | ||||||
| chr12:50473796
|
T | G | 1 | a0001c0001t0002g0080 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1668-203T>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 14/15 | chr12 | 50473796 | ||||||
| chr12:50473796
|
T | TG | 11 | a0001c0001t0001g0256a0001c0001t0001g0282a0001c0001t0002g0016others(8): Show | 11 | HG00438.hp2 HG01361.hp2 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.1668-198dupG | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr12 | 50473796 | |||||
| chr12:50473802
|
T | C | 260 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(257): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.1668-197T>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 14/15 | chr12 | 50473802 | ||||||
| chr12:50473806
|
T | TG | 14 | a0001c0001t0001g0005a0001c0001t0001g0188a0001c0001t0001g0249others(11): Show | 14 | HG00642.hp2 HG01261.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.1668-186dupG | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr12 | 50473806 | |||||
| chr12:50473807
|
GGGGGGGT others(9): Show |
G | 1 | a0001c0001t0002g0081 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1668-183_1668-168d others(18): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr12 | 50473807 | |||||
| chr12:50473808
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1668-191G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 14/15 | chr12 | 50473808 | ||||||
| chr12:50473810
|
G | C | 2 | a0001c0006t0007g0108a0001c0010t0007g0111 | 2 | HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1668-189G>C | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 14/15 | chr12 | 50473810 | ||||||
| chr12:50473813
|
G | GGT | 18 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0230others(15): Show | 18 | HG00673.hp2 HG01261.hp2 HG01928.hp1 others(15): Show |
intron_variant | MODIFIER | c.1668-186_1668-185i others(4): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 14/15 | chr12 | 50473813 | ||||||
| chr12:50473814
|
T | G | 19 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0230others(16): Show | 19 | HG00673.hp2 HG01261.hp2 HG01928.hp1 others(16): Show |
intron_variant | MODIFIER | c.1668-185T>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 14/15 | chr12 | 50473814 | ||||||
| chr12:50473814
|
T | TG | 97 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(94): Show | 97 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.1668-177dupG | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr12 | 50473814 | |||||
| chr12:50473814
|
T | TGGGGGGG others(3): Show |
1 | a0001c0001t0020g0300 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1668-179_1668-170d others(12): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr12 | 50473814 | |||||
| chr12:50473823
|
T | G | 2 | a0001c0001t0001g0024a0001c0001t0002g0115 | 2 | HG02145.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1668-176T>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 14/15 | chr12 | 50473823 | ||||||
| chr12:50473962
|
C | A | 5 | a0002c0002t0001g0207a0002c0002t0001g0215a0002c0002t0001g0253others(2): Show | 5 | HG02071.hp1 NA18979.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.1668-37C>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 14/15 | chr12 | 50473962 | ||||||
| chr12:50474215
|
A | AT | 6 | a0001c0001t0001g0004a0001c0001t0001g0256a0001c0001t0002g0039others(3): Show | 6 | HG02293.hp1 HG02293.hp2 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.1836+63dupT | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr12 | 50474215 | |||||
| chr12:50474248
|
G | A | 1 | a0001c0001t0001g0175 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1836+81G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 15/15 | chr12 | 50474248 | ||||||
| chr12:50474314
|
G | A | 126 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(123): Show | 126 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(123): Show |
intron_variant | MODIFIER | c.1836+147G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 15/15 | chr12 | 50474314 | ||||||
| chr12:50474416
|
C | T | 118 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(115): Show | 118 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(115): Show |
intron_variant | MODIFIER | c.1836+249C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 15/15 | chr12 | 50474416 | ||||||
| chr12:50474598
|
C | T | 5 | a0001c0001t0006g0273a0001c0001t0006g0274a0001c0001t0006g0275others(2): Show | 5 | HG02109.hp1 HG02559.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1836+431C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 15/15 | chr12 | 50474598 | ||||||
| chr12:50474815
|
A | T | 2 | a0001c0001t0002g0040a0001c0012t0002g0066 | 2 | HG02451.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1836+648A>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 15/15 | chr12 | 50474815 | ||||||
| chr12:50474933
|
C | T | 9 | a0001c0001t0001g0006a0001c0001t0001g0204a0001c0001t0001g0205others(6): Show | 9 | HG02027.hp1 NA18612.hp2 NA18959.hp1 others(6): Show |
intron_variant | MODIFIER | c.1837-593C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 15/15 | chr12 | 50474933 | ||||||
| chr12:50475338
|
C | T | 307 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(304): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.1837-188C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 15/15 | chr12 | 50475338 |