Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 23175 |
| ensemblid | ENSG00000134324.12 |
| hgncid | 13345 |
| symbol | LPIN1 |
| name | lipin 1 |
| refseq_nuc | NM_001349206.2 |
| refseq_prot | NP_001336135.1 |
| ensembl_nuc | ENST00000674199.1 |
| ensembl_prot | ENSP00000501331.1 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 11746632 |
| end | 11827409 |
| strand | + |
| ver | v1.2 |
| region | chr2:11746632-11827409 |
| region5000 | chr2:11741632-11832409 |
| regionname0 | LPIN1_chr2_11746632_11827409 |
| regionname5000 | LPIN1_chr2_11741632_11832409 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 926 | 268 | 81 | 51 | 91 | 13 | 30 | 62 | LPIN1_chr2_11741632_11832409 | LPIN1 | MNYVG others(921): Show |
chr2 | 11741632 | 11832409 |
| a0002 | 0/0 | 925 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | MNYVG others(920): Show |
chr2 | 11741632 | 11832409 |
| a0003 | 0/0 | 926 | 3 | 0 | 2 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | MNYVG others(921): Show |
chr2 | 11741632 | 11832409 |
| a0004 | 0/0 | 926 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | MNYVG others(921): Show |
chr2 | 11741632 | 11832409 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2778 | 230 | 57 | 42 | 91 | 11 | 27 | LPIN1_chr2_11741632_11832409 | LPIN1 | ATGAA others(2773): Show |
chr2 | 11741632 | 11832409 | ||
| a0001c0002 | 0/0 | 2778 | 13 | 12 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | ATGAA others(2773): Show |
chr2 | 11741632 | 11832409 | ||
| a0001c0003 | 0/0 | 2778 | 10 | 0 | 6 | 0 | 2 | 2 | LPIN1_chr2_11741632_11832409 | LPIN1 | ATGAA others(2773): Show |
chr2 | 11741632 | 11832409 | ||
| a0001c0004 | 0/0 | 2778 | 6 | 4 | 2 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | ATGAA others(2773): Show |
chr2 | 11741632 | 11832409 | ||
| a0001c0005 | 0/0 | 2778 | 5 | 5 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | ATGAA others(2773): Show |
chr2 | 11741632 | 11832409 | ||
| a0001c0008 | 0/0 | 2778 | 2 | 2 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | ATGAA others(2773): Show |
chr2 | 11741632 | 11832409 | ||
| a0001c0011 | 0/0 | 2778 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | ATGAA others(2773): Show |
chr2 | 11741632 | 11832409 | ||
| a0001c0013 | 0/0 | 2778 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | ATGAA others(2773): Show |
chr2 | 11741632 | 11832409 | ||
| a0002c0007 | 0/0 | 2775 | 3 | 2 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | ATGAA others(2770): Show |
chr2 | 11741632 | 11832409 | ||
| a0002c0009 | 0/0 | 2775 | 2 | 2 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | ATGAA others(2770): Show |
chr2 | 11741632 | 11832409 | ||
| a0002c0010 | 0/0 | 2775 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | ATGAA others(2770): Show |
chr2 | 11741632 | 11832409 | ||
| a0003c0006 | 0/0 | 2778 | 3 | 0 | 2 | 0 | 1 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | ATGAA others(2773): Show |
chr2 | 11741632 | 11832409 | ||
| a0004c0012 | 0/0 | 2778 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | ATGAA others(2773): Show |
chr2 | 11741632 | 11832409 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 5448 | 58 | 4 | 6 | 32 | 4 | 11 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5443): Show |
chr2 | 11741632 | 11832409 |
| a0001c0001t0002 | 0/0 | 5447 | 41 | 10 | 14 | 8 | 4 | 5 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5442): Show |
chr2 | 11741632 | 11832409 |
| a0001c0001t0003 | 0/0 | 5448 | 28 | 11 | 4 | 13 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5443): Show |
chr2 | 11741632 | 11832409 |
| a0001c0001t0004 | 0/0 | 5447 | 31 | 2 | 4 | 22 | 1 | 2 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5442): Show |
chr2 | 11741632 | 11832409 |
| a0001c0001t0005 | 0/0 | 5447 | 9 | 9 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5442): Show |
chr2 | 11741632 | 11832409 |
| a0001c0001t0006 | 0/0 | 5447 | 8 | 7 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5442): Show |
chr2 | 11741632 | 11832409 |
| a0001c0001t0007 | 0/0 | 5447 | 3 | 0 | 2 | 0 | 1 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5442): Show |
chr2 | 11741632 | 11832409 |
| a0001c0001t0008 | 0/0 | 5446 | 7 | 5 | 2 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5441): Show |
chr2 | 11741632 | 11832409 |
| a0001c0001t0009 | 0/0 | 5447 | 2 | 0 | 0 | 0 | 0 | 2 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5442): Show |
chr2 | 11741632 | 11832409 |
| a0001c0001t0010 | 0/0 | 5447 | 3 | 1 | 2 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5442): Show |
chr2 | 11741632 | 11832409 |
| a0001c0001t0011 | 0/1 | 5446 | 6 | 0 | 0 | 0 | 1 | 4 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5441): Show |
chr2 | 11741632 | 11832409 |
| a0001c0001t0012 | 0/0 | 5448 | 5 | 1 | 1 | 2 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5443): Show |
chr2 | 11741632 | 11832409 |
| a0001c0001t0013 | 0/0 | 5449 | 4 | 0 | 1 | 3 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5444): Show |
chr2 | 11741632 | 11832409 |
| a0001c0001t0014 | 0/0 | 5447 | 3 | 0 | 0 | 3 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5442): Show |
chr2 | 11741632 | 11832409 |
| a0001c0001t0016 | 0/0 | 5449 | 3 | 0 | 0 | 3 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5444): Show |
chr2 | 11741632 | 11832409 |
| a0001c0001t0017 | 0/0 | 5447 | 2 | 2 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5442): Show |
chr2 | 11741632 | 11832409 |
| a0001c0001t0018 | 0/0 | 5447 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5442): Show |
chr2 | 11741632 | 11832409 |
| a0001c0001t0019 | 0/0 | 5449 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5444): Show |
chr2 | 11741632 | 11832409 |
| a0001c0001t0020 | 0/0 | 5448 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5443): Show |
chr2 | 11741632 | 11832409 |
| a0001c0001t0021 | 0/0 | 5449 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5444): Show |
chr2 | 11741632 | 11832409 |
| a0001c0001t0022 | 0/0 | 5448 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5443): Show |
chr2 | 11741632 | 11832409 |
| a0001c0001t0023 | 0/0 | 5449 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5444): Show |
chr2 | 11741632 | 11832409 |
| a0001c0001t0024 | 0/0 | 5448 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5443): Show |
chr2 | 11741632 | 11832409 |
| a0001c0001t0025 | 0/0 | 5447 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5442): Show |
chr2 | 11741632 | 11832409 |
| a0001c0001t0026 | 0/0 | 5446 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5441): Show |
chr2 | 11741632 | 11832409 |
| a0001c0001t0027 | 0/0 | 5448 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5443): Show |
chr2 | 11741632 | 11832409 |
| a0001c0001t0028 | 0/0 | 5448 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5443): Show |
chr2 | 11741632 | 11832409 |
| a0001c0001t0029 | 0/0 | 5448 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5443): Show |
chr2 | 11741632 | 11832409 |
| a0001c0001t0031 | 0/0 | 5446 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5441): Show |
chr2 | 11741632 | 11832409 |
| a0001c0001t0033 | 0/0 | 5446 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5441): Show |
chr2 | 11741632 | 11832409 |
| a0001c0001t0036 | 0/0 | 5448 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5443): Show |
chr2 | 11741632 | 11832409 |
| a0001c0001t0037 | 0/0 | 5447 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5442): Show |
chr2 | 11741632 | 11832409 |
| a0001c0001t0038 | 0/0 | 5445 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5440): Show |
chr2 | 11741632 | 11832409 |
| a0001c0002t0002 | 0/0 | 5447 | 2 | 1 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5442): Show |
chr2 | 11741632 | 11832409 |
| a0001c0002t0003 | 0/0 | 5448 | 5 | 5 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5443): Show |
chr2 | 11741632 | 11832409 |
| a0001c0002t0006 | 0/0 | 5447 | 2 | 2 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5442): Show |
chr2 | 11741632 | 11832409 |
| a0001c0002t0008 | 0/0 | 5446 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5441): Show |
chr2 | 11741632 | 11832409 |
| a0001c0002t0015 | 0/0 | 5448 | 2 | 2 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5443): Show |
chr2 | 11741632 | 11832409 |
| a0001c0002t0030 | 0/0 | 5447 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5442): Show |
chr2 | 11741632 | 11832409 |
| a0001c0003t0001 | 0/0 | 5448 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5443): Show |
chr2 | 11741632 | 11832409 |
| a0001c0003t0002 | 0/0 | 5447 | 3 | 0 | 1 | 0 | 2 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5442): Show |
chr2 | 11741632 | 11832409 |
| a0001c0003t0009 | 0/0 | 5447 | 5 | 0 | 4 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5442): Show |
chr2 | 11741632 | 11832409 |
| a0001c0003t0014 | 0/0 | 5447 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5442): Show |
chr2 | 11741632 | 11832409 |
| a0001c0004t0006 | 0/0 | 5447 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5442): Show |
chr2 | 11741632 | 11832409 |
| a0001c0004t0007 | 0/0 | 5447 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5442): Show |
chr2 | 11741632 | 11832409 |
| a0001c0004t0010 | 0/0 | 5447 | 4 | 3 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5442): Show |
chr2 | 11741632 | 11832409 |
| a0001c0005t0007 | 0/0 | 5447 | 5 | 5 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5442): Show |
chr2 | 11741632 | 11832409 |
| a0001c0008t0005 | 0/0 | 5447 | 2 | 2 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5442): Show |
chr2 | 11741632 | 11832409 |
| a0001c0011t0015 | 0/0 | 5448 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5443): Show |
chr2 | 11741632 | 11832409 |
| a0001c0013t0001 | 0/0 | 5448 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5443): Show |
chr2 | 11741632 | 11832409 |
| a0002c0007t0011 | 0/0 | 5443 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5438): Show |
chr2 | 11741632 | 11832409 |
| a0002c0007t0034 | 0/0 | 5445 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5440): Show |
chr2 | 11741632 | 11832409 |
| a0002c0007t0035 | 0/0 | 5444 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5439): Show |
chr2 | 11741632 | 11832409 |
| a0002c0009t0002 | 0/0 | 5444 | 2 | 2 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5439): Show |
chr2 | 11741632 | 11832409 |
| a0002c0010t0005 | 0/0 | 5444 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5439): Show |
chr2 | 11741632 | 11832409 |
| a0003c0006t0004 | 0/0 | 5447 | 2 | 0 | 2 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5442): Show |
chr2 | 11741632 | 11832409 |
| a0003c0006t0032 | 0/0 | 5447 | 1 | 0 | 0 | 0 | 1 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5442): Show |
chr2 | 11741632 | 11832409 |
| a0004c0012t0001 | 0/0 | 5448 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | GTGTT others(5443): Show |
chr2 | 11741632 | 11832409 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0214 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0004g0005 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0004g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0004g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0004g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0004g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0004g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0004g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0004g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0004g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0004g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0004g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0004g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0004g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0004g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0004g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0004g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0005g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0005g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0005g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0005g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0005g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0005g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0005g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0006g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0006g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0006g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0006g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0006g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0006g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0006g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0006g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0007g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0007g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0007g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0008g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0008g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0008g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0008g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0008g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0008g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0008g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0009g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0009g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0010g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0010g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0010g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0011g0001 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0011g0088 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0011g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0011g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0011g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0012g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0012g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0012g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0012g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0012g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0013g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0013g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0013g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0013g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0014g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0014g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0014g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0016g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0016g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0016g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0017g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0017g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0018g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0019g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0020g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0021g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0022g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0023g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0024g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0025g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0026g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0027g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0028g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0029g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0031g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0033g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0036g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0037g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0001t0038g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0002t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0002t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0002t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0002t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0002t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0002t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0002t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0002t0006g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0002t0006g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0002t0008g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0002t0015g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0002t0015g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0002t0030g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0003t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0003t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0003t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0003t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0003t0009g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0003t0009g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0003t0009g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0003t0009g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0003t0009g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0003t0014g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0004t0006g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0004t0007g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0004t0010g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0004t0010g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0004t0010g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0004t0010g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0005t0007g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0005t0007g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0005t0007g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0005t0007g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0005t0007g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0008t0005g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0008t0005g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0011t0015g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0001c0013t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0002c0007t0011g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0002c0007t0034g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0002c0007t0035g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0002c0009t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0002c0009t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0002c0010t0005g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0003c0006t0004g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0003c0006t0004g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0003c0006t0032g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| a0004c0012t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0255 | EUR | GBR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0100 | EUR | GBR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG00280 | hp1 | a0001 | c0003 | t0002 | g0056 | EUR | FIN | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0253 | EUR | FIN | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0225 | EAS | CHS | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | CHS | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG00558 | hp1 | a0001 | c0001 | t0014 | g0189 | EAS | CHS | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0140 | EAS | CHS | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG00609 | hp2 | a0001 | c0001 | t0004 | g0208 | EAS | CHS | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG00639 | hp1 | a0001 | c0001 | t0031 | g0183 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG00639 | hp2 | a0001 | c0001 | t0008 | g0042 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG00673 | hp1 | a0001 | c0001 | t0004 | g0121 | EAS | CHS | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | CHS | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG00733 | hp1 | a0001 | c0003 | t0001 | g0052 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG00733 | hp2 | a0001 | c0001 | t0004 | g0200 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG00735 | hp1 | a0001 | c0001 | t0007 | g0112 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0182 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG00738 | hp1 | a0001 | c0003 | t0009 | g0139 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG00738 | hp2 | a0001 | c0001 | t0004 | g0192 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0164 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0117 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0205 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01070 | hp2 | a0001 | c0013 | t0001 | g0025 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0116 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0204 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0245 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01074 | hp2 | a0001 | c0003 | t0002 | g0090 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01081 | hp1 | a0001 | c0003 | t0009 | g0053 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0123 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01109 | hp1 | a0001 | c0001 | t0010 | g0024 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01109 | hp2 | a0001 | c0004 | t0007 | g0270 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0114 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01167 | hp2 | a0002 | c0007 | t0011 | g0029 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0202 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01175 | hp2 | a0001 | c0001 | t0006 | g0043 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01243 | hp1 | a0003 | c0006 | t0004 | g0174 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0175 | AMR | PUR | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01255 | hp1 | a0001 | c0001 | t0004 | g0193 | AMR | CLM | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0212 | AMR | CLM | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01257 | hp1 | a0001 | c0001 | t0038 | g0002 | AMR | CLM | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01257 | hp2 | a0001 | c0003 | t0009 | g0055 | AMR | CLM | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01258 | hp1 | a0001 | c0001 | t0007 | g0219 | AMR | CLM | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01258 | hp2 | a0001 | c0001 | t0008 | g0002 | AMR | CLM | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01261 | hp1 | a0001 | c0001 | t0010 | g0080 | AMR | CLM | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0057 | AMR | CLM | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | CLM | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01346 | hp2 | a0001 | c0001 | t0012 | g0249 | AMR | CLM | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01361 | hp1 | a0001 | c0001 | t0021 | g0102 | AMR | CLM | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0131 | AMR | CLM | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01433 | hp2 | a0001 | c0003 | t0009 | g0092 | AMR | CLM | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01496 | hp1 | a0003 | c0006 | t0004 | g0099 | AMR | CLM | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0072 | AMR | CLM | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0251 | EUR | IBS | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01515 | hp2 | a0001 | c0003 | t0002 | g0091 | EUR | IBS | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0186 | EUR | IBS | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | IBS | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0252 | EUR | IBS | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | IBS | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01884 | hp1 | a0001 | c0001 | t0012 | g0070 | AFR | ACB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01891 | hp1 | a0001 | c0001 | t0006 | g0041 | AFR | ACB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01891 | hp2 | a0001 | c0001 | t0008 | g0023 | AFR | ACB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01934 | hp1 | a0001 | c0004 | t0010 | g0081 | AMR | PEL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01934 | hp2 | a0001 | c0001 | t0023 | g0161 | AMR | PEL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01952 | hp1 | a0001 | c0001 | t0024 | g0176 | AMR | PEL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0203 | AMR | PEL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01981 | hp1 | a0001 | c0001 | t0013 | g0209 | AMR | PEL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0160 | AMR | PEL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0118 | AMR | PEL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0211 | AMR | PEL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02015 | hp2 | a0001 | c0001 | t0012 | g0113 | EAS | KHV | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0207 | EAS | KHV | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02055 | hp1 | a0001 | c0004 | t0006 | g0076 | AFR | ACB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02055 | hp2 | a0002 | c0007 | t0034 | g0027 | AFR | ACB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0146 | EAS | KHV | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02071 | hp1 | a0001 | c0001 | t0004 | g0265 | EAS | KHV | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02071 | hp2 | a0001 | c0001 | t0004 | g0259 | EAS | KHV | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02074 | hp2 | a0001 | c0001 | t0020 | g0126 | EAS | KHV | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02080 | hp1 | a0001 | c0001 | t0016 | g0105 | EAS | KHV | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0169 | EAS | KHV | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0149 | AFR | ACB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | ACB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02155 | hp1 | a0001 | c0001 | t0016 | g0124 | EAS | CDX | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0170 | EAS | CDX | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | CDX | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | CDX | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02257 | hp2 | a0001 | c0004 | t0010 | g0008 | AFR | ACB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | ACB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02258 | hp2 | a0001 | c0005 | t0007 | g0159 | AFR | ACB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02280 | hp1 | a0002 | c0010 | t0005 | g0012 | AFR | ACB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0087 | AFR | ACB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0082 | AFR | ACB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0046 | AFR | ACB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02523 | hp1 | a0001 | c0001 | t0027 | g0142 | EAS | KHV | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02523 | hp2 | a0004 | c0012 | t0001 | g0178 | EAS | KHV | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0220 | AFR | GWD | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02572 | hp2 | a0001 | c0002 | t0008 | g0085 | AFR | GWD | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0060 | AFR | GWD | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02615 | hp2 | a0001 | c0002 | t0006 | g0155 | AFR | GWD | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02622 | hp1 | a0001 | c0001 | t0018 | g0035 | AFR | GWD | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02622 | hp2 | a0001 | c0002 | t0015 | g0158 | AFR | GWD | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02630 | hp1 | a0001 | c0002 | t0015 | g0154 | AFR | GWD | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0033 | AFR | GWD | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0050 | AFR | GWD | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0068 | AFR | GWD | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0044 | AFR | GWD | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02723 | hp2 | a0001 | c0001 | t0006 | g0059 | AFR | GWD | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02735 | hp1 | a0001 | c0003 | t0014 | g0089 | SAS | PJL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02735 | hp2 | a0001 | c0001 | t0011 | g0119 | SAS | PJL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02738 | hp1 | a0001 | c0001 | t0029 | g0138 | SAS | PJL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02738 | hp2 | a0001 | c0001 | t0004 | g0191 | SAS | PJL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02809 | hp1 | a0001 | c0002 | t0003 | g0014 | AFR | GWD | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02809 | hp2 | a0001 | c0004 | t0010 | g0078 | AFR | GWD | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0063 | AFR | GWD | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0071 | AFR | GWD | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02896 | hp1 | a0001 | c0001 | t0017 | g0065 | AFR | GWD | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02896 | hp2 | a0001 | c0002 | t0003 | g0016 | AFR | GWD | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02897 | hp1 | a0001 | c0001 | t0017 | g0066 | AFR | GWD | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02897 | hp2 | a0001 | c0001 | t0006 | g0083 | AFR | GWD | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02922 | hp1 | a0001 | c0008 | t0005 | g0007 | AFR | ESN | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0093 | AFR | ESN | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02970 | hp1 | a0001 | c0002 | t0003 | g0017 | AFR | ESN | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02970 | hp2 | a0001 | c0005 | t0007 | g0021 | AFR | ESN | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02976 | hp1 | a0001 | c0001 | t0006 | g0166 | AFR | ESN | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02976 | hp2 | a0001 | c0001 | t0005 | g0034 | AFR | ESN | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG03017 | hp1 | a0001 | c0001 | t0011 | g0095 | SAS | PJL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG03041 | hp1 | a0001 | c0002 | t0002 | g0018 | AFR | GWD | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG03041 | hp2 | a0001 | c0001 | t0006 | g0039 | AFR | GWD | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG03098 | hp1 | a0001 | c0001 | t0006 | g0045 | AFR | MSL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0073 | AFR | MSL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | ESN | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG03130 | hp2 | a0001 | c0001 | t0028 | g0084 | AFR | ESN | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0079 | AFR | ESN | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG03139 | hp2 | a0001 | c0001 | t0022 | g0162 | AFR | ESN | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG03195 | hp1 | a0001 | c0008 | t0005 | g0006 | AFR | ESN | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0062 | AFR | ESN | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG03209 | hp1 | a0001 | c0005 | t0007 | g0153 | AFR | MSL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG03209 | hp2 | a0002 | c0009 | t0002 | g0051 | AFR | MSL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0064 | AFR | MSL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG03225 | hp2 | a0001 | c0002 | t0003 | g0019 | AFR | MSL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG03239 | hp1 | a0001 | c0001 | t0009 | g0125 | SAS | PJL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0242 | SAS | PJL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG03486 | hp1 | a0001 | c0001 | t0010 | g0075 | AFR | MSL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG03486 | hp2 | a0001 | c0001 | t0037 | g0221 | AFR | MSL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG03491 | hp1 | a0001 | c0001 | t0012 | g0163 | SAS | PJL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0269 | SAS | PJL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0262 | SAS | PJL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | PJL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0061 | AFR | ESN | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG03516 | hp2 | a0001 | c0005 | t0007 | g0156 | AFR | ESN | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG03540 | hp1 | a0001 | c0001 | t0008 | g0047 | AFR | GWD | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG03540 | hp2 | a0001 | c0001 | t0005 | g0094 | AFR | GWD | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0144 | SAS | PJL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | STU | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG03688 | hp2 | a0001 | c0001 | t0011 | g0001 | SAS | STU | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG03710 | hp1 | a0001 | c0001 | t0004 | g0005 | SAS | PJL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG03710 | hp2 | a0001 | c0001 | t0011 | g0188 | SAS | PJL | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG03831 | hp1 | a0001 | c0002 | t0002 | g0020 | SAS | BEB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | BEB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0137 | SAS | BEB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | BEB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0210 | SAS | STU | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | STU | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | STU | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG04228 | hp2 | a0001 | c0003 | t0009 | g0054 | SAS | STU | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA18522 | hp1 | a0001 | c0005 | t0007 | g0022 | AFR | YRI | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA18522 | hp2 | a0001 | c0001 | t0008 | g0049 | AFR | YRI | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0266 | EAS | CHB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | CHB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA18906 | hp1 | a0002 | c0009 | t0002 | g0026 | AFR | YRI | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA18906 | hp2 | a0001 | c0002 | t0030 | g0011 | AFR | YRI | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA18940 | hp2 | a0001 | c0001 | t0004 | g0108 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA18943 | hp1 | a0001 | c0001 | t0004 | g0196 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA18950 | hp1 | a0001 | c0001 | t0019 | g0181 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA18951 | hp1 | a0001 | c0001 | t0014 | g0271 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA18951 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA18960 | hp1 | a0001 | c0001 | t0004 | g0128 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA18960 | hp2 | a0001 | c0001 | t0014 | g0213 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA18961 | hp1 | a0001 | c0001 | t0033 | g0264 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0115 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA18965 | hp2 | a0001 | c0001 | t0004 | g0185 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA18968 | hp2 | a0001 | c0001 | t0004 | g0229 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA18975 | hp1 | a0001 | c0001 | t0012 | g0187 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA18975 | hp2 | a0001 | c0001 | t0016 | g0143 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA18982 | hp2 | a0001 | c0001 | t0004 | g0101 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA18983 | hp1 | a0001 | c0001 | t0004 | g0231 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA18989 | hp2 | a0001 | c0001 | t0004 | g0111 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA18991 | hp1 | a0001 | c0001 | t0004 | g0096 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA18991 | hp2 | a0001 | c0001 | t0013 | g0197 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA18995 | hp2 | a0001 | c0001 | t0004 | g0129 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA19000 | hp1 | a0001 | c0001 | t0013 | g0179 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA19000 | hp2 | a0001 | c0001 | t0013 | g0135 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA19004 | hp1 | a0001 | c0001 | t0004 | g0147 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA19005 | hp2 | a0001 | c0001 | t0004 | g0232 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0234 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0133 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA19030 | hp1 | a0001 | c0001 | t0005 | g0086 | AFR | LWK | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA19030 | hp2 | a0002 | c0007 | t0035 | g0028 | AFR | LWK | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA19043 | hp1 | a0001 | c0001 | t0005 | g0273 | AFR | LWK | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | LWK | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA19064 | hp1 | a0001 | c0001 | t0004 | g0150 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA19074 | hp2 | a0001 | c0001 | t0004 | g0152 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA19081 | hp1 | a0001 | c0001 | t0036 | g0260 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA19086 | hp1 | a0001 | c0001 | t0004 | g0230 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA19086 | hp2 | a0001 | c0001 | t0004 | g0151 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA19087 | hp2 | a0001 | c0001 | t0004 | g0103 | EAS | JPT | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0074 | AFR | YRI | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA19240 | hp2 | a0001 | c0002 | t0003 | g0013 | AFR | YRI | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0015 | AFR | ASW | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA20129 | hp2 | a0001 | c0004 | t0010 | g0009 | AFR | ASW | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA20752 | hp1 | a0003 | c0006 | t0032 | g0132 | EUR | TSI | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0244 | EUR | TSI | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA20805 | hp1 | a0001 | c0001 | t0007 | g0172 | EUR | TSI | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA20805 | hp2 | a0001 | c0001 | t0011 | g0001 | EUR | TSI | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA20905 | hp1 | a0001 | c0001 | t0009 | g0227 | SAS | GIH | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA20905 | hp2 | a0001 | c0001 | t0025 | g0107 | SAS | GIH | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0036 | AFR | ACB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0040 | AFR | ACB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02486 | hp1 | a0001 | c0001 | t0008 | g0010 | AFR | ACB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02486 | hp2 | a0001 | c0001 | t0008 | g0048 | AFR | ACB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02559 | hp1 | a0001 | c0002 | t0006 | g0157 | AFR | ACB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0069 | AFR | ACB | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG06807 | hp1 | a0001 | c0011 | t0015 | g0077 | AFR | USA | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0037 | AFR | USA | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0241 | AFR | USA | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0032 | AFR | USA | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA21309 | hp1 | a0001 | c0001 | t0026 | g0038 | AFR | LWK | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| NA21309 | hp2 | a0001 | c0001 | t0005 | g0097 | AFR | LWK | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0011 | g0088 | REF | REF | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0214 | REF | REF | LPIN1_chr2_11741632_11832409 | LPIN1 | chr2 | 11741632 | 11832409 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:11782200 | GTCT | G | 1 | a0002 | 6 | HG01167.hp2 HG02055.hp2 HG02280.hp1 others(3): Show |
