Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51056 |
| ensemblid | ENSG00000002549.13 |
| hgncid | 18449 |
| symbol | LAP3 |
| name | leucine aminopeptidase 3 |
| refseq_nuc | NM_015907.3 |
| refseq_prot | NP_056991.2 |
| ensembl_nuc | ENST00000226299.9 |
| ensembl_prot | ENSP00000226299.4 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 17577198 |
| end | 17607970 |
| strand | + |
| ver | v1.2 |
| region | chr4:17577198-17607970 |
| region5000 | chr4:17572198-17612970 |
| regionname0 | LAP3_chr4_17577198_17607970 |
| regionname5000 | LAP3_chr4_17572198_17612970 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1557 | 187 | 37 | 39 | 78 | 8 | 24 | LAP3_chr4_17572198_17612970 | LAP3 | ATGTT others(1552): Show |
chr4 | 17572198 | 17612970 | ||
| a0001c0002 | 1/0 | 1557 | 59 | 17 | 11 | 13 | 6 | 11 | LAP3_chr4_17572198_17612970 | LAP3 | ATGTT others(1552): Show |
chr4 | 17572198 | 17612970 | ||
| a0001c0003 | 0/0 | 1557 | 18 | 18 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | ATGTT others(1552): Show |
chr4 | 17572198 | 17612970 | ||
| a0001c0004 | 0/0 | 1557 | 15 | 13 | 1 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | ATGTT others(1552): Show |
chr4 | 17572198 | 17612970 | ||
| a0001c0005 | 0/0 | 1557 | 15 | 14 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | ATGTT others(1552): Show |
chr4 | 17572198 | 17612970 | ||
| a0001c0006 | 0/0 | 1557 | 4 | 0 | 4 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | ATGTT others(1552): Show |
chr4 | 17572198 | 17612970 | ||
| a0001c0007 | 0/0 | 1557 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | ATGTT others(1552): Show |
chr4 | 17572198 | 17612970 | ||
| a0001c0008 | 0/0 | 1557 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | ATGTT others(1552): Show |
chr4 | 17572198 | 17612970 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2209 | 167 | 36 | 36 | 64 | 8 | 22 | LAP3_chr4_17572198_17612970 | LAP3 | GCACA others(2204): Show |
chr4 | 17572198 | 17612970 |
| a0001c0001t0004 | 0/0 | 2196 | 18 | 0 | 3 | 14 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | GCGGG others(2191): Show |
chr4 | 17572198 | 17612970 |
| a0001c0001t0008 | 0/0 | 2209 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | GCACA others(2204): Show |
chr4 | 17572198 | 17612970 |
| a0001c0001t0011 | 0/0 | 2180 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | GCGGG others(2175): Show |
chr4 | 17572198 | 17612970 |
| a0001c0002t0001 | 0/0 | 2209 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | GCACA others(2204): Show |
chr4 | 17572198 | 17612970 |
| a0001c0002t0002 | 1/0 | 2209 | 53 | 12 | 11 | 12 | 6 | 11 | LAP3_chr4_17572198_17612970 | LAP3 | GCACA others(2204): Show |
chr4 | 17572198 | 17612970 |
| a0001c0002t0005 | 0/0 | 2209 | 4 | 4 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | GCACA others(2204): Show |
chr4 | 17572198 | 17612970 |
| a0001c0002t0010 | 0/0 | 2199 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | GCGGG others(2194): Show |
chr4 | 17572198 | 17612970 |
| a0001c0003t0001 | 0/0 | 2209 | 3 | 3 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | GCACA others(2204): Show |
chr4 | 17572198 | 17612970 |
| a0001c0003t0003 | 0/0 | 2199 | 15 | 15 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | GCGGG others(2194): Show |
chr4 | 17572198 | 17612970 |
| a0001c0004t0001 | 0/0 | 2209 | 13 | 11 | 1 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | GCACA others(2204): Show |
chr4 | 17572198 | 17612970 |
| a0001c0004t0007 | 0/0 | 2225 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | GCACA others(2220): Show |
chr4 | 17572198 | 17612970 |
| a0001c0004t0009 | 0/0 | 2209 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | GCACA others(2204): Show |
chr4 | 17572198 | 17612970 |
| a0001c0005t0003 | 0/0 | 2199 | 13 | 12 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | GCGGG others(2194): Show |
chr4 | 17572198 | 17612970 |
| a0001c0005t0006 | 0/0 | 2199 | 2 | 2 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | GCGGG others(2194): Show |
chr4 | 17572198 | 17612970 |
| a0001c0006t0001 | 0/0 | 2209 | 4 | 0 | 4 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | GCACA others(2204): Show |
chr4 | 17572198 | 17612970 |
| a0001c0007t0001 | 0/0 | 2209 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | GCACA others(2204): Show |
chr4 | 17572198 | 17612970 |
| a0001c0008t0002 | 0/0 | 2209 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | GCACA others(2204): Show |
chr4 | 17572198 | 17612970 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 20 | 0 | 2 | 10 | 3 | 5 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0004 | 0/0 | 8 | 1 | 2 | 2 | 1 | 2 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0006 | 0/0 | 6 | 2 | 1 | 0 | 1 | 2 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0008 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0009 | 0/0 | 4 | 1 | 1 | 0 | 2 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0014 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0038 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0004g0005 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0004g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0004g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0004g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0004g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0004g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0008g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0001t0011g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0002t0002g0002 | 1/0 | 11 | 0 | 2 | 6 | 2 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0002t0002g0003 | 0/0 | 9 | 1 | 4 | 2 | 0 | 2 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0002t0002g0024 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0002t0002g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0002t0002g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0002t0002g0032 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0002t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0002t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0002t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0002t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0002t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0002t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0002t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0002t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0002t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0002t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0002t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0002t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0002t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0002t0005g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0002t0005g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0002t0010g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0003t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0003t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0003t0003g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0003t0003g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0003t0003g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0003t0003g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0003t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0003t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0003t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0003t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0003t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0003t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0004t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0004t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0004t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0004t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0004t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0004t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0004t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0004t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0004t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0004t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0004t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0004t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0004t0007g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0004t0009g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0005t0003g0007 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0005t0003g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0005t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0005t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0005t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0005t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0005t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0005t0006g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0005t0006g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0006t0001g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0006t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0007t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| a0001c0008t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0002 | g0024 | EUR | GBR | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG00140 | hp1 | a0001 | c0002 | t0002 | g0196 | EUR | GBR | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | GBR | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG00280 | hp2 | a0001 | c0002 | t0002 | g0002 | EUR | FIN | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG00323 | hp1 | a0001 | c0002 | t0002 | g0181 | EUR | FIN | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0083 | EUR | FIN | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG00423 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | CHS | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | CHS | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG00544 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | CHS | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG00597 | hp1 | a0001 | c0002 | t0002 | g0180 | EAS | CHS | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG00609 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | CHS | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG00673 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | CHS | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG00735 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG00735 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG00738 | hp1 | a0001 | c0002 | t0002 | g0187 | AMR | PUR | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG00738 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG01099 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG01109 | hp1 | a0001 | c0005 | t0003 | g0026 | AMR | PUR | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG01169 | hp2 | a0001 | c0002 | t0002 | g0192 | AMR | PUR | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG01175 | hp1 | a0001 | c0002 | t0002 | g0191 | AMR | PUR | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG01192 | hp2 | a0001 | c0001 | t0004 | g0005 | AMR | PUR | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG01243 | hp1 | a0001 | c0004 | t0001 | g0128 | AMR | PUR | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG01255 | hp1 | a0001 | c0002 | t0002 | g0186 | AMR | CLM | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0177 | AMR | CLM | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG01361 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | CLM | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG01516 | hp1 | a0001 | c0002 | t0002 | g0002 | EUR | IBS | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG01884 | hp1 | a0001 | c0005 | t0003 | g0026 | AFR | ACB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG01884 | hp2 | a0001 | c0002 | t0002 | g0174 | AFR | ACB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG01891 | hp1 | a0001 | c0004 | t0001 | g0021 | AFR | ACB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG01891 | hp2 | a0001 | c0004 | t0001 | g0126 | AFR | ACB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG01928 | hp2 | a0001 | c0006 | t0001 | g0001 | AMR | PEL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG01943 | hp2 | a0001 | c0006 | t0001 | g0001 | AMR | PEL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG01952 | hp1 | a0001 | c0001 | t0004 | g0169 | AMR | PEL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG01978 | hp2 | a0001 | c0006 | t0001 | g0017 | AMR | PEL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02027 | hp1 | a0001 | c0002 | t0002 | g0178 | EAS | KHV | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02055 | hp1 | a0001 | c0005 | t0003 | g0156 | AFR | ACB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02055 | hp2 | a0001 | c0002 | t0002 | g0003 | AFR | ACB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0089 | EAS | KHV | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02135 | hp2 | a0001 | c0002 | t0002 | g0184 | EAS | KHV | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02145 | hp1 | a0001 | c0003 | t0003 | g0025 | AFR | ACB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02257 | hp2 | a0001 | c0004 | t0007 | g0139 | AFR | ACB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02258 | hp1 | a0001 | c0005 | t0006 | g0159 | AFR | ACB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02258 | hp2 | a0001 | c0002 | t0002 | g0189 | AFR | ACB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02280 | hp1 | a0001 | c0005 | t0003 | g0142 | AFR | ACB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02293 | hp1 | a0001 | c0006 | t0001 | g0001 | AMR | PEL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02293 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PEL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02451 | hp2 | a0001 | c0004 | t0001 | g0119 | AFR | ACB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02572 | hp2 | a0001 | c0002 | t0002 | g0031 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02615 | hp2 | a0001 | c0004 | t0001 | g0127 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02622 | hp1 | a0001 | c0003 | t0003 | g0012 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02622 | hp2 | a0001 | c0002 | t0002 | g0193 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02630 | hp1 | a0001 | c0004 | t0001 | g0124 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02630 | hp2 | a0001 | c0005 | t0003 | g0154 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02647 | hp1 | a0001 | c0002 | t0002 | g0190 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02647 | hp2 | a0001 | c0002 | t0002 | g0144 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02683 | hp1 | a0001 | c0002 | t0002 | g0003 | SAS | PJL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02698 | hp2 | a0001 | c0002 | t0002 | g0194 | SAS | PJL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02717 | hp2 | a0001 | c0005 | t0003 | g0007 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02723 | hp1 | a0001 | c0005 | t0003 | g0007 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02723 | hp2 | a0001 | c0002 | t0005 | g0002 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02809 | hp1 | a0001 | c0003 | t0003 | g0025 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02809 | hp2 | a0001 | c0002 | t0002 | g0024 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02818 | hp2 | a0001 | c0003 | t0003 | g0152 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02886 | hp1 | a0001 | c0002 | t0002 | g0145 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02895 | hp1 | a0001 | c0004 | t0001 | g0021 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02895 | hp2 | a0001 | c0003 | t0003 | g0027 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02896 | hp1 | a0001 | c0003 | t0003 | g0012 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02897 | hp1 | a0001 | c0003 | t0003 | g0027 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02922 | hp1 | a0001 | c0005 | t0003 | g0007 | AFR | ESN | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02922 | hp2 | a0001 | c0001 | t0008 | g0033 | AFR | ESN | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02965 | hp1 | a0001 | c0002 | t0010 | g0141 | AFR | ESN | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ESN | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ESN | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02970 | hp2 | a0001 | c0004 | t0009 | g0034 | AFR | ESN | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ESN | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02976 | hp2 | a0001 | c0002 | t0005 | g0183 | AFR | ESN | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG03017 | hp1 | a0001 | c0004 | t0001 | g0143 | SAS | PJL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG03098 | hp1 | a0001 | c0003 | t0001 | g0016 | AFR | MSL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG03098 | hp2 | a0001 | c0003 | t0003 | g0149 | AFR | MSL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG03130 | hp1 | a0001 | c0002 | t0005 | g0002 | AFR | ESN | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG03139 | hp1 | a0001 | c0003 | t0003 | g0148 | AFR | ESN | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG03139 | hp2 | a0001 | c0003 | t0003 | g0028 | AFR | ESN | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG03195 | hp1 | a0001 | c0005 | t0003 | g0007 | AFR | ESN | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG03195 | hp2 | a0001 | c0003 | t0001 | g0006 | AFR | ESN | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG03209 | hp1 | a0001 | c0003 | t0003 | g0028 | AFR | MSL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG03225 | hp1 | a0001 | c0003 | t0003 | g0151 | AFR | MSL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG03225 | hp2 | a0001 | c0004 | t0001 | g0121 | AFR | MSL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | MSL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG03453 | hp2 | a0001 | c0005 | t0003 | g0007 | AFR | MSL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | MSL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG03486 | hp2 | a0001 | c0004 | t0001 | g0118 | AFR | MSL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG03490 | hp1 | a0001 | c0002 | t0002 | g0195 | SAS | PJL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG03491 | hp2 | a0001 | c0002 | t0002 | g0182 | SAS | PJL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG03516 | hp1 | a0001 | c0003 | t0003 | g0150 | AFR | ESN | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG03516 | hp2 | a0001 | c0005 | t0003 | g0155 | AFR | ESN | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG03540 | hp1 | a0001 | c0003 | t0003 | g0012 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG03540 | hp2 | a0001 | c0003 | t0001 | g0016 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | MSL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG03579 | hp2 | a0001 | c0008 | t0002 | g0160 | AFR | MSL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG03654 | hp1 | a0001 | c0002 | t0002 | g0030 | SAS | PJL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG03704 | hp2 | a0001 | c0002 | t0002 | g0175 | SAS | PJL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG03710 | hp1 | a0001 | c0002 | t0002 | g0030 | SAS | PJL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | BEB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG03831 | hp2 | a0001 | c0001 | t0011 | g0005 | SAS | BEB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG03942 | hp1 | a0001 | c0002 | t0002 | g0003 | SAS | BEB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0185 | SAS | BEB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | BEB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0164 | SAS | STU | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG04199 | hp2 | a0001 | c0002 | t0002 | g0032 | SAS | STU | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG04228 | hp1 | a0001 | c0002 | t0002 | g0188 | SAS | STU | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA18522 | hp1 | a0001 | c0004 | t0001 | g0120 | AFR | YRI | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA18522 | hp2 | a0001 | c0003 | t0003 | g0153 | AFR | YRI | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA18612 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | CHB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | CHB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CHB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA18906 | hp2 | a0001 | c0002 | t0005 | g0002 | AFR | YRI | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA18939 | hp1 | a0001 | c0007 | t0001 | g0146 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA18945 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA18946 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA18950 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA18956 | hp1 | a0001 | c0001 | t0004 | g0168 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA18995 | hp1 | a0001 | c0001 | t0004 | g0163 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA18998 | hp2 | a0001 | c0001 | t0004 | g0029 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA19000 | hp2 | a0001 | c0001 | t0004 | g0167 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA19001 | hp2 | a0001 | c0002 | t0002 | g0179 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA19004 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA19012 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA19030 | hp1 | a0001 | c0005 | t0003 | g0157 | AFR | LWK | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA19030 | hp2 | a0001 | c0004 | t0001 | g0125 | AFR | LWK | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | LWK | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | LWK | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA19056 | hp1 | a0001 | c0001 | t0004 | g0029 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA19058 | hp2 | a0001 | c0001 | t0004 | g0166 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA19064 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA19068 | hp2 | a0001 | c0001 | t0004 | g0165 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA19081 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA19085 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA19240 | hp1 | a0001 | c0002 | t0002 | g0031 | AFR | YRI | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ASW | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA20129 | hp2 | a0001 | c0002 | t0002 | g0176 | AFR | ASW | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA20752 | hp1 | a0001 | c0002 | t0002 | g0032 | EUR | TSI | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG01123 | hp1 | a0001 | c0001 | t0004 | g0161 | AMR | CLM | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02486 | hp1 | a0001 | c0005 | t0003 | g0007 | AFR | ACB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG02559 | hp2 | a0001 | c0005 | t0006 | g0158 | AFR | ACB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG03471 | hp1 | a0001 | c0004 | t0001 | g0123 | AFR | MSL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG03471 | hp2 | a0001 | c0002 | t0002 | g0147 | AFR | MSL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | USA | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | USA | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA18955 | hp2 | a0001 | c0001 | t0004 | g0162 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | USA | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | USA | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | LWK | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | LWK | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0038 | REF | REF | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0002 | REF | REF | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:17579826 | C | T | 1 | a0001c0006 | 4 | HG01928.hp2 HG01943.hp2 HG01978.hp2 others(1): Show |
splice_region_variant&synonymous_variant | LOW | c.105C>T | p.Gly35Gly | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/13 | 373/2209 | 105/1560 | 35/519 | chr4 | 17579826 | |||
| chr4:17585080 | T | C | 6 | a0001c0001 a0001c0003 a0001c0004 others(3): Show |
239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
synonymous_variant | LOW | c.648T>C | p.Ala216Ala | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/13 | 916/2209 | 648/1560 | 216/519 | chr4 | 17585080 | |||
| chr4:17588882 | C | T | 1 | a0001c0005 | 15 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(12): Show |
synonymous_variant | LOW | c.768C>T | p.Asp256Asp | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/13 | 1036/2209 | 768/1560 | 256/519 | chr4 | 17588882 | |||
| chr4:17598509 | C | T | 2 | a0001c0003 a0001c0005 |
33 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(30): Show |
synonymous_variant | LOW | c.1131C>T | p.Tyr377Tyr | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/13 | 1399/2209 | 1131/1560 | 377/519 | chr4 | 17598509 | |||
| chr4:17607502 | A | G | 3 | a0001c0004 a0001c0007 a0001c0008 |
17 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(14): Show |
synonymous_variant | LOW | c.1473A>G | p.Glu491Glu | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 13/13 | 1741/2209 | 1473/1560 | 491/519 | chr4 | 17607502 | |||
| chr4:17607547 | T | G | 1 | a0001c0007 | 1 | NA18939.hp1 | synonymous_variant | LOW | c.1518T>G | p.Thr506Thr | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 13/13 | 1786/2209 | 1518/1560 | 506/519 | chr4 | 17607547 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:17577206 | A | C | 2 | a0001c0001t0008 a0001c0004t0009 |
2 | HG02922.hp2 HG02970.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-260A>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/13 | chr4 | 17577206 | |||||||
| chr4:17577209 | C | CGGGCGCA others(9): Show |
1 | a0001c0004t0007 | 1 | HG02257.hp2 | 5_prime_UTR_variant | MODIFIER | c.-242_-241insGGGGCG others(10): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/13 | 241 | INFO_REALIGN_3_PRIME | chr4 | 17577209 | |||||
| chr4:17577222 | A | C | 2 | a0001c0001t0008 a0001c0004t0009 |
2 | HG02922.hp2 HG02970.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-244A>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/13 | chr4 | 17577222 | |||||||
| chr4:17577238 | A | C | 1 | a0001c0004t0009 | 1 | HG02970.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-228A>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/13 | chr4 | 17577238 | |||||||
| chr4:17577268 | A | G | 14 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0008 others(11): Show |
240 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(237): Show |
5_prime_UTR_variant | MODIFIER | c.-198A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/13 | 198 | chr4 | 17577268 | ||||||
| chr4:17577295 | C | G | 1 | a0001c0002t0005 | 4 | HG02723.hp2 HG02976.hp2 HG03130.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-171C>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/13 | 171 | chr4 | 17577295 | ||||||
| chr4:17577352 | C | G | 1 | a0001c0002t0010 | 1 | HG02965.hp1 | 5_prime_UTR_variant | MODIFIER | c.-114C>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/13 | 114 | chr4 | 17577352 | ||||||
| chr4:17607678 | C | T | 1 | a0001c0005t0006 | 2 | HG02258.hp1 HG02559.hp2 |
3_prime_UTR_variant | MODIFIER | c.*89C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 13/13 | 89 | chr4 | 17607678 | ||||||
| chr4:17607795 | ATTT | A | 2 | a0001c0001t0004 a0001c0001t0011 |
19 | HG01123.hp1 HG01192.hp2 HG01952.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*209_*211delTTT | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 13/13 | 209 | INFO_REALIGN_3_PRIME | chr4 | 17607795 | |||||
| chr4:17607912 | G | T | 2 | a0001c0001t0004 a0001c0001t0011 |
19 | HG01123.hp1 HG01192.hp2 HG01952.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*323G>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 13/13 | 323 | chr4 | 17607912 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:17577627 | G | T | 1 | a0001c0001t0001g0197 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.102+60G>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17577627 | |||||||
| chr4:17577792 | T | C | 172 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(169): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.102+225T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17577792 | |||||||
| chr4:17577850 | C | T | 4 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(1): Show |
4 | HG01243.hp2 HG02615.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.102+283C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17577850 | |||||||
| chr4:17577908 | G | A | 1 | a0001c0002t0002g0030 | 2 | HG03654.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.102+341G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17577908 | |||||||
| chr4:17578055 | G | C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(126): Show |
185 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.102+488G>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17578055 | |||||||
| chr4:17578162 | G | T | 1 | a0001c0001t0001g0140 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.102+595G>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17578162 | |||||||
| chr4:17578163 | G | T | 1 | a0001c0001t0001g0140 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.102+596G>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17578163 | |||||||
| chr4:17578246 | G | T | 1 | a0001c0004t0007g0139 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.102+679G>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17578246 | |||||||
| chr4:17578324 | T | C | 1 | a0001c0002t0010g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.102+757T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17578324 | |||||||
| chr4:17578371 | C | T | 1 | a0001c0001t0001g0023 | 2 | HG00741.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.102+804C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17578371 | |||||||
| chr4:17578515 | G | A | 1 | a0001c0002t0002g0174 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.102+948G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17578515 | |||||||
| chr4:17578542 | TACCAC | T | 129 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(126): Show |
185 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.102+983_102+987del others(5): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 17578542 | ||||||
| chr4:17578554 | C | T | 12 | a0001c0001t0004g0005 a0001c0001t0004g0029 a0001c0001t0004g0161 others(9): Show |
19 | HG01123.hp1 HG01192.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.102+987C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17578554 | |||||||
| chr4:17578597 | C | G | 1 | a0001c0008t0002g0160 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.102+1030C>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17578597 | |||||||
| chr4:17578802 | T | C | 2 | a0001c0001t0008g0033 a0001c0004t0009g0034 |
2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.103-1022T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17578802 | |||||||
| chr4:17578872 | C | T | 16 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0129 others(13): Show |
21 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.103-952C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17578872 | |||||||
| chr4:17579013 | G | A | 2 | a0001c0001t0008g0033 a0001c0004t0009g0034 |
2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.103-811G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17579013 | |||||||
| chr4:17579120 | G | A | 12 | a0001c0001t0004g0005 a0001c0001t0004g0029 a0001c0001t0004g0161 others(9): Show |
19 | HG01123.hp1 HG01192.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.103-704G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17579120 | |||||||
| chr4:17579137 | A | G | 3 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 |
3 | HG02280.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.103-687A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17579137 | |||||||
| chr4:17579313 | C | T | 1 | a0001c0002t0002g0002 | 4 | HG00280.hp2 HG00735.hp1 HG00738.hp2 others(1): Show |
intron_variant | MODIFIER | c.103-511C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17579313 | |||||||
| chr4:17579323 | T | C | 1 | a0001c0005t0003g0142 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.103-501T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17579323 | |||||||
| chr4:17579332 | G | A | 128 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(125): Show |
184 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.103-492G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17579332 | |||||||
| chr4:17579447 | G | A | 4 | a0001c0004t0001g0021 a0001c0004t0001g0126 a0001c0004t0001g0127 others(1): Show |
5 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.103-377G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17579447 | |||||||
| chr4:17579597 | T | C | 1 | a0001c0008t0002g0160 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.103-227T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17579597 | |||||||
| chr4:17579600 | A | G | 6 | a0001c0005t0003g0007 a0001c0005t0003g0155 a0001c0005t0003g0156 others(3): Show |
11 | HG02055.hp1 HG02258.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.103-224A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17579600 | |||||||
| chr4:17579675 | C | T | 23 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(20): Show |
34 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.103-149C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17579675 | |||||||
| chr4:17579715 | A | G | 8 | a0001c0001t0001g0122 a0001c0004t0001g0118 a0001c0004t0001g0119 others(5): Show |
8 | HG02451.hp2 HG02630.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.103-109A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17579715 | |||||||
| chr4:17579719 | G | A | 1 | a0001c0004t0007g0139 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.103-105G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17579719 | |||||||
| chr4:17579763 | T | C | 1 | a0001c0001t0001g0035 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.103-61T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17579763 | |||||||
| chr4:17579967 | T | A | 12 | a0001c0001t0004g0005 a0001c0001t0004g0029 a0001c0001t0004g0161 others(9): Show |
19 | HG01123.hp1 HG01192.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.218+28T>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17579967 | |||||||
| chr4:17579994 | T | A | 128 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(125): Show |
184 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.218+55T>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17579994 | |||||||
| chr4:17580004 | C | A | 1 | a0001c0002t0010g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.218+65C>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580004 | |||||||
| chr4:17580020 | CAG | C | 102 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(99): Show |
153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.218+84_218+85delAG | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580020 | ||||||
| chr4:17580159 | G | A | 6 | a0001c0005t0003g0007 a0001c0005t0003g0155 a0001c0005t0003g0156 others(3): Show |
11 | HG02055.hp1 HG02258.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.218+220G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580159 | |||||||
| chr4:17580165 | C | CATATATA others(5): Show |
1 | a0001c0004t0001g0143 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.218+231_218+242dup others(12): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | ||||||
| chr4:17580165 | C | CATATATA others(461): Show |
1 | a0001c0004t0001g0118 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.218+239_218+240ins others(468): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | ||||||
| chr4:17580165 | C | CATATATA others(469): Show |
1 | a0001c0004t0001g0119 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.218+239_218+240ins others(476): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | ||||||
| chr4:17580165 | C | CATATATA others(117): Show |
1 | a0001c0001t0001g0129 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.218+239_218+240ins others(124): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | ||||||
| chr4:17580165 | C | CATATATA others(99): Show |
1 | a0001c0001t0001g0036 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.218+241_218+242ins others(106): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | ||||||
| chr4:17580165 | C | CATATATA others(467): Show |
1 | a0001c0004t0001g0120 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.218+241_218+242ins others(474): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | ||||||
| chr4:17580165 | C | CATATATA others(451): Show |
1 | a0001c0004t0001g0121 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.218+241_218+242ins others(458): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | ||||||
| chr4:17580165 | C | CATATATA others(136): Show |
1 | a0001c0001t0001g0037 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.218+242_218+243ins others(143): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | ||||||
| chr4:17580165 | C | CATATATA others(141): Show |
1 | a0001c0001t0001g0039 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.218+242_218+243ins others(148): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | ||||||
| chr4:17580165 | C | CATATATA others(139): Show |
1 | a0001c0001t0001g0040 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.218+242_218+243ins others(146): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | ||||||
| chr4:17580165 | C | CATATATA others(125): Show |
1 | a0001c0001t0001g0092 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.218+240_218+241ins others(132): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | ||||||
| chr4:17580165 | C | CATATATA others(115): Show |
1 | a0001c0001t0001g0093 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.218+240_218+241ins others(122): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | ||||||
| chr4:17580165 | C | CATATATA others(134): Show |
1 | a0001c0001t0001g0094 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.218+240_218+241ins others(141): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | ||||||
| chr4:17580165 | C | CATATATA others(117): Show |
3 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 |
3 | HG02129.hp1 NA18978.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.218+240_218+241ins others(124): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | ||||||
| chr4:17580165 | C | CATATATA others(130): Show |
1 | a0001c0001t0001g0102 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.218+240_218+241ins others(137): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | ||||||
| chr4:17580165 | C | CATATATA others(132): Show |
1 | a0001c0001t0001g0101 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.218+240_218+241ins others(139): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | ||||||
| chr4:17580165 | C | CATATATA others(134): Show |
2 | a0001c0001t0001g0099 a0001c0001t0001g0100 |
2 | HG02257.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.218+240_218+241ins others(141): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | ||||||
| chr4:17580165 | C | CATATATA others(138): Show |
