Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MLLFV others(719): Show |
chr12 | 50395885 | 50485004 |
| a0002 | 0/0 | 724 | 14 | 0 | 0 | 13 | 0 | 1 | 12 | LARP4_chr12_50395885_50485004 | LARP4 | MLLFV others(719): Show |
chr12 | 50395885 | 50485004 |
| a0003 | 0/0 | 724 | 11 | 0 | 2 | 4 | 1 | 4 | 2 | LARP4_chr12_50395885_50485004 | LARP4 | MLLFV others(719): Show |
chr12 | 50395885 | 50485004 |
| a0004 | 0/0 | 724 | 8 | 0 | 0 | 8 | 0 | 0 | 7 | LARP4_chr12_50395885_50485004 | LARP4 | MLLFV others(719): Show |
chr12 | 50395885 | 50485004 |
| a0005 | 0/0 | 724 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | MLLFV others(719): Show |
chr12 | 50395885 | 50485004 |
| a0006 | 0/0 | 724 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | MLLLV others(719): Show |
chr12 | 50395885 | 50485004 |
| a0007 | 0/0 | 724 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | MLLFV others(719): Show |
chr12 | 50395885 | 50485004 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2172 | 269 | 78 | 42 | 114 | 9 | 24 | LARP4_chr12_50395885_50485004 | LARP4 | ATGTT others(2167): Show |
chr12 | 50395885 | 50485004 | ||
| a0001c0005 | 0/0 | 2172 | 3 | 0 | 0 | 3 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | ATGTT others(2167): Show |
chr12 | 50395885 | 50485004 | ||
| a0001c0006 | 0/0 | 2172 | 3 | 2 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | ATGTT others(2167): Show |
chr12 | 50395885 | 50485004 | ||
| a0001c0009 | 0/0 | 2172 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | ATGTT others(2167): Show |
chr12 | 50395885 | 50485004 | ||
| a0001c0010 | 0/0 | 2172 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | ATGTT others(2167): Show |
chr12 | 50395885 | 50485004 | ||
| a0001c0011 | 0/0 | 2172 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | ATGTT others(2167): Show |
chr12 | 50395885 | 50485004 | ||
| a0001c0012 | 0/0 | 2172 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | ATGTT others(2167): Show |
chr12 | 50395885 | 50485004 | ||
| a0002c0002 | 0/0 | 2172 | 14 | 0 | 0 | 13 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | ATGTT others(2167): Show |
chr12 | 50395885 | 50485004 | ||
| a0003c0003 | 0/0 | 2172 | 11 | 0 | 2 | 4 | 1 | 4 | LARP4_chr12_50395885_50485004 | LARP4 | ATGTT others(2167): Show |
chr12 | 50395885 | 50485004 | ||
| a0004c0004 | 0/0 | 2172 | 8 | 0 | 0 | 8 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | ATGTT others(2167): Show |
chr12 | 50395885 | 50485004 | ||
| a0005c0007 | 0/0 | 2172 | 3 | 0 | 3 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | ATGTT others(2167): Show |
chr12 | 50395885 | 50485004 | ||
| a0006c0008 | 0/0 | 2172 | 2 | 2 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | ATGTT others(2167): Show |
chr12 | 50395885 | 50485004 | ||
| a0007c0013 | 0/0 | 2172 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | ATGTT others(2167): Show |
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 | AGCCG others(6437): Show |
chr12 | 50395885 | 50485004 |
| a0001c0001t0002 | 0/1 | 6442 | 118 | 8 | 21 | 66 | 9 | 13 | LARP4_chr12_50395885_50485004 | LARP4 | AGCCG others(6437): Show |
chr12 | 50395885 | 50485004 |
| a0001c0001t0003 | 1/0 | 6441 | 9 | 6 | 2 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | AGCCG others(6436): Show |
chr12 | 50395885 | 50485004 |
| a0001c0001t0004 | 0/0 | 6444 | 7 | 4 | 0 | 3 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | AGCCG others(6439): Show |
chr12 | 50395885 | 50485004 |
| a0001c0001t0005 | 0/0 | 6442 | 4 | 4 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | AGCCG others(6437): Show |
chr12 | 50395885 | 50485004 |
| a0001c0001t0006 | 0/0 | 6442 | 5 | 5 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | AGCCG others(6437): Show |
chr12 | 50395885 | 50485004 |
| a0001c0001t0008 | 0/0 | 6442 | 3 | 3 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | AGCCG others(6437): Show |
chr12 | 50395885 | 50485004 |
| a0001c0001t0009 | 0/0 | 6442 | 2 | 0 | 2 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | AGCCG others(6437): Show |
chr12 | 50395885 | 50485004 |
| a0001c0001t0010 | 0/0 | 6441 | 2 | 2 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | AGCCG others(6436): Show |
chr12 | 50395885 | 50485004 |
| a0001c0001t0011 | 0/0 | 6442 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | AGCCG others(6437): Show |
chr12 | 50395885 | 50485004 |
| a0001c0001t0012 | 0/0 | 6442 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | AGCCG others(6437): Show |
chr12 | 50395885 | 50485004 |
| a0001c0001t0013 | 0/0 | 6442 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | AGCCG others(6437): Show |
chr12 | 50395885 | 50485004 |
| a0001c0001t0014 | 0/0 | 6442 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | AGCCG others(6437): Show |
chr12 | 50395885 | 50485004 |
| a0001c0001t0015 | 0/0 | 6442 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | AGCCG others(6437): Show |
chr12 | 50395885 | 50485004 |
| a0001c0001t0016 | 0/0 | 6441 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | AGCCG others(6436): Show |
chr12 | 50395885 | 50485004 |
| a0001c0001t0017 | 0/0 | 6442 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | AGCCG others(6437): Show |
chr12 | 50395885 | 50485004 |
| a0001c0001t0018 | 0/0 | 6442 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | AGCCG others(6437): Show |
chr12 | 50395885 | 50485004 |
| a0001c0001t0019 | 0/0 | 6442 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | AGCCG others(6437): Show |
chr12 | 50395885 | 50485004 |
| a0001c0001t0020 | 0/0 | 6442 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | AGCCG others(6437): Show |
chr12 | 50395885 | 50485004 |
| a0001c0001t0021 | 0/0 | 6444 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | AGCCG others(6439): Show |
chr12 | 50395885 | 50485004 |
| a0001c0001t0022 | 0/0 | 6442 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | AGCCG others(6437): Show |
chr12 | 50395885 | 50485004 |
| a0001c0005t0001 | 0/0 | 6442 | 3 | 0 | 0 | 3 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | AGCCG others(6437): Show |
chr12 | 50395885 | 50485004 |
| a0001c0006t0007 | 0/0 | 6442 | 3 | 2 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | AGCCG others(6437): Show |
chr12 | 50395885 | 50485004 |
| a0001c0009t0001 | 0/0 | 6442 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | AGCCG others(6437): Show |
chr12 | 50395885 | 50485004 |
| a0001c0010t0007 | 0/0 | 6442 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | AGCCG others(6437): Show |
chr12 | 50395885 | 50485004 |
| a0001c0011t0002 | 0/0 | 6442 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | AGCCG others(6437): Show |
chr12 | 50395885 | 50485004 |
| a0001c0012t0002 | 0/0 | 6442 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | AGCCG others(6437): Show |
chr12 | 50395885 | 50485004 |
| a0002c0002t0001 | 0/0 | 6442 | 14 | 0 | 0 | 13 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | AGCCG others(6437): Show |
chr12 | 50395885 | 50485004 |
| a0003c0003t0001 | 0/0 | 6442 | 11 | 0 | 2 | 4 | 1 | 4 | LARP4_chr12_50395885_50485004 | LARP4 | AGCCG others(6437): Show |
chr12 | 50395885 | 50485004 |
| a0004c0004t0001 | 0/0 | 6442 | 8 | 0 | 0 | 8 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | AGCCG others(6437): Show |
chr12 | 50395885 | 50485004 |
| a0005c0007t0002 | 0/0 | 6442 | 3 | 0 | 3 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | AGCCG others(6437): Show |
chr12 | 50395885 | 50485004 |
| a0006c0008t0005 | 0/0 | 6442 | 2 | 2 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | AGCCG others(6437): Show |
chr12 | 50395885 | 50485004 |
| a0007c0013t0002 | 0/0 | 6442 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | AGCCG others(6437): Show |
chr12 | 50395885 | 50485004 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0002 | 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 | 1 | 0 | 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 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0037 | 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 |
| a0001c0001t0001g0158 | 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 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0173 | 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 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0179 | 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 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0186 | 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 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0217 | 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 |
| a0001c0001t0001g0220 | 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 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0255 | 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 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0294 | 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 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 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 | 1 | 0 | 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 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 1 | 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 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0108 | 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 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0266 | 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 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0003g0027 | 0/0 | 1 | 1 | 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 | 1/0 | 1 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0003g0033 | 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 |
| a0001c0001t0003g0036 | 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 |
| a0001c0001t0004g0151 | 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 |
| a0001c0001t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0004g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0004g0221 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0005g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0006g0272 | 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 |
| a0001c0001t0006g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0008g0159 | 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 |
| a0001c0001t0008g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0009g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0009g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0010g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0010g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0011g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0012g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0013g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0014g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0015g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0016g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0017g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0018g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0019g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0020g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0021g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0001t0022g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0005t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0005t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0005t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0006t0007g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0009t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0010t0007g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0011t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0001c0012t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0002c0002t0001g0209 | 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 |
| a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0002c0002t0001g0252 | 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 |
| a0002c0002t0001g0279 | 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 |
| a0002c0002t0001g0286 | 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 |
| a0003c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0003c0003t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0003c0003t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0003c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0003c0003t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0003c0003t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0003c0003t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0003c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0003c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0003c0003t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0003c0003t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0004c0004t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0004c0004t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0004c0004t0001g0228 | 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 |
| a0004c0004t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0004c0004t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0004c0004t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0005c0007t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0005c0007t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| a0005c0007t0002g0137 | 0/0 | 1 | 0 | 1 | 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 |
| a0006c0008t0005g0039 | 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 | g0074 | EUR | GBR | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0307 | EUR | GBR | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0107 | EUR | GBR | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG00140 | hp2 | a0003 | c0003 | t0001 | g0163 | EUR | GBR | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | CHS | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG00438 | hp2 | a0004 | c0004 | t0001 | g0240 | EAS | CHS | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | CHS | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG00544 | hp2 | a0003 | c0003 | t0001 | g0154 | EAS | CHS | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | CHS | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | PUR | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG00642 | hp2 | a0005 | c0007 | t0002 | g0137 | AMR | PUR | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | CHS | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | CHS | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG00738 | hp1 | a0005 | c0007 | t0002 | g0120 | AMR | PUR | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG00738 | hp2 | a0001 | c0001 | t0022 | g0003 | AMR | PUR | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG00741 | hp1 | a0001 | c0001 | t0009 | g0058 | AMR | PUR | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0050 | AMR | PUR | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0032 | AMR | PUR | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01069 | hp2 | a0005 | c0007 | t0002 | g0082 | AMR | PUR | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0031 | AMR | PUR | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0302 | AMR | PUR | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0069 | AMR | PUR | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01074 | hp2 | a0001 | c0001 | t0009 | g0049 | AMR | PUR | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0306 | AMR | PUR | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01106 | hp2 | a0003 | c0003 | t0001 | g0174 | AMR | PUR | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01109 | hp1 | a0001 | c0006 | t0007 | g0111 | AMR | PUR | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0060 | AMR | PUR | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0076 | AMR | PUR | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0165 | 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 | g0312 | AMR | CLM | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0006 | 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 | g0121 | AMR | CLM | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | CLM | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0309 | AMR | CLM | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | CLM | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | CLM | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0136 | AMR | CLM | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01433 | hp2 | a0001 | c0001 | t0019 | g0135 | AMR | CLM | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0311 | EUR | IBS | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0053 | EUR | IBS | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0310 | EUR | IBS | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0073 | EUR | IBS | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | ACB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0171 | AFR | ACB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0123 | AFR | ACB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01928 | hp1 | a0001 | c0001 | t0012 | g0245 | AMR | PEL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PEL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PEL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0079 | AMR | PEL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PEL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01975 | hp1 | a0003 | c0003 | t0001 | g0164 | AMR | PEL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | PEL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0083 | AMR | PEL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PEL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | KHV | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | KHV | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02040 | hp1 | a0003 | c0003 | t0001 | g0181 | EAS | KHV | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02040 | hp2 | a0001 | c0001 | t0004 | g0210 | EAS | KHV | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0170 | AFR | ACB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0286 | 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 | g0145 | EAS | KHV | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02074 | hp2 | a0001 | c0001 | t0013 | g0195 | EAS | KHV | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | KHV | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02083 | hp2 | a0001 | c0009 | t0001 | g0270 | 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 | g0214 | 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 | g0025 | AFR | ACB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0134 | AMR | PEL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | CDX | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | CDX | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | CDX | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | CDX | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0151 | AFR | ACB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02258 | hp1 | a0001 | c0001 | t0020 | g0299 | AFR | ACB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0149 | AFR | ACB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0138 | AFR | ACB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0005 | 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 | g0065 | AFR | ACB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02451 | hp2 | a0001 | c0001 | t0008 | g0159 | AFR | ACB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | KHV | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02572 | hp1 | a0001 | c0006 | t0007 | g0110 | AFR | GWD | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0036 | AFR | GWD | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0064 | SAS | PJL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0067 | SAS | PJL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0308 | AFR | GWD | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0035 | AFR | GWD | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0127 | AFR | GWD | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | GWD | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02647 | hp2 | a0001 | c0001 | t0006 | g0272 | AFR | GWD | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0075 | SAS | PJL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02683 | hp2 | a0001 | c0011 | t0002 | g0192 | SAS | PJL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02809 | hp2 | a0001 | c0001 | t0015 | g0316 | AFR | GWD | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0182 | 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 | g0283 | AFR | GWD | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02896 | hp1 | a0001 | c0001 | t0010 | g0034 | AFR | GWD | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0027 | AFR | GWD | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02897 | hp1 | a0001 | c0001 | t0010 | g0026 | AFR | GWD | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0147 | AFR | ESN | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | ESN | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02970 | hp1 | a0001 | c0001 | t0008 | g0184 | AFR | ESN | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | ESN | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ESN | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02976 | hp2 | a0006 | c0008 | t0005 | g0038 | AFR | ESN | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0081 | SAS | PJL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03017 | hp2 | a0003 | c0003 | t0001 | g0166 | SAS | PJL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | MSL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | MSL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03130 | hp1 | a0006 | c0008 | t0005 | g0039 | AFR | ESN | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0033 | AFR | ESN | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | MSL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0293 | AFR | MSL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03225 | hp1 | a0001 | c0001 | t0011 | g0313 | AFR | MSL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03225 | hp2 | a0001 | c0006 | t0007 | g0109 | AFR | MSL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | MSL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | MSL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03486 | hp1 | a0001 | c0001 | t0021 | g0300 | AFR | MSL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | MSL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0057 | SAS | PJL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0055 | SAS | PJL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | MSL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03579 | hp2 | a0001 | c0001 | t0008 | g0185 | AFR | MSL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0305 | SAS | PJL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0304 | 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 | g0224 | SAS | STU | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0054 | SAS | PJL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03834 | hp1 | a0003 | c0003 | t0001 | g0172 | SAS | BEB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0215 | SAS | BEB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03927 | hp1 | a0001 | c0001 | t0017 | g0303 | SAS | BEB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0282 | SAS | BEB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0285 | SAS | STU | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0141 | SAS | STU | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | STU | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0139 | SAS | STU | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | STU | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | STU | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG04228 | hp1 | a0003 | c0003 | t0001 | g0187 | SAS | STU | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0238 | SAS | STU | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | CHB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | CHB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | CHB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0269 | 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 | g0203 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18942 | hp2 | a0004 | c0004 | t0001 | g0201 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0287 | 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 | g0266 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0254 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18946 | hp1 | a0001 | c0001 | t0004 | g0221 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18948 | hp1 | a0001 | c0001 | t0018 | g0013 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0213 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0078 | 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 | g0115 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0118 | 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 | g0222 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18969 | hp1 | a0003 | c0003 | t0001 | g0167 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0211 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18979 | hp1 | a0004 | c0004 | t0001 | g0264 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0252 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18980 | hp2 | a0004 | c0004 | t0001 | g0228 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18989 | hp2 | a0003 | c0003 | t0001 | g0188 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18990 | hp1 | a0004 | c0004 | t0001 | g0249 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18990 | hp2 | a0002 | c0002 | t0001 | g0216 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18991 | hp1 | a0001 | c0005 | t0001 | g0011 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18992 | hp2 | a0001 | c0001 | t0014 | g0239 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0280 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0066 | 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 | g0223 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0116 | 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 | g0297 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0253 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0218 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19009 | hp1 | a0004 | c0004 | t0001 | g0199 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | LWK | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | LWK | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | LWK | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0148 | AFR | LWK | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19054 | hp1 | a0004 | c0004 | t0001 | g0242 | 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 | g0314 | 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 | g0258 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19058 | hp1 | a0002 | c0002 | t0001 | g0209 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19063 | hp1 | a0002 | c0002 | t0001 | g0212 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0279 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0225 | 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 | g0126 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19074 | hp1 | a0004 | c0004 | t0001 | g0241 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0281 | 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 | g0088 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19080 | hp1 | a0001 | c0005 | t0001 | g0009 | 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 | g0246 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19090 | hp2 | a0001 | c0005 | t0001 | g0259 | EAS | JPT | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0267 | 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 | g0140 | AFR | YRI | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | YRI | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ASW | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0153 | EUR | TSI | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0152 | EUR | TSI | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA20905 | hp1 | a0003 | c0003 | t0001 | g0180 | SAS | GIH | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0056 | SAS | GIH | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02109 | hp1 | a0001 | c0001 | t0006 | g0274 | 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 | g0173 | AFR | ACB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0084 | AFR | ACB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG02559 | hp2 | a0001 | c0001 | t0006 | g0275 | AFR | ACB | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03471 | hp1 | a0001 | c0001 | t0006 | g0273 | AFR | MSL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0150 | AFR | MSL | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | USA | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | USA | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | LWK | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| NA21309 | hp2 | a0001 | c0010 | t0007 | g0112 | AFR | LWK | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0106 | REF | REF | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0030 | REF | REF | LARP4_chr12_50395885_50485004 | LARP4 | chr12 | 50395885 | 50485004 |
| view | 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 |
| view | 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 | a0001c0006 a0001c0010 |
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 |
| view | 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 | a0001c0001t0004 a0001c0001t0021 |
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 | a0001c0001t0011 a0001c0006t0007 a0001c0010t0007 |
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 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(29): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): 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 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0009 others(10): Show |
136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): 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 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(27): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): 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 | a0001c0006t0007 a0001c0010t0007 |
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 | a0001c0006t0007 a0001c0010t0007 |
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 | a0001c0001t0020 a0001c0001t0021 |
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 | a0001c0001t0005 a0001c0001t0020 a0001c0001t0021 others(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 | a0001c0001t0020 a0001c0001t0021 |
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 |
| view | 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 | a0001c0001t0001g0317 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(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 | a0001c0001t0015g0316 | 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 | a0001c0001t0018g0013 | 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 | a0001c0001t0002g0014 | 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 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(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 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0002g0301 others(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 | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(118): 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 | a0001c0011t0002g0192 | 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 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(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 | a0001c0001t0002g0153 | 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 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
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 | a0001c0001t0002g0152 | 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 | a0001c0001t0015g0316 | 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 | a0001c0001t0004g0150 a0001c0001t0004g0151 |
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 | 257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(254): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): 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 | a0001c0001t0001g0037 | 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 | a0001c0001t0004g0150 | 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 | a0001c0001t0005g0146 a0001c0001t0005g0147 a0001c0001t0005g0148 others(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 | a0001c0001t0002g0310 a0001c0001t0002g0311 a0001c0001t0002g0312 |
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 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0145 |
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 | 305 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(302): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): 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 | 307 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(304): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): 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 | a0001c0001t0001g0298 | 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 | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(118): 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 | a0001c0001t0001g0193 a0001c0001t0005g0146 a0001c0001t0005g0147 others(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 | a0001c0001t0002g0144 | 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 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0182 others(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 | 116 | a0001c0001t0001g0012 a0001c0001t0001g0276 a0001c0001t0001g0277 others(113): Show |
116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): 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 | 98 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(95): 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 | a0001c0001t0020g0299 a0001c0001t0021g0300 |
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 | a0001c0001t0002g0040 | 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 | a0001c0001t0002g0108 | 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 | a0001c0001t0020g0299 a0001c0001t0021g0300 |
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 | a0001c0001t0006g0272 a0001c0001t0006g0273 a0001c0001t0006g0274 others(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 | a0001c0001t0020g0299 | 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 | a0001c0001t0001g0194 a0001c0001t0013g0195 |
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 | 300 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(297): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): 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 | a0003c0003t0001g0181 | 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 | 257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(254): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): 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 | 130 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(127): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): 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 | a0003c0003t0001g0180 | 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 | a0001c0001t0002g0301 | 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 | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(118): 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 | a0001c0001t0002g0107 | 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 | a0003c0003t0001g0154 | 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 | a0001c0001t0002g0041 | 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 | a0001c0001t0001g0193 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.18+5356A>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50406384 | |||||||
| chr12:50406486 | A | T | 1 | a0001c0001t0001g0037 | 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 | 124 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(121): Show |
124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): 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 | a0001c0001t0010g0034 | 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 | a0001c0001t0001g0271 a0001c0009t0001g0270 |