conservative_inframe_deletion | MODERATE | c.964_966delTCT | p.Ser322del | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 8/21 | 1013/5448 | 964/2781 | 322/926 | INFO_REALIGN_3_PRIME | chr2 | 11782200 | ||
| chr2:11802956 | C | T | 1 | a0003 | 3 | HG01243.hp1 HG01496.hp1 NA20752.hp1 |
missense_variant | MODERATE | c.1936C>T | p.Pro646Ser | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 15/21 | 1985/5448 | 1936/2781 | 646/926 | chr2 | 11802956 | |||
| chr2:11802990 | A | G | 1 | a0004 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.1970A>G | p.Asn657Ser | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 15/21 | 2019/5448 | 1970/2781 | 657/926 | chr2 | 11802990 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:11771503 | C | T | 3 | a0001c0013 a0002c0007 a0002c0009 |
6 | HG01070.hp2 HG01167.hp2 HG02055.hp2 others(3): Show |
synonymous_variant | LOW | c.420C>T | p.Ile140Ile | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 4/21 | 469/5448 | 420/2781 | 140/926 | chr2 | 11771503 | |||
| chr2:11771635 | C | T | 1 | a0001c0003 | 10 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(7): Show |
synonymous_variant | LOW | c.552C>T | p.Ile184Ile | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 4/21 | 601/5448 | 552/2781 | 184/926 | chr2 | 11771635 | |||
| chr2:11773680 | G | A | 4 | a0001c0002 a0001c0005 a0001c0008 others(1): Show |
21 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(18): Show |
synonymous_variant | LOW | c.657G>A | p.Leu219Leu | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 5/21 | 706/5448 | 657/2781 | 219/926 | chr2 | 11773680 | |||
| chr2:11804452 | C | T | 1 | a0002c0010 | 1 | HG02280.hp1 | synonymous_variant | LOW | c.2043C>T | p.Asn681Asn | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 16/21 | 2092/5448 | 2043/2781 | 681/926 | chr2 | 11804452 | |||
| chr2:11805136 | G | A | 1 | a0001c0011 | 1 | HG06807.hp1 | synonymous_variant | LOW | c.2229G>A | p.Lys743Lys | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/21 | 2278/5448 | 2229/2781 | 743/926 | chr2 | 11805136 | |||
| chr2:11815196 | G | C | 4 | a0001c0004 a0001c0005 a0002c0007 others(1): Show |
15 | HG01109.hp2 HG01167.hp2 HG01934.hp1 others(12): Show |
synonymous_variant | LOW | c.2358G>C | p.Gly786Gly | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/21 | 2407/5448 | 2358/2781 | 786/926 | chr2 | 11815196 | |||
| chr2:11820488 | G | A | 1 | a0001c0008 | 2 | HG02922.hp1 HG03195.hp1 |
synonymous_variant | LOW | c.2595G>A | p.Gln865Gln | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/21 | 2644/5448 | 2595/2781 | 865/926 | chr2 | 11820488 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:11825117 | C | T | 4 | a0001c0001t0008 a0001c0001t0037 a0001c0001t0038 others(1): Show |
10 | HG00639.hp2 HG01257.hp1 HG01258.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*326C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 326 | chr2 | 11825117 | ||||||
| chr2:11825138 | C | T | 1 | a0001c0001t0036 | 1 | NA19081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*347C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 347 | chr2 | 11825138 | ||||||
| chr2:11825216 | G | A | 3 | a0001c0001t0009 a0001c0001t0018 a0001c0003t0009 |
8 | HG00738.hp1 HG01081.hp1 HG01257.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*425G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 425 | chr2 | 11825216 | ||||||
| chr2:11825414 | A | C | 2 | a0002c0007t0034 a0002c0007t0035 |
2 | HG02055.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*623A>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 623 | chr2 | 11825414 | ||||||
| chr2:11825415 | A | G | 44 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(41): Show |
201 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(198): Show |
3_prime_UTR_variant | MODIFIER | c.*624A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 624 | chr2 | 11825415 | ||||||
| chr2:11825473 | G | C | 1 | a0001c0001t0017 | 2 | HG02896.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*682G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 682 | chr2 | 11825473 | ||||||
| chr2:11825503 | G | A | 1 | a0001c0001t0025 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*712G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 712 | chr2 | 11825503 | ||||||
| chr2:11825688 | C | T | 4 | a0001c0001t0004 a0001c0001t0033 a0003c0006t0004 others(1): Show |
35 | HG00609.hp2 HG00673.hp1 HG00733.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*897C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 897 | chr2 | 11825688 | ||||||
| chr2:11825872 | AG | A | 5 | a0001c0001t0008 a0001c0001t0026 a0001c0001t0037 others(2): Show |
11 | HG00639.hp2 HG01257.hp1 HG01258.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1082delG | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 1082 | chr2 | 11825872 | ||||||
| chr2:11826063 | G | A | 2 | a0001c0002t0015 a0001c0011t0015 |
3 | HG02622.hp2 HG02630.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1272G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 1272 | chr2 | 11826063 | ||||||
| chr2:11826191 | T | C | 23 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0006 others(20): Show |
90 | HG00423.hp1 HG00558.hp2 HG00639.hp2 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*1400T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 1400 | chr2 | 11826191 | ||||||
| chr2:11826194 | T | C | 1 | a0001c0001t0019 | 1 | NA18950.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1403T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 1403 | chr2 | 11826194 | ||||||
| chr2:11826361 | C | G | 6 | a0001c0001t0007 a0001c0001t0031 a0001c0004t0007 others(3): Show |
12 | HG00639.hp1 HG00735.hp1 HG01109.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1570C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 1570 | chr2 | 11826361 | ||||||
| chr2:11826411 | T | C | 2 | a0001c0001t0020 a0001c0001t0036 |
2 | HG02074.hp2 NA19081.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1620T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 1620 | chr2 | 11826411 | ||||||
| chr2:11826447 | G | C | 1 | a0001c0001t0018 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1656G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 1656 | chr2 | 11826447 | ||||||
| chr2:11826457 | T | C | 1 | a0001c0001t0027 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1666T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 1666 | chr2 | 11826457 | ||||||
| chr2:11826462 | C | T | 2 | a0001c0001t0023 a0001c0001t0024 |
2 | HG01934.hp2 HG01952.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1671C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 1671 | chr2 | 11826462 | ||||||
| chr2:11826490 | G | A | 4 | a0001c0001t0006 a0001c0001t0028 a0001c0002t0006 others(1): Show |
12 | HG01175.hp2 HG01891.hp1 HG02055.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1699G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 1699 | chr2 | 11826490 | ||||||
| chr2:11826513 | C | CA | 5 | a0001c0001t0013 a0001c0001t0016 a0001c0001t0019 others(2): Show |
10 | HG01361.hp1 HG01934.hp2 HG01981.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1746dupA | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 1747 | INFO_REALIGN_3_PRIME | chr2 | 11826513 | |||||
| chr2:11826513 | CA | C | 30 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(27): Show |
147 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(144): Show |
3_prime_UTR_variant | MODIFIER | c.*1746delA | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 1746 | INFO_REALIGN_3_PRIME | chr2 | 11826513 | |||||
| chr2:11826513 | CAA | C | 5 | a0001c0001t0011 a0001c0001t0031 a0001c0001t0033 others(2): Show |
9 | HG00639.hp1 HG01167.hp2 HG01257.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1745_*1746delAA | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 1745 | INFO_REALIGN_3_PRIME | chr2 | 11826513 | |||||
| chr2:11826584 | A | T | 1 | a0001c0002t0030 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1793A>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 1793 | chr2 | 11826584 | ||||||
| chr2:11826877 | C | G | 3 | a0001c0001t0009 a0001c0001t0018 a0001c0003t0009 |
8 | HG00738.hp1 HG01081.hp1 HG01257.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2086C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 2086 | chr2 | 11826877 | ||||||
| chr2:11826913 | A | G | 1 | a0001c0001t0022 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2122A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 2122 | chr2 | 11826913 | ||||||
| chr2:11826999 | T | C | 1 | a0003c0006t0032 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2208T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 2208 | chr2 | 11826999 | ||||||
| chr2:11827065 | C | G | 1 | a0001c0001t0021 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2274C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 2274 | chr2 | 11827065 | ||||||
| chr2:11827075 | A | G | 1 | a0001c0001t0029 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2284A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 2284 | chr2 | 11827075 | ||||||
| chr2:11827282 | G | A | 2 | a0001c0001t0010 a0001c0004t0010 |
7 | HG01109.hp1 HG01261.hp1 HG01934.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2491G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 21/21 | 2491 | chr2 | 11827282 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:11746723 | C | T | 1 | a0001c0001t0005g0273 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-10+52C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11746723 | |||||||
| chr2:11746791 | G | A | 19 | a0001c0001t0003g0015 a0001c0001t0008g0010 a0001c0001t0008g0023 others(16): Show |
19 | HG01109.hp1 HG01891.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.-10+120G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11746791 | |||||||
| chr2:11746792 | G | A | 6 | a0001c0001t0001g0030 a0001c0013t0001g0025 a0002c0007t0011g0029 others(3): Show |
6 | HG01070.hp2 HG01167.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10+121G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11746792 | |||||||
| chr2:11746826 | G | C | 81 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0002g0031 others(78): Show |
81 | HG00280.hp1 HG00639.hp2 HG00733.hp1 others(78): Show |
intron_variant | MODIFIER | c.-10+155G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11746826 | |||||||
| chr2:11746907 | C | T | 1 | a0001c0001t0002g0272 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-10+236C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11746907 | |||||||
| chr2:11746925 | C | T | 35 | a0001c0001t0001g0030 a0001c0001t0002g0064 a0001c0001t0002g0067 others(32): Show |
35 | HG01070.hp2 HG01109.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.-10+254C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11746925 | |||||||
| chr2:11747059 | C | T | 1 | a0001c0001t0014g0271 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-10+388C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11747059 | |||||||
| chr2:11747109 | C | T | 1 | a0001c0002t0008g0085 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-10+438C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11747109 | |||||||
| chr2:11747111 | C | T | 1 | a0001c0004t0007g0270 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-10+440C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11747111 | |||||||
| chr2:11747129 | G | C | 5 | a0001c0013t0001g0025 a0002c0007t0011g0029 a0002c0007t0034g0027 others(2): Show |
5 | HG01070.hp2 HG01167.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10+458G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11747129 | |||||||
| chr2:11747151 | C | G | 2 | a0001c0001t0001g0268 a0001c0001t0001g0269 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-10+480C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11747151 | |||||||
| chr2:11747309 | G | A | 160 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0001g0098 others(157): Show |
161 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(158): Show |
intron_variant | MODIFIER | c.-10+638G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11747309 | |||||||
| chr2:11747395 | C | T | 2 | a0001c0001t0006g0083 a0001c0001t0028g0084 |
2 | HG02897.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-10+724C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11747395 | |||||||
| chr2:11747426 | C | T | 6 | a0001c0001t0001g0263 a0001c0001t0001g0267 a0001c0001t0003g0266 others(3): Show |
7 | HG02071.hp1 HG03710.hp1 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10+755C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11747426 | |||||||
| chr2:11747428 | G | T | 17 | a0001c0001t0001g0058 a0001c0001t0002g0057 a0001c0001t0002g0071 others(14): Show |
17 | HG01261.hp1 HG01261.hp2 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.-10+757G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11747428 | |||||||
| chr2:11747805 | C | T | 10 | a0001c0002t0002g0020 a0001c0002t0006g0155 a0001c0002t0006g0157 others(7): Show |
10 | HG02258.hp2 HG02559.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.-10+1134C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11747805 | |||||||
| chr2:11747921 | A | G | 3 | a0001c0001t0004g0150 a0001c0001t0004g0151 a0001c0001t0004g0152 |
3 | NA19064.hp1 NA19074.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.-10+1250A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11747921 | |||||||
| chr2:11747927 | C | T | 1 | a0001c0001t0002g0262 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-10+1256C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11747927 | |||||||
| chr2:11748010 | A | C | 5 | a0001c0003t0001g0052 a0001c0003t0002g0056 a0001c0003t0009g0053 others(2): Show |
5 | HG00280.hp1 HG00733.hp1 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10+1339A>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11748010 | |||||||
| chr2:11748045 | G | A | 7 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0003g0036 others(4): Show |
7 | HG02109.hp1 HG02145.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10+1374G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11748045 | |||||||
| chr2:11748192 | G | A | 1 | a0001c0001t0002g0071 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-10+1521G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11748192 | |||||||
| chr2:11748325 | C | T | 3 | a0001c0001t0001g0261 a0001c0001t0004g0259 a0001c0001t0036g0260 |
3 | HG02071.hp2 NA18989.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.-10+1654C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11748325 | |||||||
| chr2:11748340 | G | A | 2 | a0001c0008t0005g0006 a0001c0008t0005g0007 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-10+1669G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11748340 | |||||||
| chr2:11748348 | C | T | 32 | a0001c0001t0001g0030 a0001c0001t0003g0015 a0001c0001t0008g0010 others(29): Show |
32 | HG01070.hp2 HG01109.hp1 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.-10+1677C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11748348 | |||||||
| chr2:11748372 | G | T | 9 | a0001c0001t0002g0064 a0001c0001t0002g0067 a0001c0001t0002g0068 others(6): Show |
9 | HG01884.hp1 HG02559.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-10+1701G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11748372 | |||||||
| chr2:11748561 | A | G | 1 | a0001c0001t0001g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-10+1890A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11748561 | |||||||
| chr2:11748631 | G | C | 1 | a0001c0001t0023g0161 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-10+1960G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11748631 | |||||||
| chr2:11748693 | C | T | 62 | a0001c0001t0001g0098 a0001c0001t0001g0109 a0001c0001t0001g0110 others(59): Show |
62 | HG00099.hp2 HG00558.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.-10+2022C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11748693 | |||||||
| chr2:11748715 | T | G | 32 | a0001c0001t0003g0015 a0001c0001t0003g0060 a0001c0001t0003g0061 others(29): Show |
32 | HG01109.hp1 HG01891.hp2 HG02257.hp2 others(29): Show |
intron_variant | MODIFIER | c.-10+2044T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11748715 | |||||||
| chr2:11748874 | A | G | 1 | a0001c0001t0011g0095 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-10+2203A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11748874 | |||||||
| chr2:11748895 | A | G | 14 | a0001c0001t0002g0071 a0001c0001t0002g0073 a0001c0001t0003g0072 others(11): Show |
14 | HG01261.hp1 HG01496.hp2 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.-10+2224A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11748895 | |||||||
| chr2:11748922 | G | T | 1 | a0001c0001t0001g0256 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-10+2251G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11748922 | |||||||
| chr2:11749007 | A | G | 7 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0003g0036 others(4): Show |
7 | HG02109.hp1 HG02145.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10+2336A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11749007 | |||||||
| chr2:11749259 | G | T | 161 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0001g0098 others(158): Show |
162 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(159): Show |
intron_variant | MODIFIER | c.-10+2588G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11749259 | |||||||
| chr2:11749286 | A | G | 4 | a0001c0001t0005g0086 a0001c0001t0005g0093 a0001c0001t0005g0094 others(1): Show |
4 | HG01109.hp2 HG02922.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+2615A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11749286 | |||||||
| chr2:11749296 | G | A | 1 | a0001c0001t0022g0162 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-10+2625G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11749296 | |||||||
| chr2:11749398 | C | T | 1 | a0001c0001t0022g0162 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-10+2727C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11749398 | |||||||
| chr2:11749403 | G | A | 14 | a0001c0001t0002g0071 a0001c0001t0002g0073 a0001c0001t0003g0072 others(11): Show |
14 | HG01261.hp1 HG01496.hp2 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.-10+2732G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11749403 | |||||||
| chr2:11749526 | G | T | 12 | a0001c0001t0003g0044 a0001c0001t0003g0050 a0001c0001t0005g0046 others(9): Show |
12 | HG00639.hp2 HG01175.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.-10+2855G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11749526 | |||||||
| chr2:11749539 | C | G | 67 | a0001c0001t0001g0098 a0001c0001t0001g0109 a0001c0001t0001g0110 others(64): Show |
67 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.-10+2868C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11749539 | |||||||
| chr2:11749783 | A | G | 1 | a0001c0001t0001g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-10+3112A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11749783 | |||||||
| chr2:11749942 | A | G | 1 | a0001c0001t0012g0070 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-10+3271A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11749942 | |||||||
| chr2:11750012 | T | C | 166 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0001g0098 others(163): Show |
167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.-10+3341T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11750012 | |||||||
| chr2:11750030 | T | C | 1 | a0001c0001t0012g0163 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-10+3359T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11750030 | |||||||
| chr2:11750087 | C | A | 1 | a0001c0001t0004g0096 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-10+3416C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11750087 | |||||||
| chr2:11750091 | C | T | 1 | a0001c0001t0012g0070 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-10+3420C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11750091 | |||||||
| chr2:11750148 | C | G | 3 | a0001c0001t0001g0058 a0001c0001t0002g0057 a0001c0001t0002g0160 |
3 | HG01261.hp2 HG01981.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-10+3477C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11750148 | |||||||
| chr2:11750181 | C | T | 14 | a0001c0002t0002g0018 a0001c0002t0002g0020 a0001c0002t0003g0016 others(11): Show |
14 | HG02258.hp2 HG02559.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.-10+3510C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11750181 | |||||||
| chr2:11750302 | C | G | 142 | a0001c0001t0001g0030 a0001c0001t0001g0098 a0001c0001t0001g0109 others(139): Show |
142 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(139): Show |
intron_variant | MODIFIER | c.-10+3631C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11750302 | |||||||
| chr2:11750472 | G | A | 3 | a0001c0001t0001g0058 a0001c0001t0002g0057 a0001c0001t0002g0160 |
3 | HG01261.hp2 HG01981.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-10+3801G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11750472 | |||||||
| chr2:11750520 | G | A | 1 | a0001c0001t0005g0097 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-10+3849G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11750520 | |||||||
| chr2:11750533 | C | T | 5 | a0001c0013t0001g0025 a0002c0007t0011g0029 a0002c0007t0034g0027 others(2): Show |
5 | HG01070.hp2 HG01167.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10+3862C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11750533 | |||||||
| chr2:11750638 | T | C | 84 | a0001c0001t0001g0098 a0001c0001t0001g0109 a0001c0001t0001g0110 others(81): Show |
84 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.-10+3967T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11750638 | |||||||
| chr2:11750698 | G | C | 1 | a0001c0001t0022g0162 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-10+4027G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11750698 | |||||||
| chr2:11750774 | G | A | 2 | a0001c0001t0002g0031 a0001c0001t0002g0032 |
2 | HG02145.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-10+4103G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11750774 | |||||||
| chr2:11750794 | A | G | 1 | a0001c0001t0001g0250 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-10+4123A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11750794 | |||||||
| chr2:11750806 | T | TAGAC | 149 | a0001c0001t0001g0030 a0001c0001t0001g0098 a0001c0001t0001g0109 others(146): Show |
149 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.-10+4137_-10+4138i others(6): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11750806 | ||||||
| chr2:11750906 | A | G | 2 | a0001c0008t0005g0006 a0001c0008t0005g0007 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-10+4235A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11750906 | |||||||
| chr2:11751198 | C | G | 1 | a0001c0001t0001g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-10+4527C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11751198 | |||||||
| chr2:11751290 | T | TGG | 125 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0001g0098 others(122): Show |
125 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.-10+4620_-10+4621d others(4): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11751290 | ||||||
| chr2:11751330 | T | C | 3 | a0001c0001t0001g0058 a0001c0001t0002g0057 a0001c0001t0002g0160 |
3 | HG01261.hp2 HG01981.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-10+4659T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11751330 | |||||||
| chr2:11751395 | G | T | 1 | a0001c0001t0012g0249 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-10+4724G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11751395 | |||||||
| chr2:11751462 | C | T | 1 | a0001c0001t0005g0273 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-10+4791C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11751462 | |||||||
| chr2:11751824 | C | G | 12 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0073 others(9): Show |
12 | HG01496.hp2 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.-10+5153C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11751824 | |||||||
| chr2:11751910 | T | C | 5 | a0001c0013t0001g0025 a0002c0007t0011g0029 a0002c0007t0034g0027 others(2): Show |
5 | HG01070.hp2 HG01167.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10+5239T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11751910 | |||||||
| chr2:11752008 | A | G | 1 | a0001c0001t0001g0256 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-10+5337A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11752008 | |||||||
| chr2:11752064 | G | A | 118 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0001g0098 others(115): Show |
118 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.-10+5393G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11752064 | |||||||
| chr2:11752284 | T | C | 1 | a0001c0001t0008g0023 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-10+5613T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11752284 | |||||||
| chr2:11752363 | A | G | 1 | a0001c0001t0001g0248 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-10+5692A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11752363 | |||||||
| chr2:11752396 | G | C | 1 | a0001c0001t0022g0162 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-10+5725G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11752396 | |||||||
| chr2:11752432 | C | CTTTTTTT others(7): Show |
3 | a0001c0001t0002g0064 a0001c0001t0017g0065 a0001c0001t0017g0066 |
3 | HG02896.hp1 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-10+5761_-10+5762i others(16): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11752432 | |||||||
| chr2:11752432 | C | CTTTTTTT others(8): Show |
5 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(2): Show |
5 | HG02559.hp2 HG02572.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10+5761_-10+5762i others(17): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11752432 | |||||||
| chr2:11752433 | A | ATTTTTTT others(1): Show |
8 | a0001c0001t0003g0044 a0001c0001t0005g0046 a0001c0001t0006g0039 others(5): Show |
8 | HG00639.hp2 HG01175.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.-10+5771_-10+5778d others(10): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11752433 | ||||||
| chr2:11752433 | A | ATTTTTTT others(2): Show |
37 | a0001c0001t0001g0098 a0001c0001t0001g0257 a0001c0001t0001g0258 others(34): Show |
37 | HG00099.hp2 HG01361.hp1 HG01496.hp1 others(34): Show |
intron_variant | MODIFIER | c.-10+5770_-10+5778d others(11): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11752433 | ||||||
| chr2:11752433 | A | ATTTTTTT others(3): Show |
44 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0127 others(41): Show |
44 | HG00099.hp1 HG00280.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.-10+5769_-10+5778d others(12): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11752433 | ||||||
| chr2:11752433 | A | ATTTTTTT others(4): Show |
13 | a0001c0001t0001g0141 a0001c0001t0001g0145 a0001c0001t0001g0148 others(10): Show |
13 | HG00558.hp2 HG00738.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.-10+5768_-10+5778d others(13): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11752433 | ||||||
| chr2:11752433 | A | ATTTTTTT others(5): Show |
8 | a0001c0001t0001g0030 a0001c0001t0005g0079 a0001c0001t0006g0083 others(5): Show |
8 | HG02257.hp2 HG02809.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.-10+5767_-10+5778d others(14): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11752433 | ||||||
| chr2:11752433 | A | ATTTTTTT others(6): Show |
10 | a0001c0001t0002g0071 a0001c0001t0003g0060 a0001c0001t0003g0082 others(7): Show |
10 | HG01261.hp1 HG01884.hp1 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.-10+5766_-10+5778d others(15): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11752433 | ||||||
| chr2:11752433 | A | ATTTTTTT others(7): Show |
6 | a0001c0001t0002g0057 a0001c0001t0002g0160 a0001c0001t0003g0061 others(3): Show |
6 | HG01167.hp2 HG01261.hp2 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10+5765_-10+5778d others(16): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11752433 | ||||||
| chr2:11752433 | A | ATTTTTTT others(8): Show |
1 | a0001c0001t0001g0058 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-10+5764_-10+5778d others(17): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11752433 | ||||||
| chr2:11752433 | A | ATTTTTTT others(9): Show |
2 | a0001c0001t0008g0023 a0001c0001t0010g0024 |
2 | HG01109.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.-10+5763_-10+5778d others(18): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11752433 | ||||||
| chr2:11752433 | A | ATTTTTTT others(11): Show |
2 | a0001c0001t0002g0073 a0001c0001t0003g0072 |
2 | HG01496.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-10+5778_-10+5779i others(20): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11752433 | ||||||
| chr2:11752433 | A | ATTTTTTT others(14): Show |
1 | a0001c0001t0005g0074 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-10+5778_-10+5779i others(23): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11752433 | ||||||
| chr2:11752433 | A | ATTTTTTT others(16): Show |
8 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0003g0036 others(5): Show |
8 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-10+5778_-10+5779i others(25): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11752433 | ||||||
| chr2:11752433 | A | ATTTTTTT others(17): Show |
1 | a0001c0001t0003g0037 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-10+5778_-10+5779i others(26): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11752433 | ||||||
| chr2:11752433 | A | T | 9 | a0001c0001t0002g0064 a0001c0001t0002g0067 a0001c0001t0002g0068 others(6): Show |
9 | HG02145.hp1 HG02559.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-10+5762A>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11752433 | |||||||
| chr2:11752433 | AT | A | 8 | a0001c0001t0002g0164 a0001c0001t0005g0086 a0001c0001t0005g0093 others(5): Show |
9 | HG01069.hp1 HG01109.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.-10+5778delT | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11752433 | ||||||
| chr2:11752433 | ATT | A | 8 | a0001c0003t0001g0052 a0001c0003t0002g0056 a0001c0003t0002g0090 others(5): Show |
8 | HG00280.hp1 HG00733.hp1 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.-10+5777_-10+5778d others(4): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11752433 | ||||||
| chr2:11752451 | A | T | 1 | a0001c0001t0003g0050 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-10+5780A>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11752451 | |||||||
| chr2:11752455 | G | A | 21 | a0001c0001t0003g0015 a0001c0002t0002g0018 a0001c0002t0002g0020 others(18): Show |
21 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.-10+5784G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11752455 | |||||||
| chr2:11752483 | G | GT | 113 | a0001c0001t0001g0098 a0001c0001t0001g0109 a0001c0001t0001g0110 others(110): Show |
113 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.-10+5813dupT | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11752483 | ||||||
| chr2:11752582 | C | T | 1 | a0001c0001t0005g0273 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-10+5911C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11752582 | |||||||
| chr2:11752588 | C | T | 79 | a0001c0001t0001g0098 a0001c0001t0001g0109 a0001c0001t0001g0110 others(76): Show |
79 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.-10+5917C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11752588 | |||||||
| chr2:11752611 | T | G | 6 | a0001c0001t0001g0165 a0001c0001t0001g0167 a0001c0001t0006g0166 others(3): Show |
6 | HG01257.hp1 HG01258.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10+5940T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11752611 | |||||||
