Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 163747 |
| ensemblid | ENSG00000162398.12 |
| hgncid | 26854 |
| symbol | LEXM |
| name | ciliary microtubule associated protein 2 |
| refseq_nuc | NM_001110533.2 |
| refseq_prot | NP_001104003.1 |
| ensembl_nuc | ENST00000371273.4 |
| ensembl_prot | ENSP00000360320.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 54806063 |
| end | 54842252 |
| strand | + |
| ver | v1.2 |
| region | chr1:54806063-54842252 |
| region5000 | chr1:54801063-54847252 |
| regionname0 | LEXM_chr1_54806063_54842252 |
| regionname5000 | LEXM_chr1_54801063_54847252 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 418 | 194 | 25 | 39 | 108 | 7 | 14 | 84 | LEXM_chr1_54801063_54847252 | LEXM | MRESQ others(413): Show |
chr1 | 54801063 | 54847252 |
| a0002 | 0/1 | 418 | 145 | 35 | 26 | 49 | 9 | 25 | 33 | LEXM_chr1_54801063_54847252 | LEXM | MRESQ others(413): Show |
chr1 | 54801063 | 54847252 |
| a0003 | 0/0 | 418 | 15 | 1 | 0 | 14 | 0 | 0 | 12 | LEXM_chr1_54801063_54847252 | LEXM | MRESQ others(413): Show |
chr1 | 54801063 | 54847252 |
| a0004 | 0/0 | 418 | 11 | 6 | 0 | 5 | 0 | 0 | 4 | LEXM_chr1_54801063_54847252 | LEXM | MRESQ others(413): Show |
chr1 | 54801063 | 54847252 |
| a0005 | 0/0 | 418 | 6 | 1 | 0 | 5 | 0 | 0 | 4 | LEXM_chr1_54801063_54847252 | LEXM | MRESQ others(413): Show |
chr1 | 54801063 | 54847252 |
| a0006 | 0/0 | 418 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | MRESQ others(413): Show |
chr1 | 54801063 | 54847252 |
| a0007 | 0/0 | 418 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | MRESQ others(413): Show |
chr1 | 54801063 | 54847252 |
| a0008 | 0/0 | 418 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | MRESQ others(413): Show |
chr1 | 54801063 | 54847252 |
| a0009 | 0/0 | 418 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | MRESQ others(413): Show |
chr1 | 54801063 | 54847252 |
| a0010 | 0/0 | 418 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LEXM_chr1_54801063_54847252 | LEXM | MRESQ others(413): Show |
chr1 | 54801063 | 54847252 |
| a0011 | 0/0 | 418 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | MRESQ others(413): Show |
chr1 | 54801063 | 54847252 |
| a0012 | 0/0 | 418 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | MRESQ others(413): Show |
chr1 | 54801063 | 54847252 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 1/0 | 1254 | 101 | 21 | 25 | 40 | 3 | 11 | LEXM_chr1_54801063_54847252 | LEXM | ATGAG others(1249): Show |
chr1 | 54801063 | 54847252 | ||
| a0001c0003 | 0/0 | 1254 | 58 | 4 | 12 | 36 | 4 | 2 | LEXM_chr1_54801063_54847252 | LEXM | ATGAG others(1249): Show |
chr1 | 54801063 | 54847252 | ||
| a0001c0004 | 0/0 | 1254 | 29 | 0 | 2 | 27 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | ATGAG others(1249): Show |
chr1 | 54801063 | 54847252 | ||
| a0001c0009 | 0/0 | 1254 | 5 | 0 | 0 | 4 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | ATGAG others(1249): Show |
chr1 | 54801063 | 54847252 | ||
| a0001c0018 | 0/0 | 1254 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | ATGAG others(1249): Show |
chr1 | 54801063 | 54847252 | ||
| a0002c0001 | 0/1 | 1254 | 114 | 25 | 19 | 39 | 8 | 22 | LEXM_chr1_54801063_54847252 | LEXM | ATGAG others(1249): Show |
chr1 | 54801063 | 54847252 | ||
| a0002c0005 | 0/0 | 1254 | 20 | 5 | 4 | 9 | 1 | 1 | LEXM_chr1_54801063_54847252 | LEXM | ATGAG others(1249): Show |
chr1 | 54801063 | 54847252 | ||
| a0002c0010 | 0/0 | 1254 | 5 | 5 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | ATGAG others(1249): Show |
chr1 | 54801063 | 54847252 | ||
| a0002c0011 | 0/0 | 1254 | 5 | 0 | 3 | 1 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | ATGAG others(1249): Show |
chr1 | 54801063 | 54847252 | ||
| a0002c0015 | 0/0 | 1254 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | ATGAG others(1249): Show |
chr1 | 54801063 | 54847252 | ||
| a0003c0006 | 0/0 | 1254 | 14 | 1 | 0 | 13 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | ATGAG others(1249): Show |
chr1 | 54801063 | 54847252 | ||
| a0003c0020 | 0/0 | 1254 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | ATGAG others(1249): Show |
chr1 | 54801063 | 54847252 | ||
| a0004c0008 | 0/0 | 1254 | 6 | 6 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | ATGAG others(1249): Show |
chr1 | 54801063 | 54847252 | ||
| a0004c0012 | 0/0 | 1254 | 5 | 0 | 0 | 5 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | ATGAG others(1249): Show |
chr1 | 54801063 | 54847252 | ||
| a0005c0007 | 0/0 | 1254 | 6 | 1 | 0 | 5 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | ATGAG others(1249): Show |
chr1 | 54801063 | 54847252 | ||
| a0006c0013 | 0/0 | 1254 | 3 | 3 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | ATGAG others(1249): Show |
chr1 | 54801063 | 54847252 | ||
| a0007c0014 | 0/0 | 1254 | 3 | 3 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | ATGAG others(1249): Show |
chr1 | 54801063 | 54847252 | ||
| a0008c0017 | 0/0 | 1254 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | ATGAG others(1249): Show |
chr1 | 54801063 | 54847252 | ||
| a0009c0019 | 0/0 | 1254 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | ATGAG others(1249): Show |
chr1 | 54801063 | 54847252 | ||
| a0010c0016 | 0/0 | 1254 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | ATGAG others(1249): Show |
chr1 | 54801063 | 54847252 | ||
| a0011c0022 | 0/0 | 1254 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | ATGAG others(1249): Show |
chr1 | 54801063 | 54847252 | ||
| a0012c0021 | 0/0 | 1254 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | ATGAG others(1249): Show |
chr1 | 54801063 | 54847252 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001 | 0/0 | 1690 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | ACAAG others(1685): Show |
chr1 | 54801063 | 54847252 |
| a0001c0002t0002 | 1/0 | 1690 | 97 | 19 | 24 | 39 | 3 | 11 | LEXM_chr1_54801063_54847252 | LEXM | ACAAG others(1685): Show |
chr1 | 54801063 | 54847252 |
| a0001c0002t0005 | 0/0 | 1690 | 2 | 2 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | ACAAG others(1685): Show |
chr1 | 54801063 | 54847252 |
| a0001c0002t0009 | 0/0 | 1690 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | ACAAG others(1685): Show |
chr1 | 54801063 | 54847252 |
| a0001c0003t0003 | 0/0 | 1690 | 55 | 4 | 11 | 34 | 4 | 2 | LEXM_chr1_54801063_54847252 | LEXM | ACAAG others(1685): Show |
chr1 | 54801063 | 54847252 |
| a0001c0003t0004 | 0/0 | 1690 | 2 | 0 | 0 | 2 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | ACAAG others(1685): Show |
chr1 | 54801063 | 54847252 |
| a0001c0003t0008 | 0/0 | 1690 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | ACAAG others(1685): Show |
chr1 | 54801063 | 54847252 |
| a0001c0004t0003 | 0/0 | 1690 | 29 | 0 | 2 | 27 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | ACAAG others(1685): Show |
chr1 | 54801063 | 54847252 |
| a0001c0009t0002 | 0/0 | 1690 | 5 | 0 | 0 | 4 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | ACAAG others(1685): Show |
chr1 | 54801063 | 54847252 |
| a0001c0018t0003 | 0/0 | 1690 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | ACAAG others(1685): Show |
chr1 | 54801063 | 54847252 |
| a0002c0001t0001 | 0/1 | 1690 | 113 | 25 | 19 | 39 | 7 | 22 | LEXM_chr1_54801063_54847252 | LEXM | ACAAG others(1685): Show |
chr1 | 54801063 | 54847252 |
| a0002c0001t0007 | 0/0 | 1690 | 1 | 0 | 0 | 0 | 1 | 0 | LEXM_chr1_54801063_54847252 | LEXM | ACAAG others(1685): Show |
chr1 | 54801063 | 54847252 |
| a0002c0005t0004 | 0/0 | 1690 | 20 | 5 | 4 | 9 | 1 | 1 | LEXM_chr1_54801063_54847252 | LEXM | ACAAG others(1685): Show |
chr1 | 54801063 | 54847252 |
| a0002c0010t0001 | 0/0 | 1690 | 5 | 5 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | ACAAG others(1685): Show |
chr1 | 54801063 | 54847252 |
| a0002c0011t0004 | 0/0 | 1690 | 5 | 0 | 3 | 1 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | ACAAG others(1685): Show |
chr1 | 54801063 | 54847252 |
| a0002c0015t0001 | 0/0 | 1690 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | ACAAG others(1685): Show |
chr1 | 54801063 | 54847252 |
| a0003c0006t0001 | 0/0 | 1690 | 14 | 1 | 0 | 13 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | ACAAG others(1685): Show |
chr1 | 54801063 | 54847252 |
| a0003c0020t0004 | 0/0 | 1690 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | ACAAG others(1685): Show |
chr1 | 54801063 | 54847252 |
| a0004c0008t0001 | 0/0 | 1690 | 5 | 5 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | ACAAG others(1685): Show |
chr1 | 54801063 | 54847252 |
| a0004c0008t0006 | 0/0 | 1690 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | ACAAG others(1685): Show |
chr1 | 54801063 | 54847252 |
| a0004c0012t0004 | 0/0 | 1690 | 5 | 0 | 0 | 5 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | ACAAG others(1685): Show |
chr1 | 54801063 | 54847252 |
| a0005c0007t0001 | 0/0 | 1690 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | ACAAG others(1685): Show |
chr1 | 54801063 | 54847252 |
| a0005c0007t0002 | 0/0 | 1690 | 5 | 1 | 0 | 4 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | ACAAG others(1685): Show |
chr1 | 54801063 | 54847252 |
| a0006c0013t0002 | 0/0 | 1690 | 3 | 3 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | ACAAG others(1685): Show |
chr1 | 54801063 | 54847252 |
| a0007c0014t0003 | 0/0 | 1690 | 3 | 3 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | ACAAG others(1685): Show |
chr1 | 54801063 | 54847252 |
| a0008c0017t0001 | 0/0 | 1690 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | ACAAG others(1685): Show |
chr1 | 54801063 | 54847252 |
| a0009c0019t0002 | 0/0 | 1690 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | ACAAG others(1685): Show |
chr1 | 54801063 | 54847252 |
| a0010c0016t0001 | 0/0 | 1690 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | ACAAG others(1685): Show |
chr1 | 54801063 | 54847252 |
| a0011c0022t0001 | 0/0 | 1690 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | ACAAG others(1685): Show |
chr1 | 54801063 | 54847252 |
| a0012c0021t0004 | 0/0 | 1690 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | ACAAG others(1685): Show |
chr1 | 54801063 | 54847252 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0005 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0006 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0014 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0015 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0020 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0044 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0047 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0049 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0223 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0005g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0002t0009g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0003t0003g0009 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0003t0003g0012 | 0/0 | 5 | 0 | 3 | 0 | 2 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0003t0003g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0003t0003g0019 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0003t0003g0023 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0003t0003g0024 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0003t0003g0042 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0003t0003g0045 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0003t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0003t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0003t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0003t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0003t0003g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0003t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0003t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0003t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0003t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0003t0003g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0003t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0003t0003g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0003t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0003t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0003t0003g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0003t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0003t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0003t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0003t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0003t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0003t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0003t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0003t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0003t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0003t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0003t0004g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0003t0008g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0004t0003g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0004t0003g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0004t0003g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0004t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0004t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0004t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0004t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0004t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0004t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0004t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0004t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0004t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0004t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0004t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0004t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0004t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0004t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0004t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0004t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0004t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0004t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0004t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0009t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0009t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0009t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0009t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0009t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0001c0018t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0001 | 0/0 | 11 | 3 | 3 | 5 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0002 | 0/0 | 7 | 0 | 0 | 2 | 1 | 4 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0003 | 0/0 | 7 | 0 | 2 | 2 | 1 | 2 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0008 | 0/0 | 6 | 0 | 1 | 2 | 3 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0018 | 0/0 | 4 | 2 | 0 | 2 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0021 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0038 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0150 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0001t0007g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0005t0004g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0005t0004g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0005t0004g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0005t0004g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0005t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0005t0004g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0005t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0005t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0005t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0005t0004g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0005t0004g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0005t0004g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0005t0004g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0005t0004g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0005t0004g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0010t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0010t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0010t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0010t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0011t0004g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0011t0004g0033 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0011t0004g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0011t0004g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0002c0015t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0003c0006t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0003c0006t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0003c0006t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0003c0006t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0003c0006t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0003c0006t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0003c0006t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0003c0006t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0003c0006t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0003c0006t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0003c0006t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0003c0006t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0003c0020t0004g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0004c0008t0001g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0004c0008t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0004c0008t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0004c0008t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0004c0008t0006g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0004c0012t0004g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0004c0012t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0004c0012t0004g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0005c0007t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0005c0007t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0005c0007t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0005c0007t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0005c0007t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0005c0007t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0006c0013t0002g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0006c0013t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0007c0014t0003g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0007c0014t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0008c0017t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0009c0019t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0010c0016t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0011c0022t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| a0012c0021t0004g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0001 | t0001 | g0003 | EUR | GBR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG00099 | hp2 | a0001 | c0003 | t0003 | g0012 | EUR | GBR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG00140 | hp1 | a0001 | c0003 | t0003 | g0042 | EUR | GBR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG00140 | hp2 | a0002 | c0001 | t0001 | g0134 | EUR | GBR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG00280 | hp1 | a0002 | c0001 | t0001 | g0008 | EUR | FIN | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG00280 | hp2 | a0001 | c0002 | t0002 | g0020 | EUR | FIN | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG00323 | hp1 | a0001 | c0003 | t0003 | g0185 | EUR | FIN | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG00323 | hp2 | a0002 | c0001 | t0007 | g0002 | EUR | FIN | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG00408 | hp1 | a0001 | c0002 | t0002 | g0230 | EAS | CHS | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG00408 | hp2 | a0001 | c0004 | t0003 | g0004 | EAS | CHS | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG00423 | hp1 | a0002 | c0001 | t0001 | g0034 | EAS | CHS | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG00423 | hp2 | a0001 | c0002 | t0002 | g0229 | EAS | CHS | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG00438 | hp1 | a0002 | c0001 | t0001 | g0034 | EAS | CHS | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG00438 | hp2 | a0001 | c0004 | t0003 | g0181 | EAS | CHS | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG00544 | hp1 | a0001 | c0003 | t0003 | g0197 | EAS | CHS | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG00544 | hp2 | a0002 | c0001 | t0001 | g0011 | EAS | CHS | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG00558 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | CHS | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG00558 | hp2 | a0002 | c0005 | t0004 | g0031 | EAS | CHS | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG00609 | hp1 | a0001 | c0004 | t0003 | g0163 | EAS | CHS | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG00609 | hp2 | a0001 | c0004 | t0003 | g0159 | EAS | CHS | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG00621 | hp1 | a0001 | c0002 | t0002 | g0231 | EAS | CHS | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG00621 | hp2 | a0001 | c0003 | t0003 | g0209 | EAS | CHS | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG00639 | hp1 | a0002 | c0001 | t0001 | g0135 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG00639 | hp2 | a0001 | c0002 | t0002 | g0049 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG00642 | hp1 | a0002 | c0001 | t0001 | g0100 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG00642 | hp2 | a0002 | c0001 | t0001 | g0001 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG00673 | hp1 | a0002 | c0001 | t0001 | g0011 | EAS | CHS | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG00673 | hp2 | a0001 | c0003 | t0004 | g0028 | EAS | CHS | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG00735 | hp1 | a0001 | c0003 | t0003 | g0012 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG00735 | hp2 | a0002 | c0001 | t0001 | g0084 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG00741 | hp1 | a0001 | c0002 | t0002 | g0020 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG00741 | hp2 | a0008 | c0017 | t0001 | g0002 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0187 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01069 | hp2 | a0001 | c0002 | t0002 | g0059 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01070 | hp1 | a0001 | c0002 | t0002 | g0217 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01070 | hp2 | a0001 | c0003 | t0003 | g0184 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01071 | hp1 | a0001 | c0002 | t0002 | g0220 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0188 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01074 | hp1 | a0001 | c0003 | t0003 | g0192 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01074 | hp2 | a0002 | c0001 | t0001 | g0127 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01099 | hp1 | a0001 | c0002 | t0002 | g0015 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01099 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01106 | hp1 | a0002 | c0001 | t0001 | g0078 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01106 | hp2 | a0001 | c0003 | t0003 | g0012 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01109 | hp1 | a0002 | c0001 | t0001 | g0001 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01109 | hp2 | a0001 | c0003 | t0003 | g0186 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0102 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01167 | hp2 | a0001 | c0002 | t0002 | g0027 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01168 | hp1 | a0002 | c0001 | t0001 | g0145 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01168 | hp2 | a0001 | c0004 | t0003 | g0041 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01169 | hp1 | a0001 | c0004 | t0003 | g0041 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01169 | hp2 | a0001 | c0002 | t0002 | g0027 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01175 | hp1 | a0002 | c0001 | t0001 | g0092 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01175 | hp2 | a0002 | c0005 | t0004 | g0146 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01192 | hp1 | a0001 | c0003 | t0003 | g0012 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01192 | hp2 | a0002 | c0001 | t0001 | g0153 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01243 | hp1 | a0002 | c0001 | t0001 | g0038 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01243 | hp2 | a0002 | c0005 | t0004 | g0068 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01255 | hp1 | a0002 | c0001 | t0001 | g0070 | AMR | CLM | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | CLM | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01256 | hp1 | a0001 | c0003 | t0008 | g0195 | AMR | CLM | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01256 | hp2 | a0001 | c0002 | t0002 | g0050 | AMR | CLM | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01257 | hp1 | a0002 | c0005 | t0004 | g0036 | AMR | CLM | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0044 | AMR | CLM | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01258 | hp1 | a0002 | c0005 | t0004 | g0036 | AMR | CLM | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01258 | hp2 | a0001 | c0002 | t0002 | g0050 | AMR | CLM | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01261 | hp1 | a0002 | c0001 | t0001 | g0003 | AMR | CLM | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01261 | hp2 | a0002 | c0001 | t0001 | g0001 | AMR | CLM | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01346 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | CLM | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01346 | hp2 | a0002 | c0001 | t0001 | g0090 | AMR | CLM | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01361 | hp1 | a0001 | c0003 | t0003 | g0009 | AMR | CLM | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01361 | hp2 | a0001 | c0002 | t0002 | g0020 | AMR | CLM | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01433 | hp1 | a0001 | c0003 | t0003 | g0042 | AMR | CLM | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01433 | hp2 | a0002 | c0001 | t0001 | g0008 | AMR | CLM | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01515 | hp1 | a0002 | c0001 | t0001 | g0002 | EUR | IBS | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01515 | hp2 | a0001 | c0003 | t0003 | g0012 | EUR | IBS | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01516 | hp1 | a0001 | c0002 | t0002 | g0020 | EUR | IBS | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01516 | hp2 | a0002 | c0001 | t0001 | g0008 | EUR | IBS | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01884 | hp1 | a0009 | c0019 | t0002 | g0065 | AFR | ACB | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01884 | hp2 | a0004 | c0008 | t0001 | g0051 | AFR | ACB | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01891 | hp1 | a0001 | c0002 | t0002 | g0103 | AFR | ACB | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01891 | hp2 | a0001 | c0002 | t0002 | g0063 | AFR | ACB | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01934 | hp1 | a0001 | c0002 | t0002 | g0015 | AMR | PEL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01934 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01978 | hp1 | a0001 | c0002 | t0002 | g0015 | AMR | PEL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01978 | hp2 | a0002 | c0011 | t0004 | g0165 | AMR | PEL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01981 | hp1 | a0002 | c0001 | t0001 | g0003 | AMR | PEL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01981 | hp2 | a0001 | c0002 | t0002 | g0015 | AMR | PEL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01993 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG01993 | hp2 | a0002 | c0001 | t0001 | g0137 | AMR | PEL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02004 | hp1 | a0001 | c0002 | t0002 | g0015 | AMR | PEL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02004 | hp2 | a0001 | c0003 | t0003 | g0023 | AMR | PEL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02015 | hp1 | a0002 | c0001 | t0001 | g0121 | EAS | KHV | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02015 | hp2 | a0002 | c0001 | t0001 | g0011 | EAS | KHV | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02027 | hp1 | a0002 | c0001 | t0001 | g0021 | EAS | KHV | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02027 | hp2 | a0001 | c0004 | t0003 | g0004 | EAS | KHV | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02040 | hp1 | a0004 | c0012 | t0004 | g0236 | EAS | KHV | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02040 | hp2 | a0002 | c0011 | t0004 | g0033 | EAS | KHV | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02055 | hp1 | a0002 | c0001 | t0001 | g0021 | AFR | ACB | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02055 | hp2 | a0002 | c0001 | t0001 | g0098 | AFR | ACB | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02056 | hp1 | a0001 | c0002 | t0002 | g0228 | EAS | KHV | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02056 | hp2 | a0001 | c0003 | t0003 | g0024 | EAS | KHV | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02071 | hp1 | a0002 | c0001 | t0001 | g0120 | EAS | KHV | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02071 | hp2 | a0001 | c0003 | t0003 | g0199 | EAS | KHV | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02074 | hp1 | a0002 | c0001 | t0001 | g0038 | EAS | KHV | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02074 | hp2 | a0003 | c0006 | t0001 | g0246 | EAS | KHV | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02080 | hp1 | a0001 | c0003 | t0003 | g0207 | EAS | KHV | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02080 | hp2 | a0001 | c0003 | t0003 | g0019 | EAS | KHV | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02083 | hp1 | a0002 | c0005 | t0004 | g0067 | EAS | KHV | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02083 | hp2 | a0001 | c0004 | t0003 | g0053 | EAS | KHV | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02132 | hp1 | a0002 | c0001 | t0001 | g0144 | EAS | KHV | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0016 | EAS | KHV | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02135 | hp1 | a0001 | c0003 | t0003 | g0210 | EAS | KHV | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02135 | hp2 | a0001 | c0003 | t0003 | g0019 | EAS | KHV | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02145 | hp1 | a0002 | c0001 | t0001 | g0018 | AFR | ACB | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02145 | hp2 | a0002 | c0001 | t0001 | g0017 | AFR | ACB | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02148 | hp1 | a0001 | c0003 | t0003 | g0023 | AMR | PEL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02148 | hp2 | a0002 | c0011 | t0004 | g0004 | AMR | PEL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02155 | hp1 | a0002 | c0005 | t0004 | g0091 | EAS | CDX | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02155 | hp2 | a0001 | c0004 | t0003 | g0164 | EAS | CDX | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02165 | hp1 | a0003 | c0006 | t0001 | g0245 | EAS | CDX | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02165 | hp2 | a0002 | c0005 | t0004 | g0031 | EAS | CDX | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02257 | hp1 | a0004 | c0008 | t0006 | g0248 | AFR | ACB | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02257 | hp2 | a0002 | c0001 | t0001 | g0001 | AFR | ACB | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02293 | hp1 | a0002 | c0011 | t0004 | g0169 | AMR | PEL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02293 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02300 | hp1 | a0001 | c0003 | t0003 | g0023 | AMR | PEL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02300 | hp2 | a0002 | c0001 | t0001 | g0097 | AMR | PEL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02451 | hp1 | a0006 | c0013 | t0002 | g0030 | AFR | ACB | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02451 | hp2 | a0002 | c0010 | t0001 | g0123 | AFR | ACB | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02523 | hp1 | a0002 | c0001 | t0001 | g0011 | EAS | KHV | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02523 | hp2 | a0001 | c0002 | t0002 | g0227 | EAS | KHV | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02572 | hp1 | a0002 | c0001 | t0001 | g0143 | AFR | GWD | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02572 | hp2 | a0002 | c0001 | t0001 | g0138 | AFR | GWD | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02602 | hp1 | a0001 | c0003 | t0003 | g0198 | SAS | PJL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02602 | hp2 | a0002 | c0001 | t0001 | g0002 | SAS | PJL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02615 | hp1 | a0002 | c0005 | t0004 | g0032 | AFR | GWD | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02615 | hp2 | a0002 | c0001 | t0001 | g0140 | AFR | GWD | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02622 | hp1 | a0001 | c0002 | t0002 | g0052 | AFR | GWD | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02622 | hp2 | a0001 | c0002 | t0002 | g0014 | AFR | GWD | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02647 | hp1 | a0004 | c0008 | t0001 | g0249 | AFR | GWD | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02647 | hp2 | a0002 | c0001 | t0001 | g0131 | AFR | GWD | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02698 | hp1 | a0002 | c0001 | t0001 | g0074 | SAS | PJL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02698 | hp2 | a0001 | c0002 | t0002 | g0119 | SAS | PJL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02717 | hp1 | a0001 | c0002 | t0002 | g0043 | AFR | GWD | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02717 | hp2 | a0002 | c0005 | t0004 | g0022 | AFR | GWD | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02723 | hp1 | a0004 | c0008 | t0001 | g0051 | AFR | GWD | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02723 | hp2 | a0006 | c0013 | t0002 | g0104 | AFR | GWD | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02735 | hp1 | a0002 | c0015 | t0001 | g0133 | SAS | PJL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02735 | hp2 | a0002 | c0001 | t0001 | g0002 | SAS | PJL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0049 | SAS | PJL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02738 | hp2 | a0002 | c0005 | t0004 | g0093 | SAS | PJL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02809 | hp1 | a0004 | c0008 | t0001 | g0250 | AFR | GWD | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02809 | hp2 | a0001 | c0002 | t0002 | g0043 | AFR | GWD | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02818 | hp1 | a0002 | c0001 | t0001 | g0018 | AFR | GWD | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02818 | hp2 | a0001 | c0002 | t0002 | g0014 | AFR | GWD | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02886 | hp1 | a0006 | c0013 | t0002 | g0030 | AFR | GWD | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02886 | hp2 | a0001 | c0002 | t0002 | g0215 | AFR | GWD | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02895 | hp1 | a0002 | c0001 | t0001 | g0094 | AFR | GWD | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02895 | hp2 | a0001 | c0002 | t0002 | g0226 | AFR | GWD | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02897 | hp1 | a0002 | c0001 | t0001 | g0035 | AFR | GWD | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02897 | hp2 | a0001 | c0003 | t0003 | g0191 | AFR | GWD | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02922 | hp1 | a0007 | c0014 | t0003 | g0046 | AFR | ESN | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02922 | hp2 | a0002 | c0001 | t0001 | g0083 | AFR | ESN | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02970 | hp1 | a0002 | c0005 | t0004 | g0022 | AFR | ESN | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02970 | hp2 | a0002 | c0010 | t0001 | g0029 | AFR | ESN | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02976 | hp1 | a0002 | c0001 | t0001 | g0001 | AFR | ESN | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02976 | hp2 | a0001 | c0002 | t0002 | g0048 | AFR | ESN | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG03017 | hp1 | a0001 | c0002 | t0002 | g0222 | SAS | PJL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG03017 | hp2 | a0002 | c0001 | t0001 | g0002 | SAS | PJL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG03041 | hp1 | a0002 | c0001 | t0001 | g0001 | AFR | GWD | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG03041 | hp2 | a0002 | c0001 | t0001 | g0152 | AFR | GWD | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG03098 | hp1 | a0001 | c0002 | t0002 | g0014 | AFR | MSL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG03098 | hp2 | a0001 | c0002 | t0002 | g0232 | AFR | MSL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG03130 | hp1 | a0007 | c0014 | t0003 | g0203 | AFR | ESN | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG03130 | hp2 | a0002 | c0005 | t0004 | g0022 | AFR | ESN | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG03139 | hp1 | a0002 | c0005 | t0004 | g0032 | AFR | ESN | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG03139 | hp2 | a0002 | c0001 | t0001 | g0099 | AFR | ESN | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG03209 | hp1 | a0001 | c0003 | t0003 | g0024 | AFR | MSL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG03209 | hp2 | a0002 | c0001 | t0001 | g0079 | AFR | MSL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG03239 | hp1 | a0001 | c0002 | t0002 | g0219 | SAS | PJL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG03239 | hp2 | a0002 | c0001 | t0001 | g0088 | SAS | PJL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG03453 | hp1 | a0007 | c0014 | t0003 | g0046 | AFR | MSL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG03453 | hp2 | a0001 | c0002 | t0002 | g0101 | AFR | MSL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG03486 | hp1 | a0001 | c0002 | t0002 | g0014 | AFR | MSL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG03486 | hp2 | a0002 | c0001 | t0001 | g0017 | AFR | MSL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG03490 | hp1 | a0001 | c0002 | t0002 | g0218 | SAS | PJL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG03490 | hp2 | a0001 | c0002 | t0002 | g0047 | SAS | PJL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG03492 | hp1 | a0002 | c0001 | t0001 | g0148 | SAS | PJL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG03492 | hp2 | a0001 | c0002 | t0002 | g0047 | SAS | PJL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG03516 | hp1 | a0002 | c0001 | t0001 | g0040 | AFR | ESN | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG03516 | hp2 | a0003 | c0006 | t0001 | g0234 | AFR | ESN | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG03540 | hp1 | a0002 | c0010 | t0001 | g0142 | AFR | GWD | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0216 | AFR | GWD | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG03579 | hp1 | a0001 | c0002 | t0005 | g0062 | AFR | MSL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG03579 | hp2 | a0002 | c0001 | t0001 | g0017 | AFR | MSL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG03654 | hp1 | a0001 | c0003 | t0003 | g0194 | SAS | PJL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG03654 | hp2 | a0002 | c0001 | t0001 | g0003 | SAS | PJL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG03669 | hp1 | a0002 | c0001 | t0001 | g0155 | SAS | PJL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG03669 | hp2 | a0001 | c0009 | t0002 | g0168 | SAS | PJL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG03704 | hp1 | a0002 | c0001 | t0001 | g0002 | SAS | PJL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG03704 | hp2 | a0001 | c0002 | t0002 | g0006 | SAS | PJL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG03710 | hp1 | a0002 | c0001 | t0001 | g0072 | SAS | PJL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG03710 | hp2 | a0002 | c0001 | t0001 | g0086 | SAS | PJL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG03834 | hp1 | a0001 | c0002 | t0002 | g0111 | SAS | BEB | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG03834 | hp2 | a0002 | c0001 | t0001 | g0129 | SAS | BEB | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG03927 | hp1 | a0002 | c0001 | t0001 | g0154 | SAS | BEB | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG03927 | hp2 | a0001 | c0002 | t0002 | g0221 | SAS | BEB | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG03942 | hp1 | a0002 | c0001 | t0001 | g0139 | SAS | BEB | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG03942 | hp2 | a0002 | c0001 | t0001 | g0087 | SAS | BEB | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG04115 | hp1 | a0010 | c0016 | t0001 | g0167 | SAS | STU | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG04115 | hp2 | a0002 | c0001 | t0001 | g0071 | SAS | STU | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG04184 | hp1 | a0002 | c0001 | t0001 | g0073 | SAS | BEB | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG04184 | hp2 | a0002 | c0011 | t0004 | g0033 | SAS | BEB | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG04199 | hp1 | a0002 | c0001 | t0001 | g0149 | SAS | STU | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG04199 | hp2 | a0002 | c0001 | t0001 | g0003 | SAS | STU | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG04204 | hp1 | a0002 | c0001 | t0001 | g0147 | SAS | STU | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG04204 | hp2 | a0002 | c0001 | t0001 | g0126 | SAS | STU | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18522 | hp1 | a0001 | c0002 | t0005 | g0214 | AFR | YRI | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18522 | hp2 | a0001 | c0002 | t0002 | g0048 | AFR | YRI | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18747 | hp1 | a0001 | c0002 | t0002 | g0058 | EAS | CHB | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18747 | hp2 | a0005 | c0007 | t0001 | g0066 | EAS | CHB | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18939 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18939 | hp2 | a0001 | c0003 | t0003 | g0019 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18940 | hp1 | a0001 | c0002 | t0002 | g0115 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18940 | hp2 | a0001 | c0004 | t0003 | g0175 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18941 | hp1 | a0003 | c0006 | t0001 | g0235 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18941 | hp2 | a0002 | c0001 | t0001 | g0075 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18943 | hp1 | a0002 | c0005 | t0004 | g0105 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18943 | hp2 | a0001 | c0004 | t0003 | g0166 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18944 | hp1 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18944 | hp2 | a0002 | c0001 | t0001 | g0095 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18946 | hp1 | a0003 | c0006 | t0001 | g0025 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18946 | hp2 | a0002 | c0005 | t0004 | g0106 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18947 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18947 | hp2 | a0004 | c0012 | t0004 | g0026 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18948 | hp1 | a0001 | c0003 | t0003 | g0009 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18948 | hp2 | a0001 | c0002 | t0002 | g0112 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18949 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18949 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18950 | hp1 | a0004 | c0012 | t0004 | g0026 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18950 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18951 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18951 | hp2 | a0001 | c0003 | t0003 | g0206 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18952 | hp1 | a0001 | c0004 | t0003 | g0037 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18952 | hp2 | a0002 | c0001 | t0001 | g0096 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18953 | hp1 | a0001 | c0003 | t0003 | g0009 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18953 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18954 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18954 | hp2 | a0001 | c0004 | t0003 | g0037 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18956 | hp1 | a0001 | c0003 | t0003 | g0056 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18956 | hp2 | a0001 | c0018 | t0003 | g0178 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18957 | hp1 | a0003 | c0006 | t0001 | g0237 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18957 | hp2 | a0002 | c0001 | t0001 | g0003 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18960 | hp1 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18960 | hp2 | a0001 | c0003 | t0003 | g0013 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18961 | hp1 | a0001 | c0004 | t0003 | g0179 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18961 | hp2 | a0002 | c0001 | t0001 | g0039 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18962 | hp1 | a0002 | c0005 | t0004 | g0081 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18962 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18963 | hp1 | a0002 | c0001 | t0001 | g0089 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18963 | hp2 | a0001 | c0004 | t0003 | g0054 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18964 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18964 | hp2 | a0001 | c0004 | t0003 | g0180 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18965 | hp1 | a0001 | c0009 | t0002 | g0171 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18965 | hp2 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18967 | hp1 | a0001 | c0004 | t0003 | g0004 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18967 | hp2 | a0002 | c0001 | t0001 | g0151 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18968 | hp1 | a0002 | c0001 | t0001 | g0003 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18968 | hp2 | a0001 | c0003 | t0003 | g0193 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18969 | hp1 | a0001 | c0002 | t0002 | g0109 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18969 | hp2 | a0001 | c0004 | t0003 | g0177 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18970 | hp1 | a0002 | c0001 | t0001 | g0018 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18970 | hp2 | a0002 | c0001 | t0001 | g0082 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18971 | hp1 | a0001 | c0009 | t0002 | g0173 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18971 | hp2 | a0001 | c0009 | t0002 | g0170 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18972 | hp1 | a0002 | c0005 | t0004 | g0080 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18972 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18975 | hp1 | a0001 | c0002 | t0002 | g0118 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18975 | hp2 | a0001 | c0003 | t0003 | g0117 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18978 | hp1 | a0001 | c0002 | t0002 | g0224 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18978 | hp2 | a0001 | c0002 | t0002 | g0116 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18979 | hp1 | a0001 | c0004 | t0003 | g0172 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18979 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18980 | hp1 | a0002 | c0001 | t0001 | g0077 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18980 | hp2 | a0001 | c0003 | t0003 | g0009 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18981 | hp1 | a0004 | c0012 | t0004 | g0244 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18981 | hp2 | a0001 | c0002 | t0002 | g0057 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18983 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18983 | hp2 | a0001 | c0003 | t0003 | g0213 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18985 | hp1 | a0003 | c0006 | t0001 | g0243 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18985 | hp2 | a0005 | c0007 | t0002 | g0201 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18987 | hp1 | a0002 | c0001 | t0001 | g0011 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18987 | hp2 | a0001 | c0003 | t0003 | g0024 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18988 | hp1 | a0001 | c0003 | t0003 | g0009 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18988 | hp2 | a0002 | c0001 | t0001 | g0018 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18989 | hp1 | a0002 | c0001 | t0001 | g0008 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18989 | hp2 | a0001 | c0002 | t0002 | g0113 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18990 | hp1 | a0011 | c0022 | t0001 | g0076 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18990 | hp2 | a0003 | c0006 | t0001 | g0241 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18994 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18994 | hp2 | a0001 | c0004 | t0003 | g0162 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18995 | hp1 | a0001 | c0004 | t0003 | g0157 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18995 | hp2 | a0001 | c0004 | t0003 | g0160 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18997 | hp1 | a0001 | c0002 | t0002 | g0208 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18997 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18999 | hp1 | a0001 | c0003 | t0003 | g0013 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18999 | hp2 | a0001 | c0003 | t0003 | g0204 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19000 | hp1 | a0003 | c0006 | t0001 | g0242 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19000 | hp2 | a0001 | c0004 | t0003 | g0004 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19001 | hp1 | a0001 | c0003 | t0003 | g0202 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19001 | hp2 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19002 | hp1 | a0001 | c0009 | t0002 | g0158 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19002 | hp2 | a0001 | c0003 | t0003 | g0013 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19005 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19005 | hp2 | a0001 | c0004 | t0003 | g0174 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19009 | hp1 | a0001 | c0004 | t0003 | g0156 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19009 | hp2 | a0005 | c0007 | t0002 | g0055 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19010 | hp1 | a0002 | c0001 | t0001 | g0125 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19010 | hp2 | a0001 | c0003 | t0003 | g0212 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19011 | hp1 | a0001 | c0004 | t0003 | g0161 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19011 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19012 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19012 | hp2 | a0001 | c0003 | t0003 | g0009 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19030 | hp1 | a0001 | c0002 | t0002 | g0225 | AFR | LWK | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19030 | hp2 | a0001 | c0003 | t0003 | g0045 | AFR | LWK | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19043 | hp1 | a0001 | c0003 | t0003 | g0190 | AFR | LWK | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19043 | hp2 | a0002 | c0001 | t0001 | g0035 | AFR | LWK | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19056 | hp1 | a0002 | c0001 | t0001 | g0124 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19056 | hp2 | a0001 | c0003 | t0003 | g0013 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19062 | hp1 | a0001 | c0002 | t0002 | g0114 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19062 | hp2 | a0001 | c0004 | t0003 | g0176 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19064 | hp1 | a0001 | c0003 | t0003 | g0045 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19064 | hp2 | a0002 | c0001 | t0001 | g0021 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19066 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19066 | hp2 | a0003 | c0006 | t0001 | g0025 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19068 | hp1 | a0002 | c0001 | t0001 | g0182 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19068 | hp2 | a0004 | c0012 | t0004 | g0026 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19070 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19070 | hp2 | a0001 | c0004 | t0003 | g0004 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19076 | hp1 | a0001 | c0003 | t0004 | g0028 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19076 | hp2 | a0003 | c0006 | t0001 | g0239 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19077 | hp1 | a0001 | c0003 | t0003 | g0183 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19077 | hp2 | a0003 | c0006 | t0001 | g0240 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19078 | hp1 | a0001 | c0002 | t0002 | g0064 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19078 | hp2 | a0005 | c0007 | t0002 | g0211 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19079 | hp1 | a0002 | c0001 | t0001 | g0039 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19079 | hp2 | a0001 | c0004 | t0003 | g0004 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19080 | hp1 | a0002 | c0001 | t0001 | g0008 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19080 | hp2 | a0002 | c0005 | t0004 | g0085 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19082 | hp1 | a0001 | c0003 | t0003 | g0196 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19082 | hp2 | a0001 | c0002 | t0002 | g0107 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19085 | hp1 | a0001 | c0003 | t0003 | g0019 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19085 | hp2 | a0001 | c0003 | t0003 | g0013 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19086 | hp1 | a0001 | c0003 | t0003 | g0205 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19086 | hp2 | a0003 | c0006 | t0001 | g0025 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19087 | hp1 | a0002 | c0001 | t0001 | g0132 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19087 | hp2 | a0001 | c0003 | t0003 | g0189 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19090 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19090 | hp2 | a0003 | c0020 | t0004 | g0247 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19091 | hp1 | a0005 | c0007 | t0002 | g0108 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19091 | hp2 | a0003 | c0006 | t0001 | g0238 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19240 | hp1 | a0004 | c0008 | t0001 | g0233 | AFR | YRI | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA19240 | hp2 | a0002 | c0010 | t0001 | g0029 | AFR | YRI | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA20129 | hp1 | a0012 | c0021 | t0004 | g0251 | AFR | ASW | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA20129 | hp2 | a0005 | c0007 | t0002 | g0061 | AFR | ASW | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA20752 | hp1 | a0001 | c0002 | t0002 | g0044 | EUR | TSI | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA20752 | hp2 | a0002 | c0001 | t0001 | g0008 | EUR | TSI | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA20805 | hp1 | a0002 | c0005 | t0004 | g0141 | EUR | TSI | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA20805 | hp2 | a0002 | c0001 | t0001 | g0130 | EUR | TSI | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA20905 | hp1 | a0001 | c0002 | t0002 | g0110 | SAS | GIH | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA20905 | hp2 | a0002 | c0001 | t0001 | g0128 | SAS | GIH | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02109 | hp1 | a0002 | c0001 | t0001 | g0136 | AFR | ACB | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02109 | hp2 | a0001 | c0002 | t0002 | g0069 | AFR | ACB | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02486 | hp1 | a0002 | c0001 | t0001 | g0040 | AFR | ACB | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG02486 | hp2 | a0002 | c0010 | t0001 | g0122 | AFR | ACB | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG03471 | hp1 | a0002 | c0001 | t0001 | g0017 | AFR | MSL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| HG03471 | hp2 | a0001 | c0002 | t0002 | g0014 | AFR | MSL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18955 | hp1 | a0001 | c0002 | t0009 | g0200 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| NA18955 | hp2 | a0001 | c0002 | t0002 | g0060 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| homoSapiens | chm13v2 | a0002 | c0001 | t0001 | g0150 | REF | REF | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0223 | REF | REF | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:54806172 | C | T | 4 | a0003 a0004 a0011 others(1): Show |
28 | HG01884.hp2 HG02040.hp1 HG02074.hp2 others(25): Show |
missense_variant | MODERATE | c.56C>T | p.Thr19Met | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 1/10 | 110/1690 | 56/1257 | 19/418 | chr1 | 54806172 | |||
| chr1:54807061 | C | G | 1 | a0009 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.170C>G | p.Ser57Cys | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 2/10 | 224/1690 | 170/1257 | 57/418 | chr1 | 54807061 | |||
| chr1:54807070 | A | G | 1 | a0007 | 3 | HG02922.hp1 HG03130.hp1 HG03453.hp1 |
missense_variant | MODERATE | c.179A>G | p.Tyr60Cys | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 2/10 | 233/1690 | 179/1257 | 60/418 | chr1 | 54807070 | |||
| chr1:54807907 | G | T | 4 | a0002 a0008 a0010 others(1): Show |
147 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
missense_variant | MODERATE | c.376G>T | p.Gly126Cys | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/10 | 430/1690 | 376/1257 | 126/418 | chr1 | 54807907 | |||
| chr1:54811819 | A | C | 1 | a0008 | 1 | HG00741.hp2 | missense_variant | MODERATE | c.506A>C | p.Tyr169Ser | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 5/10 | 560/1690 | 506/1257 | 169/418 | chr1 | 54811819 | |||
| chr1:54812145 | G | A | 1 | a0009 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.718G>A | p.Gly240Ser | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 6/10 | 772/1690 | 718/1257 | 240/418 | chr1 | 54812145 | |||
| chr1:54813968 | G | T | 2 | a0006 a0012 |
4 | HG02451.hp1 HG02723.hp2 HG02886.hp1 others(1): Show |
missense_variant | MODERATE | c.917G>T | p.Arg306Leu | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 7/10 | 971/1690 | 917/1257 | 306/418 | chr1 | 54813968 | |||
| chr1:54815017 | G | A | 2 | a0003 a0005 |
21 | HG02074.hp2 HG02165.hp1 HG03516.hp2 others(18): Show |
missense_variant | MODERATE | c.1028G>A | p.Cys343Tyr | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/10 | 1082/1690 | 1028/1257 | 343/418 | chr1 | 54815017 | |||
| chr1:54841851 | A | T | 1 | a0010 | 1 | HG04115.hp1 | missense_variant | MODERATE | c.1235A>T | p.Tyr412Phe | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 10/10 | 1289/1690 | 1235/1257 | 412/418 | chr1 | 54841851 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:54807080 | A | G | 1 | a0009c0019 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.189A>G | p.Gln63Gln | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 2/10 | 243/1690 | 189/1257 | 63/418 | chr1 | 54807080 | |||
| chr1:54807630 | G | A | 1 | a0009c0019 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.297G>A | p.Thr99Thr | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 3/10 | 351/1690 | 297/1257 | 99/418 | chr1 | 54807630 | |||
| chr1:54807645 | A | C | 1 | a0001c0018 | 1 | NA18956.hp2 | synonymous_variant | LOW | c.312A>C | p.Leu104Leu | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 3/10 | 366/1690 | 312/1257 | 104/418 | chr1 | 54807645 | |||
| chr1:54811841 | C | T | 5 | a0001c0004 a0001c0009 a0001c0018 others(2): Show |
41 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(38): Show |
synonymous_variant | LOW | c.528C>T | p.Tyr176Tyr | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 5/10 | 582/1690 | 528/1257 | 176/418 | chr1 | 54811841 | |||
| chr1:54811880 | C | T | 1 | a0002c0010 | 5 | HG02451.hp2 HG02486.hp2 HG02970.hp2 others(2): Show |
synonymous_variant | LOW | c.567C>T | p.Ser189Ser | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 5/10 | 621/1690 | 567/1257 | 189/418 | chr1 | 54811880 | |||
| chr1:54817048 | G | C | 1 | a0002c0015 | 1 | HG02735.hp1 | synonymous_variant | LOW | c.1110G>C | p.Arg370Arg | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/10 | 1164/1690 | 1110/1257 | 370/418 | chr1 | 54817048 | |||
| chr1:54841828 | A | G | 9 | a0001c0003 a0001c0004 a0001c0018 others(6): Show |
123 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(120): Show |
synonymous_variant | LOW | c.1212A>G | p.Gly404Gly | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 10/10 | 1266/1690 | 1212/1257 | 404/418 | chr1 | 54841828 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:54806071 | C | T | 1 | a0001c0002t0009 | 1 | NA18955.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-46C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 1/10 | chr1 | 54806071 | |||||||
| chr1:54806078 | C | T | 1 | a0001c0003t0008 | 1 | HG01256.hp1 | 5_prime_UTR_variant | MODIFIER | c.-39C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 1/10 | 39 | chr1 | 54806078 | ||||||
| chr1:54806101 | A | G | 18 | a0001c0002t0001 a0001c0003t0004 a0002c0001t0001 others(15): Show |
178 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
5_prime_UTR_variant | MODIFIER | c.-16A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 1/10 | 16 | chr1 | 54806101 | ||||||
| chr1:54841967 | C | T | 11 | a0001c0003t0003 a0001c0003t0004 a0001c0003t0008 others(8): Show |
123 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*94C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 10/10 | 94 | chr1 | 54841967 | ||||||
| chr1:54842020 | C | A | 11 | a0001c0003t0003 a0001c0003t0004 a0001c0003t0008 others(8): Show |
123 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*147C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 10/10 | 147 | chr1 | 54842020 | ||||||
| chr1:54842059 | C | T | 1 | a0002c0001t0007 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*186C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 10/10 | 186 | chr1 | 54842059 | ||||||
| chr1:54842141 | G | C | 2 | a0001c0002t0005 a0004c0008t0006 |
3 | HG02257.hp1 HG03579.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*268G>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 10/10 | 268 | chr1 | 54842141 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:54806262 | A | G | 22 | a0003c0006t0001g0025 a0003c0006t0001g0234 a0003c0006t0001g0235 others(19): Show |
27 | HG01884.hp2 HG02040.hp1 HG02074.hp2 others(24): Show |
intron_variant | MODIFIER | c.104+42A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 1/9 | chr1 | 54806262 | |||||||
| chr1:54806263 | G | A | 1 | a0001c0002t0002g0052 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.104+43G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 1/9 | chr1 | 54806263 | |||||||
| chr1:54806313 | C | T | 1 | a0004c0008t0001g0051 | 2 | HG01884.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.104+93C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 1/9 | chr1 | 54806313 | |||||||
| chr1:54806340 | G | C | 1 | a0001c0004t0003g0053 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.104+120G>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 1/9 | chr1 | 54806340 | |||||||
| chr1:54806399 | C | A | 1 | a0004c0008t0001g0233 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.104+179C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 1/9 | chr1 | 54806399 | |||||||
| chr1:54806506 | T | C | 16 | a0003c0006t0001g0025 a0003c0006t0001g0234 a0003c0006t0001g0235 others(13): Show |
20 | HG02040.hp1 HG02074.hp2 HG02165.hp1 others(17): Show |
intron_variant | MODIFIER | c.104+286T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 1/9 | chr1 | 54806506 | |||||||
| chr1:54806507 | G | A | 6 | a0004c0008t0001g0051 a0004c0008t0001g0233 a0004c0008t0001g0249 others(3): Show |
7 | HG01884.hp2 HG02257.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.104+287G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 1/9 | chr1 | 54806507 | |||||||
| chr1:54806663 | A | T | 15 | a0001c0002t0002g0224 a0001c0002t0002g0225 a0001c0002t0002g0226 others(12): Show |
16 | HG00408.hp1 HG00423.hp2 HG00621.hp1 others(13): Show |
intron_variant | MODIFIER | c.105-333A>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 1/9 | chr1 | 54806663 | |||||||
| chr1:54806750 | A | G | 31 | a0001c0002t0002g0224 a0001c0002t0002g0225 a0001c0002t0002g0226 others(28): Show |
36 | HG00408.hp1 HG00423.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.105-246A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 1/9 | chr1 | 54806750 | |||||||
| chr1:54806807 | G | GCGGGT | 15 | a0001c0002t0002g0224 a0001c0002t0002g0225 a0001c0002t0002g0226 others(12): Show |
16 | HG00408.hp1 HG00423.hp2 HG00621.hp1 others(13): Show |
intron_variant | MODIFIER | c.105-189_105-188ins others(5): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 1/9 | chr1 | 54806807 | |||||||
| chr1:54806807 | GTGGGTGG others(3): Show |
G | 1 | a0001c0004t0003g0054 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.105-188_105-179del others(10): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 1/9 | chr1 | 54806807 | |||||||
| chr1:54806808 | T | C | 236 | a0001c0002t0001g0102 a0001c0002t0002g0005 a0001c0002t0002g0006 others(233): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.105-188T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 1/9 | chr1 | 54806808 | |||||||
| chr1:54806808 | T | G | 15 | a0001c0002t0002g0224 a0001c0002t0002g0225 a0001c0002t0002g0226 others(12): Show |
16 | HG00408.hp1 HG00423.hp2 HG00621.hp1 others(13): Show |
intron_variant | MODIFIER | c.105-188T>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 1/9 | chr1 | 54806808 | |||||||
| chr1:54806818 | G | C | 1 | a0001c0004t0003g0054 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.105-178G>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 1/9 | chr1 | 54806818 | |||||||
| chr1:54806848 | A | G | 41 | a0001c0002t0002g0015 a0001c0002t0002g0020 a0001c0002t0002g0049 others(38): Show |
55 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.105-148A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 1/9 | chr1 | 54806848 | |||||||
| chr1:54806905 | C | T | 5 | a0001c0002t0002g0014 a0001c0002t0002g0048 a0001c0002t0002g0215 others(2): Show |
10 | HG02622.hp2 HG02818.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.105-91C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 1/9 | chr1 | 54806905 | |||||||
| chr1:54806970 | C | G | 41 | a0001c0002t0002g0015 a0001c0002t0002g0020 a0001c0002t0002g0049 others(38): Show |
55 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.105-26C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 1/9 | chr1 | 54806970 | |||||||
| chr1:54807313 | C | A | 1 | a0005c0007t0002g0055 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.193-213C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 2/9 | chr1 | 54807313 | |||||||
| chr1:54807344 | G | A | 1 | a0001c0003t0003g0056 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.193-182G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 2/9 | chr1 | 54807344 | |||||||
| chr1:54807486 | C | T | 4 | a0004c0008t0001g0051 a0004c0008t0001g0249 a0004c0008t0001g0250 others(1): Show |
5 | HG01884.hp2 HG02647.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.193-40C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 2/9 | chr1 | 54807486 | |||||||
| chr1:54807713 | T | G | 11 | a0001c0002t0002g0005 a0001c0002t0002g0016 a0001c0002t0002g0027 others(8): Show |
20 | HG01069.hp2 HG01099.hp2 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.357+23T>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 3/9 | chr1 | 54807713 | |||||||
| chr1:54807749 | A | T | 45 | a0001c0002t0002g0043 a0001c0002t0002g0044 a0001c0002t0002g0047 others(42): Show |
71 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.357+59A>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 3/9 | chr1 | 54807749 | |||||||
| chr1:54807765 | C | T | 1 | a0002c0001t0001g0182 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.357+75C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 3/9 | chr1 | 54807765 | |||||||
| chr1:54808190 | C | T | 1 | a0004c0008t0006g0248 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.480+179C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808190 | |||||||
| chr1:54808369 | C | T | 1 | a0001c0003t0003g0213 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.480+358C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808369 | |||||||
| chr1:54808379 | G | A | 49 | a0001c0002t0002g0043 a0001c0002t0002g0044 a0001c0002t0002g0047 others(46): Show |
76 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.480+368G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808379 | |||||||
| chr1:54808405 | C | G | 242 | a0001c0002t0001g0102 a0001c0002t0002g0006 a0001c0002t0002g0007 others(239): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.480+394C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808405 | |||||||
| chr1:54808528 | C | T | 3 | a0004c0008t0001g0249 a0004c0008t0001g0250 a0012c0021t0004g0251 |
3 | HG02647.hp1 HG02809.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.480+517C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808528 | |||||||
| chr1:54808563 | T | A | 1 | a0002c0005t0004g0068 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.480+552T>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808563 | |||||||
| chr1:54808607 | G | A | 10 | a0001c0002t0002g0014 a0001c0002t0002g0048 a0001c0002t0002g0069 others(7): Show |
16 | HG01884.hp2 HG02109.hp2 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.480+596G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808607 | |||||||
| chr1:54808611 | C | CGGGGGG | 15 | a0001c0004t0003g0004 a0001c0004t0003g0053 a0001c0004t0003g0160 others(12): Show |
20 | HG00408.hp2 HG00609.hp1 HG01978.hp2 others(17): Show |
intron_variant | MODIFIER | c.480+600_480+601ins others(6): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808611 | |||||||
| chr1:54808611 | C | CGGGGGGG | 7 | a0001c0004t0003g0172 a0001c0004t0003g0174 a0001c0004t0003g0175 others(4): Show |
7 | NA18940.hp2 NA18956.hp2 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.480+600_480+601ins others(7): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808611 | |||||||
| chr1:54808611 | C | CGGGGGGG others(3): Show |
1 | a0001c0004t0003g0054 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.480+600_480+601ins others(10): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808611 | |||||||
| chr1:54808611 | C | CGGGGGGG others(4): Show |
3 | a0001c0004t0003g0179 a0001c0004t0003g0180 a0001c0004t0003g0181 |
3 | HG00438.hp2 NA18961.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.480+600_480+601ins others(11): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808611 | |||||||
| chr1:54808612 | C | CGGGGG | 20 | a0002c0001t0001g0002 a0002c0001t0001g0011 a0002c0001t0001g0121 others(17): Show |
31 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.480+602_480+606dup others(5): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 54808612 | ||||||
| chr1:54808612 | C | CGGGGGGG | 23 | a0001c0002t0002g0064 a0001c0004t0003g0037 a0002c0001t0001g0008 others(20): Show |
38 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.480+606_480+607ins others(7): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 54808612 | ||||||
| chr1:54808612 | C | CGGGGGGG others(3): Show |
3 | a0002c0001t0001g0038 a0002c0001t0001g0151 a0002c0001t0001g0152 |
4 | HG01243.hp1 HG02074.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.480+606_480+607ins others(10): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 54808612 | ||||||
| chr1:54808612 | C | CGGGGGGG others(4): Show |
2 | a0002c0001t0001g0039 a0002c0001t0001g0153 |
3 | HG01192.hp2 NA18961.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.480+606_480+607ins others(11): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 54808612 | ||||||
| chr1:54808612 | C | CGGGGGGG others(5): Show |
1 | a0002c0001t0001g0154 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.480+606_480+607ins others(12): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 54808612 | ||||||
| chr1:54808612 | C | G | 33 | a0001c0004t0003g0004 a0001c0004t0003g0041 a0001c0004t0003g0053 others(30): Show |
40 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.480+601C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808612 | |||||||
| chr1:54808616 | GGA | G | 26 | a0001c0002t0002g0006 a0001c0002t0002g0007 a0001c0002t0002g0010 others(23): Show |
41 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.480+607_480+608del others(2): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 54808616 | ||||||
| chr1:54808618 | A | C | 25 | a0001c0003t0003g0009 a0001c0003t0003g0183 a0001c0003t0003g0196 others(22): Show |
37 | HG00140.hp2 HG00544.hp2 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.480+607A>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808618 | |||||||
| chr1:54808618 | A | G | 94 | a0001c0002t0002g0064 a0001c0004t0003g0004 a0001c0004t0003g0037 others(91): Show |
132 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.480+607A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808618 | |||||||
| chr1:54808703 | C | T | 28 | a0001c0004t0003g0004 a0001c0004t0003g0037 a0001c0004t0003g0041 others(25): Show |
35 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.480+692C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808703 | |||||||
| chr1:54808719 | T | TG | 6 | a0001c0004t0003g0156 a0001c0004t0003g0172 a0002c0001t0001g0070 others(3): Show |
6 | HG01255.hp1 HG02109.hp1 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.480+713dupG | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 54808719 | ||||||
| chr1:54808791 | A | C | 144 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(141): Show |
211 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.480+780A>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808791 | |||||||
| chr1:54808801 | A | G | 1 | a0001c0003t0003g0212 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.480+790A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808801 | |||||||
| chr1:54808826 | G | T | 2 | a0006c0013t0002g0030 a0006c0013t0002g0104 |
3 | HG02451.hp1 HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.480+815G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808826 | |||||||
| chr1:54808840 | G | T | 1 | a0005c0007t0002g0055 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.480+829G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808840 | |||||||
| chr1:54808853 | G | A | 1 | a0001c0003t0003g0213 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.480+842G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808853 | |||||||
| chr1:54808856 | C | T | 2 | a0001c0002t0002g0226 a0001c0002t0002g0232 |
2 | HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.480+845C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808856 | |||||||
| chr1:54808962 | C | T | 9 | a0001c0002t0002g0225 a0001c0002t0002g0226 a0001c0002t0002g0227 others(6): Show |
9 | HG00408.hp1 HG00423.hp2 HG00621.hp1 others(6): Show |
intron_variant | MODIFIER | c.480+951C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808962 | |||||||
| chr1:54808985 | T | G | 203 | a0001c0002t0002g0043 a0001c0002t0002g0044 a0001c0002t0002g0047 others(200): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.480+974T>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808985 | |||||||
| chr1:54808987 | T | C | 203 | a0001c0002t0002g0043 a0001c0002t0002g0044 a0001c0002t0002g0047 others(200): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.480+976T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808987 | |||||||
| chr1:54808989 | T | C | 203 | a0001c0002t0002g0043 a0001c0002t0002g0044 a0001c0002t0002g0047 others(200): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.480+978T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808989 | |||||||
| chr1:54808990 | G | GCCTACTC others(104): Show |
92 | a0001c0002t0002g0064 a0001c0002t0002g0225 a0001c0002t0002g0226 others(89): Show |
138 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.480+979_480+980ins others(111): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808990 | |||||||
| chr1:54808990 | G | GCCTACTC others(104): Show |
1 | a0002c0001t0001g0100 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.480+979_480+980ins others(111): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808990 | |||||||
| chr1:54808990 | G | GCCTACTC others(104): Show |
1 | a0001c0004t0003g0157 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.480+979_480+980ins others(111): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808990 | |||||||
| chr1:54808990 | G | GCCTACTC others(104): Show |
89 | a0001c0002t0002g0043 a0001c0002t0002g0044 a0001c0002t0002g0047 others(86): Show |
129 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.480+979_480+980ins others(111): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808990 | |||||||
| chr1:54808990 | G | GCCTACTC others(104): Show |
19 | a0001c0002t0002g0224 a0001c0004t0003g0179 a0001c0004t0003g0181 others(16): Show |
23 | HG00438.hp2 HG02040.hp1 HG02074.hp2 others(20): Show |
intron_variant | MODIFIER | c.480+979_480+980ins others(111): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808990 | |||||||
| chr1:54808990 | G | GCCTACTC others(105): Show |
1 | a0001c0018t0003g0178 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.480+979_480+980ins others(112): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808990 | |||||||