1 | a0001c0001t0001g0098 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.218+240_218+241ins others(145): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | ||||||
| chr4:17580165 | C | CATATATA others(137): Show |
1 | a0001c0001t0001g0103 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.218+240_218+241ins others(144): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | ||||||
| chr4:17580165 | C | CATATATA others(117): Show |
5 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0105 others(2): Show |
9 | HG00597.hp2 HG02015.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.218+240_218+241ins others(124): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | ||||||
| chr4:17580165 | C | CATATATA others(133): Show |
1 | a0001c0001t0001g0104 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.218+240_218+241ins others(140): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | ||||||
| chr4:17580165 | C | CATATATA others(143): Show |
1 | a0001c0001t0001g0108 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.218+240_218+241ins others(150): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | ||||||
| chr4:17580165 | C | CATATATA others(136): Show |
1 | a0001c0001t0001g0109 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.218+240_218+241ins others(143): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | ||||||
| chr4:17580165 | C | CATATATA others(137): Show |
1 | a0001c0001t0001g0111 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.218+240_218+241ins others(144): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | ||||||
| chr4:17580165 | C | CATATATA others(143): Show |
1 | a0001c0001t0001g0110 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.218+240_218+241ins others(150): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | ||||||
| chr4:17580165 | C | CATATATA others(119): Show |
2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | HG01255.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.218+240_218+241ins others(126): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | ||||||
| chr4:17580165 | C | CATATATA others(139): Show |
1 | a0001c0001t0001g0115 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.218+240_218+241ins others(146): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | ||||||
| chr4:17580165 | C | CATATATA others(141): Show |
1 | a0001c0001t0001g0114 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.218+240_218+241ins others(148): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | ||||||
| chr4:17580165 | C | CATATATA others(147): Show |
1 | a0001c0001t0001g0116 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.218+240_218+241ins others(154): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | ||||||
| chr4:17580165 | C | CATATATA others(143): Show |
1 | a0001c0001t0001g0117 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.218+240_218+241ins others(150): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | ||||||
| chr4:17580165 | C | CATATATA others(115): Show |
1 | a0001c0001t0001g0135 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.218+238_218+239ins others(122): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | ||||||
| chr4:17580165 | C | CATATATA others(29): Show |
2 | a0001c0005t0006g0158 a0001c0005t0006g0159 |
2 | HG02258.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.218+234_218+235ins others(36): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | ||||||
| chr4:17580178 | A | G | 1 | a0001c0005t0003g0157 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.218+239A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580178 | |||||||
| chr4:17580182 | G | A | 125 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(122): Show |
194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.218+243G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580182 | |||||||
| chr4:17580184 | A | AT | 36 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0039 others(33): Show |
40 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.218+259dupT | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATATACAC others(121): Show |
1 | a0001c0004t0001g0126 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(128): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATATACAC others(115): Show |
1 | a0001c0004t0001g0127 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(122): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATATACAC others(117): Show |
1 | a0001c0004t0001g0021 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(124): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATATACAC others(116): Show |
2 | a0001c0004t0001g0021 a0001c0004t0001g0128 |
2 | HG01243.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.218+246_218+247ins others(123): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATATACAT others(194): Show |
1 | a0001c0004t0009g0034 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(201): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATATATAC others(121): Show |
1 | a0001c0001t0001g0022 | 2 | HG02451.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.218+246_218+247ins others(128): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATATATAC others(148): Show |
1 | a0001c0001t0008g0033 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(155): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATATATAT others(118): Show |
3 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 |
3 | HG02280.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.218+246_218+247ins others(125): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATATATAT others(116): Show |
1 | a0001c0001t0001g0131 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(123): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATATATAT others(121): Show |
1 | a0001c0001t0001g0132 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(128): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATATATAT others(127): Show |
1 | a0001c0001t0001g0130 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(134): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATATATAT others(123): Show |
2 | a0001c0001t0001g0011 a0001c0001t0001g0133 |
4 | HG02109.hp2 NA18906.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+246_218+247ins others(130): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATATATAT others(121): Show |
1 | a0001c0001t0001g0011 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(128): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATATATAT others(454): Show |
1 | a0001c0001t0001g0122 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(461): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATATATAT others(151): Show |
1 | a0001c0001t0001g0134 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(158): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATATATAT others(458): Show |
1 | a0001c0004t0001g0125 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(465): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATATATAT others(460): Show |
1 | a0001c0004t0001g0123 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(467): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATATATAT others(452): Show |
1 | a0001c0004t0001g0124 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(459): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATATATAT others(29): Show |
1 | a0001c0005t0003g0007 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(36): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATATATAT others(27): Show |
1 | a0001c0005t0003g0156 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(34): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATATATAT others(25): Show |
1 | a0001c0005t0003g0007 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(32): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATATATAT others(23): Show |
2 | a0001c0005t0003g0007 a0001c0005t0003g0155 |
3 | HG02486.hp1 HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.218+246_218+247ins others(30): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATATATAT others(21): Show |
1 | a0001c0005t0003g0007 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(28): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATATATAT others(19): Show |
1 | a0001c0005t0003g0007 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(26): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATATATAT others(12): Show |
1 | a0001c0007t0001g0146 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(19): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATATGTGT others(132): Show |
1 | a0001c0001t0001g0088 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(139): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATATGTGT others(134): Show |
1 | a0001c0001t0001g0018 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(141): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATATGTGT others(137): Show |
2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.218+246_218+247ins others(144): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATATGTGT others(143): Show |
1 | a0001c0001t0001g0006 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(150): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATATGTGT others(138): Show |
1 | a0001c0001t0001g0197 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(145): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATATGTGT others(136): Show |
1 | a0001c0001t0001g0018 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(143): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATATGTGT others(142): Show |
1 | a0001c0001t0001g0082 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(149): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATATGTGT others(137): Show |
1 | a0001c0001t0001g0001 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(144): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATATGTGT others(144): Show |
1 | a0001c0001t0001g0045 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(151): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(126): Show |
1 | a0001c0001t0001g0017 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(133): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(132): Show |
2 | a0001c0001t0001g0008 a0001c0001t0001g0023 |
2 | HG01433.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.218+246_218+247ins others(139): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(131): Show |
1 | a0001c0001t0001g0009 | 3 | HG00140.hp2 HG01256.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.218+246_218+247ins others(138): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(129): Show |
1 | a0001c0001t0001g0009 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(136): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(127): Show |
1 | a0001c0001t0001g0079 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(134): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(139): Show |
1 | a0001c0001t0001g0004 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(146): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(137): Show |
1 | a0001c0001t0001g0015 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(144): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(133): Show |
1 | a0001c0001t0001g0056 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(140): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(134): Show |
2 | a0001c0001t0001g0019 a0001c0001t0001g0090 |
2 | HG01123.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.218+246_218+247ins others(141): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(132): Show |
1 | a0001c0001t0001g0061 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(139): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(138): Show |
1 | a0001c0001t0001g0075 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(145): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(132): Show |
1 | a0001c0001t0001g0091 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(139): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(137): Show |
1 | a0001c0001t0001g0015 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(144): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(141): Show |
1 | a0001c0001t0001g0064 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(148): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(143): Show |
1 | a0001c0006t0001g0001 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(150): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(141): Show |
1 | a0001c0001t0001g0004 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(148): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(137): Show |
1 | a0001c0001t0001g0065 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(144): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(135): Show |
2 | a0001c0001t0001g0067 a0001c0001t0001g0071 |
2 | HG01261.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.218+246_218+247ins others(142): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(133): Show |
2 | a0001c0001t0001g0006 a0001c0001t0001g0057 |
2 | HG01515.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.218+246_218+247ins others(140): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(129): Show |
1 | a0001c0001t0001g0048 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(136): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(142): Show |
2 | a0001c0001t0001g0001 a0001c0001t0001g0004 |
2 | NA18942.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.218+246_218+247ins others(149): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(158): Show |
1 | a0001c0003t0001g0016 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(165): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(160): Show |
1 | a0001c0003t0001g0016 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(167): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(140): Show |
3 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0003t0001g0006 |
3 | HG03195.hp2 HG03239.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.218+246_218+247ins others(147): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(138): Show |
4 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(1): Show |
4 | HG01978.hp1 HG01981.hp2 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+246_218+247ins others(145): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(136): Show |
5 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0086 others(2): Show |
7 | HG01516.hp2 HG02071.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.218+246_218+247ins others(143): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(134): Show |
1 | a0001c0001t0001g0140 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(141): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(122): Show |
1 | a0001c0001t0001g0004 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(129): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(118): Show |
2 | a0001c0001t0001g0006 a0001c0001t0001g0043 |
3 | HG02074.hp2 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.218+246_218+247ins others(125): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(145): Show |
1 | a0001c0001t0001g0001 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(152): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(136): Show |
1 | a0001c0001t0001g0001 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(143): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(134): Show |
1 | a0001c0001t0001g0001 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(141): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(136): Show |
2 | a0001c0001t0001g0001 a0001c0001t0001g0004 |
2 | HG02148.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.218+246_218+247ins others(143): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(138): Show |
1 | a0001c0001t0001g0083 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(145): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(131): Show |
1 | a0001c0001t0001g0066 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(138): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(133): Show |
1 | a0001c0001t0001g0004 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(140): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(136): Show |
1 | a0001c0001t0001g0001 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(143): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(145): Show |
1 | a0001c0006t0001g0001 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(152): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(135): Show |
1 | a0001c0001t0001g0052 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(142): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(144): Show |
1 | a0001c0001t0001g0047 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(151): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(140): Show |
2 | a0001c0001t0001g0044 a0001c0001t0001g0054 |
2 | NA18946.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.218+246_218+247ins others(147): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(138): Show |
3 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0058 |
3 | HG01943.hp1 NA18984.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.218+246_218+247ins others(145): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(136): Show |
1 | a0001c0001t0001g0014 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(143): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(138): Show |
3 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0062 |
3 | HG01928.hp1 HG02273.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.218+246_218+247ins others(145): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(143): Show |
1 | a0001c0006t0001g0001 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(150): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(137): Show |
2 | a0001c0001t0001g0055 a0001c0001t0001g0063 |
2 | HG01169.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.218+246_218+247ins others(144): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(135): Show |
1 | a0001c0001t0001g0001 | 2 | HG00609.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.218+246_218+247ins others(142): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(144): Show |
1 | a0001c0001t0001g0013 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(151): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(142): Show |
1 | a0001c0001t0001g0001 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(149): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(140): Show |
2 | a0001c0001t0001g0008 a0001c0001t0001g0023 |
3 | HG00741.hp1 HG00741.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.218+246_218+247ins others(147): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(140): Show |
1 | a0001c0001t0001g0001 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(147): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(141): Show |
1 | a0001c0001t0001g0078 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(148): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(142): Show |
1 | a0001c0001t0001g0077 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(149): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(139): Show |
1 | a0001c0001t0001g0004 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(146): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(146): Show |
2 | a0001c0001t0001g0013 a0001c0001t0001g0085 |
2 | NA18956.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.218+246_218+247ins others(153): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(144): Show |
2 | a0001c0001t0001g0001 a0001c0001t0001g0059 |
2 | HG00544.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.218+246_218+247ins others(151): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(142): Show |