| chr2:11752635 | T | G | 113 | a0001c0001t0001g0098 a0001c0001t0001g0109 a0001c0001t0001g0110 others(110): Show |
113 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.-10+5964T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11752635 | |||||||
| chr2:11752652 | C | T | 4 | a0001c0003t0002g0090 a0001c0003t0002g0091 a0001c0003t0009g0092 others(1): Show |
4 | HG01074.hp2 HG01433.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+5981C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11752652 | |||||||
| chr2:11752678 | G | A | 3 | a0001c0001t0001g0168 a0001c0001t0003g0169 a0001c0001t0003g0170 |
3 | HG02132.hp2 HG02155.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.-10+6007G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11752678 | |||||||
| chr2:11752789 | T | A | 3 | a0001c0001t0001g0058 a0001c0001t0002g0057 a0001c0001t0002g0160 |
3 | HG01261.hp2 HG01981.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-10+6118T>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11752789 | |||||||
| chr2:11752871 | T | C | 132 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0001g0098 others(129): Show |
132 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.-10+6200T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11752871 | |||||||
| chr2:11752906 | G | C | 1 | a0001c0001t0005g0273 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-10+6235G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11752906 | |||||||
| chr2:11753036 | T | C | 4 | a0001c0001t0001g0030 a0001c0001t0008g0023 a0001c0001t0010g0024 others(1): Show |
4 | HG01109.hp1 HG01891.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+6365T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11753036 | |||||||
| chr2:11753087 | T | C | 146 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0001g0098 others(143): Show |
146 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.-10+6416T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11753087 | |||||||
| chr2:11753113 | G | A | 1 | a0001c0003t0009g0139 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-10+6442G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11753113 | |||||||
| chr2:11753206 | G | GGGCTTTG others(2): Show |
129 | a0001c0001t0001g0030 a0001c0001t0001g0098 a0001c0001t0001g0109 others(126): Show |
129 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.-10+6539_-10+6547d others(11): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11753206 | ||||||
| chr2:11753274 | A | G | 1 | a0001c0001t0001g0247 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-10+6603A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11753274 | |||||||
| chr2:11753326 | T | A | 10 | a0001c0002t0002g0020 a0001c0002t0006g0155 a0001c0002t0006g0157 others(7): Show |
10 | HG02258.hp2 HG02559.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.-10+6655T>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11753326 | |||||||
| chr2:11753379 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-10+6708C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11753379 | |||||||
| chr2:11753390 | G | A | 4 | a0001c0003t0002g0090 a0001c0003t0002g0091 a0001c0003t0009g0092 others(1): Show |
4 | HG01074.hp2 HG01433.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+6719G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11753390 | |||||||
| chr2:11753491 | T | A | 3 | a0001c0001t0005g0093 a0001c0001t0005g0094 a0001c0004t0007g0270 |
3 | HG01109.hp2 HG02922.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-10+6820T>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11753491 | |||||||
| chr2:11753578 | C | T | 1 | a0001c0001t0026g0038 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-10+6907C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11753578 | |||||||
| chr2:11753692 | C | G | 4 | a0001c0001t0001g0030 a0001c0001t0008g0023 a0001c0001t0010g0024 others(1): Show |
4 | HG01109.hp1 HG01891.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+7021C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11753692 | |||||||
| chr2:11753895 | C | A | 1 | a0001c0001t0005g0273 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-10+7224C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11753895 | |||||||
| chr2:11753916 | G | C | 1 | a0001c0001t0001g0263 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-10+7245G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11753916 | |||||||
| chr2:11753944 | G | A | 4 | a0001c0001t0001g0030 a0001c0001t0008g0023 a0001c0001t0010g0024 others(1): Show |
4 | HG01109.hp1 HG01891.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+7273G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11753944 | |||||||
| chr2:11754084 | C | T | 2 | a0001c0001t0002g0164 a0001c0001t0002g0245 |
2 | HG01069.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.-10+7413C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11754084 | |||||||
| chr2:11754223 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-10+7552G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11754223 | |||||||
| chr2:11754316 | C | T | 1 | a0001c0001t0029g0138 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-10+7645C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11754316 | |||||||
| chr2:11754401 | C | G | 3 | a0001c0001t0001g0243 a0001c0001t0002g0242 a0001c0001t0004g0244 |
3 | HG01081.hp2 HG03239.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-10+7730C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11754401 | |||||||
| chr2:11754458 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-10+7787G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11754458 | |||||||
| chr2:11754463 | G | A | 1 | a0001c0001t0003g0140 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-10+7792G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11754463 | |||||||
| chr2:11754504 | C | G | 1 | a0001c0001t0001g0255 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-10+7833C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11754504 | |||||||
| chr2:11754591 | G | A | 1 | a0001c0001t0004g0259 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-10+7920G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11754591 | |||||||
| chr2:11754601 | T | C | 6 | a0001c0013t0001g0025 a0002c0007t0011g0029 a0002c0007t0034g0027 others(3): Show |
6 | HG01070.hp2 HG01167.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10+7930T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11754601 | |||||||
| chr2:11754670 | A | G | 1 | a0001c0001t0005g0046 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-10+7999A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11754670 | |||||||
| chr2:11754676 | A | G | 7 | a0001c0001t0003g0015 a0001c0002t0003g0013 a0001c0002t0003g0014 others(4): Show |
7 | HG02280.hp1 HG02809.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10+8005A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11754676 | |||||||
| chr2:11754817 | C | T | 62 | a0001c0001t0001g0098 a0001c0001t0001g0109 a0001c0001t0001g0110 others(59): Show |
62 | HG00099.hp2 HG00558.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.-10+8146C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11754817 | |||||||
| chr2:11754840 | C | G | 1 | a0001c0001t0026g0038 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-10+8169C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11754840 | |||||||
| chr2:11754976 | A | AT | 7 | a0001c0001t0001g0240 a0001c0001t0002g0137 a0001c0001t0004g0108 others(4): Show |
7 | HG02559.hp1 HG03098.hp1 HG03942.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10+8322dupT | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11754976 | ||||||
| chr2:11754980 | T | C | 3 | a0001c0001t0004g0150 a0001c0001t0004g0151 a0001c0001t0004g0152 |
3 | NA19064.hp1 NA19074.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.-10+8309T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11754980 | |||||||
| chr2:11755028 | C | A | 1 | a0001c0001t0036g0260 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-10+8357C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11755028 | |||||||
| chr2:11755045 | A | G | 1 | a0001c0001t0005g0273 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-10+8374A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11755045 | |||||||
| chr2:11755103 | C | T | 1 | a0001c0001t0012g0070 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-10+8432C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11755103 | |||||||
| chr2:11755115 | G | A | 4 | a0001c0001t0001g0030 a0001c0001t0008g0023 a0001c0001t0010g0024 others(1): Show |
4 | HG01109.hp1 HG01891.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+8444G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11755115 | |||||||
| chr2:11755157 | C | T | 1 | a0001c0001t0012g0163 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-10+8486C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11755157 | |||||||
| chr2:11755177 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-10+8506C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11755177 | |||||||
| chr2:11755262 | C | T | 5 | a0001c0001t0005g0093 a0001c0001t0005g0094 a0001c0001t0011g0001 others(2): Show |
6 | HG01109.hp2 HG02922.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10+8591C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11755262 | |||||||
| chr2:11755354 | GT | G | 3 | a0001c0001t0001g0058 a0001c0001t0002g0057 a0001c0001t0002g0160 |
3 | HG01261.hp2 HG01981.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-10+8687delT | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11755354 | ||||||
| chr2:11755360 | C | T | 1 | a0001c0001t0003g0037 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-10+8689C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11755360 | |||||||
| chr2:11755374 | G | A | 1 | a0001c0001t0002g0003 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-10+8703G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11755374 | |||||||
| chr2:11755479 | G | A | 1 | a0001c0001t0007g0172 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-10+8808G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11755479 | |||||||
| chr2:11755570 | C | T | 1 | a0001c0001t0005g0273 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-10+8899C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11755570 | |||||||
| chr2:11755723 | C | CT | 20 | a0001c0001t0001g0148 a0001c0001t0001g0239 a0001c0001t0003g0015 others(17): Show |
20 | HG00639.hp2 HG01175.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.-10+9068dupT | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11755723 | ||||||
| chr2:11755723 | CT | C | 6 | a0001c0001t0001g0030 a0001c0001t0001g0173 a0001c0001t0002g0242 others(3): Show |
6 | HG00733.hp1 HG01109.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10+9068delT | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11755723 | ||||||
| chr2:11755828 | T | C | 6 | a0001c0013t0001g0025 a0002c0007t0011g0029 a0002c0007t0034g0027 others(3): Show |
6 | HG01070.hp2 HG01167.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10+9157T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11755828 | |||||||
| chr2:11755869 | G | A | 1 | a0001c0001t0002g0242 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-10+9198G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11755869 | |||||||
| chr2:11755903 | A | G | 11 | a0001c0001t0001g0030 a0001c0001t0002g0064 a0001c0001t0002g0067 others(8): Show |
11 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.-10+9232A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11755903 | |||||||
| chr2:11755922 | C | T | 1 | a0001c0001t0001g0238 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-10+9251C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11755922 | |||||||
| chr2:11755944 | G | A | 2 | a0001c0001t0011g0001 a0001c0001t0011g0095 |
3 | HG03017.hp1 HG03688.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-10+9273G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11755944 | |||||||
| chr2:11756012 | C | A | 6 | a0001c0003t0001g0052 a0001c0003t0002g0056 a0001c0003t0009g0053 others(3): Show |
6 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10+9341C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11756012 | |||||||
| chr2:11756012 | C | T | 6 | a0001c0013t0001g0025 a0002c0007t0011g0029 a0002c0007t0034g0027 others(3): Show |
6 | HG01070.hp2 HG01167.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10+9341C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11756012 | |||||||
| chr2:11756038 | A | G | 11 | a0001c0001t0001g0058 a0001c0001t0002g0057 a0001c0001t0002g0064 others(8): Show |
11 | HG01109.hp1 HG01261.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.-10+9367A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11756038 | |||||||
| chr2:11756099 | C | T | 10 | a0001c0003t0001g0052 a0001c0003t0002g0056 a0001c0003t0002g0090 others(7): Show |
10 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.-10+9428C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11756099 | |||||||
| chr2:11756113 | G | A | 1 | a0001c0002t0003g0016 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-9-9420G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11756113 | |||||||
| chr2:11756114 | T | G | 13 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0002g0057 others(10): Show |
13 | HG01109.hp1 HG01261.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-9-9419T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11756114 | |||||||
| chr2:11756352 | C | T | 1 | a0001c0001t0004g0108 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-9-9181C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11756352 | |||||||
| chr2:11756357 | A | C | 13 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0002g0057 others(10): Show |
13 | HG01109.hp1 HG01261.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-9-9176A>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11756357 | |||||||
| chr2:11756513 | C | G | 1 | a0001c0001t0001g0237 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-9-9020C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11756513 | |||||||
| chr2:11756676 | C | T | 1 | a0001c0001t0012g0070 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-9-8857C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11756676 | |||||||
| chr2:11756712 | C | T | 1 | a0001c0001t0004g0147 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-9-8821C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11756712 | |||||||
| chr2:11756849 | G | A | 156 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0001g0098 others(153): Show |
157 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(154): Show |
intron_variant | MODIFIER | c.-9-8684G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11756849 | |||||||
| chr2:11757034 | G | A | 6 | a0001c0013t0001g0025 a0002c0007t0011g0029 a0002c0007t0034g0027 others(3): Show |
6 | HG01070.hp2 HG01167.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9-8499G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11757034 | |||||||
| chr2:11757099 | C | T | 53 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0002g0057 others(50): Show |
54 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.-9-8434C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11757099 | |||||||
| chr2:11757486 | G | T | 21 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0003g0062 others(18): Show |
22 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.-9-8047G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11757486 | |||||||
| chr2:11757623 | T | A | 1 | a0001c0001t0005g0034 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-9-7910T>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11757623 | |||||||
| chr2:11757786 | C | G | 1 | a0001c0001t0001g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-9-7747C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11757786 | |||||||
| chr2:11757813 | A | AT | 65 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0002g0057 others(62): Show |
66 | HG00280.hp1 HG00639.hp2 HG00733.hp1 others(63): Show |
intron_variant | MODIFIER | c.-9-7720_-9-7719ins others(1): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11757813 | |||||||
| chr2:11757813 | A | T | 23 | a0001c0001t0005g0273 a0001c0001t0012g0070 a0001c0002t0002g0018 others(20): Show |
23 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(20): Show |
intron_variant | MODIFIER | c.-9-7720A>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11757813 | |||||||
| chr2:11757932 | TCCGCTTC others(2): Show |
T | 4 | a0001c0003t0002g0090 a0001c0003t0002g0091 a0001c0003t0009g0092 others(1): Show |
4 | HG01074.hp2 HG01433.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9-7598_-9-7590del others(9): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11757932 | ||||||
| chr2:11757967 | T | A | 2 | a0001c0001t0005g0273 a0001c0001t0012g0070 |
2 | HG01884.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-9-7566T>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11757967 | |||||||
| chr2:11757986 | G | A | 13 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0002g0057 others(10): Show |
13 | HG01109.hp1 HG01261.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-9-7547G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11757986 | |||||||
| chr2:11758130 | C | T | 1 | a0001c0001t0002g0236 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-9-7403C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11758130 | |||||||
| chr2:11758261 | G | GT | 28 | a0001c0001t0001g0058 a0001c0001t0002g0031 a0001c0001t0002g0032 others(25): Show |
28 | HG01109.hp1 HG01261.hp1 HG01261.hp2 others(25): Show |
intron_variant | MODIFIER | c.-9-7261dupT | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11758261 | ||||||
| chr2:11758273 | G | T | 6 | a0001c0013t0001g0025 a0002c0007t0011g0029 a0002c0007t0034g0027 others(3): Show |
6 | HG01070.hp2 HG01167.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9-7260G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11758273 | |||||||
| chr2:11758274 | A | T | 1 | a0001c0001t0001g0235 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-9-7259A>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11758274 | |||||||
| chr2:11758323 | A | G | 1 | a0001c0001t0002g0134 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-9-7210A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11758323 | |||||||
| chr2:11758355 | G | T | 1 | a0001c0001t0003g0133 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-9-7178G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11758355 | |||||||
| chr2:11758565 | A | G | 13 | a0001c0001t0002g0071 a0001c0001t0003g0015 a0001c0001t0003g0082 others(10): Show |
13 | HG01261.hp1 HG01934.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-9-6968A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11758565 | |||||||
| chr2:11758613 | T | G | 5 | a0001c0013t0001g0025 a0002c0007t0011g0029 a0002c0007t0034g0027 others(2): Show |
5 | HG01070.hp2 HG01167.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9-6920T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11758613 | |||||||
| chr2:11758756 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-9-6777C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11758756 | |||||||
| chr2:11758805 | C | T | 88 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0002g0057 others(85): Show |
89 | HG00280.hp1 HG00639.hp2 HG00733.hp1 others(86): Show |
intron_variant | MODIFIER | c.-9-6728C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11758805 | |||||||
| chr2:11758962 | T | C | 88 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0002g0057 others(85): Show |
89 | HG00280.hp1 HG00639.hp2 HG00733.hp1 others(86): Show |
intron_variant | MODIFIER | c.-9-6571T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11758962 | |||||||
| chr2:11759049 | T | C | 88 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0002g0057 others(85): Show |
89 | HG00280.hp1 HG00639.hp2 HG00733.hp1 others(86): Show |
intron_variant | MODIFIER | c.-9-6484T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759049 | |||||||
| chr2:11759118 | A | T | 1 | a0001c0004t0010g0009 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-9-6415A>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759118 | |||||||
| chr2:11759123 | G | T | 13 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0002g0057 others(10): Show |
13 | HG01109.hp1 HG01261.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-9-6410G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759123 | |||||||
| chr2:11759123 | GCTTTCTT others(6): Show |
G | 1 | a0001c0001t0011g0001 | 2 | HG03688.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-9-6397_-9-6385del others(13): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11759123 | ||||||
| chr2:11759123 | GCTTTCTT others(10): Show |
G | 1 | a0001c0001t0011g0095 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-9-6397_-9-6381del others(17): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11759123 | ||||||
| chr2:11759127 | T | G | 4 | a0001c0001t0002g0003 a0001c0001t0002g0175 a0001c0001t0004g0033 others(1): Show |
5 | HG01243.hp2 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9-6406T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759127 | |||||||
| chr2:11759133 | T | TTTC | 3 | a0001c0001t0002g0204 a0001c0002t0003g0019 a0001c0004t0010g0009 |
3 | HG01071.hp2 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-9-6398_-9-6397ins others(3): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11759133 | ||||||
| chr2:11759133 | T | TTTTC | 48 | a0001c0001t0001g0004 a0001c0001t0001g0184 a0001c0001t0001g0223 others(45): Show |
48 | HG00639.hp1 HG00673.hp1 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.-9-6344_-9-6341dup others(4): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11759133 | ||||||
| chr2:11759133 | T | TTTTCTTT others(1): Show |
19 | a0001c0001t0001g0004 a0001c0001t0001g0216 a0001c0001t0001g0240 others(16): Show |
19 | HG01175.hp1 HG01346.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.-9-6348_-9-6341dup others(8): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11759133 | ||||||
| chr2:11759133 | T | TTTTCTTT others(5): Show |
6 | a0001c0001t0001g0226 a0001c0001t0003g0225 a0001c0001t0014g0189 others(3): Show |
6 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9-6352_-9-6341dup others(12): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11759133 | ||||||
| chr2:11759133 | TTTTC | T | 51 | a0001c0001t0001g0098 a0001c0001t0001g0136 a0001c0001t0001g0145 others(48): Show |
52 | HG00280.hp1 HG00280.hp2 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.-9-6344_-9-6341del others(4): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11759133 | ||||||
| chr2:11759133 | TTTTCTTT others(1): Show |
T | 38 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0127 others(35): Show |
38 | HG00609.hp1 HG00733.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.-9-6348_-9-6341del others(8): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11759133 | ||||||
| chr2:11759133 | TTTTCTTT others(5): Show |
T | 9 | a0001c0001t0001g0030 a0001c0001t0001g0141 a0001c0001t0001g0173 others(6): Show |
9 | HG00733.hp1 HG01346.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-9-6352_-9-6341del others(12): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11759133 | ||||||
| chr2:11759133 | TTTTCTTT others(9): Show |
T | 3 | a0001c0001t0002g0203 a0001c0001t0003g0044 a0001c0001t0004g0241 |
3 | HG01978.hp1 HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-9-6356_-9-6341del others(16): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11759133 | ||||||
| chr2:11759133 | TTTTCTTT others(13): Show |
T | 2 | a0001c0001t0002g0220 a0001c0001t0037g0221 |
2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-9-6360_-9-6341del others(20): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11759133 | ||||||
| chr2:11759133 | TTTTCTTT others(17): Show |
T | 1 | a0001c0001t0026g0038 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-9-6364_-9-6341del others(24): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11759133 | ||||||
| chr2:11759140 | T | G | 1 | a0001c0001t0011g0001 | 2 | HG03688.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-9-6393T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759140 | |||||||
| chr2:11759144 | T | G | 1 | a0001c0001t0011g0095 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-9-6389T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759144 | |||||||
| chr2:11759145 | C | A | 2 | a0001c0001t0003g0015 a0001c0001t0006g0083 |
2 | HG02897.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-9-6388C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759145 | |||||||
| chr2:11759177 | CTTTCTTT others(6): Show |
C | 3 | a0001c0013t0001g0025 a0002c0007t0011g0029 a0002c0009t0002g0026 |
3 | HG01070.hp2 HG01167.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-9-6340_-9-6328del others(13): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11759177 | ||||||
| chr2:11759190 | T | TTTCTTTC others(8): Show |
1 | a0001c0005t0007g0156 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-9-6341_-9-6340ins others(15): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11759190 | ||||||
| chr2:11759346 | T | C | 1 | a0001c0001t0001g0110 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-9-6187T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759346 | |||||||
| chr2:11759351 | C | T | 2 | a0001c0001t0005g0273 a0001c0001t0012g0070 |
2 | HG01884.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-9-6182C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759351 | |||||||
| chr2:11759437 | G | A | 13 | a0001c0001t0002g0071 a0001c0001t0003g0015 a0001c0001t0003g0082 others(10): Show |
13 | HG01261.hp1 HG01934.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-9-6096G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759437 | |||||||
| chr2:11759529 | C | T | 1 | a0001c0001t0003g0234 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-9-6004C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759529 | |||||||
| chr2:11759569 | T | C | 1 | a0001c0002t0030g0011 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-9-5964T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759569 | |||||||
| chr2:11759586 | A | G | 1 | a0001c0001t0001g0237 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-9-5947A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759586 | |||||||
| chr2:11759666 | A | G | 12 | a0001c0001t0003g0044 a0001c0001t0003g0050 a0001c0001t0005g0046 others(9): Show |
12 | HG00639.hp2 HG01175.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.-9-5867A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759666 | |||||||
| chr2:11759685 | G | A | 1 | a0001c0001t0002g0031 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-9-5848G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759685 | |||||||
| chr2:11759709 | C | CG | 36 | a0001c0001t0001g0141 a0001c0001t0001g0148 a0001c0001t0001g0165 others(33): Show |
36 | HG00735.hp1 HG00735.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.-9-5820dupG | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11759709 | ||||||
| chr2:11759710 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-9-5823G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759710 | |||||||
| chr2:11759758 | T | C | 13 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0002g0057 others(10): Show |
13 | HG01109.hp1 HG01261.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-9-5775T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759758 | |||||||
| chr2:11759759 | G | A | 12 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0002g0057 others(9): Show |
12 | HG01109.hp1 HG01261.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.-9-5774G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759759 | |||||||
| chr2:11759769 | G | GCCCCCCA others(40): Show |
1 | a0001c0001t0001g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-9-5717_-9-5671dup others(47): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11759769 | ||||||
| chr2:11759787 | G | A | 2 | a0001c0001t0002g0164 a0001c0001t0002g0245 |
2 | HG01069.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.-9-5746G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759787 | |||||||
| chr2:11759817 | C | T | 1 | a0001c0001t0026g0038 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-9-5716C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759817 | |||||||
| chr2:11759843 | G | A | 13 | a0001c0001t0002g0071 a0001c0001t0003g0015 a0001c0001t0003g0082 others(10): Show |
13 | HG01261.hp1 HG01934.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-9-5690G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759843 | |||||||
| chr2:11759850 | C | T | 6 | a0001c0013t0001g0025 a0002c0007t0011g0029 a0002c0007t0034g0027 others(3): Show |
6 | HG01070.hp2 HG01167.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9-5683C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759850 | |||||||
| chr2:11759870 | C | T | 1 | a0001c0002t0030g0011 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-9-5663C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759870 | |||||||
| chr2:11759895 | C | T | 1 | a0001c0003t0002g0056 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-9-5638C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759895 | |||||||
| chr2:11759899 | C | T | 1 | a0001c0003t0009g0139 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-9-5634C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759899 | |||||||
| chr2:11759924 | G | A | 1 | a0001c0001t0006g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-9-5609G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759924 | |||||||
| chr2:11759946 | G | T | 5 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0003g0062 others(2): Show |
5 | HG02615.hp1 HG02723.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9-5587G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759946 | |||||||
| chr2:11759963 | C | T | 1 | a0001c0001t0001g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-9-5570C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759963 | |||||||
| chr2:11759964 | G | A | 6 | a0001c0001t0005g0086 a0001c0001t0005g0093 a0001c0001t0005g0094 others(3): Show |
7 | HG01109.hp2 HG02922.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9-5569G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11759964 | |||||||
| chr2:11760086 | G | A | 2 | a0001c0001t0006g0083 a0001c0001t0028g0084 |
2 | HG02897.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-9-5447G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11760086 | |||||||
| chr2:11760102 | T | G | 12 | a0001c0001t0003g0044 a0001c0001t0003g0050 a0001c0001t0005g0046 others(9): Show |
12 | HG00639.hp2 HG01175.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.-9-5431T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11760102 | |||||||
| chr2:11760156 | C | T | 27 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0003g0062 others(24): Show |
28 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.-9-5377C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11760156 | |||||||
| chr2:11760165 | G | A | 6 | a0001c0002t0003g0013 a0001c0002t0003g0014 a0001c0002t0030g0011 others(3): Show |
6 | HG02280.hp1 HG02809.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9-5368G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11760165 | |||||||
| chr2:11760278 | G | A | 2 | a0001c0001t0005g0273 a0001c0001t0012g0070 |
2 | HG01884.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-9-5255G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11760278 | |||||||
| chr2:11760319 | G | A | 2 | a0001c0001t0006g0039 a0001c0001t0006g0041 |
2 | HG01891.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-9-5214G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11760319 | |||||||
| chr2:11760354 | G | A | 1 | a0001c0001t0001g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-9-5179G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11760354 | |||||||
| chr2:11760383 | C | T | 6 | a0001c0013t0001g0025 a0002c0007t0011g0029 a0002c0007t0034g0027 others(3): Show |
6 | HG01070.hp2 HG01167.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9-5150C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11760383 | |||||||
| chr2:11760438 | A | G | 13 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0002g0057 others(10): Show |
13 | HG01109.hp1 HG01261.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-9-5095A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11760438 | |||||||
| chr2:11760633 | G | C | 1 | a0001c0001t0005g0273 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-9-4900G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11760633 | |||||||
| chr2:11760800 | G | A | 1 | a0001c0001t0031g0183 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-9-4733G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11760800 | |||||||
| chr2:11760838 | G | A | 12 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0002g0057 others(9): Show |
12 | HG01109.hp1 HG01261.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.-9-4695G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11760838 | |||||||
| chr2:11760858 | G | C | 2 | a0001c0001t0008g0023 a0001c0001t0010g0024 |
2 | HG01109.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.-9-4675G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11760858 | |||||||
| chr2:11760883 | G | A | 1 | a0001c0001t0001g0184 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-9-4650G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11760883 | |||||||
| chr2:11760934 | C | T | 5 | a0001c0001t0002g0233 a0001c0001t0004g0230 a0001c0001t0004g0231 others(2): Show |
5 | NA18747.hp2 NA18983.hp1 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9-4599C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11760934 | |||||||
| chr2:11761168 | TTTAGAG | T | 35 | a0001c0001t0003g0044 a0001c0001t0003g0050 a0001c0001t0005g0046 others(32): Show |
35 | HG00639.hp2 HG01175.hp2 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.-9-4358_-9-4353del others(6): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11761168 | ||||||
| chr2:11761235 | A | C | 21 | a0001c0002t0002g0018 a0001c0002t0002g0020 a0001c0002t0003g0013 others(18): Show |
21 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.-9-4298A>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11761235 | |||||||
| chr2:11761544 | G | A | 1 | a0001c0001t0012g0113 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-9-3989G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11761544 | |||||||
| chr2:11761564 | CT | C | 3 | a0001c0001t0001g0058 a0001c0001t0002g0057 a0001c0001t0002g0160 |
3 | HG01261.hp2 HG01981.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-9-3967delT | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11761564 | ||||||
| chr2:11761616 | T | C | 1 | a0001c0001t0004g0033 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-9-3917T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11761616 | |||||||
| chr2:11761682 | G | C | 1 | a0001c0001t0003g0050 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-9-3851G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11761682 | |||||||
| chr2:11761730 | G | A | 63 | a0001c0001t0001g0098 a0001c0001t0001g0109 a0001c0001t0001g0110 others(60): Show |
63 | HG00099.hp2 HG00558.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.-9-3803G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11761730 | |||||||
| chr2:11761936 | G | A | 2 | a0001c0001t0002g0064 a0001c0001t0002g0067 |
2 | HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-9-3597G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11761936 | |||||||
| chr2:11761942 | A | G | 1 | a0001c0001t0026g0038 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-9-3591A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11761942 | |||||||