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 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0198 |
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 | a0001c0001t0001g0182 | 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 | a0001c0001t0002g0042 a0001c0001t0002g0113 |
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 | a0001c0001t0001g0037 | 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 | a0001c0001t0002g0042 a0001c0001t0002g0113 |
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 | a0001c0001t0002g0108 a0001c0001t0002g0114 |
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 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0145 |
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 | a0001c0001t0002g0043 a0001c0001t0002g0044 a0001c0001t0002g0045 others(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 | a0004c0004t0001g0199 | 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 | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(118): 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 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(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 | a0001c0001t0001g0269 a0001c0001t0001g0292 |
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 | 159 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0021 others(156): Show |
159 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(156): 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 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0160 others(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 | a0001c0001t0001g0200 a0001c0001t0001g0202 a0001c0001t0001g0276 others(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 | a0001c0001t0001g0196 | 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 | a0001c0006t0007g0109 a0001c0006t0007g0110 a0001c0006t0007g0111 others(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 | a0001c0001t0004g0150 a0001c0001t0004g0151 |
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 | a0001c0010t0007g0112 | 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 | a0001c0001t0006g0272 a0001c0001t0006g0273 a0001c0001t0006g0274 |
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 | a0001c0001t0002g0040 a0001c0001t0002g0093 a0001c0001t0002g0094 others(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 | 130 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(127): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): 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 | a0001c0001t0004g0150 a0001c0001t0004g0151 |
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 | a0003c0003t0001g0181 | 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 | 307 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(304): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): 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 | a0001c0001t0002g0145 | 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 | a0001c0001t0001g0002 | 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 | a0001c0001t0002g0306 a0001c0001t0002g0307 a0001c0001t0002g0309 |
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 | a0001c0006t0007g0109 a0001c0006t0007g0110 a0001c0006t0007g0111 others(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 | a0001c0001t0002g0050 a0001c0001t0005g0146 a0001c0001t0005g0147 others(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 | a0001c0001t0006g0272 a0001c0001t0006g0273 a0001c0001t0006g0274 others(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 | a0001c0001t0002g0118 | 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 | a0001c0001t0011g0313 | 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 | a0001c0001t0004g0150 | 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 | 119 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(116): Show |
119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.18+8780A>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50409808 | |||||||
| chr12:50409935 | C | G | 257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(254): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): 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 | a0001c0001t0001g0250 a0001c0001t0002g0088 a0001c0001t0002g0089 others(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 | a0001c0001t0001g0024 a0001c0001t0002g0040 a0001c0001t0002g0051 others(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 | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(122): 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 | a0003c0003t0001g0163 | 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 | a0001c0001t0001g0012 a0001c0001t0001g0194 a0001c0001t0001g0246 others(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 | a0001c0001t0001g0165 a0001c0001t0001g0200 a0001c0001t0002g0016 others(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 | a0001c0001t0006g0272 a0001c0001t0006g0273 a0001c0001t0006g0274 others(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 | a0001c0001t0001g0202 a0001c0001t0001g0276 a0001c0001t0012g0245 |
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 | a0001c0001t0003g0033 | 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 | a0001c0001t0003g0033 | 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 | a0001c0001t0001g0173 | 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 | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(120): 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 | a0001c0006t0007g0109 a0001c0006t0007g0110 a0001c0006t0007g0111 others(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 | a0001c0001t0002g0128 | 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 | a0001c0006t0007g0109 a0001c0006t0007g0110 a0001c0006t0007g0111 |
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 | 307 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(304): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): 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 | a0003c0003t0001g0166 | 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 | 307 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(304): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): 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 | a0001c0001t0002g0053 a0001c0001t0002g0097 |
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 | a0001c0001t0001g0178 a0001c0001t0001g0191 |
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 | a0001c0001t0020g0299 a0001c0001t0021g0300 |
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 | a0001c0006t0007g0109 a0001c0006t0007g0110 a0001c0006t0007g0111 others(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 | a0001c0001t0002g0054 | 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 | a0001c0006t0007g0109 | 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 | a0003c0003t0001g0163 | 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 | a0001c0001t0001g0182 | 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 | a0001c0001t0006g0272 a0001c0001t0006g0273 a0001c0001t0006g0274 others(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 | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(114): 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 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(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 | a0001c0001t0001g0298 | 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 | a0001c0001t0002g0117 | 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 | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(109): 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 | a0001c0006t0007g0109 a0001c0006t0007g0110 a0001c0006t0007g0111 others(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 | 127 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(124): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): 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 | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(114): 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 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0277 others(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 | a0001c0001t0001g0173 | 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 | 257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(254): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): 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 | a0001c0001t0001g0007 a0001c0001t0001g0161 |
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 | a0001c0006t0007g0109 a0001c0006t0007g0110 a0001c0006t0007g0111 |
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 | a0003c0003t0001g0172 | 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 | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(113): 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 | a0001c0001t0020g0299 a0001c0001t0021g0300 |
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 | a0001c0006t0007g0110 | 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 | a0001c0001t0001g0227 a0001c0001t0001g0282 |
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 | a0001c0006t0007g0109 a0001c0006t0007g0110 a0001c0006t0007g0111 others(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 | a0001c0001t0006g0272 a0001c0001t0006g0273 a0001c0001t0006g0274 others(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 | a0001c0001t0001g0186 | 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 | a0001c0001t0002g0053 a0001c0001t0002g0085 a0001c0001t0002g0086 others(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 | 126 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(123): Show |
126 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(123): 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 | a0001c0001t0002g0142 | 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 | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(114): 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 | a0001c0001t0001g0162 | 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 | a0001c0001t0001g0186 | 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 | a0001c0001t0002g0134 | 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 | 257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(254): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): 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 | a0001c0001t0004g0170 a0001c0001t0004g0171 |
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 | a0001c0001t0001g0182 | 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 | a0001c0001t0004g0170 a0001c0001t0004g0171 |
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 | a0001c0001t0013g0195 | 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 | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(114): 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 | a0001c0001t0001g0261 | 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 | a0006c0008t0005g0038 a0006c0008t0005g0039 |
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 | a0001c0001t0002g0141 | 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 | a0001c0006t0007g0109 a0001c0006t0007g0110 a0001c0006t0007g0111 others(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 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(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 | a0001c0001t0002g0053 a0001c0001t0002g0097 |
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 | a0001c0001t0006g0272 a0001c0001t0006g0273 a0001c0001t0006g0274 others(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 | a0006c0008t0005g0038 a0006c0008t0005g0039 |
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 | a0001c0001t0015g0316 | 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 | a0001c0001t0006g0272 a0001c0001t0006g0273 a0001c0001t0006g0274 others(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 | a0001c0001t0006g0272 a0001c0001t0006g0273 a0001c0001t0006g0274 others(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 | a0001c0001t0020g0299 a0001c0001t0021g0300 |
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 | a0001c0001t0002g0084 a0001c0001t0002g0140 |
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 | a0001c0001t0015g0316 | 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 | a0001c0001t0004g0150 a0001c0001t0004g0151 |
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 | a0001c0001t0001g0244 | 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 | a0001c0001t0002g0050 a0001c0001t0009g0049 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(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 | a0001c0001t0001g0227 a0001c0001t0001g0282 |
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 | a0003c0003t0001g0154 | 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 | a0001c0001t0001g0261 | 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 | a0001c0001t0002g0043 | 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 | a0001c0001t0020g0299 a0001c0001t0021g0300 |
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 | a0001c0001t0004g0150 a0001c0001t0004g0151 |
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 | a0002c0002t0001g0218 a0003c0003t0001g0181 |
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 | a0003c0003t0001g0154 | 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 | 130 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(127): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.19-6980G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50420782 | |||||||
| chr12:50420947 | C | CTTTT | 115 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(112): 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 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(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 |
13 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0012 others(10): 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 | a0001c0001t0020g0299 a0001c0001t0021g0300 |
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 | a0001c0001t0005g0147 a0001c0001t0005g0148 |
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 | a0001c0001t0005g0146 a0001c0001t0005g0149 |
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 | 307 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(304): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): 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 | a0001c0001t0015g0316 | 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 | a0001c0001t0001g0207 | 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 | a0001c0001t0001g0196 | 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 | a0001c0001t0001g0269 a0001c0001t0001g0292 |
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 | a0001c0001t0001g0037 | 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 | a0001c0001t0004g0150 a0001c0001t0004g0151 |
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 | 124 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(121): Show |
124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): 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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0037 a0001c0001t0001g0186 others(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 | a0001c0001t0003g0028 a0001c0001t0003g0035 |
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 | a0001c0001t0001g0265 a0001c0001t0001g0298 a0001c0001t0015g0316 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(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 | 37 | a0001c0001t0001g0001 a0001c0001t0001g0197 a0001c0001t0001g0198 others(34): 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 | 125 | a0001c0001t0001g0023 a0001c0001t0002g0014 a0001c0001t0002g0015 others(122): Show |
125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): 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 | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(118): 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 | a0001c0006t0007g0109 a0001c0006t0007g0110 a0001c0006t0007g0111 others(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 | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(118): 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 | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(118): 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 | a0001c0001t0002g0116 | 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 | a0001c0001t0001g0232 a0001c0001t0001g0262 a0001c0001t0002g0042 others(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 | a0001c0001t0002g0128 a0001c0001t0002g0302 a0001c0001t0003g0027 others(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 | 86 | a0001c0001t0001g0001 a0001c0001t0001g0196 a0001c0001t0001g0198 others(83): 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 | 35 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0023 others(32): Show |
35 | HG00140.hp2 HG00544.hp2 HG01069.hp1 others(32): 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 | a0001c0001t0001g0162 a0001c0001t0001g0168 a0001c0001t0001g0173 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(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 | a0001c0001t0001g0182 a0003c0003t0001g0180 |
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 | a0001c0001t0006g0272 a0001c0001t0006g0273 a0001c0001t0006g0274 |
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 | a0001c0006t0007g0109 a0001c0006t0007g0110 a0001c0006t0007g0111 others(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 | a0001c0001t0006g0293 | 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 | a0001c0001t0003g0028 a0001c0001t0003g0029 a0001c0001t0003g0033 others(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 | a0001c0001t0002g0116 | 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 | a0001c0001t0002g0266 a0001c0001t0002g0267 |
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 | a0001c0001t0002g0266 a0001c0001t0002g0267 |
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 | a0001c0001t0020g0299 a0001c0001t0021g0300 |