| chr1:54808997 | C | G | 1 | a0001c0018t0003g0178 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.480+986C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808997 | |||||||
| chr1:54809095 | T | C | 1 | a0003c0006t0001g0234 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.480+1084T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54809095 | |||||||
| chr1:54809109 | A | G | 1 | a0001c0002t0002g0052 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.480+1098A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54809109 | |||||||
| chr1:54809160 | A | C | 1 | a0001c0002t0002g0225 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.480+1149A>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54809160 | |||||||
| chr1:54809160 | A | G | 1 | a0012c0021t0004g0251 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.480+1149A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54809160 | |||||||
| chr1:54809234 | C | A | 55 | a0001c0002t0002g0043 a0001c0002t0002g0044 a0001c0002t0002g0047 others(52): Show |
86 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.480+1223C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54809234 | |||||||
| chr1:54809275 | A | G | 2 | a0002c0001t0001g0099 a0002c0001t0001g0135 |
2 | HG00639.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.480+1264A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54809275 | |||||||
| chr1:54809294 | T | C | 51 | a0001c0002t0002g0224 a0001c0004t0003g0004 a0001c0004t0003g0037 others(48): Show |
63 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.480+1283T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54809294 | |||||||
| chr1:54809434 | C | A | 1 | a0001c0002t0002g0109 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.480+1423C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54809434 | |||||||
| chr1:54809435 | G | A | 1 | a0001c0002t0002g0109 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.480+1424G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54809435 | |||||||
| chr1:54809482 | T | C | 250 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(247): Show |
378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.480+1471T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54809482 | |||||||
| chr1:54809649 | A | C | 1 | a0001c0018t0003g0178 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.480+1638A>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54809649 | |||||||
| chr1:54809669 | G | A | 14 | a0001c0002t0002g0006 a0001c0002t0002g0007 a0001c0002t0002g0010 others(11): Show |
28 | HG00558.hp1 HG03704.hp2 HG03834.hp1 others(25): Show |
intron_variant | MODIFIER | c.480+1658G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54809669 | |||||||
| chr1:54809763 | C | A | 1 | a0001c0003t0003g0183 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.480+1752C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54809763 | |||||||
| chr1:54809856 | C | G | 1 | a0001c0002t0002g0118 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.480+1845C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54809856 | |||||||
| chr1:54809856 | C | T | 1 | a0002c0001t0001g0098 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.480+1845C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54809856 | |||||||
| chr1:54809875 | G | GA | 241 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(238): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.480+1873dupA | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 54809875 | ||||||
| chr1:54809885 | C | A | 249 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(246): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.480+1874C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54809885 | |||||||
| chr1:54809957 | G | C | 85 | a0001c0002t0002g0064 a0002c0001t0001g0001 a0002c0001t0001g0002 others(82): Show |
131 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.481-1837G>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54809957 | |||||||
| chr1:54810095 | C | T | 5 | a0001c0002t0002g0047 a0001c0002t0002g0208 a0001c0003t0003g0207 others(2): Show |
6 | HG00621.hp2 HG02080.hp1 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.481-1699C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54810095 | |||||||
| chr1:54810096 | G | A | 1 | a0001c0003t0003g0184 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.481-1698G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54810096 | |||||||
| chr1:54810158 | T | G | 51 | a0001c0002t0002g0224 a0001c0004t0003g0004 a0001c0004t0003g0037 others(48): Show |
63 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.481-1636T>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54810158 | |||||||
| chr1:54810368 | T | G | 1 | a0001c0003t0003g0185 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.481-1426T>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54810368 | |||||||
| chr1:54810370 | T | A | 2 | a0001c0002t0002g0227 a0002c0001t0001g0120 |
2 | HG02071.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.481-1424T>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54810370 | |||||||
| chr1:54810371 | C | T | 12 | a0001c0002t0002g0005 a0001c0002t0002g0016 a0001c0002t0002g0027 others(9): Show |
21 | HG01069.hp2 HG01099.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.481-1423C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54810371 | |||||||
| chr1:54810473 | G | A | 1 | a0001c0004t0003g0163 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.481-1321G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54810473 | |||||||
| chr1:54810572 | C | T | 1 | a0002c0015t0001g0133 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.481-1222C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54810572 | |||||||
| chr1:54810615 | T | C | 1 | a0009c0019t0002g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.481-1179T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54810615 | |||||||
| chr1:54810684 | A | G | 1 | a0002c0001t0001g0149 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.481-1110A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54810684 | |||||||
| chr1:54810878 | G | A | 3 | a0002c0001t0001g0072 a0002c0001t0001g0136 a0002c0001t0001g0137 |
3 | HG01993.hp2 HG02109.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.481-916G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54810878 | |||||||
| chr1:54811014 | G | A | 55 | a0001c0002t0002g0043 a0001c0002t0002g0044 a0001c0002t0002g0047 others(52): Show |
86 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.481-780G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54811014 | |||||||
| chr1:54811057 | T | C | 1 | a0004c0008t0001g0051 | 2 | HG01884.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.481-737T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54811057 | |||||||
| chr1:54811320 | C | G | 1 | a0001c0003t0003g0206 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.481-474C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54811320 | |||||||
| chr1:54811525 | G | A | 12 | a0001c0002t0002g0015 a0001c0002t0002g0020 a0001c0002t0002g0049 others(9): Show |
22 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.481-269G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54811525 | |||||||
| chr1:54811582 | C | T | 3 | a0003c0006t0001g0245 a0003c0006t0001g0246 a0003c0020t0004g0247 |
3 | HG02074.hp2 HG02165.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.481-212C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54811582 | |||||||
| chr1:54811673 | C | G | 3 | a0002c0001t0001g0097 a0002c0001t0001g0148 a0002c0005t0004g0036 |
4 | HG01257.hp1 HG01258.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.481-121C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54811673 | |||||||
| chr1:54811674 | G | A | 1 | a0002c0001t0001g0073 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.481-120G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54811674 | |||||||
| chr1:54811751 | G | C | 1 | a0009c0019t0002g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.481-43G>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54811751 | |||||||
| chr1:54811757 | T | A | 84 | a0001c0002t0002g0064 a0002c0001t0001g0001 a0002c0001t0001g0002 others(81): Show |
130 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.481-37T>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54811757 | |||||||
| chr1:54811778 | C | T | 33 | a0001c0004t0003g0004 a0001c0004t0003g0037 a0001c0004t0003g0041 others(30): Show |
41 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.481-16C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54811778 | |||||||
| chr1:54811784 | C | T | 1 | a0002c0001t0001g0096 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.481-10C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54811784 | |||||||
| chr1:54811785 | G | GC | 6 | a0001c0002t0002g0014 a0001c0002t0002g0048 a0001c0002t0002g0069 others(3): Show |
11 | HG02109.hp2 HG02622.hp2 HG02818.hp2 others(8): Show |
splice_region_variant&intron_variant | LOW | c.481-5dupC | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 54811785 | ||||||
| chr1:54811972 | C | T | 2 | a0002c0001t0001g0011 a0002c0001t0001g0132 |
6 | HG00544.hp2 HG00673.hp1 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.618+41C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 5/9 | chr1 | 54811972 | |||||||
| chr1:54812008 | G | A | 2 | a0002c0001t0001g0040 a0002c0001t0001g0138 |
3 | HG02486.hp1 HG02572.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.619-38G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 5/9 | chr1 | 54812008 | |||||||
| chr1:54812292 | C | T | 1 | a0004c0008t0001g0233 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.762+103C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 6/9 | chr1 | 54812292 | |||||||
| chr1:54812386 | C | T | 1 | a0002c0001t0001g0095 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.762+197C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 6/9 | chr1 | 54812386 | |||||||
| chr1:54812646 | T | TGAGGTAG others(301): Show |
1 | a0009c0019t0002g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.762+470_762+471ins others(308): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 54812646 | ||||||
| chr1:54812721 | G | C | 154 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(151): Show |
226 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.762+532G>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 6/9 | chr1 | 54812721 | |||||||
| chr1:54812766 | C | T | 2 | a0002c0001t0001g0035 a0002c0001t0001g0094 |
3 | HG02895.hp1 HG02897.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.762+577C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 6/9 | chr1 | 54812766 | |||||||
| chr1:54813104 | A | G | 5 | a0001c0002t0002g0014 a0001c0002t0002g0048 a0001c0002t0002g0069 others(2): Show |
10 | HG02109.hp2 HG02622.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.763-710A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 6/9 | chr1 | 54813104 | |||||||
| chr1:54813117 | C | T | 4 | a0001c0002t0002g0027 a0002c0001t0001g0092 a0002c0001t0001g0147 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.763-697C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 6/9 | chr1 | 54813117 | |||||||
| chr1:54813141 | CT | C | 126 | a0001c0002t0002g0005 a0001c0002t0002g0014 a0001c0002t0002g0016 others(123): Show |
181 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.763-660delT | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 54813141 | ||||||
| chr1:54813168 | G | A | 77 | a0001c0002t0002g0005 a0001c0002t0002g0014 a0001c0002t0002g0016 others(74): Show |
120 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.763-646G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 6/9 | chr1 | 54813168 | |||||||
| chr1:54813191 | A | G | 1 | a0001c0002t0002g0103 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.763-623A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 6/9 | chr1 | 54813191 | |||||||
| chr1:54813392 | C | A | 3 | a0003c0006t0001g0234 a0004c0008t0006g0248 a0012c0021t0004g0251 |
3 | HG02257.hp1 HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.763-422C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 6/9 | chr1 | 54813392 | |||||||
| chr1:54813649 | T | G | 40 | a0001c0002t0001g0102 a0001c0002t0002g0052 a0001c0003t0003g0019 others(37): Show |
52 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.763-165T>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 6/9 | chr1 | 54813649 | |||||||
| chr1:54813672 | CCCGGCCT | C | 251 | a0001c0002t0001g0102 a0001c0002t0002g0005 a0001c0002t0002g0006 others(248): Show |
379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.763-130_763-124del others(7): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 54813672 | ||||||
| chr1:54813749 | A | G | 1 | a0001c0002t0002g0014 | 5 | HG02622.hp2 HG02818.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.763-65A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 6/9 | chr1 | 54813749 | |||||||
| chr1:54813750 | G | C | 1 | a0001c0002t0002g0014 | 5 | HG02622.hp2 HG02818.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.763-64G>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 6/9 | chr1 | 54813750 | |||||||
| chr1:54814015 | G | A | 5 | a0001c0003t0003g0012 a0001c0003t0003g0042 a0001c0003t0003g0184 others(2): Show |
11 | HG00099.hp2 HG00140.hp1 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.924+40G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 7/9 | chr1 | 54814015 | |||||||
| chr1:54814071 | G | T | 57 | a0001c0002t0001g0102 a0001c0002t0002g0047 a0001c0002t0002g0103 others(54): Show |
86 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.924+96G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 7/9 | chr1 | 54814071 | |||||||
| chr1:54814180 | T | C | 50 | a0001c0002t0002g0047 a0001c0002t0002g0208 a0001c0002t0009g0200 others(47): Show |
75 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.924+205T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 7/9 | chr1 | 54814180 | |||||||
| chr1:54814225 | A | G | 2 | a0003c0006t0001g0234 a0005c0007t0002g0061 |
2 | HG03516.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.924+250A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 7/9 | chr1 | 54814225 | |||||||
| chr1:54814228 | G | A | 1 | a0001c0003t0003g0189 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.924+253G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 7/9 | chr1 | 54814228 | |||||||
| chr1:54814305 | G | A | 1 | a0003c0006t0001g0234 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.924+330G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 7/9 | chr1 | 54814305 | |||||||
| chr1:54814352 | C | A | 1 | a0001c0002t0001g0102 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.924+377C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 7/9 | chr1 | 54814352 | |||||||
| chr1:54814376 | CCGCCCAA others(24): Show |
C | 1 | a0001c0003t0003g0202 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.924+402_924+432del others(31): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 7/9 | chr1 | 54814376 | |||||||
| chr1:54814382 | A | C | 1 | a0001c0002t0002g0064 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.924+407A>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 7/9 | chr1 | 54814382 | |||||||
| chr1:54814398 | C | T | 2 | a0001c0002t0002g0006 a0001c0002t0002g0113 |
3 | NA18950.hp2 NA18989.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.924+423C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 7/9 | chr1 | 54814398 | |||||||
| chr1:54814412 | AAGCAGGC others(14): Show |
A | 1 | a0001c0003t0003g0190 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.924+447_924+467del others(21): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr1 | 54814412 | ||||||
| chr1:54814463 | G | A | 2 | a0001c0002t0002g0043 a0001c0003t0003g0186 |
3 | HG01109.hp2 HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.925-451G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 7/9 | chr1 | 54814463 | |||||||
| chr1:54814750 | G | A | 1 | a0001c0004t0003g0164 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.925-164G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 7/9 | chr1 | 54814750 | |||||||
| chr1:54814762 | C | T | 2 | a0003c0006t0001g0234 a0005c0007t0002g0061 |
2 | HG03516.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.925-152C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 7/9 | chr1 | 54814762 | |||||||
| chr1:54814909 | C | T | 1 | a0001c0002t0005g0214 | 1 | NA18522.hp1 | splice_region_variant&intron_variant | LOW | c.925-5C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 7/9 | chr1 | 54814909 | |||||||
| chr1:54815118 | G | A | 2 | a0002c0001t0001g0097 a0002c0001t0001g0148 |
2 | HG02300.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1050+79G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54815118 | |||||||
| chr1:54815124 | C | T | 2 | a0006c0013t0002g0030 a0006c0013t0002g0104 |
3 | HG02451.hp1 HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1050+85C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54815124 | |||||||
| chr1:54815151 | C | A | 1 | a0003c0006t0001g0235 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1050+112C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54815151 | |||||||
| chr1:54815257 | T | C | 2 | a0006c0013t0002g0030 a0006c0013t0002g0104 |
3 | HG02451.hp1 HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1050+218T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54815257 | |||||||
| chr1:54815333 | A | T | 16 | a0001c0002t0002g0015 a0001c0002t0002g0020 a0001c0002t0002g0044 others(13): Show |
26 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.1050+294A>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54815333 | |||||||
| chr1:54815458 | TCC | T | 103 | a0001c0002t0002g0006 a0001c0002t0002g0007 a0001c0002t0002g0010 others(100): Show |
162 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.1050+420_1050+421d others(4): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54815458 | |||||||
| chr1:54815459 | C | T | 135 | a0001c0002t0002g0005 a0001c0002t0002g0015 a0001c0002t0002g0016 others(132): Show |
198 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.1050+420C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54815459 | |||||||
| chr1:54815534 | C | G | 1 | a0001c0004t0003g0177 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1050+495C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54815534 | |||||||
| chr1:54815646 | T | A | 1 | a0001c0002t0002g0118 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1050+607T>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54815646 | |||||||
| chr1:54815781 | G | T | 2 | a0001c0002t0002g0227 a0001c0002t0002g0231 |
2 | HG00621.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.1050+742G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54815781 | |||||||
| chr1:54815858 | A | G | 132 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(129): Show |
204 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.1050+819A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54815858 | |||||||
| chr1:54816019 | G | C | 2 | a0006c0013t0002g0030 a0006c0013t0002g0104 |
3 | HG02451.hp1 HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1051-970G>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54816019 | |||||||
| chr1:54816034 | A | G | 6 | a0001c0002t0009g0200 a0001c0003t0003g0013 a0001c0003t0003g0212 others(3): Show |
11 | HG00558.hp2 HG02165.hp2 NA18943.hp1 others(8): Show |
intron_variant | MODIFIER | c.1051-955A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54816034 | |||||||
| chr1:54816174 | G | A | 85 | a0001c0002t0002g0208 a0001c0002t0009g0200 a0001c0003t0003g0009 others(82): Show |
124 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.1051-815G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54816174 | |||||||
| chr1:54816236 | C | G | 14 | a0001c0002t0002g0015 a0001c0002t0002g0020 a0001c0002t0002g0044 others(11): Show |
24 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.1051-753C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54816236 | |||||||
| chr1:54816245 | C | T | 1 | a0001c0002t0002g0222 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1051-744C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54816245 | |||||||
| chr1:54816292 | C | T | 115 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(112): Show |
185 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.1051-697C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54816292 | |||||||
| chr1:54816318 | A | G | 137 | a0001c0002t0001g0102 a0001c0002t0002g0014 a0001c0002t0002g0015 others(134): Show |
195 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.1051-671A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54816318 | |||||||
| chr1:54816341 | C | T | 120 | a0001c0002t0001g0102 a0001c0002t0002g0014 a0001c0002t0002g0015 others(117): Show |
176 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.1051-648C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54816341 | |||||||
| chr1:54816396 | A | G | 2 | a0006c0013t0002g0030 a0006c0013t0002g0104 |
3 | HG02451.hp1 HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1051-593A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54816396 | |||||||
| chr1:54816560 | T | A | 112 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(109): Show |
181 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.1051-429T>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54816560 | |||||||
| chr1:54816570 | T | C | 2 | a0001c0002t0002g0110 a0001c0002t0002g0111 |
2 | HG03834.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1051-419T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54816570 | |||||||
| chr1:54816621 | T | C | 9 | a0003c0006t0001g0237 a0003c0006t0001g0238 a0003c0006t0001g0245 others(6): Show |
9 | HG02074.hp2 HG02165.hp1 NA18957.hp1 others(6): Show |
intron_variant | MODIFIER | c.1051-368T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54816621 | |||||||
| chr1:54816623 | T | C | 1 | a0001c0002t0001g0102 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1051-366T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54816623 | |||||||
| chr1:54816637 | A | G | 112 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(109): Show |
181 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.1051-352A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54816637 | |||||||
| chr1:54816717 | A | G | 1 | a0001c0003t0003g0202 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1051-272A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54816717 | |||||||
| chr1:54816780 | A | T | 1 | a0001c0002t0002g0103 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1051-209A>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54816780 | |||||||
| chr1:54816883 | A | G | 112 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(109): Show |
181 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.1051-106A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54816883 | |||||||
| chr1:54816911 | C | G | 21 | a0003c0006t0001g0025 a0003c0006t0001g0234 a0003c0006t0001g0235 others(18): Show |
24 | HG02074.hp2 HG02165.hp1 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.1051-78C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54816911 | |||||||
| chr1:54816931 | C | T | 1 | a0002c0011t0004g0169 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1051-58C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54816931 | |||||||
| chr1:54817155 | G | A | 3 | a0001c0002t0002g0052 a0004c0008t0001g0249 a0004c0008t0001g0250 |
3 | HG02622.hp1 HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1184+33G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54817155 | |||||||
| chr1:54817161 | G | A | 1 | a0001c0004t0003g0041 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1184+39G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54817161 | |||||||
| chr1:54817262 | G | A | 1 | a0001c0002t0002g0103 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1184+140G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54817262 | |||||||
| chr1:54817306 | A | C | 112 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(109): Show |
181 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.1184+184A>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54817306 | |||||||
| chr1:54817403 | T | G | 112 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(109): Show |
181 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.1184+281T>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54817403 | |||||||
| chr1:54817477 | C | T | 1 | a0002c0001t0001g0134 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1184+355C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54817477 | |||||||
| chr1:54817693 | A | G | 1 | a0004c0008t0001g0051 | 2 | HG01884.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1184+571A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54817693 | |||||||
| chr1:54817724 | AT | A | 219 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(216): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.1184+615delT | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54817724 | ||||||
| chr1:54817737 | T | G | 112 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(109): Show |
181 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.1184+615T>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54817737 | |||||||
| chr1:54817755 | ATGAGGAC others(7): Show |
A | 112 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(109): Show |
181 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.1184+647_1184+660d others(16): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54817755 | ||||||
| chr1:54817762 | C | T | 1 | a0001c0002t0001g0102 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1184+640C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54817762 | |||||||
| chr1:54817955 | T | C | 52 | a0001c0002t0002g0208 a0001c0002t0009g0200 a0001c0003t0003g0009 others(49): Show |
80 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.1184+833T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54817955 | |||||||