1 | a0001c0001t0001g0049 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(149): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(145): Show |
1 | a0001c0001t0001g0080 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(152): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(144): Show |
1 | a0001c0001t0001g0060 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(151): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(141): Show |
1 | a0001c0001t0001g0041 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(148): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(184): Show |
1 | a0001c0001t0001g0042 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(191): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(180): Show |
1 | a0001c0001t0001g0046 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(187): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(211): Show |
1 | a0001c0001t0001g0006 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(218): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(208): Show |
1 | a0001c0001t0001g0074 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(215): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(190): Show |
1 | a0001c0001t0001g0006 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(197): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTAT others(190): Show |
1 | a0001c0001t0001g0072 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(197): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTGT others(134): Show |
1 | a0001c0001t0001g0035 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(141): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTGT others(141): Show |
1 | a0001c0001t0001g0001 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(148): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTGT others(137): Show |
1 | a0001c0001t0001g0068 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(144): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTGT others(132): Show |
1 | a0001c0001t0001g0076 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(139): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTGT others(136): Show |
1 | a0001c0001t0001g0073 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(143): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTGT others(139): Show |
1 | a0001c0001t0001g0001 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(146): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTGT others(145): Show |
1 | a0001c0006t0001g0017 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(152): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTGT others(135): Show |
1 | a0001c0001t0001g0081 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(142): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | ATGTGTGT others(148): Show |
1 | a0001c0001t0001g0084 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(155): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | ||||||
| chr4:17580184 | A | G | 1 | a0001c0002t0010g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.218+245A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580184 | |||||||
| chr4:17580184 | A | T | 1 | a0001c0001t0001g0037 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.218+245A>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580184 | |||||||
| chr4:17580185 | T | TATATATA others(44): Show |
2 | a0001c0001t0001g0170 a0001c0005t0003g0142 |
2 | HG02280.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.218+246_218+247ins others(51): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580185 | |||||||
| chr4:17580185 | T | TATATATA others(40): Show |
1 | a0001c0005t0003g0154 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(47): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580185 | |||||||
| chr4:17580185 | T | TATATATA others(42): Show |
1 | a0001c0003t0003g0012 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(49): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580185 | |||||||
| chr4:17580185 | T | TATATATA others(40): Show |
1 | a0001c0003t0003g0025 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(47): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580185 | |||||||
| chr4:17580185 | T | TATATATA others(38): Show |
1 | a0001c0003t0003g0151 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(45): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580185 | |||||||
| chr4:17580185 | T | TATATATA others(36): Show |
1 | a0001c0003t0003g0025 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(43): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580185 | |||||||
| chr4:17580185 | T | TATATATA others(34): Show |
1 | a0001c0003t0003g0152 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(41): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580185 | |||||||
| chr4:17580185 | T | TATATATA others(32): Show |
1 | a0001c0003t0003g0028 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(39): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580185 | |||||||
| chr4:17580185 | T | TATATATA others(26): Show |
1 | a0001c0004t0007g0139 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(33): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580185 | |||||||
| chr4:17580185 | T | TATATATA others(30): Show |
3 | a0001c0003t0003g0012 a0001c0003t0003g0027 a0001c0003t0003g0148 |
5 | HG02622.hp1 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.218+246_218+247ins others(37): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580185 | |||||||
| chr4:17580185 | T | TATATATA others(28): Show |
1 | a0001c0003t0003g0028 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(35): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580185 | |||||||
| chr4:17580185 | T | TATATATA others(22): Show |
3 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 |
3 | HG01243.hp2 HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.218+246_218+247ins others(29): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580185 | |||||||
| chr4:17580185 | T | TATATATA others(26): Show |
1 | a0001c0003t0003g0153 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(33): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580185 | |||||||
| chr4:17580185 | T | TATATATA others(24): Show |
2 | a0001c0003t0003g0149 a0001c0003t0003g0150 |
2 | HG03098.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.218+246_218+247ins others(31): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580185 | |||||||
| chr4:17580185 | T | TATATATA others(8): Show |
1 | a0001c0005t0003g0026 | 2 | HG01109.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.218+246_218+247ins others(15): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580185 | |||||||
| chr4:17580185 | T | TATATATA others(6): Show |
2 | a0001c0001t0004g0029 a0001c0001t0011g0005 |
3 | HG03831.hp2 NA18998.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.218+246_218+247ins others(13): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580185 | |||||||
| chr4:17580185 | T | TATATATA others(4): Show |
5 | a0001c0001t0004g0005 a0001c0001t0004g0162 a0001c0001t0004g0163 others(2): Show |
9 | NA18945.hp1 NA18955.hp2 NA18956.hp1 others(6): Show |
intron_variant | MODIFIER | c.218+246_218+247ins others(11): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580185 | |||||||
| chr4:17580185 | T | TATATATG others(2): Show |
6 | a0001c0001t0004g0005 a0001c0001t0004g0161 a0001c0001t0004g0164 others(3): Show |
7 | HG01123.hp1 HG01192.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.218+246_218+247ins others(9): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580185 | |||||||
| chr4:17580186 | T | A | 3 | a0001c0005t0003g0007 a0001c0005t0003g0155 a0001c0005t0003g0156 |
8 | HG02055.hp1 HG02486.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.218+247T>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580186 | |||||||
| chr4:17580331 | T | C | 1 | a0001c0002t0002g0144 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.218+392T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580331 | |||||||
| chr4:17580334 | A | G | 1 | a0001c0004t0007g0139 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.218+395A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580334 | |||||||
| chr4:17580428 | G | A | 102 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(99): Show |
153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.218+489G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580428 | |||||||
| chr4:17580729 | A | G | 16 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0129 others(13): Show |
21 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.218+790A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580729 | |||||||
| chr4:17580819 | T | C | 171 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(168): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.218+880T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580819 | |||||||
| chr4:17580897 | G | A | 1 | a0001c0001t0001g0041 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.219-863G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580897 | |||||||
| chr4:17580917 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.219-843A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580917 | |||||||
| chr4:17580996 | G | A | 11 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0095 others(8): Show |
15 | HG00438.hp1 HG00597.hp2 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.219-764G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580996 | |||||||
| chr4:17581011 | T | C | 1 | a0001c0001t0004g0161 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.219-749T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17581011 | |||||||
| chr4:17581108 | G | A | 12 | a0001c0001t0004g0005 a0001c0001t0004g0029 a0001c0001t0004g0161 others(9): Show |
19 | HG01123.hp1 HG01192.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.219-652G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17581108 | |||||||
| chr4:17581167 | G | A | 12 | a0001c0001t0004g0005 a0001c0001t0004g0029 a0001c0001t0004g0161 others(9): Show |
19 | HG01123.hp1 HG01192.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.219-593G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17581167 | |||||||
| chr4:17581181 | G | A | 1 | a0001c0004t0001g0143 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.219-579G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17581181 | |||||||
| chr4:17581241 | A | G | 3 | a0001c0003t0003g0012 a0001c0003t0003g0027 a0001c0003t0003g0028 |
7 | HG02622.hp1 HG02895.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.219-519A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17581241 | |||||||
| chr4:17581292 | G | A | 1 | a0001c0002t0002g0175 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.219-468G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17581292 | |||||||
| chr4:17581307 | C | T | 1 | a0001c0002t0002g0196 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.219-453C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17581307 | |||||||
| chr4:17581360 | T | C | 1 | a0001c0004t0001g0143 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.219-400T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17581360 | |||||||
| chr4:17581377 | A | G | 8 | a0001c0001t0001g0122 a0001c0004t0001g0118 a0001c0004t0001g0119 others(5): Show |
8 | HG02451.hp2 HG02630.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.219-383A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17581377 | |||||||
| chr4:17581458 | G | A | 1 | a0001c0003t0003g0148 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.219-302G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17581458 | |||||||
| chr4:17581497 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.219-263G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17581497 | |||||||
| chr4:17581514 | G | A | 1 | a0001c0004t0001g0143 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.219-246G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17581514 | |||||||
| chr4:17581523 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.219-237G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17581523 | |||||||
| chr4:17581577 | TA | T | 17 | a0001c0001t0004g0005 a0001c0001t0004g0029 a0001c0001t0004g0161 others(14): Show |
24 | HG01123.hp1 HG01192.hp2 HG01952.hp1 others(21): Show |
intron_variant | MODIFIER | c.219-169delA | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17581577 | ||||||
| chr4:17581577 | TAA | T | 128 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(125): Show |
184 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.219-170_219-169del others(2): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17581577 | ||||||
| chr4:17581725 | A | G | 3 | a0001c0005t0003g0026 a0001c0005t0003g0142 a0001c0005t0003g0154 |
4 | HG01109.hp1 HG01884.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.219-35A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17581725 | |||||||
| chr4:17581738 | C | T | 2 | a0001c0001t0001g0173 a0001c0004t0007g0139 |
2 | HG01243.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.219-22C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17581738 | |||||||
| chr4:17581743 | A | G | 12 | a0001c0001t0004g0005 a0001c0001t0004g0029 a0001c0001t0004g0161 others(9): Show |
19 | HG01123.hp1 HG01192.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.219-17A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17581743 | |||||||
| chr4:17582183 | A | C | 128 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(125): Show |
184 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.274-105A>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 3/12 | chr4 | 17582183 | |||||||
| chr4:17582412 | T | A | 6 | a0001c0005t0003g0007 a0001c0005t0003g0155 a0001c0005t0003g0156 others(3): Show |
11 | HG02055.hp1 HG02258.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.379+19T>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 4/12 | chr4 | 17582412 | |||||||
| chr4:17582550 | G | A | 1 | a0001c0002t0002g0176 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.379+157G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 4/12 | chr4 | 17582550 | |||||||
| chr4:17582813 | G | GT | 2 | a0001c0001t0001g0019 a0001c0001t0001g0090 |
3 | HG01123.hp2 HG02698.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.379+421dupT | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 17582813 | ||||||
| chr4:17582910 | C | A | 1 | a0001c0001t0001g0043 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.379+517C>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 4/12 | chr4 | 17582910 | |||||||
| chr4:17582939 | A | G | 1 | a0001c0003t0003g0153 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.380-544A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 4/12 | chr4 | 17582939 | |||||||
| chr4:17583391 | G | C | 128 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(125): Show |
184 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.380-92G>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 4/12 | chr4 | 17583391 | |||||||
| chr4:17583468 | C | T | 9 | a0001c0005t0003g0007 a0001c0005t0003g0026 a0001c0005t0003g0142 others(6): Show |
15 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.380-15C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 4/12 | chr4 | 17583468 | |||||||
| chr4:17583658 | TAGG | T | 23 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(20): Show |
34 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.539+23_539+25delAG others(1): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 17583658 | ||||||
| chr4:17583744 | G | A | 1 | a0001c0001t0004g0029 | 2 | NA18998.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.539+102G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 5/12 | chr4 | 17583744 | |||||||
| chr4:17583860 | C | A | 26 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0122 others(23): Show |
31 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.539+218C>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 5/12 | chr4 | 17583860 | |||||||
| chr4:17583876 | T | C | 2 | a0001c0001t0008g0033 a0001c0004t0009g0034 |
2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.539+234T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 5/12 | chr4 | 17583876 | |||||||
| chr4:17583883 | A | G | 12 | a0001c0001t0004g0005 a0001c0001t0004g0029 a0001c0001t0004g0161 others(9): Show |
19 | HG01123.hp1 HG01192.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.539+241A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 5/12 | chr4 | 17583883 | |||||||
| chr4:17584002 | T | C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(161): Show |
238 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.539+360T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 5/12 | chr4 | 17584002 | |||||||
| chr4:17584361 | T | C | 127 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(124): Show |
183 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.540-611T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 5/12 | chr4 | 17584361 | |||||||
| chr4:17584418 | A | T | 4 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(1): Show |
4 | HG01243.hp2 HG02615.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.540-554A>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 5/12 | chr4 | 17584418 | |||||||
| chr4:17584451 | C | T | 3 | a0001c0001t0001g0018 a0001c0001t0001g0088 a0001c0001t0001g0197 |
4 | HG02970.hp1 HG02976.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.540-521C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 5/12 | chr4 | 17584451 | |||||||
| chr4:17584787 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.540-185C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 5/12 | chr4 | 17584787 | |||||||
| chr4:17584850 | A | G | 1 | a0001c0008t0002g0160 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.540-122A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 5/12 | chr4 | 17584850 | |||||||
| chr4:17584893 | G | C | 1 | a0001c0001t0001g0044 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.540-79G>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 5/12 | chr4 | 17584893 | |||||||
| chr4:17584937 | G | A | 1 | a0001c0001t0001g0044 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.540-35G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 5/12 | chr4 | 17584937 | |||||||
| chr4:17585150 | G | A | 7 | a0001c0004t0001g0118 a0001c0004t0001g0119 a0001c0004t0001g0120 others(4): Show |
7 | HG02451.hp2 HG02630.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.704+14G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17585150 | |||||||
| chr4:17585218 | T | G | 10 | a0001c0003t0003g0012 a0001c0003t0003g0025 a0001c0003t0003g0027 others(7): Show |
15 | HG02145.hp1 HG02622.hp1 HG02809.hp1 others(12): Show |
intron_variant | MODIFIER | c.704+82T>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17585218 | |||||||
| chr4:17585264 | G | T | 2 | a0001c0001t0001g0114 a0001c0001t0001g0115 |
2 | HG01257.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.704+128G>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17585264 | |||||||
| chr4:17585334 | A | G | 127 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(124): Show |
183 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.704+198A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17585334 | |||||||
| chr4:17585395 | A | G | 2 | a0001c0002t0002g0032 a0001c0002t0002g0175 |
3 | HG03704.hp2 HG04199.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.704+259A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17585395 | |||||||
| chr4:17585435 | A | AT | 116 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(113): Show |
180 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.704+318dupT | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 17585435 | ||||||