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 | a0001c0001t0020g0299 | 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 | a0001c0001t0005g0146 a0001c0001t0005g0147 a0001c0001t0005g0148 others(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 | a0001c0001t0021g0300 | 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 | a0001c0001t0002g0019 | 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 | a0001c0001t0003g0033 | 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 | a0001c0006t0007g0109 a0001c0006t0007g0110 a0001c0006t0007g0111 others(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 | a0001c0001t0002g0069 | 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 | a0001c0001t0002g0117 | 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 | a0001c0001t0001g0024 | 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 | a0001c0001t0004g0150 a0001c0001t0004g0151 |
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 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(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 | a0001c0001t0002g0152 | 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 | a0001c0006t0007g0109 a0001c0006t0007g0110 a0001c0006t0007g0111 others(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 | a0001c0001t0001g0255 a0001c0001t0001g0281 a0001c0001t0001g0285 others(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 | a0001c0001t0001g0260 | 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 | a0001c0001t0004g0150 a0001c0001t0004g0151 |
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 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0198 |
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 | a0001c0001t0004g0170 a0001c0001t0004g0171 |
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 | a0003c0003t0001g0166 a0003c0003t0001g0187 |
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 | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(114): 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 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0198 others(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 | a0001c0001t0002g0123 a0001c0001t0002g0152 a0001c0001t0009g0058 |
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 | a0001c0006t0007g0109 a0001c0006t0007g0110 a0001c0006t0007g0111 others(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 | a0001c0001t0002g0308 | 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 | a0001c0001t0020g0299 a0001c0001t0021g0300 |
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 | a0001c0001t0002g0305 | 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 | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(114): 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 | a0006c0008t0005g0038 a0006c0008t0005g0039 |
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 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0198 |
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 | a0001c0001t0002g0014 | 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 | a0001c0001t0002g0067 | 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 | a0001c0001t0002g0084 | 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 | a0001c0001t0002g0085 a0001c0001t0002g0098 |
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 | a0004c0004t0001g0199 | 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 | a0001c0001t0006g0272 a0001c0001t0006g0273 a0001c0001t0006g0274 |
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 | a0001c0001t0002g0080 | 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 | a0005c0007t0002g0082 a0005c0007t0002g0120 a0005c0007t0002g0137 |
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 | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(116): 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 | a0001c0001t0020g0299 a0001c0001t0021g0300 |
2 | HG02258.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.19-1236T>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 1/15 | chr12 | 50426526 | |||||||
| chr12:50426605 | T | C | 3 | a0001c0001t0001g0175 a0001c0001t0001g0189 a0001c0001t0001g0190 |
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 | a0001c0001t0001g0298 | 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 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0220 others(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 | a0001c0001t0001g0023 | 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 | a0001c0001t0002g0114 | 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 | 70 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(67): Show |
70 | HG00738.hp1 HG01069.hp2 HG01346.hp1 others(67): 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 | a0001c0001t0001g0010 a0001c0001t0001g0022 a0001c0001t0001g0223 others(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 | a0001c0001t0002g0042 a0001c0001t0002g0047 a0001c0001t0002g0048 others(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 | a0001c0001t0002g0052 a0001c0001t0002g0086 a0001c0001t0002g0100 others(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 | a0001c0001t0002g0066 a0001c0001t0009g0049 |
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 | a0001c0001t0002g0040 a0001c0001t0002g0094 a0001c0001t0002g0132 |
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 | a0001c0001t0002g0108 a0001c0001t0002g0128 |
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 | a0001c0001t0002g0302 | 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 | a0001c0001t0002g0145 | 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 | a0001c0001t0001g0190 a0001c0001t0001g0193 a0001c0001t0001g0205 others(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 | 10 | a0001c0001t0001g0001 a0001c0001t0001g0175 a0001c0001t0001g0189 others(7): 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 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(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 | a0001c0001t0001g0165 a0001c0001t0001g0168 a0001c0001t0001g0169 others(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 | a0001c0001t0001g0037 a0001c0001t0005g0146 a0001c0001t0005g0147 others(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 | a0001c0001t0001g0207 | 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 | a0001c0001t0002g0041 a0001c0001t0002g0059 a0001c0001t0002g0107 others(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 | a0001c0001t0001g0269 a0001c0001t0001g0292 |
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 | a0001c0006t0007g0109 a0001c0006t0007g0110 a0001c0006t0007g0111 |
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 | a0001c0001t0001g0229 | 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 | a0001c0001t0001g0196 a0001c0001t0001g0243 a0001c0001t0001g0285 others(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 | a0001c0001t0001g0298 a0001c0001t0003g0028 a0001c0001t0003g0029 others(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 | a0001c0001t0004g0150 | 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 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(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 | a0001c0001t0004g0171 a0006c0008t0005g0038 a0006c0008t0005g0039 |
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 | a0001c0001t0005g0146 a0001c0001t0005g0147 a0001c0001t0005g0148 others(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 | a0001c0006t0007g0109 a0001c0006t0007g0110 |
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 | a0001c0010t0007g0112 | 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 | a0001c0001t0002g0068 | 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 | a0001c0001t0002g0017 a0001c0001t0002g0045 a0001c0001t0002g0053 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(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 | a0001c0001t0001g0217 | 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 | a0001c0001t0015g0316 | 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 | 300 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(297): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): 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 | a0001c0001t0004g0150 a0001c0001t0004g0151 a0001c0001t0005g0146 others(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 | a0001c0006t0007g0109 a0001c0006t0007g0110 a0001c0006t0007g0111 others(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 | ||||||
| chr12:50427555 | C | T | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(113): 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 | a0001c0001t0002g0305 a0001c0001t0002g0310 a0001c0001t0002g0311 others(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 | a0001c0001t0001g0178 a0001c0001t0001g0191 |
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 | a0001c0001t0002g0066 | 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 | 274 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(271): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(271): 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 | 22 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0182 others(19): 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 | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(113): 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 | a0001c0001t0002g0056 | 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 | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(113): 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 | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(113): 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 | a0001c0001t0002g0042 a0001c0001t0002g0113 |
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 | a0001c0001t0002g0052 a0001c0001t0002g0071 a0001c0001t0002g0077 others(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 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(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 | a0001c0001t0002g0080 | 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 | 305 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(302): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.322+352C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 3/15 | chr12 | 50429442 | |||||||
| chr12:50429476 | G | A | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(113): 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 | a0001c0010t0007g0112 | 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 | a0001c0001t0002g0302 | 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 | a0001c0001t0002g0053 a0001c0001t0002g0097 |
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 | a0001c0001t0020g0299 a0001c0001t0021g0300 |
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 | a0001c0006t0007g0109 a0001c0006t0007g0110 a0001c0006t0007g0111 others(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 | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(250): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): 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 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(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 | 135 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(132): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.323-343delG | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 3/15 | chr12 | 50430151 | |||||||
| chr12:50430152 | G | A | 4 | a0001c0006t0007g0109 a0001c0006t0007g0110 a0001c0006t0007g0111 others(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 | a0001c0001t0001g0200 | 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 | a0001c0001t0001g0232 a0001c0001t0001g0234 a0001c0001t0001g0235 others(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 | a0001c0001t0020g0299 a0001c0001t0021g0300 |
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 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(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 | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(113): 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 | a0001c0001t0002g0076 | 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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(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 | a0001c0001t0002g0145 | 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 | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(113): 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 | a0001c0001t0001g0260 | 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 | 2 | a0001c0001t0001g0001 a0001c0001t0001g0244 |
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 | a0001c0001t0001g0160 | 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 | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(113): 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 | a0001c0001t0001g0214 a0001c0001t0001g0255 |
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 | a0001c0001t0004g0171 | 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 | 257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(254): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.398+1394T>G | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 4/15 | chr12 | 50431964 | |||||||
| chr12:50431976 | G | A | 135 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(132): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): 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 | a0001c0001t0015g0316 | 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 | a0001c0001t0015g0316 | 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 | a0001c0001t0001g0037 | 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 | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(113): 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 | a0001c0001t0002g0145 | 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 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(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 | 122 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(119): Show |
122 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(119): 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 | a0001c0001t0001g0178 a0001c0001t0001g0191 a0001c0001t0002g0043 others(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 | a0001c0001t0003g0035 | 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 | a0001c0001t0001g0225 | 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 | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(113): 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 | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(89): 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 | a0001c0001t0001g0012 a0001c0001t0001g0198 a0001c0001t0001g0243 others(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 | a0001c0001t0001g0165 a0001c0001t0001g0175 a0001c0001t0001g0189 others(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 | 116 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(113): Show |
116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): 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 | a0001c0001t0002g0267 | 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 | 104 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(101): 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 | a0001c0001t0002g0108 a0001c0001t0002g0114 |
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 | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(115): 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 | 135 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(132): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): 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 | a0001c0001t0001g0238 | 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 | a0001c0001t0001g0224 | 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 | a0001c0001t0014g0239 | 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 | a0001c0006t0007g0111 | 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 | a0001c0006t0007g0109 | 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 | a0001c0001t0001g0246 a0001c0001t0001g0290 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(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 | 260 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(257): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): 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 | a0006c0008t0005g0038 a0006c0008t0005g0039 |
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 | a0001c0001t0002g0043 | 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 | a0001c0001t0002g0131 | 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 | a0001c0001t0015g0316 | 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 | a0001c0006t0007g0109 a0001c0006t0007g0110 a0001c0006t0007g0111 others(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 | a0001c0001t0002g0083 | 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 | a0002c0002t0001g0209 | 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 | 257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(254): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): 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 | 257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(254): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): 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 | a0001c0001t0003g0027 a0001c0001t0003g0028 a0001c0001t0003g0029 others(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 | a0001c0001t0020g0299 a0001c0001t0021g0300 |
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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(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 | a0001c0001t0001g0023 a0001c0001t0001g0157 a0001c0001t0001g0158 others(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 | 11 | a0001c0001t0001g0001 a0001c0001t0001g0156 a0001c0001t0001g0160 others(8): 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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0162 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(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 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0198 others(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 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(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 | 120 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0040 others(117): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): 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 | a0001c0001t0002g0122 a0001c0001t0002g0126 |
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 | a0001c0001t0001g0294 a0001c0001t0001g0295 |