| chr2:11762086 | C | T | 6 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0003g0062 others(3): Show |
6 | HG02451.hp1 HG02615.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9-3447C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11762086 | |||||||
| chr2:11762217 | T | C | 2 | a0001c0001t0008g0023 a0001c0001t0010g0024 |
2 | HG01109.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.-9-3316T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11762217 | |||||||
| chr2:11762334 | G | A | 1 | a0001c0001t0002g0137 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-9-3199G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11762334 | |||||||
| chr2:11762374 | A | C | 1 | a0001c0001t0001g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-9-3159A>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11762374 | |||||||
| chr2:11762380 | C | T | 9 | a0001c0001t0001g0263 a0001c0001t0001g0267 a0001c0001t0003g0266 others(6): Show |
10 | HG01884.hp1 HG02071.hp1 HG03710.hp1 others(7): Show |
intron_variant | MODIFIER | c.-9-3153C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11762380 | |||||||
| chr2:11762655 | A | G | 1 | a0001c0001t0026g0038 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-9-2878A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11762655 | |||||||
| chr2:11762885 | G | T | 1 | a0001c0001t0001g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-9-2648G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11762885 | |||||||
| chr2:11763035 | C | T | 6 | a0001c0013t0001g0025 a0002c0007t0011g0029 a0002c0007t0034g0027 others(3): Show |
6 | HG01070.hp2 HG01167.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9-2498C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11763035 | |||||||
| chr2:11763043 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-9-2490C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11763043 | |||||||
| chr2:11763313 | G | A | 22 | a0001c0001t0005g0074 a0001c0002t0002g0018 a0001c0002t0002g0020 others(19): Show |
22 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.-9-2220G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11763313 | |||||||
| chr2:11763452 | C | T | 1 | a0001c0001t0012g0113 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-9-2081C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11763452 | |||||||
| chr2:11763536 | T | C | 2 | a0001c0001t0001g0238 a0001c0001t0004g0185 |
2 | HG00673.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.-9-1997T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11763536 | |||||||
| chr2:11763555 | G | A | 1 | a0001c0001t0001g0110 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-9-1978G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11763555 | |||||||
| chr2:11763589 | T | C | 10 | a0001c0003t0001g0052 a0001c0003t0002g0056 a0001c0003t0002g0090 others(7): Show |
10 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.-9-1944T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11763589 | |||||||
| chr2:11763671 | C | A | 1 | a0001c0001t0001g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-9-1862C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11763671 | |||||||
| chr2:11763688 | C | T | 6 | a0001c0013t0001g0025 a0002c0007t0011g0029 a0002c0007t0034g0027 others(3): Show |
6 | HG01070.hp2 HG01167.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9-1845C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11763688 | |||||||
| chr2:11763702 | C | T | 10 | a0001c0003t0001g0052 a0001c0003t0002g0056 a0001c0003t0002g0090 others(7): Show |
10 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.-9-1831C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11763702 | |||||||
| chr2:11763714 | C | T | 6 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0003g0062 others(3): Show |
6 | HG02615.hp1 HG02723.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9-1819C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11763714 | |||||||
| chr2:11763728 | A | T | 150 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0001g0098 others(147): Show |
151 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(148): Show |
intron_variant | MODIFIER | c.-9-1805A>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11763728 | |||||||
| chr2:11763729 | G | C | 150 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0001g0098 others(147): Show |
151 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(148): Show |
intron_variant | MODIFIER | c.-9-1804G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11763729 | |||||||
| chr2:11763730 | T | C | 1 | a0001c0001t0005g0273 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-9-1803T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11763730 | |||||||
| chr2:11763848 | G | A | 1 | a0001c0001t0003g0266 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-9-1685G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11763848 | |||||||
| chr2:11763854 | G | GTCC | 150 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0001g0098 others(147): Show |
151 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(148): Show |
intron_variant | MODIFIER | c.-9-1675_-9-1673dup others(3): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11763854 | ||||||
| chr2:11763964 | A | AGT | 20 | a0001c0001t0001g0004 a0001c0001t0001g0030 a0001c0001t0001g0109 others(17): Show |
21 | HG00609.hp1 HG00735.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.-9-1546_-9-1545dup others(2): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11763964 | ||||||
| chr2:11763964 | A | AGTGT | 58 | a0001c0001t0001g0098 a0001c0001t0001g0110 a0001c0001t0001g0127 others(55): Show |
58 | HG00099.hp2 HG00558.hp2 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.-9-1548_-9-1545dup others(4): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11763964 | ||||||
| chr2:11763964 | A | AGTGTGT | 6 | a0001c0001t0001g0136 a0001c0001t0002g0071 a0001c0001t0002g0134 others(3): Show |
6 | HG01261.hp1 HG01934.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9-1550_-9-1545dup others(6): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11763964 | ||||||
| chr2:11763964 | A | AGTGTGTG others(1): Show |
11 | a0001c0001t0002g0057 a0001c0001t0002g0160 a0001c0001t0003g0015 others(8): Show |
11 | HG01261.hp2 HG01981.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-9-1552_-9-1545dup others(8): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11763964 | ||||||
| chr2:11763964 | A | AGTGTGTG others(3): Show |
17 | a0001c0001t0001g0058 a0001c0001t0008g0023 a0001c0001t0010g0024 others(14): Show |
17 | HG01070.hp2 HG01109.hp1 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.-9-1554_-9-1545dup others(10): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11763964 | ||||||
| chr2:11763964 | A | AGTGTGTG others(5): Show |
14 | a0001c0002t0006g0155 a0001c0002t0006g0157 a0001c0002t0015g0154 others(11): Show |
14 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.-9-1556_-9-1545dup others(12): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11763964 | ||||||
| chr2:11763964 | A | AGTGTGTG others(7): Show |
10 | a0001c0002t0002g0018 a0001c0002t0002g0020 a0001c0002t0003g0016 others(7): Show |
10 | HG01433.hp2 HG02258.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.-9-1558_-9-1545dup others(14): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11763964 | ||||||
| chr2:11763964 | A | T | 5 | a0001c0001t0005g0093 a0001c0001t0005g0094 a0001c0001t0005g0273 others(2): Show |
6 | HG02922.hp2 HG03017.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9-1569A>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11763964 | |||||||
| chr2:11763987 | G | A | 2 | a0001c0001t0001g0237 a0001c0001t0002g0236 |
2 | HG04228.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.-9-1546G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11763987 | |||||||
| chr2:11763987 | G | GTA | 8 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0073 others(5): Show |
8 | HG01496.hp2 HG01516.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-9-1528_-9-1527dup others(2): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11763987 | ||||||
| chr2:11763987 | GTA | G | 4 | a0001c0001t0002g0262 a0001c0001t0003g0044 a0001c0001t0008g0042 others(1): Show |
4 | HG00639.hp2 HG02723.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9-1528_-9-1527del others(2): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11763987 | ||||||
| chr2:11763989 | A | G | 131 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0001g0098 others(128): Show |
132 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.-9-1544A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11763989 | |||||||
| chr2:11763991 | A | G | 53 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0001g0141 others(50): Show |
54 | HG01070.hp2 HG01109.hp1 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.-9-1542A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11763991 | |||||||
| chr2:11763993 | A | G | 31 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0002g0057 others(28): Show |
32 | HG01070.hp2 HG01109.hp1 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.-9-1540A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11763993 | |||||||
| chr2:11763995 | A | G | 26 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0002g0057 others(23): Show |
27 | HG01070.hp2 HG01109.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.-9-1538A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11763995 | |||||||
| chr2:11763997 | A | G | 15 | a0001c0001t0001g0058 a0001c0001t0002g0057 a0001c0001t0002g0160 others(12): Show |
16 | HG01070.hp2 HG01109.hp2 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.-9-1536A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11763997 | |||||||
| chr2:11763999 | A | G | 6 | a0001c0001t0005g0093 a0001c0001t0005g0094 a0001c0001t0005g0273 others(3): Show |
7 | HG01109.hp2 HG02922.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9-1534A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11763999 | |||||||
| chr2:11764001 | A | G | 6 | a0001c0001t0005g0093 a0001c0001t0005g0094 a0001c0001t0005g0273 others(3): Show |
7 | HG01109.hp2 HG02922.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9-1532A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11764001 | |||||||
| chr2:11764016 | G | A | 62 | a0001c0001t0001g0098 a0001c0001t0001g0109 a0001c0001t0001g0110 others(59): Show |
62 | HG00099.hp2 HG00558.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.-9-1517G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11764016 | |||||||
| chr2:11764034 | G | C | 1 | a0001c0001t0012g0187 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-9-1499G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11764034 | |||||||
| chr2:11764054 | A | ATG | 11 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0226 others(8): Show |
11 | HG00423.hp1 HG00423.hp2 HG00673.hp2 others(8): Show |
intron_variant | MODIFIER | c.-9-1455_-9-1454dup others(2): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11764054 | ||||||
| chr2:11764054 | ATG | A | 5 | a0001c0001t0005g0046 a0001c0001t0006g0045 a0001c0001t0008g0048 others(2): Show |
5 | HG02451.hp2 HG02486.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9-1455_-9-1454del others(2): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11764054 | ||||||
| chr2:11764054 | ATGTG | A | 11 | a0001c0002t0008g0085 a0001c0002t0030g0011 a0001c0003t0002g0090 others(8): Show |
11 | HG00738.hp1 HG01074.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.-9-1457_-9-1454del others(4): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11764054 | ||||||
| chr2:11764072 | G | A | 1 | a0001c0001t0001g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-9-1461G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11764072 | |||||||
| chr2:11764074 | G | A | 1 | a0001c0001t0001g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-9-1459G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11764074 | |||||||
| chr2:11764074 | GTGTGTA | G | 16 | a0001c0001t0005g0093 a0001c0001t0005g0094 a0001c0001t0011g0001 others(13): Show |
17 | HG02258.hp2 HG02559.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.-9-1457_-9-1452del others(6): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11764074 | ||||||
| chr2:11764074 | GTGTGTAT others(3): Show |
G | 2 | a0001c0001t0005g0273 a0001c0001t0012g0070 |
2 | HG01884.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-9-1457_-9-1448del others(10): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11764074 | ||||||
| chr2:11764076 | G | A | 13 | a0001c0001t0001g0030 a0001c0001t0003g0044 a0001c0001t0003g0050 others(10): Show |
13 | HG01175.hp2 HG01891.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-9-1457G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11764076 | |||||||
| chr2:11764076 | G | GTATA | 6 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0203 others(3): Show |
6 | HG01496.hp2 HG01978.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9-1456_-9-1455ins others(4): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11764076 | ||||||
| chr2:11764078 | G | A | 54 | a0001c0001t0001g0030 a0001c0001t0002g0031 a0001c0001t0002g0032 others(51): Show |
54 | HG00558.hp2 HG00639.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.-9-1455G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11764078 | |||||||
| chr2:11764078 | G | GTA | 48 | a0001c0001t0001g0004 a0001c0001t0001g0165 a0001c0001t0001g0167 others(45): Show |
50 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.-9-1430_-9-1429dup others(2): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11764078 | ||||||
| chr2:11764078 | G | GTATA | 5 | a0001c0001t0001g0240 a0001c0001t0002g0164 a0001c0001t0002g0245 others(2): Show |
5 | HG01069.hp1 HG01074.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9-1432_-9-1429dup others(4): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11764078 | ||||||
| chr2:11764078 | G | GTATATA | 3 | a0001c0001t0001g0190 a0001c0001t0001g0263 a0001c0001t0004g0005 |
3 | HG01361.hp2 HG03710.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.-9-1434_-9-1429dup others(6): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11764078 | ||||||
| chr2:11764078 | G | GTGTATAT others(1): Show |
5 | a0001c0001t0001g0248 a0001c0001t0001g0267 a0001c0001t0004g0005 others(2): Show |
5 | HG02056.hp1 HG02071.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9-1454_-9-1453ins others(8): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11764078 | ||||||
| chr2:11764078 | G | GTGTATAT others(3): Show |
2 | a0001c0001t0003g0266 a0001c0001t0033g0264 |
2 | NA18747.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.-9-1454_-9-1453ins others(10): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11764078 | ||||||
| chr2:11764078 | GTA | G | 7 | a0001c0001t0007g0172 a0001c0001t0026g0038 a0001c0013t0001g0025 others(4): Show |
7 | HG01070.hp2 HG01167.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9-1430_-9-1429del others(2): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11764078 | ||||||
| chr2:11764078 | GTATA | G | 6 | a0001c0001t0001g0058 a0001c0001t0001g0243 a0001c0001t0002g0057 others(3): Show |
6 | HG01081.hp2 HG01261.hp2 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9-1432_-9-1429del others(4): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11764078 | ||||||
| chr2:11764078 | GTATATAT others(1): Show |
G | 6 | a0001c0001t0002g0064 a0001c0001t0002g0067 a0001c0001t0002g0068 others(3): Show |
6 | HG02559.hp2 HG02717.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9-1436_-9-1429del others(8): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11764078 | ||||||
| chr2:11764080 | A | G | 4 | a0001c0001t0001g0130 a0001c0001t0001g0224 a0001c0001t0025g0107 others(1): Show |
4 | HG01243.hp1 HG02015.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9-1453A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11764080 | |||||||
| chr2:11764086 | A | G | 1 | a0001c0001t0001g0222 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-9-1447A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11764086 | |||||||
| chr2:11764091 | T | C | 2 | a0001c0002t0002g0018 a0001c0002t0003g0019 |
2 | HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-9-1442T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11764091 | |||||||
| chr2:11764093 | T | C | 4 | a0001c0002t0002g0018 a0001c0002t0003g0019 a0001c0002t0030g0011 others(1): Show |
4 | HG02280.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9-1440T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11764093 | |||||||
| chr2:11764095 | T | C | 19 | a0001c0002t0002g0018 a0001c0002t0002g0020 a0001c0002t0003g0013 others(16): Show |
19 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.-9-1438T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11764095 | |||||||
| chr2:11764097 | T | C | 30 | a0001c0001t0001g0136 a0001c0001t0002g0114 a0001c0001t0002g0116 others(27): Show |
30 | HG01069.hp2 HG01071.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.-9-1436T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11764097 | |||||||
| chr2:11764097 | T | TAC | 46 | a0001c0001t0001g0098 a0001c0001t0001g0109 a0001c0001t0001g0110 others(43): Show |
46 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.-9-1435_-9-1434ins others(2): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11764097 | ||||||
| chr2:11764099 | T | C | 89 | a0001c0001t0001g0098 a0001c0001t0001g0109 a0001c0001t0001g0110 others(86): Show |
89 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.-9-1434T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11764099 | |||||||
| chr2:11764099 | T | TACAC | 5 | a0001c0001t0001g0130 a0001c0001t0001g0268 a0001c0001t0001g0269 others(2): Show |
5 | HG01243.hp1 HG03491.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9-1433_-9-1432ins others(4): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11764099 | ||||||
| chr2:11764101 | T | C | 105 | a0001c0001t0001g0098 a0001c0001t0001g0109 a0001c0001t0001g0110 others(102): Show |
105 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.-9-1432T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11764101 | |||||||
| chr2:11764101 | T | TAC | 6 | a0001c0001t0003g0061 a0001c0001t0003g0062 a0001c0001t0003g0063 others(3): Show |
6 | HG02723.hp2 HG02886.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9-1431_-9-1430ins others(2): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11764101 | ||||||
| chr2:11764103 | T | C | 124 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0001g0098 others(121): Show |
124 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.-9-1430T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11764103 | |||||||
| chr2:11764103 | T | TAC | 3 | a0001c0001t0003g0037 a0001c0001t0008g0042 a0001c0001t0008g0047 |
3 | HG00639.hp2 HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-9-1414_-9-1413dup others(2): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11764103 | ||||||
| chr2:11764103 | T | TACACACA others(1): Show |
7 | a0001c0001t0003g0015 a0001c0001t0003g0082 a0001c0001t0006g0083 others(4): Show |
7 | HG02257.hp2 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9-1420_-9-1413dup others(8): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11764103 | ||||||
| chr2:11764103 | T | TATAC | 3 | a0001c0001t0003g0036 a0001c0001t0005g0034 a0001c0001t0018g0035 |
3 | HG02109.hp1 HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-9-1429_-9-1428ins others(4): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11764103 | ||||||
| chr2:11764103 | T | TATACACA others(3): Show |
3 | a0001c0001t0010g0080 a0001c0004t0010g0081 a0001c0011t0015g0077 |
3 | HG01261.hp1 HG01934.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-9-1429_-9-1428ins others(10): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11764103 | ||||||
| chr2:11764103 | T | TATATACA others(5): Show |
2 | a0001c0001t0002g0071 a0001c0004t0010g0078 |
2 | HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-9-1429_-9-1428ins others(12): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11764103 | ||||||
| chr2:11764105 | C | T | 7 | a0001c0001t0001g0267 a0001c0001t0003g0266 a0001c0001t0004g0005 others(4): Show |
8 | HG02071.hp1 HG03710.hp1 NA18747.hp1 others(5): Show |
intron_variant | MODIFIER | c.-9-1428C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11764105 | |||||||
| chr2:11764328 | G | A | 4 | a0001c0001t0001g0168 a0001c0001t0003g0169 a0001c0001t0003g0170 others(1): Show |
4 | HG02132.hp2 HG02155.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9-1205G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11764328 | |||||||
| chr2:11764360 | T | C | 155 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0001g0098 others(152): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.-9-1173T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11764360 | |||||||
| chr2:11764436 | T | G | 1 | a0001c0001t0002g0137 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-9-1097T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11764436 | |||||||
| chr2:11764535 | C | T | 2 | a0001c0001t0002g0220 a0001c0001t0037g0221 |
2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-9-998C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11764535 | |||||||
| chr2:11764536 | A | G | 1 | a0001c0001t0026g0038 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-9-997A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11764536 | |||||||
| chr2:11764617 | G | T | 6 | a0001c0013t0001g0025 a0002c0007t0011g0029 a0002c0007t0034g0027 others(3): Show |
6 | HG01070.hp2 HG01167.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9-916G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11764617 | |||||||
| chr2:11764894 | A | G | 14 | a0001c0002t0002g0018 a0001c0002t0002g0020 a0001c0002t0003g0016 others(11): Show |
14 | HG02258.hp2 HG02559.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.-9-639A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11764894 | |||||||
| chr2:11765191 | T | C | 67 | a0001c0001t0001g0098 a0001c0001t0001g0109 a0001c0001t0001g0110 others(64): Show |
67 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.-9-342T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11765191 | |||||||
| chr2:11765264 | G | C | 1 | a0001c0001t0005g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-9-269G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11765264 | |||||||
| chr2:11765291 | T | C | 1 | a0001c0003t0001g0052 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-9-242T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11765291 | |||||||
| chr2:11765341 | C | T | 1 | a0001c0001t0012g0070 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-9-192C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11765341 | |||||||
| chr2:11765372 | C | T | 14 | a0001c0002t0002g0018 a0001c0002t0002g0020 a0001c0002t0003g0016 others(11): Show |
14 | HG02258.hp2 HG02559.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.-9-161C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11765372 | |||||||
| chr2:11765413 | A | G | 1 | a0001c0001t0003g0087 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-9-120A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11765413 | |||||||
| chr2:11765510 | GT | G | 150 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0001g0098 others(147): Show |
151 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(148): Show |
intron_variant | MODIFIER | c.-9-14delT | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr2 | 11765510 | ||||||
| chr2:11765512 | T | G | 2 | a0001c0001t0002g0031 a0001c0001t0002g0032 |
2 | HG02145.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-9-21T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 1/20 | chr2 | 11765512 | |||||||
| chr2:11765750 | C | T | 62 | a0001c0001t0001g0098 a0001c0001t0001g0109 a0001c0001t0001g0110 others(59): Show |
62 | HG00099.hp2 HG00558.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.192+17C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | chr2 | 11765750 | |||||||
| chr2:11765819 | T | C | 1 | a0001c0001t0001g0184 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.192+86T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | chr2 | 11765819 | |||||||
| chr2:11765880 | T | C | 5 | a0001c0013t0001g0025 a0002c0007t0011g0029 a0002c0007t0034g0027 others(2): Show |
5 | HG01070.hp2 HG01167.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.192+147T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | chr2 | 11765880 | |||||||
| chr2:11765904 | C | T | 14 | a0001c0001t0001g0030 a0001c0001t0002g0064 a0001c0001t0002g0067 others(11): Show |
14 | HG02559.hp2 HG02615.hp1 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.192+171C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | chr2 | 11765904 | |||||||
| chr2:11765923 | G | A | 5 | a0001c0001t0001g0130 a0001c0001t0001g0268 a0001c0001t0001g0269 others(2): Show |
5 | HG02738.hp1 HG03491.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.192+190G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | chr2 | 11765923 | |||||||
| chr2:11765930 | A | C | 13 | a0001c0001t0002g0071 a0001c0001t0003g0015 a0001c0001t0003g0082 others(10): Show |
13 | HG01261.hp1 HG01934.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.192+197A>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | chr2 | 11765930 | |||||||
| chr2:11765968 | G | A | 1 | a0001c0002t0003g0014 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.192+235G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | chr2 | 11765968 | |||||||
| chr2:11766111 | C | T | 13 | a0001c0001t0002g0071 a0001c0001t0003g0015 a0001c0001t0003g0082 others(10): Show |
13 | HG01261.hp1 HG01934.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.192+378C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | chr2 | 11766111 | |||||||
| chr2:11766258 | T | C | 6 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0003g0062 others(3): Show |
6 | HG02615.hp1 HG02723.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.192+525T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | chr2 | 11766258 | |||||||
| chr2:11766261 | C | A | 10 | a0001c0003t0001g0052 a0001c0003t0002g0056 a0001c0003t0002g0090 others(7): Show |
10 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.192+528C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | chr2 | 11766261 | |||||||
| chr2:11766262 | G | A | 1 | a0001c0001t0003g0234 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.192+529G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | chr2 | 11766262 | |||||||
| chr2:11766291 | G | GC | 12 | a0001c0001t0003g0044 a0001c0001t0003g0050 a0001c0001t0005g0046 others(9): Show |
12 | HG00639.hp2 HG01175.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.192+560dupC | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr2 | 11766291 | ||||||
| chr2:11766370 | A | G | 1 | a0001c0001t0005g0273 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.192+637A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | chr2 | 11766370 | |||||||
| chr2:11766378 | G | A | 5 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(2): Show |
5 | HG00099.hp1 HG00280.hp2 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.192+645G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | chr2 | 11766378 | |||||||
| chr2:11766549 | G | T | 1 | a0001c0001t0002g0233 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.192+816G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | chr2 | 11766549 | |||||||
| chr2:11766623 | C | T | 1 | a0001c0001t0004g0033 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.192+890C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | chr2 | 11766623 | |||||||
| chr2:11766762 | AACAAAC | A | 87 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0002g0057 others(84): Show |
88 | HG00280.hp1 HG00639.hp2 HG00733.hp1 others(85): Show |
intron_variant | MODIFIER | c.193-993_193-988del others(6): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr2 | 11766762 | ||||||
| chr2:11766768 | CACAA | C | 3 | a0001c0001t0001g0165 a0001c0001t0006g0166 a0001c0001t0022g0162 |
3 | HG02257.hp1 HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.193-969_193-966del others(4): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr2 | 11766768 | ||||||
| chr2:11766768 | CACAAACA others(5): Show |
C | 3 | a0001c0001t0001g0141 a0001c0001t0001g0145 a0001c0001t0003g0140 |
3 | HG00558.hp2 NA19009.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.193-977_193-966del others(12): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr2 | 11766768 | ||||||
| chr2:11766903 | G | A | 6 | a0001c0001t0002g0064 a0001c0001t0002g0067 a0001c0001t0002g0068 others(3): Show |
6 | HG02559.hp2 HG02717.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.193-860G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | chr2 | 11766903 | |||||||
| chr2:11766915 | C | T | 1 | a0001c0001t0005g0093 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.193-848C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | chr2 | 11766915 | |||||||
| chr2:11766988 | A | AG | 16 | a0001c0001t0005g0093 a0001c0001t0005g0094 a0001c0001t0005g0273 others(13): Show |
17 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.193-770dupG | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr2 | 11766988 | ||||||
| chr2:11766995 | C | G | 2 | a0001c0001t0008g0023 a0001c0001t0010g0024 |
2 | HG01109.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.193-768C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | chr2 | 11766995 | |||||||
| chr2:11767077 | C | G | 5 | a0001c0013t0001g0025 a0002c0007t0011g0029 a0002c0007t0034g0027 others(2): Show |
5 | HG01070.hp2 HG01167.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.193-686C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | chr2 | 11767077 | |||||||
| chr2:11767109 | A | G | 2 | a0001c0001t0007g0172 a0001c0001t0007g0219 |
2 | HG01258.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.193-654A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | chr2 | 11767109 | |||||||
| chr2:11767124 | G | A | 1 | a0001c0001t0005g0273 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.193-639G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | chr2 | 11767124 | |||||||
| chr2:11767140 | T | C | 1 | a0001c0001t0024g0176 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.193-623T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | chr2 | 11767140 | |||||||
| chr2:11767386 | C | G | 1 | a0001c0001t0012g0070 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.193-377C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | chr2 | 11767386 | |||||||
| chr2:11767666 | C | G | 3 | a0001c0001t0005g0093 a0001c0001t0005g0094 a0001c0004t0007g0270 |
3 | HG01109.hp2 HG02922.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.193-97C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | chr2 | 11767666 | |||||||
| chr2:11767716 | C | T | 17 | a0001c0001t0005g0093 a0001c0001t0005g0094 a0001c0001t0005g0273 others(14): Show |
18 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.193-47C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | chr2 | 11767716 | |||||||
| chr2:11767720 | G | T | 1 | a0001c0001t0012g0070 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.193-43G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 2/20 | chr2 | 11767720 | |||||||
| chr2:11768012 | T | C | 5 | a0001c0001t0001g0058 a0001c0001t0002g0057 a0001c0001t0002g0160 others(2): Show |
5 | HG01109.hp1 HG01261.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.288+154T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11768012 | |||||||
| chr2:11768158 | C | T | 1 | a0001c0001t0005g0093 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.288+300C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11768158 | |||||||
| chr2:11768184 | T | A | 11 | a0001c0001t0001g0058 a0001c0001t0002g0057 a0001c0001t0002g0160 others(8): Show |
11 | HG01070.hp2 HG01109.hp1 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.288+326T>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11768184 | |||||||
| chr2:11768663 | A | G | 1 | a0001c0001t0002g0100 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.288+805A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11768663 | |||||||
| chr2:11768664 | T | C | 1 | a0001c0001t0002g0100 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.288+806T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11768664 | |||||||
| chr2:11768795 | G | A | 3 | a0001c0001t0001g0058 a0001c0001t0002g0057 a0001c0001t0002g0160 |
3 | HG01261.hp2 HG01981.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.288+937G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11768795 | |||||||
| chr2:11768830 | G | A | 1 | a0001c0001t0001g0256 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.288+972G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11768830 | |||||||
| chr2:11768852 | C | T | 146 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0001g0098 others(143): Show |
147 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(144): Show |
intron_variant | MODIFIER | c.288+994C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11768852 | |||||||
| chr2:11768922 | C | T | 1 | a0001c0004t0006g0076 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.288+1064C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11768922 | |||||||
| chr2:11768967 | C | A | 1 | a0001c0001t0003g0115 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.288+1109C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11768967 | |||||||
| chr2:11768976 | C | A | 6 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0003g0062 others(3): Show |
6 | HG02615.hp1 HG02723.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.288+1118C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11768976 | |||||||
| chr2:11769005 | G | A | 33 | a0001c0001t0003g0044 a0001c0001t0003g0050 a0001c0001t0005g0046 others(30): Show |
34 | HG00280.hp1 HG00639.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.288+1147G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11769005 | |||||||
| chr2:11769013 | CA | C | 15 | a0001c0001t0005g0093 a0001c0001t0005g0094 a0001c0001t0011g0001 others(12): Show |
16 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.288+1157delA | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr2 | 11769013 | ||||||
| chr2:11769016 | C | T | 15 | a0001c0001t0005g0093 a0001c0001t0005g0094 a0001c0001t0011g0001 others(12): Show |
16 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.288+1158C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11769016 | |||||||
| chr2:11769017 | A | G | 15 | a0001c0001t0005g0093 a0001c0001t0005g0094 a0001c0001t0011g0001 others(12): Show |
16 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.288+1159A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11769017 | |||||||
| chr2:11769267 | G | A | 11 | a0001c0001t0001g0058 a0001c0001t0002g0057 a0001c0001t0002g0160 others(8): Show |
11 | HG01070.hp2 HG01109.hp1 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.288+1409G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11769267 | |||||||
| chr2:11769400 | G | T | 1 | a0001c0002t0008g0085 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.288+1542G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11769400 | |||||||
| chr2:11769545 | A | G | 2 | a0001c0001t0008g0023 a0001c0001t0010g0024 |
2 | HG01109.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.288+1687A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11769545 | |||||||
| chr2:11769591 | AT | A | 9 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0003g0062 others(6): Show |
9 | HG01884.hp1 HG02615.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.288+1744delT | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr2 | 11769591 | ||||||