| chr4:17585435 | A | ATT | 14 | a0001c0001t0001g0017 a0001c0001t0001g0041 a0001c0001t0001g0083 others(11): Show |
14 | HG00323.hp2 HG01952.hp1 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.704+317_704+318dup others(2): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 17585435 | ||||||
| chr4:17585514 | T | A | 127 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(124): Show |
183 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.704+378T>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17585514 | |||||||
| chr4:17585610 | A | G | 1 | a0001c0001t0001g0082 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.704+474A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17585610 | |||||||
| chr4:17585639 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.704+503G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17585639 | |||||||
| chr4:17585715 | C | T | 3 | a0001c0002t0002g0024 a0001c0002t0002g0144 a0001c0002t0002g0145 |
4 | HG00099.hp1 HG02647.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.704+579C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17585715 | |||||||
| chr4:17585738 | C | T | 127 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(124): Show |
183 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.704+602C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17585738 | |||||||
| chr4:17585942 | C | T | 127 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(124): Show |
183 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.704+806C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17585942 | |||||||
| chr4:17586148 | C | T | 7 | a0001c0004t0001g0118 a0001c0004t0001g0119 a0001c0004t0001g0120 others(4): Show |
7 | HG02451.hp2 HG02630.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.704+1012C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17586148 | |||||||
| chr4:17586162 | G | A | 1 | a0001c0004t0001g0143 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.704+1026G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17586162 | |||||||
| chr4:17586292 | CT | C | 5 | a0001c0001t0001g0022 a0001c0004t0001g0021 a0001c0004t0001g0126 others(2): Show |
7 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.704+1158delT | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 17586292 | ||||||
| chr4:17586380 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.704+1244A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17586380 | |||||||
| chr4:17586697 | A | G | 142 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(139): Show |
205 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.704+1561A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17586697 | |||||||
| chr4:17586722 | G | A | 23 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(20): Show |
34 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.704+1586G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17586722 | |||||||
| chr4:17586814 | A | G | 127 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(124): Show |
183 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.704+1678A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17586814 | |||||||
| chr4:17586965 | G | C | 1 | a0001c0003t0003g0149 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.704+1829G>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17586965 | |||||||
| chr4:17587092 | A | G | 1 | a0001c0001t0001g0081 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.705-1727A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17587092 | |||||||
| chr4:17587130 | A | G | 5 | a0001c0001t0001g0040 a0001c0001t0001g0077 a0001c0001t0001g0078 others(2): Show |
5 | HG00438.hp2 HG00673.hp2 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.705-1689A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17587130 | |||||||
| chr4:17587143 | G | A | 1 | a0001c0004t0009g0034 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.705-1676G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17587143 | |||||||
| chr4:17587148 | G | T | 4 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(1): Show |
4 | HG01243.hp2 HG02615.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.705-1671G>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17587148 | |||||||
| chr4:17587155 | C | T | 23 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(20): Show |
34 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.705-1664C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17587155 | |||||||
| chr4:17587207 | T | C | 1 | a0001c0002t0002g0177 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.705-1612T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17587207 | |||||||
| chr4:17587289 | C | T | 3 | a0001c0002t0002g0024 a0001c0002t0002g0144 a0001c0002t0002g0145 |
4 | HG00099.hp1 HG02647.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.705-1530C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17587289 | |||||||
| chr4:17587327 | G | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(162): Show |
239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.705-1492G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17587327 | |||||||
| chr4:17587413 | C | T | 1 | a0001c0004t0001g0127 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.705-1406C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17587413 | |||||||
| chr4:17587429 | G | GT | 15 | a0001c0001t0004g0005 a0001c0001t0004g0029 a0001c0001t0004g0161 others(12): Show |
22 | HG01123.hp1 HG01192.hp2 HG01952.hp1 others(19): Show |
intron_variant | MODIFIER | c.705-1374dupT | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 17587429 | ||||||
| chr4:17587429 | G | GTT | 15 | a0001c0003t0003g0012 a0001c0003t0003g0025 a0001c0003t0003g0027 others(12): Show |
21 | HG01109.hp1 HG01884.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.705-1375_705-1374d others(4): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 17587429 | ||||||
| chr4:17587429 | G | GTTT | 9 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(6): Show |
13 | HG01243.hp2 HG02258.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.705-1376_705-1374d others(5): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 17587429 | ||||||
| chr4:17587429 | GTTTT | G | 127 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(124): Show |
183 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.705-1377_705-1374d others(6): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 17587429 | ||||||
| chr4:17587436 | T | G | 2 | a0001c0001t0001g0105 a0001c0001t0001g0112 |
2 | NA18950.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.705-1383T>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17587436 | |||||||
| chr4:17587437 | T | A | 1 | a0001c0001t0001g0046 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.705-1382T>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17587437 | |||||||
| chr4:17587667 | T | C | 10 | a0001c0003t0003g0012 a0001c0003t0003g0025 a0001c0003t0003g0027 others(7): Show |
15 | HG02145.hp1 HG02622.hp1 HG02809.hp1 others(12): Show |
intron_variant | MODIFIER | c.705-1152T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17587667 | |||||||
| chr4:17587706 | G | T | 1 | a0001c0002t0002g0174 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.705-1113G>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17587706 | |||||||
| chr4:17587752 | G | A | 1 | a0001c0004t0001g0143 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.705-1067G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17587752 | |||||||
| chr4:17587758 | A | G | 2 | a0001c0003t0003g0148 a0001c0003t0003g0152 |
2 | HG02818.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.705-1061A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17587758 | |||||||
| chr4:17587934 | C | T | 170 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(167): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.705-885C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17587934 | |||||||
| chr4:17587936 | G | C | 1 | a0001c0004t0007g0139 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.705-883G>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17587936 | |||||||
| chr4:17587944 | A | AT | 14 | a0001c0001t0001g0113 a0001c0001t0004g0168 a0001c0003t0003g0012 others(11): Show |
19 | HG01255.hp2 HG02145.hp1 HG02622.hp1 others(16): Show |
intron_variant | MODIFIER | c.705-861dupT | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 17587944 | ||||||
| chr4:17587944 | AT | A | 9 | a0001c0001t0008g0033 a0001c0004t0001g0118 a0001c0004t0001g0119 others(6): Show |
9 | HG02451.hp2 HG02630.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.705-861delT | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 17587944 | ||||||
| chr4:17588201 | CT | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(116): Show |
175 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.705-606delT | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 17588201 | ||||||
| chr4:17588579 | A | C | 4 | a0001c0004t0001g0021 a0001c0004t0001g0126 a0001c0004t0001g0127 others(1): Show |
5 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.705-240A>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17588579 | |||||||
| chr4:17588596 | A | G | 165 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(162): Show |
239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.705-223A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17588596 | |||||||
| chr4:17588657 | T | G | 1 | a0001c0003t0003g0149 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.705-162T>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17588657 | |||||||
| chr4:17588684 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.705-135A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17588684 | |||||||
| chr4:17588769 | T | C | 1 | a0001c0001t0001g0097 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.705-50T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17588769 | |||||||
| chr4:17588816 | T | C | 17 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0122 others(14): Show |
22 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(19): Show |
splice_region_variant&intron_variant | LOW | c.705-3T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17588816 | |||||||
| chr4:17589018 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.863+41A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17589018 | |||||||
| chr4:17589048 | G | A | 72 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(69): Show |
111 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.863+71G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17589048 | |||||||
| chr4:17589053 | TTTTGG | T | 3 | a0001c0002t0002g0024 a0001c0002t0002g0144 a0001c0002t0002g0145 |
4 | HG00099.hp1 HG02647.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.863+81_863+85delGT others(3): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 17589053 | ||||||
| chr4:17589063 | AT | A | 146 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(143): Show |
213 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.863+101delT | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 17589063 | ||||||
| chr4:17589111 | A | T | 127 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(124): Show |
183 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.863+134A>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17589111 | |||||||
| chr4:17589161 | A | C | 7 | a0001c0004t0001g0118 a0001c0004t0001g0119 a0001c0004t0001g0120 others(4): Show |
7 | HG02451.hp2 HG02630.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.863+184A>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17589161 | |||||||
| chr4:17589272 | G | A | 1 | a0001c0001t0004g0029 | 2 | NA18998.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.863+295G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17589272 | |||||||
| chr4:17589332 | A | C | 1 | a0001c0007t0001g0146 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.863+355A>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17589332 | |||||||
| chr4:17589389 | G | T | 9 | a0001c0001t0008g0033 a0001c0004t0001g0118 a0001c0004t0001g0119 others(6): Show |
9 | HG02451.hp2 HG02630.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.863+412G>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17589389 | |||||||
| chr4:17589565 | T | C | 1 | a0001c0001t0001g0047 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.863+588T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17589565 | |||||||
| chr4:17589794 | C | T | 1 | a0001c0001t0001g0134 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.863+817C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17589794 | |||||||
| chr4:17589821 | T | C | 1 | a0001c0008t0002g0160 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.863+844T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17589821 | |||||||
| chr4:17589845 | C | T | 10 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0122 others(7): Show |
15 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.863+868C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17589845 | |||||||
| chr4:17590004 | T | G | 10 | a0001c0003t0003g0012 a0001c0003t0003g0025 a0001c0003t0003g0027 others(7): Show |
15 | HG02145.hp1 HG02622.hp1 HG02809.hp1 others(12): Show |
intron_variant | MODIFIER | c.863+1027T>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17590004 | |||||||
| chr4:17590025 | A | G | 127 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(124): Show |
183 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.863+1048A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17590025 | |||||||
| chr4:17590121 | C | A | 1 | a0001c0004t0007g0139 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.863+1144C>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17590121 | |||||||
| chr4:17590123 | A | G | 1 | a0001c0004t0007g0139 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.863+1146A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17590123 | |||||||
| chr4:17590217 | G | A | 7 | a0001c0004t0001g0118 a0001c0004t0001g0119 a0001c0004t0001g0120 others(4): Show |
7 | HG02451.hp2 HG02630.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.863+1240G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17590217 | |||||||
| chr4:17590276 | C | T | 7 | a0001c0004t0001g0118 a0001c0004t0001g0119 a0001c0004t0001g0120 others(4): Show |
7 | HG02451.hp2 HG02630.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.863+1299C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17590276 | |||||||
| chr4:17590587 | T | G | 2 | a0001c0004t0001g0021 a0001c0004t0001g0128 |
3 | HG01243.hp1 HG01891.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.863+1610T>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17590587 | |||||||
| chr4:17590657 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.863+1680C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17590657 | |||||||
| chr4:17590664 | C | T | 1 | a0001c0001t0004g0167 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.863+1687C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17590664 | |||||||
| chr4:17590665 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.863+1688G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17590665 | |||||||
| chr4:17590688 | C | T | 1 | a0001c0004t0001g0124 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.863+1711C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17590688 | |||||||
| chr4:17590765 | G | A | 1 | a0001c0005t0003g0157 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.863+1788G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17590765 | |||||||
| chr4:17590776 | T | A | 1 | a0001c0007t0001g0146 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.863+1799T>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17590776 | |||||||
| chr4:17590840 | G | C | 2 | a0001c0001t0008g0033 a0001c0004t0009g0034 |
2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.863+1863G>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17590840 | |||||||
| chr4:17590845 | C | T | 4 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(1): Show |
4 | HG01243.hp2 HG02615.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.863+1868C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17590845 | |||||||
| chr4:17590898 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.863+1921A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17590898 | |||||||
| chr4:17590923 | CT | C | 128 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(125): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.863+1971delT | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 17590923 | ||||||
| chr4:17590923 | CTT | C | 40 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0011 others(37): Show |
57 | HG01109.hp1 HG01123.hp1 HG01192.hp2 others(54): Show |
intron_variant | MODIFIER | c.863+1970_863+1971d others(4): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 17590923 | ||||||
| chr4:17590925 | T | A | 1 | a0001c0002t0002g0178 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.863+1948T>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17590925 | |||||||
| chr4:17590951 | T | G | 1 | a0001c0002t0002g0178 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.863+1974T>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17590951 | |||||||
| chr4:17591103 | A | G | 1 | a0001c0008t0002g0160 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.863+2126A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17591103 | |||||||
| chr4:17591113 | G | C | 1 | a0001c0001t0001g0045 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.863+2136G>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17591113 | |||||||
| chr4:17591199 | C | T | 2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.863+2222C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17591199 | |||||||
| chr4:17591215 | T | C | 1 | a0001c0001t0001g0099 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.863+2238T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17591215 | |||||||
| chr4:17591244 | T | C | 1 | a0001c0001t0001g0099 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.863+2267T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17591244 | |||||||
| chr4:17591298 | G | A | 1 | a0001c0002t0010g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.863+2321G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17591298 | |||||||
| chr4:17591358 | G | A | 1 | a0001c0004t0007g0139 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.863+2381G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17591358 | |||||||
| chr4:17591490 | G | T | 9 | a0001c0005t0003g0007 a0001c0005t0003g0026 a0001c0005t0003g0142 others(6): Show |
15 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.863+2513G>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17591490 | |||||||
| chr4:17591609 | T | C | 15 | a0001c0001t0004g0005 a0001c0001t0004g0029 a0001c0001t0004g0161 others(12): Show |
22 | HG01123.hp1 HG01192.hp2 HG01952.hp1 others(19): Show |
intron_variant | MODIFIER | c.863+2632T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17591609 | |||||||
| chr4:17591673 | G | C | 2 | a0001c0001t0001g0019 a0001c0001t0001g0090 |
3 | HG01123.hp2 HG02698.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.863+2696G>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17591673 | |||||||
| chr4:17591739 | G | T | 9 | a0001c0001t0008g0033 a0001c0004t0001g0118 a0001c0004t0001g0119 others(6): Show |
9 | HG02451.hp2 HG02630.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.863+2762G>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17591739 | |||||||
| chr4:17591812 | T | C | 28 | a0001c0001t0004g0005 a0001c0001t0004g0029 a0001c0001t0004g0161 others(25): Show |