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 | a0001c0001t0021g0300 | 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 | a0001c0001t0020g0299 | 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 | 289 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(286): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): 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 | a0001c0001t0001g0162 a0001c0001t0002g0053 a0001c0001t0002g0084 others(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 | a0001c0001t0001g0200 | 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 | a0001c0006t0007g0111 a0001c0010t0007g0112 |
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 | a0001c0006t0007g0109 a0001c0006t0007g0110 |
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 | a0001c0001t0001g0257 | 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 | a0001c0001t0001g0257 | 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 | a0001c0001t0001g0220 a0001c0001t0002g0094 a0001c0001t0006g0272 others(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 | a0001c0001t0001g0257 | 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 | a0001c0006t0007g0109 a0001c0006t0007g0110 a0001c0006t0007g0111 others(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 | a0001c0006t0007g0109 a0001c0006t0007g0110 a0001c0006t0007g0111 others(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 | a0001c0001t0003g0035 | 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 | a0001c0001t0005g0146 a0001c0001t0005g0147 a0001c0001t0005g0148 others(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 | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(220): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): 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 | a0001c0006t0007g0110 a0001c0006t0007g0111 a0001c0010t0007g0112 |
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 | a0001c0001t0005g0148 | 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 | a0001c0001t0001g0276 | 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 | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(256): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): 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 | a0001c0001t0006g0272 a0001c0001t0006g0273 a0001c0001t0006g0274 others(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 | a0001c0001t0004g0150 a0001c0001t0004g0151 |
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 | a0001c0001t0003g0031 a0001c0001t0003g0032 |
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 | a0001c0001t0002g0100 a0001c0001t0020g0299 a0001c0001t0021g0300 |
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 | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(250): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): 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 | a0001c0001t0015g0316 | 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 | a0001c0001t0001g0175 a0001c0001t0001g0189 a0001c0001t0001g0190 |
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 | a0001c0001t0003g0028 a0001c0001t0003g0029 |
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 | a0001c0006t0007g0109 a0001c0006t0007g0110 a0001c0006t0007g0111 |
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 | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(117): 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 | a0001c0006t0007g0109 a0001c0006t0007g0110 a0001c0006t0007g0111 others(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 | a0003c0003t0001g0154 | 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 | a0001c0001t0015g0316 | 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 | a0001c0001t0001g0165 a0001c0001t0001g0168 a0001c0001t0001g0169 others(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 | a0001c0001t0005g0146 a0001c0001t0005g0147 a0001c0001t0005g0148 others(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 | 123 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(120): Show |
123 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(120): 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 | a0001c0001t0002g0084 a0001c0001t0002g0090 a0001c0001t0002g0107 others(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 | a0001c0001t0002g0083 | 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 | a0001c0001t0002g0059 a0001c0001t0002g0068 |
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 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(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 | a0001c0001t0004g0203 | 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 | a0006c0008t0005g0038 a0006c0008t0005g0039 |
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 | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(117): 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 | a0001c0010t0007g0112 | 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 | a0001c0001t0001g0226 | 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 | a0001c0001t0020g0299 a0001c0001t0021g0300 |
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 | a0001c0001t0006g0293 | 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 | a0001c0001t0019g0135 | 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 | a0001c0006t0007g0109 a0001c0006t0007g0110 a0001c0006t0007g0111 others(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 | a0001c0001t0002g0103 a0001c0001t0002g0121 |
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 | a0001c0001t0001g0173 | 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 | a0001c0006t0007g0109 a0001c0006t0007g0110 a0001c0006t0007g0111 others(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 | a0001c0001t0002g0067 a0001c0001t0002g0099 |
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 | a0001c0001t0001g0278 | 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 | a0001c0006t0007g0109 a0001c0006t0007g0110 a0001c0006t0007g0111 others(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 | a0001c0001t0002g0044 a0001c0001t0002g0301 a0001c0006t0007g0111 others(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 | a0001c0006t0007g0109 a0001c0006t0007g0110 a0001c0006t0007g0111 others(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 | a0001c0001t0002g0070 | 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 | a0001c0001t0020g0299 a0001c0001t0021g0300 |
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 | a0001c0001t0001g0291 | 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 | a0001c0001t0001g0294 a0001c0001t0001g0295 |
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 | 260 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(257): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): 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 | a0001c0001t0002g0153 | 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 | a0001c0001t0001g0243 a0001c0001t0001g0285 a0001c0001t0001g0291 others(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 | a0001c0001t0001g0317 | 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 | a0001c0001t0015g0316 | 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 | a0001c0001t0008g0159 a0001c0001t0008g0184 a0001c0001t0008g0185 |
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 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0263 others(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 | a0001c0001t0002g0088 a0001c0001t0002g0090 a0001c0001t0002g0091 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0001t0005g0146 a0001c0001t0005g0147 a0001c0001t0005g0148 others(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 | a0001c0001t0002g0084 a0001c0001t0002g0140 |
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 | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(113): 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 | a0001c0001t0004g0150 a0001c0001t0004g0151 |
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 | 298 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(295): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): 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 | a0001c0001t0002g0143 | 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 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0145 |
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 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0145 |
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 | a0001c0001t0001g0269 | 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 | a0001c0001t0002g0041 | 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 | 131 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(128): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): 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 | a0001c0001t0002g0047 | 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 | a0001c0001t0004g0150 a0001c0001t0004g0151 |
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 | 132 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(129): Show |
132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): 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 | a0001c0001t0006g0275 | 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 | a0001c0001t0001g0265 | 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 | a0001c0001t0001g0037 a0001c0001t0001g0175 a0001c0001t0001g0208 others(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 | a0001c0001t0001g0278 | 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 | a0001c0001t0002g0055 a0001c0001t0002g0056 |
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 | a0001c0001t0002g0046 a0001c0001t0002g0048 a0001c0001t0002g0116 |
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 | 255 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(252): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): 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 | a0001c0006t0007g0109 a0001c0006t0007g0110 a0001c0006t0007g0111 others(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 | a0001c0001t0001g0233 | 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 | a0001c0001t0006g0272 | 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 | a0001c0001t0001g0230 | 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 | a0001c0001t0001g0198 | 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 | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(248): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): 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 | a0001c0001t0001g0250 | 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 | a0001c0001t0001g0198 | 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 | a0003c0003t0001g0172 | 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 | a0002c0002t0001g0213 | 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 | a0001c0010t0007g0112 | 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 | a0001c0001t0001g0265 | 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 | a0001c0001t0002g0251 | 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 | a0001c0001t0001g0243 | 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 | a0002c0002t0001g0254 | 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 | a0001c0001t0001g0037 | 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 | a0001c0001t0004g0221 | 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 | a0001c0001t0001g0197 a0001c0001t0001g0229 |
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 | a0003c0003t0001g0154 | 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 | a0001c0001t0001g0282 | 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 | a0001c0001t0001g0315 | 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 | a0001c0001t0001g0236 | 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 | a0001c0001t0020g0299 a0001c0001t0021g0300 |
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 | a0001c0001t0006g0274 | 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 | a0001c0001t0001g0219 | 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 | a0002c0002t0001g0279 | 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 | a0004c0004t0001g0201 | 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 | a0001c0001t0001g0291 | 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 | a0003c0003t0001g0180 | 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 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
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 | a0001c0001t0001g0217 | 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 | a0001c0001t0001g0193 | 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 | a0001c0001t0004g0150 | 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 | a0001c0001t0001g0295 a0001c0001t0001g0317 |
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 | a0004c0004t0001g0249 | 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 | a0001c0001t0001g0022 | 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 | a0001c0001t0001g0191 | 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 | a0002c0002t0001g0218 | 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 | a0001c0001t0001g0182 | 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 | a0001c0001t0001g0231 | 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 | a0003c0003t0001g0181 | 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 | a0001c0001t0006g0273 | 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 | a0001c0001t0006g0293 | 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 | a0004c0004t0001g0228 | 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 | a0002c0002t0001g0215 | 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 | a0001c0001t0001g0021 | 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 | a0001c0001t0001g0283 | 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 | a0001c0001t0004g0171 | 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 | a0003c0003t0001g0164 | 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 | a0001c0001t0008g0159 | 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 | a0001c0001t0022g0003 | 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 | a0001c0001t0002g0266 | 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 | a0002c0002t0001g0287 | 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 | a0001c0001t0001g0178 | 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 | a0001c0001t0001g0237 | 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 | a0001c0001t0020g0299 a0001c0001t0021g0300 |
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 | a0001c0001t0001g0294 | 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 | a0003c0003t0001g0163 | 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 | a0004c0004t0001g0241 | 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 | a0001c0001t0003g0031 | 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 | a0001c0001t0001g0244 | 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 | a0001c0001t0003g0032 | 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 | a0001c0001t0001g0235 | 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 | a0001c0001t0001g0261 | 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 | a0002c0002t0001g0286 | 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 | a0001c0001t0012g0245 | 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 | a0001c0001t0011g0313 | 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 | a0001c0001t0001g0314 a0002c0002t0001g0209 |
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 | a0003c0003t0001g0166 | 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 | a0001c0001t0008g0185 a0003c0003t0001g0167 |
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 | a0001c0001t0001g0160 a0001c0001t0008g0184 |
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 | a0001c0001t0002g0267 a0002c0002t0001g0252 |
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 | a0001c0001t0016g0258 | 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 | a0001c0001t0001g0226 | 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 | a0001c0010t0007g0112 | 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 | a0001c0001t0001g0233 | 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 | a0001c0001t0004g0151 | 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 | a0001c0001t0001g0255 | 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 | a0004c0004t0001g0199 | 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 | a0002c0002t0001g0211 | 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 | a0002c0002t0001g0280 | 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 | a0001c0001t0001g0202 | 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 | a0001c0001t0001g0173 | 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 | a0001c0001t0001g0234 | 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 | a0003c0003t0001g0187 | 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 | a0001c0001t0001g0284 | 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 | a0001c0001t0001g0025 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0277 a0002c0002t0001g0253 |
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 | a0003c0003t0001g0188 | 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 | a0001c0001t0001g0012 | 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 | a0001c0001t0001g0260 a0001c0001t0001g0281 |
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 | a0001c0001t0001g0288 | 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 | a0001c0006t0007g0109 | 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 | a0001c0001t0001g0204 | 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 | a0001c0001t0001g0289 | 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 | a0004c0004t0001g0240 | 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 | a0001c0001t0001g0232 a0001c0001t0001g0238 |
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 | a0004c0004t0001g0264 | 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 |
2 | a0001c0001t0001g0001 a0004c0004t0001g0242 |