| chr2:11769603 | A | T | 1 | a0001c0001t0002g0100 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.288+1745A>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11769603 | |||||||
| chr2:11770265 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.289-1107G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11770265 | |||||||
| chr2:11770314 | A | T | 1 | a0001c0001t0009g0227 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.289-1058A>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11770314 | |||||||
| chr2:11770370 | C | G | 1 | a0001c0001t0005g0097 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.289-1002C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11770370 | |||||||
| chr2:11770432 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.289-940C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11770432 | |||||||
| chr2:11770495 | C | T | 13 | a0001c0001t0003g0044 a0001c0001t0003g0050 a0001c0001t0005g0046 others(10): Show |
13 | HG00639.hp2 HG01175.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.289-877C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11770495 | |||||||
| chr2:11770592 | C | T | 59 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0002g0057 others(56): Show |
59 | HG01070.hp2 HG01109.hp1 HG01167.hp2 others(56): Show |
intron_variant | MODIFIER | c.289-780C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11770592 | |||||||
| chr2:11770625 | A | G | 2 | a0001c0001t0006g0083 a0001c0001t0028g0084 |
2 | HG02897.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.289-747A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11770625 | |||||||
| chr2:11770673 | A | G | 1 | a0001c0001t0012g0070 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.289-699A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11770673 | |||||||
| chr2:11770775 | T | C | 14 | a0001c0001t0001g0030 a0001c0001t0002g0064 a0001c0001t0002g0067 others(11): Show |
14 | HG02559.hp2 HG02615.hp1 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.289-597T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11770775 | |||||||
| chr2:11770877 | C | T | 88 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0002g0057 others(85): Show |
89 | HG00280.hp1 HG00639.hp2 HG00733.hp1 others(86): Show |
intron_variant | MODIFIER | c.289-495C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11770877 | |||||||
| chr2:11770929 | TACA | T | 21 | a0001c0002t0002g0018 a0001c0002t0002g0020 a0001c0002t0003g0013 others(18): Show |
21 | HG02258.hp2 HG02280.hp1 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.289-442_289-440del others(3): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | chr2 | 11770929 | |||||||
| chr2:11770948 | GTCTT | G | 15 | a0001c0001t0005g0093 a0001c0001t0005g0094 a0001c0001t0011g0001 others(12): Show |
16 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.289-420_289-417del others(4): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr2 | 11770948 | ||||||
| chr2:11771820 | G | A | 5 | a0001c0001t0005g0093 a0001c0001t0005g0094 a0001c0001t0011g0001 others(2): Show |
6 | HG01109.hp2 HG02922.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.596+141G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 4/20 | chr2 | 11771820 | |||||||
| chr2:11771831 | G | T | 16 | a0001c0001t0005g0093 a0001c0001t0005g0094 a0001c0001t0011g0001 others(13): Show |
17 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.596+152G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 4/20 | chr2 | 11771831 | |||||||
| chr2:11771855 | C | G | 15 | a0001c0001t0005g0093 a0001c0001t0005g0094 a0001c0001t0011g0001 others(12): Show |
16 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.596+176C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 4/20 | chr2 | 11771855 | |||||||
| chr2:11772010 | C | T | 23 | a0001c0001t0001g0058 a0001c0001t0002g0057 a0001c0001t0002g0160 others(20): Show |
23 | HG00639.hp2 HG01070.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.596+331C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 4/20 | chr2 | 11772010 | |||||||
| chr2:11772072 | G | A | 1 | a0001c0001t0012g0070 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.596+393G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 4/20 | chr2 | 11772072 | |||||||
| chr2:11772119 | C | G | 1 | a0001c0001t0026g0038 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.596+440C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 4/20 | chr2 | 11772119 | |||||||
| chr2:11772196 | C | T | 16 | a0001c0001t0005g0093 a0001c0001t0005g0094 a0001c0001t0011g0001 others(13): Show |
17 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.596+517C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 4/20 | chr2 | 11772196 | |||||||
| chr2:11772225 | C | G | 6 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0003g0062 others(3): Show |
6 | HG02615.hp1 HG02723.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.596+546C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 4/20 | chr2 | 11772225 | |||||||
| chr2:11772257 | T | G | 1 | a0001c0001t0001g0168 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.596+578T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 4/20 | chr2 | 11772257 | |||||||
| chr2:11772265 | G | A | 1 | a0001c0001t0001g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.596+586G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 4/20 | chr2 | 11772265 | |||||||
| chr2:11772281 | G | T | 1 | a0001c0001t0012g0070 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.596+602G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 4/20 | chr2 | 11772281 | |||||||
| chr2:11772367 | A | G | 6 | a0001c0001t0002g0064 a0001c0001t0002g0067 a0001c0001t0002g0068 others(3): Show |
6 | HG02559.hp2 HG02717.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.596+688A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 4/20 | chr2 | 11772367 | |||||||
| chr2:11772403 | C | G | 3 | a0001c0001t0001g0058 a0001c0001t0002g0057 a0001c0001t0002g0160 |
3 | HG01261.hp2 HG01981.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.596+724C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 4/20 | chr2 | 11772403 | |||||||
| chr2:11772509 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.596+830C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 4/20 | chr2 | 11772509 | |||||||
| chr2:11772670 | G | A | 5 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0003g0062 others(2): Show |
5 | HG02615.hp1 HG02723.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.597-950G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 4/20 | chr2 | 11772670 | |||||||
| chr2:11772779 | C | T | 8 | a0001c0001t0001g0030 a0001c0001t0002g0064 a0001c0001t0002g0067 others(5): Show |
8 | HG02559.hp2 HG02717.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.597-841C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 4/20 | chr2 | 11772779 | |||||||
| chr2:11772932 | CTCTA | C | 162 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0001g0098 others(159): Show |
163 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(160): Show |
intron_variant | MODIFIER | c.597-683_597-680del others(4): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr2 | 11772932 | ||||||
| chr2:11772965 | G | A | 3 | a0001c0002t0003g0013 a0001c0002t0003g0014 a0002c0010t0005g0012 |
3 | HG02280.hp1 HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.597-655G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 4/20 | chr2 | 11772965 | |||||||
| chr2:11773119 | C | T | 120 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0001g0098 others(117): Show |
120 | HG00099.hp2 HG00558.hp2 HG00609.hp1 others(117): Show |
intron_variant | MODIFIER | c.597-501C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 4/20 | chr2 | 11773119 | |||||||
| chr2:11773260 | G | A | 45 | a0001c0001t0001g0058 a0001c0001t0002g0057 a0001c0001t0002g0160 others(42): Show |
46 | HG00280.hp1 HG00639.hp2 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.597-360G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 4/20 | chr2 | 11773260 | |||||||
| chr2:11773303 | G | C | 2 | a0003c0006t0004g0099 a0003c0006t0004g0174 |
2 | HG01243.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.597-317G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 4/20 | chr2 | 11773303 | |||||||
| chr2:11773312 | C | T | 62 | a0001c0001t0001g0098 a0001c0001t0001g0109 a0001c0001t0001g0110 others(59): Show |
62 | HG00099.hp2 HG00558.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.597-308C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 4/20 | chr2 | 11773312 | |||||||
| chr2:11773422 | C | G | 2 | a0001c0002t0006g0155 a0001c0002t0006g0157 |
2 | HG02559.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.597-198C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 4/20 | chr2 | 11773422 | |||||||
| chr2:11773602 | T | A | 8 | a0001c0001t0001g0030 a0001c0001t0002g0064 a0001c0001t0002g0067 others(5): Show |
8 | HG02559.hp2 HG02717.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.597-18T>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 4/20 | chr2 | 11773602 | |||||||
| chr2:11773775 | T | A | 1 | a0001c0001t0001g0235 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.722+30T>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 5/20 | chr2 | 11773775 | |||||||
| chr2:11773793 | A | T | 1 | a0001c0001t0003g0234 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.722+48A>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 5/20 | chr2 | 11773793 | |||||||
| chr2:11774091 | G | A | 1 | a0001c0001t0004g0111 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.722+346G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 5/20 | chr2 | 11774091 | |||||||
| chr2:11774681 | C | T | 1 | a0001c0001t0012g0070 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.722+936C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 5/20 | chr2 | 11774681 | |||||||
| chr2:11774815 | C | T | 61 | a0001c0001t0001g0098 a0001c0001t0001g0109 a0001c0001t0001g0110 others(58): Show |
61 | HG00099.hp2 HG00558.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.722+1070C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 5/20 | chr2 | 11774815 | |||||||
| chr2:11774948 | G | T | 3 | a0001c0001t0001g0058 a0001c0001t0002g0057 a0001c0001t0002g0160 |
3 | HG01261.hp2 HG01981.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.723-1138G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 5/20 | chr2 | 11774948 | |||||||
| chr2:11774965 | T | TAAAA | 13 | a0001c0001t0001g0030 a0001c0001t0002g0064 a0001c0001t0002g0067 others(10): Show |
13 | HG02559.hp2 HG02615.hp1 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.723-1108_723-1105d others(6): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr2 | 11774965 | ||||||
| chr2:11775095 | A | T | 150 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0001g0098 others(147): Show |
151 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(148): Show |
intron_variant | MODIFIER | c.723-991A>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 5/20 | chr2 | 11775095 | |||||||
| chr2:11775119 | A | G | 1 | a0001c0001t0006g0083 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.723-967A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 5/20 | chr2 | 11775119 | |||||||
| chr2:11775158 | A | C | 150 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0001g0098 others(147): Show |
151 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(148): Show |
intron_variant | MODIFIER | c.723-928A>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 5/20 | chr2 | 11775158 | |||||||
| chr2:11775314 | A | G | 1 | a0001c0001t0003g0106 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.723-772A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 5/20 | chr2 | 11775314 | |||||||
| chr2:11775334 | A | G | 6 | a0001c0001t0002g0064 a0001c0001t0002g0067 a0001c0001t0002g0068 others(3): Show |
6 | HG02559.hp2 HG02717.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.723-752A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 5/20 | chr2 | 11775334 | |||||||
| chr2:11775404 | C | T | 1 | a0001c0001t0004g0033 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.723-682C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 5/20 | chr2 | 11775404 | |||||||
| chr2:11775414 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.723-672G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 5/20 | chr2 | 11775414 | |||||||
| chr2:11775481 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.723-605G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 5/20 | chr2 | 11775481 | |||||||
| chr2:11775569 | C | A | 1 | a0001c0001t0001g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.723-517C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 5/20 | chr2 | 11775569 | |||||||
| chr2:11775640 | G | T | 1 | a0001c0001t0001g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.723-446G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 5/20 | chr2 | 11775640 | |||||||
| chr2:11775777 | T | TTCTTTAT others(2307): Show |
1 | a0001c0001t0017g0065 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.723-296_723-295ins others(2314): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr2 | 11775777 | ||||||
| chr2:11775777 | T | TTCTTTAT others(2306): Show |
1 | a0001c0001t0017g0066 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.723-296_723-295ins others(2313): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr2 | 11775777 | ||||||
| chr2:11775777 | T | TTCTTTAT others(2305): Show |
3 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 |
3 | HG02559.hp2 HG02717.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.723-296_723-295ins others(2312): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr2 | 11775777 | ||||||
| chr2:11775777 | T | TTCTTTAT others(2304): Show |
1 | a0001c0001t0002g0064 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.723-296_723-295ins others(2311): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr2 | 11775777 | ||||||
| chr2:11775881 | T | TTATATAT others(29): Show |
1 | a0001c0001t0012g0249 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.723-203_723-168dup others(36): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr2 | 11775881 | ||||||
| chr2:11775883 | A | ATATATAA others(29): Show |
1 | a0001c0001t0005g0079 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.723-191_723-156dup others(36): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr2 | 11775883 | ||||||
| chr2:11775915 | T | C | 12 | a0001c0001t0003g0044 a0001c0001t0003g0050 a0001c0001t0005g0046 others(9): Show |
12 | HG00639.hp2 HG01175.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.723-171T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 5/20 | chr2 | 11775915 | |||||||
| chr2:11775929 | TTATA | T | 12 | a0001c0001t0003g0044 a0001c0001t0003g0050 a0001c0001t0005g0046 others(9): Show |
12 | HG00639.hp2 HG01175.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.723-152_723-149del others(4): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr2 | 11775929 | ||||||
| chr2:11776229 | A | G | 12 | a0001c0001t0003g0044 a0001c0001t0003g0050 a0001c0001t0005g0046 others(9): Show |
12 | HG00639.hp2 HG01175.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.830+36A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11776229 | |||||||
| chr2:11776395 | T | C | 1 | a0002c0010t0005g0012 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.830+202T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11776395 | |||||||
| chr2:11776406 | C | T | 14 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0127 others(11): Show |
14 | HG00609.hp1 HG02056.hp2 NA18943.hp2 others(11): Show |
intron_variant | MODIFIER | c.830+213C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11776406 | |||||||
| chr2:11776432 | AT | A | 16 | a0001c0001t0001g0030 a0001c0001t0002g0064 a0001c0001t0002g0067 others(13): Show |
16 | HG00558.hp1 HG01516.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.830+254delT | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr2 | 11776432 | ||||||
| chr2:11776622 | A | G | 5 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0003g0062 others(2): Show |
5 | HG02615.hp1 HG02723.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.830+429A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11776622 | |||||||
| chr2:11776678 | C | T | 1 | a0001c0001t0012g0070 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.830+485C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11776678 | |||||||
| chr2:11776893 | G | T | 14 | a0001c0001t0002g0071 a0001c0001t0003g0015 a0001c0001t0003g0082 others(11): Show |
14 | HG01261.hp1 HG01934.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.830+700G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11776893 | |||||||
| chr2:11776979 | A | G | 14 | a0001c0001t0002g0071 a0001c0001t0003g0015 a0001c0001t0003g0082 others(11): Show |
14 | HG01261.hp1 HG01934.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.830+786A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11776979 | |||||||
| chr2:11776990 | T | A | 90 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0002g0003 others(87): Show |
92 | HG00280.hp1 HG00639.hp2 HG00733.hp1 others(89): Show |
intron_variant | MODIFIER | c.830+797T>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11776990 | |||||||
| chr2:11777139 | C | A | 1 | a0001c0001t0004g0259 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.830+946C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11777139 | |||||||
| chr2:11777152 | T | C | 63 | a0001c0001t0001g0098 a0001c0001t0001g0109 a0001c0001t0001g0110 others(60): Show |
63 | HG00099.hp2 HG00558.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.830+959T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11777152 | |||||||
| chr2:11777240 | T | G | 1 | a0003c0006t0004g0099 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.830+1047T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11777240 | |||||||
| chr2:11777386 | G | A | 14 | a0001c0001t0001g0030 a0001c0001t0002g0064 a0001c0001t0002g0067 others(11): Show |
14 | HG02559.hp2 HG02615.hp1 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.830+1193G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11777386 | |||||||
| chr2:11777393 | G | A | 118 | a0001c0001t0001g0098 a0001c0001t0001g0109 a0001c0001t0001g0110 others(115): Show |
120 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.830+1200G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11777393 | |||||||
| chr2:11777402 | A | G | 1 | a0001c0001t0001g0228 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.830+1209A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11777402 | |||||||
| chr2:11777431 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.830+1238C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11777431 | |||||||
| chr2:11777583 | C | T | 1 | a0001c0001t0026g0038 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.830+1390C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11777583 | |||||||
| chr2:11777651 | C | T | 1 | a0001c0001t0012g0187 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.830+1458C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11777651 | |||||||
| chr2:11777719 | C | T | 7 | a0001c0013t0001g0025 a0002c0007t0011g0029 a0002c0007t0034g0027 others(4): Show |
7 | HG01070.hp2 HG01167.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.830+1526C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11777719 | |||||||
| chr2:11777779 | T | C | 89 | a0001c0001t0001g0098 a0001c0001t0001g0109 a0001c0001t0001g0110 others(86): Show |
89 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.830+1586T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11777779 | |||||||
| chr2:11777907 | A | G | 20 | a0001c0001t0002g0071 a0001c0001t0005g0086 a0001c0001t0008g0010 others(17): Show |
20 | HG01261.hp1 HG01934.hp1 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.831-1612A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11777907 | |||||||
| chr2:11778025 | C | T | 1 | a0001c0001t0005g0079 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.831-1494C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11778025 | |||||||
| chr2:11778138 | G | GT | 144 | a0001c0001t0001g0058 a0001c0001t0001g0098 a0001c0001t0001g0109 others(141): Show |
146 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(143): Show |
intron_variant | MODIFIER | c.831-1381_831-1380i others(3): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11778138 | |||||||
| chr2:11778139 | G | T | 9 | a0001c0001t0001g0030 a0001c0001t0003g0060 a0001c0001t0003g0061 others(6): Show |
9 | HG00639.hp2 HG02615.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.831-1380G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11778139 | |||||||
| chr2:11778144 | G | C | 144 | a0001c0001t0001g0058 a0001c0001t0001g0098 a0001c0001t0001g0109 others(141): Show |
146 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(143): Show |
intron_variant | MODIFIER | c.831-1375G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11778144 | |||||||
| chr2:11778582 | G | A | 2 | a0001c0001t0001g0130 a0001c0001t0025g0107 |
2 | HG04199.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.831-937G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11778582 | |||||||
| chr2:11778638 | C | T | 1 | a0001c0004t0010g0081 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.831-881C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11778638 | |||||||
| chr2:11778871 | G | A | 21 | a0001c0001t0002g0064 a0001c0001t0002g0067 a0001c0001t0002g0068 others(18): Show |
21 | HG01175.hp2 HG01891.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.831-648G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11778871 | |||||||
| chr2:11778962 | T | C | 1 | a0001c0001t0004g0033 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.831-557T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11778962 | |||||||
| chr2:11779049 | A | G | 85 | a0001c0001t0001g0058 a0001c0001t0001g0098 a0001c0001t0001g0130 others(82): Show |
87 | HG00099.hp2 HG01070.hp2 HG01109.hp1 others(84): Show |
intron_variant | MODIFIER | c.831-470A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11779049 | |||||||
| chr2:11779372 | G | A | 44 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0127 others(41): Show |
44 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.831-147G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 6/20 | chr2 | 11779372 | |||||||
| chr2:11779775 | G | T | 1 | a0001c0001t0012g0070 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.957+130G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 7/20 | chr2 | 11779775 | |||||||
| chr2:11779881 | CT | C | 16 | a0001c0001t0003g0044 a0001c0001t0003g0050 a0001c0001t0005g0046 others(13): Show |
16 | HG01175.hp2 HG01891.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.957+250delT | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr2 | 11779881 | ||||||
| chr2:11779894 | T | G | 6 | a0001c0001t0001g0190 a0001c0001t0004g0191 a0001c0001t0004g0192 others(3): Show |
6 | HG00738.hp2 HG01255.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.957+249T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 7/20 | chr2 | 11779894 | |||||||
| chr2:11779898 | TGA | T | 10 | a0001c0003t0001g0052 a0001c0003t0002g0056 a0001c0003t0002g0090 others(7): Show |
10 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.957+256_957+257del others(2): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr2 | 11779898 | ||||||
| chr2:11779924 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.957+279G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 7/20 | chr2 | 11779924 | |||||||
| chr2:11780021 | C | G | 62 | a0001c0001t0001g0098 a0001c0001t0001g0130 a0001c0001t0001g0268 others(59): Show |
62 | HG00099.hp2 HG01175.hp2 HG01243.hp1 others(59): Show |
intron_variant | MODIFIER | c.957+376C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 7/20 | chr2 | 11780021 | |||||||
| chr2:11780073 | G | C | 46 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0127 others(43): Show |
46 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.957+428G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 7/20 | chr2 | 11780073 | |||||||
| chr2:11780081 | G | A | 3 | a0001c0001t0003g0015 a0001c0001t0003g0082 a0001c0001t0005g0079 |
3 | HG02451.hp1 HG03139.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.957+436G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 7/20 | chr2 | 11780081 | |||||||
| chr2:11780095 | G | A | 1 | a0001c0001t0002g0194 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.957+450G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 7/20 | chr2 | 11780095 | |||||||
| chr2:11780171 | G | A | 2 | a0001c0002t0015g0154 a0001c0002t0015g0158 |
2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.957+526G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 7/20 | chr2 | 11780171 | |||||||
| chr2:11780415 | G | C | 2 | a0001c0005t0007g0021 a0001c0005t0007g0022 |
2 | HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.957+770G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 7/20 | chr2 | 11780415 | |||||||
| chr2:11780619 | G | A | 3 | a0001c0001t0003g0015 a0001c0001t0003g0082 a0001c0001t0005g0079 |
3 | HG02451.hp1 HG03139.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.957+974G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 7/20 | chr2 | 11780619 | |||||||
| chr2:11780658 | G | A | 2 | a0001c0001t0001g0109 a0001c0001t0003g0146 |
2 | HG00609.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.957+1013G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 7/20 | chr2 | 11780658 | |||||||
| chr2:11780864 | G | C | 1 | a0001c0001t0007g0219 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.957+1219G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 7/20 | chr2 | 11780864 | |||||||
| chr2:11781237 | G | A | 1 | a0001c0001t0002g0242 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.958-964G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 7/20 | chr2 | 11781237 | |||||||
| chr2:11781364 | A | C | 2 | a0001c0001t0001g0130 a0001c0001t0025g0107 |
2 | HG04199.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.958-837A>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 7/20 | chr2 | 11781364 | |||||||
| chr2:11781379 | A | G | 1 | a0001c0001t0002g0003 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.958-822A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 7/20 | chr2 | 11781379 | |||||||
| chr2:11781571 | T | C | 263 | a0001c0001t0001g0004 a0001c0001t0001g0030 a0001c0001t0001g0058 others(260): Show |
267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.958-630T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 7/20 | chr2 | 11781571 | |||||||
| chr2:11781770 | G | T | 1 | a0001c0001t0001g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.958-431G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 7/20 | chr2 | 11781770 | |||||||
| chr2:11781928 | A | G | 64 | a0001c0001t0001g0098 a0001c0001t0001g0130 a0001c0001t0001g0268 others(61): Show |
66 | HG00099.hp2 HG00738.hp2 HG01167.hp2 others(63): Show |
intron_variant | MODIFIER | c.958-273A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 7/20 | chr2 | 11781928 | |||||||
| chr2:11782005 | A | G | 1 | a0001c0001t0012g0070 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.958-196A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 7/20 | chr2 | 11782005 | |||||||
| chr2:11782622 | A | C | 1 | a0001c0002t0008g0085 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1264+115A>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 8/20 | chr2 | 11782622 | |||||||
| chr2:11782729 | A | G | 63 | a0001c0001t0001g0058 a0001c0001t0001g0109 a0001c0001t0001g0110 others(60): Show |
63 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.1264+222A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 8/20 | chr2 | 11782729 | |||||||
| chr2:11782780 | C | T | 29 | a0001c0001t0001g0098 a0001c0001t0001g0130 a0001c0001t0001g0268 others(26): Show |
29 | HG00099.hp2 HG00738.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.1264+273C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 8/20 | chr2 | 11782780 | |||||||
| chr2:11782861 | C | T | 44 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0127 others(41): Show |
44 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.1264+354C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 8/20 | chr2 | 11782861 | |||||||
| chr2:11783053 | C | T | 58 | a0001c0001t0001g0098 a0001c0001t0001g0130 a0001c0001t0001g0268 others(55): Show |
60 | HG00099.hp2 HG00738.hp2 HG01175.hp2 others(57): Show |
intron_variant | MODIFIER | c.1264+546C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 8/20 | chr2 | 11783053 | |||||||
| chr2:11783135 | C | T | 1 | a0001c0001t0003g0082 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1264+628C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 8/20 | chr2 | 11783135 | |||||||
| chr2:11783209 | C | T | 6 | a0001c0003t0001g0052 a0001c0003t0002g0056 a0001c0003t0009g0053 others(3): Show |
6 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.1265-620C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 8/20 | chr2 | 11783209 | |||||||
| chr2:11783219 | G | A | 3 | a0001c0001t0005g0273 a0001c0001t0008g0042 a0001c0001t0008g0047 |
3 | HG00639.hp2 HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1265-610G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 8/20 | chr2 | 11783219 | |||||||
| chr2:11783282 | A | G | 44 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0127 others(41): Show |
44 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.1265-547A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 8/20 | chr2 | 11783282 | |||||||
| chr2:11783292 | A | G | 165 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0001g0098 others(162): Show |
167 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(164): Show |
intron_variant | MODIFIER | c.1265-537A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 8/20 | chr2 | 11783292 | |||||||
| chr2:11783497 | C | T | 19 | a0001c0001t0001g0058 a0001c0001t0002g0057 a0001c0001t0002g0160 others(16): Show |
19 | HG01109.hp1 HG01175.hp2 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.1265-332C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 8/20 | chr2 | 11783497 | |||||||
| chr2:11783526 | C | T | 5 | a0001c0001t0002g0194 a0001c0001t0003g0211 a0001c0001t0003g0212 others(2): Show |
5 | HG00423.hp1 HG01255.hp2 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.1265-303C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 8/20 | chr2 | 11783526 | |||||||
| chr2:11783549 | A | G | 23 | a0001c0001t0001g0058 a0001c0001t0002g0057 a0001c0001t0002g0160 others(20): Show |
23 | HG01109.hp1 HG01175.hp2 HG01261.hp2 others(20): Show |
intron_variant | MODIFIER | c.1265-280A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 8/20 | chr2 | 11783549 | |||||||
| chr2:11783761 | A | G | 1 | a0001c0001t0001g0145 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1265-68A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 8/20 | chr2 | 11783761 | |||||||
| chr2:11784033 | G | A | 1 | a0001c0001t0009g0125 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1358+111G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 9/20 | chr2 | 11784033 | |||||||
| chr2:11784167 | G | A | 43 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0127 others(40): Show |
43 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.1358+245G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 9/20 | chr2 | 11784167 | |||||||
| chr2:11784289 | GTGAGACT others(53): Show |
G | 48 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0127 others(45): Show |
48 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.1358+369_1358+428d others(62): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr2 | 11784289 | ||||||
| chr2:11784303 | C | CA | 21 | a0001c0001t0001g0030 a0001c0001t0002g0003 a0001c0001t0002g0031 others(18): Show |
21 | HG01175.hp1 HG01496.hp2 HG01517.hp2 others(18): Show |
intron_variant | MODIFIER | c.1358+402dupA | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr2 | 11784303 | ||||||
| chr2:11784303 | C | CAA | 45 | a0001c0001t0001g0098 a0001c0001t0001g0268 a0001c0001t0001g0269 others(42): Show |
45 | HG00738.hp2 HG01167.hp2 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.1358+401_1358+402d others(4): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr2 | 11784303 | ||||||
| chr2:11784303 | C | CAAA | 11 | a0001c0001t0002g0100 a0001c0001t0004g0191 a0001c0001t0005g0086 others(8): Show |
11 | HG00099.hp2 HG01109.hp2 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.1358+400_1358+402d others(5): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr2 | 11784303 | ||||||
| chr2:11784303 | C | CAAAAA | 8 | a0001c0001t0001g0058 a0001c0001t0002g0057 a0001c0001t0002g0064 others(5): Show |
8 | HG01109.hp1 HG01261.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1358+398_1358+402d others(7): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr2 | 11784303 | ||||||
| chr2:11784303 | C | CACAAAAA | 9 | a0001c0001t0003g0044 a0001c0001t0003g0050 a0001c0001t0005g0046 others(6): Show |
9 | HG01891.hp1 HG02451.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1358+382_1358+383i others(9): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr2 | 11784303 | ||||||
| chr2:11784303 | CA | C | 11 | a0001c0001t0002g0205 a0001c0001t0003g0060 a0001c0001t0003g0061 others(8): Show |
11 | HG01070.hp1 HG01515.hp2 HG01993.hp2 others(8): Show |
intron_variant | MODIFIER | c.1358+402delA | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr2 | 11784303 | ||||||
| chr2:11784352 | C | T | 48 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0127 others(45): Show |
48 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.1358+430C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 9/20 | chr2 | 11784352 | |||||||
| chr2:11784438 | C | T | 1 | a0001c0001t0002g0032 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1359-448C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 9/20 | chr2 | 11784438 | |||||||
| chr2:11784502 | T | C | 1 | a0001c0001t0001g0237 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1359-384T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 9/20 | chr2 | 11784502 | |||||||
| chr2:11784692 | T | G | 14 | a0001c0001t0003g0044 a0001c0001t0003g0050 a0001c0001t0005g0046 others(11): Show |
14 | HG01175.hp2 HG01891.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1359-194T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 9/20 | chr2 | 11784692 | |||||||
| chr2:11784813 | T | C | 1 | a0001c0001t0002g0149 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1359-73T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 9/20 | chr2 | 11784813 | |||||||
| chr2:11784824 | T | C | 162 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0001g0098 others(159): Show |
165 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(162): Show |
intron_variant | MODIFIER | c.1359-62T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 9/20 | chr2 | 11784824 | |||||||
| chr2:11784835 | C | G | 2 | a0001c0002t0002g0018 a0001c0002t0003g0019 |
2 | HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1359-51C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 9/20 | chr2 | 11784835 | |||||||
| chr2:11785209 | A | G | 51 | a0001c0001t0001g0098 a0001c0001t0001g0130 a0001c0001t0001g0268 others(48): Show |
53 | HG00099.hp2 HG00738.hp2 HG01109.hp2 others(50): Show |
intron_variant | MODIFIER | c.1549+133A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 10/20 | chr2 | 11785209 | |||||||
| chr2:11785372 | T | C | 2 | a0001c0002t0015g0154 a0001c0002t0015g0158 |
2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1549+296T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 10/20 | chr2 | 11785372 | |||||||
| chr2:11785403 | G | C | 1 | a0001c0001t0005g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1549+327G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 10/20 | chr2 | 11785403 | |||||||