| chr1:54817975 | A | ATCAATAG others(18): Show |
1 | a0001c0003t0003g0202 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1184+856_1184+880d others(27): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54817975 | ||||||
| chr1:54818045 | A | G | 112 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(109): Show |
181 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.1184+923A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818045 | |||||||
| chr1:54818085 | T | C | 140 | a0001c0002t0001g0102 a0001c0002t0002g0014 a0001c0002t0002g0015 others(137): Show |
199 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.1184+963T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818085 | |||||||
| chr1:54818335 | T | C | 17 | a0003c0006t0001g0025 a0003c0006t0001g0235 a0003c0006t0001g0237 others(14): Show |
19 | HG02074.hp2 HG02165.hp1 NA18747.hp2 others(16): Show |
intron_variant | MODIFIER | c.1184+1213T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818335 | |||||||
| chr1:54818385 | C | T | 249 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(246): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1184+1263C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818385 | |||||||
| chr1:54818386 | T | C | 111 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(108): Show |
180 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.1184+1264T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818386 | |||||||
| chr1:54818391 | C | G | 11 | a0001c0002t0002g0014 a0001c0002t0002g0048 a0001c0002t0002g0052 others(8): Show |
17 | HG01884.hp2 HG02109.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.1184+1269C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818391 | |||||||
| chr1:54818481 | A | T | 113 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(110): Show |
182 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.1184+1359A>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818481 | |||||||
| chr1:54818522 | C | T | 113 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(110): Show |
182 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.1184+1400C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818522 | |||||||
| chr1:54818588 | G | A | 115 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(112): Show |
184 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.1184+1466G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818588 | |||||||
| chr1:54818617 | G | A | 115 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(112): Show |
184 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.1184+1495G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818617 | |||||||
| chr1:54818628 | G | GA | 1 | a0001c0003t0003g0023 | 3 | HG02004.hp2 HG02148.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1184+1507dupA | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54818628 | ||||||
| chr1:54818732 | C | G | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1610C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818732 | |||||||
| chr1:54818735 | G | C | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1613G>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818735 | |||||||
| chr1:54818736 | C | T | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1614C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818736 | |||||||
| chr1:54818737 | A | T | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1615A>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818737 | |||||||
| chr1:54818739 | G | T | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1617G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818739 | |||||||
| chr1:54818740 | C | T | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1618C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818740 | |||||||
| chr1:54818741 | A | T | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1619A>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818741 | |||||||
| chr1:54818742 | C | T | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1620C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818742 | |||||||
| chr1:54818743 | C | A | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1621C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818743 | |||||||
| chr1:54818745 | C | T | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1623C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818745 | |||||||
| chr1:54818746 | C | G | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1624C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818746 | |||||||
| chr1:54818748 | C | T | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1626C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818748 | |||||||
| chr1:54818749 | A | T | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1627A>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818749 | |||||||
| chr1:54818750 | C | A | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1628C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818750 | |||||||
| chr1:54818751 | C | A | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1629C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818751 | |||||||
| chr1:54818752 | C | A | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1630C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818752 | |||||||
| chr1:54818752 | C | T | 1 | a0002c0001t0001g0070 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1184+1630C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818752 | |||||||
| chr1:54818753 | G | T | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1631G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818753 | |||||||
| chr1:54818754 | G | T | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1632G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818754 | |||||||
| chr1:54818755 | C | A | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1633C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818755 | |||||||
| chr1:54818756 | T | A | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1634T>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818756 | |||||||
| chr1:54818762 | T | A | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1640T>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818762 | |||||||
| chr1:54818763 | T | C | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1641T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818763 | |||||||
| chr1:54818764 | G | A | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1642G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818764 | |||||||
| chr1:54818764 | GT | G | 114 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(111): Show |
183 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.1184+1644delT | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54818764 | ||||||
| chr1:54818766 | T | A | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1644T>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818766 | |||||||
| chr1:54818779 | G | T | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1657G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818779 | |||||||
| chr1:54818781 | C | A | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1659C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818781 | |||||||
| chr1:54818789 | T | C | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1667T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818789 | |||||||
| chr1:54818790 | G | A | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1668G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818790 | |||||||
| chr1:54818796 | T | G | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1674T>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818796 | |||||||
| chr1:54818807 | G | T | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1685G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818807 | |||||||
| chr1:54818808 | G | T | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1686G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818808 | |||||||
| chr1:54818813 | G | C | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1691G>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818813 | |||||||
| chr1:54818818 | C | A | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1696C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818818 | |||||||
| chr1:54818822 | A | T | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1700A>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818822 | |||||||
| chr1:54818823 | G | T | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1701G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818823 | |||||||
| chr1:54818826 | C | A | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1704C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818826 | |||||||
| chr1:54818829 | G | T | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1707G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818829 | |||||||
| chr1:54818830 | C | T | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1708C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818830 | |||||||
| chr1:54818834 | C | A | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1712C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818834 | |||||||
| chr1:54818835 | T | A | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1713T>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818835 | |||||||
| chr1:54818836 | G | T | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1714G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818836 | |||||||
| chr1:54818837 | C | A | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1715C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818837 | |||||||
| chr1:54818840 | G | C | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1718G>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818840 | |||||||
| chr1:54818842 | C | T | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1720C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818842 | |||||||
| chr1:54818847 | C | G | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1725C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818847 | |||||||
| chr1:54818848 | C | G | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1726C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818848 | |||||||
| chr1:54818850 | C | G | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1728C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818850 | |||||||
| chr1:54818851 | C | A | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1729C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818851 | |||||||
| chr1:54818854 | A | G | 137 | a0001c0002t0001g0102 a0001c0002t0002g0014 a0001c0002t0002g0015 others(134): Show |
196 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.1184+1732A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818854 | |||||||
| chr1:54818860 | T | C | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1738T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818860 | |||||||
| chr1:54818861 | G | A | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1739G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818861 | |||||||
| chr1:54818865 | T | A | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1743T>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818865 | |||||||
| chr1:54818866 | T | A | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1744T>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818866 | |||||||
| chr1:54818868 | C | T | 30 | a0001c0003t0003g0019 a0001c0003t0003g0204 a0001c0003t0003g0205 others(27): Show |
40 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.1184+1746C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818868 | |||||||
| chr1:54818870 | G | A | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1748G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818870 | |||||||
| chr1:54818871 | G | A | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1749G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818871 | |||||||
| chr1:54818877 | G | A | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1755G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818877 | |||||||
| chr1:54818879 | C | A | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1757C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818879 | |||||||
| chr1:54818883 | G | T | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1761G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818883 | |||||||
| chr1:54818885 | G | A | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1763G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818885 | |||||||
| chr1:54818886 | G | T | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1764G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818886 | |||||||
| chr1:54818887 | C | A | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1765C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818887 | |||||||
| chr1:54818890 | G | T | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1768G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818890 | |||||||
| chr1:54818891 | C | A | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1769C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818891 | |||||||
| chr1:54818894 | C | A | 1 | a0001c0004t0003g0176 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1772C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818894 | |||||||
| chr1:54818980 | T | C | 1 | a0001c0002t0002g0116 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1184+1858T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818980 | |||||||
| chr1:54819081 | C | A | 127 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(124): Show |
199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1184+1959C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54819081 | |||||||
| chr1:54819114 | G | T | 2 | a0006c0013t0002g0030 a0006c0013t0002g0104 |
3 | HG02451.hp1 HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1184+1992G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54819114 | |||||||
| chr1:54819118 | C | A | 1 | a0001c0002t0005g0214 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1184+1996C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54819118 | |||||||
| chr1:54819352 | G | A | 4 | a0001c0002t0002g0016 a0001c0002t0002g0057 a0001c0002t0002g0058 others(1): Show |
7 | HG02132.hp2 NA18747.hp1 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+2230G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54819352 | |||||||
| chr1:54819353 | C | A | 4 | a0001c0002t0002g0016 a0001c0002t0002g0057 a0001c0002t0002g0058 others(1): Show |
7 | HG02132.hp2 NA18747.hp1 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+2231C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54819353 | |||||||
| chr1:54819365 | G | A | 1 | a0002c0001t0001g0078 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1184+2243G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54819365 | |||||||
| chr1:54819444 | C | T | 7 | a0001c0002t0002g0007 a0001c0002t0002g0010 a0001c0002t0002g0047 others(4): Show |
17 | HG00558.hp1 HG03490.hp2 HG03492.hp2 others(14): Show |
intron_variant | MODIFIER | c.1184+2322C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54819444 | |||||||
| chr1:54819533 | C | T | 53 | a0001c0002t0002g0208 a0001c0002t0009g0200 a0001c0003t0003g0009 others(50): Show |
82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1184+2411C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54819533 | |||||||
| chr1:54819570 | T | C | 1 | a0001c0002t0002g0225 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1184+2448T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54819570 | |||||||
| chr1:54819573 | G | A | 1 | a0001c0002t0002g0218 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1184+2451G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54819573 | |||||||
| chr1:54819647 | A | C | 2 | a0006c0013t0002g0030 a0006c0013t0002g0104 |
3 | HG02451.hp1 HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1184+2525A>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54819647 | |||||||
| chr1:54819812 | T | TTTTCTTT others(24): Show |
1 | a0001c0002t0002g0208 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1184+2699_1184+270 others(35): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54819812 | ||||||
| chr1:54819812 | T | TTTTCTTT others(17): Show |
1 | a0001c0003t0003g0191 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1184+2699_1184+270 others(28): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54819812 | ||||||
| chr1:54819812 | T | TTTTCTTT others(21): Show |
5 | a0001c0003t0003g0024 a0001c0003t0003g0117 a0001c0003t0003g0192 others(2): Show |
9 | HG01074.hp1 HG02056.hp2 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.1184+2699_1184+270 others(32): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54819812 | ||||||
| chr1:54819812 | T | TTTTCTTT others(25): Show |
19 | a0001c0003t0003g0009 a0001c0003t0003g0012 a0001c0003t0003g0013 others(16): Show |
36 | HG00099.hp2 HG00558.hp2 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.1184+2699_1184+270 others(36): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54819812 | ||||||
| chr1:54819812 | T | TTTTCTTT others(29): Show |
16 | a0001c0002t0009g0200 a0001c0003t0003g0183 a0001c0003t0003g0184 others(13): Show |
19 | HG00544.hp1 HG00673.hp2 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.1184+2699_1184+270 others(40): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54819812 | ||||||
| chr1:54819812 | T | TTTTCTTT others(33): Show |
5 | a0001c0003t0003g0199 a0001c0004t0003g0162 a0002c0005t0004g0022 others(2): Show |
7 | HG02071.hp2 HG02717.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+2699_1184+270 others(44): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54819812 | ||||||
| chr1:54819812 | T | TTTTCTTT others(37): Show |
4 | a0001c0003t0003g0042 a0001c0003t0003g0045 a0001c0003t0003g0190 others(1): Show |
7 | HG00140.hp1 HG01433.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+2699_1184+270 others(48): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54819812 | ||||||
| chr1:54819812 | T | TTTTCTTT others(45): Show |
1 | a0002c0001t0001g0139 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1184+2699_1184+270 others(56): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54819812 | ||||||
| chr1:54819814 | T | C | 1 | a0001c0003t0003g0185 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1184+2692T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54819814 | |||||||
| chr1:54819814 | TTCTTTCT others(3): Show |
T | 1 | a0002c0001t0001g0078 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1184+2704_1184+271 others(14): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54819814 | ||||||
| chr1:54819824 | C | CTT | 52 | a0001c0002t0002g0208 a0001c0002t0009g0200 a0001c0003t0003g0009 others(49): Show |
81 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.1184+2703_1184+270 others(6): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54819824 | ||||||
| chr1:54819824 | C | CTTTTTCT others(21): Show |
1 | a0001c0003t0003g0185 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1184+2703_1184+270 others(32): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54819824 | ||||||
| chr1:54819824 | CTCTT | C | 2 | a0006c0013t0002g0030 a0006c0013t0002g0104 |
3 | HG02451.hp1 HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1184+2714_1184+271 others(8): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54819824 | ||||||
| chr1:54819832 | TTCTTTC | T | 29 | a0001c0002t0001g0102 a0001c0002t0002g0014 a0001c0002t0002g0048 others(26): Show |
36 | HG00408.hp1 HG00423.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.1184+2718_1184+272 others(10): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54819832 | ||||||
| chr1:54819835 | TTTCTCTT others(11): Show |
T | 15 | a0001c0002t0002g0015 a0001c0002t0002g0020 a0001c0002t0002g0044 others(12): Show |
25 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.1184+2717_1184+273 others(22): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54819835 | ||||||
| chr1:54819839 | TCTTTCTT others(7): Show |
T | 29 | a0001c0002t0002g0215 a0001c0003t0003g0019 a0001c0003t0003g0204 others(26): Show |
39 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.1184+2718_1184+273 others(18): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54819839 | |||||||
| chr1:54819860 | CCTTCCT | C | 29 | a0001c0002t0001g0102 a0001c0002t0002g0014 a0001c0002t0002g0048 others(26): Show |
36 | HG00408.hp1 HG00423.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.1184+2741_1184+274 others(10): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54819860 | ||||||
| chr1:54819864 | CCT | C | 43 | a0001c0002t0002g0020 a0001c0002t0002g0044 a0001c0002t0002g0049 others(40): Show |
59 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.1184+2747_1184+274 others(6): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54819864 | ||||||
| chr1:54819868 | TCTTTC | T | 1 | a0001c0002t0002g0015 | 5 | HG01099.hp1 HG01934.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.1184+2747_1184+275 others(9): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54819868 | |||||||
| chr1:54819876 | CCT | C | 1 | a0001c0002t0002g0015 | 5 | HG01099.hp1 HG01934.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.1184+2755_1184+275 others(6): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54819876 | |||||||
| chr1:54819928 | A | ATT | 72 | a0001c0002t0001g0102 a0001c0002t0002g0014 a0001c0002t0002g0015 others(69): Show |
99 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.1184+2807_1184+280 others(6): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54819928 | ||||||
| chr1:54819930 | A | C | 72 | a0001c0002t0001g0102 a0001c0002t0002g0014 a0001c0002t0002g0015 others(69): Show |
99 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.1184+2808A>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54819930 | |||||||
| chr1:54819934 | C | T | 72 | a0001c0002t0001g0102 a0001c0002t0002g0014 a0001c0002t0002g0015 others(69): Show |
99 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.1184+2812C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54819934 | |||||||
| chr1:54819935 | T | C | 72 | a0001c0002t0001g0102 a0001c0002t0002g0014 a0001c0002t0002g0015 others(69): Show |
99 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.1184+2813T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54819935 | |||||||
| chr1:54819945 | G | T | 73 | a0001c0002t0001g0102 a0001c0002t0002g0014 a0001c0002t0002g0015 others(70): Show |
100 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.1184+2823G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54819945 | |||||||
| chr1:54819948 | C | T | 1 | a0002c0011t0004g0165 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1184+2826C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54819948 | |||||||
| chr1:54819952 | T | C | 1 | a0002c0011t0004g0165 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1184+2830T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54819952 | |||||||
| chr1:54819978 | T | C | 72 | a0001c0002t0001g0102 a0001c0002t0002g0014 a0001c0002t0002g0015 others(69): Show |
98 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.1184+2856T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54819978 | |||||||
| chr1:54819980 | C | T | 72 | a0001c0002t0001g0102 a0001c0002t0002g0014 a0001c0002t0002g0015 others(69): Show |
98 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.1184+2858C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54819980 | |||||||
| chr1:54819982 | C | CTTTT | 14 | a0001c0002t0002g0015 a0001c0002t0002g0020 a0001c0002t0002g0044 others(11): Show |
24 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.1184+2861_1184+286 others(8): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54819982 | ||||||
| chr1:54819982 | C | T | 58 | a0001c0002t0001g0102 a0001c0002t0002g0014 a0001c0002t0002g0048 others(55): Show |
74 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.1184+2860C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54819982 | |||||||
| chr1:54820009 | T | C | 73 | a0001c0002t0001g0102 a0001c0002t0002g0014 a0001c0002t0002g0015 others(70): Show |
100 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.1184+2887T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54820009 | |||||||
| chr1:54820017 | T | C | 73 | a0001c0002t0001g0102 a0001c0002t0002g0014 a0001c0002t0002g0015 others(70): Show |
100 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.1184+2895T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54820017 | |||||||
| chr1:54820017 | T | TTTCC | 3 | a0002c0001t0001g0035 a0002c0001t0001g0094 a0002c0001t0001g0140 |
4 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1184+2911_1184+291 others(8): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54820017 | ||||||
| chr1:54820017 | TTTCC | T | 53 | a0001c0002t0002g0208 a0001c0002t0009g0200 a0001c0003t0003g0009 others(50): Show |
82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1184+2911_1184+291 others(8): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54820017 | ||||||
| chr1:54820033 | C | A | 49 | a0001c0002t0001g0102 a0001c0002t0002g0052 a0001c0002t0002g0224 others(46): Show |
61 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.1184+2911C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54820033 | |||||||
| chr1:54820041 | A | ATTCC | 16 | a0001c0002t0002g0015 a0001c0002t0002g0020 a0001c0002t0002g0044 others(13): Show |
25 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.1184+2927_1184+293 others(8): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54820041 | ||||||
| chr1:54820041 | A | C | 57 | a0001c0002t0001g0102 a0001c0002t0002g0014 a0001c0002t0002g0048 others(54): Show |
75 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.1184+2919A>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54820041 | |||||||
| chr1:54820071 | CCCTT | C | 49 | a0001c0002t0002g0015 a0001c0002t0002g0020 a0001c0002t0002g0044 others(46): Show |