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 | a0001c0001t0003g0033 | 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 | a0001c0001t0001g0263 | 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 | a0001c0001t0004g0170 | 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 | a0001c0001t0002g0268 | 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 | a0001c0001t0001g0189 | 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 | a0001c0001t0001g0155 | 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 | a0001c0001t0001g0278 | 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 | a0001c0001t0001g0276 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0227 |
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 | a0001c0001t0001g0207 | 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 | a0001c0001t0001g0165 | 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 | a0001c0001t0001g0223 | 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 | a0001c0001t0001g0262 | 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 | a0001c0001t0001g0298 | 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 | a0001c0001t0001g0214 a0001c0001t0004g0203 |
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 | a0001c0001t0015g0316 | 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 | a0001c0001t0003g0036 | 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 | a0001c0001t0003g0027 a0001c0001t0010g0034 |
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 | a0001c0001t0003g0029 a0001c0001t0003g0035 |
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 | a0001c0001t0010g0026 | 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 | a0001c0001t0001g0297 | 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 | a0001c0001t0001g0222 | 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 | a0001c0001t0001g0175 | 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 | a0001c0001t0001g0196 a0001c0001t0004g0210 |
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 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0183 |
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 | a0001c0001t0001g0271 | 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 | a0001c0001t0001g0200 a0001c0001t0001g0220 a0001c0001t0001g0224 others(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 | a0001c0001t0001g0169 | 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 | a0001c0001t0001g0248 | 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 | a0001c0001t0001g0246 | 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 | a0002c0002t0001g0216 | 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 | a0001c0001t0001g0179 | 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 | a0003c0003t0001g0174 | 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 | a0001c0006t0007g0111 | 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 | a0001c0001t0002g0124 | 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 | a0001c0001t0002g0088 | 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 | a0001c0001t0001g0010 | 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 | a0001c0001t0014g0239 | 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 | a0001c0001t0001g0247 a0001c0001t0001g0256 |
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 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0004 | 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 | a0001c0001t0001g0194 | 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 | a0001c0001t0001g0257 a0001c0001t0001g0285 |
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 | a0001c0001t0001g0156 a0001c0001t0001g0161 a0001c0001t0001g0162 |
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 | a0001c0001t0002g0051 | 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 | a0001c0001t0001g0269 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0206 a0001c0001t0001g0290 |
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 | a0001c0001t0001g0168 | 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 | a0001c0001t0001g0292 | 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 | a0001c0001t0002g0063 | 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 | a0001c0001t0002g0123 | 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 | a0001c0001t0002g0068 | 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 | a0001c0001t0002g0059 | 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 | a0001c0001t0002g0062 | 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 | a0001c0001t0002g0116 | 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 | a0001c0001t0002g0143 | 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 | a0001c0001t0002g0014 | 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 | a0001c0001t0002g0129 | 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 | a0001c0001t0001g0232 a0001c0001t0001g0238 a0001c0001t0001g0298 |
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 | a0001c0001t0001g0208 | 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 | a0001c0005t0001g0009 a0002c0002t0001g0212 |
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 | a0001c0001t0001g0177 | 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 | a0001c0001t0001g0190 | 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 | a0001c0001t0013g0195 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0205 |
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 | a0001c0001t0001g0186 | 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 | a0001c0001t0002g0066 | 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 | a0001c0001t0002g0061 | 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 | a0001c0001t0002g0048 | 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 | a0001c0001t0002g0152 | 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 | a0001c0001t0002g0075 a0001c0001t0002g0080 |
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 | a0001c0001t0002g0017 | 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 | a0001c0001t0002g0145 | 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 | a0001c0001t0002g0079 | 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 | a0001c0001t0002g0125 | 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(68): Show |
3 | a0001c0001t0002g0015 a0001c0001t0002g0078 a0001c0001t0002g0105 |
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 | a0001c0001t0002g0076 | 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 | a0001c0001t0002g0060 | 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 | a0001c0001t0002g0113 | 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 | a0001c0001t0001g0214 a0001c0001t0001g0262 a0001c0001t0001g0298 others(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 | a0001c0005t0001g0011 | 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 | a0001c0001t0002g0108 | 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 | a0001c0001t0002g0114 | 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 | a0001c0001t0002g0046 | 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 | a0001c0001t0002g0040 | 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 | a0001c0001t0002g0070 a0001c0001t0002g0093 |
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 | a0001c0001t0002g0089 | 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 | a0001c0001t0002g0057 | 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 | a0001c0009t0001g0270 | 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 | a0001c0001t0002g0054 a0001c0001t0002g0084 a0001c0001t0002g0107 others(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 | a0001c0001t0002g0142 | 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 | a0001c0001t0002g0052 a0001c0001t0002g0086 |
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 | a0001c0001t0002g0115 a0001c0001t0002g0130 |
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 | a0001c0001t0002g0128 | 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 | a0001c0001t0002g0098 a0001c0001t0002g0121 a0001c0001t0002g0138 others(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 | a0001c0001t0002g0050 | 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 | a0001c0001t0002g0306 | 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 | a0001c0001t0002g0131 | 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 | a0001c0001t0002g0118 | 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 | a0001c0001t0002g0016 a0001c0001t0002g0018 a0001c0001t0002g0117 others(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 | a0001c0001t0002g0136 a0001c0001t0002g0310 |
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 | a0001c0001t0002g0085 a0001c0001t0009g0049 |
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 | a0001c0001t0002g0139 | 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 | a0001c0001t0002g0304 | 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 | a0001c0001t0002g0311 | 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 | a0001c0001t0002g0074 a0001c0001t0009g0058 a0001c0001t0019g0135 |
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 | a0001c0001t0018g0013 | 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 | a0001c0001t0002g0056 | 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 | a0001c0001t0002g0127 | 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 | a0001c0001t0002g0309 | 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 | a0001c0001t0002g0308 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0194 a0001c0001t0001g0247 others(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 | a0001c0006t0007g0110 | 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 | a0001c0001t0002g0044 | 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 | a0001c0001t0002g0072 | 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 | a0001c0001t0002g0119 | 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 | a0001c0001t0002g0019 a0001c0001t0002g0094 a0001c0001t0002g0132 others(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 | a0001c0001t0002g0045 | 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 | a0001c0001t0002g0073 | 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 | a0006c0008t0005g0038 | 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 | a0001c0001t0002g0071 | 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 | a0006c0008t0005g0039 | 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 | a0001c0001t0002g0077 | 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 | a0001c0001t0002g0043 | 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 | a0001c0001t0002g0047 | 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 | a0005c0007t0002g0137 | 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 | a0001c0001t0002g0067 | 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 | a0001c0001t0006g0275 | 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 | a0001c0001t0002g0064 a0001c0001t0002g0069 |
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 | a0001c0012t0002g0065 | 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 | a0001c0001t0002g0042 | 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 | a0005c0007t0002g0082 | 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 | a0001c0001t0002g0041 a0001c0001t0002g0305 |
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 | a0001c0001t0002g0302 a0007c0013t0002g0101 |
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 | a0001c0001t0017g0303 | 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 | a0001c0001t0002g0307 | 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 | a0001c0001t0002g0301 | 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 | a0001c0001t0002g0083 | 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 | a0001c0001t0002g0020 | 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 | a0005c0007t0002g0120 | 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 | a0001c0001t0002g0144 | 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 | a0001c0001t0002g0053 | 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 | a0001c0001t0005g0149 | 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 | a0001c0001t0002g0055 | 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 | a0001c0001t0001g0298 a0001c0001t0002g0108 |
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 | a0001c0001t0005g0148 | 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 | a0001c0001t0005g0147 | 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 | a0001c0001t0002g0122 a0001c0001t0002g0153 |
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 | a0001c0001t0002g0312 | 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 | a0001c0001t0001g0296 | 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 | a0001c0001t0002g0141 | 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 | a0001c0001t0002g0081 | 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 | a0001c0001t0002g0126 | 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 | a0001c0001t0021g0300 | 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 | a0001c0001t0021g0300 | 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 | a0001c0001t0021g0300 | 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 | a0001c0001t0021g0300 | 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 | a0001c0001t0021g0300 | 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 | a0001c0001t0021g0300 | 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 | a0001c0001t0004g0203 a0001c0001t0006g0272 a0001c0001t0015g0316 others(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 | a0001c0001t0001g0160 a0001c0001t0002g0084 a0001c0001t0003g0028 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0190 others(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 | a0001c0001t0001g0178 a0001c0001t0001g0191 a0001c0001t0004g0170 others(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 | a0001c0001t0001g0177 a0001c0001t0001g0189 a0001c0001t0004g0151 others(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 | a0001c0001t0001g0155 a0001c0001t0001g0158 a0001c0001t0001g0175 others(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 | a0001c0001t0001g0156 a0001c0001t0001g0162 a0001c0001t0001g0182 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0157 a0001c0001t0001g0161 others(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 | a0001c0001t0001g0168 a0001c0001t0001g0186 |
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 | a0001c0001t0001g0220 | 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 | a0001c0001t0002g0268 | 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 | a0002c0002t0001g0287 | 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 | a0001c0001t0001g0024 a0001c0001t0001g0298 a0001c0001t0002g0017 others(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 | a0001c0001t0002g0017 a0001c0001t0002g0069 a0001c0001t0002g0073 others(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 | a0001c0001t0001g0023 a0001c0001t0002g0046 a0001c0001t0002g0048 others(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 | a0001c0001t0001g0022 a0001c0001t0002g0044 a0001c0001t0002g0045 others(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 | a0001c0001t0001g0219 a0001c0010t0007g0112 |
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 | a0001c0001t0001g0314 a0001c0001t0022g0003 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0250 a0001c0001t0001g0271 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0222 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0224 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0200 a0001c0001t0001g0202 others(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 | a0001c0001t0001g0207 a0001c0001t0012g0245 a0001c0001t0016g0258 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0206 others(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 | a0001c0001t0001g0255 a0001c0001t0001g0276 a0002c0002t0001g0252 |
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 | a0001c0001t0001g0247 | 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 | a0002c0002t0001g0211 a0002c0002t0001g0279 |
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 | a0001c0001t0001g0214 | 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 | a0001c0005t0001g0011 | 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 | a0001c0001t0001g0260 | 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 | a0001c0001t0001g0288 a0001c0001t0001g0296 |
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 | a0001c0001t0001g0278 | 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 | a0001c0001t0002g0251 | 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 | a0001c0001t0001g0232 a0001c0001t0001g0237 a0001c0001t0001g0262 others(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 | a0001c0001t0001g0226 | 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 | a0001c0001t0001g0196 | 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 | a0001c0001t0001g0231 a0001c0001t0001g0265 a0001c0001t0001g0283 others(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 | a0001c0001t0004g0171 | 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 | a0001c0001t0001g0173 a0001c0001t0001g0229 |
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 | a0001c0001t0001g0233 a0001c0001t0001g0256 |
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 | a0001c0001t0001g0238 | 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 | a0001c0001t0001g0284 | 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 | a0001c0001t0001g0236 a0001c0001t0001g0315 |
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 | a0001c0001t0001g0197 | 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 | a0001c0001t0001g0263 | 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 | a0001c0001t0001g0230 | 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 | a0001c0001t0001g0234 a0001c0001t0001g0317 |
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 | a0001c0001t0001g0235 a0001c0001t0014g0239 |
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 | a0001c0001t0001g0198 | 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 | a0001c0001t0001g0001 | 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 | a0001c0001t0001g0001 | 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 | a0001c0001t0015g0316 | 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 | a0001c0001t0001g0244 | 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 | a0001c0001t0001g0024 a0001c0001t0001g0298 |
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 | 39 | a0001c0001t0002g0014 a0001c0001t0002g0017 a0001c0001t0002g0051 others(36): Show |