| chr2:11785430 | T | G | 6 | a0001c0001t0005g0086 a0001c0001t0005g0093 a0001c0001t0005g0094 others(3): Show |
6 | HG02922.hp1 HG02922.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1549+354T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 10/20 | chr2 | 11785430 | |||||||
| chr2:11785656 | C | T | 53 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0127 others(50): Show |
53 | HG00558.hp2 HG00609.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.1549+580C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 10/20 | chr2 | 11785656 | |||||||
| chr2:11785666 | A | T | 6 | a0001c0001t0005g0086 a0001c0001t0005g0093 a0001c0001t0005g0094 others(3): Show |
6 | HG02922.hp1 HG02922.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1549+590A>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 10/20 | chr2 | 11785666 | |||||||
| chr2:11785765 | T | G | 61 | a0001c0001t0001g0058 a0001c0001t0001g0109 a0001c0001t0001g0110 others(58): Show |
61 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.1549+689T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 10/20 | chr2 | 11785765 | |||||||
| chr2:11785774 | G | A | 1 | a0001c0001t0001g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1549+698G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 10/20 | chr2 | 11785774 | |||||||
| chr2:11785809 | C | T | 1 | a0001c0001t0002g0186 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1549+733C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 10/20 | chr2 | 11785809 | |||||||
| chr2:11785937 | A | T | 1 | a0001c0001t0002g0210 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1549+861A>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 10/20 | chr2 | 11785937 | |||||||
| chr2:11785938 | C | T | 1 | a0001c0001t0002g0210 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1549+862C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 10/20 | chr2 | 11785938 | |||||||
| chr2:11786157 | G | C | 6 | a0001c0001t0005g0086 a0001c0001t0005g0093 a0001c0001t0005g0094 others(3): Show |
6 | HG02922.hp1 HG02922.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1550-917G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 10/20 | chr2 | 11786157 | |||||||
| chr2:11786245 | T | G | 1 | a0004c0012t0001g0178 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1550-829T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 10/20 | chr2 | 11786245 | |||||||
| chr2:11786315 | G | A | 1 | a0001c0001t0008g0047 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1550-759G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 10/20 | chr2 | 11786315 | |||||||
| chr2:11786479 | A | G | 6 | a0001c0002t0008g0085 a0002c0007t0011g0029 a0002c0007t0034g0027 others(3): Show |
6 | HG01167.hp2 HG02055.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1550-595A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 10/20 | chr2 | 11786479 | |||||||
| chr2:11786568 | C | T | 2 | a0001c0002t0015g0154 a0001c0002t0015g0158 |
2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1550-506C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 10/20 | chr2 | 11786568 | |||||||
| chr2:11786706 | C | T | 1 | a0001c0002t0008g0085 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1550-368C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 10/20 | chr2 | 11786706 | |||||||
| chr2:11786728 | C | A | 1 | a0001c0001t0002g0144 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1550-346C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 10/20 | chr2 | 11786728 | |||||||
| chr2:11786844 | C | T | 1 | a0001c0002t0002g0018 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1550-230C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 10/20 | chr2 | 11786844 | |||||||
| chr2:11786957 | A | G | 1 | a0001c0001t0003g0087 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1550-117A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 10/20 | chr2 | 11786957 | |||||||
| chr2:11787326 | A | C | 1 | a0001c0001t0011g0188 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1643+159A>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 11/20 | chr2 | 11787326 | |||||||
| chr2:11787376 | A | G | 1 | a0001c0001t0003g0106 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1643+209A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 11/20 | chr2 | 11787376 | |||||||
| chr2:11787392 | C | CT | 12 | a0001c0001t0001g0141 a0001c0001t0001g0257 a0001c0001t0001g0258 others(9): Show |
12 | HG00673.hp1 HG00735.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.1643+230dupT | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr2 | 11787392 | ||||||
| chr2:11787392 | C | CTT | 33 | a0001c0001t0001g0058 a0001c0001t0001g0109 a0001c0001t0001g0110 others(30): Show |
33 | HG00558.hp2 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.1643+229_1643+230d others(4): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr2 | 11787392 | ||||||
| chr2:11787392 | C | CTTT | 9 | a0001c0001t0002g0137 a0001c0001t0002g0144 a0001c0001t0003g0146 others(6): Show |
9 | HG02055.hp2 HG02056.hp2 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.1643+228_1643+230d others(5): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr2 | 11787392 | ||||||
| chr2:11787392 | C | CTTTTTTT others(5): Show |
3 | a0001c0001t0005g0086 a0001c0001t0005g0093 a0001c0001t0005g0094 |
3 | HG02922.hp2 HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1643+230_1643+231i others(14): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr2 | 11787392 | ||||||
| chr2:11787392 | C | CTTTTTTT others(13): Show |
1 | a0001c0008t0005g0006 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1643+230_1643+231i others(22): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr2 | 11787392 | ||||||
| chr2:11787392 | C | CTTTTTTT others(14): Show |
1 | a0001c0002t0030g0011 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1643+230_1643+231i others(23): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr2 | 11787392 | ||||||
| chr2:11787392 | C | CTTTTTTT others(18): Show |
1 | a0001c0008t0005g0007 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1643+230_1643+231i others(27): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr2 | 11787392 | ||||||
| chr2:11787396 | TTC | T | 15 | a0001c0001t0002g0003 a0001c0001t0002g0149 a0001c0001t0008g0023 others(12): Show |
16 | HG00738.hp1 HG01109.hp1 HG01516.hp2 others(13): Show |
intron_variant | MODIFIER | c.1643+231_1643+232d others(4): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr2 | 11787396 | ||||||
| chr2:11787397 | TC | T | 63 | a0001c0001t0001g0098 a0001c0001t0001g0130 a0001c0001t0002g0032 others(60): Show |
63 | HG00280.hp1 HG00639.hp2 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.1643+231delC | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 11/20 | chr2 | 11787397 | |||||||
| chr2:11787398 | C | T | 85 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0001g0109 others(82): Show |
85 | HG00099.hp2 HG00558.hp2 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.1643+231C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 11/20 | chr2 | 11787398 | |||||||
| chr2:11787566 | C | T | 43 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0127 others(40): Show |
43 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.1643+399C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 11/20 | chr2 | 11787566 | |||||||
| chr2:11787615 | G | A | 2 | a0001c0002t0015g0154 a0001c0002t0015g0158 |
2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1643+448G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 11/20 | chr2 | 11787615 | |||||||
| chr2:11787626 | C | G | 2 | a0001c0002t0015g0154 a0001c0002t0015g0158 |
2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1643+459C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 11/20 | chr2 | 11787626 | |||||||
| chr2:11787781 | G | A | 2 | a0001c0002t0015g0154 a0001c0002t0015g0158 |
2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1644-606G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 11/20 | chr2 | 11787781 | |||||||
| chr2:11787857 | C | T | 2 | a0001c0001t0002g0031 a0001c0001t0002g0032 |
2 | HG02145.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1644-530C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 11/20 | chr2 | 11787857 | |||||||
| chr2:11787865 | T | C | 1 | a0001c0001t0001g0248 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1644-522T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 11/20 | chr2 | 11787865 | |||||||
| chr2:11787898 | G | A | 2 | a0001c0001t0006g0083 a0001c0001t0028g0084 |
2 | HG02897.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1644-489G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 11/20 | chr2 | 11787898 | |||||||
| chr2:11787940 | C | CA | 39 | a0001c0001t0001g0030 a0001c0001t0002g0031 a0001c0001t0002g0032 others(36): Show |
39 | HG00639.hp2 HG01175.hp2 HG01496.hp2 others(36): Show |
intron_variant | MODIFIER | c.1644-432dupA | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr2 | 11787940 | ||||||
| chr2:11788123 | C | T | 6 | a0001c0001t0002g0064 a0001c0001t0002g0067 a0001c0001t0002g0068 others(3): Show |
6 | HG02559.hp2 HG02717.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1644-264C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 11/20 | chr2 | 11788123 | |||||||
| chr2:11788172 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1644-215G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 11/20 | chr2 | 11788172 | |||||||
| chr2:11788188 | T | C | 5 | a0001c0001t0001g0058 a0001c0001t0002g0057 a0001c0001t0002g0160 others(2): Show |
5 | HG01261.hp2 HG01981.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1644-199T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 11/20 | chr2 | 11788188 | |||||||
| chr2:11788287 | G | A | 2 | a0001c0001t0008g0023 a0001c0001t0010g0024 |
2 | HG01109.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.1644-100G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 11/20 | chr2 | 11788287 | |||||||
| chr2:11788351 | C | T | 3 | a0001c0001t0005g0273 a0001c0001t0008g0042 a0001c0001t0008g0047 |
3 | HG00639.hp2 HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1644-36C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 11/20 | chr2 | 11788351 | |||||||
| chr2:11788543 | G | A | 5 | a0002c0007t0011g0029 a0002c0007t0034g0027 a0002c0007t0035g0028 others(2): Show |
5 | HG01167.hp2 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1713+87G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11788543 | |||||||
| chr2:11788682 | G | A | 5 | a0001c0001t0002g0233 a0001c0001t0004g0230 a0001c0001t0004g0231 others(2): Show |
5 | NA18747.hp2 NA18983.hp1 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.1713+226G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11788682 | |||||||
| chr2:11788732 | G | C | 1 | a0001c0001t0004g0191 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1713+276G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11788732 | |||||||
| chr2:11788997 | G | A | 1 | a0001c0001t0013g0135 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1713+541G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11788997 | |||||||
| chr2:11789140 | A | G | 1 | a0001c0001t0001g0237 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1713+684A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11789140 | |||||||
| chr2:11789186 | G | A | 1 | a0001c0002t0008g0085 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1713+730G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11789186 | |||||||
| chr2:11789198 | G | C | 1 | a0001c0001t0012g0070 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1713+742G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11789198 | |||||||
| chr2:11789202 | A | T | 105 | a0001c0001t0001g0030 a0001c0001t0001g0098 a0001c0001t0001g0130 others(102): Show |
107 | HG00099.hp2 HG00639.hp2 HG00738.hp2 others(104): Show |
intron_variant | MODIFIER | c.1713+746A>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11789202 | |||||||
| chr2:11789267 | T | TTG | 5 | a0001c0001t0001g0267 a0001c0001t0004g0208 a0001c0001t0013g0209 others(2): Show |
5 | HG00609.hp2 HG01934.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.1713+830_1713+831d others(4): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr2 | 11789267 | ||||||
| chr2:11789273 | G | A | 164 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0001g0098 others(161): Show |
166 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(163): Show |
intron_variant | MODIFIER | c.1713+817G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11789273 | |||||||
| chr2:11789333 | G | A | 3 | a0001c0001t0003g0015 a0001c0001t0003g0082 a0001c0001t0005g0079 |
3 | HG02451.hp1 HG03139.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1713+877G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11789333 | |||||||
| chr2:11789338 | T | C | 44 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0127 others(41): Show |
44 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.1713+882T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11789338 | |||||||
| chr2:11789357 | G | A | 12 | a0001c0001t0001g0030 a0001c0001t0002g0031 a0001c0001t0002g0032 others(9): Show |
12 | HG01496.hp2 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1713+901G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11789357 | |||||||
| chr2:11789386 | C | T | 6 | a0001c0001t0002g0064 a0001c0001t0002g0067 a0001c0001t0002g0068 others(3): Show |
6 | HG02559.hp2 HG02717.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1713+930C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11789386 | |||||||
| chr2:11789484 | G | A | 1 | a0001c0001t0002g0032 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1713+1028G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11789484 | |||||||
| chr2:11789486 | A | G | 6 | a0001c0002t0008g0085 a0002c0007t0011g0029 a0002c0007t0034g0027 others(3): Show |
6 | HG01167.hp2 HG02055.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1713+1030A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11789486 | |||||||
| chr2:11789492 | A | T | 1 | a0001c0001t0001g0109 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1713+1036A>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11789492 | |||||||
| chr2:11789528 | ACATGTGT others(5): Show |
A | 2 | a0001c0001t0002g0057 a0001c0001t0002g0160 |
2 | HG01261.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.1713+1081_1713+109 others(16): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr2 | 11789528 | ||||||
| chr2:11789571 | T | C | 29 | a0001c0001t0001g0098 a0001c0001t0001g0130 a0001c0001t0001g0268 others(26): Show |
29 | HG00099.hp2 HG00738.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.1713+1115T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11789571 | |||||||
| chr2:11789575 | C | T | 4 | a0001c0001t0002g0073 a0001c0001t0003g0072 a0001c0001t0026g0038 others(1): Show |
4 | HG01496.hp2 HG02055.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1713+1119C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11789575 | |||||||
| chr2:11789577 | T | C | 4 | a0001c0001t0002g0073 a0001c0001t0003g0072 a0001c0001t0026g0038 others(1): Show |
4 | HG01496.hp2 HG02055.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1713+1121T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11789577 | |||||||
| chr2:11789610 | C | T | 1 | a0001c0001t0003g0072 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1713+1154C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11789610 | |||||||
| chr2:11789614 | G | A | 142 | a0001c0001t0001g0030 a0001c0001t0001g0098 a0001c0001t0001g0109 others(139): Show |
144 | HG00099.hp2 HG00558.hp2 HG00609.hp1 others(141): Show |
intron_variant | MODIFIER | c.1713+1158G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11789614 | |||||||
| chr2:11790133 | C | G | 6 | a0001c0001t0001g0165 a0001c0001t0001g0167 a0001c0001t0006g0166 others(3): Show |
6 | HG01257.hp1 HG01258.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.1713+1677C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11790133 | |||||||
| chr2:11790153 | A | G | 133 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0001g0098 others(130): Show |
135 | HG00099.hp2 HG00558.hp2 HG00609.hp1 others(132): Show |
intron_variant | MODIFIER | c.1713+1697A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11790153 | |||||||
| chr2:11790207 | G | A | 2 | a0001c0001t0008g0042 a0001c0001t0008g0047 |
2 | HG00639.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1714-1707G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11790207 | |||||||
| chr2:11790274 | G | A | 2 | a0001c0001t0007g0112 a0001c0001t0009g0125 |
2 | HG00735.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1714-1640G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11790274 | |||||||
| chr2:11790370 | C | T | 10 | a0001c0003t0001g0052 a0001c0003t0002g0056 a0001c0003t0002g0090 others(7): Show |
10 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.1714-1544C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11790370 | |||||||
| chr2:11790377 | A | G | 1 | a0001c0001t0012g0249 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1714-1537A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11790377 | |||||||
| chr2:11790406 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1714-1508C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11790406 | |||||||
| chr2:11790798 | C | G | 1 | a0001c0001t0001g0235 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1714-1116C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11790798 | |||||||
| chr2:11790931 | G | A | 2 | a0001c0002t0015g0154 a0001c0002t0015g0158 |
2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1714-983G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11790931 | |||||||
| chr2:11790986 | A | T | 21 | a0001c0001t0003g0044 a0001c0001t0003g0050 a0001c0001t0005g0046 others(18): Show |
21 | HG01167.hp2 HG01175.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.1714-928A>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11790986 | |||||||
| chr2:11791159 | T | C | 1 | a0001c0001t0001g0246 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1714-755T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11791159 | |||||||
| chr2:11791227 | C | T | 1 | a0001c0001t0010g0024 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1714-687C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11791227 | |||||||
| chr2:11791255 | G | A | 2 | a0001c0008t0005g0006 a0001c0008t0005g0007 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1714-659G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11791255 | |||||||
| chr2:11791306 | A | C | 1 | a0001c0001t0004g0265 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1714-608A>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11791306 | |||||||
| chr2:11791372 | A | G | 43 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0127 others(40): Show |
43 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.1714-542A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11791372 | |||||||
| chr2:11791596 | A | G | 3 | a0001c0001t0001g0030 a0001c0001t0002g0031 a0001c0001t0002g0032 |
3 | HG02145.hp2 NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1714-318A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11791596 | |||||||
| chr2:11791647 | G | T | 4 | a0001c0003t0002g0090 a0001c0003t0002g0091 a0001c0003t0009g0092 others(1): Show |
4 | HG01074.hp2 HG01433.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.1714-267G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | chr2 | 11791647 | |||||||
| chr2:11791805 | A | AT | 44 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0127 others(41): Show |
44 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.1714-100dupT | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr2 | 11791805 | ||||||
| chr2:11792047 | G | T | 164 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0001g0098 others(161): Show |
166 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(163): Show |
intron_variant | MODIFIER | c.1806+41G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 13/20 | chr2 | 11792047 | |||||||
| chr2:11792209 | T | C | 164 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0001g0098 others(161): Show |
166 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(163): Show |
intron_variant | MODIFIER | c.1806+203T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 13/20 | chr2 | 11792209 | |||||||
| chr2:11792388 | C | T | 4 | a0001c0003t0002g0090 a0001c0003t0002g0091 a0001c0003t0009g0092 others(1): Show |
4 | HG01074.hp2 HG01433.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.1806+382C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 13/20 | chr2 | 11792388 | |||||||
| chr2:11792513 | G | T | 1 | a0002c0009t0002g0051 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1806+507G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 13/20 | chr2 | 11792513 | |||||||
| chr2:11792587 | T | A | 3 | a0001c0001t0003g0015 a0001c0001t0003g0082 a0001c0001t0005g0079 |
3 | HG02451.hp1 HG03139.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1806+581T>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 13/20 | chr2 | 11792587 | |||||||
| chr2:11792621 | G | A | 1 | a0001c0001t0003g0140 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1806+615G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 13/20 | chr2 | 11792621 | |||||||
| chr2:11792810 | C | T | 1 | a0001c0013t0001g0025 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1806+804C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 13/20 | chr2 | 11792810 | |||||||
| chr2:11793120 | C | T | 2 | a0001c0001t0004g0259 a0001c0001t0036g0260 |
2 | HG02071.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1806+1114C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 13/20 | chr2 | 11793120 | |||||||
| chr2:11793174 | A | G | 1 | a0001c0001t0026g0038 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1806+1168A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 13/20 | chr2 | 11793174 | |||||||
| chr2:11793260 | A | G | 48 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0127 others(45): Show |
48 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.1806+1254A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 13/20 | chr2 | 11793260 | |||||||
| chr2:11793604 | C | T | 12 | a0001c0001t0002g0064 a0001c0001t0002g0067 a0001c0001t0002g0068 others(9): Show |
12 | HG02559.hp2 HG02717.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.1806+1598C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 13/20 | chr2 | 11793604 | |||||||
| chr2:11793909 | AGG | A | 3 | a0001c0001t0005g0273 a0001c0001t0008g0042 a0001c0001t0008g0047 |
3 | HG00639.hp2 HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1807-1496_1807-149 others(6): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr2 | 11793909 | ||||||
| chr2:11794047 | G | A | 2 | a0001c0008t0005g0006 a0001c0008t0005g0007 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1807-1361G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 13/20 | chr2 | 11794047 | |||||||
| chr2:11794057 | G | A | 1 | a0001c0001t0012g0070 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1807-1351G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 13/20 | chr2 | 11794057 | |||||||
| chr2:11794073 | C | G | 25 | a0001c0001t0001g0030 a0001c0001t0002g0031 a0001c0001t0002g0032 others(22): Show |
25 | HG00639.hp2 HG01496.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.1807-1335C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 13/20 | chr2 | 11794073 | |||||||
| chr2:11794122 | C | A | 10 | a0001c0003t0001g0052 a0001c0003t0002g0056 a0001c0003t0002g0090 others(7): Show |
10 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.1807-1286C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 13/20 | chr2 | 11794122 | |||||||
| chr2:11794539 | T | C | 1 | a0001c0001t0002g0236 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1807-869T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 13/20 | chr2 | 11794539 | |||||||
| chr2:11794561 | C | T | 10 | a0001c0001t0001g0216 a0001c0001t0001g0224 a0001c0001t0001g0248 others(7): Show |
11 | HG02015.hp1 HG02040.hp1 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.1807-847C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 13/20 | chr2 | 11794561 | |||||||
| chr2:11794630 | C | T | 2 | a0001c0001t0007g0172 a0001c0001t0007g0219 |
2 | HG01258.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1807-778C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 13/20 | chr2 | 11794630 | |||||||
| chr2:11794641 | CAGAG | C | 57 | a0001c0001t0001g0098 a0001c0001t0001g0130 a0001c0001t0001g0268 others(54): Show |
59 | HG00099.hp2 HG00639.hp2 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.1807-765_1807-762d others(6): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr2 | 11794641 | ||||||
| chr2:11794718 | C | A | 1 | a0001c0001t0002g0220 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1807-690C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 13/20 | chr2 | 11794718 | |||||||
| chr2:11794726 | G | A | 2 | a0001c0002t0015g0154 a0001c0002t0015g0158 |
2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1807-682G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 13/20 | chr2 | 11794726 | |||||||
| chr2:11794888 | C | G | 10 | a0001c0003t0001g0052 a0001c0003t0002g0056 a0001c0003t0002g0090 others(7): Show |
10 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.1807-520C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 13/20 | chr2 | 11794888 | |||||||
| chr2:11795150 | C | T | 1 | a0001c0001t0002g0149 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1807-258C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 13/20 | chr2 | 11795150 | |||||||
| chr2:11795160 | T | C | 1 | a0001c0002t0008g0085 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1807-248T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 13/20 | chr2 | 11795160 | |||||||
| chr2:11795528 | C | T | 1 | a0001c0001t0005g0079 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1886+41C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11795528 | |||||||
| chr2:11795546 | G | C | 1 | a0001c0002t0008g0085 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1886+59G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11795546 | |||||||
| chr2:11795874 | A | G | 1 | a0001c0001t0016g0143 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1886+387A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11795874 | |||||||
| chr2:11795890 | A | G | 6 | a0001c0001t0003g0015 a0001c0001t0003g0082 a0001c0001t0005g0079 others(3): Show |
6 | HG02451.hp1 HG02572.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1886+403A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11795890 | |||||||
| chr2:11796014 | C | T | 1 | a0001c0001t0011g0119 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1886+527C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11796014 | |||||||
| chr2:11796216 | G | A | 1 | a0001c0001t0012g0070 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1886+729G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11796216 | |||||||
| chr2:11796394 | C | G | 6 | a0001c0001t0002g0064 a0001c0001t0002g0067 a0001c0001t0002g0068 others(3): Show |
6 | HG02559.hp2 HG02717.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1886+907C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11796394 | |||||||
| chr2:11796465 | C | G | 29 | a0001c0001t0001g0141 a0001c0001t0001g0145 a0001c0001t0001g0148 others(26): Show |
29 | HG00558.hp2 HG00673.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.1886+978C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11796465 | |||||||
| chr2:11796514 | T | C | 3 | a0001c0001t0005g0273 a0001c0001t0008g0042 a0001c0001t0008g0047 |
3 | HG00639.hp2 HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1886+1027T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11796514 | |||||||
| chr2:11796556 | G | A | 2 | a0001c0001t0002g0220 a0001c0001t0037g0221 |
2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1886+1069G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11796556 | |||||||
| chr2:11796672 | A | G | 150 | a0001c0001t0001g0030 a0001c0001t0001g0058 a0001c0001t0001g0098 others(147): Show |
152 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(149): Show |
intron_variant | MODIFIER | c.1886+1185A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11796672 | |||||||
| chr2:11796770 | C | T | 1 | a0001c0001t0016g0143 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1886+1283C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11796770 | |||||||
| chr2:11796791 | C | T | 20 | a0001c0001t0003g0044 a0001c0001t0003g0050 a0001c0001t0005g0046 others(17): Show |
20 | HG01167.hp2 HG01175.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.1886+1304C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11796791 | |||||||
| chr2:11796906 | T | G | 1 | a0001c0001t0005g0273 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1886+1419T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11796906 | |||||||
| chr2:11796915 | C | T | 1 | a0001c0001t0004g0244 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1886+1428C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11796915 | |||||||
| chr2:11797032 | G | C | 87 | a0001c0001t0001g0058 a0001c0001t0001g0098 a0001c0001t0001g0130 others(84): Show |
89 | HG00099.hp2 HG00639.hp2 HG00738.hp2 others(86): Show |
intron_variant | MODIFIER | c.1886+1545G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11797032 | |||||||
| chr2:11797123 | C | T | 16 | a0001c0001t0002g0064 a0001c0001t0002g0067 a0001c0001t0002g0068 others(13): Show |
16 | HG00639.hp2 HG02559.hp2 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.1886+1636C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11797123 | |||||||
| chr2:11797211 | G | C | 5 | a0001c0001t0002g0233 a0001c0001t0004g0230 a0001c0001t0004g0231 others(2): Show |
5 | NA18747.hp2 NA18983.hp1 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.1886+1724G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11797211 | |||||||
| chr2:11797222 | C | A | 1 | a0001c0001t0006g0039 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1886+1735C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11797222 | |||||||
| chr2:11797308 | G | C | 1 | a0001c0002t0002g0018 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1886+1821G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11797308 | |||||||
| chr2:11797648 | CA | C | 6 | a0001c0001t0002g0064 a0001c0001t0002g0067 a0001c0001t0002g0068 others(3): Show |
6 | HG02559.hp2 HG02717.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1886+2163delA | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr2 | 11797648 | ||||||
| chr2:11797687 | A | G | 6 | a0001c0001t0002g0064 a0001c0001t0002g0067 a0001c0001t0002g0068 others(3): Show |
6 | HG02559.hp2 HG02717.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1886+2200A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11797687 | |||||||
| chr2:11797829 | T | C | 1 | a0001c0001t0001g0127 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1886+2342T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11797829 | |||||||
| chr2:11798250 | C | T | 1 | a0001c0002t0030g0011 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1886+2763C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11798250 | |||||||
| chr2:11798360 | G | A | 5 | a0001c0001t0002g0194 a0001c0001t0003g0211 a0001c0001t0003g0212 others(2): Show |
5 | HG00423.hp1 HG01255.hp2 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.1886+2873G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11798360 | |||||||
| chr2:11798586 | C | A | 2 | a0001c0002t0002g0018 a0001c0002t0003g0019 |
2 | HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1886+3099C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11798586 | |||||||
| chr2:11798615 | T | G | 8 | a0001c0001t0001g0127 a0001c0001t0004g0111 a0001c0001t0004g0128 others(5): Show |
8 | NA18960.hp1 NA18989.hp2 NA18995.hp2 others(5): Show |
intron_variant | MODIFIER | c.1886+3128T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11798615 | |||||||
| chr2:11798664 | T | C | 1 | a0001c0001t0006g0166 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1886+3177T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11798664 | |||||||
| chr2:11798670 | C | T | 2 | a0001c0001t0002g0220 a0001c0001t0037g0221 |
2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1886+3183C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11798670 | |||||||
| chr2:11798731 | G | A | 2 | a0001c0002t0015g0154 a0001c0002t0015g0158 |
2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1886+3244G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11798731 | |||||||
| chr2:11798775 | T | TA | 8 | a0001c0001t0001g0058 a0001c0001t0002g0057 a0001c0001t0002g0160 others(5): Show |
8 | HG01167.hp2 HG01261.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1886+3302dupA | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr2 | 11798775 | ||||||
| chr2:11798820 | G | A | 95 | a0001c0001t0001g0030 a0001c0001t0001g0098 a0001c0001t0001g0130 others(92): Show |
97 | HG00099.hp2 HG00639.hp2 HG00738.hp2 others(94): Show |
intron_variant | MODIFIER | c.1886+3333G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11798820 | |||||||
| chr2:11798848 | C | G | 10 | a0001c0003t0001g0052 a0001c0003t0002g0056 a0001c0003t0002g0090 others(7): Show |
10 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.1886+3361C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11798848 | |||||||
| chr2:11798892 | G | A | 32 | a0001c0001t0001g0141 a0001c0001t0001g0145 a0001c0001t0001g0148 others(29): Show |
32 | HG00558.hp2 HG00673.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.1886+3405G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11798892 | |||||||
| chr2:11798993 | T | C | 1 | a0001c0001t0004g0231 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1886+3506T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11798993 | |||||||
| chr2:11799030 | T | G | 12 | a0001c0001t0001g0030 a0001c0001t0002g0031 a0001c0001t0002g0032 others(9): Show |
12 | HG01496.hp2 HG02109.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1886+3543T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11799030 | |||||||
| chr2:11799292 | G | C | 1 | a0001c0001t0001g0226 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1887-3615G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11799292 | |||||||
| chr2:11799391 | T | C | 5 | a0002c0007t0011g0029 a0002c0007t0034g0027 a0002c0007t0035g0028 others(2): Show |
5 | HG01167.hp2 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1887-3516T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11799391 | |||||||
| chr2:11799432 | CCT | C | 73 | a0001c0001t0001g0030 a0001c0001t0001g0098 a0001c0001t0001g0130 others(70): Show |
75 | HG00099.hp2 HG00639.hp2 HG00738.hp2 others(72): Show |
intron_variant | MODIFIER | c.1887-3473_1887-347 others(6): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr2 | 11799432 | ||||||
| chr2:11799482 | C | T | 1 | a0001c0001t0016g0124 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1887-3425C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11799482 | |||||||
| chr2:11799483 | G | A | 7 | a0001c0001t0003g0015 a0001c0001t0003g0060 a0001c0001t0003g0061 others(4): Show |
7 | HG02451.hp1 HG02615.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1887-3424G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11799483 | |||||||
| chr2:11799504 | G | C | 1 | a0001c0001t0005g0074 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1887-3403G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11799504 | |||||||
| chr2:11799505 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1887-3402C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11799505 | |||||||