36 | HG01123.hp1 HG01192.hp2 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.863+2835T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17591812 | |||||||
| chr4:17591822 | C | T | 1 | a0001c0002t0002g0193 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.863+2845C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17591822 | |||||||
| chr4:17591971 | CT | C | 127 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(124): Show |
183 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.863+2996delT | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 17591971 | ||||||
| chr4:17591982 | G | T | 125 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(122): Show |
181 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.863+3005G>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17591982 | |||||||
| chr4:17592034 | T | C | 1 | a0001c0001t0001g0132 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.863+3057T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17592034 | |||||||
| chr4:17592168 | C | A | 1 | a0001c0001t0001g0009 | 4 | HG00140.hp2 HG01256.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.863+3191C>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17592168 | |||||||
| chr4:17592226 | G | C | 127 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(124): Show |
183 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.864-3184G>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17592226 | |||||||
| chr4:17592282 | A | G | 165 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(162): Show |
239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.864-3128A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17592282 | |||||||
| chr4:17592342 | G | A | 127 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(124): Show |
183 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.864-3068G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17592342 | |||||||
| chr4:17592344 | C | CTTCT | 170 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(167): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.864-3062_864-3059d others(6): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 17592344 | ||||||
| chr4:17592355 | G | T | 127 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(124): Show |
183 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.864-3055G>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17592355 | |||||||
| chr4:17592375 | A | G | 1 | a0001c0001t0001g0068 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.864-3035A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17592375 | |||||||
| chr4:17592462 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.864-2948A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17592462 | |||||||
| chr4:17592478 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.864-2932T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17592478 | |||||||
| chr4:17592614 | A | T | 5 | a0001c0001t0001g0011 a0001c0001t0001g0122 a0001c0001t0001g0130 others(2): Show |
8 | HG02109.hp2 HG02559.hp1 HG03579.hp1 others(5): Show |
intron_variant | MODIFIER | c.864-2796A>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17592614 | |||||||
| chr4:17592840 | G | A | 1 | a0001c0002t0010g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.864-2570G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17592840 | |||||||
| chr4:17592863 | C | T | 12 | a0001c0001t0004g0005 a0001c0001t0004g0029 a0001c0001t0004g0161 others(9): Show |
19 | HG01123.hp1 HG01192.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.864-2547C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17592863 | |||||||
| chr4:17592869 | G | A | 1 | a0001c0002t0010g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.864-2541G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17592869 | |||||||
| chr4:17592876 | T | C | 1 | a0001c0007t0001g0146 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.864-2534T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17592876 | |||||||
| chr4:17593006 | C | T | 1 | a0001c0002t0002g0192 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.864-2404C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17593006 | |||||||
| chr4:17593076 | G | C | 1 | a0001c0001t0001g0106 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.864-2334G>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17593076 | |||||||
| chr4:17593079 | T | C | 117 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(114): Show |
168 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.864-2331T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17593079 | |||||||
| chr4:17593261 | C | T | 1 | a0001c0004t0009g0034 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.864-2149C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17593261 | |||||||
| chr4:17593312 | C | G | 4 | a0001c0004t0001g0021 a0001c0004t0001g0126 a0001c0004t0001g0127 others(1): Show |
5 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.864-2098C>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17593312 | |||||||
| chr4:17593453 | C | G | 3 | a0001c0005t0003g0026 a0001c0005t0003g0142 a0001c0005t0003g0154 |
4 | HG01109.hp1 HG01884.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.864-1957C>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17593453 | |||||||
| chr4:17593522 | CAT | C | 101 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(98): Show |
152 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.864-1887_864-1886d others(4): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17593522 | |||||||
| chr4:17593565 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.864-1845G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17593565 | |||||||
| chr4:17593589 | A | G | 1 | a0001c0002t0010g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.864-1821A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17593589 | |||||||
| chr4:17593609 | G | GT | 13 | a0001c0002t0002g0189 a0001c0002t0002g0190 a0001c0002t0002g0191 others(10): Show |
18 | HG00140.hp1 HG01175.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.864-1781dupT | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 17593609 | ||||||
| chr4:17593609 | G | GTT | 10 | a0001c0001t0004g0005 a0001c0001t0004g0029 a0001c0001t0004g0164 others(7): Show |
17 | HG01192.hp2 HG01952.hp1 HG03098.hp2 others(14): Show |
intron_variant | MODIFIER | c.864-1782_864-1781d others(4): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 17593609 | ||||||
| chr4:17593609 | G | GTTTTT | 5 | a0001c0005t0003g0007 a0001c0005t0003g0026 a0001c0005t0003g0142 others(2): Show |
11 | HG01109.hp1 HG01884.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.864-1785_864-1781d others(7): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 17593609 | ||||||
| chr4:17593609 | G | GTTTTTTT | 83 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(80): Show |
131 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.864-1787_864-1781d others(9): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 17593609 | ||||||
| chr4:17593609 | G | GTTTTTTT others(1): Show |
36 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0040 others(33): Show |
44 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.864-1788_864-1781d others(10): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 17593609 | ||||||
| chr4:17593609 | G | GTTTTTTT others(3): Show |
2 | a0001c0001t0001g0173 a0001c0007t0001g0146 |
2 | HG01243.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.864-1790_864-1781d others(12): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 17593609 | ||||||
| chr4:17593609 | G | GTTTTTTT others(4): Show |
6 | a0001c0004t0001g0118 a0001c0004t0001g0119 a0001c0004t0001g0120 others(3): Show |
6 | HG02257.hp2 HG02451.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.864-1791_864-1781d others(13): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 17593609 | ||||||
| chr4:17593609 | G | GTTTTTTT others(5): Show |
3 | a0001c0004t0001g0121 a0001c0004t0001g0125 a0001c0004t0009g0034 |
3 | HG02970.hp2 HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.864-1792_864-1781d others(14): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 17593609 | ||||||
| chr4:17593609 | GT | G | 5 | a0001c0002t0002g0179 a0001c0004t0001g0021 a0001c0004t0001g0126 others(2): Show |
6 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.864-1781delT | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 17593609 | ||||||
| chr4:17593631 | A | G | 1 | a0001c0002t0002g0188 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.864-1779A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17593631 | |||||||
| chr4:17593637 | T | C | 1 | a0001c0008t0002g0160 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.864-1773T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17593637 | |||||||
| chr4:17593697 | G | A | 1 | a0001c0002t0002g0176 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.864-1713G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17593697 | |||||||
| chr4:17593738 | G | C | 3 | a0001c0005t0003g0007 a0001c0005t0003g0155 a0001c0005t0003g0156 |
8 | HG02055.hp1 HG02486.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.864-1672G>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17593738 | |||||||
| chr4:17593742 | A | T | 116 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(113): Show |
167 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.864-1668A>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17593742 | |||||||
| chr4:17593845 | T | C | 7 | a0001c0004t0001g0118 a0001c0004t0001g0119 a0001c0004t0001g0120 others(4): Show |
7 | HG02451.hp2 HG02630.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.864-1565T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17593845 | |||||||
| chr4:17593913 | A | G | 2 | a0001c0001t0001g0060 a0001c0001t0001g0066 |
2 | HG01192.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.864-1497A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17593913 | |||||||
| chr4:17593971 | G | C | 1 | a0001c0001t0001g0066 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.864-1439G>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17593971 | |||||||
| chr4:17593975 | G | A | 15 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(12): Show |
20 | HG01243.hp2 HG02145.hp1 HG02615.hp1 others(17): Show |
intron_variant | MODIFIER | c.864-1435G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17593975 | |||||||
| chr4:17594149 | CA | C | 7 | a0001c0004t0001g0118 a0001c0004t0001g0119 a0001c0004t0001g0120 others(4): Show |
7 | HG02451.hp2 HG02630.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.864-1258delA | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 17594149 | ||||||
| chr4:17594206 | T | TA | 7 | a0001c0004t0001g0118 a0001c0004t0001g0119 a0001c0004t0001g0120 others(4): Show |
7 | HG02451.hp2 HG02630.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.864-1203dupA | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 17594206 | ||||||
| chr4:17594298 | A | G | 1 | a0001c0002t0010g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.864-1112A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17594298 | |||||||
| chr4:17594384 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.864-1026G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17594384 | |||||||
| chr4:17594568 | G | A | 1 | a0001c0004t0007g0139 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.864-842G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17594568 | |||||||
| chr4:17594621 | T | G | 1 | a0001c0004t0009g0034 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.864-789T>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17594621 | |||||||
| chr4:17594682 | A | G | 4 | a0001c0004t0001g0021 a0001c0004t0001g0126 a0001c0004t0001g0127 others(1): Show |
5 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.864-728A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17594682 | |||||||
| chr4:17594838 | A | G | 3 | a0001c0001t0001g0008 a0001c0001t0001g0059 a0001c0001t0001g0084 |
7 | HG00741.hp1 HG01071.hp2 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.864-572A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17594838 | |||||||
| chr4:17594878 | T | C | 4 | a0001c0004t0001g0021 a0001c0004t0001g0126 a0001c0004t0001g0127 others(1): Show |
5 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.864-532T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17594878 | |||||||
| chr4:17594969 | C | T | 1 | a0001c0004t0009g0034 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.864-441C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17594969 | |||||||
| chr4:17594985 | A | C | 12 | a0001c0001t0004g0005 a0001c0001t0004g0029 a0001c0001t0004g0161 others(9): Show |
19 | HG01123.hp1 HG01192.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.864-425A>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17594985 | |||||||
| chr4:17595073 | C | T | 12 | a0001c0001t0004g0005 a0001c0001t0004g0029 a0001c0001t0004g0161 others(9): Show |
19 | HG01123.hp1 HG01192.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.864-337C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17595073 | |||||||
| chr4:17595213 | G | A | 1 | a0001c0007t0001g0146 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.864-197G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17595213 | |||||||
| chr4:17595281 | G | T | 1 | a0001c0003t0003g0151 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.864-129G>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17595281 | |||||||
| chr4:17595317 | C | T | 5 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(2): Show |
5 | HG01243.hp2 HG02615.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.864-93C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17595317 | |||||||
| chr4:17595328 | G | A | 43 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0122 others(40): Show |
60 | HG00099.hp1 HG01123.hp1 HG01192.hp2 others(57): Show |
intron_variant | MODIFIER | c.864-82G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17595328 | |||||||
| chr4:17595332 | C | A | 15 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(12): Show |
20 | HG01243.hp2 HG02145.hp1 HG02615.hp1 others(17): Show |
intron_variant | MODIFIER | c.864-78C>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17595332 | |||||||
| chr4:17595390 | C | T | 1 | a0001c0001t0001g0020 | 2 | NA18942.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.864-20C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17595390 | |||||||
| chr4:17595639 | T | C | 1 | a0001c0001t0001g0106 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.988+105T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 8/12 | chr4 | 17595639 | |||||||
| chr4:17595654 | C | T | 1 | a0001c0002t0010g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.988+120C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 8/12 | chr4 | 17595654 | |||||||
| chr4:17595868 | C | A | 1 | a0001c0001t0008g0033 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.988+334C>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 8/12 | chr4 | 17595868 | |||||||
| chr4:17595926 | A | G | 161 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(158): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.988+392A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 8/12 | chr4 | 17595926 | |||||||
| chr4:17596019 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.988+485A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 8/12 | chr4 | 17596019 | |||||||
| chr4:17596076 | C | T | 1 | a0001c0004t0001g0143 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.988+542C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 8/12 | chr4 | 17596076 | |||||||
| chr4:17596084 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.988+550C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 8/12 | chr4 | 17596084 | |||||||
| chr4:17596339 | G | A | 1 | a0001c0001t0001g0092 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.989-707G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 8/12 | chr4 | 17596339 | |||||||
| chr4:17596355 | T | G | 1 | a0001c0002t0010g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.989-691T>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 8/12 | chr4 | 17596355 | |||||||
| chr4:17596402 | C | T | 4 | a0001c0004t0001g0021 a0001c0004t0001g0126 a0001c0004t0001g0127 others(1): Show |
5 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.989-644C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 8/12 | chr4 | 17596402 | |||||||
| chr4:17596454 | C | T | 3 | a0001c0004t0001g0021 a0001c0004t0001g0126 a0001c0004t0001g0128 |
4 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.989-592C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 8/12 | chr4 | 17596454 | |||||||
| chr4:17596462 | C | T | 4 | a0001c0004t0001g0021 a0001c0004t0001g0126 a0001c0004t0001g0127 others(1): Show |
5 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.989-584C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 8/12 | chr4 | 17596462 | |||||||
| chr4:17596519 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.989-527A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 8/12 | chr4 | 17596519 | |||||||
| chr4:17596581 | T | C | 19 | a0001c0002t0010g0141 a0001c0004t0001g0118 a0001c0004t0001g0119 others(16): Show |
25 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.989-465T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 8/12 | chr4 | 17596581 | |||||||
| chr4:17596690 | G | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0049 |
3 | NA18956.hp2 NA18971.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.989-356G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 8/12 | chr4 | 17596690 | |||||||
| chr4:17596732 | T | G | 9 | a0001c0004t0001g0118 a0001c0004t0001g0119 a0001c0004t0001g0120 others(6): Show |
9 | HG02451.hp2 HG02630.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.989-314T>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 8/12 | chr4 | 17596732 | |||||||
| chr4:17596736 | T | C | 1 | a0001c0002t0002g0180 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.989-310T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 8/12 | chr4 | 17596736 | |||||||
| chr4:17596740 | C | T | 4 | a0001c0004t0001g0021 a0001c0004t0001g0126 a0001c0004t0001g0127 others(1): Show |
5 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.989-306C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 8/12 | chr4 | 17596740 | |||||||
| chr4:17596761 | G | A | 102 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(99): Show |
153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.989-285G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 8/12 | chr4 | 17596761 | |||||||
| chr4:17597217 | G | A | 2 | a0001c0002t0002g0181 a0001c0002t0002g0182 |
2 | HG00323.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1077+83G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 9/12 | chr4 | 17597217 | |||||||
| chr4:17597268 | T | A | 1 | a0001c0003t0001g0016 | 2 | HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1077+134T>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 9/12 | chr4 | 17597268 | |||||||
| chr4:17597397 | G | A | 5 | a0001c0001t0001g0019 a0001c0001t0001g0035 a0001c0001t0001g0073 others(2): Show |
6 | HG01123.hp2 HG02698.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1077+263G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 9/12 | chr4 | 17597397 | |||||||
| chr4:17597410 | G | A | 9 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(6): Show |
10 | HG01243.hp2 HG02145.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1077+276G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 9/12 | chr4 | 17597410 | |||||||