39 | HG00099.hp1 HG00673.hp1 HG01074.hp2 others(36): 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 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0018 others(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 | a0001c0001t0002g0020 a0001c0001t0002g0053 a0001c0001t0002g0055 others(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 | a0001c0001t0002g0072 a0001c0001t0002g0100 a0001c0001t0002g0108 others(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 | a0003c0003t0001g0167 | 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 | a0001c0001t0001g0217 | 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 | a0001c0001t0001g0193 a0001c0006t0007g0111 |
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 | a0001c0001t0004g0210 a0002c0002t0001g0280 |
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 | a0001c0001t0001g0194 | 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 | a0001c0001t0001g0204 a0001c0001t0001g0223 a0001c0001t0001g0281 others(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 | a0001c0001t0001g0225 a0001c0001t0001g0248 |
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 | a0001c0001t0001g0246 | 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 | a0001c0001t0013g0195 | 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 | a0001c0001t0001g0037 a0001c0001t0001g0155 a0001c0001t0001g0156 others(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 | a0001c0001t0001g0204 a0001c0001t0001g0217 a0001c0001t0001g0248 others(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 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0160 others(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 | a0001c0001t0001g0204 a0001c0001t0001g0217 |
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 | a0001c0001t0001g0173 | 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 | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(121): 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 | a0001c0001t0020g0299 a0001c0001t0021g0300 |
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 | a0001c0001t0004g0151 | 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 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0001c0001t0001g0231 others(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 | a0001c0001t0008g0159 a0001c0001t0008g0184 |
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 | a0001c0006t0007g0110 | 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 | a0001c0001t0002g0074 a0001c0001t0002g0302 a0001c0001t0002g0305 others(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 | a0001c0001t0005g0146 a0001c0001t0005g0147 a0001c0001t0005g0148 others(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 | a0001c0001t0020g0299 a0001c0001t0021g0300 |
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 | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(117): 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 | 125 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(122): Show |
125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): 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 | a0001c0001t0001g0007 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(117): 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 | a0001c0001t0015g0316 | 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 | a0001c0001t0001g0193 | 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 | 122 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(119): 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 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0234 others(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 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(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 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0204 others(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 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(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 | 131 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(128): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): 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 | a0001c0001t0002g0103 a0001c0001t0002g0121 |
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 | 131 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(128): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): 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 | a0001c0006t0007g0109 a0001c0006t0007g0110 a0001c0006t0007g0111 others(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 | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(117): 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 | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(250): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): 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 | a0001c0006t0007g0109 a0001c0006t0007g0110 a0001c0006t0007g0111 others(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 | a0001c0006t0007g0109 a0001c0006t0007g0110 a0001c0006t0007g0111 others(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 | a0001c0001t0001g0204 a0001c0001t0001g0223 a0001c0001t0001g0225 others(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 | a0001c0001t0001g0204 a0001c0001t0001g0223 a0001c0001t0001g0225 others(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 | a0001c0001t0002g0057 | 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 | 125 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(122): Show |
125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): 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 | a0001c0001t0002g0304 | 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 | a0003c0003t0001g0181 | 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 | a0001c0001t0001g0024 | 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 | a0001c0001t0004g0150 a0001c0001t0004g0151 |
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 | a0001c0001t0002g0128 | 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 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0234 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0227 a0001c0001t0001g0232 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(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 | 9 | a0001c0001t0001g0001 a0001c0001t0001g0224 a0001c0001t0001g0233 others(6): 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 | 147 | a0001c0001t0001g0022 a0001c0001t0001g0037 a0001c0001t0001g0155 others(144): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): 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 | a0001c0001t0001g0165 a0001c0001t0001g0168 a0001c0001t0001g0173 others(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 | a0001c0001t0001g0165 a0001c0001t0001g0168 a0001c0001t0001g0169 others(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 | a0001c0001t0005g0146 a0001c0001t0005g0147 a0001c0001t0005g0148 others(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 | 131 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(128): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.805-3441C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50450019 | |||||||
| chr12:50450021 | C | T | 125 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(122): Show |
125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): 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 | a0001c0001t0002g0077 | 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 | a0004c0004t0001g0201 | 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 | a0003c0003t0001g0180 | 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 | 257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(254): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.805-2985G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | chr12 | 50450475 | |||||||
| chr12:50450512 | T | G | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(113): 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 | a0001c0001t0001g0219 | 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 | a0001c0001t0001g0285 | 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 | a0001c0001t0001g0175 a0001c0001t0001g0189 a0001c0001t0001g0190 |
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 | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(117): 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 | a0001c0006t0007g0109 a0001c0006t0007g0110 a0001c0006t0007g0111 others(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 | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(117): 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 | 257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(254): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): 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 | a0001c0001t0003g0027 | 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 | a0001c0001t0003g0027 | 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 | a0001c0001t0003g0027 | 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 | a0001c0001t0005g0146 a0001c0001t0005g0147 a0001c0001t0005g0148 others(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 | a0001c0001t0010g0026 a0001c0001t0010g0034 |
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 | a0001c0001t0001g0196 | 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 | a0001c0001t0017g0303 | 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 | a0001c0001t0001g0160 | 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 | a0001c0001t0001g0269 a0001c0001t0001g0292 |
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 | a0001c0001t0002g0043 | 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 | a0001c0001t0004g0203 | 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 | 135 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(132): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): 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 | a0001c0001t0001g0002 a0001c0001t0001g0191 a0001c0001t0002g0131 others(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 | a0001c0006t0007g0109 a0001c0006t0007g0110 a0001c0006t0007g0111 others(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 | a0001c0001t0002g0108 | 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 | a0001c0001t0002g0069 | 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 | a0001c0001t0001g0246 a0001c0001t0001g0290 |
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 | a0001c0010t0007g0112 | 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 | a0001c0001t0001g0205 | 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 | a0001c0001t0001g0260 | 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 | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(113): 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 | 137 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(134): Show |
137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): 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 | a0001c0001t0004g0150 | 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 | a0001c0001t0001g0288 | 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 | a0001c0001t0002g0051 a0001c0001t0002g0144 |
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 | a0001c0001t0002g0070 a0001c0001t0002g0072 a0001c0001t0002g0080 others(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 | a0001c0001t0002g0304 | 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 | 257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(254): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): 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 | a0001c0001t0002g0076 | 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 | a0001c0001t0002g0076 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0205 a0001c0001t0001g0206 others(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 | a0003c0003t0001g0166 a0003c0003t0001g0187 |
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 | a0001c0001t0002g0078 | 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 | a0001c0001t0005g0146 a0001c0001t0005g0147 a0001c0001t0005g0148 others(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 | a0001c0001t0001g0025 | 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 | a0001c0001t0001g0276 | 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 | a0001c0001t0002g0305 | 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 | a0001c0001t0004g0150 a0001c0001t0004g0151 |
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 | a0001c0001t0001g0037 | 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 | 129 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(126): Show |
129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): 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 | 2 | a0001c0001t0001g0001 a0001c0001t0001g0244 |
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 | a0001c0001t0001g0025 | 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 | a0001c0001t0002g0060 | 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 | 134 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(131): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): 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 | a0002c0002t0001g0212 | 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 | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(114): 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 | a0001c0001t0001g0007 | 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 | a0001c0001t0002g0125 | 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 | a0001c0001t0001g0024 a0001c0001t0001g0176 a0001c0001t0001g0222 others(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 | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): 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 | a0001c0001t0001g0202 a0001c0001t0001g0207 a0001c0001t0001g0227 others(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 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0168 others(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 | 294 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(291): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.1121+2806A>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 10/15 | chr12 | 50457223 | |||||||
| chr12:50457251 | G | T | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(113): 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 | a0001c0001t0001g0193 | 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 | a0001c0001t0015g0316 | 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 | a0001c0001t0001g0012 | 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 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0001c0001t0001g0231 others(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 | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(256): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): 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 | a0003c0003t0001g0164 | 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 | a0001c0001t0001g0198 | 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 | a0001c0001t0001g0037 a0001c0001t0001g0156 a0001c0001t0001g0157 others(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 | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(125): 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 | 108 | a0001c0001t0001g0237 a0001c0001t0001g0288 a0001c0001t0002g0014 others(105): Show |
108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): 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 | a0001c0001t0002g0052 a0001c0001t0002g0068 a0001c0001t0002g0071 others(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 | a0001c0001t0003g0027 a0001c0001t0003g0028 a0001c0001t0003g0029 others(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 | a0001c0001t0015g0316 | 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 | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(105): 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 | a0001c0001t0001g0248 a0001c0001t0001g0281 a0001c0001t0001g0288 others(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 | a0001c0001t0001g0037 a0001c0001t0002g0076 a0001c0006t0007g0109 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(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 | a0001c0001t0011g0313 | 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 | a0001c0001t0001g0227 a0001c0001t0001g0282 |
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 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0234 others(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 | a0001c0001t0003g0035 | 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 | a0001c0001t0001g0283 | 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 | a0001c0001t0006g0272 a0001c0001t0006g0273 a0001c0001t0006g0274 others(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 | a0001c0001t0001g0012 | 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 | a0001c0001t0020g0299 a0001c0001t0021g0300 |
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 | a0001c0001t0001g0177 | 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 | a0001c0001t0001g0243 a0001c0001t0001g0285 a0001c0001t0001g0291 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(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 | a0001c0001t0002g0088 | 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 | a0002c0002t0001g0216 | 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 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(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 | a0001c0001t0001g0023 a0001c0001t0001g0037 a0001c0001t0001g0177 others(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 | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(103): 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 | a0001c0001t0002g0054 a0001c0001t0002g0062 a0001c0001t0002g0063 others(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 | 92 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(89): Show |