66 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.1184+2960_1184+296 others(8): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54820071 | ||||||
| chr1:54820082 | T | C | 25 | a0001c0002t0001g0102 a0001c0002t0002g0014 a0001c0002t0002g0048 others(22): Show |
34 | HG00408.hp1 HG01167.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.1184+2960T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54820082 | |||||||
| chr1:54820086 | C | T | 25 | a0001c0002t0001g0102 a0001c0002t0002g0014 a0001c0002t0002g0048 others(22): Show |
34 | HG00408.hp1 HG01167.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.1184+2964C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54820086 | |||||||
| chr1:54820089 | C | CTTCT | 32 | a0001c0002t0002g0224 a0001c0002t0002g0225 a0001c0002t0002g0226 others(29): Show |
39 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.1184+2980_1184+298 others(8): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54820089 | ||||||
| chr1:54820089 | C | T | 25 | a0001c0002t0001g0102 a0001c0002t0002g0014 a0001c0002t0002g0048 others(22): Show |
34 | HG00408.hp1 HG01167.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.1184+2967C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54820089 | |||||||
| chr1:54820098 | TTCTTTCT others(5): Show |
T | 2 | a0002c0001t0001g0017 a0009c0019t0002g0065 |
5 | HG01884.hp1 HG02145.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1184+2980_1184+299 others(16): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54820098 | ||||||
| chr1:54820102 | T | C | 104 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(101): Show |
170 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.1184+2980T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54820102 | |||||||
| chr1:54820106 | C | T | 17 | a0001c0002t0002g0015 a0001c0002t0002g0020 a0001c0002t0002g0044 others(14): Show |
27 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.1184+2984C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54820106 | |||||||
| chr1:54820108 | CTCTCTCT others(5): Show |
C | 104 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(101): Show |
169 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.1184+2990_1184+300 others(16): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54820108 | ||||||
| chr1:54820108 | CTCTCTCT others(9): Show |
C | 1 | a0001c0002t0002g0016 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1184+2990_1184+300 others(20): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54820108 | ||||||
| chr1:54820112 | C | CTCTT | 1 | a0003c0006t0001g0025 | 3 | NA18946.hp1 NA19066.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1184+3014_1184+301 others(8): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54820112 | ||||||
| chr1:54820112 | C | CTCTTTCT others(5): Show |
12 | a0003c0006t0001g0235 a0003c0006t0001g0240 a0003c0006t0001g0241 others(9): Show |
13 | HG02165.hp1 HG02451.hp1 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.1184+3006_1184+301 others(16): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54820112 | ||||||
| chr1:54820112 | C | CTCTTTCT others(9): Show |
2 | a0003c0006t0001g0237 a0003c0006t0001g0246 |
2 | HG02074.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.1184+3002_1184+301 others(20): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54820112 | ||||||
| chr1:54820112 | C | CTCTTTCT others(13): Show |
2 | a0003c0006t0001g0238 a0003c0020t0004g0247 |
2 | NA19090.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1184+2998_1184+301 others(24): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54820112 | ||||||
| chr1:54820112 | CTCTTTCT others(1): Show |
C | 53 | a0001c0002t0002g0208 a0001c0002t0009g0200 a0001c0003t0003g0009 others(50): Show |
82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1184+3010_1184+301 others(12): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54820112 | ||||||
| chr1:54820116 | T | C | 74 | a0001c0002t0001g0102 a0001c0002t0002g0014 a0001c0002t0002g0015 others(71): Show |
104 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.1184+2994T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54820116 | |||||||
| chr1:54820124 | T | C | 53 | a0001c0002t0002g0208 a0001c0002t0009g0200 a0001c0003t0003g0009 others(50): Show |
82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1184+3002T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54820124 | |||||||
| chr1:54820132 | T | C | 73 | a0001c0002t0001g0102 a0001c0002t0002g0014 a0001c0002t0002g0015 others(70): Show |
100 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.1184+3010T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54820132 | |||||||
| chr1:54820136 | T | C | 126 | a0001c0002t0001g0102 a0001c0002t0002g0014 a0001c0002t0002g0015 others(123): Show |
182 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.1184+3014T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54820136 | |||||||
| chr1:54820148 | C | CCCTT | 40 | a0001c0002t0001g0102 a0001c0002t0002g0224 a0001c0002t0002g0225 others(37): Show |
50 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.1184+3044_1184+304 others(8): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54820148 | ||||||
| chr1:54820258 | C | T | 17 | a0001c0002t0002g0015 a0001c0002t0002g0020 a0001c0002t0002g0044 others(14): Show |
27 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.1184+3136C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54820258 | |||||||
| chr1:54820287 | T | G | 1 | a0002c0001t0001g0137 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1184+3165T>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54820287 | |||||||
| chr1:54820584 | C | G | 2 | a0001c0002t0002g0226 a0001c0002t0002g0232 |
2 | HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1184+3462C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54820584 | |||||||
| chr1:54820750 | C | T | 1 | a0002c0001t0001g0131 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1184+3628C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54820750 | |||||||
| chr1:54820771 | TTTTG | T | 5 | a0001c0003t0003g0012 a0001c0003t0003g0042 a0001c0003t0003g0184 others(2): Show |
11 | HG00099.hp2 HG00140.hp1 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.1184+3662_1184+366 others(8): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54820771 | ||||||
| chr1:54820799 | C | T | 13 | a0001c0002t0001g0102 a0001c0002t0002g0224 a0001c0002t0002g0225 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG00621.hp1 others(10): Show |
intron_variant | MODIFIER | c.1184+3677C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54820799 | |||||||
| chr1:54820872 | G | A | 72 | a0001c0002t0001g0102 a0001c0002t0002g0014 a0001c0002t0002g0015 others(69): Show |
99 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.1184+3750G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54820872 | |||||||
| chr1:54820960 | G | A | 53 | a0001c0002t0002g0208 a0001c0002t0009g0200 a0001c0003t0003g0009 others(50): Show |
82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1184+3838G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54820960 | |||||||
| chr1:54821170 | T | C | 53 | a0001c0002t0002g0208 a0001c0002t0009g0200 a0001c0003t0003g0009 others(50): Show |
82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1184+4048T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54821170 | |||||||
| chr1:54821180 | G | A | 17 | a0001c0002t0002g0015 a0001c0002t0002g0020 a0001c0002t0002g0044 others(14): Show |
27 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.1184+4058G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54821180 | |||||||
| chr1:54821200 | A | ATTGT | 53 | a0001c0002t0002g0208 a0001c0002t0009g0200 a0001c0003t0003g0009 others(50): Show |
82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1184+4080_1184+408 others(8): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54821200 | ||||||
| chr1:54821208 | G | C | 1 | a0002c0001t0001g0100 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1184+4086G>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54821208 | |||||||
| chr1:54821219 | G | GC | 126 | a0001c0002t0001g0102 a0001c0002t0002g0014 a0001c0002t0002g0015 others(123): Show |
182 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.1184+4097_1184+409 others(5): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54821219 | |||||||
| chr1:54821275 | T | A | 1 | a0004c0008t0006g0248 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1184+4153T>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54821275 | |||||||
| chr1:54821343 | G | C | 2 | a0007c0014t0003g0046 a0007c0014t0003g0203 |
3 | HG02922.hp1 HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+4221G>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54821343 | |||||||
| chr1:54821414 | G | A | 107 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(104): Show |
176 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.1184+4292G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54821414 | |||||||
| chr1:54821732 | T | C | 53 | a0001c0002t0002g0208 a0001c0002t0009g0200 a0001c0003t0003g0009 others(50): Show |
82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1184+4610T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54821732 | |||||||
| chr1:54821816 | T | A | 73 | a0001c0002t0001g0102 a0001c0002t0002g0014 a0001c0002t0002g0015 others(70): Show |
100 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.1184+4694T>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54821816 | |||||||
| chr1:54821854 | T | G | 17 | a0003c0006t0001g0025 a0003c0006t0001g0235 a0003c0006t0001g0237 others(14): Show |
19 | HG02074.hp2 HG02165.hp1 NA18747.hp2 others(16): Show |
intron_variant | MODIFIER | c.1184+4732T>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54821854 | |||||||
| chr1:54821878 | TCTTATTT others(311): Show |
T | 53 | a0001c0002t0002g0208 a0001c0002t0009g0200 a0001c0003t0003g0009 others(50): Show |
82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1184+4768_1184+508 others(4): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54821878 | ||||||
| chr1:54821886 | C | CT | 38 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(35): Show |
63 | HG00544.hp2 HG00558.hp1 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.1184+4794dupT | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54821886 | ||||||
| chr1:54821886 | C | CTT | 7 | a0001c0002t0002g0005 a0001c0003t0003g0186 a0002c0001t0001g0001 others(4): Show |
10 | HG01109.hp1 HG01109.hp2 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.1184+4793_1184+479 others(6): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54821886 | ||||||
| chr1:54821886 | CT | C | 20 | a0001c0002t0002g0006 a0001c0002t0002g0112 a0002c0001t0001g0034 others(17): Show |
21 | HG00423.hp1 HG02074.hp2 HG02165.hp1 others(18): Show |
intron_variant | MODIFIER | c.1184+4794delT | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54821886 | ||||||
| chr1:54821886 | CTT | C | 8 | a0001c0002t0002g0063 a0001c0002t0002g0064 a0001c0002t0002g0103 others(5): Show |
9 | HG01891.hp1 HG01891.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1184+4793_1184+479 others(6): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54821886 | ||||||
| chr1:54821886 | CTTTT | C | 9 | a0001c0002t0002g0225 a0001c0002t0002g0229 a0001c0004t0003g0004 others(6): Show |
9 | HG00423.hp2 HG00438.hp2 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.1184+4791_1184+479 others(8): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54821886 | ||||||
| chr1:54821886 | CTTTTT | C | 30 | a0001c0002t0002g0050 a0001c0002t0002g0224 a0001c0002t0002g0226 others(27): Show |
40 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.1184+4790_1184+479 others(9): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54821886 | ||||||
| chr1:54821886 | CTTTTTT | C | 21 | a0001c0002t0002g0014 a0001c0002t0002g0015 a0001c0002t0002g0020 others(18): Show |
30 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.1184+4789_1184+479 others(10): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54821886 | ||||||
| chr1:54821886 | CTTTTTTT | C | 18 | a0001c0002t0002g0014 a0001c0002t0002g0016 a0001c0002t0002g0027 others(15): Show |
28 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.1184+4788_1184+479 others(11): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54821886 | ||||||
| chr1:54821886 | CTTTTTTT others(2): Show |
C | 3 | a0002c0001t0001g0017 a0002c0001t0001g0143 a0009c0019t0002g0065 |
6 | HG01884.hp1 HG02145.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1184+4786_1184+479 others(13): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54821886 | ||||||
| chr1:54821886 | CTTTTTTT others(5): Show |
C | 1 | a0001c0004t0003g0159 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1184+4783_1184+479 others(16): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54821886 | ||||||
| chr1:54821929 | C | T | 2 | a0006c0013t0002g0030 a0006c0013t0002g0104 |
3 | HG02451.hp1 HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1184+4807C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54821929 | |||||||
| chr1:54821960 | G | A | 16 | a0001c0002t0002g0015 a0001c0002t0002g0020 a0001c0002t0002g0044 others(13): Show |
26 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.1184+4838G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54821960 | |||||||
| chr1:54822010 | C | T | 73 | a0001c0002t0001g0102 a0001c0002t0002g0014 a0001c0002t0002g0015 others(70): Show |
100 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.1184+4888C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54822010 | |||||||
| chr1:54822048 | A | G | 1 | a0001c0002t0002g0103 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1184+4926A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54822048 | |||||||
| chr1:54822108 | C | T | 1 | a0004c0008t0001g0051 | 2 | HG01884.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1184+4986C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54822108 | |||||||
| chr1:54822140 | C | T | 50 | a0001c0002t0001g0102 a0001c0002t0002g0016 a0001c0002t0002g0027 others(47): Show |
64 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.1184+5018C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54822140 | |||||||
| chr1:54822144 | C | T | 73 | a0001c0002t0001g0102 a0001c0002t0002g0014 a0001c0002t0002g0015 others(70): Show |
100 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.1184+5022C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54822144 | |||||||
| chr1:54822164 | C | T | 1 | a0001c0002t0005g0062 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1184+5042C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54822164 | |||||||
| chr1:54822182 | G | A | 19 | a0003c0006t0001g0025 a0003c0006t0001g0235 a0003c0006t0001g0237 others(16): Show |
22 | HG02074.hp2 HG02165.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.1184+5060G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54822182 | |||||||
| chr1:54822188 | G | A | 1 | a0001c0002t0002g0052 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1184+5066G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54822188 | |||||||
| chr1:54822189 | C | T | 1 | a0002c0001t0001g0084 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1184+5067C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54822189 | |||||||
| chr1:54822288 | G | C | 53 | a0001c0002t0002g0208 a0001c0002t0009g0200 a0001c0003t0003g0009 others(50): Show |
82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1184+5166G>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54822288 | |||||||
| chr1:54822311 | G | T | 53 | a0001c0002t0002g0208 a0001c0002t0009g0200 a0001c0003t0003g0009 others(50): Show |
82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1184+5189G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54822311 | |||||||
| chr1:54822382 | G | GT | 61 | a0001c0002t0002g0014 a0001c0002t0002g0048 a0001c0002t0002g0052 others(58): Show |
96 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.1184+5272dupT | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54822382 | ||||||
| chr1:54822382 | G | T | 1 | a0001c0003t0003g0196 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1184+5260G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54822382 | |||||||
| chr1:54822430 | A | C | 33 | a0001c0009t0002g0170 a0001c0009t0002g0171 a0002c0001t0001g0002 others(30): Show |
54 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.1184+5308A>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54822430 | |||||||
| chr1:54822628 | T | C | 2 | a0002c0001t0001g0082 a0002c0001t0001g0151 |
2 | NA18967.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.1184+5506T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54822628 | |||||||
| chr1:54822936 | T | C | 53 | a0001c0002t0002g0208 a0001c0002t0009g0200 a0001c0003t0003g0009 others(50): Show |
82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1184+5814T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54822936 | |||||||
| chr1:54822950 | T | C | 1 | a0004c0008t0001g0249 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1184+5828T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54822950 | |||||||
| chr1:54823058 | C | T | 127 | a0001c0002t0001g0102 a0001c0002t0002g0014 a0001c0002t0002g0015 others(124): Show |
183 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.1184+5936C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54823058 | |||||||
| chr1:54823162 | T | C | 1 | a0001c0002t0005g0214 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1184+6040T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54823162 | |||||||
| chr1:54823179 | C | T | 32 | a0001c0002t0002g0014 a0001c0002t0002g0015 a0001c0002t0002g0020 others(29): Show |
49 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.1184+6057C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54823179 | |||||||
| chr1:54823325 | T | C | 53 | a0001c0002t0002g0208 a0001c0002t0009g0200 a0001c0003t0003g0009 others(50): Show |
82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1184+6203T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54823325 | |||||||
| chr1:54823345 | CT | C | 9 | a0001c0002t0002g0016 a0001c0002t0002g0027 a0001c0002t0002g0057 others(6): Show |
13 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1184+6234delT | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54823345 | ||||||
| chr1:54823413 | C | T | 1 | a0001c0002t0002g0050 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1184+6291C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54823413 | |||||||
| chr1:54823506 | A | G | 127 | a0001c0002t0001g0102 a0001c0002t0002g0014 a0001c0002t0002g0015 others(124): Show |
183 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.1184+6384A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54823506 | |||||||
| chr1:54823632 | C | A | 17 | a0001c0002t0002g0015 a0001c0002t0002g0020 a0001c0002t0002g0044 others(14): Show |
27 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.1184+6510C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54823632 | |||||||
| chr1:54823942 | TTTTG | T | 4 | a0001c0002t0002g0016 a0001c0002t0002g0057 a0001c0002t0002g0058 others(1): Show |
7 | HG02132.hp2 NA18747.hp1 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+6836_1184+683 others(8): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54823942 | ||||||
| chr1:54824053 | G | A | 41 | a0001c0002t0001g0102 a0001c0002t0002g0103 a0001c0002t0002g0224 others(38): Show |
51 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.1184+6931G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54824053 | |||||||
| chr1:54824087 | T | G | 73 | a0001c0002t0001g0102 a0001c0002t0002g0014 a0001c0002t0002g0015 others(70): Show |
100 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.1184+6965T>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54824087 | |||||||
| chr1:54824088 | C | G | 41 | a0001c0002t0001g0102 a0001c0002t0002g0103 a0001c0002t0002g0224 others(38): Show |
51 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.1184+6966C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54824088 | |||||||
| chr1:54824242 | A | G | 127 | a0001c0002t0001g0102 a0001c0002t0002g0014 a0001c0002t0002g0015 others(124): Show |
183 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.1184+7120A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54824242 | |||||||
| chr1:54824319 | T | G | 42 | a0001c0002t0001g0102 a0001c0002t0002g0103 a0001c0002t0002g0224 others(39): Show |
52 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.1184+7197T>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54824319 | |||||||
| chr1:54824337 | C | T | 1 | a0001c0003t0004g0028 | 2 | HG00673.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.1184+7215C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54824337 | |||||||
| chr1:54824394 | TG | T | 127 | a0001c0002t0001g0102 a0001c0002t0002g0014 a0001c0002t0002g0015 others(124): Show |
183 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.1184+7277delG | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54824394 | ||||||
| chr1:54824540 | G | A | 3 | a0002c0001t0001g0017 a0002c0001t0001g0143 a0009c0019t0002g0065 |
6 | HG01884.hp1 HG02145.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1184+7418G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54824540 | |||||||
| chr1:54824572 | T | A | 251 | a0001c0002t0001g0102 a0001c0002t0002g0005 a0001c0002t0002g0006 others(248): Show |
379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.1184+7450T>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54824572 | |||||||
| chr1:54824656 | AGT | A | 16 | a0001c0002t0002g0015 a0001c0002t0002g0020 a0001c0002t0002g0044 others(13): Show |
26 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.1184+7537_1184+753 others(6): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54824656 | ||||||
| chr1:54824659 | G | A | 1 | a0001c0002t0002g0103 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1184+7537G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54824659 | |||||||
| chr1:54824723 | C | T | 53 | a0001c0002t0002g0208 a0001c0002t0009g0200 a0001c0003t0003g0009 others(50): Show |
82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1184+7601C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54824723 | |||||||
| chr1:54824724 | T | C | 53 | a0001c0002t0002g0208 a0001c0002t0009g0200 a0001c0003t0003g0009 others(50): Show |
82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1184+7602T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54824724 | |||||||
| chr1:54824757 | G | C | 19 | a0001c0003t0003g0019 a0001c0003t0003g0204 a0001c0003t0003g0205 others(16): Show |
28 | HG00408.hp2 HG00609.hp1 HG01978.hp2 others(25): Show |
intron_variant | MODIFIER | c.1184+7635G>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54824757 | |||||||
| chr1:54824811 | T | C | 1 | a0001c0009t0002g0170 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1184+7689T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54824811 | |||||||
| chr1:54824835 | T | C | 6 | a0001c0002t0002g0007 a0001c0002t0002g0047 a0001c0002t0002g0109 others(3): Show |
12 | HG03490.hp2 HG03492.hp2 NA18940.hp1 others(9): Show |
intron_variant | MODIFIER | c.1184+7713T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54824835 | |||||||
| chr1:54825035 | G | A | 1 | a0004c0008t0006g0248 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1184+7913G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54825035 | |||||||
| chr1:54825041 | CT | C | 33 | a0001c0002t0002g0052 a0001c0002t0002g0069 a0001c0002t0002g0225 others(30): Show |
39 | HG00408.hp1 HG00423.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.1184+7945delT | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54825041 | ||||||
| chr1:54825041 | CTT | C | 83 | a0001c0002t0002g0005 a0001c0002t0002g0014 a0001c0002t0002g0043 others(80): Show |
136 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.1184+7944_1184+794 others(6): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54825041 | ||||||
| chr1:54825041 | CTTT | C | 57 | a0001c0002t0002g0006 a0001c0002t0002g0007 a0001c0002t0002g0010 others(54): Show |
87 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.1184+7943_1184+794 others(7): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54825041 | ||||||
| chr1:54825041 | CTTTTTTT others(2): Show |
C | 55 | a0001c0002t0002g0208 a0001c0002t0005g0062 a0001c0002t0009g0200 others(52): Show |
84 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.1184+7937_1184+794 others(13): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54825041 | ||||||
| chr1:54825041 | CTTTTTTT others(8): Show |
C | 17 | a0001c0002t0002g0015 a0001c0002t0002g0020 a0001c0002t0002g0044 others(14): Show |
27 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.1184+7931_1184+794 others(19): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54825041 | ||||||
| chr1:54825070 | G | A | 16 | a0003c0006t0001g0025 a0003c0006t0001g0237 a0003c0006t0001g0238 others(13): Show |
18 | HG02074.hp2 HG02165.hp1 NA18747.hp2 others(15): Show |
intron_variant | MODIFIER | c.1184+7948G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54825070 | |||||||
| chr1:54825096 | C | G | 53 | a0001c0002t0002g0208 a0001c0002t0009g0200 a0001c0003t0003g0009 others(50): Show |
82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1184+7974C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54825096 | |||||||
| chr1:54825136 | C | T | 11 | a0001c0002t0002g0014 a0001c0002t0002g0048 a0001c0002t0002g0052 others(8): Show |
17 | HG01884.hp2 HG02109.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.1184+8014C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54825136 | |||||||
| chr1:54825176 | G | A | 1 | a0002c0001t0001g0126 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1184+8054G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54825176 | |||||||
| chr1:54825339 | C | T | 74 | a0001c0002t0001g0102 a0001c0002t0002g0014 a0001c0002t0002g0015 others(71): Show |
101 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1184+8217C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54825339 | |||||||