| chr2:11799567 | A | G | 1 | a0001c0002t0002g0020 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1887-3340A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11799567 | |||||||
| chr2:11799850 | C | T | 47 | a0001c0001t0001g0098 a0001c0001t0001g0130 a0001c0001t0001g0268 others(44): Show |
49 | HG00099.hp2 HG00738.hp2 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.1887-3057C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11799850 | |||||||
| chr2:11800002 | C | T | 1 | a0003c0006t0032g0132 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1887-2905C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11800002 | |||||||
| chr2:11800020 | C | T | 6 | a0001c0001t0001g0165 a0001c0001t0001g0167 a0001c0001t0006g0166 others(3): Show |
6 | HG01257.hp1 HG01258.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.1887-2887C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11800020 | |||||||
| chr2:11800045 | G | A | 30 | a0001c0001t0001g0141 a0001c0001t0001g0145 a0001c0001t0001g0148 others(27): Show |
30 | HG00558.hp2 HG00673.hp1 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.1887-2862G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11800045 | |||||||
| chr2:11800191 | C | T | 1 | a0001c0001t0007g0219 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1887-2716C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11800191 | |||||||
| chr2:11800309 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1887-2598C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11800309 | |||||||
| chr2:11800359 | A | G | 1 | a0001c0001t0012g0070 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1887-2548A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11800359 | |||||||
| chr2:11800414 | T | G | 1 | a0003c0006t0004g0099 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1887-2493T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11800414 | |||||||
| chr2:11800468 | C | T | 1 | a0001c0001t0005g0093 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1887-2439C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11800468 | |||||||
| chr2:11800469 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1887-2438G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11800469 | |||||||
| chr2:11800649 | G | A | 3 | a0001c0001t0002g0057 a0001c0001t0002g0118 a0001c0001t0002g0160 |
3 | HG01261.hp2 HG01981.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.1887-2258G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11800649 | |||||||
| chr2:11800661 | T | G | 253 | a0001c0001t0001g0004 a0001c0001t0001g0030 a0001c0001t0001g0058 others(250): Show |
257 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.1887-2246T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11800661 | |||||||
| chr2:11800693 | G | A | 145 | a0001c0001t0001g0004 a0001c0001t0001g0030 a0001c0001t0001g0058 others(142): Show |
147 | HG00280.hp1 HG00423.hp2 HG00558.hp1 others(144): Show |
intron_variant | MODIFIER | c.1887-2214G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11800693 | |||||||
| chr2:11800720 | G | A | 56 | a0001c0001t0001g0110 a0001c0001t0001g0130 a0001c0001t0001g0145 others(53): Show |
57 | HG00099.hp1 HG00099.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.1887-2187G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11800720 | |||||||
| chr2:11800893 | C | T | 2 | a0001c0008t0005g0006 a0001c0008t0005g0007 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1887-2014C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11800893 | |||||||
| chr2:11800959 | T | A | 1 | a0001c0001t0001g0258 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1887-1948T>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11800959 | |||||||
| chr2:11801007 | T | G | 1 | a0001c0001t0003g0072 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1887-1900T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11801007 | |||||||
| chr2:11801020 | T | A | 1 | a0002c0009t0002g0051 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1887-1887T>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11801020 | |||||||
| chr2:11801022 | A | G | 13 | a0001c0001t0003g0036 a0001c0001t0003g0044 a0001c0001t0003g0050 others(10): Show |
13 | HG01109.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1887-1885A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11801022 | |||||||
| chr2:11801134 | G | A | 1 | a0001c0001t0005g0079 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1887-1773G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11801134 | |||||||
| chr2:11801256 | A | G | 6 | a0001c0001t0018g0035 a0001c0008t0005g0006 a0001c0008t0005g0007 others(3): Show |
6 | HG01167.hp2 HG02055.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1887-1651A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11801256 | |||||||
| chr2:11801337 | G | A | 1 | a0001c0001t0007g0219 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1887-1570G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11801337 | |||||||
| chr2:11801352 | C | T | 1 | a0001c0001t0005g0097 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1887-1555C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11801352 | |||||||
| chr2:11801424 | A | G | 1 | a0001c0004t0010g0081 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1887-1483A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11801424 | |||||||
| chr2:11801520 | G | A | 3 | a0001c0004t0007g0270 a0001c0005t0007g0021 a0001c0005t0007g0022 |
3 | HG01109.hp2 HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1887-1387G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11801520 | |||||||
| chr2:11801535 | T | C | 1 | a0001c0001t0025g0107 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1887-1372T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11801535 | |||||||
| chr2:11801563 | G | C | 1 | a0001c0001t0001g0145 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1887-1344G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11801563 | |||||||
| chr2:11801571 | G | C | 1 | a0001c0001t0001g0201 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1887-1336G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11801571 | |||||||
| chr2:11801681 | G | A | 5 | a0001c0008t0005g0006 a0001c0008t0005g0007 a0002c0007t0011g0029 others(2): Show |
5 | HG01167.hp2 HG02055.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1887-1226G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11801681 | |||||||
| chr2:11801863 | A | G | 47 | a0001c0001t0001g0190 a0001c0001t0002g0071 a0001c0001t0002g0073 others(44): Show |
47 | HG00733.hp1 HG00733.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.1887-1044A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11801863 | |||||||
| chr2:11802121 | AG | A | 3 | a0001c0005t0007g0153 a0001c0005t0007g0156 a0001c0005t0007g0159 |
3 | HG02258.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1887-784delG | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr2 | 11802121 | ||||||
| chr2:11802123 | G | T | 3 | a0001c0005t0007g0153 a0001c0005t0007g0156 a0001c0005t0007g0159 |
3 | HG02258.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1887-784G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11802123 | |||||||
| chr2:11802124 | C | A | 3 | a0001c0005t0007g0153 a0001c0005t0007g0156 a0001c0005t0007g0159 |
3 | HG02258.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1887-783C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11802124 | |||||||
| chr2:11802125 | A | G | 3 | a0001c0005t0007g0153 a0001c0005t0007g0156 a0001c0005t0007g0159 |
3 | HG02258.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1887-782A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11802125 | |||||||
| chr2:11802127 | T | G | 3 | a0001c0005t0007g0153 a0001c0005t0007g0156 a0001c0005t0007g0159 |
3 | HG02258.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1887-780T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11802127 | |||||||
| chr2:11802128 | T | G | 3 | a0001c0005t0007g0153 a0001c0005t0007g0156 a0001c0005t0007g0159 |
3 | HG02258.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1887-779T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11802128 | |||||||
| chr2:11802240 | A | G | 10 | a0001c0001t0002g0071 a0001c0001t0006g0039 a0001c0001t0006g0041 others(7): Show |
10 | HG01261.hp1 HG01891.hp1 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.1887-667A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11802240 | |||||||
| chr2:11802354 | G | A | 3 | a0001c0001t0006g0059 a0001c0002t0006g0155 a0001c0002t0006g0157 |
3 | HG02559.hp1 HG02615.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1887-553G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11802354 | |||||||
| chr2:11802365 | T | C | 5 | a0001c0001t0001g0190 a0001c0001t0005g0074 a0001c0001t0007g0112 others(2): Show |
5 | HG00735.hp1 HG01258.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.1887-542T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11802365 | |||||||
| chr2:11802593 | T | A | 1 | a0001c0001t0003g0225 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1887-314T>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 14/20 | chr2 | 11802593 | |||||||
| chr2:11803154 | C | A | 3 | a0001c0005t0007g0153 a0001c0005t0007g0156 a0001c0005t0007g0159 |
3 | HG02258.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2013+121C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 15/20 | chr2 | 11803154 | |||||||
| chr2:11803181 | T | C | 4 | a0001c0004t0010g0008 a0001c0004t0010g0009 a0001c0004t0010g0078 others(1): Show |
4 | HG01934.hp1 HG02257.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2013+148T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 15/20 | chr2 | 11803181 | |||||||
| chr2:11803236 | G | A | 1 | a0001c0001t0002g0032 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2013+203G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 15/20 | chr2 | 11803236 | |||||||
| chr2:11803249 | G | C | 1 | a0001c0001t0004g0129 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2013+216G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 15/20 | chr2 | 11803249 | |||||||
| chr2:11803387 | T | C | 2 | a0001c0001t0001g0004 a0001c0001t0001g0240 |
3 | NA18963.hp1 NA18978.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.2013+354T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 15/20 | chr2 | 11803387 | |||||||
| chr2:11803607 | T | C | 2 | a0001c0008t0005g0006 a0001c0008t0005g0007 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2013+574T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 15/20 | chr2 | 11803607 | |||||||
| chr2:11803657 | A | G | 1 | a0001c0001t0003g0082 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2013+624A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 15/20 | chr2 | 11803657 | |||||||
| chr2:11803941 | AT | A | 7 | a0001c0001t0002g0064 a0001c0001t0002g0067 a0001c0001t0002g0068 others(4): Show |
7 | HG02559.hp2 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.2014-480delT | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr2 | 11803941 | ||||||
| chr2:11804197 | A | G | 1 | a0001c0011t0015g0077 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2014-226A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 15/20 | chr2 | 11804197 | |||||||
| chr2:11804206 | A | G | 3 | a0001c0005t0007g0153 a0001c0005t0007g0156 a0001c0005t0007g0159 |
3 | HG02258.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2014-217A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 15/20 | chr2 | 11804206 | |||||||
| chr2:11804610 | T | C | 5 | a0001c0004t0006g0076 a0001c0004t0010g0008 a0001c0004t0010g0009 others(2): Show |
5 | HG01934.hp1 HG02055.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.2162+39T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 16/20 | chr2 | 11804610 | |||||||
| chr2:11804620 | TG | T | 81 | a0001c0001t0001g0177 a0001c0001t0002g0071 a0001c0001t0002g0073 others(78): Show |
81 | HG00423.hp1 HG00558.hp2 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.2162+54delG | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 11804620 | ||||||
| chr2:11804655 | C | G | 2 | a0001c0008t0005g0006 a0001c0008t0005g0007 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2162+84C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 16/20 | chr2 | 11804655 | |||||||
| chr2:11804782 | G | A | 1 | a0001c0002t0002g0020 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2162+211G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 16/20 | chr2 | 11804782 | |||||||
| chr2:11804830 | C | A | 1 | a0001c0001t0007g0172 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2163-240C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 16/20 | chr2 | 11804830 | |||||||
| chr2:11804982 | G | GT | 7 | a0001c0001t0001g0127 a0001c0001t0001g0171 a0001c0001t0002g0073 others(4): Show |
7 | HG02735.hp2 HG03098.hp2 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.2163-72dupT | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 11804982 | ||||||
| chr2:11804982 | G | GTT | 5 | a0001c0001t0004g0150 a0001c0001t0004g0152 a0001c0004t0007g0270 others(2): Show |
5 | HG01109.hp2 HG02970.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.2163-73_2163-72dup others(2): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr2 | 11804982 | ||||||
| chr2:11804985 | T | G | 2 | a0001c0002t0015g0154 a0001c0002t0015g0158 |
2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.2163-85T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 16/20 | chr2 | 11804985 | |||||||
| chr2:11805369 | A | C | 1 | a0003c0006t0032g0132 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2249+213A>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11805369 | |||||||
| chr2:11805374 | C | T | 3 | a0001c0001t0002g0071 a0001c0001t0010g0075 a0001c0001t0010g0080 |
3 | HG01261.hp1 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2249+218C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11805374 | |||||||
| chr2:11805407 | C | A | 53 | a0001c0001t0001g0177 a0001c0001t0002g0194 a0001c0001t0003g0036 others(50): Show |
53 | HG00423.hp1 HG00558.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.2249+251C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11805407 | |||||||
| chr2:11805603 | T | C | 2 | a0001c0001t0010g0024 a0001c0001t0026g0038 |
2 | HG01109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2249+447T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11805603 | |||||||
| chr2:11805713 | G | C | 3 | a0001c0001t0006g0040 a0001c0001t0006g0083 a0001c0001t0028g0084 |
3 | HG02109.hp2 HG02897.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2249+557G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11805713 | |||||||
| chr2:11806004 | C | T | 18 | a0001c0001t0001g0136 a0001c0001t0001g0148 a0001c0001t0001g0184 others(15): Show |
19 | HG00673.hp2 HG02015.hp1 HG02056.hp1 others(16): Show |
intron_variant | MODIFIER | c.2249+848C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11806004 | |||||||
| chr2:11806009 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2249+853A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11806009 | |||||||
| chr2:11806011 | A | T | 3 | a0001c0001t0002g0071 a0001c0001t0010g0075 a0001c0001t0010g0080 |
3 | HG01261.hp1 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2249+855A>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11806011 | |||||||
| chr2:11806644 | T | G | 5 | a0001c0004t0006g0076 a0001c0004t0010g0008 a0001c0004t0010g0009 others(2): Show |
5 | HG01934.hp1 HG02055.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.2249+1488T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11806644 | |||||||
| chr2:11806660 | A | G | 5 | a0001c0001t0002g0071 a0001c0001t0010g0024 a0001c0001t0010g0075 others(2): Show |
5 | HG01109.hp1 HG01261.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2249+1504A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11806660 | |||||||
| chr2:11806678 | A | C | 1 | a0001c0001t0003g0015 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2249+1522A>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11806678 | |||||||
| chr2:11806685 | A | T | 1 | a0001c0001t0003g0015 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2249+1529A>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11806685 | |||||||
| chr2:11806863 | T | C | 3 | a0001c0004t0007g0270 a0001c0005t0007g0021 a0001c0005t0007g0022 |
3 | HG01109.hp2 HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2249+1707T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11806863 | |||||||
| chr2:11806878 | A | G | 1 | a0001c0001t0003g0082 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2249+1722A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11806878 | |||||||
| chr2:11806908 | A | G | 4 | a0001c0001t0003g0082 a0001c0001t0008g0048 a0001c0001t0008g0049 others(1): Show |
4 | HG02451.hp1 HG02486.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2249+1752A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11806908 | |||||||
| chr2:11807012 | T | C | 4 | a0001c0001t0003g0082 a0001c0001t0008g0048 a0001c0001t0008g0049 others(1): Show |
4 | HG02451.hp1 HG02486.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2249+1856T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11807012 | |||||||
| chr2:11807064 | C | A | 2 | a0001c0001t0006g0083 a0001c0001t0028g0084 |
2 | HG02897.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2249+1908C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11807064 | |||||||
| chr2:11807077 | T | C | 83 | a0001c0001t0001g0177 a0001c0001t0002g0071 a0001c0001t0002g0073 others(80): Show |
83 | HG00423.hp1 HG00558.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.2249+1921T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11807077 | |||||||
| chr2:11807106 | T | C | 1 | a0001c0001t0003g0082 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2249+1950T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11807106 | |||||||
| chr2:11807156 | T | C | 2 | a0001c0002t0002g0018 a0001c0002t0003g0019 |
2 | HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2249+2000T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11807156 | |||||||
| chr2:11807274 | T | C | 57 | a0001c0001t0001g0177 a0001c0001t0002g0194 a0001c0001t0003g0015 others(54): Show |
57 | HG00423.hp1 HG00558.hp2 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.2249+2118T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11807274 | |||||||
| chr2:11807306 | G | A | 3 | a0001c0001t0003g0087 a0001c0001t0005g0079 a0001c0002t0030g0011 |
3 | HG02280.hp2 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2249+2150G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11807306 | |||||||
| chr2:11807512 | A | AT | 16 | a0001c0001t0002g0164 a0001c0001t0002g0245 a0001c0001t0004g0103 others(13): Show |
16 | HG00733.hp1 HG00733.hp2 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.2249+2372dupT | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr2 | 11807512 | ||||||
| chr2:11807928 | T | C | 1 | a0001c0001t0004g0121 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2249+2772T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11807928 | |||||||
| chr2:11808059 | C | T | 3 | a0001c0001t0002g0071 a0001c0001t0010g0075 a0001c0001t0010g0080 |
3 | HG01261.hp1 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2249+2903C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11808059 | |||||||
| chr2:11808120 | A | C | 2 | a0001c0001t0017g0065 a0001c0001t0017g0066 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2249+2964A>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11808120 | |||||||
| chr2:11808245 | A | G | 1 | a0001c0001t0012g0113 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2249+3089A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11808245 | |||||||
| chr2:11808256 | C | G | 2 | a0001c0001t0003g0170 a0001c0001t0016g0105 |
2 | HG02080.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.2249+3100C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11808256 | |||||||
| chr2:11808276 | G | T | 1 | a0001c0001t0003g0140 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2249+3120G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11808276 | |||||||
| chr2:11808299 | G | T | 1 | a0001c0001t0001g0246 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2249+3143G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11808299 | |||||||
| chr2:11808334 | G | A | 1 | a0001c0001t0004g0208 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2249+3178G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11808334 | |||||||
| chr2:11808586 | A | G | 2 | a0001c0008t0005g0006 a0001c0008t0005g0007 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2249+3430A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11808586 | |||||||
| chr2:11808639 | C | T | 14 | a0001c0001t0004g0200 a0001c0001t0004g0244 a0001c0001t0009g0125 others(11): Show |
14 | HG00733.hp1 HG00733.hp2 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.2249+3483C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11808639 | |||||||
| chr2:11808707 | C | A | 1 | a0001c0011t0015g0077 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2249+3551C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11808707 | |||||||
| chr2:11808749 | C | T | 1 | a0001c0001t0003g0082 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2249+3593C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11808749 | |||||||
| chr2:11808870 | C | CA | 13 | a0001c0001t0001g0058 a0001c0001t0002g0071 a0001c0001t0002g0137 others(10): Show |
13 | HG01261.hp1 HG02040.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.2249+3730dupA | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr2 | 11808870 | ||||||
| chr2:11808870 | C | CAA | 6 | a0001c0001t0010g0024 a0001c0004t0006g0076 a0001c0004t0010g0008 others(3): Show |
6 | HG01109.hp1 HG01934.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.2249+3729_2249+373 others(6): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr2 | 11808870 | ||||||
| chr2:11808884 | AAAG | A | 13 | a0001c0001t0004g0200 a0001c0001t0004g0244 a0001c0001t0009g0125 others(10): Show |
13 | HG00733.hp1 HG00733.hp2 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.2249+3730_2249+373 others(7): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr2 | 11808884 | ||||||
| chr2:11809137 | C | CAAAACTA others(1260): Show |
7 | a0001c0001t0005g0093 a0001c0001t0008g0002 a0001c0001t0008g0010 others(4): Show |
7 | HG01257.hp1 HG01258.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.2249+3999_2249+400 others(1271): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr2 | 11809137 | ||||||
| chr2:11809137 | C | CAAAACTA others(1259): Show |
1 | a0001c0001t0005g0074 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2249+3999_2249+400 others(1270): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr2 | 11809137 | ||||||
| chr2:11809137 | C | CAAAACTA others(1259): Show |
1 | a0001c0011t0015g0077 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2249+3999_2249+400 others(1270): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr2 | 11809137 | ||||||
| chr2:11809137 | C | CAAAACTA others(1259): Show |
3 | a0001c0001t0002g0073 a0001c0001t0008g0042 a0001c0001t0008g0047 |
3 | HG00639.hp2 HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2249+3999_2249+400 others(1270): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr2 | 11809137 | ||||||
| chr2:11809312 | A | T | 1 | a0001c0001t0002g0210 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2249+4156A>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11809312 | |||||||
| chr2:11809331 | G | C | 25 | a0001c0001t0002g0071 a0001c0001t0003g0015 a0001c0001t0004g0200 others(22): Show |
25 | HG00733.hp1 HG00733.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.2249+4175G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11809331 | |||||||
| chr2:11809422 | C | CT | 8 | a0001c0002t0002g0018 a0001c0002t0003g0019 a0001c0004t0007g0270 others(5): Show |
8 | HG01109.hp2 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.2249+4276dupT | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr2 | 11809422 | ||||||
| chr2:11809519 | C | A | 2 | a0001c0001t0008g0042 a0001c0001t0008g0047 |
2 | HG00639.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2249+4363C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11809519 | |||||||
| chr2:11809703 | A | C | 5 | a0001c0004t0006g0076 a0001c0004t0010g0008 a0001c0004t0010g0009 others(2): Show |
5 | HG01934.hp1 HG02055.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.2249+4547A>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11809703 | |||||||
| chr2:11809743 | G | A | 1 | a0001c0003t0009g0053 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2249+4587G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11809743 | |||||||
| chr2:11809909 | A | T | 1 | a0001c0001t0003g0015 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2249+4753A>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11809909 | |||||||
| chr2:11810216 | A | G | 270 | a0001c0001t0001g0004 a0001c0001t0001g0030 a0001c0001t0001g0058 others(267): Show |
274 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.2250-4872A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11810216 | |||||||
| chr2:11810369 | A | G | 2 | a0001c0001t0002g0215 a0001c0001t0002g0236 |
2 | NA18997.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.2250-4719A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11810369 | |||||||
| chr2:11810385 | GA | G | 14 | a0001c0001t0004g0200 a0001c0001t0004g0244 a0001c0001t0009g0125 others(11): Show |
14 | HG00733.hp1 HG00733.hp2 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.2250-4702delA | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11810385 | |||||||
| chr2:11810387 | G | C | 1 | a0001c0001t0001g0201 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2250-4701G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11810387 | |||||||
| chr2:11810516 | G | A | 2 | a0001c0001t0017g0065 a0001c0001t0017g0066 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2250-4572G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11810516 | |||||||
| chr2:11810588 | A | T | 1 | a0001c0001t0002g0100 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2250-4500A>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11810588 | |||||||
| chr2:11810630 | G | T | 21 | a0001c0001t0002g0073 a0001c0001t0005g0074 a0001c0001t0005g0093 others(18): Show |
21 | HG00639.hp2 HG01109.hp2 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.2250-4458G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11810630 | |||||||
| chr2:11810717 | C | G | 1 | a0001c0001t0002g0175 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2250-4371C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11810717 | |||||||
| chr2:11810872 | C | T | 1 | a0001c0001t0004g0151 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2250-4216C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11810872 | |||||||
| chr2:11811227 | A | G | 1 | a0001c0001t0001g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2250-3861A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11811227 | |||||||
| chr2:11811324 | G | A | 14 | a0001c0001t0004g0200 a0001c0001t0004g0244 a0001c0001t0009g0125 others(11): Show |
14 | HG00733.hp1 HG00733.hp2 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.2250-3764G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11811324 | |||||||
| chr2:11811420 | A | T | 1 | a0004c0012t0001g0178 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2250-3668A>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11811420 | |||||||
| chr2:11811502 | C | T | 3 | a0001c0001t0008g0048 a0001c0001t0008g0049 a0002c0009t0002g0051 |
3 | HG02486.hp2 HG03209.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2250-3586C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11811502 | |||||||
| chr2:11811507 | A | G | 1 | a0001c0001t0005g0074 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2250-3581A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11811507 | |||||||
| chr2:11811539 | A | G | 1 | a0001c0001t0026g0038 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2250-3549A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11811539 | |||||||
| chr2:11811593 | C | A | 1 | a0001c0001t0003g0106 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2250-3495C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11811593 | |||||||
| chr2:11811841 | T | C | 95 | a0001c0001t0001g0030 a0001c0001t0001g0177 a0001c0001t0001g0190 others(92): Show |
95 | HG00423.hp1 HG00558.hp2 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.2250-3247T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11811841 | |||||||
| chr2:11811899 | C | T | 3 | a0001c0001t0004g0230 a0001c0001t0004g0231 a0001c0001t0004g0232 |
3 | NA18983.hp1 NA19005.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.2250-3189C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11811899 | |||||||
| chr2:11811941 | T | C | 5 | a0001c0001t0002g0073 a0001c0001t0003g0234 a0001c0001t0005g0074 others(2): Show |
5 | HG00639.hp2 HG03098.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.2250-3147T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11811941 | |||||||
| chr2:11811970 | C | T | 4 | a0001c0004t0010g0008 a0001c0004t0010g0009 a0001c0004t0010g0078 others(1): Show |
4 | HG01934.hp1 HG02257.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2250-3118C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11811970 | |||||||
| chr2:11812253 | G | GT | 11 | a0001c0001t0003g0036 a0001c0001t0003g0037 a0001c0001t0003g0050 others(8): Show |
11 | HG01496.hp2 HG02109.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.2250-2830dupT | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr2 | 11812253 | ||||||
| chr2:11812255 | T | A | 11 | a0001c0001t0001g0110 a0001c0001t0001g0127 a0001c0001t0004g0096 others(8): Show |
11 | NA18943.hp1 NA18943.hp2 NA18960.hp1 others(8): Show |
intron_variant | MODIFIER | c.2250-2833T>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11812255 | |||||||
| chr2:11812263 | C | T | 1 | a0001c0001t0012g0070 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2250-2825C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11812263 | |||||||
| chr2:11812444 | G | T | 1 | a0001c0001t0001g0224 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2250-2644G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11812444 | |||||||
| chr2:11812496 | A | T | 40 | a0001c0001t0001g0184 a0001c0001t0001g0224 a0001c0001t0002g0194 others(37): Show |
40 | HG00423.hp1 HG00558.hp2 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.2250-2592A>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11812496 | |||||||
| chr2:11812610 | G | A | 1 | a0001c0001t0001g0148 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2250-2478G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11812610 | |||||||
| chr2:11812711 | T | C | 3 | a0001c0002t0015g0154 a0001c0002t0015g0158 a0001c0011t0015g0077 |
3 | HG02622.hp2 HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2250-2377T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11812711 | |||||||
| chr2:11812787 | C | T | 6 | a0001c0001t0002g0071 a0001c0001t0003g0087 a0001c0001t0005g0079 others(3): Show |
6 | HG02280.hp2 HG02886.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.2250-2301C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11812787 | |||||||
| chr2:11812807 | C | T | 1 | a0001c0001t0009g0227 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2250-2281C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11812807 | |||||||
| chr2:11812939 | G | C | 2 | a0001c0001t0001g0254 a0001c0001t0002g0131 |
2 | HG01099.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.2250-2149G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11812939 | |||||||
| chr2:11812979 | G | A | 2 | a0001c0003t0001g0052 a0001c0003t0014g0089 |
2 | HG00733.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.2250-2109G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11812979 | |||||||
| chr2:11813172 | G | A | 2 | a0001c0001t0002g0100 a0001c0003t0002g0091 |
2 | HG00099.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.2250-1916G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11813172 | |||||||
| chr2:11813195 | A | G | 31 | a0001c0001t0002g0194 a0001c0001t0003g0036 a0001c0001t0003g0037 others(28): Show |
31 | HG00423.hp1 HG00558.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.2250-1893A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11813195 | |||||||
| chr2:11813281 | G | C | 1 | a0001c0001t0001g0109 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2250-1807G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11813281 | |||||||
| chr2:11813302 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2250-1786C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11813302 | |||||||
| chr2:11813416 | C | T | 1 | a0001c0001t0002g0215 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2250-1672C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11813416 | |||||||
| chr2:11813461 | C | T | 2 | a0001c0001t0005g0074 a0001c0001t0005g0093 |
2 | HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2250-1627C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11813461 | |||||||
| chr2:11813771 | C | T | 3 | a0001c0005t0007g0153 a0001c0005t0007g0156 a0001c0005t0007g0159 |
3 | HG02258.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2250-1317C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11813771 | |||||||
| chr2:11813774 | C | T | 5 | a0001c0001t0018g0035 a0001c0003t0009g0053 a0001c0003t0009g0054 others(2): Show |
5 | HG00738.hp1 HG01081.hp1 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.2250-1314C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11813774 | |||||||
| chr2:11813873 | C | T | 3 | a0002c0007t0011g0029 a0002c0007t0034g0027 a0002c0007t0035g0028 |
3 | HG01167.hp2 HG02055.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2250-1215C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11813873 | |||||||
| chr2:11814057 | G | T | 30 | a0001c0001t0003g0036 a0001c0001t0003g0037 a0001c0001t0003g0044 others(27): Show |
30 | HG00423.hp1 HG00558.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.2250-1031G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11814057 | |||||||
| chr2:11814243 | C | T | 2 | a0001c0001t0005g0074 a0001c0001t0005g0093 |
2 | HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2250-845C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11814243 | |||||||
| chr2:11814244 | G | A | 2 | a0001c0001t0005g0074 a0001c0001t0005g0093 |
2 | HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2250-844G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11814244 | |||||||
| chr2:11814372 | A | G | 77 | a0001c0001t0002g0071 a0001c0001t0003g0015 a0001c0001t0003g0036 others(74): Show |
77 | HG00423.hp1 HG00558.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.2250-716A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11814372 | |||||||
| chr2:11814511 | C | T | 1 | a0001c0001t0002g0149 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2250-577C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11814511 | |||||||
| chr2:11814512 | A | ATG | 35 | a0001c0001t0001g0110 a0001c0001t0001g0165 a0001c0001t0001g0173 others(32): Show |
35 | HG00738.hp1 HG01069.hp2 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.2250-539_2250-538d others(4): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr2 | 11814512 | ||||||
| chr2:11814512 | A | ATGTG | 60 | a0001c0001t0001g0004 a0001c0001t0001g0058 a0001c0001t0001g0098 others(57): Show |
61 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.2250-541_2250-538d others(6): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr2 | 11814512 | ||||||
| chr2:11814512 | A | ATGTGTG | 6 | a0001c0001t0001g0145 a0001c0001t0008g0042 a0001c0001t0013g0135 others(3): Show |
6 | HG00639.hp2 HG02523.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.2250-543_2250-538d others(8): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr2 | 11814512 | ||||||