92 | HG00099.hp1 HG00597.hp2 HG00642.hp2 others(89): 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 | a0001c0001t0002g0043 a0001c0001t0002g0044 a0001c0001t0002g0045 others(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 | a0001c0001t0002g0305 a0001c0001t0002g0310 a0001c0001t0002g0311 others(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 | a0001c0006t0007g0109 a0001c0006t0007g0110 a0001c0006t0007g0111 others(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 | a0001c0001t0015g0316 | 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 | a0001c0001t0002g0128 | 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 | a0001c0001t0002g0081 | 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 | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(114): 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 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(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 | a0001c0001t0011g0313 | 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 | a0001c0001t0001g0178 a0001c0001t0001g0191 a0003c0003t0001g0154 others(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 | a0001c0001t0021g0300 | 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 | a0002c0002t0001g0215 a0002c0002t0001g0218 |
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 | a0001c0006t0007g0109 a0001c0006t0007g0110 a0001c0006t0007g0111 others(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 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(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 | a0001c0001t0006g0272 a0001c0001t0006g0273 a0001c0001t0006g0274 others(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 | a0001c0001t0002g0073 a0001c0001t0002g0307 |
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 | a0006c0008t0005g0038 a0006c0008t0005g0039 |
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 | a0001c0001t0004g0150 a0001c0001t0004g0151 |
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 | a0001c0001t0004g0170 a0001c0001t0004g0171 |
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 | a0001c0001t0006g0272 a0001c0001t0006g0273 a0001c0001t0006g0274 others(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 | a0001c0001t0019g0135 | 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 | a0001c0006t0007g0109 a0001c0006t0007g0110 a0001c0006t0007g0111 others(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 | a0001c0001t0001g0196 | 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 | 137 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(134): Show |
137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): 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 | a0002c0002t0001g0209 a0002c0002t0001g0212 a0002c0002t0001g0216 others(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 | a0001c0001t0002g0064 | 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 | a0002c0002t0001g0209 a0002c0002t0001g0211 a0002c0002t0001g0212 others(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 | a0001c0001t0014g0239 | 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 | a0001c0001t0002g0077 | 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 | a0001c0001t0001g0037 | 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 | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(114): 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 | a0001c0001t0002g0308 | 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 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(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 | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(247): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): 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 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(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 | a0001c0001t0001g0282 a0001c0001t0006g0272 a0001c0001t0006g0273 others(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 | a0001c0001t0011g0313 | 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 | a0001c0001t0002g0078 | 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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(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 | 137 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(134): Show |
137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): 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 | a0001c0001t0002g0053 | 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 | a0001c0001t0002g0152 | 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 | a0001c0001t0001g0037 | 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 | a0001c0001t0002g0144 | 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 | a0001c0001t0002g0069 | 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 | a0001c0001t0002g0041 a0001c0012t0002g0065 |
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 | a0001c0001t0001g0025 a0001c0001t0001g0037 a0001c0001t0001g0155 others(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 | a0001c0001t0001g0261 | 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 | a0006c0008t0005g0038 a0006c0008t0005g0039 |
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 | 262 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(259): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): 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 | a0001c0001t0001g0025 a0001c0001t0001g0037 a0001c0001t0001g0155 others(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 | a0001c0001t0001g0157 a0001c0001t0001g0162 a0001c0001t0001g0165 others(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 | 141 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(138): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): 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 | a0001c0001t0001g0007 a0001c0001t0002g0044 |
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 | a0003c0003t0001g0163 | 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 | a0001c0001t0001g0261 | 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 | a0006c0008t0005g0038 a0006c0008t0005g0039 |
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 | a0004c0004t0001g0201 | 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 | a0001c0001t0015g0316 | 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 | a0001c0001t0001g0197 a0001c0001t0001g0198 |
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 | a0001c0001t0010g0026 a0001c0001t0010g0034 |
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 | 136 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(133): Show |
136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): 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 | a0001c0006t0007g0109 a0001c0006t0007g0110 a0001c0006t0007g0111 others(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 | 300 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(297): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.1384-2113G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 12/15 | chr12 | 50464846 | |||||||
| chr12:50465037 | C | T | 134 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(131): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): 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 | a0001c0001t0004g0150 a0001c0001t0004g0151 |
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 | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(109): 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 | a0003c0003t0001g0181 | 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 | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(113): 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 | 128 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0040 others(125): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): 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 | a0001c0001t0002g0046 a0001c0001t0002g0121 a0001c0001t0002g0305 others(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 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(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 | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(109): 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 | 135 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(132): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.1384-1565G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 12/15 | chr12 | 50465394 | |||||||
| chr12:50465499 | G | A | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(113): 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 | a0001c0001t0001g0231 | 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 | a0001c0001t0006g0272 a0001c0001t0006g0273 a0001c0001t0006g0274 others(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 | a0001c0001t0001g0182 | 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 | a0001c0001t0001g0200 | 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 | 137 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(134): Show |
137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): 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 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0002g0096 |
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 | a0001c0001t0004g0150 a0001c0001t0004g0151 |
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 | a0001c0001t0001g0165 a0001c0001t0001g0168 a0001c0001t0001g0169 others(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 | a0001c0001t0004g0150 | 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 | a0001c0001t0003g0027 a0001c0001t0003g0028 a0001c0001t0003g0029 others(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 | a0001c0001t0002g0014 | 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 | a0001c0001t0001g0278 | 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 | 300 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(297): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.1545+641G>A | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 13/15 | chr12 | 50467761 | |||||||
| chr12:50467857 | G | GT | 135 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(132): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): 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 | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(109): 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 | 136 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(133): Show |
136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): 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 | a0001c0001t0004g0221 | 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 | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(114): 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 | 136 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(133): Show |
136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): 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 | a0005c0007t0002g0120 | 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 | 128 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(125): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): 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 | a0001c0001t0006g0273 | 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 | 300 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(297): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): 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 | a0001c0001t0001g0285 | 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 | a0001c0001t0002g0310 a0001c0001t0002g0311 |
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 | a0001c0001t0002g0081 | 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 | a0001c0001t0004g0150 a0001c0001t0004g0151 |
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 | a0001c0001t0001g0179 | 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 | 133 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0234 others(130): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): 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 | a0001c0001t0001g0207 a0001c0001t0002g0017 a0001c0001t0002g0020 others(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 | a0001c0001t0001g0156 a0001c0001t0001g0158 a0001c0001t0001g0220 others(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 | a0001c0001t0002g0067 a0001c0001t0002g0069 a0001c0001t0002g0073 others(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 | a0001c0001t0002g0107 a0001c0001t0002g0138 |
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 | a0001c0001t0001g0162 | 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 | a0004c0004t0001g0201 | 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 | a0001c0001t0009g0049 a0001c0001t0009g0058 |
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 | 125 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(122): Show |
125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): 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 | a0001c0001t0001g0317 | 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 | a0001c0001t0015g0316 | 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 | a0001c0001t0005g0146 a0001c0001t0005g0147 a0001c0001t0005g0148 others(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 | 314 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(311): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): 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 | a0001c0001t0004g0170 a0001c0001t0004g0171 |
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 | a0001c0001t0010g0026 a0001c0001t0010g0034 |
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 | a0001c0001t0012g0245 | 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 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0001c0001t0001g0283 |
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 | a0001c0001t0002g0073 a0001c0001t0002g0307 |
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 | a0001c0001t0009g0058 | 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 | a0001c0001t0010g0026 a0001c0001t0010g0034 |
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 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(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 | a0001c0001t0015g0316 | 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 | a0001c0001t0001g0224 | 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 | a0001c0001t0002g0268 | 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 | a0001c0001t0001g0207 | 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 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(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 | a0001c0001t0015g0316 | 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 | a0001c0001t0001g0200 a0001c0001t0001g0269 a0001c0001t0001g0292 |
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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(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 | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(113): 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 | a0001c0001t0020g0299 a0001c0001t0021g0300 |
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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 |
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 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 |
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 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0198 |
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 | a0001c0001t0001g0197 a0001c0001t0001g0198 |
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 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0277 others(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 | a0001c0001t0001g0219 | 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 | a0001c0006t0007g0111 | 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 | 128 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(125): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): 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 | a0001c0001t0020g0299 a0001c0001t0021g0300 |
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 | a0001c0001t0002g0059 a0001c0001t0002g0068 |
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 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(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 | a0001c0001t0002g0079 | 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 | a0001c0001t0001g0255 a0001c0001t0001g0281 a0001c0001t0002g0017 others(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 | 258 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(255): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): 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 | a0001c0001t0001g0006 a0001c0001t0001g0189 a0001c0001t0001g0248 others(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 | a0001c0001t0002g0080 | 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 | a0001c0001t0001g0037 | 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 | a0001c0006t0007g0109 a0001c0010t0007g0112 |
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 | a0001c0001t0001g0176 a0001c0001t0001g0178 a0001c0001t0001g0231 others(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 | a0001c0001t0001g0176 a0001c0001t0001g0178 a0001c0001t0001g0231 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(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 | a0001c0001t0020g0299 | 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 | a0001c0001t0001g0025 a0001c0001t0002g0116 |
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 | a0002c0002t0001g0209 a0002c0002t0001g0216 a0002c0002t0001g0252 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0255 a0001c0001t0002g0040 others(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 | a0001c0001t0001g0177 | 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 | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(122): 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 | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(114): 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 | a0001c0001t0006g0272 a0001c0001t0006g0273 a0001c0001t0006g0274 others(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 | a0001c0001t0002g0041 a0001c0012t0002g0065 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0205 a0001c0001t0001g0206 others(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 | 305 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(302): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.1837-188C>T | LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 15/15 | chr12 | 50475338 |