| chr4:17597463 | T | G | 1 | a0001c0001t0001g0132 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1077+329T>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 9/12 | chr4 | 17597463 | |||||||
| chr4:17597714 | A | T | 2 | a0001c0004t0001g0143 a0001c0007t0001g0146 |
2 | HG03017.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.1077+580A>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 9/12 | chr4 | 17597714 | |||||||
| chr4:17597800 | G | A | 1 | a0001c0002t0002g0189 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1078-656G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 9/12 | chr4 | 17597800 | |||||||
| chr4:17597848 | G | T | 1 | a0001c0002t0010g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1078-608G>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 9/12 | chr4 | 17597848 | |||||||
| chr4:17597877 | G | T | 161 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(158): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.1078-579G>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 9/12 | chr4 | 17597877 | |||||||
| chr4:17597901 | C | A | 1 | a0001c0002t0010g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1078-555C>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 9/12 | chr4 | 17597901 | |||||||
| chr4:17597901 | C | T | 3 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 |
3 | HG02280.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1078-555C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 9/12 | chr4 | 17597901 | |||||||
| chr4:17597919 | A | C | 7 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(4): Show |
7 | HG02145.hp2 HG02280.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1078-537A>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 9/12 | chr4 | 17597919 | |||||||
| chr4:17598070 | G | A | 1 | a0001c0001t0001g0022 | 2 | HG02451.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1078-386G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 9/12 | chr4 | 17598070 | |||||||
| chr4:17598139 | C | T | 1 | a0001c0001t0001g0058 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1078-317C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 9/12 | chr4 | 17598139 | |||||||
| chr4:17598191 | G | T | 1 | a0001c0002t0010g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1078-265G>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 9/12 | chr4 | 17598191 | |||||||
| chr4:17598206 | C | T | 1 | a0001c0002t0010g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1078-250C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 9/12 | chr4 | 17598206 | |||||||
| chr4:17598214 | G | A | 131 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(128): Show |
189 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.1078-242G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 9/12 | chr4 | 17598214 | |||||||
| chr4:17598271 | G | T | 103 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(100): Show |
154 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.1078-185G>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 9/12 | chr4 | 17598271 | |||||||
| chr4:17598377 | C | T | 1 | a0001c0001t0001g0080 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1078-79C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 9/12 | chr4 | 17598377 | |||||||
| chr4:17598395 | G | T | 1 | a0001c0002t0002g0187 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1078-61G>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 9/12 | chr4 | 17598395 | |||||||
| chr4:17598761 | C | CT | 117 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(114): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.1180+212dupT | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 17598761 | ||||||
| chr4:17598775 | C | T | 4 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(1): Show |
4 | HG00673.hp2 NA18960.hp1 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.1180+217C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17598775 | |||||||
| chr4:17598787 | C | CT | 5 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(2): Show |
5 | HG01243.hp2 HG02615.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1180+230dupT | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 17598787 | ||||||
| chr4:17598883 | C | T | 3 | a0001c0001t0001g0020 a0001c0001t0001g0105 a0001c0001t0001g0112 |
4 | NA18942.hp2 NA18950.hp2 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.1180+325C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17598883 | |||||||
| chr4:17598890 | C | T | 1 | a0001c0005t0003g0157 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1180+332C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17598890 | |||||||
| chr4:17598916 | T | G | 5 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(2): Show |
5 | HG01243.hp2 HG02615.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1180+358T>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17598916 | |||||||
| chr4:17598958 | G | A | 1 | a0001c0004t0001g0143 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1180+400G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17598958 | |||||||
| chr4:17598983 | C | A | 116 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(113): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.1180+425C>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17598983 | |||||||
| chr4:17598984 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1180+426C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17598984 | |||||||
| chr4:17599035 | G | T | 1 | a0001c0007t0001g0146 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1180+477G>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17599035 | |||||||
| chr4:17599046 | A | C | 1 | a0001c0001t0001g0079 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1180+488A>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17599046 | |||||||
| chr4:17599105 | A | C | 169 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(166): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.1180+547A>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17599105 | |||||||
| chr4:17599260 | C | T | 3 | a0001c0004t0001g0143 a0001c0004t0007g0139 a0001c0007t0001g0146 |
3 | HG02257.hp2 HG03017.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.1180+702C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17599260 | |||||||
| chr4:17599261 | A | G | 137 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(134): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.1180+703A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17599261 | |||||||
| chr4:17599291 | C | A | 2 | a0001c0001t0001g0050 a0001c0001t0001g0061 |
2 | HG01433.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.1180+733C>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17599291 | |||||||
| chr4:17599428 | C | T | 5 | a0001c0001t0001g0011 a0001c0001t0001g0122 a0001c0001t0001g0130 others(2): Show |
8 | HG02109.hp2 HG02559.hp1 HG03579.hp1 others(5): Show |
intron_variant | MODIFIER | c.1180+870C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17599428 | |||||||
| chr4:17599434 | G | T | 1 | a0001c0004t0009g0034 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1180+876G>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17599434 | |||||||
| chr4:17599484 | C | T | 3 | a0001c0001t0001g0035 a0001c0001t0001g0073 a0001c0001t0001g0076 |
3 | HG02717.hp1 HG02886.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1180+926C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17599484 | |||||||
| chr4:17599521 | C | T | 2 | a0001c0001t0001g0081 a0001c0001t0001g0096 |
2 | HG02129.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.1180+963C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17599521 | |||||||
| chr4:17599532 | C | T | 1 | a0001c0008t0002g0160 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1180+974C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17599532 | |||||||
| chr4:17599533 | T | C | 1 | a0001c0008t0002g0160 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1180+975T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17599533 | |||||||
| chr4:17599536 | A | AAAAAT | 11 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0173 others(8): Show |
12 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.1180+997_1180+1001 others(8): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 17599536 | ||||||
| chr4:17599536 | A | AAAAATAA others(3): Show |
1 | a0001c0001t0001g0172 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1180+992_1180+1001 others(13): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 17599536 | ||||||
| chr4:17599554 | A | G | 1 | a0001c0004t0009g0034 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1180+996A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17599554 | |||||||
| chr4:17599704 | A | AC | 7 | a0001c0004t0001g0118 a0001c0004t0001g0119 a0001c0004t0001g0120 others(4): Show |
7 | HG02451.hp2 HG02630.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.1180+1147dupC | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 17599704 | ||||||
| chr4:17599760 | A | T | 1 | a0001c0004t0007g0139 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1180+1202A>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17599760 | |||||||
| chr4:17599820 | C | T | 3 | a0001c0001t0001g0018 a0001c0001t0001g0088 a0001c0001t0001g0197 |
4 | HG02970.hp1 HG02976.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1180+1262C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17599820 | |||||||
| chr4:17599876 | C | T | 4 | a0001c0001t0001g0058 a0001c0004t0001g0143 a0001c0004t0007g0139 others(1): Show |
4 | HG02257.hp2 HG03017.hp1 NA18939.hp1 others(1): Show |
intron_variant | MODIFIER | c.1180+1318C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17599876 | |||||||
| chr4:17600133 | A | T | 1 | a0001c0001t0001g0058 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1180+1575A>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17600133 | |||||||
| chr4:17600274 | A | G | 9 | a0001c0004t0001g0118 a0001c0004t0001g0119 a0001c0004t0001g0120 others(6): Show |
9 | HG02451.hp2 HG02630.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.1180+1716A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17600274 | |||||||
| chr4:17600361 | T | C | 1 | a0001c0003t0001g0016 | 2 | HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1180+1803T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17600361 | |||||||
| chr4:17600382 | T | G | 3 | a0001c0005t0003g0007 a0001c0005t0003g0155 a0001c0005t0003g0156 |
8 | HG02055.hp1 HG02486.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1180+1824T>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17600382 | |||||||
| chr4:17600410 | G | C | 121 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(118): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.1180+1852G>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17600410 | |||||||
| chr4:17600450 | C | T | 9 | a0001c0004t0001g0118 a0001c0004t0001g0119 a0001c0004t0001g0120 others(6): Show |
9 | HG02451.hp2 HG02630.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.1180+1892C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17600450 | |||||||
| chr4:17600518 | A | C | 9 | a0001c0004t0001g0118 a0001c0004t0001g0119 a0001c0004t0001g0120 others(6): Show |
9 | HG02451.hp2 HG02630.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.1180+1960A>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17600518 | |||||||
| chr4:17600560 | T | C | 1 | a0001c0002t0010g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1180+2002T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17600560 | |||||||
| chr4:17600594 | C | G | 5 | a0001c0005t0003g0007 a0001c0005t0003g0155 a0001c0005t0003g0156 others(2): Show |
10 | HG02055.hp1 HG02258.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1180+2036C>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17600594 | |||||||
| chr4:17600629 | G | A | 4 | a0001c0001t0001g0011 a0001c0001t0001g0122 a0001c0001t0001g0130 others(1): Show |
7 | HG02109.hp2 HG02559.hp1 HG03579.hp1 others(4): Show |
intron_variant | MODIFIER | c.1180+2071G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17600629 | |||||||
| chr4:17600673 | G | A | 9 | a0001c0004t0001g0118 a0001c0004t0001g0119 a0001c0004t0001g0120 others(6): Show |
9 | HG02451.hp2 HG02630.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.1180+2115G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17600673 | |||||||
| chr4:17600738 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1180+2180A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17600738 | |||||||
| chr4:17600782 | C | T | 1 | a0001c0004t0009g0034 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1180+2224C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17600782 | |||||||
| chr4:17600840 | G | T | 9 | a0001c0004t0001g0118 a0001c0004t0001g0119 a0001c0004t0001g0120 others(6): Show |
9 | HG02451.hp2 HG02630.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.1180+2282G>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17600840 | |||||||
| chr4:17600896 | C | T | 1 | a0001c0002t0010g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1180+2338C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17600896 | |||||||
| chr4:17600898 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1180+2340C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17600898 | |||||||
| chr4:17601134 | C | A | 4 | a0001c0004t0001g0021 a0001c0004t0001g0126 a0001c0004t0001g0127 others(1): Show |
5 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.1180+2576C>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17601134 | |||||||
| chr4:17601136 | C | T | 9 | a0001c0004t0001g0118 a0001c0004t0001g0119 a0001c0004t0001g0120 others(6): Show |
9 | HG02451.hp2 HG02630.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.1180+2578C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17601136 | |||||||
| chr4:17601153 | T | C | 3 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 |
3 | HG02280.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1180+2595T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17601153 | |||||||
| chr4:17601188 | C | T | 1 | a0001c0004t0007g0139 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1180+2630C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17601188 | |||||||
| chr4:17601346 | G | C | 1 | a0001c0002t0002g0031 | 2 | HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1180+2788G>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17601346 | |||||||
| chr4:17601348 | G | A | 2 | a0001c0001t0001g0051 a0001c0001t0001g0062 |
2 | HG01928.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.1180+2790G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17601348 | |||||||
| chr4:17601414 | T | C | 5 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(2): Show |
5 | HG01243.hp2 HG02615.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1180+2856T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17601414 | |||||||
| chr4:17601461 | T | G | 7 | a0001c0004t0001g0118 a0001c0004t0001g0119 a0001c0004t0001g0120 others(4): Show |
7 | HG02451.hp2 HG02630.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.1180+2903T>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17601461 | |||||||
| chr4:17601534 | C | A | 1 | a0001c0001t0001g0093 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1180+2976C>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17601534 | |||||||
| chr4:17601539 | A | C | 1 | a0001c0004t0009g0034 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1180+2981A>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17601539 | |||||||
| chr4:17601556 | T | C | 8 | a0001c0004t0001g0118 a0001c0004t0001g0119 a0001c0004t0001g0120 others(5): Show |
8 | HG02451.hp2 HG02630.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.1180+2998T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17601556 | |||||||
| chr4:17601565 | A | G | 2 | a0001c0001t0001g0022 a0001c0003t0001g0016 |
4 | HG02451.hp1 HG03098.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1180+3007A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17601565 | |||||||
| chr4:17601586 | G | A | 7 | a0001c0004t0001g0021 a0001c0004t0001g0126 a0001c0004t0001g0127 others(4): Show |
8 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1181-3002G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17601586 | |||||||
| chr4:17601695 | C | T | 150 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(147): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.1181-2893C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17601695 | |||||||
| chr4:17601722 | A | G | 14 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0175 others(11): Show |
23 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.1181-2866A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17601722 | |||||||
| chr4:17601801 | C | T | 150 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(147): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.1181-2787C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17601801 | |||||||
| chr4:17601820 | T | C | 1 | a0001c0002t0002g0184 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1181-2768T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17601820 | |||||||
| chr4:17601835 | C | T | 1 | a0001c0004t0001g0143 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1181-2753C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17601835 | |||||||
| chr4:17601863 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1181-2725T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17601863 | |||||||
| chr4:17601875 | C | T | 12 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(9): Show |
13 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.1181-2713C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17601875 | |||||||
| chr4:17601950 | A | T | 7 | a0001c0004t0001g0118 a0001c0004t0001g0119 a0001c0004t0001g0120 others(4): Show |
7 | HG02451.hp2 HG02630.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.1181-2638A>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17601950 | |||||||
| chr4:17602012 | T | C | 4 | a0001c0004t0001g0021 a0001c0004t0001g0126 a0001c0004t0001g0127 others(1): Show |
5 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.1181-2576T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17602012 | |||||||
| chr4:17602044 | C | T | 1 | a0001c0003t0003g0028 | 2 | HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1181-2544C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17602044 | |||||||
| chr4:17602286 | C | T | 2 | a0001c0001t0001g0057 a0001c0001t0001g0071 |
2 | HG01261.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1181-2302C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17602286 | |||||||
| chr4:17602345 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1181-2243G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17602345 | |||||||
| chr4:17602349 | T | C | 5 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(2): Show |
5 | HG01243.hp2 HG02615.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1181-2239T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17602349 | |||||||
| chr4:17602524 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1181-2064A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17602524 | |||||||
| chr4:17602629 | C | T | 2 | a0001c0001t0001g0048 a0001c0001t0001g0065 |
2 | HG00423.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.1181-1959C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17602629 | |||||||
| chr4:17602672 | G | C | 116 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(113): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.1181-1916G>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17602672 | |||||||
| chr4:17602678 | A | G | 9 | a0001c0004t0001g0118 a0001c0004t0001g0119 a0001c0004t0001g0120 others(6): Show |