| chr2:11814512 | A | ATGTGTGT others(1): Show |
5 | a0001c0001t0002g0236 a0001c0004t0006g0076 a0001c0004t0007g0270 others(2): Show |
5 | HG01109.hp2 HG02055.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.2250-545_2250-538d others(10): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr2 | 11814512 | ||||||
| chr2:11814512 | A | G | 2 | a0001c0001t0002g0149 a0001c0001t0027g0142 |
2 | HG02145.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.2250-576A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11814512 | |||||||
| chr2:11814512 | ATG | A | 33 | a0001c0001t0001g0127 a0001c0001t0002g0057 a0001c0001t0002g0104 others(30): Show |
34 | HG00609.hp2 HG00673.hp1 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.2250-539_2250-538d others(4): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr2 | 11814512 | ||||||
| chr2:11814512 | ATGTG | A | 10 | a0001c0001t0001g0239 a0001c0001t0001g0243 a0001c0001t0002g0194 others(7): Show |
10 | HG01081.hp2 HG01496.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.2250-541_2250-538d others(6): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr2 | 11814512 | ||||||
| chr2:11814512 | ATGTGTG | A | 3 | a0001c0001t0010g0024 a0001c0001t0010g0075 a0001c0001t0010g0080 |
3 | HG01109.hp1 HG01261.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2250-543_2250-538d others(8): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr2 | 11814512 | ||||||
| chr2:11814567 | TTGTTTTA others(16): Show |
T | 1 | a0002c0010t0005g0012 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2250-519_2250-497d others(25): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr2 | 11814567 | ||||||
| chr2:11814732 | G | A | 2 | a0001c0001t0008g0048 a0001c0001t0008g0049 |
2 | HG02486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2250-356G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11814732 | |||||||
| chr2:11814816 | T | C | 23 | a0001c0001t0003g0015 a0001c0001t0008g0002 a0001c0001t0008g0010 others(20): Show |
23 | HG00639.hp2 HG00738.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.2250-272T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11814816 | |||||||
| chr2:11815014 | T | C | 11 | a0001c0001t0008g0002 a0001c0001t0008g0010 a0001c0001t0008g0023 others(8): Show |
11 | HG00639.hp2 HG01257.hp1 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2250-74T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 17/20 | chr2 | 11815014 | |||||||
| chr2:11815334 | G | A | 3 | a0001c0001t0002g0236 a0001c0001t0013g0179 a0001c0001t0013g0197 |
3 | NA18991.hp2 NA18997.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.2402+94G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11815334 | |||||||
| chr2:11815477 | C | T | 5 | a0001c0001t0002g0057 a0001c0001t0002g0160 a0001c0001t0011g0001 others(2): Show |
6 | HG01261.hp2 HG01981.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.2402+237C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11815477 | |||||||
| chr2:11815576 | C | T | 2 | a0001c0003t0001g0052 a0001c0003t0014g0089 |
2 | HG00733.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.2402+336C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11815576 | |||||||
| chr2:11815741 | A | G | 2 | a0001c0001t0005g0074 a0001c0001t0005g0093 |
2 | HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2402+501A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11815741 | |||||||
| chr2:11815786 | C | G | 1 | a0001c0001t0001g0201 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2402+546C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11815786 | |||||||
| chr2:11815906 | G | A | 1 | a0001c0001t0002g0215 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2402+666G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11815906 | |||||||
| chr2:11816120 | T | G | 3 | a0001c0002t0015g0154 a0001c0002t0015g0158 a0001c0011t0015g0077 |
3 | HG02622.hp2 HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2402+880T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11816120 | |||||||
| chr2:11816205 | C | T | 1 | a0001c0001t0002g0068 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2402+965C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11816205 | |||||||
| chr2:11816251 | C | T | 1 | a0001c0001t0020g0126 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2402+1011C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11816251 | |||||||
| chr2:11816261 | G | T | 5 | a0001c0001t0002g0064 a0001c0001t0002g0067 a0001c0001t0002g0068 others(2): Show |
5 | HG02559.hp2 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.2402+1021G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11816261 | |||||||
| chr2:11816392 | T | C | 30 | a0001c0001t0003g0036 a0001c0001t0003g0037 a0001c0001t0003g0044 others(27): Show |
30 | HG00423.hp1 HG00558.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.2402+1152T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11816392 | |||||||
| chr2:11816619 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2402+1379A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11816619 | |||||||
| chr2:11816629 | C | T | 6 | a0001c0001t0002g0071 a0001c0001t0003g0087 a0001c0001t0005g0079 others(3): Show |
6 | HG02280.hp2 HG02886.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.2402+1389C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11816629 | |||||||
| chr2:11816741 | C | CT | 8 | a0001c0001t0007g0112 a0001c0001t0007g0172 a0001c0001t0007g0219 others(5): Show |
8 | HG00735.hp1 HG01258.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.2402+1519dupT | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr2 | 11816741 | ||||||
| chr2:11816741 | CT | C | 47 | a0001c0001t0001g0243 a0001c0001t0001g0251 a0001c0001t0001g0269 others(44): Show |
47 | HG00423.hp1 HG00558.hp2 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.2402+1519delT | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr2 | 11816741 | ||||||
| chr2:11816749 | T | C | 30 | a0001c0001t0003g0036 a0001c0001t0003g0037 a0001c0001t0003g0044 others(27): Show |
30 | HG00423.hp1 HG00558.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.2402+1509T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11816749 | |||||||
| chr2:11816829 | T | C | 3 | a0001c0005t0007g0153 a0001c0005t0007g0156 a0001c0005t0007g0159 |
3 | HG02258.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2402+1589T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11816829 | |||||||
| chr2:11816920 | C | A | 6 | a0001c0001t0008g0048 a0001c0001t0008g0049 a0001c0002t0015g0154 others(3): Show |
6 | HG02486.hp2 HG02622.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.2402+1680C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11816920 | |||||||
| chr2:11816920 | C | G | 8 | a0001c0001t0009g0125 a0001c0001t0009g0227 a0001c0001t0018g0035 others(5): Show |
8 | HG00738.hp1 HG01081.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.2402+1680C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11816920 | |||||||
| chr2:11816921 | C | A | 31 | a0001c0001t0003g0036 a0001c0001t0003g0037 a0001c0001t0003g0044 others(28): Show |
31 | HG00423.hp1 HG00558.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.2402+1681C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11816921 | |||||||
| chr2:11817090 | A | G | 1 | a0001c0001t0010g0024 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2402+1850A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11817090 | |||||||
| chr2:11817092 | G | C | 2 | a0001c0001t0013g0179 a0001c0001t0013g0197 |
2 | NA18991.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.2402+1852G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11817092 | |||||||
| chr2:11817144 | A | G | 24 | a0001c0001t0001g0256 a0001c0001t0002g0144 a0001c0001t0002g0210 others(21): Show |
24 | HG00423.hp1 HG00558.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.2402+1904A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11817144 | |||||||
| chr2:11817187 | C | T | 1 | a0002c0009t0002g0051 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2402+1947C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11817187 | |||||||
| chr2:11817586 | A | AT | 13 | a0001c0001t0005g0046 a0001c0001t0006g0039 a0001c0001t0006g0040 others(10): Show |
13 | HG01175.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.2403-1888dupT | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr2 | 11817586 | ||||||
| chr2:11817628 | T | C | 3 | a0001c0001t0010g0024 a0001c0001t0010g0075 a0001c0001t0010g0080 |
3 | HG01109.hp1 HG01261.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2403-1856T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11817628 | |||||||
| chr2:11817643 | G | T | 8 | a0001c0001t0009g0125 a0001c0001t0009g0227 a0001c0001t0018g0035 others(5): Show |
8 | HG00738.hp1 HG01081.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.2403-1841G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11817643 | |||||||
| chr2:11817655 | C | T | 3 | a0001c0001t0003g0036 a0001c0002t0003g0013 a0001c0002t0003g0014 |
3 | HG02109.hp1 HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2403-1829C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11817655 | |||||||
| chr2:11817696 | A | G | 5 | a0001c0001t0010g0024 a0001c0001t0010g0075 a0001c0001t0010g0080 others(2): Show |
5 | HG01109.hp1 HG01261.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.2403-1788A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11817696 | |||||||
| chr2:11817704 | T | C | 5 | a0001c0001t0010g0024 a0001c0001t0010g0075 a0001c0001t0010g0080 others(2): Show |
5 | HG01109.hp1 HG01261.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.2403-1780T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11817704 | |||||||
| chr2:11817730 | C | T | 3 | a0001c0002t0015g0154 a0001c0002t0015g0158 a0001c0011t0015g0077 |
3 | HG02622.hp2 HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2403-1754C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11817730 | |||||||
| chr2:11817760 | G | C | 123 | a0001c0001t0002g0003 a0001c0001t0002g0100 a0001c0001t0002g0114 others(120): Show |
124 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.2403-1724G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11817760 | |||||||
| chr2:11817797 | A | G | 7 | a0001c0001t0010g0024 a0001c0001t0010g0075 a0001c0001t0010g0080 others(4): Show |
7 | HG01109.hp1 HG01261.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.2403-1687A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11817797 | |||||||
| chr2:11817803 | CTGTAG | C | 7 | a0001c0001t0010g0024 a0001c0001t0010g0075 a0001c0001t0010g0080 others(4): Show |
7 | HG01109.hp1 HG01261.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.2403-1674_2403-167 others(9): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr2 | 11817803 | ||||||
| chr2:11817919 | A | G | 100 | a0001c0001t0003g0015 a0001c0001t0003g0036 a0001c0001t0003g0037 others(97): Show |
100 | HG00423.hp1 HG00558.hp2 HG00639.hp1 others(97): Show |
intron_variant | MODIFIER | c.2403-1565A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11817919 | |||||||
| chr2:11817926 | T | C | 1 | a0001c0001t0005g0273 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2403-1558T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11817926 | |||||||
| chr2:11817929 | CTCAAAAA others(2): Show |
C | 7 | a0001c0001t0010g0024 a0001c0001t0010g0075 a0001c0001t0010g0080 others(4): Show |
7 | HG01109.hp1 HG01261.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.2403-1554_2403-154 others(13): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11817929 | |||||||
| chr2:11817931 | C | CA | 60 | a0001c0001t0001g0109 a0001c0001t0001g0141 a0001c0001t0001g0148 others(57): Show |
60 | HG00423.hp2 HG00609.hp1 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.2403-1524dupA | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr2 | 11817931 | ||||||
| chr2:11817931 | C | CAA | 8 | a0001c0001t0005g0273 a0001c0001t0006g0041 a0001c0001t0008g0010 others(5): Show |
8 | HG01433.hp2 HG01891.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.2403-1525_2403-152 others(6): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr2 | 11817931 | ||||||
| chr2:11817931 | CA | C | 29 | a0001c0001t0001g0251 a0001c0001t0002g0032 a0001c0001t0002g0064 others(26): Show |
29 | HG00423.hp1 HG00558.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.2403-1524delA | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr2 | 11817931 | ||||||
| chr2:11817931 | CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0005g0074 a0001c0001t0005g0093 |
2 | HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2403-1533_2403-152 others(14): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr2 | 11817931 | ||||||
| chr2:11817931 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0005g0097 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2403-1534_2403-152 others(15): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr2 | 11817931 | ||||||
| chr2:11818021 | C | T | 1 | a0001c0001t0002g0031 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2403-1463C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11818021 | |||||||
| chr2:11818022 | G | A | 3 | a0001c0001t0017g0065 a0001c0001t0017g0066 a0002c0009t0002g0051 |
3 | HG02896.hp1 HG02897.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2403-1462G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11818022 | |||||||
| chr2:11818067 | G | A | 8 | a0001c0001t0009g0125 a0001c0001t0009g0227 a0001c0001t0018g0035 others(5): Show |
8 | HG00738.hp1 HG01081.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.2403-1417G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11818067 | |||||||
| chr2:11818128 | C | T | 3 | a0001c0001t0004g0230 a0001c0001t0004g0231 a0001c0001t0004g0232 |
3 | NA18983.hp1 NA19005.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.2403-1356C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11818128 | |||||||
| chr2:11818195 | A | G | 12 | a0001c0001t0006g0039 a0001c0001t0006g0040 a0001c0001t0006g0041 others(9): Show |
12 | HG01175.hp2 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.2403-1289A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11818195 | |||||||
| chr2:11818197 | C | G | 2 | a0001c0001t0017g0065 a0001c0001t0017g0066 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2403-1287C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11818197 | |||||||
| chr2:11818213 | C | A | 6 | a0001c0001t0005g0273 a0001c0002t0015g0154 a0001c0002t0015g0158 others(3): Show |
6 | HG02622.hp2 HG02630.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2403-1271C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11818213 | |||||||
| chr2:11818451 | A | T | 8 | a0001c0001t0009g0125 a0001c0001t0009g0227 a0001c0001t0018g0035 others(5): Show |
8 | HG00738.hp1 HG01081.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.2403-1033A>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11818451 | |||||||
| chr2:11818495 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2403-989C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11818495 | |||||||
| chr2:11818510 | CT | C | 14 | a0001c0001t0003g0082 a0001c0001t0007g0112 a0001c0001t0007g0172 others(11): Show |
14 | HG00639.hp1 HG00735.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.2403-963delT | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr2 | 11818510 | ||||||
| chr2:11818514 | T | A | 7 | a0001c0001t0010g0024 a0001c0001t0010g0075 a0001c0001t0010g0080 others(4): Show |
7 | HG01109.hp1 HG01261.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.2403-970T>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11818514 | |||||||
| chr2:11818640 | T | C | 2 | a0002c0007t0034g0027 a0002c0007t0035g0028 |
2 | HG02055.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2403-844T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11818640 | |||||||
| chr2:11818644 | G | A | 80 | a0001c0001t0003g0015 a0001c0001t0003g0036 a0001c0001t0003g0037 others(77): Show |
80 | HG00423.hp1 HG00558.hp2 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.2403-840G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11818644 | |||||||
| chr2:11818659 | A | G | 7 | a0001c0001t0010g0024 a0001c0001t0010g0075 a0001c0001t0010g0080 others(4): Show |
7 | HG01109.hp1 HG01261.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.2403-825A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11818659 | |||||||
| chr2:11818674 | A | G | 1 | a0001c0001t0004g0033 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2403-810A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11818674 | |||||||
| chr2:11818807 | C | T | 1 | a0001c0002t0002g0018 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2403-677C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11818807 | |||||||
| chr2:11819043 | T | TAC | 17 | a0001c0001t0001g0145 a0001c0001t0002g0116 a0001c0001t0002g0134 others(14): Show |
17 | HG01070.hp1 HG01071.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.2403-416_2403-415d others(4): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr2 | 11819043 | ||||||
| chr2:11819043 | TAC | T | 43 | a0001c0001t0002g0118 a0001c0001t0003g0015 a0001c0001t0003g0036 others(40): Show |
43 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.2403-416_2403-415d others(4): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr2 | 11819043 | ||||||
| chr2:11819043 | TACAC | T | 27 | a0001c0001t0003g0082 a0001c0001t0003g0106 a0001c0001t0003g0115 others(24): Show |
27 | HG00423.hp1 HG00558.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.2403-418_2403-415d others(6): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr2 | 11819043 | ||||||
| chr2:11819045 | C | A | 2 | a0001c0001t0004g0200 a0001c0001t0004g0244 |
2 | HG00733.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.2403-439C>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11819045 | |||||||
| chr2:11819055 | C | T | 1 | a0001c0004t0007g0270 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2403-429C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11819055 | |||||||
| chr2:11819138 | A | G | 39 | a0001c0001t0003g0015 a0001c0001t0003g0036 a0001c0001t0003g0037 others(36): Show |
39 | HG00423.hp1 HG00558.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.2403-346A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11819138 | |||||||
| chr2:11819178 | C | T | 7 | a0001c0001t0010g0024 a0001c0001t0010g0075 a0001c0001t0010g0080 others(4): Show |
7 | HG01109.hp1 HG01261.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.2403-306C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11819178 | |||||||
| chr2:11819184 | G | A | 6 | a0001c0001t0005g0273 a0001c0002t0015g0154 a0001c0002t0015g0158 others(3): Show |
6 | HG02622.hp2 HG02630.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2403-300G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11819184 | |||||||
| chr2:11819256 | C | T | 100 | a0001c0001t0003g0015 a0001c0001t0003g0036 a0001c0001t0003g0037 others(97): Show |
100 | HG00423.hp1 HG00558.hp2 HG00639.hp1 others(97): Show |
intron_variant | MODIFIER | c.2403-228C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11819256 | |||||||
| chr2:11819275 | C | T | 2 | a0001c0001t0005g0046 a0002c0010t0005g0012 |
2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.2403-209C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11819275 | |||||||
| chr2:11819286 | T | C | 2 | a0002c0007t0034g0027 a0002c0007t0035g0028 |
2 | HG02055.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2403-198T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11819286 | |||||||
| chr2:11819363 | A | G | 2 | a0001c0001t0001g0239 a0001c0001t0004g0108 |
2 | NA18940.hp1 NA18940.hp2 |
intron_variant | MODIFIER | c.2403-121A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 18/20 | chr2 | 11819363 | |||||||
| chr2:11819779 | T | C | 100 | a0001c0001t0003g0015 a0001c0001t0003g0036 a0001c0001t0003g0037 others(97): Show |
100 | HG00423.hp1 HG00558.hp2 HG00639.hp1 others(97): Show |
intron_variant | MODIFIER | c.2517+181T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 19/20 | chr2 | 11819779 | |||||||
| chr2:11819803 | G | A | 7 | a0001c0001t0010g0024 a0001c0001t0010g0075 a0001c0001t0010g0080 others(4): Show |
7 | HG01109.hp1 HG01261.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.2517+205G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 19/20 | chr2 | 11819803 | |||||||
| chr2:11819824 | A | G | 24 | a0001c0001t0005g0273 a0001c0001t0008g0002 a0001c0001t0008g0010 others(21): Show |
24 | HG00639.hp2 HG01109.hp1 HG01257.hp1 others(21): Show |
intron_variant | MODIFIER | c.2517+226A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 19/20 | chr2 | 11819824 | |||||||
| chr2:11819857 | A | G | 26 | a0001c0001t0003g0082 a0001c0001t0003g0087 a0001c0001t0003g0106 others(23): Show |
26 | HG00423.hp1 HG00558.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.2517+259A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 19/20 | chr2 | 11819857 | |||||||
| chr2:11819903 | A | G | 6 | a0001c0001t0005g0273 a0001c0002t0015g0154 a0001c0002t0015g0158 others(3): Show |
6 | HG02622.hp2 HG02630.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2517+305A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 19/20 | chr2 | 11819903 | |||||||
| chr2:11819958 | C | T | 1 | a0001c0001t0029g0138 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2517+360C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 19/20 | chr2 | 11819958 | |||||||
| chr2:11819999 | G | A | 1 | a0001c0001t0026g0038 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2517+401G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 19/20 | chr2 | 11819999 | |||||||
| chr2:11820001 | T | G | 2 | a0001c0001t0005g0074 a0001c0001t0005g0093 |
2 | HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2517+403T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 19/20 | chr2 | 11820001 | |||||||
| chr2:11820025 | G | A | 7 | a0001c0001t0010g0024 a0001c0001t0010g0075 a0001c0001t0010g0080 others(4): Show |
7 | HG01109.hp1 HG01261.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.2518-386G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 19/20 | chr2 | 11820025 | |||||||
| chr2:11820107 | C | T | 7 | a0001c0001t0010g0024 a0001c0001t0010g0075 a0001c0001t0010g0080 others(4): Show |
7 | HG01109.hp1 HG01261.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.2518-304C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 19/20 | chr2 | 11820107 | |||||||
| chr2:11820285 | A | G | 3 | a0001c0001t0005g0074 a0001c0001t0005g0093 a0001c0001t0005g0097 |
3 | HG02922.hp2 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2518-126A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 19/20 | chr2 | 11820285 | |||||||
| chr2:11820388 | T | C | 2 | a0001c0001t0003g0146 a0001c0001t0003g0225 |
2 | HG00423.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.2518-23T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 19/20 | chr2 | 11820388 | |||||||
| chr2:11820646 | T | C | 1 | a0001c0001t0026g0038 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2621+132T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11820646 | |||||||
| chr2:11820658 | C | G | 1 | a0001c0001t0001g0238 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2621+144C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11820658 | |||||||
| chr2:11820778 | A | C | 1 | a0001c0001t0010g0075 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2621+264A>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11820778 | |||||||
| chr2:11820783 | G | C | 1 | a0001c0001t0001g0218 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2621+269G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11820783 | |||||||
| chr2:11820983 | C | T | 3 | a0001c0001t0005g0074 a0001c0001t0005g0093 a0001c0001t0005g0097 |
3 | HG02922.hp2 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2621+469C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11820983 | |||||||
| chr2:11821164 | T | G | 6 | a0001c0001t0005g0273 a0001c0002t0015g0154 a0001c0002t0015g0158 others(3): Show |
6 | HG02622.hp2 HG02630.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2621+650T>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11821164 | |||||||
| chr2:11821230 | T | TG | 23 | a0001c0001t0006g0039 a0001c0001t0006g0040 a0001c0001t0006g0041 others(20): Show |
23 | HG00639.hp2 HG01175.hp2 HG01257.hp1 others(20): Show |
intron_variant | MODIFIER | c.2621+718dupG | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr2 | 11821230 | ||||||
| chr2:11821282 | T | C | 7 | a0001c0001t0010g0024 a0001c0001t0010g0075 a0001c0001t0010g0080 others(4): Show |
7 | HG01109.hp1 HG01261.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.2621+768T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11821282 | |||||||
| chr2:11821287 | T | C | 7 | a0001c0001t0010g0024 a0001c0001t0010g0075 a0001c0001t0010g0080 others(4): Show |
7 | HG01109.hp1 HG01261.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.2621+773T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11821287 | |||||||
| chr2:11821288 | G | A | 1 | a0001c0001t0010g0080 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2621+774G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11821288 | |||||||
| chr2:11821314 | C | T | 1 | a0001c0001t0003g0207 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2621+800C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11821314 | |||||||
| chr2:11821385 | T | C | 7 | a0001c0001t0010g0024 a0001c0001t0010g0075 a0001c0001t0010g0080 others(4): Show |
7 | HG01109.hp1 HG01261.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.2621+871T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11821385 | |||||||
| chr2:11821440 | T | C | 7 | a0001c0001t0010g0024 a0001c0001t0010g0075 a0001c0001t0010g0080 others(4): Show |
7 | HG01109.hp1 HG01261.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.2621+926T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11821440 | |||||||
| chr2:11821471 | C | T | 2 | a0001c0001t0008g0042 a0001c0001t0008g0047 |
2 | HG00639.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2621+957C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11821471 | |||||||
| chr2:11821495 | C | T | 3 | a0001c0005t0007g0153 a0001c0005t0007g0156 a0001c0005t0007g0159 |
3 | HG02258.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2621+981C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11821495 | |||||||
| chr2:11821564 | G | T | 36 | a0001c0001t0003g0015 a0001c0001t0003g0036 a0001c0001t0003g0037 others(33): Show |
36 | HG00423.hp1 HG00558.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.2621+1050G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11821564 | |||||||
| chr2:11821565 | G | A | 1 | a0001c0001t0002g0149 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2621+1051G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11821565 | |||||||
| chr2:11821570 | T | C | 1 | a0001c0001t0005g0273 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2621+1056T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11821570 | |||||||
| chr2:11821593 | G | C | 1 | a0001c0001t0001g0253 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2621+1079G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11821593 | |||||||
| chr2:11821648 | G | C | 1 | a0001c0001t0037g0221 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2621+1134G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11821648 | |||||||
| chr2:11821670 | G | T | 7 | a0001c0001t0010g0024 a0001c0001t0010g0075 a0001c0001t0010g0080 others(4): Show |
7 | HG01109.hp1 HG01261.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.2621+1156G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11821670 | |||||||
| chr2:11821728 | C | T | 7 | a0001c0001t0010g0024 a0001c0001t0010g0075 a0001c0001t0010g0080 others(4): Show |
7 | HG01109.hp1 HG01261.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.2621+1214C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11821728 | |||||||
| chr2:11821732 | G | C | 1 | a0001c0001t0012g0070 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2621+1218G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11821732 | |||||||
| chr2:11821915 | G | A | 3 | a0001c0004t0007g0270 a0001c0005t0007g0021 a0001c0005t0007g0022 |
3 | HG01109.hp2 HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2621+1401G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11821915 | |||||||
| chr2:11821951 | C | G | 23 | a0001c0001t0006g0039 a0001c0001t0006g0040 a0001c0001t0006g0041 others(20): Show |
23 | HG00639.hp2 HG01175.hp2 HG01257.hp1 others(20): Show |
intron_variant | MODIFIER | c.2621+1437C>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11821951 | |||||||
| chr2:11822277 | C | CA | 20 | a0001c0001t0001g0098 a0001c0001t0001g0184 a0001c0001t0002g0071 others(17): Show |
20 | HG01257.hp1 HG01258.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.2621+1787dupA | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr2 | 11822277 | ||||||
| chr2:11822277 | CA | C | 90 | a0001c0001t0001g0257 a0001c0001t0001g0269 a0001c0001t0002g0149 others(87): Show |
91 | HG00558.hp2 HG00609.hp2 HG00673.hp1 others(88): Show |
intron_variant | MODIFIER | c.2621+1787delA | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr2 | 11822277 | ||||||
| chr2:11822277 | CAA | C | 32 | a0001c0001t0003g0015 a0001c0001t0003g0036 a0001c0001t0003g0037 others(29): Show |
32 | HG00423.hp1 HG01255.hp2 HG01433.hp2 others(29): Show |
intron_variant | MODIFIER | c.2621+1786_2621+178 others(6): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr2 | 11822277 | ||||||
| chr2:11822382 | G | A | 7 | a0001c0001t0010g0024 a0001c0001t0010g0075 a0001c0001t0010g0080 others(4): Show |
7 | HG01109.hp1 HG01261.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.2621+1868G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11822382 | |||||||
| chr2:11822427 | G | A | 2 | a0001c0001t0005g0046 a0002c0010t0005g0012 |
2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.2621+1913G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11822427 | |||||||
| chr2:11822433 | G | C | 4 | a0001c0001t0007g0112 a0001c0001t0007g0172 a0001c0001t0007g0219 others(1): Show |
4 | HG00639.hp1 HG00735.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.2621+1919G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11822433 | |||||||
| chr2:11822484 | C | T | 1 | a0001c0001t0003g0170 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2621+1970C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11822484 | |||||||
| chr2:11822487 | A | G | 87 | a0001c0001t0003g0015 a0001c0001t0003g0036 a0001c0001t0003g0037 others(84): Show |
87 | HG00423.hp1 HG00558.hp2 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.2621+1973A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11822487 | |||||||
| chr2:11822521 | A | G | 2 | a0002c0007t0034g0027 a0002c0007t0035g0028 |
2 | HG02055.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2621+2007A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11822521 | |||||||
| chr2:11822861 | T | C | 3 | a0001c0005t0007g0153 a0001c0005t0007g0156 a0001c0005t0007g0159 |
3 | HG02258.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2622-1771T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11822861 | |||||||
| chr2:11822895 | G | A | 1 | a0002c0010t0005g0012 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2622-1737G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11822895 | |||||||
| chr2:11822960 | T | C | 1 | a0001c0001t0002g0118 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2622-1672T>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11822960 | |||||||
| chr2:11823142 | C | T | 2 | a0001c0001t0005g0046 a0002c0010t0005g0012 |
2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.2622-1490C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11823142 | |||||||
| chr2:11823145 | A | C | 3 | a0001c0001t0012g0163 a0001c0001t0029g0138 a0001c0002t0002g0020 |
3 | HG02738.hp1 HG03491.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.2622-1487A>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11823145 | |||||||
| chr2:11823236 | G | A | 39 | a0001c0001t0003g0015 a0001c0001t0003g0036 a0001c0001t0003g0037 others(36): Show |
39 | HG00423.hp1 HG00558.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.2622-1396G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11823236 | |||||||
| chr2:11823251 | G | A | 8 | a0001c0001t0009g0125 a0001c0001t0009g0227 a0001c0001t0018g0035 others(5): Show |
8 | HG00738.hp1 HG01081.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.2622-1381G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11823251 | |||||||
| chr2:11823294 | G | GCC | 87 | a0001c0001t0003g0015 a0001c0001t0003g0036 a0001c0001t0003g0037 others(84): Show |
87 | HG00423.hp1 HG00558.hp2 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.2622-1337_2622-133 others(6): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr2 | 11823294 | ||||||
| chr2:11823329 | G | A | 6 | a0001c0001t0005g0273 a0001c0002t0015g0154 a0001c0002t0015g0158 others(3): Show |
6 | HG02622.hp2 HG02630.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2622-1303G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11823329 | |||||||
| chr2:11823509 | TATTAAAT others(16): Show |
T | 31 | a0001c0001t0006g0039 a0001c0001t0006g0040 a0001c0001t0006g0041 others(28): Show |
31 | HG00639.hp2 HG00738.hp1 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.2622-1119_2622-109 others(27): Show |
LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr2 | 11823509 | ||||||
| chr2:11823527 | G | A | 6 | a0001c0001t0005g0273 a0001c0002t0015g0154 a0001c0002t0015g0158 others(3): Show |
6 | HG02622.hp2 HG02630.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2622-1105G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11823527 | |||||||
| chr2:11823821 | G | A | 1 | a0001c0003t0009g0053 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2622-811G>A | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11823821 | |||||||
| chr2:11823821 | G | C | 2 | a0001c0001t0004g0151 a0001c0001t0004g0152 |
2 | NA19074.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.2622-811G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11823821 | |||||||
| chr2:11823883 | A | C | 1 | a0001c0001t0004g0202 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2622-749A>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11823883 | |||||||
| chr2:11824003 | G | T | 7 | a0001c0001t0001g0030 a0001c0001t0001g0165 a0001c0001t0001g0167 others(4): Show |
7 | HG00733.hp1 HG01884.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.2622-629G>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11824003 | |||||||
| chr2:11824277 | A | T | 2 | a0002c0007t0034g0027 a0002c0007t0035g0028 |
2 | HG02055.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2622-355A>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11824277 | |||||||
| chr2:11824335 | G | C | 7 | a0001c0001t0010g0024 a0001c0001t0010g0075 a0001c0001t0010g0080 others(4): Show |
7 | HG01109.hp1 HG01261.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.2622-297G>C | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11824335 | |||||||
| chr2:11824410 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2622-222C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11824410 | |||||||
| chr2:11824460 | C | T | 12 | a0001c0001t0006g0039 a0001c0001t0006g0040 a0001c0001t0006g0041 others(9): Show |
12 | HG01175.hp2 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.2622-172C>T | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11824460 | |||||||
| chr2:11824461 | A | G | 18 | a0001c0001t0005g0273 a0001c0001t0006g0039 a0001c0001t0006g0040 others(15): Show |
18 | HG01175.hp2 HG01891.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.2622-171A>G | LPIN1 | ENSG00000134324.12 | transcript | ENST00000674199.1 | protein_coding | 20/20 | chr2 | 11824461 |