| chr1:54825342 | C | T | 1 | a0004c0008t0006g0248 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1184+8220C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54825342 | |||||||
| chr1:54825384 | G | A | 1 | a0002c0001t0001g0124 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1184+8262G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54825384 | |||||||
| chr1:54825432 | T | A | 2 | a0007c0014t0003g0046 a0007c0014t0003g0203 |
3 | HG02922.hp1 HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+8310T>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54825432 | |||||||
| chr1:54825785 | G | A | 2 | a0001c0003t0003g0189 a0001c0003t0003g0193 |
2 | NA18968.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.1184+8663G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54825785 | |||||||
| chr1:54826177 | C | T | 1 | a0001c0003t0003g0191 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1184+9055C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54826177 | |||||||
| chr1:54826481 | G | C | 17 | a0001c0002t0002g0015 a0001c0002t0002g0020 a0001c0002t0002g0044 others(14): Show |
27 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.1184+9359G>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54826481 | |||||||
| chr1:54826538 | C | T | 1 | a0001c0002t0002g0221 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1184+9416C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54826538 | |||||||
| chr1:54826691 | C | A | 1 | a0002c0001t0001g0154 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1184+9569C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54826691 | |||||||
| chr1:54826815 | A | G | 1 | a0012c0021t0004g0251 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1184+9693A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54826815 | |||||||
| chr1:54826875 | C | T | 53 | a0001c0002t0002g0208 a0001c0002t0009g0200 a0001c0003t0003g0009 others(50): Show |
82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1184+9753C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54826875 | |||||||
| chr1:54826927 | A | G | 3 | a0002c0001t0001g0017 a0002c0001t0001g0143 a0009c0019t0002g0065 |
6 | HG01884.hp1 HG02145.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1184+9805A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54826927 | |||||||
| chr1:54826940 | C | T | 9 | a0001c0002t0002g0016 a0001c0002t0002g0027 a0001c0002t0002g0057 others(6): Show |
13 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1184+9818C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54826940 | |||||||
| chr1:54827027 | C | T | 1 | a0002c0001t0001g0078 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1184+9905C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54827027 | |||||||
| chr1:54827211 | A | G | 53 | a0001c0002t0002g0208 a0001c0002t0009g0200 a0001c0003t0003g0009 others(50): Show |
82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1184+10089A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54827211 | |||||||
| chr1:54827340 | C | G | 1 | a0002c0001t0001g0088 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1184+10218C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54827340 | |||||||
| chr1:54827383 | C | G | 11 | a0001c0002t0002g0014 a0001c0002t0002g0048 a0001c0002t0002g0052 others(8): Show |
17 | HG01884.hp2 HG02109.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.1184+10261C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54827383 | |||||||
| chr1:54827705 | G | A | 4 | a0001c0002t0002g0052 a0004c0008t0001g0051 a0004c0008t0001g0249 others(1): Show |
5 | HG01884.hp2 HG02622.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1184+10583G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54827705 | |||||||
| chr1:54828022 | A | G | 1 | a0012c0021t0004g0251 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1184+10900A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54828022 | |||||||
| chr1:54828067 | T | G | 42 | a0001c0002t0001g0102 a0001c0002t0002g0103 a0001c0002t0002g0224 others(39): Show |
52 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.1184+10945T>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54828067 | |||||||
| chr1:54828116 | A | G | 1 | a0002c0005t0004g0091 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1184+10994A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54828116 | |||||||
| chr1:54828178 | T | C | 1 | a0002c0001t0001g0100 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1184+11056T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54828178 | |||||||
| chr1:54828210 | T | G | 1 | a0002c0001t0001g0095 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1184+11088T>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54828210 | |||||||
| chr1:54828243 | A | C | 4 | a0005c0007t0002g0055 a0005c0007t0002g0108 a0005c0007t0002g0201 others(1): Show |
4 | NA18985.hp2 NA19009.hp2 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.1184+11121A>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54828243 | |||||||
| chr1:54828268 | C | T | 1 | a0004c0008t0006g0248 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1184+11146C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54828268 | |||||||
| chr1:54828297 | AAATT | A | 28 | a0001c0003t0003g0019 a0001c0003t0003g0204 a0001c0003t0003g0205 others(25): Show |
38 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.1184+11180_1184+11 others(10): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54828297 | ||||||
| chr1:54828325 | AT | A | 12 | a0001c0002t0001g0102 a0001c0002t0002g0224 a0001c0002t0002g0225 others(9): Show |
12 | HG00408.hp1 HG00423.hp2 HG00621.hp1 others(9): Show |
intron_variant | MODIFIER | c.1184+11214delT | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54828325 | ||||||
| chr1:54828365 | C | T | 11 | a0001c0002t0001g0102 a0001c0002t0002g0224 a0001c0002t0002g0225 others(8): Show |
11 | HG00408.hp1 HG00423.hp2 HG00621.hp1 others(8): Show |
intron_variant | MODIFIER | c.1184+11243C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54828365 | |||||||
| chr1:54828477 | A | G | 1 | a0002c0001t0001g0098 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1184+11355A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54828477 | |||||||
| chr1:54828661 | A | T | 1 | a0001c0003t0008g0195 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1184+11539A>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54828661 | |||||||
| chr1:54828675 | C | T | 4 | a0001c0002t0002g0208 a0001c0003t0003g0209 a0001c0003t0003g0210 others(1): Show |
4 | HG00621.hp2 HG02083.hp1 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.1184+11553C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54828675 | |||||||
| chr1:54828696 | C | A | 1 | a0002c0001t0001g0100 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1184+11574C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54828696 | |||||||
| chr1:54828714 | C | T | 1 | a0002c0001t0001g0084 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1184+11592C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54828714 | |||||||
| chr1:54828785 | A | G | 1 | a0001c0003t0003g0198 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1184+11663A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54828785 | |||||||
| chr1:54828831 | A | G | 1 | a0001c0002t0002g0227 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1184+11709A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54828831 | |||||||
| chr1:54828850 | T | A | 3 | a0001c0002t0002g0052 a0004c0008t0001g0249 a0004c0008t0001g0250 |
3 | HG02622.hp1 HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1184+11728T>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54828850 | |||||||
| chr1:54828927 | T | C | 1 | a0001c0002t0002g0225 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1184+11805T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54828927 | |||||||
| chr1:54829049 | T | C | 110 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(107): Show |
180 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.1184+11927T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54829049 | |||||||
| chr1:54829081 | G | A | 1 | a0002c0001t0001g0145 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1184+11959G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54829081 | |||||||
| chr1:54829275 | C | T | 28 | a0001c0003t0003g0019 a0001c0003t0003g0204 a0001c0003t0003g0205 others(25): Show |
38 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.1184+12153C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54829275 | |||||||
| chr1:54829300 | A | G | 53 | a0001c0002t0002g0208 a0001c0002t0009g0200 a0001c0003t0003g0009 others(50): Show |
82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1184+12178A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54829300 | |||||||
| chr1:54829330 | A | G | 53 | a0001c0002t0002g0208 a0001c0002t0009g0200 a0001c0003t0003g0009 others(50): Show |
82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1184+12208A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54829330 | |||||||
| chr1:54829347 | A | T | 14 | a0001c0002t0002g0015 a0001c0002t0002g0020 a0001c0002t0002g0044 others(11): Show |
24 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.1184+12225A>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54829347 | |||||||
| chr1:54829585 | G | A | 11 | a0001c0002t0001g0102 a0001c0002t0002g0224 a0001c0002t0002g0225 others(8): Show |
11 | HG00408.hp1 HG00423.hp2 HG00621.hp1 others(8): Show |
intron_variant | MODIFIER | c.1185-12216G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54829585 | |||||||
| chr1:54829589 | T | C | 1 | a0001c0009t0002g0171 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1185-12212T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54829589 | |||||||
| chr1:54829908 | T | G | 1 | a0002c0001t0001g0071 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1185-11893T>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54829908 | |||||||
| chr1:54830137 | T | C | 14 | a0001c0002t0002g0015 a0001c0002t0002g0020 a0001c0002t0002g0044 others(11): Show |
24 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.1185-11664T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54830137 | |||||||
| chr1:54830177 | T | C | 9 | a0001c0002t0002g0016 a0001c0002t0002g0027 a0001c0002t0002g0057 others(6): Show |
13 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1185-11624T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54830177 | |||||||
| chr1:54830249 | T | A | 16 | a0001c0002t0002g0015 a0001c0002t0002g0020 a0001c0002t0002g0044 others(13): Show |
26 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.1185-11552T>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54830249 | |||||||
| chr1:54830258 | T | C | 53 | a0001c0002t0002g0208 a0001c0002t0009g0200 a0001c0003t0003g0009 others(50): Show |
82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1185-11543T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54830258 | |||||||
| chr1:54830441 | C | G | 53 | a0001c0002t0002g0208 a0001c0002t0009g0200 a0001c0003t0003g0009 others(50): Show |
82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1185-11360C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54830441 | |||||||
| chr1:54830551 | G | T | 4 | a0001c0002t0002g0052 a0004c0008t0001g0051 a0004c0008t0001g0249 others(1): Show |
5 | HG01884.hp2 HG02622.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1185-11250G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54830551 | |||||||
| chr1:54830560 | T | C | 74 | a0001c0002t0001g0102 a0001c0002t0002g0014 a0001c0002t0002g0015 others(71): Show |
101 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1185-11241T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54830560 | |||||||
| chr1:54830591 | A | G | 127 | a0001c0002t0001g0102 a0001c0002t0002g0014 a0001c0002t0002g0015 others(124): Show |
183 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.1185-11210A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54830591 | |||||||
| chr1:54830663 | G | A | 16 | a0001c0002t0002g0015 a0001c0002t0002g0020 a0001c0002t0002g0044 others(13): Show |
26 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.1185-11138G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54830663 | |||||||
| chr1:54830752 | G | A | 1 | a0002c0010t0001g0122 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1185-11049G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54830752 | |||||||
| chr1:54830810 | A | C | 236 | a0001c0002t0001g0102 a0001c0002t0002g0005 a0001c0002t0002g0006 others(233): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.1185-10991A>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54830810 | |||||||
| chr1:54830837 | T | C | 3 | a0002c0001t0001g0017 a0002c0001t0001g0143 a0009c0019t0002g0065 |
6 | HG01884.hp1 HG02145.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1185-10964T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54830837 | |||||||
| chr1:54830943 | T | C | 1 | a0001c0002t0002g0027 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1185-10858T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54830943 | |||||||
| chr1:54831042 | G | A | 1 | a0004c0008t0001g0051 | 2 | HG01884.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1185-10759G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54831042 | |||||||
| chr1:54831132 | A | T | 4 | a0002c0010t0001g0029 a0002c0010t0001g0122 a0002c0010t0001g0123 others(1): Show |
5 | HG02451.hp2 HG02486.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1185-10669A>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54831132 | |||||||
| chr1:54831347 | A | C | 2 | a0001c0002t0002g0217 a0001c0002t0002g0220 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1185-10454A>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54831347 | |||||||
| chr1:54831363 | A | T | 1 | a0002c0001t0001g0087 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1185-10438A>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54831363 | |||||||
| chr1:54831426 | G | A | 1 | a0006c0013t0002g0030 | 2 | HG02451.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1185-10375G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54831426 | |||||||
| chr1:54831463 | G | A | 2 | a0001c0002t0001g0102 a0005c0007t0002g0061 |
2 | HG01167.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1185-10338G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54831463 | |||||||
| chr1:54831482 | G | A | 4 | a0002c0010t0001g0029 a0002c0010t0001g0122 a0002c0010t0001g0123 others(1): Show |
5 | HG02451.hp2 HG02486.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1185-10319G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54831482 | |||||||
| chr1:54831640 | C | T | 41 | a0001c0002t0001g0102 a0001c0002t0002g0103 a0001c0002t0002g0224 others(38): Show |
51 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.1185-10161C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54831640 | |||||||
| chr1:54831684 | A | G | 2 | a0001c0002t0002g0187 a0001c0002t0002g0188 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1185-10117A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54831684 | |||||||
| chr1:54831709 | C | T | 1 | a0001c0002t0002g0064 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1185-10092C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54831709 | |||||||
| chr1:54831939 | C | T | 2 | a0001c0002t0002g0043 a0001c0003t0003g0186 |
3 | HG01109.hp2 HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1185-9862C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54831939 | |||||||
| chr1:54831978 | C | G | 1 | a0001c0004t0003g0164 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1185-9823C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54831978 | |||||||
| chr1:54832005 | C | G | 41 | a0001c0002t0001g0102 a0001c0002t0002g0103 a0001c0002t0002g0224 others(38): Show |
51 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.1185-9796C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54832005 | |||||||
| chr1:54832037 | G | T | 2 | a0001c0002t0001g0102 a0005c0007t0002g0061 |
2 | HG01167.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1185-9764G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54832037 | |||||||
| chr1:54832126 | T | C | 4 | a0002c0010t0001g0029 a0002c0010t0001g0122 a0002c0010t0001g0123 others(1): Show |
5 | HG02451.hp2 HG02486.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1185-9675T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54832126 | |||||||
| chr1:54832311 | A | G | 97 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(94): Show |
160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.1185-9490A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54832311 | |||||||
| chr1:54832358 | TAGTTAAC others(1): Show |
T | 127 | a0001c0002t0001g0102 a0001c0002t0002g0014 a0001c0002t0002g0015 others(124): Show |
183 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.1185-9434_1185-942 others(12): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54832358 | ||||||
| chr1:54832375 | C | T | 1 | a0002c0001t0001g0147 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1185-9426C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54832375 | |||||||
| chr1:54832618 | C | T | 1 | a0001c0004t0003g0166 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1185-9183C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54832618 | |||||||
| chr1:54832634 | A | G | 1 | a0002c0001t0001g0086 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1185-9167A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54832634 | |||||||
| chr1:54832720 | G | T | 16 | a0003c0006t0001g0025 a0003c0006t0001g0237 a0003c0006t0001g0238 others(13): Show |
18 | HG02074.hp2 HG02165.hp1 NA18747.hp2 others(15): Show |
intron_variant | MODIFIER | c.1185-9081G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54832720 | |||||||
| chr1:54832822 | G | A | 1 | a0001c0003t0003g0204 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1185-8979G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54832822 | |||||||
| chr1:54832835 | C | T | 17 | a0001c0002t0002g0015 a0001c0002t0002g0020 a0001c0002t0002g0044 others(14): Show |
27 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.1185-8966C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54832835 | |||||||
| chr1:54832993 | C | T | 1 | a0004c0008t0006g0248 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1185-8808C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54832993 | |||||||
| chr1:54833016 | CA | C | 17 | a0001c0002t0002g0015 a0001c0002t0002g0020 a0001c0002t0002g0044 others(14): Show |
27 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.1185-8774delA | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54833016 | ||||||
| chr1:54833139 | A | T | 1 | a0001c0003t0003g0194 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1185-8662A>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54833139 | |||||||
| chr1:54833289 | C | T | 1 | a0001c0002t0002g0230 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1185-8512C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54833289 | |||||||
| chr1:54833332 | A | G | 53 | a0001c0002t0002g0208 a0001c0002t0009g0200 a0001c0003t0003g0009 others(50): Show |
82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1185-8469A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54833332 | |||||||
| chr1:54833466 | C | T | 74 | a0001c0002t0001g0102 a0001c0002t0002g0014 a0001c0002t0002g0015 others(71): Show |
101 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1185-8335C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54833466 | |||||||
| chr1:54833671 | T | C | 42 | a0001c0002t0001g0102 a0001c0002t0002g0103 a0001c0002t0002g0224 others(39): Show |
52 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.1185-8130T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54833671 | |||||||
| chr1:54833730 | C | T | 1 | a0001c0002t0002g0111 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1185-8071C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54833730 | |||||||
| chr1:54833796 | C | T | 74 | a0001c0002t0001g0102 a0001c0002t0002g0014 a0001c0002t0002g0015 others(71): Show |
101 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1185-8005C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54833796 | |||||||
| chr1:54833820 | T | C | 109 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(106): Show |
179 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.1185-7981T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54833820 | |||||||
| chr1:54833841 | CT | C | 53 | a0001c0002t0002g0208 a0001c0002t0009g0200 a0001c0003t0003g0009 others(50): Show |
82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1185-7950delT | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54833841 | ||||||
| chr1:54833851 | T | A | 1 | a0002c0001t0001g0143 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1185-7950T>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54833851 | |||||||
| chr1:54833913 | T | C | 1 | a0001c0002t0005g0062 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1185-7888T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54833913 | |||||||
| chr1:54833983 | G | A | 17 | a0001c0002t0002g0006 a0001c0002t0002g0007 a0001c0002t0002g0010 others(14): Show |
32 | HG00558.hp1 HG02080.hp1 HG03490.hp2 others(29): Show |
intron_variant | MODIFIER | c.1185-7818G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54833983 | |||||||
| chr1:54833987 | A | G | 1 | a0002c0001t0001g0155 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1185-7814A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54833987 | |||||||
| chr1:54834190 | A | T | 3 | a0002c0001t0001g0017 a0002c0001t0001g0143 a0009c0019t0002g0065 |
6 | HG01884.hp1 HG02145.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1185-7611A>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54834190 | |||||||
| chr1:54834674 | C | T | 1 | a0002c0001t0001g0149 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1185-7127C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54834674 | |||||||
| chr1:54834828 | G | A | 127 | a0001c0002t0001g0102 a0001c0002t0002g0014 a0001c0002t0002g0015 others(124): Show |
183 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.1185-6973G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54834828 | |||||||
| chr1:54834855 | G | A | 16 | a0003c0006t0001g0025 a0003c0006t0001g0237 a0003c0006t0001g0238 others(13): Show |
18 | HG02074.hp2 HG02165.hp1 NA18747.hp2 others(15): Show |
intron_variant | MODIFIER | c.1185-6946G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54834855 | |||||||
| chr1:54834869 | G | C | 1 | a0001c0002t0002g0059 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1185-6932G>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54834869 | |||||||
| chr1:54834881 | A | C | 127 | a0001c0002t0001g0102 a0001c0002t0002g0014 a0001c0002t0002g0015 others(124): Show |
183 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.1185-6920A>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54834881 | |||||||
| chr1:54834941 | A | G | 127 | a0001c0002t0001g0102 a0001c0002t0002g0014 a0001c0002t0002g0015 others(124): Show |
183 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.1185-6860A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54834941 | |||||||
| chr1:54835129 | G | A | 125 | a0001c0002t0001g0102 a0001c0002t0002g0014 a0001c0002t0002g0015 others(122): Show |
181 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.1185-6672G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54835129 | |||||||
| chr1:54835182 | GGTTT | G | 41 | a0001c0002t0001g0102 a0001c0002t0002g0103 a0001c0002t0002g0224 others(38): Show |
51 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.1185-6606_1185-660 others(8): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54835182 | ||||||
| chr1:54835259 | T | G | 202 | a0001c0002t0001g0102 a0001c0002t0002g0005 a0001c0002t0002g0006 others(199): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.1185-6542T>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54835259 | |||||||
| chr1:54835322 | GCTGGGAC others(4551): Show |
G | 2 | a0004c0008t0001g0249 a0004c0008t0001g0250 |
2 | HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1185-6461_1185-190 others(4): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54835322 | ||||||
| chr1:54835352 | T | C | 89 | a0001c0002t0001g0102 a0001c0002t0002g0014 a0001c0002t0002g0015 others(86): Show |
118 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.1185-6449T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54835352 | |||||||
| chr1:54835547 | T | C | 185 | a0001c0002t0001g0102 a0001c0002t0002g0005 a0001c0002t0002g0006 others(182): Show |
277 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.1185-6254T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54835547 | |||||||
| chr1:54835636 | T | C | 92 | a0001c0002t0001g0102 a0001c0002t0002g0014 a0001c0002t0002g0015 others(89): Show |
124 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.1185-6165T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54835636 | |||||||
| chr1:54835765 | C | T | 15 | a0001c0002t0002g0015 a0001c0002t0002g0020 a0001c0002t0002g0044 others(12): Show |
25 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.1185-6036C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54835765 | |||||||
| chr1:54835805 | A | G | 101 | a0001c0002t0001g0102 a0001c0002t0002g0014 a0001c0002t0002g0015 others(98): Show |
137 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.1185-5996A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54835805 | |||||||
| chr1:54835842 | A | G | 12 | a0001c0002t0001g0102 a0001c0002t0002g0224 a0001c0002t0002g0225 others(9): Show |
12 | HG00408.hp1 HG00423.hp2 HG00621.hp1 others(9): Show |
intron_variant | MODIFIER | c.1185-5959A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54835842 | |||||||
| chr1:54836011 | T | G | 172 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(169): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1185-5790T>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54836011 | |||||||
| chr1:54836067 | G | T | 2 | a0001c0002t0005g0214 a0004c0008t0006g0248 |