9 | HG02451.hp2 HG02630.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.1181-1910A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17602678 | |||||||
| chr4:17602726 | G | T | 4 | a0001c0004t0001g0021 a0001c0004t0001g0126 a0001c0004t0001g0127 others(1): Show |
5 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.1181-1862G>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17602726 | |||||||
| chr4:17602831 | T | G | 9 | a0001c0004t0001g0118 a0001c0004t0001g0119 a0001c0004t0001g0120 others(6): Show |
9 | HG02451.hp2 HG02630.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.1181-1757T>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17602831 | |||||||
| chr4:17602833 | C | T | 1 | a0001c0002t0010g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1181-1755C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17602833 | |||||||
| chr4:17602846 | G | A | 1 | a0001c0007t0001g0146 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1181-1742G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17602846 | |||||||
| chr4:17602871 | G | A | 1 | a0001c0002t0010g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1181-1717G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17602871 | |||||||
| chr4:17602881 | A | G | 137 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(134): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.1181-1707A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17602881 | |||||||
| chr4:17602928 | C | T | 9 | a0001c0004t0001g0118 a0001c0004t0001g0119 a0001c0004t0001g0120 others(6): Show |
9 | HG02451.hp2 HG02630.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.1181-1660C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17602928 | |||||||
| chr4:17602966 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1181-1622G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17602966 | |||||||
| chr4:17602992 | A | G | 5 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(2): Show |
5 | HG01243.hp2 HG02615.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1181-1596A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17602992 | |||||||
| chr4:17603034 | G | A | 1 | a0001c0002t0010g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1181-1554G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17603034 | |||||||
| chr4:17603036 | G | A | 7 | a0001c0004t0001g0021 a0001c0004t0001g0126 a0001c0004t0001g0127 others(4): Show |
8 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1181-1552G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17603036 | |||||||
| chr4:17603082 | T | C | 137 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(134): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.1181-1506T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17603082 | |||||||
| chr4:17603179 | T | C | 137 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(134): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.1181-1409T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17603179 | |||||||
| chr4:17603202 | A | G | 137 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(134): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.1181-1386A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17603202 | |||||||
| chr4:17603505 | CT | C | 148 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(145): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.1181-1067delT | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 17603505 | ||||||
| chr4:17603535 | G | A | 7 | a0001c0004t0001g0118 a0001c0004t0001g0119 a0001c0004t0001g0120 others(4): Show |
7 | HG02451.hp2 HG02630.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.1181-1053G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17603535 | |||||||
| chr4:17603646 | G | C | 3 | a0001c0005t0003g0026 a0001c0005t0003g0142 a0001c0005t0003g0154 |
4 | HG01109.hp1 HG01884.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1181-942G>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17603646 | |||||||
| chr4:17603669 | C | G | 9 | a0001c0004t0001g0118 a0001c0004t0001g0119 a0001c0004t0001g0120 others(6): Show |
9 | HG02451.hp2 HG02630.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.1181-919C>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17603669 | |||||||
| chr4:17603671 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1181-917C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17603671 | |||||||
| chr4:17603724 | G | C | 116 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(113): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.1181-864G>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17603724 | |||||||
| chr4:17603779 | G | A | 9 | a0001c0004t0001g0118 a0001c0004t0001g0119 a0001c0004t0001g0120 others(6): Show |
9 | HG02451.hp2 HG02630.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.1181-809G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17603779 | |||||||
| chr4:17603813 | C | CT | 11 | a0001c0001t0004g0005 a0001c0001t0004g0029 a0001c0001t0004g0161 others(8): Show |
18 | HG01123.hp1 HG01192.hp2 HG01952.hp1 others(15): Show |
intron_variant | MODIFIER | c.1181-763dupT | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 17603813 | ||||||
| chr4:17603813 | CT | C | 9 | a0001c0004t0001g0118 a0001c0004t0001g0119 a0001c0004t0001g0120 others(6): Show |
9 | HG02451.hp2 HG02630.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.1181-763delT | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 17603813 | ||||||
| chr4:17603822 | T | C | 2 | a0001c0002t0010g0141 a0001c0008t0002g0160 |
2 | HG02965.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1181-766T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17603822 | |||||||
| chr4:17603824 | TTCTTTCT others(3): Show |
T | 2 | a0001c0001t0001g0053 a0001c0001t0001g0104 |
2 | HG01952.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.1181-762_1181-753d others(12): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 17603824 | ||||||
| chr4:17603826 | CTTTCTTT others(2): Show |
C | 114 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(111): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.1181-758_1181-750d others(11): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 17603826 | ||||||
| chr4:17603834 | C | CT | 8 | a0001c0004t0001g0118 a0001c0004t0001g0119 a0001c0004t0001g0120 others(5): Show |
8 | HG02451.hp2 HG02630.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.1181-744dupT | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 17603834 | ||||||
| chr4:17603835 | T | C | 2 | a0001c0001t0001g0053 a0001c0001t0001g0104 |
2 | HG01952.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.1181-753T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17603835 | |||||||
| chr4:17603863 | A | G | 4 | a0001c0001t0001g0011 a0001c0001t0001g0122 a0001c0001t0001g0130 others(1): Show |
7 | HG02109.hp2 HG02559.hp1 HG03579.hp1 others(4): Show |
intron_variant | MODIFIER | c.1181-725A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17603863 | |||||||
| chr4:17603912 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1181-676C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17603912 | |||||||
| chr4:17603978 | G | C | 2 | a0001c0004t0001g0143 a0001c0007t0001g0146 |
2 | HG03017.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.1181-610G>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17603978 | |||||||
| chr4:17603991 | T | C | 9 | a0001c0004t0001g0118 a0001c0004t0001g0119 a0001c0004t0001g0120 others(6): Show |
9 | HG02451.hp2 HG02630.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.1181-597T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17603991 | |||||||
| chr4:17604009 | C | T | 3 | a0001c0001t0001g0056 a0001c0001t0001g0069 a0001c0001t0001g0070 |
3 | HG01361.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1181-579C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17604009 | |||||||
| chr4:17604019 | A | C | 137 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(134): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.1181-569A>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17604019 | |||||||
| chr4:17604177 | C | T | 7 | a0001c0004t0001g0118 a0001c0004t0001g0119 a0001c0004t0001g0120 others(4): Show |
7 | HG02451.hp2 HG02630.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.1181-411C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17604177 | |||||||
| chr4:17604198 | G | C | 116 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(113): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.1181-390G>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17604198 | |||||||
| chr4:17604245 | C | T | 1 | a0001c0002t0010g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1181-343C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17604245 | |||||||
| chr4:17604270 | C | CA | 19 | a0001c0001t0001g0035 a0001c0001t0001g0045 a0001c0001t0001g0049 others(16): Show |
20 | HG01109.hp2 HG01257.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.1181-296dupA | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 17604270 | ||||||
| chr4:17604270 | C | CAA | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(3): Show |
6 | HG01243.hp2 HG02615.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1181-297_1181-296d others(4): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 17604270 | ||||||
| chr4:17604270 | C | CAAA | 12 | a0001c0004t0001g0021 a0001c0004t0001g0118 a0001c0004t0001g0119 others(9): Show |
13 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1181-298_1181-296d others(5): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 17604270 | ||||||
| chr4:17604270 | C | CAAAAAAA others(4): Show |
1 | a0001c0004t0001g0143 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1181-306_1181-296d others(13): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 17604270 | ||||||
| chr4:17604270 | CA | C | 20 | a0001c0001t0001g0011 a0001c0001t0001g0070 a0001c0001t0001g0075 others(17): Show |
27 | HG00323.hp2 HG01255.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.1181-296delA | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 17604270 | ||||||
| chr4:17604270 | CAA | C | 11 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(8): Show |
13 | HG00099.hp1 HG02280.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.1181-297_1181-296d others(4): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 17604270 | ||||||
| chr4:17604292 | A | G | 1 | a0001c0001t0001g0134 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1181-296A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17604292 | |||||||
| chr4:17604327 | GT | G | 116 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(113): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.1181-259delT | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 17604327 | ||||||
| chr4:17604336 | T | C | 116 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(113): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.1181-252T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17604336 | |||||||
| chr4:17604773 | G | A | 2 | a0001c0005t0006g0158 a0001c0005t0006g0159 |
2 | HG02258.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1260+106G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | chr4 | 17604773 | |||||||
| chr4:17604778 | T | C | 1 | a0001c0005t0003g0157 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1260+111T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | chr4 | 17604778 | |||||||
| chr4:17604883 | C | T | 5 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(2): Show |
5 | HG01243.hp2 HG02615.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1260+216C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | chr4 | 17604883 | |||||||
| chr4:17605036 | G | A | 99 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(96): Show |
148 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.1260+369G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | chr4 | 17605036 | |||||||
| chr4:17605118 | C | CCA | 19 | a0001c0002t0002g0176 a0001c0003t0003g0012 a0001c0003t0003g0025 others(16): Show |
24 | HG02145.hp1 HG02451.hp2 HG02622.hp1 others(21): Show |
intron_variant | MODIFIER | c.1260+481_1260+482d others(4): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 17605118 | ||||||
| chr4:17605118 | C | CCACA | 4 | a0001c0001t0004g0164 a0001c0005t0003g0026 a0001c0005t0003g0142 others(1): Show |
5 | HG01109.hp1 HG01884.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1260+479_1260+482d others(6): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 17605118 | ||||||
| chr4:17605118 | CCA | C | 19 | a0001c0001t0001g0022 a0001c0001t0001g0043 a0001c0001t0001g0056 others(16): Show |
28 | HG00099.hp1 HG01243.hp1 HG01361.hp1 others(25): Show |
intron_variant | MODIFIER | c.1260+481_1260+482d others(4): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 17605118 | ||||||
| chr4:17605118 | CCACA | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(109): Show |
164 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.1260+479_1260+482d others(6): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 17605118 | ||||||
| chr4:17605148 | A | C | 6 | a0001c0004t0001g0021 a0001c0004t0001g0126 a0001c0004t0001g0127 others(3): Show |
7 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.1260+481A>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | chr4 | 17605148 | |||||||
| chr4:17605229 | CTG | C | 7 | a0001c0004t0001g0021 a0001c0004t0001g0126 a0001c0004t0001g0127 others(4): Show |
8 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1260+565_1260+566d others(4): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 17605229 | ||||||
| chr4:17605270 | T | G | 9 | a0001c0004t0001g0118 a0001c0004t0001g0119 a0001c0004t0001g0120 others(6): Show |
9 | HG02451.hp2 HG02630.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.1260+603T>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | chr4 | 17605270 | |||||||
| chr4:17605333 | C | T | 3 | a0001c0001t0001g0055 a0001c0001t0001g0063 a0001c0001t0001g0109 |
3 | HG00733.hp1 HG01169.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.1260+666C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | chr4 | 17605333 | |||||||
| chr4:17605400 | G | A | 3 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0080 |
3 | NA18960.hp1 NA19081.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1260+733G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | chr4 | 17605400 | |||||||
| chr4:17605444 | G | T | 8 | a0001c0004t0001g0118 a0001c0004t0001g0119 a0001c0004t0001g0120 others(5): Show |
8 | HG02451.hp2 HG02630.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.1260+777G>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | chr4 | 17605444 | |||||||
| chr4:17605524 | T | C | 1 | a0001c0002t0010g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1260+857T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | chr4 | 17605524 | |||||||
| chr4:17605580 | TA | T | 116 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(113): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.1260+915delA | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 17605580 | ||||||
| chr4:17605676 | C | T | 1 | a0001c0002t0010g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1260+1009C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | chr4 | 17605676 | |||||||
| chr4:17605681 | A | C | 3 | a0001c0004t0001g0143 a0001c0004t0007g0139 a0001c0007t0001g0146 |
3 | HG02257.hp2 HG03017.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.1260+1014A>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | chr4 | 17605681 | |||||||
| chr4:17605700 | T | C | 137 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(134): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.1260+1033T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | chr4 | 17605700 | |||||||
| chr4:17605718 | G | A | 2 | a0001c0001t0001g0022 a0001c0003t0001g0016 |
4 | HG02451.hp1 HG03098.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1260+1051G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | chr4 | 17605718 | |||||||
| chr4:17605752 | C | T | 1 | a0001c0002t0002g0185 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1261-1077C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | chr4 | 17605752 | |||||||
| chr4:17605954 | T | C | 12 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(9): Show |
13 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.1261-875T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | chr4 | 17605954 | |||||||
| chr4:17606097 | C | G | 9 | a0001c0004t0001g0118 a0001c0004t0001g0119 a0001c0004t0001g0120 others(6): Show |
9 | HG02451.hp2 HG02630.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.1261-732C>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | chr4 | 17606097 | |||||||
| chr4:17606150 | T | C | 12 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(9): Show |
13 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.1261-679T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | chr4 | 17606150 | |||||||
| chr4:17606208 | G | T | 1 | a0001c0001t0001g0091 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1261-621G>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | chr4 | 17606208 | |||||||
| chr4:17606374 | C | T | 5 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(2): Show |
5 | HG01243.hp2 HG02615.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1261-455C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | chr4 | 17606374 | |||||||
| chr4:17606394 | C | T | 9 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(6): Show |
10 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.1261-435C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | chr4 | 17606394 | |||||||
| chr4:17606395 | G | A | 1 | a0001c0004t0001g0126 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1261-434G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | chr4 | 17606395 | |||||||
| chr4:17606484 | G | A | 3 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0002t0002g0185 |
3 | HG03491.hp1 HG03492.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1261-345G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | chr4 | 17606484 | |||||||
| chr4:17606673 | TA | T | 9 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(6): Show |
10 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.1261-154delA | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 17606673 | ||||||
| chr4:17606676 | T | C | 116 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(113): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.1261-153T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | chr4 | 17606676 | |||||||
| chr4:17606700 | A | G | 1 | a0001c0004t0007g0139 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1261-129A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | chr4 | 17606700 | |||||||
| chr4:17606997 | A | G | 116 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(113): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.1370+59A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 12/12 | chr4 | 17606997 | |||||||
| chr4:17607018 | T | C | 1 | a0001c0001t0001g0132 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1370+80T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 12/12 | chr4 | 17607018 | |||||||
| chr4:17607137 | G | A | 2 | a0001c0001t0001g0019 a0001c0001t0001g0090 |
3 | HG01123.hp2 HG02698.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1370+199G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 12/12 | chr4 | 17607137 | |||||||
| chr4:17607261 | C | G | 150 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(147): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.1371-139C>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 12/12 | chr4 | 17607261 |