2 | HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1185-5734G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54836067 | |||||||
| chr1:54836262 | CTCCCGCC others(17): Show |
C | 1 | a0001c0004t0003g0161 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1185-5538_1185-551 others(28): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54836262 | |||||||
| chr1:54836263 | T | G | 154 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(151): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.1185-5538T>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54836263 | |||||||
| chr1:54836282 | CGCCTGCC others(17): Show |
C | 249 | a0001c0002t0001g0102 a0001c0002t0002g0005 a0001c0002t0002g0006 others(246): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1185-5494_1185-547 others(28): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54836282 | ||||||
| chr1:54836299 | G | A | 1 | a0001c0004t0003g0161 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1185-5502G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54836299 | |||||||
| chr1:54836306 | T | C | 1 | a0001c0004t0003g0161 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1185-5495T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54836306 | |||||||
| chr1:54836355 | C | T | 1 | a0002c0001t0001g0018 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1185-5446C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54836355 | |||||||
| chr1:54836407 | T | C | 4 | a0002c0010t0001g0029 a0002c0010t0001g0122 a0002c0010t0001g0123 others(1): Show |
5 | HG02451.hp2 HG02486.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1185-5394T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54836407 | |||||||
| chr1:54836596 | CAGA | C | 27 | a0001c0002t0002g0015 a0001c0002t0002g0020 a0001c0002t0002g0044 others(24): Show |
41 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(38): Show |
intron_variant | MODIFIER | c.1185-5202_1185-520 others(7): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54836596 | ||||||
| chr1:54836664 | C | T | 1 | a0002c0001t0001g0011 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1185-5137C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54836664 | |||||||
| chr1:54836716 | G | T | 57 | a0001c0002t0001g0102 a0001c0002t0002g0015 a0001c0002t0002g0020 others(54): Show |
81 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.1185-5085G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54836716 | |||||||
| chr1:54836784 | G | T | 1 | a0002c0001t0001g0003 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1185-5017G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54836784 | |||||||
| chr1:54836807 | G | A | 1 | a0002c0010t0001g0142 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1185-4994G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54836807 | |||||||
| chr1:54837024 | A | G | 155 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(152): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.1185-4777A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54837024 | |||||||
| chr1:54837046 | A | C | 155 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(152): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.1185-4755A>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54837046 | |||||||
| chr1:54837054 | T | A | 1 | a0002c0001t0001g0148 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1185-4747T>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54837054 | |||||||
| chr1:54837159 | C | T | 1 | a0001c0002t0002g0020 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1185-4642C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54837159 | |||||||
| chr1:54837206 | C | A | 1 | a0004c0008t0001g0233 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1185-4595C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54837206 | |||||||
| chr1:54837668 | G | T | 29 | a0001c0002t0002g0043 a0001c0009t0002g0168 a0002c0001t0001g0001 others(26): Show |
40 | HG00423.hp1 HG00438.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.1185-4133G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54837668 | |||||||
| chr1:54837766 | A | G | 155 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(152): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.1185-4035A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54837766 | |||||||
| chr1:54837790 | A | G | 250 | a0001c0002t0001g0102 a0001c0002t0002g0005 a0001c0002t0002g0006 others(247): Show |
378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.1185-4011A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54837790 | |||||||
| chr1:54837845 | C | G | 155 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(152): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.1185-3956C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54837845 | |||||||
| chr1:54837880 | G | T | 1 | a0001c0002t0002g0103 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1185-3921G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54837880 | |||||||
| chr1:54837908 | T | TA | 155 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(152): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.1185-3893_1185-389 others(5): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54837908 | |||||||
| chr1:54838073 | G | A | 1 | a0001c0002t0002g0015 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1185-3728G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54838073 | |||||||
| chr1:54838079 | A | T | 55 | a0001c0002t0002g0208 a0001c0002t0009g0200 a0001c0003t0003g0009 others(52): Show |
84 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.1185-3722A>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54838079 | |||||||
| chr1:54838109 | T | G | 155 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(152): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.1185-3692T>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54838109 | |||||||
| chr1:54838110 | A | G | 1 | a0001c0002t0002g0103 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1185-3691A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54838110 | |||||||
| chr1:54838126 | G | A | 1 | a0001c0002t0002g0114 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1185-3675G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54838126 | |||||||
| chr1:54838129 | A | G | 1 | a0001c0002t0002g0114 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1185-3672A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54838129 | |||||||
| chr1:54838280 | C | T | 15 | a0001c0002t0002g0015 a0001c0002t0002g0020 a0001c0002t0002g0044 others(12): Show |
25 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.1185-3521C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54838280 | |||||||
| chr1:54838317 | T | C | 2 | a0001c0002t0005g0214 a0004c0008t0006g0248 |
2 | HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1185-3484T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54838317 | |||||||
| chr1:54838345 | C | T | 1 | a0002c0001t0001g0011 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1185-3456C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54838345 | |||||||
| chr1:54838347 | G | A | 155 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(152): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.1185-3454G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54838347 | |||||||
| chr1:54838360 | G | A | 20 | a0001c0002t0002g0014 a0001c0002t0002g0048 a0001c0002t0002g0052 others(17): Show |
27 | HG02074.hp2 HG02165.hp1 HG02622.hp1 others(24): Show |
intron_variant | MODIFIER | c.1185-3441G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54838360 | |||||||
| chr1:54838361 | T | C | 1 | a0002c0001t0001g0155 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1185-3440T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54838361 | |||||||
| chr1:54838375 | T | C | 246 | a0001c0002t0001g0102 a0001c0002t0002g0005 a0001c0002t0002g0006 others(243): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.1185-3426T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54838375 | |||||||
| chr1:54838376 | G | C | 1 | a0005c0007t0002g0211 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1185-3425G>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54838376 | |||||||
| chr1:54838485 | T | A | 1 | a0001c0002t0002g0114 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1185-3316T>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54838485 | |||||||
| chr1:54838485 | T | TA | 158 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(155): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.1185-3305dupA | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54838485 | ||||||
| chr1:54838495 | A | T | 42 | a0001c0002t0001g0102 a0001c0002t0002g0101 a0001c0002t0002g0103 others(39): Show |
56 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.1185-3306A>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54838495 | |||||||
| chr1:54838659 | A | G | 1 | a0001c0002t0002g0052 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1185-3142A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54838659 | |||||||
| chr1:54838682 | A | T | 1 | a0002c0001t0001g0124 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1185-3119A>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54838682 | |||||||
| chr1:54838740 | T | C | 28 | a0001c0003t0003g0019 a0001c0003t0003g0204 a0001c0003t0003g0205 others(25): Show |
38 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.1185-3061T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54838740 | |||||||
| chr1:54838785 | C | T | 1 | a0001c0002t0002g0103 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1185-3016C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54838785 | |||||||
| chr1:54838935 | T | TG | 155 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(152): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.1185-2860dupG | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54838935 | ||||||
| chr1:54839010 | A | G | 155 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(152): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.1185-2791A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54839010 | |||||||
| chr1:54839050 | C | T | 14 | a0001c0002t0001g0102 a0001c0002t0002g0101 a0001c0002t0002g0103 others(11): Show |
18 | HG00408.hp1 HG00423.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.1185-2751C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54839050 | |||||||
| chr1:54839051 | G | A | 4 | a0002c0010t0001g0029 a0002c0010t0001g0122 a0002c0010t0001g0123 others(1): Show |
5 | HG02451.hp2 HG02486.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1185-2750G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54839051 | |||||||
| chr1:54839130 | GA | G | 155 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(152): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.1185-2663delA | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54839130 | ||||||
| chr1:54839163 | C | T | 9 | a0001c0002t0002g0016 a0001c0002t0002g0027 a0001c0002t0002g0057 others(6): Show |
13 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1185-2638C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54839163 | |||||||
| chr1:54839297 | G | A | 100 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(97): Show |
163 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.1185-2504G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54839297 | |||||||
| chr1:54839362 | A | T | 154 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(151): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.1185-2439A>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54839362 | |||||||
| chr1:54839386 | A | T | 155 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(152): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.1185-2415A>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54839386 | |||||||
| chr1:54839397 | C | CAG | 250 | a0001c0002t0001g0102 a0001c0002t0002g0005 a0001c0002t0002g0006 others(247): Show |
378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.1185-2403_1185-240 others(6): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54839397 | ||||||
| chr1:54839412 | C | G | 155 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(152): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.1185-2389C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54839412 | |||||||
| chr1:54839495 | A | C | 1 | a0002c0001t0001g0100 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1185-2306A>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54839495 | |||||||
| chr1:54839522 | C | T | 2 | a0001c0003t0003g0186 a0002c0005t0004g0032 |
2 | HG01109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1185-2279C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54839522 | |||||||
| chr1:54839534 | C | T | 1 | a0001c0003t0003g0193 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1185-2267C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54839534 | |||||||
| chr1:54839540 | A | G | 155 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(152): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.1185-2261A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54839540 | |||||||
| chr1:54839557 | T | C | 15 | a0001c0002t0002g0015 a0001c0002t0002g0020 a0001c0002t0002g0044 others(12): Show |
25 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.1185-2244T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54839557 | |||||||
| chr1:54839585 | C | T | 8 | a0001c0004t0003g0037 a0001c0004t0003g0054 a0001c0004t0003g0157 others(5): Show |
9 | HG00438.hp2 HG00609.hp2 NA18952.hp1 others(6): Show |
intron_variant | MODIFIER | c.1185-2216C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54839585 | |||||||
| chr1:54839850 | G | A | 100 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(97): Show |
163 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.1185-1951G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54839850 | |||||||
| chr1:54839858 | C | T | 4 | a0001c0003t0003g0186 a0002c0005t0004g0022 a0002c0005t0004g0032 others(1): Show |
7 | HG01109.hp2 HG01243.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-1943C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54839858 | |||||||
| chr1:54839893 | G | A | 100 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(97): Show |
163 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.1185-1908G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54839893 | |||||||
| chr1:54839940 | T | C | 1 | a0010c0016t0001g0167 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1185-1861T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54839940 | |||||||
| chr1:54840058 | T | G | 155 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(152): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.1185-1743T>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54840058 | |||||||
| chr1:54840094 | A | C | 155 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(152): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.1185-1707A>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54840094 | |||||||
| chr1:54840141 | TAGTC | T | 21 | a0001c0009t0002g0168 a0002c0001t0001g0021 a0002c0001t0001g0034 others(18): Show |
27 | HG00423.hp1 HG00438.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.1185-1655_1185-165 others(8): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54840141 | ||||||
| chr1:54840182 | C | T | 1 | a0002c0011t0004g0033 | 2 | HG02040.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1185-1619C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54840182 | |||||||
| chr1:54840208 | G | C | 55 | a0001c0002t0002g0208 a0001c0002t0009g0200 a0001c0003t0003g0009 others(52): Show |
84 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.1185-1593G>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54840208 | |||||||
| chr1:54840394 | C | T | 1 | a0001c0002t0002g0232 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1185-1407C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54840394 | |||||||
| chr1:54840718 | T | A | 12 | a0001c0002t0001g0102 a0001c0002t0002g0052 a0001c0002t0002g0101 others(9): Show |
16 | HG01167.hp1 HG01884.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1185-1083T>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54840718 | |||||||
| chr1:54840728 | A | G | 1 | a0001c0002t0002g0219 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1185-1073A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54840728 | |||||||
| chr1:54840756 | A | C | 156 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(153): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.1185-1045A>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54840756 | |||||||
| chr1:54840759 | C | G | 1 | a0001c0002t0002g0226 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1185-1042C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54840759 | |||||||
| chr1:54840828 | T | A | 1 | a0002c0001t0001g0144 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1185-973T>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54840828 | |||||||
| chr1:54840945 | G | A | 192 | a0001c0002t0001g0102 a0001c0002t0002g0005 a0001c0002t0002g0006 others(189): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.1185-856G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54840945 | |||||||
| chr1:54840963 | C | G | 1 | a0001c0002t0002g0114 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1185-838C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54840963 | |||||||
| chr1:54840964 | G | C | 1 | a0001c0002t0002g0114 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1185-837G>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54840964 | |||||||
| chr1:54840970 | AGAGACAG others(4): Show |
A | 1 | a0003c0006t0001g0246 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-829_1185-819d others(13): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54840970 | ||||||
| chr1:54840982 | G | T | 1 | a0003c0006t0001g0246 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-819G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54840982 | |||||||
| chr1:54840985 | G | C | 1 | a0003c0006t0001g0246 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-816G>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54840985 | |||||||
| chr1:54840986 | C | T | 1 | a0003c0006t0001g0246 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-815C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54840986 | |||||||
| chr1:54840992 | T | C | 1 | a0003c0006t0001g0246 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-809T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54840992 | |||||||
| chr1:54840994 | G | A | 1 | a0003c0006t0001g0246 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-807G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54840994 | |||||||
| chr1:54840995 | T | C | 1 | a0003c0006t0001g0246 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-806T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54840995 | |||||||
| chr1:54840997 | G | A | 1 | a0003c0006t0001g0246 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-804G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54840997 | |||||||
| chr1:54840998 | A | C | 1 | a0003c0006t0001g0246 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-803A>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54840998 | |||||||
| chr1:54841001 | T | C | 1 | a0003c0006t0001g0246 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-800T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841001 | |||||||
| chr1:54841008 | T | A | 1 | a0003c0006t0001g0246 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-793T>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841008 | |||||||
| chr1:54841012 | G | A | 1 | a0003c0006t0001g0246 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-789G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841012 | |||||||
| chr1:54841013 | C | G | 1 | a0003c0006t0001g0246 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-788C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841013 | |||||||
| chr1:54841015 | T | G | 1 | a0003c0006t0001g0246 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-786T>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841015 | |||||||
| chr1:54841016 | G | A | 1 | a0003c0006t0001g0246 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-785G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841016 | |||||||
| chr1:54841017 | G | T | 1 | a0003c0006t0001g0246 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-784G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841017 | |||||||
| chr1:54841018 | G | C | 1 | a0003c0006t0001g0246 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-783G>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841018 | |||||||
| chr1:54841019 | G | T | 1 | a0003c0006t0001g0246 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-782G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841019 | |||||||
| chr1:54841022 | G | C | 1 | a0003c0006t0001g0246 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-779G>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841022 | |||||||
| chr1:54841030 | G | A | 1 | a0003c0006t0001g0246 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-771G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841030 | |||||||
| chr1:54841032 | C | G | 1 | a0003c0006t0001g0246 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-769C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841032 | |||||||
| chr1:54841033 | C | A | 1 | a0003c0006t0001g0246 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-768C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841033 | |||||||
| chr1:54841035 | T | G | 1 | a0003c0006t0001g0246 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-766T>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841035 | |||||||
| chr1:54841036 | G | A | 1 | a0003c0006t0001g0246 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-765G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841036 | |||||||
| chr1:54841038 | G | A | 1 | a0003c0006t0001g0246 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-763G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841038 | |||||||
| chr1:54841039 | C | G | 1 | a0003c0006t0001g0246 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-762C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841039 | |||||||
| chr1:54841041 | T | G | 1 | a0003c0006t0001g0246 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-760T>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841041 | |||||||
| chr1:54841043 | G | A | 1 | a0003c0006t0001g0246 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-758G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841043 | |||||||
| chr1:54841060 | A | G | 62 | a0001c0002t0002g0107 a0001c0002t0002g0112 a0001c0002t0002g0208 others(59): Show |
91 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.1185-741A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841060 | |||||||
| chr1:54841066 | T | C | 88 | a0001c0002t0002g0107 a0001c0002t0002g0112 a0001c0002t0002g0208 others(85): Show |
127 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.1185-735T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841066 | |||||||
| chr1:54841085 | G | A | 21 | a0001c0002t0002g0015 a0001c0002t0002g0020 a0001c0002t0002g0044 others(18): Show |
30 | HG00280.hp2 HG00741.hp1 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.1185-716G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841085 | |||||||
| chr1:54841261 | C | T | 3 | a0001c0002t0002g0063 a0001c0002t0002g0064 a0004c0008t0001g0233 |
3 | HG01891.hp2 NA19078.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1185-540C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841261 | |||||||
| chr1:54841344 | G | A | 1 | a0001c0003t0003g0205 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1185-457G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841344 | |||||||
| chr1:54841345 | A | G | 1 | a0001c0003t0003g0205 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1185-456A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841345 | |||||||
| chr1:54841352 | G | A | 1 | a0001c0003t0003g0209 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1185-449G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841352 | |||||||
| chr1:54841368 | C | T | 1 | a0001c0004t0003g0163 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1185-433C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841368 | |||||||
| chr1:54841382 | T | G | 2 | a0001c0002t0002g0069 a0001c0002t0002g0216 |
2 | HG02109.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1185-419T>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841382 | |||||||
| chr1:54841386 | A | C | 7 | a0001c0002t0005g0062 a0001c0002t0005g0214 a0002c0010t0001g0029 others(4): Show |
8 | HG02257.hp1 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1185-415A>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841386 | |||||||
| chr1:54841387 | G | A | 4 | a0002c0010t0001g0029 a0002c0010t0001g0122 a0002c0010t0001g0123 others(1): Show |
5 | HG02451.hp2 HG02486.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1185-414G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841387 | |||||||
| chr1:54841409 | G | A | 3 | a0001c0002t0002g0052 a0004c0008t0001g0249 a0004c0008t0001g0250 |
3 | HG02622.hp1 HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1185-392G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841409 | |||||||
| chr1:54841480 | G | A | 1 | a0001c0002t0005g0062 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1185-321G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841480 | |||||||
| chr1:54841659 | G | T | 16 | a0001c0002t0002g0208 a0003c0006t0001g0025 a0003c0006t0001g0237 others(13): Show |
18 | HG02074.hp2 HG02165.hp1 NA18747.hp2 others(15): Show |
intron_variant | MODIFIER | c.1185-142G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841659 | |||||||
| chr1:54841784 | T | C | 1 | a0002c0001t0001g0128 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1185-17T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841784 |